Patent classifications
B01J23/22
Process for the production of nitric acid with tertiary abatement of N2O and NOx
A nitric acid production process, comprising tertiary abatement of N2O and NOx on a tail gas withdrawn from an absorption stage, said abatement including passing the tail gas over a sequence of a deN2O stage comprising a Fe-z catalyst and a deNOx stage comprising a V2O5-TiO2 catalyst in the presence of gaseous ammonia, wherein the tail gas at the inlet of deN2O stage and the tail gas at the inlet of deNOx stage have a temperature greater than 400° C.
Exhaust gas purifying catalyst
This exhaust gas purifying catalyst is provided with a substrate 10 and a catalyst layer 20 formed on a surface of the substrate 10. The catalyst layer 20 contains zeolite particles 22 that support a metal, and a rare earth element-containing compound 24 that contains a rare earth element. The rare earth element-containing compound 24 is added in such an amount that the molar ratio of the rare earth element relative to Si contained in the zeolite 22 is 0.001 to 0.014 in terms of oxides.
Nitrogen oxide reduction catalyst regenerable at low temperature
Provided is a nitrogen oxide (NO.sub.X) reduction catalyst including an active site including at least one of a metal vanadate expressed by [Chemical Formula 1] and a metal vanadate expressed by [Chemical Formula 2], and a support for loading the active site thereon.
(M.sub.1).sub.XV.sub.2O.sub.X+5 [Chemical Formula 1] (where M.sub.1 denotes one selected from among manganese (Mn), cobalt (Co), and nickel (Ni), and X denotes a real number having a value between 1 and 3.)
(M.sub.2).sub.YVO.sub.4 [Chemical Formula 2] (where M.sub.2 denotes one selected from among lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), promethium (Pm), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), and lutetium (Lu), and Y denotes a real number having a value between 0.5 and 1.5).
Nitrogen oxide reduction catalyst regenerable at low temperature
Provided is a nitrogen oxide (NO.sub.X) reduction catalyst including an active site including at least one of a metal vanadate expressed by [Chemical Formula 1] and a metal vanadate expressed by [Chemical Formula 2], and a support for loading the active site thereon.
(M.sub.1).sub.XV.sub.2O.sub.X+5 [Chemical Formula 1] (where M.sub.1 denotes one selected from among manganese (Mn), cobalt (Co), and nickel (Ni), and X denotes a real number having a value between 1 and 3.)
(M.sub.2).sub.YVO.sub.4 [Chemical Formula 2] (where M.sub.2 denotes one selected from among lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), promethium (Pm), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), and lutetium (Lu), and Y denotes a real number having a value between 0.5 and 1.5).
CATALYST WITH A CORE-SHELL STRUCTURE FOR METHANE OXIDATION, METHOD OF PREPARING THE SAME AND METHOD OF OXIDIZING METHANE USING THE SAME
A catalyst with a core-shell structure for methane oxidation, a method of preparing the catalyst, and a method of methane oxidation using the catalyst are disclosed. The catalyst includes a core structure consisting of a nano-support and core nanoparticles; and a shell coating layer coated on the core structure in which the core nanoparticles have a particle diameter smaller than that of the nano-support and are coated on the nano-support to form a core structure. The catalyst has excellent thermal stability during methane oxidation reaction at high temperature and an effect of increasing methane conversion and formaldehyde selectivity.
CATALYST WITH A CORE-SHELL STRUCTURE FOR METHANE OXIDATION, METHOD OF PREPARING THE SAME AND METHOD OF OXIDIZING METHANE USING THE SAME
A catalyst with a core-shell structure for methane oxidation, a method of preparing the catalyst, and a method of methane oxidation using the catalyst are disclosed. The catalyst includes a core structure consisting of a nano-support and core nanoparticles; and a shell coating layer coated on the core structure in which the core nanoparticles have a particle diameter smaller than that of the nano-support and are coated on the nano-support to form a core structure. The catalyst has excellent thermal stability during methane oxidation reaction at high temperature and an effect of increasing methane conversion and formaldehyde selectivity.
Method for cleaning viscose production off-gases and catalysts for use in the method
A method for cleaning an off-gas from viscose production, essentially containing H.sub.2S and CS.sub.2, comprises passing the gas through a catalytic reactor containing a direct oxidation type catalyst, such as V.sub.2O.sub.5 on silica, to convert H.sub.2S in the gas to elemental sulfur, SO.sub.2 or mixtures thereof, either via the oxygen present in the gas or via oxygen added to the gas stream. Elemental sulfur and SO.sub.2 are removed from the effluent gas from the catalytic reactor, and the unconverted CS.sub.2 is recycled to the viscose production process.
Method for cleaning viscose production off-gases and catalysts for use in the method
A method for cleaning an off-gas from viscose production, essentially containing H.sub.2S and CS.sub.2, comprises passing the gas through a catalytic reactor containing a direct oxidation type catalyst, such as V.sub.2O.sub.5 on silica, to convert H.sub.2S in the gas to elemental sulfur, SO.sub.2 or mixtures thereof, either via the oxygen present in the gas or via oxygen added to the gas stream. Elemental sulfur and SO.sub.2 are removed from the effluent gas from the catalytic reactor, and the unconverted CS.sub.2 is recycled to the viscose production process.
DOPED CARBONACEOUS MATERIALS FOR PHOTOCATALYTIC REMOVAL OF POLLUTANTS UNDER VISIBLE LIGHT, MAKING METHODS AND APPLICATIONS OF SAME
A method of synthesizing a doped carbonaceous material includes mixing a carbon precursor material with at least one dopant to form a homogeneous/heterogeneous mixture; and subjecting the mixture to pyrolysis in an inert atmosphere to obtain the doped carbonaceous material. A method of purifying water includes providing an amount of the doped carbonaceous material in the water as a photocatalyst; and illuminating the water containing the doped carbonaceous material with visible light such that under visible light illumination, the doped carbonaceous material generates excitons (electron-hole pairs) and has high electron affinity, which react with oxygen and water adsorbed on its surface forming reactive oxygen species (ROS), such as hydroxyl radicals and superoxide radicals, singlet oxygen, hydrogen peroxide, that, in turn, decompose pollutants and micropollutants.
DOPED CARBONACEOUS MATERIALS FOR PHOTOCATALYTIC REMOVAL OF POLLUTANTS UNDER VISIBLE LIGHT, MAKING METHODS AND APPLICATIONS OF SAME
A method of synthesizing a doped carbonaceous material includes mixing a carbon precursor material with at least one dopant to form a homogeneous/heterogeneous mixture; and subjecting the mixture to pyrolysis in an inert atmosphere to obtain the doped carbonaceous material. A method of purifying water includes providing an amount of the doped carbonaceous material in the water as a photocatalyst; and illuminating the water containing the doped carbonaceous material with visible light such that under visible light illumination, the doped carbonaceous material generates excitons (electron-hole pairs) and has high electron affinity, which react with oxygen and water adsorbed on its surface forming reactive oxygen species (ROS), such as hydroxyl radicals and superoxide radicals, singlet oxygen, hydrogen peroxide, that, in turn, decompose pollutants and micropollutants.