Method to produce catalytically active nanocomposite coatings

Abstract

A nanocomposite coating and method of making and using the coating. The nanocomposite coating is disposed on a base material, such as a metal or ceramic; and the nanocomposite consists essentially of a matrix of an alloy selected from the group of Cu, Ni, Pd, Pt and Re which are catalytically active for cracking of carbon bonds in oils and greases and a grain structure selected from the group of borides, carbides and nitrides.

Claims

1. A method for lubricating materials in wear contact, comprising the steps of: providing a base material; disposing a nanocomposite coating on the base material, the nanocomposite consisting essentially of a microstructural matrix of a catalytically active alloy with grains embedded in the microstructural, the microstructural matrix selected from the group of Cu, Ni, Pd, Pt and Re and mixtures thereof and the grains selected from the group of transition metal carbides, transition metal nitrides, transition metal carbo-nitrides, transition metal borides, refractory metal carbides, refractory metal nitrides, refractory metal carbo-nitrides, refractory metal borides disposing an oil on the nanocomposite coating; engaging the nanocomposite coating with a surface, the oil disposed therebetween; cracking carbon bonds of the oil; forming a carbon film disposed between the coating and the surface, thereby lubricating the nanocomposite coating.

2. The method as defined in claim 1 wherein the alloy is about 1% to 10% by weight and the grains from about 90% to 99% by weight.

3. The method as defined in claim 1 wherein the base material is selected from the group of a metal and a ceramic.

4. The method as defined in claim 1 wherein the base material comprises a steel based material.

5. The method as defined in claim 1 wherein the oil is essentially free of additives.

6. The method as defined in claim 1 where the carbon film consists essentially of diamond like carbon.

7. The method as defined in claim 1 where the grains are selected from the group of refractory metal carbides, carbo-nitrides, nitrides and borides.

8. A method for lubricating materials in wear contact, comprising the steps of: providing a base material; disposing a nanocomposite coating on the base material, the nanocomposite consisting essentially of about 1% to 10% by weight a microstructural matrix of a catalytically active alloy with about 90% to 99% by weight grains embedded in therein, the microstructural matrix selected from the group of Cu, Ni, Pd, Pt and Re and mixtures thereof and the grains selected from the group of transition metal carbides, transition metal nitrides, transition metal carbo-nitrides, transition metal borides, refractory metal carbides, refractory metal nitrides, refractory metal carbo-nitrides, refractory metal borides; disposing a hydrocarbon on the nanocomposite coating; engaging the nanocomposite coating with a surface, the hydrocarbon disposed therebetween; forming a carbon film disposed between the coating and the surface, thereby lubricating the nanocomposite coating.

9. The method as defined in claim 8 wherein the base material is selected from the group of a metal and a ceramic.

10. The method as defined in claim 8 wherein the base material comprises a steel based material.

11. The method as defined in claim 8 wherein the hydrocarbon is an oil.

12. The method as defined in claim 8 where the carbon film consists essentially of diamond like carbon.

13. The method as defined in claim 8 where the grains are selected from the group of refractory metal carbides, carbo-nitrides, nitrides and borides.

14. A method for lubricating materials in wear contact, comprising the steps of: providing a base material; disposing a nanocomposite coating on the base material, the nanocomposite consisting essentially of a microstructural matrix of a catalytically active alloy with grains embedded in the microstructural, the microstructural matrix selected from the group of Cu, Ni, Pd, Pt and Re and mixtures thereof and the grains selected from the group of transition metal carbides, transition metal nitrides, transition metal carbo-nitrides, transition metal borides, refractory metal carbides, refractory metal nitrides, refractory metal carbo-nitrides, refractory metal borides disposing a hydrocarbon on the nanocomposite coating; engaging the nanocomposite coating with a surface, the hydrocarbon disposed therebetween; forming a carbon film disposed between the coating and the surface, thereby lubricating the nanocomposite coating.

15. The method as defined in claim 14 wherein the alloy is about 1% to 10% by weight and the grains from about 90% to 99% by weight.

16. The method as defined in claim 14 wherein the base material is selected from the group of a metal and a ceramic.

17. The method as defined in claim 14 wherein the base material comprises a steel based material.

18. The method as defined in claim 14 where the carbon film consists essentially of diamond like carbon.

19. The method as defined in claim 14 where the grains are selected from the group of refractory metal carbides, carbo-nitrides, nitrides and borides.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 illustrates scuffing performance of a steel/steel test pair in synthetic PAO oil and also on insert micrograph of the wear area B60315B—Scuffing Steel vs steel PAO10;

(2) FIG. 2 illustrates scuffing performance of a 0.5% ZDDP/PAO-10 synthetic oil mixture (B60317A Scuffing2 C60314 Low SHC vs Low SHC PAO10);

(3) FIG. 3A illustrates scuffing performance of a steel/steel test pair in fully formulated Mobil 1 oil (090202C Mobil 1 5w40 H60 fs 10 1000 rpm); FIG. 3B illustrates a schematic of the test pair; and FIG. 3C shows the mechanical scuffing on the block side;

(4) FIG. 4 illustrates scuffing performance of a coating of an embodiment of the invention on a steel/steel test pair with pure PAO oil (B60317A Scuffing2 C60314 Low SHC vs Low SHC PAO100;

(5) FIG. 5A is a schematic illustration of a preferred form of a nanocomposite microstructure with MoN grains and grain boundaries of catalytically active metal alloys of the invention; FIG. 5B(1) shows an SEM micrograph of a nanocomposite layer (“NL”); FIG. 5B(2) shows a schematic of the typical columnar growth of such layers; FIG. 5B(3) shows the nanocomposite layer deposited on a base layer (“BL”); FIG. 5B(4) shows a layer magnification view of 5B(3) and FIG. 5B(5) shows yet a layer magnification of 5B(3); FIG. 5C(1) shows a high magnification view of the BL portion after acid etching; FIG. 5C(2) shows yet another high magnification view of the BL and NL portions; and FIG. 5C(3) shows a transmission electron microscope view of the nanocomposition layer at high magnification;

(6) FIG. 6A illustrates a block on ring wear scuff test system with a black, shiny carbon based film on the surface undergoing wear testing; FIG. 6B illustrates a schematic of the test system; and FIG. 6C illustrates a layer of lubricant derived carbon film on the test block;

(7) FIG. 7 illustrates a lubricant derived carbon based film formed on the ball and disk sides of a steel test pair having a catalytically active coating (C60314 Low SHC Flat vs C60314 Low SHC Ball (9.5 mm Rad) Pure PAO 10, 20 N load, 50 rpm, 38 mm track diameter CS60328A—Starved Condition);

(8) FIG. 8 illustrates Raman spectra of a carbon film (labeled curve 4) formed on a wear track of a disk coated with catalytically active coatings tested in pure PAO-10 base oil and also shown are comparison spectra of diamond (1), graphite (1725-1) labeled curve (2), LDC film B60316 low SHC PAO10 in WT test, an LDC film (8), an LDC film (29) and an LDC film (30);

(9) FIG. 9 shows further comparison Raman spectra for diamond (2), LDC film (4) C90204 N3 FC20 M2 steel test, LDC film (6) C81120 N3FC12 M2 steel test, graphite (1), LDC film (7) C81119 N3FC26 M2 steel test and LDC film (5) P60411 NFC6 440C steel; and

(10) FIG. 10A shows a TEM micrograph of LDC film particles, FIG. 10B shows the raw diffraction pattern from the LDC film and FIG. 10C shows an EELS spectrum of the LDC film.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

(11) The invention is directed to methods of preparation of catalytically active nanocomposite coatings. Rather than add lubricant additives, which have substantial deleterious effects, the method of the invention concerns depositing of catalytically active metal based films on engine or machine parts which are in contact and moving while in contact. Various catalytically active coatings are therefore deposited by any one of various conventional deposition methodologies, such as, PVD, CVD and ALD. Such selected hard/soft-phase nanocomposite coatings enable substantial improvement of scuff and wear resistance for engine or machinery with sliding contact.

(12) In FIG. 1 is shown the scuffing performance of a steel on steel test pair in a conventional pure synthetic oil (PAO). As can be seen from the data, the steel/steel pair undergoes substantial, rapid scuffing at a load of 400 Newtons “(N)”. In FIG. 2, it can be seen that the addition of a conventional additive, 0.5% ZDDP-containing PAO oil, causes the scuffing behavior to improve dramatically. In FIG. 3 is shown data for fully formulated engine oil, such as Mobil 1; and the scuffing load is increased to about 1400 N. Such an oil is fully formulated with several oil additives, including ZDDP and MoTDC. This can be compared to the performance in FIG. 1 showing a substantial improvement thereover.

(13) In order to overcome the disadvantages of such additives, the engine or machine components can be coated at selected friction points, to provide a film which is a nanocomposite of catalytically active ingredients, generally including one or more of Cu, Ni, Pd, Pt and Re as a matrix and grains of a transition or refractory metal nitride, carbide, carbo-nitrides and borides. As shown in FIG. 4, a nanocomposite coating of formulation MoN—Cu (with 2 wt. % Cu) results in greatly improved scuffing performance even compared to Mobil 1, generally acknowledged as the best engine oil available. As shown in FIG. 5, the coating has a preferred microstructure with nano-sized grains, such as, for example, a molybdenum nitride phase with grain boundaries of the catalytically active metal phase, such as, Cu, Ni, Pd, Pt, and Re, and alloy combinations thereof. The weight percentages of the most preferred nanocomposite includes about 1-10% by weight for the matrix and 90-99% by weight the nano-sized grains. Tests performed on various nanocomposites also determined that the alloy composition must be adjusted to compositions which achieve a threshold catalytic activity which enables cracking of the carbon chain in the oil used to create the diamond-like carbon material at the wear interface.

(14) In order to evaluate the nature of the coating, tests were performed on a metal test component as shown in FIG. 6. Tests were performed on rubbing surfaces on a block side of a steel test pair which provided the performance data of FIG. 4. The surfaces of the sliding test pair exhibited a shiny film. Likewise, such a shiny film was formed in the test system of a sliding surface of a ball and disk shown in FIG. 7 in which pure PAO-10 oil was the lubricant used. The shiny film was examined using Raman spectroscopy, and the Raman features of FIG. 8 are quite similar to that of a diamond-like carbon film.

(15) In FIG. 8, B60316 is an internal experiment number for reference purposes only. Low SHC is the coating tested. It is made out of Mo—N—Cu produced by the PVD method. The numbers 8, 29 and 30 in the figures are for Raman spectrum taken from the black area after a block on ring tribology test, showing that the test produces Diamond Like Carbon species on the tested surfaces.

(16) FIG. 9 shows a further comparison of the Raman spectra for crystalline diamond (1), crystalline graphite (1), a conventional graphite; LDC film (4) on test system C90204 N3 FC20 M2 steel; LDC film (6) C81120 N3 FC12 M2 steel; LDC film (7) C81119 N3 FC26 M2 steel; and LDC film (5) P60411 NF C6 440C steel. C90204, C81120, C81119, P60411 and P60411 are internal experimental numbers; and are also reference numbers used to track those coatings in our system. N3FC20, N3FC12 and N3FC26 are hydrogenated Diamond Like Carbon Coatings produced by reactive PVD method. The higher the number (e.g. 12, 20, 26) the higher the CH.sub.4 gas flow during the deposition; or the higher the number, the higher the hydrogen content in the LDC film. P60411 is also an internal experiment number. NFC6 also is a Diamond Like Carbon (here LDC layers as described before) coating produced by Plasma Assisted Chemical Vapor Deposition (PA-CVD). All above LDC films are made out of carbon and hydrogen only. M2 steel and 440C steel are well-known steels for the substrate materials.

(17) Diamond and graphite (graphite reference is for a disordered graphite in FIGS. 8 and 9) are used as a Raman reference in the graphs.

(18) FIG. 10A shows transmission electron microscopy of on LDC film; FIG. 10B shows an electron diffraction pattern of FIG. 10A; and FIG. 10C shows electron energy loss spectrum for FIG. 10A all of which illustrate the DLC character of the product lubricating media produced by use of the nanocomposite in contact with an oil during wear tests. The following non-limiting Example illustrates one method of preparation.

EXAMPLE

(19) This is an example of preparation of a nanocomposite coating of Mo—N—Cu done by Magnetron sputtering.

(20) Process-ID: xxx

(21) Cathode 2: Mo

(22) Cathode 1: Mo—Cu (20% at. Cu)

(23) TABLE-US-00001 Remaining Time (seconds) Main Sub Parameters Heating 25200 Heating_Startpress.[mPa]6 Roughpump1 Tablespeed[%]15 Turbo1speed[%]100 Heater[W]8000 Press.lim.1[mPa]6 Press.lim.2[mPa]6 Testinterval[s]5400 20400 Heater[W]Heater[W]2500 20400 Turbo1speed[%]Turbo1speed[%]66 Etching 19800 Etching_Argon[mln]200 Turbo1speed[%]66 Tablespeed[%]30 19790 MF-tableControlmode7 Setpoint550 Frequency[kHz]240 Rev.time[ns]1600 Coating 16200 Coating_Argon[mln]150 N2[mln]0 Heater[W]0 Tablespeed[%]30 Turbo1speed[%]66 16190 DC-tableControlmode7 (Voltage) Setpoint 200 V 16190 DCcathode2[W]DCcathode2[W]2500 16180 Rampcath .2Startvalue[W]2500 Endvalue[W]8000 Stepwidth[W]250 Int.val.time[sec]20 15680 DCcathode1[W]DCcathode1[W]500 15670 Rampcath.1Startvalue[W]500 Endvalue[W]4000 Stepwidth[W]100 Int.val.time[sec]15 15070 DC-tableControlmode7 (Voltage) Setpoint 100 V 15070 N2Startvalue[mln]150 15060 Nitrogen control Set press[mPa] 600 Cooling 1800 Cooling_Vent.temp.[° C.]145

(24) The foregoing description of embodiments of the present invention have been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the present invention to the precise form disclosed, and modifications and variations are possible in light of the above teachings or may be acquired from practice of the present invention. The embodiments were chosen and described in order to explain the principles of the present invention and its practical application to enable one skilled in the art to utilize the present invention in various embodiments, and with various modifications, as are suited to the particular use contemplated.