Patent classifications
C07C2523/50
Palladium-Based Supported Hydrogenation Catalyst, And Preparation Method And Application Thereof
The present invention relates to a palladium-based supported hydrogenation catalyst and a preparation method and application thereof. The catalyst is prepared by the following method: impregnating an Al.sub.2O.sub.3-containing carrier with an organic solution containing a bipyridine derivative having hydroxy group, optionally drying followed by impregnating with a mixed solution containing the main active component palladium ions and the auxiliary active component M.sup.n+ ions, where M is one selected from Ag, Au, Ni, Pb and Cu; and then optionally drying, and calcining to obtain the catalyst. The preparation method provided by the present invention allows Pd atoms and M atoms to be highly uniformly dispersed on the carrier, which overcomes the adverse impact of the surface tension of the impregnation solution and the solvation effect on the dispersibility of active components. The palladium-based supported hydrogenation catalyst provided by the present invention has excellent hydrogenation activity, ethylene selectivity and anti-coking performance, and can be used in a selective hydrogenation process of C2 fraction.
Processes for Dehydrogenating Alkanes and Alkyl Aromatic Hydrocarbons
A hydrocarbon can be contacted with dehydrogenation catalyst particles to produce an effluent that can include coked catalyst particles and dehydrogenated hydrocarbon(s). A first stream rich in coked catalyst particles and a second stream rich in dehydrogenated hydrocarbon(s) and containing entrained catalyst particles can be separated from the effluent. The second stream can be contacted with a first quench medium to produce a cooled stream. The cooled stream can be contacted with a second quench medium within a quench tower. A gaseous stream that includes the dehydrogenated hydrocarbon(s), a first quench medium stream, and a slurry stream that includes the second quench medium and the entrained catalyst particles can be separated from the tower. The first quench medium can be recycled. The entrained catalyst particles can be separated from the slurry to provide recovered second quench medium and recovered entrained catalyst particles. The recovered second quench medium can be recycled.
Cross-coupling of unactivated secondary boronic acids
Provided are methods for site- and stereo-retentive cross-couplings with unactivated secondary boronic acids, which methods are particularly useful in building block-based approach for small molecule synthesis. Also provided is a method of forming an air-stable chiral secondary boronic acid.
SINGLE STEP CONVERSION OF ETHANOL TO BUTADIENE
A process for producing 1,3-butadiene (BD) from ethanol in a single step by s7 passing a mixture containing ethanol in a gas phase over a multifunctional catalyst having a transition metal dispersion of at least 30% on a silica metal oxide support. In some examples the multifunctional catalyst comprises a silica metal oxide having a surface area of at least 200 m2/g. The multifunctional catalyst can include a transition metal oxide, a silica metal oxide made from a high purity silica gel, mesoporous silica and fumed silica, such as high purity SBA16, SBA15, or Davisil grade 646.
SULFUR TERMINATED ORGANOSILICA MATERIALS AND USES THEREOF
Provided herein are compositions and methods for use of an organosilica material comprising a copolymer of at least one monomer of Formula [R.sup.1R.sup.2SiCH.sub.2].sub.3 (I), wherein, R.sup.1 represents a C.sub.1-C.sub.4 alkoxy group; and R.sup.2 is a C.sub.1-C.sub.4 alkoxy group or a C.sub.1-C.sub.4 alkyl group; and at least one other monomer of Formula [(Z.sup.1O).sub.xZ.sup.2.sub.3-xSiZ.sup.3SZ.sup.4] (II), wherein, Z.sup.1 represents a hydrolysable functional group; Z.sup.2 represents a C.sub.1-C.sub.10 alkyl or aryl group; Z.sup.3 represents a C.sub.2-C.sub.11 cyclic or linear hydrocarbon; Z.sup.4 is either H or O.sub.3H; and x represents any one of integers 1, 2, and 3. The composition may be used as a support material to covalently attach transition metal cations, as a sorbent for olefin/paraffin separations, as a catalyst support for hydrogenation reactions, as a precursor for highly dispersed metal nanoparticles, or as a polar sorbent for crude feeds.
Process and catalyst for methane conversion to aromatics
A process and catalyst for use therein for the production of aromatics via the oxidative coupling of methane and methane co-aromatization with higher hydrocarbons in a single reaction stage. First, methane is partially converted to ethane and ethylene on an OCM catalyst component, and the OCM intermediate mixture containing methane, ethane and ethylene is subsequently converted into aromatics on an aromatization catalyst component. The reaction may be conducted at 550-850 C. and at about 50 psig. The claimed process and catalyst used therein achieves high methane conversion at lower temperatures (less than 800 C.), higher methane conversion into the aromatic products and significant reductions in production cost when compared to the traditional two (or more) step processes.
CATALYST FOR 1,3-BUTADIENE PRODUCTION FROM ETHANOL
The present invention relates to a catalyst for the conversion of ethanol to 1,3-butadiene comprising a support, characterized in that silver (Ag) and copper (Cu) are present on the support in metal form, to a process for producing such a catalyst, to the use of such a catalyst for the conversion of ethanol to 1,3-butadiene, and to a process for the catalytic conversion of ethanol to 1,3-butadiene using such a catalyst.
REACTOR FOR OXYGEN-FREE DIRECT CONVERSION OF METHANE AND METHOD FOR PREPARING ETHYLENE USING THE SAME
The present invention relates to a oxygen-free direct conversion of methane reactor and a method for producing ethylene using the same. More specifically, the invention provides a oxygen-free direct conversion of methane reactor and a method for producing ethylene from methane, wherein the reactor is selectively heated to save energy, prevent overheating with high responsiveness, and minimize coke formation, thereby achieving high methane conversion rate and high ethylene yield at a high reaction rate. The method also allows for the production of ethylene and aromatic compounds.
Silver-cerium oxide composite catalyst supported on an alkaline carrier and method for producing the same
Conventionally, a silver-cerium oxide composite containing a silver particle and cerium oxide covering the surface of the silver particle has been synthesized through a multi-stage process, and is disadvantageous not only in that there is a need to use an organic solvent and a surfactant, causing the time and cost to be increased, but also in that there is a possibility that fulminating silver is formed, leading to a problem about the safety. A method for producing a catalyst having a silver-cerium oxide composite and an alkaline carrier having supported thereon the oxide composite, the silver-cerium oxide composite containing a silver particle and cerium oxide covering the surface of the silver particle, the method having preparing a mixture containing a silver compound, a cerium compound, and an alkaline carrier, and drying the mixture is provided.
Hydrocarbon conversion process
The invention relates to processes for converting a mixture of hydrocarbon and sulfur-containing molecules such as mercaptans into products comprising acetylene, ethylene, and hydrogen sulfide, to processes utilizing the acetylene and ethylene resulting from the conversion, and to equipment useful for such processes.