MOS2- or WS2-filled hollow ZnS hexagonal nanotubes as core-shell structured solid lubricants and lubricant modifiers for space mechanisms

Abstract

A process for making solid lubricants or lubricant additives or lubricant modifiers may include synthesizing two-dimensional (2D) nanoplatelets, nanorods, or nanowires of MoO.sub.3 and WO.sub.3. The process may also include creating hollow hexagonal ZnO nanotubes by refluxing a mixture of zinc nitrate and urea at a predefined temperature or a range of temperatures for a predefined period or periods of time. The process may further include growing the hollow hexagonal ZnO nanotubes around platelets, nanorods, or nanowires of the MoO.sub.3 or WO.sub.3. The process may also include creating a solid lubricant in a core-shell configuration from the hollow hexagonal ZnS nanotubes with an embedded hexagonal core of MoS.sub.2 or WS.sub.2.

Claims

1. A process for producing solid lubricants, comprising: synthesizing three-dimensional (3D) nanoplatelets, nanorods, or nanowires of MoO.sub.3 and WO.sub.3; creating hollow hexagonal ZnO nanotubes by refluxing a mixture of zinc nitrate and urea at a predefined temperature or a range of temperatures for a predefined period or periods of time; growing the hollow hexagonal ZnO nanotubes around platelets, nanorods, or nanowires of the MoO.sub.3 or WO.sub.3; and sulfidation of the hexagonal ZnO nanotubes, and the platelets, nanorods, or nanowires of the MoO.sub.3 or WO.sub.3, creating a solid lubricant in a core-shell configuration from the hollow hexagonal ZnS nanotubes with an embedded hexagonal core of MoS.sub.2 or WS.sub.2.

2. The process of claim 1, wherein the creating of the hollow hexagonal ZnO nanotubes comprises: dissolving urea in deionized water to make urea solution.

3. The process of claim 2, wherein the creating of the hollow hexagonal ZnO nanotubes comprises: heating the urea solution to near boiling point, such that the urea solution begins to reflux.

4. The process of claim 3, wherein the creating of the hollow hexagonal ZnO nanotubes comprises: adding a zinc nitrate solution to the refluxing urea solution and boiling a mixture of the zinc nitrate solution and the refluxed urea solution for a predefined period of time.

5. The process of claim 4, wherein the creating of the hollow hexagonal ZnO nanotubes comprises: rapidly cooling the mixture resulting from the boiling, and collecting a precipitate from the resulting mixture by a centrifuge and drying the precipitate.

6. The process of claim 1, wherein the growing of the hollow hexagonal ZnO nanotubes around platelets, nanorods, or nanowires of the MoO.sub.3 or WO.sub.3 comprises: dissolving urea in deionized water to make urea solution.

7. The process of claim 6, wherein the growing of the hollow hexagonal ZnO nanotubes around platelets, nanorods, or nanowires of the MoO.sub.3 or WO.sub.3 comprises: adding platelets or nanorods of MoO.sub.3 or nanobundles or nanoplates of WO.sub.3 to the urea solution being refluxed for a predefined period of time.

8. The process of claim 7, wherein the growing of the hollow hexagonal ZnO nanotubes around platelets, nanorods, or nanowires of the MoO.sub.3 or WO.sub.3 comprises: adding zinc nitrate solution to the refluxing urea solution and boiling a mixture of the zinc nitrate solution and the refluxing urea solution for a predefined period of time.

9. The process of claim 8, wherein the growing of the hollow hexagonal ZnO nanotubes around platelets, nanorods, or nanowires of the MoO.sub.3 or WO.sub.3 comprises: rapidly cooling the mixture resulting from the boiling, and collecting a precipitate from the resulting mixture by a centrifuge and drying the precipitate.

10. The process of claim 1, wherein the creating of the solid lubricant in a core-shell configuration comprises: placing the core-shell configuration in a porcelain or ceramic boat wrapped in a perforated aluminum foil.

11. The process of claim 10, wherein the creating of the solid lubricant in a core-shell configuration comprises: heating the porcelain or ceramic boat in a horizontal furnace for a predefined period of time and at a predefined temperature.

12. The process of claim 11, wherein the heating of the porcelain or ceramic boat further comprises: replacing the remnant air with inert non-reacting ambient air prior to sulfidation by controlling the flow rate of N.sub.2 within the horizontal furnace to expel remnant air from inside of the horizontal furnace.

13. The process of claim 12, wherein the heating of the porcelain or ceramic boat further comprises: increasing temperature of the horizontal furnace to a predefined temperature and holding the temperature constant for a predefined period of time to ensure completion of the sulfidation.

14. The process of claim 13, wherein the heating of the porcelain or ceramic boat further comprises: extracting a sample from the boat after the sulfidation is complete.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) In order that the advantages of certain embodiments of the invention will be readily understood to those skilled in the art, a more particular description of the invention briefly described above will be rendered by reference to specific embodiments that are illustrated in the appended drawings. While it should be understood that these drawings depict only typical embodiments of the invention and are not therefore to be considered to be limiting of its scope, the invention will be described and explained with additional specificity and detail through the use of the accompanying drawings, in which:

(2) FIG. 1 is a flow diagram illustrating a process for creating solid lubricants for space mechanisms, according to an embodiment of the present invention.

(3) FIGS. 2A-C are SEM images of hollow hexagonal nanotubes of ZnO made by refluxing a mixture of zinc nitrate and urea at 110 C. for 35 min., according to an embodiment of the present invention.

(4) FIGS. 3A-B are illustrative schematics of a composite of hollow ZnO nanotubes and, MoO.sub.3 or WO.sub.3 nanorods/nanoplatelets/nanowires in a core-shell configuration, according to an embodiment of the present invention.

(5) FIGS. 4A-B are illustrative schematics of an anticipated composite of a hexagonal ZnS shell around hexagonal MoS.sub.2 or WS.sub.2 core structure of a solid lubricant, according to an embodiment of the present invention.

DETAILED DESCRIPTION OF THE EMBODIMENTS

(6) Certain solids such as zinc sulfide (ZnS), or transition metal chalcogenides, such as molybdenum disulfide (MoS.sub.2), and tungsten disulfide (WS.sub.2), along with Teflon and graphite flakes, are excellent lubricants with exceptionally low friction coefficient. Further, these lubricants are increasingly used to minimize the maintenance costs. The low friction coefficient of these lubricants is due to low interplanar shear strength, and in some cases, low hardness.

(7) The lubricating behavior of transition metal chalcogenides, such as ZnS, MoS.sub.2 and WS.sub.2, stems from their interlayer mechanical weakness that is intrinsic to their sheet-like two-dimensional (2D) crystal structure. Interestingly, the three lubricant sulfides described herein are isostructural. The wurtzite form of ZnS has a hexagonal unit cell with a=3.25 and c=5.2 (c/a ratio1.60, close to the ideal c/a=1.633 value for hexagonal cell). MoS.sub.2 and WS.sub.2 also crystallize in hexagonal structure where a sheet of Mo (or W) atoms is sandwiched between every two layers of hexagonally packed sulfur atoms (S-M-S . . . S-M-S . . . S-M-S S-M-S) with a high c/a ratio (a=3.16 , c=12.29 for MoS.sub.2 and a=3.16 , c=18.50 for WS.sub.2). The relative value of their respective a parameter (slightly higher in the case of ZnS than that of MoS.sub.2 and WS.sub.2) indicates that both MoS.sub.2 and WS.sub.2 could be easily accommodated within ZnS, if the latter could be produced in a hollow hexagonal motif. Such a core-shell configuration could augment interlamellar shearing, leading to better interplanar slip in the composite.

(8) Some embodiments generally pertain to developing chalcogenide nanocomposites under mild and benign experimental conditions from simple and readily available chemicals, without resorting to the use of exotic, pricey and bulky precursors.

(9) FIG. 1 is a flow diagram illustrating a process 100 for creating solid lubricants for space mechanisms, according to an embodiment of the present invention. In some embodiments, the process begins at 102 with the synthesis of two-dimensional (2D) MoO.sub.3 and WO.sub.3 nanoplatelets/nanowires. At 104, pristine hexagonal hollow ZnO nanotubes are prepared, and at 106, 3D hexagonal hollow ZnO nanotubes (shell) around the 2D MoO.sub.3 and WO.sub.3 nanoplatelets/nanowires (core) are prepared. At 108, sulfidation of the core-shell under mild condition via vapor phase transport at approximately 400-450 C. is conducted, wherein hexagonal MoS.sub.2 and WS.sub.2 platelets/nanowires are formed and embedded within the hollow ZnS hexagons. At 110, the intended composite solid lubricant structure is created with anticipated amelioration in its efficacy to lower the coefficient of friction and enhance the antiwear aspect of various space mechanisms such as actuators, motors, gimbals, etc.

(10) Synthesis of 2D MoO.sub.3 Platelets

(11) An example of synthesizing 2D MoO.sub.3 platelets is described below. For example, small coupons are cut from a molybdenum (Mo) foil and heated in static air at 600 C. for approximately two hour. Due to large volume change (e.g., going from metal to metal oxide), the metal coupons disintegrate into small debris. Scanning electron microscopy (SEM) imaging and X-ray diffraction (XRD) is performed to discern for morphological changes and confirm the formation of MoO.sub.3 phase. The debris is heated for 1 hour at 450 C. in a gas mixture containing 1 percent of CO in N.sub.2, followed by natural cooling in air. SEM and XRD indicate the formation of very thin and sharp 2D platelets of MoO.sub.3.

(12) Synthesis of 2D MoO.sub.3 Nanorods and/or Nanoplates

(13) In one example, 2D MoO.sub.3 nanorods and/or nanoplates are synthesized by the reduction of peroxymolybdic solution with hexamethylenetetramine (HMTA). The peroxomolybdic solution is prepared by dissolving Mo powder in hydrogen peroxide (H.sub.2O.sub.2) under vigorous stirring. HMTA solutions of varying molarity are prepared to study the influence of HMTA strength on the morphology of the resulting MoO.sub.3 particles. HMTA solution is slowly added to the peroxomolybdic solution under constant stirring, when a precipitate is formed. The precipitate is separated by a centrifuge, and dried at 70 C.

(14) In another example, ammonium molybdate is dissolved in DI water, followed by the addition of urea (20 wt. %) and sonicated in a water bath maintained at 65-70 C. The pH is adjusted to 3.0 by adding nitric acid while sonicating. The precipitate is collected by the centrifuge and dried at 70 C.

(15) Synthesis of 3D WO.sub.3 Nanobundles/Nanoribbons/Nanowires

(16) In one example, small coupons are cut from a tungsten (W) foil and heated in static air for 2 hour at 800 C. Due to large volume change (e.g., going from metal to metal oxide), the metal coupons disintegrate into small debris. SEM and XRD is performed to discern for morphological changes and confirm the formation of WO.sub.3. In another example, W foil is heated for 2 hour at 800 C. in different CO/CO.sub.2 buffer mixtures and SEM and XRD is performed on the resulting product.

(17) In yet another example, 6M HCl is added drop wise to 100 mL of a 15 mM solution of Na.sub.2WO.sub.4. 2H.sub.2O is cooled to a temperature of 5-10 C., and stirred constantly. The suspension is centrifuged, washed repeatedly to attain a pH of 6 and is poured into 200-300 mL DI water and ultrasonicated for 2 hour. It is aged for 24 to 48 hour at room temperature for crystallization.

(18) In yet another example, 2M HCl is added drop wise to 20 mL Na.sub.2WO.sub.4. 2H.sub.2O solution under constant stirring until a pale yellow precipitate is formed. The precipitate is transferred to 60 mL of 2M HCl and stirred continuously for 24 hour, followed by aging for 96 hour at 80 C. The precipitate is filtered, washed with DI water several times, and calcined at 500 C. for 2 hour in air (e.g., heating rate: 5 C./min)

(19) Synthesis of Hollow Hexagonal ZnO Nanorods

(20) Following is an embodiment of the procedure for synthesizing hollow hexagonal ZnO nanorods. For example, 0.17 M urea solution is made by dissolving 4.9 g urea in 480 ml DI water. It is heated, allowed to come to near boiling and refluxed for approximately 20 min. at 110 C. 1.1 M solution of zinc nitrate (3.27 g dissolved in 20 ml DI water) is added to the refluxing urea solution, and the mixture (e.g., the combination of the zinc nitrate solution and the refluxing urea solution) is boiled for additional 15 min. In some embodiments, the mixture is allowed to boil for 20 to 25 min. instead of 15 min., after adding zinc nitrate solution. The resulting mixture is rapidly cooled and the precipitate collected by a centrifuge and dried. See, for example, FIGS. 2A-C, which are SEM images (200A-C) of hollow hexagonal ZnO made by refluxing zinc nitrate-urea mixture at 110 C. for 35 min, according to an embodiment of the present invention.

(21) Synthesis of Hollow Hexagonal ZnO Nanorods Around MoO.sub.3/WO.sub.3 Platelets and/or Nanorods

(22) The following discussion is an embodiment of the present invention for the synthesis of 3D hollow hexagonal ZnO nanorods around 2D MoO.sub.3/WO.sub.3 platelets and/or 3D nanorods. For example, 0.17 M urea solution is made by dissolving 4.9 g urea in 480 ml DI water. MoO.sub.3 platelets/nanorods or WO.sub.3 nanobundles/nanoplates prepared by the processes described above under the sections SYNTHESIS OF 2D MoO.sub.3 PLATELETS and SYNTHESIS OF 3D WO.sub.3 NANOBUNDLES/NANORIBBONS/NANOWIRES may be added to the urea solution being refluxed for approximately 20 min near boiling. 1.1 M solution of zinc nitrate made by dissolving 3.27 g zinc nitrate hexahydrate in 20 ml of DI water is added to the refluxing solution (i.e., the urea solution), and the entire mixture may be boiled for additional 15 min. In some embodiments, the entire mixture is boiled for 20 to 25 min. instead of 15 min. The resulting mixture is rapidly cooled and the precipitate is collected by a centrifuge and dried. Growth of hollow ZnO nanorods around MoO.sub.3 and/or WO.sub.3 platelets or nanowires or nanorods entrapped within them may be confirmed by SEM and TEM (transmission electron microscopy).

(23) FIGS. 3A-B illustrate the schematics 300A-B of the anticipated structure of the ZnO/MoO.sub.3 or ZnO/WO.sub.3 composite resulting from the aforementioned procedure, according to an embodiment of the present invention. In this embodiment, hollow ZnO nanotubes 302 grow from aqueous solution around the nanoplatelets, nanowires or nanorods of MoO.sub.3 and/or WO.sub.3 304.

(24) Synthesis of ZnSXS.sub.2 Composite in Shell-Core Configuration

(25) The following discussion is an embodiment for the synthesis of ZnSXS.sub.2 composites in shell-core configuration by subjection the ZnOXO.sub.3 composite (where XMo or W) made by a procedure discussed above with respect to FIGS. 3A-C, by a co-sulfidation step described in the following. In some embodiments, the ZnOXO.sub.3 shell-core composite is placed in a porcelain/ceramic boat which is wrapped in a perforated Al-foil. The boat is placed in a horizontal furnace and heated at 200 C. for 2 hour in dry N.sub.2 at small flow rate in order to expel remnant air from the furnace interior and replace with an inert non-reacting ambient, prior to sulfidation. In one embodiment, a bubbler containing an aqueous ammonium sulfide solution ((NH.sub.4).sub.2S, 0.1 M) is placed between a compressed N.sub.2 gas cylinder and the furnace. One end of a bubbler containing aqueous (NH.sub.4).sub.2S solution (0.1 M) is attached to the nitrogen bottle, while the other end is connected to the tube in the furnace that contains the boat. With N.sub.2 bubbling through the aqueous sulfide solution, the furnace temperature may be increased to 400 C. and held at 400 C. for 4 hour to ensure completion of the process of sulfidation of the contents of the boat via gas phase transport of the sulfiding agent, (NH.sub.4).sub.2S. The furnace is turned off and allowed to cool to ambient temperature in N.sub.2 flow. The sample is extracted from the boat and characterized by XRD, SEM, and TEM.

(26) FIGS. 4A-B illustrate the schematics 400A-B of the anticipated structure of the ZnS/MoS.sub.2 or ZnS/WS.sub.2 composite solid lubricant resulting from the aforementioned procedure, according to an embodiment of the present invention. Hollow ZnO nanorods transform into corresponding ZnS 402, retaining their hexagonal structure, while the embedded MoO.sub.3 and/or WO.sub.3 nanoplatelets and nanowires 404 upon sulfidation are converted into corresponding sulfides (also hexagonal) and stay lodged within the ZnS cage.

(27) It will be readily understood by those skilled in the art that the components of various embodiments of the present invention, as generally described and illustrated in the figures herein, may be arranged and designed in a wide variety of different configurations. Thus, the detailed description of the embodiments, as represented in the attached figures, do not limit the scope of the invention as claimed, but is merely a representative of the selected embodiments of the invention.

(28) The features, structures, or characteristics of the invention described throughout this specification may be combined in any suitable manner in one or more embodiments. For example, reference throughout this specification to certain embodiments, some embodiments, or similar language means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, the appearance of the phrases in certain embodiments, in some embodiment, in other embodiments, or similar language throughout this specification do not necessarily all refer to the same group of embodiments and, the described features, structures, or characteristics may be combined in any suitable manner in one or more embodiments.

(29) It should be noted that reference throughout this specification to features, advantages, or similar language does not imply that all of the features and advantages that may be realized with the present invention should be or are in any single embodiment of the invention. Rather, language referring to the features and advantages is understood to mean that a specific feature, advantage, or characteristic described in connection with an embodiment is included in at least one embodiment of the present invention. Thus, the discussion of the features and advantages, and similar language, throughout this specification may, but do not necessarily, refer to the same embodiment.

(30) Furthermore, the described features, advantages, and characteristics of the invention may be combined in any suitable manner in one or more embodiments. One skilled in the relevant art will recognize that the invention can be practiced without one or more of the specific features or advantages of a particular embodiment. In other instances, additional features and advantages may be recognized in certain embodiments that may not be present in all embodiments of the invention.

(31) One having ordinary skill in the art will readily understand that the invention as discussed above may be practiced with steps in a different order, and/or with hardware elements in configurations which are different than those which are disclosed. Therefore, although the invention has been described based upon these preferred embodiments, it would be apparent to those of skill in the art that certain modifications, variations, and alternative constructions would be apparent, while remaining within the spirit and scope of the invention. In order to determine the metes and bounds of the invention, therefore, reference should be made to the appended claims.