Patent classifications
B01J27/232
METHODS AND MATERIALS FOR DIRECT NOX DECOMPOSITION IN LEAN EXHAUST GASES
A noble metal-free lanthanum transition metal perovskite catalyst material. The noble metal-free lanthanum transition metal perovskite catalyst material may include a two phase mixture of a lanthanum transition metal perovskite with an alkali or alkaline earth metal carbonate, a lanthanum transition metal perovskite doped with an alkali or alkaline earth metal, or a combination thereof. The lanthanum transition metal perovskite catalyst material provides direct decomposition of NOx into N.sub.2 and O.sub.2 without the presence of a noble metal and in the presence of excess O.sub.2.
Method for producing trifluoroethylene
A method to stably produce trifluoroethylene with a high selectivity by reacting 1,1,1,2-tetrafluoroethane with a solid reactant and suppressing the formation of by-products such as polymer carbon is provided. In the method, a material gas containing 1,1,1,2-tetrafluoroethane passes through a layer consisting of a particulate solid reactant having an average particle size of from 1 μm to 5,000 μm to bring the solid reactant and 1,1,1,2-tetrafluoroethane into contact with each other in a state where the layer consisting of the solid reactant is fluidized.
Method for producing trifluoroethylene
A method to stably produce trifluoroethylene with a high selectivity by reacting 1,1,1,2-tetrafluoroethane with a solid reactant and suppressing the formation of by-products such as polymer carbon is provided. In the method, a material gas containing 1,1,1,2-tetrafluoroethane passes through a layer consisting of a particulate solid reactant having an average particle size of from 1 μm to 5,000 μm to bring the solid reactant and 1,1,1,2-tetrafluoroethane into contact with each other in a state where the layer consisting of the solid reactant is fluidized.
METATHESIS CATALYST AND PROCESS FOR PRODUCING OLEFIN
The present invention provides a catalyst comprising a transition metal, an inorganic support, a zeolite, and a layered double hydroxide. Using of the catalyst according to the present invention in an olefin production process exhibits high activity and high selectivity with decreased deactivation rate, therefore longer reaction cycle can be performed and catalyst life is prolonged.
CATALYST SYSTEM FOR OLEFIN METATHESIS
The present invention relates to a catalyst system for olefin metathesis, the catalyst system comprising: a) a first system zone substantially comprising a layered double hydroxide; and b) a second system zone comprising a metathesis catalyst.
CATALYST SYSTEM FOR OLEFIN METATHESIS
The present invention relates to a catalyst system for olefin metathesis, the catalyst system comprising: a) a first system zone substantially comprising a layered double hydroxide; and b) a second system zone comprising a metathesis catalyst.
Process for preparing propylene oxide
A continuous process for the preparation of propylene oxide, comprising (i) providing a liquid feed stream comprising propene, hydrogen peroxide, acetonitrile, water, optionally propane, and at least one dissolved potassium salt; (ii) passing the feed stream provided in (i) into an epoxidation reactor comprising a catalyst comprising a titanium zeolite of structure type MWW, and subjecting the feed stream to epoxidation reaction conditions in the epoxidation reactor, obtaining a reaction mixture comprising propylene oxide, acetonitrile, water, the at least one potassium salt, optionally propene, and optionally pane; (iii) removing an effluent stream from the epoxidation reactor, the effluent stream comprising propylene oxide, acetonitrile, water, at least a portion of the at least one potassium salt, optionally propene, and optionally propane.
Process for preparing propylene oxide
A continuous process for the preparation of propylene oxide, comprising (i) providing a liquid feed stream comprising propene, hydrogen peroxide, acetonitrile, water, optionally propane, and at least one dissolved potassium salt; (ii) passing the feed stream provided in (i) into an epoxidation reactor comprising a catalyst comprising a titanium zeolite of structure type MWW, and subjecting the feed stream to epoxidation reaction conditions in the epoxidation reactor, obtaining a reaction mixture comprising propylene oxide, acetonitrile, water, the at least one potassium salt, optionally propene, and optionally pane; (iii) removing an effluent stream from the epoxidation reactor, the effluent stream comprising propylene oxide, acetonitrile, water, at least a portion of the at least one potassium salt, optionally propene, and optionally propane.
METHOD FOR PRODUCING METAL CARBONATE AND CATALYST FOR PRODUCING THE SAME
A method for producing metal carbonate is disclosed. The method includes the following steps of providing a first mixture of metal and a catalyst containing iron, NO groups, and N-containing ligands first; then introducing carbon dioxide to the first mixture to form a second mixture and obtaining a product. The method described here can improve the yield and decrease the cost of metal carbonate production.
Method for producing porous molded body, method for producing catalyst for α-olefin dimerization, method for producing α-olefin dimer, porous molded body, and catalyst for α-olefin dimerization
Provided is a method of producing a porous molded body, the method including: the step of obtaining a molded body by molding a raw material that contains from 1 part by mass to 100 parts by mass of a bicarbonate compound (A) represented by AHCO.sub.3 (wherein, A represents Na or K) and from 0 parts by mass to 99 parts by mass of a compound (B) represented by B.sub.nX (wherein, B represents Na or K; X represents CO.sub.3, SO.sub.4, SiO.sub.3, F, Cl, or Br; and n represents an integer of 1 or 2 as determined by the valence of X) (provided that a total amount of (A) and (B) is 100 parts by mass); and the step of obtaining a porous molded body by performing a heat treatment of the molded body in a temperature range of from 100° C. to 500° C. and an atmosphere that contains water vapor in an amount of from 1.0 g/m.sup.3 to 750,000 g/m.sup.3 and thereby thermally decomposing not less than 90% by mass of the bicarbonate compound (A).