Ti-Zr alloy powder and anode containing the same

Abstract

A Ti-Zr alloy in powder form is described. Sintered pellets and capacitor anodes containing the Ti-Zr alloy powder of the present invention are further described.

Description

[Technical Field]

[0001] This application claims the benefit under 35 U.S.C. §119(e) of prior U.S. Provisional Patent Application No. 62 / 839,807, filed April 29, 2019, the entirety of which is incorporated herein by reference.

[0002] The present invention relates to titanium-zirconium (Ti-Zr) alloy powders and the use of these alloy powders to form sintered pellets and capacitor anodes, etc. Methods of making the same are further described. [Background technology]

[0003] While tantalum and sometimes niobium have been readily used in powder form to form sintered pellets and ultimately capacitor anodes, the use of alternative materials is desirable for a variety of reasons, including cost. Another reason is that the use of materials with higher dielectric constants compared to tantalum oxide allows for higher theoretical CV / g at equivalent CV / cc. Also, while metals such as titanium oxide can have high leakage, as shown in the present invention, zirconium titanium alloys can have lower leakage compared to titanium.

[0004] As described in Patent Document 1, pure titanium has been considered for use as a capacitor electrode material, given that its oxide has a high dielectric constant and other favorable properties, such as corrosion resistance and low density. However, it has been difficult to create a dielectric oxide film on the titanium surface that is excellent in terms of leakage current at high voltages. These drawbacks of titanium have prevented its widespread use as an electrode suitable for electrolytic capacitors, despite its high dielectric constant and good sinterability. Furthermore, porous titanium may exhibit poor leakage current performance when formed into solid electrolytic capacitors.

[0005] Although Patent Document 2 describes a mixture of titanium powder and zirconium powder for use in the anode, the material identified as an alloy in this patent is a powder metallurgy product that is a mixture of sintered powders, and is not a particle or material that has a Ti-Zr phase, which is typically a solid solution of titanium and zirconium.

[0006] Thus, there is a need to develop true alloys of titanium and zirconium and to provide products made from such alloys that overcome one or more of the problems / disadvantages discussed above. [Prior art documents] [Patent documents]

[0007] [Patent Document 1] U.S. Patent No. 3,599,053 [Patent Document 2] U.S. Patent No. 3,649,880 Summary of the Invention

[0008] The present invention is characterized by providing a titanium-zirconium alloy in the form of a powder or particles, which is a solid solution of titanium and zirconium.

[0009] Another feature of the present invention is to provide a titanium-zirconium alloy in powder or particulate form that can be utilized to form sintered pellets.

[0010] The present invention is also characterized by providing a titanium-zirconium alloy having a dendritic structure or a nodular shape.

[0011] The present invention further features a titanium-zirconium alloy powder useful for forming anodes for capacitors.

[0012] To achieve these and other advantages, and in accordance with the purpose of the present invention, as embodied and outlined herein, the present invention provides a Ti-Zr alloy in powder form. The Ti-Zr alloy powder can have a dendritic structure and / or a nodular morphology. The Ti-Zr alloy powder can be substantially free of other elements (other than Ti and Zr). The Ti-Zr alloy powder has one or more advantageous properties that make it useful for forming sintered pellets and ultimately anodes, and can therefore provide one or more suitable capacitor properties, such as leakage control and / or other anode-related properties.

[0013] Furthermore, the present invention relates to a titanium-zirconium (Ti-Zr) alloy powder having an atomic ratio of Ti to Zr of 10:90 to 90:10. The Ti-Zr alloy powder can have an average primary particle size of 500 nm to 2 microns. The Ti-Zr alloy powder can further include a Ti-Zr oxide layer on the Ti-Zr alloy powder. The Ti-Zr alloy powder can further include phosphorus. Further options and details of the Ti-Zr alloy powder are provided herein.

[0014] Additional features and advantages of the invention will be set forth in part in the description that follows, and in part will be obvious from the description, or may be learned by the practice of the invention. The objectives and other advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the description and appended claims.

[0015] It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are intended to provide further explanation of the invention as claimed.

[0016] The accompanying drawings, which are incorporated herein by reference, illustrate some of the features of the present invention and, together with the description, serve to explain the principles of the invention. [Brief explanation of the drawings]

[0017] [Figure 1] 1A and 1B show SEM images of an example of the Ti—Zr alloy powder of the present invention, with FIG. 1B being at a higher magnification. [Figure 2] 1A-1D illustrate exemplary portions of a process for forming the Ti-Zr alloy powder of the present invention. [Figure 3] 1 is a schematic diagram illustrating an embodiment of various steps leading to the formation of the Ti—Zr alloy powder of the present invention. [Figure 4A] FIG. 4A shows XRD analyses from examples of the present invention showing a) pure zirconium, b) Ti-15 at. % and Zr-85 at. %; c) Ti-40 at. % and Zr-60 at. %; and d) Ti-50 at. % and Zr-50 at. %. [Figure 4B] FIG. 4B shows XRD analyses from examples of the present invention showing a) pure zirconium, b) Ti-15 at. % and Zr-85 at. %; c) Ti-40 at. % and Zr-60 at. %; and d) Ti-50 at. % and Zr-50 at. %. DETAILED DESCRIPTION OF THE INVENTION

[0018] The present invention relates to a Ti-Zr alloy powder. The Ti-Zr alloy powder is not a simple physical mixture of titanium and zirconium, nor does the Ti-Zr alloy powder of the present invention contemplate a mechanical mixture of the two elements. Instead, the Ti-Zr alloy powder of the present invention is a powder comprising a plurality of particles, each or substantially all of which have at least a Ti-Zr phase, typically a solid solution of titanium and zirconium.

[0019] The Ti-Zr alloy powder can have a dendritic structure. The Ti-Zr alloy powder can have a nodular morphology. The Ti-Zr alloy powder can have both a dendritic structure and a nodular morphology. For purposes of the present invention, a dendritic shape or morphology is understood to be particles having a branched structure and / or irregular winding movement of individual branches. This term is understood in the art; see, for example, "Modeling Dendritic Shapes Using Path Planning" by Lingxhu et al. Further examples of dendritic shapes and morphologies are shown in Figures 1A and 1B.

[0020] The Ti—Zr alloy powder can have an atomic ratio of Ti to Zr of about 10:90 to about 90:10, for example, but not limited to, an atomic ratio of Ti to Zr of 20:80 to 80:20, or 30:70 to 70:30, or 40:60 to 60:40. As a further example, the Ti—Zr alloy powder can include 50 atomic % Zr, or about 20 atomic % to about 40 atomic % Zr, or about 30 atomic % to about 40 atomic % Zr. As a further example, the Ti—Zr alloy powder can include 50 atomic % Ti, or about 20 atomic % to about 40 atomic % Ti, or about 30 atomic % to about 40 atomic % Ti.

[0021] The Ti—Zr alloy powder optionally comprises at least 60 atomic %, or at least 70 atomic %, or at least 80 atomic %, or at least 90 atomic %, or at least 95 atomic %, or at least 99 atomic % of a primary Ti—Zr phase. For example, the Ti—Zr alloy powder can comprise between about 10 atomic % and 99.99 atomic %, or between about 10 atomic % and 95 atomic %, or between about 10 atomic % and 90 atomic %, etc. of a primary Ti—Zr phase.

[0022] The Ti-Zr alloy powder may be particles consisting of a single-phase homogeneous solid solution of Ti and Zr.

[0023] Titanium-zirconium alloy powders may optionally be considered binary Ti-Zr alloy powders.

[0024] The Ti-Zr alloy powder can include less than 500 ppm of titanium or zirconium individual particles, or both, for example, less than 400 ppm, less than 300 ppm, less than 200 ppm, less than 100 ppm, less than 50 ppm, less than 25 ppm, less than 10 ppm, less than 5 ppm, or less than 1 ppm of titanium or zirconium individual particles, or both.

[0025] The Ti—Zr alloy powder of the present invention can be a powder that is substantially free of elements other than Ti and Zr. For example, non-gaseous elements other than Ti and Zr (e.g., non-gaseous general elements or non-gaseous metal elements) present in the Ti—Zr alloy powder can be present in an amount of less than 1 wt %, based on the weight of the alloy powder, for example, about 0.1 ppm to about 500 ppm, or about 1 ppm to 250 ppm, or about 1 ppm to 100 ppm, or about 1 ppm to 50 ppm, or less than 50 ppm, or less than 25 ppm, or less than 500 ppm.

[0026] The Ti-Zr alloy powder can include less than 50 ppm of elemental carbon, for example, less than 40 ppm of carbon, less than 30 ppm of carbon, less than 20 ppm of carbon, less than 10 ppm of carbon, less than 5 ppm of carbon, less than 1 ppm of carbon, for example, 0 ppm to 49 ppm, or 0.1 ppm to 20 ppm, or 0.1 ppm to 2 ppm of carbon.

[0027] The titanium-zirconium alloy powder can optionally have an oxygen content of about 0.1 wt % to about 5 wt % (e.g., about 0.1 wt % to about 4 wt %, about 0.1 wt % to about 3 wt %, about 0.1 wt % to about 2 wt %, about 0.1 wt % to about 1 wt %, about 0.2 wt % to about 5 wt %, about 0.3 wt % to about 5 wt %, about 0.5 wt % to about 5 wt %, about 1 wt % to about 5 wt %) based on the weight of the powder.

[0028] The titanium-zirconium alloy powder can optionally have a nitrogen content of about 0.01 wt % to about 20 wt % (e.g., about 0.01 wt % to about 15 wt %, about 0.01 wt % to about 10 wt %, about 0.01 wt % to about 5 wt %, about 0.01 wt % to about 1 wt %, about 0.05 wt % to about 20 wt %, about 0.1 wt % to about 20 wt %, about 0.5 wt % to about 20 wt %, about 1 wt % to about 20 wt %) based on the weight of the powder.

[0029] The titanium-zirconium alloy powder can optionally have a phosphorus content of about 0.001 wt % to about 5 wt % (e.g., about 0.1 wt % to about 4 wt %, about 0.1 wt % to about 3 wt %, about 0.1 wt % to about 2 wt %, about 0.1 wt % to about 1 wt %, about 0.2 wt % to about 5 wt %, about 0.3 wt % to about 5 wt %, about 0.5 wt % to about 5 wt %, about 1 wt % to about 5 wt %) based on the weight of the powder.

[0030] The titanium-zirconium alloy powder can optionally have a hydrogen content of about 0.001 wt % to about 5 wt % (e.g., about 0.1 wt % to about 4 wt %, about 0.1 wt % to about 3 wt %, about 0.1 wt % to about 2 wt %, about 0.1 wt % to about 1 wt %, about 0.2 wt % to about 5 wt %, about 0.3 wt % to about 5 wt %, about 0.5 wt % to about 5 wt %, about 1 wt % to about 5 wt %) based on the weight of the powder.

[0031] The use of gases such as nitrogen, phosphorus, and / or hydrogen can further serve as passivators to further stabilize the Ti—Zr alloy powder.

[0032] The titanium-zirconium alloy powder (excluding any oxide layer) can optionally consist of less than 500 ppm of elements other than Ti, Zr, O, and P, e.g., less than 100 ppm (e.g., 0 ppm to 99 ppm, 1 ppm to 75 ppm, 1 ppm to 50 ppm, 1 ppm to 25 ppm, 1 ppm to 10 ppm, less than 5 ppm) of elements other than Ti, Zr, O, and P. The titanium-zirconium alloy powder (excluding any oxide layer) can consist of less than 500 ppm of elements other than Ti, Zr, O, N, H, and P, e.g., less than 100 ppm of elements other than Ti, Zr, O, N, H, and P. These ppm limits listed herein can apply to one, more than one, or all of the listed elements.

[0033] The Ti—Zr alloy powder may optionally further comprise a Ti—Zr oxide layer on the titanium-zirconium alloy powder.

[0034] The Ti—Zr oxide layer can have a thickness of about 1 nm to about 20 nm or more, for example, about 5 nm to about 20 nm, or about 10 nm to about 20 nm.

[0035] If a Ti—Zr oxide layer is present, the Ti—Zr oxide layer can optionally partially encapsulate or completely coat the titanium-zirconium alloy powder. For example, greater than 95%, or greater than 99%, or greater than 99.9%, or 100% by volume of the Ti—Zr powder can have an oxide layer on its surface that covers greater than 50%, 60%, 70%, 80%, 90%, 95%, 99%, or 100% of the effective outer surface area of ​​the Ti—Zr powder.

[0036] The Ti—Zr oxide layer can optionally further include phosphorus. If present, phosphorus can be present at a level of about 1 ppm to 5000 ppm, or about 50 ppm to about 5000 ppm, for example, about 100 ppm to 4000 ppm, or 200 ppm to about 5000 ppm, or about 100 ppm to 3000 ppm, or about 100 ppm to 2000 ppm, or about 100 ppm to 1000 ppm, or about 100 ppm to 500 ppm.

[0037] With respect to particle size and particle size distribution, the Ti—Zr can have a variety of particle sizes and / or particle size distributions.

[0038] The Ti—Zr alloy powder of the present invention can have an average primary particle size of about 500 nm to about 2 microns, or less than this range, or more than this range, including, but not limited to, about 600 nm to 2 microns, 600 nm to 1.5 microns, and 600 nm to 1 micron.

[0039] For example, the titanium-zirconium alloy powder may have a D10 and D90 within 35% of the D50. The titanium-zirconium alloy powder may have a D10 and D90 within 25% of the D50.

[0040] The titanium-zirconium alloy powder may have a D10 of about 0.3 microns to about 10 microns (e.g., about 0.5 microns to about 7 microns, or about 1 micron to about 5 microns, or about 2 microns to about 8 microns) and / or a D10 of about 0.5 microns to about 400 microns (e.g., about 0.5 microns to about 300 microns, about 0.5 microns to about 200 microns, about 0.5 microns to about 100 microns, about 0.5 microns to about 50 microns, about 1 micron to about 400 microns, about 5 microns to about 400 microns, about 10 microns to about 400 microns, about 20 microns to about 400 microns, about 50 microns to about 400 microns, about 100 microns to about 4 00 microns), and / or a D90 of about 1 micron to about 700 microns (e.g., about 1 micron to about 600 microns, about 1 micron to about 500 microns, about 1 micron to about 400 microns, about 1 micron to about 300 microns, about 1 micron to about 200 microns, about 1 micron to about 200 microns, about 1 micron to about 100 microns, about 5 microns to about 700 microns, about 10 microns to about 700 microns, about 20 microns to about 700 microns, about 40 microns to about 700 microns, about 50 microns to about 700 microns, about 75 microns to about 700 microns, about 100 microns to about 700 microns).

[0041] The titanium-zirconium alloy powder is approximately 0.1 m 2 / g ~ approx. 20 m 2 / g or more BET surface area, e.g., about 0.5 m 2 / g ~ approx. 20 m 2 / g, approx. 1 m 2 / g ~ approx. 20 m 2 / g, approx. 3 m 2 / g ~ approx. 20 m 2 / g, approx. 5 m 2 / g ~ approx. 20 m 2 / g, approx. 0.1 m 2 / g ~ approx. 15 m 2 / g, approx. 0.1 m 2 / g ~ approx. 10 m 2 / g, approx. 0.1 m 2 / g ~ approx. 5 m 2 / g, or approximately 0.3 m 2 / g ~ approx. 2 m 2 / g BET surface area.

[0042] As a further example, the Ti-Zr alloy powder may have an average particle size of about 400 nm to 600 nm, or 500 nm to 600 nm, and a 5 mm 2 / g or less.

[0043] Titanium-zirconium alloy powders can optionally be considered non-oxide metal powders (excluding any oxide layers that may be present). In other words, Ti—Zr powders optionally do not contain oxides as part of the alloy itself.

[0044] The Ti—Zr alloy powder of the present invention can have a fractal dimension of about 1.9 to about 3, for example, about 2 to about 3, or about 2.0 to 2.95, or about 2.2 to 2.8, or about 2 to about 2.2. The fractal dimension can be calculated, for example, using the Hausdorff method or the Minkowski-Bouligant method, or can be determined using a modified box-counting method and a numerical calibration curve provided by Wozniak et al. in "Journal of Aerosol Science" (ISSN: 0021-8502, Vol: 47, Page: 12-26), the entire contents of which are incorporated herein by reference.

[0045] The Ti—Zr alloy powder of the present invention can have one or more of the following parameters, and any combination of these parameters can be present in the Ti—Zr alloy powder. Average particle size: 500 nm to 2 microns Mesh size (US): -400~-40 Scott density: approx. 6 g / in 3 ~approximately 30 g / in 3 (e.g., 6 g / in 3 ~13 g / in 3 ).

[0046] As noted above, the Ti—Zr alloy powders of the present invention can have a purity of at least 99 wt.% (relative to Ti—Zr), e.g., at least 99.5 wt.%, at least 99.9 wt.%, at least 99.99 wt.%, at least 99.995 wt.%, etc., where the weight percent is by weight of the alloy powder (excluding any oxide or other layers that may be present).

[0047] The Ti—Zr alloy powder of the present invention can be porous or can have porous properties.

[0048] The Ti—Zr alloy powder of the present invention can be non-agglomerated or agglomerated. In the case of agglomerated, the size of the agglomerates can be about 10 to about 500,000 primary particles.

[0049] The Ti—Zr alloy powder can be optionally doped with one or more dopants, such as nitrogen, phosphorus, carbon, boron, and / or hydrogen, or any combination thereof. The amount of dopant that can be present in the Ti—Zr alloy powder of the present invention can be any suitable amount, such as about 10 ppm to 1000 ppm, e.g., about 50 ppm to 1000 ppm, about 100 ppm to 1000 ppm, about 200 ppm to 1000 ppm, about 350 ppm to 1000 ppm, or more. The dopant can be present as a solid solution or as a compound with other dopants, including metal elements or oxygen.

[0050] The Ti-Zr alloy powder of the present invention can be formed into sintered pellets and used to form anodes, which can ultimately be present as part of a capacitor. The capacitor, or the anode within the capacitor, can be wet or dry.

[0051] In the present invention, the sintered pellets can comprise, consist essentially of, consist of, or include the pressed and sintered Ti-Zr alloy powder of the present invention. For example, the Ti-Zr alloy powder can be pressed into any size or shape, e.g., cylindrical, square, or other geometric shape, preferably a shape suitable for anode purposes. The Ti-Zr powder of the present invention can be pressed to form, for example, a green compact, and the pressing can be performed at a density of about 1.2 g / cm. 3 ~Approx. 3.0 g / cm 3 Sintering to form sintered pellets can be carried out at a temperature of about 400°C to about 1200°C. The sintering time can be any time suitable for forming sintered pellets, for example, about 1 minute to 60 minutes or more.

[0052] The sintered pellet may optionally further include a lead wire at least partially embedded in the sintered pellet, which may be a metal lead wire, such as a lead wire having a Ti-Zr alloy material, or titanium itself, or zirconium itself, or other conductive material such as tantalum, or niobium, or aluminum.

[0053] As mentioned above, the present invention further relates to a capacitor anode comprising at least one sintered pellet of the present invention. As mentioned above, the pellet can have any shape or size. The capacitor anode of the present invention can have a capacitance of at least 1,000 μFV / g. The capacitance can be, for example, at least 5,000 μFV / g, at least 10,000 μFV / g, e.g., from about 1,000 μFV / g to about 50,000 μFV / g, from about 10,000 μFV / g to about 100,000 μFV / g, from about 50,000 μFV / g to about 150,000 μFV / g, or from about 1,000 μFV / g to about 260,000 μFV / g or more.

[0054] The capacitor anodes of the present invention can have a DC leakage of less than 15 nA / μFV, e.g., less than 10 nA / μFV, or less than 5 nA / μFV, e.g., between about 0.1 nA / μFV and 5 nA / μFV, or between 0.1 nA / μFV and 10 nA / μFV.

[0055] According to the present invention, anodizing a sintered pellet or a capacitor anode forms an anodic oxide film on the anode surface. According to the present invention, this anodic film comprises, consists essentially of, or consists of one or more oxides. The one or more oxides may be amorphous, non-amorphous, or solely amorphous. According to the present invention, oxide crystals may optionally be largely avoided, absent, or at such a low level that they do not affect the overall performance of the capacitor anode. For example, if oxide crystals are present, they may be less than 5% by volume, or less than 1% by volume, based on the total volume of the anodic film.

[0056] The anodic film can be, comprise, be part of, or be considered to be a passivation layer, and can have a thickness of from about 5 nm to about 600 nm, or from about 20 nm to about 600 nm or more.

[0057] The anode of the present invention can have a cumulative porosity of about 0.1 mL / g to about 0.6 mL / g, for example, about 0.1 mL / g to about 0.5 mL / g, or about 0.2 mL / g to about 0.4 mL / g.

[0058] The present invention further relates to a method for forming a capacitor anode containing the Ti—Zr alloy powder of the present invention. The method includes forming the Ti—Zr alloy powder into the shape of the anode and sintering it at a suitable sintering temperature, e.g., about 400°C to about 1200°C, for about 1 minute to about 30 minutes or more. Optionally, the sintered material can then be anodized at an anodization voltage of, e.g., about 10 volts to about 200 volts, or about 10 volts to about 75 volts or more, and at a formation temperature of about 10°C to about 80°C. Other formation voltages and / or other formation temperatures can be used. The anode can then be annealed, e.g., at a temperature of about 300°C to about 350°C, for about 10 minutes to about 60 minutes or more. The anode can then be optionally manganized, e.g., at a temperature of 220°C to about 280°C, or other temperatures.

[0059] In forming the anode, the Ti—Zr alloy powder can be mixed with at least one binder and / or at least one lubricant to form a pressed anode. Thus, the pressed anode can comprise, consist essentially of, or consist of pressed Ti—Zr alloy powder of the present invention with at least one binder and / or at least one lubricant.

[0060] In forming the Ti-Zr alloy powder of the present invention, a flame particle formation process, such as that described in U.S. Pat. Nos. 7,442,227 and 5,498,446, the entireties of which are incorporated herein by reference, is preferably used. More specifically, an alkali metal feed, preferably a sodium feed, is injected into a flame reactor, and separate feeds of a titanium-containing halide and a zirconium-containing halide are also introduced into the flame reactor as one or more feeds. The Ti-containing halide can be TiCl4, and the Zr-containing halide can be ZrCl4. These three feeds are then introduced (e.g., injected) into the flame reactor. The titanium halide and zirconium halide-containing feeds can be combined before entering the flame reactor, or can be introduced separately into the flame reactor. The introduction of the feeds can typically be carried out under an inert gas environment, such as argon. In the flame reactor, the various feeds can optionally be converted to steam, or the feeds can be fed to the reactor as steam. Titanium and zirconium halides are typically reacted with an alkali metal in the presence of a halide, such as sodium chloride, to form a Ti-Zr alloy powder. For example, as shown in Figure 3, primary particles can nucleate and grow, eventually forming strong aggregates of these particles, which can be coated with a salt, such as sodium chloride, and finally solidifying to form a Ti-Zr alloy powder coated with the salt, e.g., sodium chloride. Excess sodium is then removed using various techniques, and the Ti-Zr alloy particles coated with a salt, such as sodium chloride, are typically collected via a particle collector or filter. This collection can be performed in an inert gas environment or other non-reactive environment. Optionally, further heat treatment in an inert gas environment or vacuum environment can be used to increase the primary particle size. Finally, the sodium chloride can be removed (e.g., by washing, dissolution, or sublimation), and the Ti-Zr alloy powder is recovered.

[0061] One preferred method of introducing the reactants into the flame reactor is shown in Figure 2. As can be seen in Figure 2, a flow straightener can be used to maintain the feed in the proper direction and alignment, and preferably the reactants are sheathed in an inert environment as shown in Figure 2.

[0062] XRDs of example Ti-Zr alloys of the present invention are shown in Figures 4A and 4B and compared to pure zirconium.

[0063] The present invention will be further clarified by the following examples, which are intended to be exemplary of the present invention. [Example]

[0064] Example 1 Salt-encapsulated alloy powder with a Ti to Zr mass ratio of 27:63 was produced by the flame synthesis process described in U.S. Patent No. 7,442,227, as shown in Figure 2. Vaporous titanium chloride and zirconium chloride (halides) were introduced into a reactor along with argon through a central tube, such that the mass ratio of TiCl4 to ZrCl4 was 0.67. A concentric Ar flow was placed between the halides and an excess of vaporized sodium. As described in U.S. Patent No. 7,442,227, the sodium chloride by-product acted as a condensable vapor material that inhibited particle sintering behavior. The salt-encapsulated metal powder was collected and washed with deionized water to remove the sodium chloride coating. Dilute nitric acid was used to aid particle settling. This washing process introduced a thin oxide passivation layer on the particle surface, which was maintained even when the particles were dried under vacuum. The resulting zirconium-titanium alloy was then added to a 2.0 g / cm 3 The sample was pressed to a density of 0.1 M and sintered under vacuum at 500° C. for 30 min. Anodization was carried out in a 0.1 M electrolyte of ammonium pentaborate using a voltage of 30 V at 25° C. for 18 h.

[0065] The leakage current of the resulting anode was measured in a 10 wt % phosphoric acid solution after 2 minutes of application of a DC voltage of 21 V. The capacitance was also measured in the same phosphoric acid solution at a frequency of 100 Hz and a bias of 2 V.

[0066] The capacitance was 260 mFV / g and the leakage current was 7 nA / CV.

[0067] Example 2 The salt-coated alloy powder with a mass ratio of Ti to Zr of 27:63 was prepared by a flame synthesis process and washed as in Example 1, then pressed and sintered at 500°C for 30 min as in Example 1. Anodization was carried out in a 0.1 M electrolyte of ammonium pentaborate using a voltage of 10 V at 25°C for 12 h.

[0068] The leakage current of the resulting anode was measured in a 10 wt % phosphoric acid solution after 2 minutes of application of a DC voltage of 7 V. The capacitance was also measured in the same phosphoric acid solution at a frequency of 100 Hz and a bias of 2 V.

[0069] The capacitance was 140 mFV / g and the leakage current was 120 nA / CV.

[0070] Example 3 A salt-coated alloy powder with a 15:85 mass ratio of Ti to Zr was produced by a flame synthesis process using 2.5 wt. % nitrogen doping, similar to Example 1, except for the amount of reactants and the nitrogen doping. The nitrogen doping was achieved by introducing a small amount of nitrogen into the argon flow between the halide and the concentric sodium vapor flow. It was determined that all of the nitrogen had reacted with the powder. The resulting powder was washed as in Example 1 and then resuspended in 1.7 g / cm. 3 The alloy was pressed into a 0.1 M ammonium pentaborate electrolyte and sintered at 550°C for 30 minutes. The XRD of the alloy is shown in Figures 4A and 4B. Anodization was carried out in a 0.1 M ammonium pentaborate electrolyte at 25°C for 6 hours using a voltage of 30 V.

[0071] The leakage current of the resulting anode was measured in a 10 wt % phosphoric acid solution after 2 minutes of application of a DC voltage of 21 V. The capacitance was also measured in the same phosphoric acid solution at a frequency of 100 Hz and a bias of 2 V.

[0072] The capacitance was 200 mFV / g and the leakage current was 340 nA / CV.

[0073] Example 4 Salt-coated alloy powders with a Ti to Zr mass ratio of 27:63 were produced by flame synthesis as in Example 1, and the product was divided into six lots. Sodium chloride was removed from the surface of the alloy powder using a dilute solution of either nitric acid, hydrogen peroxide, sulfuric acid, phosphoric acid, ammonium pentaborate, or sodium acetate. The resulting powders were then pressed and sintered at 500°C for 30 minutes as in Example 1. Anodization was performed in a 0.1 M ammonium pentaborate electrolyte at 25°C for 24 hours using a voltage of 30 V.

[0074] The leakage current of the resulting anode was measured in a 10 wt % phosphoric acid solution after 2 minutes of application of a DC voltage of 7 V. The capacitance was also measured in the same phosphoric acid solution at a frequency of 100 Hz and a bias of 2 V.

[0075] When the broken anodes were excluded, the difference in mean anode capacitance was found to be not statistically significant, but the leakage results are summarized in the table below.

[0076] [Table 1]

[0077] Powders treated with an initial wash of phosphoric acid, then further washed with both deionized water and nitric acid, and then dried were found to have significant phosphorus doping.

[0078] The present invention encompasses the following aspects / embodiments / features in any order and / or in any combination: 1. The present invention relates to a titanium-zirconium (Ti—Zr) alloy powder having an atomic ratio of Ti to Zr of 10:90 to 90:10 and an average primary particle size of 550 nm to 2 microns. 2. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, further comprising a Ti—Zr oxide layer on the titanium-zirconium alloy powder. 3. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the Ti—Zr oxide layer further comprises phosphorus. 4. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the Ti—Zr oxide layer further comprises phosphorus at a level from about 50 ppm to about 5000 ppm. 5. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the Ti—Zr oxide layer further comprises phosphorus at a level from about 200 ppm to about 5000 ppm. 6. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, further comprising a Ti—Zr oxide layer on the titanium-zirconium alloy powder, and the Ti—Zr oxide layer has a thickness of about 5 nm to about 20 nm. 7. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, further comprising a Ti—Zr oxide layer completely coating the titanium-zirconium alloy powder. 8. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the particles consist of a single-phase homogeneous solid solution of Ti and Zr. 9. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the titanium-zirconium alloy contains less than 50 ppm carbon. 10. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the titanium-zirconium alloy contains less than 500 ppm of individual particles of titanium or zirconium, or both. 11. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, having a D10 and D90 within 35% of D50. 12. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, having a D10 and D90 within 25% of D50. 13. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, having a D10 from about 0.3 microns to about 10 microns, a D50 from about 0.5 microns to about 400 microns, and a D90 from about 1 micron to about 700 microns. 14. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, having an oxygen content of about 0.1% to about 5% by weight. 15. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, having a nitrogen content of about 0.01% to about 20% by weight. 16. Approximately 0.1 m 2 / g ~ approx. 20 m 2 / g BET surface area of ​​the titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect. 17. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the titanium-zirconium alloy powder, excluding any oxide layer present, is a non-metal oxide powder. 18. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, which is a binary Ti—Zr alloy powder. 19. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the titanium-zirconium alloy contains elements other than Ti, Zr, O, N, H, and P in amounts of less than 500 ppm. 20. The titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect, wherein the titanium-zirconium alloy contains elements other than Ti, Zr, O, and P in an amount of less than 100 ppm. 21. A sintered pellet comprising the titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect formed and sintered into the shape of a pellet. 22. A capacitor anode comprising pressed and sintered titanium-zirconium alloy powder of any preceding or following embodiment / feature / aspect. 23. An electrolytic capacitor comprising the capacitor anode of any preceding or following embodiment / feature / aspect. 24. A method of forming a capacitor anode comprising a Ti—Zr alloy of any preceding or following embodiment / feature / aspect, comprising: forming the Ti—Zr alloy into the shape of an anode and sintering it at a temperature of about 400° C. to about 1200° C. for at least 1 minute; Anodizing at about 16 volts to about 200 volts; annealing the anode at a temperature of about 300°C to about 350°C for about 10 minutes to about 60 minutes; manganizing the anode; A method comprising:

[0079] The present invention may include any combination of these various features or embodiments described above and / or below in sentences and / or paragraphs. Any combination of features disclosed herein is considered to be part of the invention, and no limitations are intended with respect to features that may be combined.

[0080] Applicants specifically incorporate the entire contents of all cited references in this disclosure. Furthermore, when an amount, concentration, or other value or parameter is given as either a range, a preferred range, or a list of a preferred upper value and a preferred lower value, this is understood to specifically disclose all ranges consisting of any pairing of any range upper limit or preferred value with any range lower limit or preferred value, regardless of whether the ranges are separately disclosed. When a range of numerical values ​​is recited herein, unless otherwise specified, it is intended that the range include its endpoints, and all integers and fractions within the range. It is not intended that the scope of the invention be limited to the specific values ​​recited when defining a range.

[0081] Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims and their equivalents. [Explanation of symbols]

[0082] Drawing translation Figure 2 Sheath Argon Sodium+Argon Flow Straighteners Rectifier Co-Flow Argon Flame Figure 3 Na Feed Argon MClx Feed 1 MClx Feed 1 MClx Feed 2 MClx Feed 2 Flame Reactor Particle Collection (Filters) M coated with NaCl Excess Na Mitigation Excess Na Argon to exhaust / recycle MClx+Na Vapor MClx+Na Vapor Flame Nucleation and growth of primary particles Formation of aggregates Condensation of NaCl on Larger Particles Scavenging of Smaller Aggregates by Salt Droplets Further aggregation in molten NaCl Solidification of NaCl, Some M unencapsulated Collector System Temperature Figure 4A Zr metal Zr metal Ti 15 Zr 85 Alloy Ti 15 Zr 85 Alloy Ti 40 Zr 60 Alloy Ti 40 Zr 60 Alloy Ti 50 Zr 50 Alloy Ti 50 Zr 50 Alloy CPS counts per second Theta-2Theta (deg) Figure 4B Zr metal Zr metal Ti 15 Zr 85 Alloy Ti 15 Zr 85 Alloy Ti 40 Zr 60 Alloy Ti 40 Zr 60 Alloy Ti 50 Zr 50 Alloy Ti 50 Zr 50 Alloy CPS counts per second Theta-2Theta (deg)

Claims

1. Titanium-zirconium (Ti-Zr) alloy powder having an atomic ratio of Ti to Zr of 10:90 to 90:10, a dendritic structure, and a D50 of 1 micron to 400 microns.

2. 10. The titanium-zirconium alloy powder according to claim 1, further comprising a Ti-Zr oxide layer on the titanium-zirconium alloy powder.

3. 3. The titanium-zirconium alloy powder according to claim 2, wherein the Ti—Zr oxide layer further contains phosphorus.

4. 3. The titanium-zirconium alloy powder of claim 2, wherein the Ti—Zr oxide layer further comprises phosphorus at a level of 50 ppm to 5000 ppm by weight.

5. 3. The titanium-zirconium alloy powder of claim 2, wherein the Ti—Zr oxide layer further comprises phosphorus at a level of 200 ppm to 5000 ppm by weight.

6. 2. The titanium-zirconium alloy powder according to claim 1, further comprising a Ti—Zr oxide layer on the titanium-zirconium alloy powder, the Ti—Zr oxide layer having a thickness of 5 nm to 20 nm.

7. 10. The titanium-zirconium alloy powder of claim 1, further comprising a Ti-Zr oxide layer completely coating the titanium-zirconium alloy powder.

8. 2. The titanium-zirconium alloy powder according to claim 1, wherein the particles consist of a single-phase homogeneous solid solution of Ti and Zr.

9. 2. The titanium-zirconium alloy powder of claim 1, wherein the titanium-zirconium alloy contains less than 50 ppm by weight of carbon.

10. 2. The titanium-zirconium alloy powder according to claim 1, wherein the titanium-zirconium alloy powder contains at least 0 ppm by weight and less than 500 ppm by weight of individual particles of titanium or zirconium, or both.

11. 2. The titanium-zirconium alloy powder of claim 1, having a D10 and a D90 within 35% of D50.

12. 2. The titanium-zirconium alloy powder of claim 1, having a D10 and a D90 within 25% of D50.

13. The titanium-zirconium alloy powder of claim 1 having a D10 of 0.3 microns to 10 microns and a D90 of 1 micron to 700 microns.

14. The titanium-zirconium alloy powder of claim 1 having an oxygen content of 0.1% to 5% by weight.

15. The titanium-zirconium alloy powder of claim 1 having a nitrogen content of 0.01% to 20% by weight.

16. 0.1 m 2 / g~20m 2 10. The titanium-zirconium alloy powder of claim 1, having a BET surface area of ​​1000 nm / g.

17. 2. The titanium-zirconium alloy powder of claim 1, which is a binary Ti-Zr alloy powder.

18. 2. The titanium-zirconium alloy powder according to claim 1, wherein the titanium-zirconium alloy contains elements other than Ti, Zr, O, N, H, and P in an amount of less than 500 ppm by weight.

19. 2. The titanium-zirconium alloy powder according to claim 1, wherein the titanium-zirconium alloy contains elements other than Ti, Zr, O, and P in an amount of less than 100 ppm by weight.

20. 10. A sintered pellet comprising the titanium-zirconium alloy powder of claim 1 formed into a pellet shape and sintered.

21. A capacitor anode comprising the pressed and sintered titanium-zirconium alloy powder of claim 1.

22. 22. An electrolytic capacitor comprising the capacitor anode of claim 21.

23. A method for forming a capacitor anode comprising a Ti—Zr alloy, comprising: forming the Ti-Zr alloy powder according to claim 1 into an anode shape and sintering it at a temperature of 400°C to 1200°C for at least 1 minute; Anodizing at 16 to 200 volts, annealing the anode at a temperature of 300°C to 350°C for 10 minutes to 60 minutes; manganizing the anode; A method comprising:

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