Abstract:
A method of making metallic carbide powders includes heating a non-static solid reactant mixture of a metal oxide and a source of carbon to a first elevated temperature which is sufficient to cause at least partial carburization of the mixture. The heating is performed in a non-reducing atmosphere having a total pressure of at least one atmosphere for a sufficient time to form a partially-carburized mixture. The source of carbon is employed at a level which is less than the stoichiometric amount needed to produce the metallic carbide. The method may further include admixing a sufficient level of a source of carbon to the partially-carburized mixture to form an adjusted mixture having a total carbon content of the stoichiometric amount needed to make the metallic carbide and carburizing the adjusted mixture in a hydrogen-containing atmosphere at a second elevated temperature which is sufficient to cause the adjusted mixture to form the metallic carbide having a particle size of less than 0.2 micrometers in diameter.
Abstract:
A low temperature method for synthesizing micrograin tungsten carbide particles having an average diameter of 0.05 to 0.2 mu m includes the programmed heating of tungsten trioxide powder or other material containing tungsten in a flowing molecular hydrogen atmosphere having a constant proportion of molecular methane. The heating program is carried out at two different heating rates, the first being higher than the second. The first heating rate is 5 DEG C to 50 DEG C per minute from 25 DEG C to 535 DEG C. The second heating rate is 1 DEG C to 10 DEG C per minute from 535 DEG C to about 850 DEG C. The last temperature is then held until conversion of the tungsten trioxide or other tungsten-containing material to tungsten carbide is complete, typically from about 15 minutes to 3 hours.
Abstract:
A multi-phase cemented ceramic material useful for metal working, including ferrous metals, titanium, aluminum and other metals. The material preferably has a microstructure which includes platelets, a range of grain sizes which yields superior hardness and other characteristics, and a low tungsten concentration within the binder phase. The preferred composition includes ultrafine WC, an ultrafine solid solution of (Ti, Ta, W)C, and a cobalt binder. Platelets are formed in situ, eliminating the need to add them during manufacture for improving toughness.
Abstract:
Prepare silicon nitride-silicon carbide composite powders by carbothermal reduction of crystalline silica powder, carbon powder and, optionally, crystalline silicon nitride powder. The crystalline silicon carbide portion of the composite powders has a mean number diameter less than about 700 nanometers and contains nitrogen. The composite powders may be used to prepare sintered ceramic bodies and self-reinforced silicon nitride ceramic bodies.
Abstract:
A method for making submicrometer metallic carbides and submicrometer solid solution metallic carbides from a source of at least one metallic oxide and carbon involves the rapid heating of a reactive particulate mixture of the source(s) and carbon in order to achieve a resulting particulate size of less than 1 micrometer. The rapid heating may produce either a finished product or a precursor. If a precursor is produced, it may be admixed with additional carbon and subjected to a second rapid heating step to prepare a finished product. Submicrometer sized metallic carbides and solid solution metallic carbides were suitable for use in commercial ceramic applications. The smaller sized particles produce a product having superior toughness and hardness.
Abstract:
A transition metal carbide-Group VIII metal powder comprising discrete particles of a transition metal carbide and Group VIII metal wherein: substantially all of the particles have a size of at most 0.4 micrometer; the transition metal carbide is selected from carbides of the group consistig of tungsten, titanium, tantalum, molybdenum, zirconium, hafnium, vanadium, niobium, chromium, mixtures and solid solutions thereof; and the Group VIII metal is selected from the group consisting of iron, cobalt, nickel, mixtures and solid solutions thereof. Said powders were produced by heating an admixture comprising a finishing source of carbon (for example, acetylene black), a source of a group VIII metal (for example, Co3O4), and a particulate precursor to a temperature of 1173K to 1773K for a time sufficient to form a transition metal carbide-Group VIII metal powder, wherein at least 25 percent by weight of the carbide precursor is carburized in forming the transition metal carbide of the transition metal carbide-Group VIII metal powder. The particulate precursor generally contains less than 2.5 percent oxygen by weight and contains compounds which undergo carburization such as a transition metal (for example, W), lower valence transition metal carbide (W2C) to form the transition metal carbide (for example, WC)-Group VIII metal powder.
Abstract:
Ceramic-ceramic and ceramic-metal composite materials are disclosed which contain at least two ceramic phases and at least one metallic phase. At least one of these ceramic phases is a metal boride or mixture of metal borides and another of the ceramic phases is a metallic nitride, metallic carbide, or a mixture of metallic nitride and a metallic carbide. These composite materials may be made by a combustion synthesis process which includes the step of igniting a mixture of at least one element selected from titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, aluminum and silicon, or a combination of two or more thereof, at least one boron compound selected from boron nitride, boron carbide, or a combination thereof and an ignition temperature reducing amount of a metal selected from iron, cobalt, nickel, copper, aluminum, silicon, palladium, platinum, silver, gold, ruthenium, rhodium, osmium, and iridium, or a mixture of two or more thereof, provided that at least one of the aforementioned elements is different from at least one of the aforementioned metals. This process permits a high degree of control over the microstructure of the product and relatively low pressures are required to obtain high composite material density. A densified product having high density and a finely grained microstructure may be obtained by applying mechanical pressure during combustion synthesis. The composites have improved hardness, toughness, strength, resistance to wear, and resistance to catastrophic failure.
Abstract:
A method of making metallic carbide powders includes heating a non-static solid reactant mixture of a metal oxide and a source of carbon to a first elevated temperature which is sufficient to cause at least partial carburization of the mixture. The heating is performed in a non-reducing atmosphere having a total pressure of at least one atmosphere for a sufficient time to form a partially-carburized mixture. The source of carbon is employed at a level which is less than the stoichiometric amount needed to produce the metallic carbide. The method may further include admixing a sufficient level of a source of carbon to the partially-carburized mixture to form an adjusted mixture having a total carbon content of the stoichiometric amount needed to make the metallic carbide and carburizing the adjusted mixture in a hydrogen-containing atmosphere at a second elevated temperature which is sufficient to cause the adjusted mixture to form the metallic carbide having a particle size of less than 0.2 micrometers in diameter.
Abstract:
A method for forming monotungsten carbide, comprising heating a solid, non-elemental tungsten-containing material in a flowing atmosphere containing molecular hydrogen and molecular methane for a time sufficient to convert substantially all of the tungsten-containing material to monotungsten carbide, The heating brings the temperature of the tungsten-containing material to a first elevated temperature of from about 520 to about 550 DEG C. and, subsequently, at a rate of from about 3 to about 10 DEG C. per minute, the heating brings the temperature from the first elevated temperature to a second elevated temperature of about 800 to about 900 DEG C. Thereafter the temperature is held at the second elevated temperature for at least about 15 minutes. At least about 50 weight percent of the monotungsten carbide formed is formed while holding the temperature at the second elevated temperature.