Provided are: a cleaning agent for a denitration catalyst; and a denitration catalyst regeneration method and a denitration catalyst regeneration system which make it possible to efficiently remove matter adhering to a surface of a catalyst and to greatly restore catalytic performance. The regeneration method includes: a prewashing step (S12) of washing a denitration catalyst with water; a liquid agent cleaning step (S14) of immersing the denitration catalyst washed with water in a liquid agent containing an inorganic acid and a fluorine compound; a step of recovering the denitration catalyst from the liquid agent; and a finish washing step (S16) of washing the denitration catalyst recovered from the liquid agent with a finish cleaning liquid which is water or sulfamic acid-containing water.

The invention relates to a catalyst composition suitable for the dehydrogenation of paraffins having 2-8 carbon atoms comprising zinc oxide and titanium dioxide, optionally further comprising oxides of cerium (Ce), dysprosium (Dy), erbium (Er), europium (Eu), gadolinium (Gd), lanthanum (La), neodymium (Nd), praseodymium (Pr), samarium (Sm), terbium (Tb), ytterbium (Yb), yttrium (Y), tungsten (W) and Zirconium (Zr) or mixtures thereof, wherein said catalyst composition is substantially free of chromium and platinum. The catalysts possess unique combinations of activity, selectivity, and stability. Methods for preparing improved dehydrogenation catalysts and a process for dehydrogenating paraffins having 2-8 carbon atoms, comprising contacting the mixed metal oxide catalyst with paraffins are also described. The catalyst may also be disposed on a porous support in an attrition-resistant form and used in a fluidized bed reactor.

A method and apparatus (1) for treating a filter (2) for filtering particulate matter from exhaust gas and a treated filter (2) are described. A reservoir (3) containing a dry powder (4) is provided. A vacuum generator (6) establishes a primary gas flow through a porous structure of the filter (2) by applying a pressure reduction to an outlet face of the filter (2). A spray device (7) receives the dry powder (4) from a transport device (8) and sprays the dry powder (4) towards the inlet face of the filter (2). A controller (9) is configured to control operation of at least the vacuum generator (6) and the spray device (7). The dry powder (4) comprises or consists of a metal compound for forming by thermal decomposition a metal oxide.

A method and apparatus (1) for treating a filter (2) for filtering particulate matter from exhaust gas and a treated filter (2) are described. A reservoir (3) containing a dry powder (4) is provided. A vacuum generator (6) establishes a primary gas flow through a porous structure of the filter (2) by applying a pressure reduction to an outlet face of the filter (2). A spray device (7) receives the dry powder (4) from a transport device (8) and sprays the dry powder (4) towards the inlet face of the filter (2). A controller (9) is configured to control operation of at least the vacuum generator (6) and the spray device (7). The dry powder (4) comprises or consists of a metal compound for forming by thermal decomposition a metal oxide.

A process for the fluorination of a chlorinated C3 alkane or alkene compound having at least one chlorine atom into a fluorinated C3 alkane or alkene compound having at least one fluorine atom includes the following steps: a) contacting, in a reactor, the chlorinated compound with hydrogen fluoride in gas phase in the presence of a fluorination catalyst to produce a fluorinated compound, and b) regenerating the fluorination catalyst used in step a). The step (b) of regenerating the fluorination catalyst comprises (c) the treatment of said fluorination catalyst with an oxidizing agent-containing gas flow to form an oxidized fluorination catalyst, and (d) the treatment of the oxidized fluorination catalyst obtained in step (c) with a gaseous mixture comprising a reducing agent and an inert gas. The catalyst regenerated in step b) is reused in step a) and the reducing agent is selected from C.sub.1-C.sub.10 hydrohalocarbons.

A process for the fluorination of a chlorinated C3 alkane or alkene compound having at least one chlorine atom into a fluorinated C3 alkane or alkene compound having at least one fluorine atom includes the following steps: a) contacting, in a reactor, the chlorinated compound with hydrogen fluoride in gas phase in the presence of a fluorination catalyst to produce a fluorinated compound, and b) regenerating the fluorination catalyst used in step a). The step (b) of regenerating the fluorination catalyst comprises (c) the treatment of said fluorination catalyst with an oxidizing agent-containing gas flow to form an oxidized fluorination catalyst, and (d) the treatment of the oxidized fluorination catalyst obtained in step (c) with a gaseous mixture comprising a reducing agent and an inert gas. The catalyst regenerated in step b) is reused in step a) and the reducing agent is selected from C.sub.1-C.sub.10 hydrohalocarbons.

A molybdenum-vanadium bimetal oxide catalyst having a molecular formula of Mo.sub.1V.sub.y, where y represents an atomic molar ratio of vanadium and molybdenum. An oxygen support Mo.sub.1V.sub.y is prepared by an impregnation method including impregnation, drying, calcination, and tablet pressing. In the dehydrogenation reaction of a light alkane to an alkene over the supported molybdenum-vanadium bimetal oxide, the reaction temperature is 450° C.-550° C. Propane can be oxidized and dehydrogenated to produce propylene with a high activity and high selectivity. A conversion rate of propane remains at 30%-40%, and a selectivity for propylene is 80%-90%. A fresh oxygen support changes from a high-valence state to a low-valence state after reacting with propane. A low-valence state oxygen support reacts with air or oxygen to be oxidized to a high-valence state, and recovers lattice oxygen and cycles again.

The present invention relates to preparation of catalyst for production of olefinic hydrocarbons by dehydrogenation of their corresponding paraffins, particularly propylene from propane, comprising a metal oxide or combination of metal oxides utilizing spent catalyst from Fluid Catalytic Cracking (FCC)/Resid Fluid Catalytic Cracking (RFCC) processes. The metal oxides are possibly from transition metal group, particularly from groups VB, VIB, VIII, and Lanthanide series, and at least one metal from alkali group. The catalyst support used is spent catalyst or modified spent catalyst or combination thereof. The said catalyst can be used for both non-oxidative Propane Dehydrogenation (PDH) and Oxidative Propane Dehydrogenation (OPDH) process in the presence of CO.sub.2.

The present invention relates to preparation of catalyst for production of olefinic hydrocarbons by dehydrogenation of their corresponding paraffins, particularly propylene from propane, comprising a metal oxide or combination of metal oxides utilizing spent catalyst from Fluid Catalytic Cracking (FCC)/Resid Fluid Catalytic Cracking (RFCC) processes. The metal oxides are possibly from transition metal group, particularly from groups VB, VIB, VIII, and Lanthanide series, and at least one metal from alkali group. The catalyst support used is spent catalyst or modified spent catalyst or combination thereof. The said catalyst can be used for both non-oxidative Propane Dehydrogenation (PDH) and Oxidative Propane Dehydrogenation (OPDH) process in the presence of CO.sub.2.

Systems and methods are provided for using oxycombustion to provide heat within a reverse flow reactor environment. The oxygen for the oxycombustion can be provided by oxygen stored in an oxygen storage component in the reactor. By using an oxygen storage component to provide the oxygen for combustion during the regeneration step, heat can be added to a reverse flow reactor while reducing or minimizing addition of diluents and while avoiding the need for an air separation unit. As a result, a regeneration flue gas can be formed that is substantially composed of CO.sub.2 and/or H.sub.2O without requiring the additional cost of creating a substantially pure oxygen-containing gas flow.