Patent classifications
B01J35/50
SELECTIVE HYDROGENATION METHODS
The present disclosure relates to methods for selectively hydrogenating acetylene, to methods for starting up a selective hydrogenation reactor, and to hydrogenation catalysts useful in such methods. In one aspect, the disclosure provides a method for selectively hydrogenating acetylene, the method comprising contacting a catalyst composition with a process gas. The catalyst composition comprises a porous support, palladium, and one or more ionic liquids. The process gas includes ethylene, present in the process gas in an amount of at least 20 mol. %; acetylene, present in the process gas in an amount of at least 1 ppm; and 0 to 190 ppm or at least 600 ppm carbon monoxide. At least 90% of the acetylene present in the process gas is hydrogenated, and the selective hydrogenation is conducted without thermal runaway.
SELECTIVE HYDROGENATION METHODS AND CATALYSTS
The present disclosure relates to methods for selectively hydrogenating acetylene, to methods for starting up a selective hydrogenation reactor, and to hydrogenation catalysts useful in such methods. In one aspect, the disclosure provides a method for selectively hydrogenating acetylene, the method comprising contacting a catalyst composition with a process gas. The catalyst composition comprises a porous support, palladium, and one or more ionic liquids. The process gas includes ethylene, present in the process gas in an amount of at least 20 mol. %; and acetylene, present in the process gas in an amount of at least 1 ppm. At least 90% of the acetylene present in the process gas is hydrogenated, and the selective hydrogenation is conducted without thermal runaway. Notably, the process gas is contacted with the catalyst at a gas hourly space velocity (GHSV) based on total catalyst volume in one bed or multiple beds of at least 7,100 h.sup.1.
METHOD FOR PRODUCING ALIPHATIC LINEAR PRIMARY ALCOHOLS
Provided are a method of preparing a linear primary alcohol, a catalyst for converting an -olefin into an alcohol, and a method of converting an -olefin into a linear primary alcohol, and the method of preparing a linear primary alcohol according to the present invention includes: charging a reactor with a heterogeneous catalyst including a cobalt oxide and a C.sub.n olefin (S1); bringing the heterogeneous catalyst including a cobalt oxide into contact with the C.sub.n olefin (S2); and supplying the reactor with a synthetic gas to obtain a C.sub.n+1 alcohol (S3).
Ag-Pd CORE-SHELL PARTICLE AND USE THEREOF
The manufacturing method provided by the present invention provides a powder material substantially comprising AgPd core-shell particles consisting of Ag core particles containing silver as a principal constituent element and a Pd shell containing palladium as a principal constituent element covering at least part of the surface of the Ag core particles, wherein hydroquinone and/or a quinone is attached to the surface of the AgPd core-shell particles.
Typically, when the powder material is in a dispersed state in a specific medium, a Z average particle diameter (D.sub.DLS) based on the dynamic light scattering (DLS) method is 0.1 m to 2 m, and the polydispersity index (PDI) based on the dynamic light scattering method is 0.4 or lower.
Method for the hydrotreatment of diesel cuts using a catalyst made from an amorphous mesoporous alumina having high connectivity
There is described a hydroprocessing process of at least one gas oil cut having a weighted mean temperature (TMP) between 240 C. and 350 C. using a catalyst comprising at least one metal of the group VIB and/or at least one metal of the group VIII of the periodic classification and a support comprising an amorphous mesoporous alumina having a connectivity (Z) greater than 2.7, the hydroprocessing process operating at a temperature between 250 C. and 400 C., at a total pressure between 2 MPa and 10 MPa with a ratio of hydrogen volume to volume of hydrocarbon-containing feedstock between 100 and 800 litres per litre and at an Hourly Volume Rate (HVR) which is defined by the ratio of the volume flow rate of liquid hydrocarbon-containing feedstock to volume of catalyst fed into the reactor between 1 and 10 h.sup.1.
Multistage body having a plurality of flow channels
Described is a new multilevel article comprising a multitude of ducts and, in each duct in the direction of flow, at least one area which generates turbulence, forms an open duct section, is connected to the duct wall, and forms a baffle for the incoming flow and a stall strip for the outgoing flow. The described article has a plurality of successive interconnected duct structures which form a step-like transition in relation to each other in the direct of flow.
A COMPOSITION COMPRISING A ZEOLITIC MATERIAL SUPPORTED ON A SUPPORT MATERIAL
A composition comprising a support material which comprises silicon carbide on the surface of which a zeolitic material of the AEI/CHA family is supported, wherein at least 99 weight-% of the framework structure of the zeolitic material consist of a tetravalent element Y which is one or more of Si, Ge, Ti, Sn and V; a trivalent element X which is one or more of Al, Ga, In, and B; O; and H.
Mesoporous and macroporous nickel-based catalyst having a median macropore diameter of greater than 200 nm and its use with regard to hydrogenation
The invention relates to a supported catalyst that comprises an oxide substrate that is for the most part calcined aluminum and an active phase that comprises nickel, with the nickel content being between 5 and 65% by weight of said element in relation to the total mass of the catalyst, with said active phase not comprising a metal from group VIB, the nickel particles having a diameter that is less than or equal to 20 nm, said catalyst having a median mesopore diameter of between 8 nm and 25 nm, a median macropore diameter of greater than 200 nm, a mesopore volume that is measured by mercury porosimetry that is greater than or equal to 0.30 mL/g, and a total pore volume that is measured by mercury porosimetry that is greater than or equal to 0.34 mL/g. The invention also relates to the method for preparation of said catalyst and its use in a hydrogenation method.
Catalyst support, recycle reactor and method for releasing hydrogen
A catalyst support may be provided that comprises: an inner core, which includes at least one phase change material; a coating layer around the inner core, which includes at least one metal oxide; a catalytically active layer, which is positioned in interstices of the coating layer and/or lying on the coating layer, wherein at least one catalytically active substance is included in the catalytically active layer; and a supporting layer which is positioned under the coating layer. A recycle reactor may be provided comprising a reservoir for accommodating a chemical hydrogen storage substance; the catalyst support; a screw conveyor for input and transport of the catalyst support; and a heating device with which the catalyst support can be heated. A method for releasing hydrogen from a chemical hydrogen storage substance may be provided.
Method for preparing supported catalyst for heterogeneous catalytic ozonation
A method for preparing a catalyst, including: 1) uniformly mixing attapulgite, lithium-manganese spinel (LiMn spinel), manganese dioxide powders to form mixed raw material; adding water to the mixed raw material; stirring and mixing the mixed raw material and the water for between 5 and 15 min to yield a reaction mixture; 2) feeding the reaction mixture in 1) to a pelletizer to prepare spherical particles or hollow cylindrical particles; drying the spherical particles or the hollow cylindrical particles to yield a precursor; 3) heating the precursor in a muffle furnace, and calcining the precursor to yield a crude catalyst; 4) mixing the crude catalyst with an acid solution; alternating between ultrasound and microwave to wash the crude catalyst; and 5) washing the crude catalyst in 4) with water; and drying the catalyst for 12 hrs in air at 105 C.