A composition of an indium oxide catalyst including an alkali dopant and a method for producing an indium oxide catalyst including an alkali dopant. The alkali dopant may include a cation of Li.sup.+, Na.sup.+, K.sup.+, Rb.sup.+, Cs.sup.+, and Fr.sup.+. The method for producing the indium oxide catalyst including an alkali dopant includes mixing a solution of an indium salt with a base to form precipitated indium hydroxide, contacting the precipitated indium hydroxide with a solution including an alkali metal salt to produce an indium hydroxide solution, and calcinating the indium hydroxide solution to form indium oxide; thereby forming the indium oxide catalyst including an alkali dopant.

A catalytic composition from earth-abundant transition metal salts and biomass is disclosed. A calcined catalytic composition formed from soybean powder and ammonium molybdate is specifically exemplified herein. Methods for making the catalytic composition are disclosed as are electrodes for hydrogen evolution reactions comprising the catalytic composition.

A one-step process to synthesize narrow band gap TiO.sub.2TiC core-shell particles is described. A mixture of a fuel source, particularly a hydrocarbon, and a titanium precursor is detonated with a source of oxygen in a constant volume reaction vessel to produce TiO.sub.2TiC core-shell particles. This process can synthesize TiO.sub.2TiC core-shell structures with tailored morphology, size, phase, absorption behavior, and other hybrid morphologies with different properties depending on the Ti/C ratio used in the feed.

A one-step process to synthesize narrow band gap TiO.sub.2TiC core-shell particles is described. A mixture of a fuel source, particularly a hydrocarbon, and a titanium precursor is detonated with a source of oxygen in a constant volume reaction vessel to produce TiO.sub.2TiC core-shell particles. This process can synthesize TiO.sub.2TiC core-shell structures with tailored morphology, size, phase, absorption behavior, and other hybrid morphologies with different properties depending on the Ti/C ratio used in the feed.

A process for facilitating the unloading of a fixed bed of cobalt/metal oxide catalyst particles from a reactor tube by (i) feeding a gas comprising 10 to 30 (vol/vol) percent of oxygen to the reactor tube with a GHSV for oxygen of 0.5 to 50 Nl/l/hr, and (ii) removing the catalyst particles from the reactor tube. In the fixed bed of catalyst particles to which the oxygen comprising gas is fed in step (i) at most 10 mole % of the element cobalt is present in Co3O4 and/or CoO, calculated on the total amount of moles of cobalt in the catalyst particles.

A process for facilitating the unloading of a fixed bed of cobalt/metal oxide catalyst particles from a reactor tube by (i) feeding a gas comprising 10 to 30 (vol/vol) percent of oxygen to the reactor tube with a GHSV for oxygen of 0.5 to 50 Nl/l/hr, and (ii) removing the catalyst particles from the reactor tube. In the fixed bed of catalyst particles to which the oxygen comprising gas is fed in step (i) at most 10 mole % of the element cobalt is present in Co3O4 and/or CoO, calculated on the total amount of moles of cobalt in the catalyst particles.

A method for producing a tetrafluoroolefin, such as 2,3,3,3-tetrafluoropropene (HFO-1234yf), comprises dehydrofluorinating a pentafluoroalkane in a gas phase in the presence of a catalyst comprising chromium oxyfluoride. In a preferred embodiment, 2,3,3,3-tetrafluoropropene (HFO-1234yf) is produced by forming a catalyst comprising chromium oxyfluoride by calcining CrF.sub.3.xH.sub.2O, where x is 1-10, in the presence of a flowing gas comprising nitrogen to form a calcined chromium oxyfluoride, and dehydrofluorinating 1,1,1,2,2-pentafluoropropane (HFC-245cb) in a gas phase in the presence of the catalyst to form the 2,3,3,3-tetrafluoropropene (HFO-1234yf).

A method for producing a tetrafluoroolefin, such as 2,3,3,3-tetrafluoropropene (HFO-1234yf), comprises dehydrofluorinating a pentafluoroalkane in a gas phase in the presence of a catalyst comprising chromium oxyfluoride. In a preferred embodiment, 2,3,3,3-tetrafluoropropene (HFO-1234yf) is produced by forming a catalyst comprising chromium oxyfluoride by calcining CrF.sub.3.xH.sub.2O, where x is 1-10, in the presence of a flowing gas comprising nitrogen to form a calcined chromium oxyfluoride, and dehydrofluorinating 1,1,1,2,2-pentafluoropropane (HFC-245cb) in a gas phase in the presence of the catalyst to form the 2,3,3,3-tetrafluoropropene (HFO-1234yf).

An SCR-active zeolite catalyst and a method for producing same. To produce the catalyst, an Fe ion-exchanged zeolite is initially subjected to a first temperature treatment within a range of 300 to 600 C. in a reducing hydrocarbon atmosphere such that the oxidation state of the Fe ions decreases and/or the dispersity of the Fe ions on the zeolite increases, whereupon the reduced zeolite is subjected to a second temperature treatment within a range of 300 to 600 C. in an oxidizing atmosphere such that hydrocarbon residues or carbon residues are oxidatively removed, the zeolite being calcined to obtain a catalyst material during the two temperature treatments. Iron contained in the zeolite is stabilized in an oxidation state of less than +3 and/or the dispersity of the Fe ions on the zeolite is permanently increased such that a high SCR activity is achieved within a temperature range of less than 300 C.

The present invention relates to a method for producing supported catalysts, comprising: providing a metal foam element A, which consists of metallic cobalt, an alloy of nickel and cobalt, or an arrangement of layers of nickel and cobalt, lying one over the other; applying an aluminum-containing powder MP to metal foam element A in order to obtain metal foam element AX; thermally treating metal foam element AX to achieve alloy formation between metal foam element A and aluminum-containing powder MP, in order to obtain metal foam element B; oxidatively treating metal foam element B, in order to obtain metal foam element C; and applying a catalytically active layer, comprising at least one support oxide and at least one catalytically active component, to at least part of the surface of metal foam element C, in order to obtain a supported catalyst. The present invention further relates to the supported catalysts that can be obtained using the method and to the use of said supported catalysts in chemical transformations.