The present invention discloses a method of preparing a catalyst for low-temperature synergistic catalytic purification of NO.sub.x and HCN in a flue gas, and the use thereof. Citric acid is dissolved in ethanol to obtain a citric acid/ethanol solution; tetrabutyl titanate is added, mixed uniformly to obtain a tetrabutyl titanate-citric acid/ethanol solution; glacial acetic acid is added dropwise to react for 30-40 min to obtain a solution A; the metal salt solution was added dropwise into the solution A, mixed uniformly and added with nitric acid, ammonium hydroxide is added dropwise to adjust the pH value, and the temperature is raised at a constant speed to obtain a gel B; dried and then then baked at a temperature of 300-500° C. for 3-4 h, cooled in the furnace, pulverized, tableted and sieved to obtain the catalyst for the low-temperature synergistic catalytic purification of NO.sub.x and HCN in the flue gas.

Compositions of manganese accumulating plants.

Compositions of manganese accumulating plants.

This invention relates to a supported catalyst for synthesizing ammonia (NH3) from nitrogen gas (N2) and hydrogen gas (H2), method of making the support, and methods of decorating the support with the catalyst.

[Solution] The present invention relates to a method for partially oxidizing an alkane, including contacting an alkane with a supported catalyst in a presence of an oxidizer to convert the alkane into an aldehyde, wherein the supported catalyst is composed of a bimetallic oxide and a support carrying the bimetallic oxide, and the bimetallic oxide is represented by the following formula and includes oxygen and two metals selected from metals of groups 8 to 10 of the periodic table:

A.sub.mB.sub.nO.sub.x wherein the bimetallic oxide and support are each a metal selected from metallic elements of groups 8 to 10 of the periodic table; the bimetallic oxide and support are not the same metallic element; m, n, and x mean amounts ((mmol)) of the bimetallic oxide, the support, and oxygen, respectively, per 1 g of the supported catalyst; m is more than 0 [mmol/g-cat] and less than 1 [mmol/g-cat]; n is more than 0 [mmol/g-cat] and less than 1 [mmol/g-cat]; and x is a value [mmol/g-cat] satisfying oxidation states of the bimetallic oxide and the support.

Methods of depolymerizing polyolefin-based material into useful petrochemical products using supported metal oxides and heat are described. The supported metal oxides improve the depolymerization reaction by decreasing the half time for the depolymerization, which results in a higher depolymerization rate and a shorter residence time in the depolymerization unit, allowing for a predictable depolymerization reaction, and decreasing the branching or aromatic formations in the product.

A metal oxide catalyst synthesized using supercritical carbon dioxide extraction is provided, wherein the metal oxide catalyst includes an active site containing at least one type of metal oxide and a support for loading the active site and the metal oxide is an oxide of a metal selected from the group consisting of transition metals (atomic number 21 to 29, 39 to 47, 72 to 79, or 104 to 108), lanthanide (atomic number 57 to 71), post-transition metals (atomic number 13, 30 to 31, 48 to 50, 80 to 84, and 112), and metalloids (atomic number 14, 32 to 33, 51 to 52, and 85) in the periodic table, and a combination thereof.

A metal oxide catalyst synthesized using supercritical carbon dioxide extraction is provided, wherein the metal oxide catalyst includes an active site containing at least one type of metal oxide and a support for loading the active site and the metal oxide is an oxide of a metal selected from the group consisting of transition metals (atomic number 21 to 29, 39 to 47, 72 to 79, or 104 to 108), lanthanide (atomic number 57 to 71), post-transition metals (atomic number 13, 30 to 31, 48 to 50, 80 to 84, and 112), and metalloids (atomic number 14, 32 to 33, 51 to 52, and 85) in the periodic table, and a combination thereof.

High surface area, high entropy oxides comprising multiple metal cations in a single-phase fluorite lattice material enables intrinsic catalytic activity without platinum group metals, tunable oxygen storage capacity, and thermal stability. These properties can be obtained through a facile sol-gel synthesis to provide a low-temperature route for production of phase-pure multi-cationic oxides. The resulting materials achieved significantly higher surface area and catalytic performance, taking advantage of all the properties endowed by the various cations in the composition.

High surface area, high entropy oxides comprising multiple metal cations in a single-phase fluorite lattice material enables intrinsic catalytic activity without platinum group metals, tunable oxygen storage capacity, and thermal stability. These properties can be obtained through a facile sol-gel synthesis to provide a low-temperature route for production of phase-pure multi-cationic oxides. The resulting materials achieved significantly higher surface area and catalytic performance, taking advantage of all the properties endowed by the various cations in the composition.