This porous copper body includes: a skeleton which is formed of a sintered body of a plurality of copper fibers and has a three-dimensional network structure, wherein the copper fibers forming the skeleton consist of copper or a copper alloy, and the copper fibers have a diameter R in a range of 0.01 mm to 1.0 mm, a ratio L/R of a length L to the diameter R in a range of 4 to 200, and a circularity of a cross section orthogonal to a length direction in a range of 0.2 to 0.9, and the porous copper body has a porosity of 50% to 95%.

In one embodiment, a physical vapor deposition device includes a phase change material sputtering target includes a primary matrix and at least one additional phase. The primary matrix includes at least one element from Group VI of the periodic table excluding oxygen and one or more elements from Group IV or Group V of the periodic table. The additional phase is substantially homogenously dispersed in the primary matrix.

In one embodiment, a physical vapor deposition device includes a phase change material sputtering target includes a primary matrix and at least one additional phase. The primary matrix includes at least one element from Group VI of the periodic table excluding oxygen and one or more elements from Group IV or Group V of the periodic table. The additional phase is substantially homogenously dispersed in the primary matrix.

A process for manufacturing ceramic-metal composite material, comprises dissolving ceramic powder into water to obtain an aqueous solution of ceramic; mixing metal powder having a multimodal particle size where largest particle size is one fourth of the minimum dimension of a device, with the aqueous solution of ceramic to obtain a powder containing ceramic precipitated on the surface of metal particles; mixing the powder containing ceramic precipitated on the surface of the metal particles, with ceramic powder having a particle size below 50 m, to obtain a powder mixture; adding saturated aqueous solution of ceramic to the powder mixture to obtain an aqueous composition containing ceramic and metal; compressing the aqueous composition to form a disc of ceramic-metal composite material containing ceramic and metal; and removing water from the ceramic-metal composite material; wherein ceramic content of the disc is 10 vol-% to 35 vol-%. Alternatively, ceramic-ceramic composite material may be manufactured.

Methods of forming a bulk metallic glass disclosed. The methods include packing a metallic glass-forming alloy powder to form a green body; heating the green body to a temperature between the glass transition temperature and the melting point of the metallic glass-forming alloy to form a heated green body; and cooling the heated green body to a temperature below the glass transition temperature of the metallic glass-forming alloy to form the bulk metallic glass. The methods of forming a bulk metallic glass also include packing one or more layers of an amorphous foil to form a green body; heating the green body to a temperature between the glass transition temperature and the melting point of the metallic glass-forming alloy to form a heated green body; and cooling the heated green body to a temperature below the glass transition temperature of the metallic glass-forming alloy to form the bulk metallic glass.

A device for treating crude oil or heavy fuel oil with a method that can lower the pour point to at least 0 C. Crude oil or heavy fuel oil treated thusly maintains this property for at least one year. The device for lowering the pour point of crude oil or heavy fuel oil uses a specific ionization method. The method is conducted by passing a heated medium through the main ionization device which is grounded and which includes three parallelly connected segments whereby each segment includes a protective copper tube inside which a protective insulating shell is situated, inside which a copper housing is situated. In each copper housing there is one cylindrical-shaped external core in which an internal core is placed, and the external core and internal core are manufactured as two different alloys by composition. Also described is a process for casting the external core and internal core.

Methods of preparing Zr based metallic using Zr sponge refined by a refining process are described. An exemplary method includes heating Zr sponge in a processing chamber with an electron-beam-heating apparatus or an arc-melting apparatus under a desired pressure condition to release volatile contaminants from the Zr sponge, introducing a purge gas into the processing chamber and permitting the purge gas to intermingle with at least some of the released volatile contaminants, evacuating the processing chamber to extract at least some of the purge gas and released volatile contaminants, repeating the heating of the Zr sponge, the introducing of the purge gas, and the evacuating of the processing chamber release and evacuate additional volatile contaminants from the Zr sponge to provide a processed Zr sponge with enhanced purity, and melting the processed Zr sponge with multiple other alloy constituents to provide a Zr-based metallic alloy.

The invention relates to a nickel-based alloy having a microstructure with a matrix of -phase and precipitates of -phase. The -phase comprises a percentage by volume of from 50 vol % to 80 vol % in the temperature range of from 1000 C. to 1100 C. The nickel-based alloy comprises 8 to 13 at % aluminum, 3 to 14 at % cobalt, 4 to 12 at % chromium, 0.6 to 8 at % molybdenum, 0 to 6 at % rhenium, 0.5 to 4 at % tantalum, 0.5 to 4 at % titanium, 0.3 to 3.5 at % tungsten, 0 to 4 at % germanium, 0 to 0.6 at % hafnium, 0 to 4 at % ruthenium, balance nickel and unavoidable impurities. The concentrations of molybdenum and tungsten are selected such that the percentage X of molybdenum and tungsten in the -phase, X=0.84 C.sub.Mo+C.sub.W, is greater than 5.5 at % at a temperature of from 1000 C. to 1100 C., C.sub.Mo and C.sub.W being the concentrations of molybdenum and tungsten in at %.

The invention relates to a nickel-based alloy having a microstructure with a matrix of -phase and precipitates of -phase. The -phase comprises a percentage by volume of from 50 vol % to 80 vol % in the temperature range of from 1000 C. to 1100 C. The nickel-based alloy comprises 8 to 13 at % aluminum, 3 to 14 at % cobalt, 4 to 12 at % chromium, 0.6 to 8 at % molybdenum, 0 to 6 at % rhenium, 0.5 to 4 at % tantalum, 0.5 to 4 at % titanium, 0.3 to 3.5 at % tungsten, 0 to 4 at % germanium, 0 to 0.6 at % hafnium, 0 to 4 at % ruthenium, balance nickel and unavoidable impurities. The concentrations of molybdenum and tungsten are selected such that the percentage X of molybdenum and tungsten in the -phase, X=0.84 C.sub.Mo+C.sub.W, is greater than 5.5 at % at a temperature of from 1000 C. to 1100 C., C.sub.Mo and C.sub.W being the concentrations of molybdenum and tungsten in at %.

High-density thermodynamically stable nanostructured copper-based metallic systems, and methods of making, are presented herein. A ternary high-density thermodynamically stable nanostructured copper-based metallic system includes: a solvent of copper (Cu) metal; that comprises 50 to 95 atomic percent (at. %) of the metallic system; a first solute metal dispersed in the solvent that comprises 0.01 to 50 at. % of the metallic system; and a second solute metal dispersed in the solvent that comprises 0.01 to 50 at. % of the metallic system. The internal grain size of the solvent is suppressed to no more than 250 nm at 98% of the melting point temperature of the solvent and the solute metals remain uniformly dispersed in the solvent at that temperature. Processes for forming these metallic systems include: subjecting powder metals to a high-energy milling process, and consolidating the resultant powder metal subjected to the milling to form a bulk material.