Methods and compostions involving high specific surface area carbides and nitrides
AssigneeThe Board of Trustees of the Leland Stanford Junior University, Stanford University
InventorsMichel Boudart, Shigeo T. Oyama, Leo Volpe
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Abstract
Methods and compostions produced thereby are provided concerning the preparation and use of high specific surface area carbides and nitrides. The carbides and nitrides can be obtained by thermal reduction of oxides in the presence of a source of carbon and nitrogen respectively, with relatively slow progressive temperature increases prior to completion of the reaction, followed by quenching. Novel metastable carbides can be obtained by carburization of nitrides having high surface area, which nitrides can be prepared by the above-described process.
Claims18
A high specific surface area metal carbide or nitride, wherein said metal is molybdenum, tungsten, titanium, chromium, zirconium, niobium, vanadium, tantalum, hafnium, or rhenium, said carbides and nitrides being prepared from the respective metal oxides and resulting in at least a 5-fold increase in surface area over that of said oxide, produced by a method which comprises:
- heating said oxide substantially uniformly and continuously at a rate in the range of 0.1.degree. to 5.degree. C./min for at least 20 minutes in the presence of a reducing environment and a source of carbon or nitrogen from a temperature at least 25.degree. C. prior to substantial completion of formation of said carbide or nitride, and through a temperature range wherein reduction of said oxide and reaction with carbon or nitrogen of said source occurs to form a carbide or nitride reaction product, respectively, whereby an effluent is formed comprising an unreacted portion of said source and gases resulting from reaction of said source with said oxide, and wherein said heating continues to a final temperature until said reaction is substantially complete as evidenced by the substantial absence of change in the composition of said effluent;
- lowering the temperature of the reaction product by at least 25.degree. C. by stopping the heating after reaching the final temperature or after maintaining the final temperature for the lesser of about one hour or about 50 percent of the time of said heating;
- and
- wherein said carbide or nitride is characterized by a particle of a size in the range of about 1 to 15 nm and having a specific surface area of at least about 40 m.sup.2 /g when measured by BET method.
A method for preparing a thermodynamically metastable metal carbide, wherein said metal is molybdenum, vanadium, tungsten, titanium, chromium, zirconium, niobium, tantalum, hafnium, rhenium, said method comprising:
- heating a nitride having a particle size in the range of about 1 to 15 nm and a specific surface area of at least about 40 m.sup.2 /g when measured by BET method in the presence of a carbon source at a temperature in the range of about 500.degree.-1500.degree. C. for a sufficient time to substantially displace all of the nitrogen with carbon, wherein a thermodynamically metastable carbide is formed;
- and
- isolating said thermodynamically metastable carbide having substantially the same crystal structure as said nitride.
A catalyst consisting essentially of a face-centered cubic molybdenum or tungsten carbide having crystals of a mean diameter in the range of about 1-15 nm, and having a specific surface area of at least 40 m.sup.2 /g when measured by BET method.
A high specific surface area metal carbide or nitride, wherein said metal is molybdenum, tungsten, titanium, chromium, zirconium, niobium, vanadium, tantalum, hafnium, or rhenium, said carbides and nitrides being prepared from the respective metal oxides and resulting in at least a 5-fold increase in surface area over that of said oxide, produced by a method which comprises:
- heating said oxide uniformly and continuously at a rate in the range of about 0.1.degree. to 5.degree. C./min for at least 20 minutes in the presence of a reducing environment and a source of carbon or nitrogen from a temperature at least 25.degree. C. prior to completion of formation of said carbide or nitride, and through a temperature range wherein reduction of said oxide and reaction with carbon and nitrogen of said source occurs to form a carbide or nitride reaction product, respectively, whereby an effluent is formed comprising an excess unreacted portion of said source and gases resulting from reaction of said source with said oxide, and wherein said heating continues to a final temperature until said reaction is complete as evidence by the absence of change in the composition of said effluent;
- lowering the temperature of the reaction product by a least 25.degree. C. by stopping the heating after reaching the final temperature or after maintaining the final temperature for the lesser of about one hour or about 50% of the time of said heating;
- and
- wherein said carbide or nitride is further characterized by a particle of a size in the range of about 1 to 15 nm and having a specific surface area of at least about 40 m.sup.2 /g when measured by BET method.
A method for preparing a thermodynamically metastable metal carbide, wherein said metal is molybdenum, vanadium, tungsten, titanium, chromium, zirconium, niobium, tantalum, hafnium or rhenium, said method comprising:
- heating a nitride having a particle size in the range of about 1 to 15 nm and specific surface area of at least about 40 m.sup.2 /g when measured by BET method, in the presence of a carbon source at a temperature range of about 500.degree.-1500.degree. C. for a sufficient time to substantially displace all of the nitrogen with carbon, wherein a thermodynamically metastable carbide is formed;
- and
- isolating said thermodynamically metastable carbide having substantially the same crystal structure as said nitride.
Dependencies are inferred from the claim text.