Patent classifications
B01J2531/845
Compositions and methods for selective carbonylation of heterocyclic compounds
Compositions comprising metal organic frameworks and related methods and uses are generally provided, including use in selective carbonylation of heterocyclic compounds.
METHOD FOR SYNTHESIZING DIHYDROXYL-TERMINATED POLYPHENYLENE OXIDE OLIGOMER
Disclosed is a method for synthesizing dihydroxyl-terminated polyphenylene oxide oligomer. The method for synthesizing dihydroxyl-terminated polyphenylene oxide oligomer, comprising oxidatively copolymerizing monohydric phenol and dihydric phenol in the presence of a metal-polyethyleneimine complex as a catalyst, to obtain the dihydroxyl-terminated polyphenylene oxide oligomer. The synthesizing method of the present disclosure uses a metal-polyethyleneimine complex as a catalyst, which has a milder catalytic activity, can effectively promote the reaction between the dihydric phenol and the monohydric phenol, increases the hydroxyl content of the product, meanwhile reduces the amount of the residual dihydric phenol monomer in the product, so that the quality of the product can be improved. The dihydroxyl-terminated polyphenylene oxide oligomer prepared can be used as additive and copolymerization block in other thermoplastic plastics, thermoplastic elastomers and thermosetting materials, thereby improving the performances of the material, such as thermal performance, adhesion, mechanical property, chemical resistance, and electrical property.
METHOD FOR CONVERTING MONOISOCYANATES TO UREAS
Organic isocyanates are converted to ureas by heating in the presence of certain cobalt, magnesium, chromium and lanthanide series organometallic catalysts. The process requires no water or other reactants. The process is particularly useful for removing small quantities of monoisocyanates from a solvent stream recovered from a polyisocyanate manufacturing process. The urea compounds in some instances can be recycled back into the polyisocyanate manufacturing process and reacted with polyisocyanate compounds to form biurets.
Fuel cell electrode having porous carbon core with macrocyclic metal chelates thereon
The invention concerns a method for manufacturing of an electrocatalyst comprising a porous carbon support material, a catalytic material in the form of at least one type of metal, and macrocyclic compounds chemically bound to the carbon support and capable of forming complexes with single metal ions of said metal or metals, said method comprising the steps of: i) providing a template capable of acting as pore structure directing agent during formation of a highly porous electrically conducting templated carbon substrate, ii) mixing the template with one or several precursor substances of the catalytic material, the macrocyclic compounds and carbon, iii) exposing the mixture of the template and the precursor substances to a carbonization process during which the precursors react and transform the mixture into a carbonized template composite in winch the carbon part of the composite is chemically bound to macrocyclic compounds present in complexes with the metal or metals. The invention also concerns an electrocatalyst for electrochemical reactions, a method for manufacturing of a membrane electrode assembly using such an electrocatalyst and to a fuel cell making use of such an electrocatalyst.
Process for the hydroformylation of olefins using a cobalt precatalyst and a diphosphine ligand
Process for the hydroformylation of olefins using a cobalt precatalyst and a diphosphine ligand.
Reactive membrane networks for CWA protection
A membrane includes a first layer, and a second layer coupled to the first layer. The second layer includes a network of catalytic sites, each catalytic site having a catalytic center characterized by promoting a chemical reaction of a target material. A method of forming a chemically reactive membrane includes applying a first solution to a structure, the first solution includes a macrocyclic ligand having electron-donating ligands and a side functional group for crosslinking, crosslinking a plurality of the macrocyclic ligand to form a first network of crosslinked macrocyclic ligands, and applying a second solution to the structure, the second solution comprising a catalytic center. Each catalytic center complexes with the electron-donating ligands of each macrocyclic ligand to form catalytic sites in the first network of crosslinked macrocyclic ligands.
PORPHYRIN-BASED CATALYSTS FOR WATER SPLITTING
The porphyrin-based catalysts for water splitting are composites of porphyrin or metalloporphyrin active ingredients, conductive carbon (e.g., graphene sheets, vapor grown carbon fiber, carbon black, etc.), and a polymer or binder that may be coated on a glassy carbon electrode. The polymer or binder may be Nafion oil or polyvinylidine difluoride. The porphyrin may be a porphyrin having a transition metal or hydrogen at its center, and may be halogenated and/or have a thiophene substituent.
Catalytic carbon fiber preparation methods
A method of producing a catalytic carbon fiber may include: providing a carbon fiber and an aminated macrocycle, mixing the carbon fiber and the aminated macrocycle with a solvent; and reacting the carbon fiber and the aminated macrocycle to form an amide bond between the carbon fiber and the aminated macrocycle thereby forming the catalytic carbon fiber.
Catalytic carbon fiber preparation methods
A method of producing a catalytic carbon fiber may include: oxidizing a virgin carbon fiber to produce an oxidized carbon fiber; reacting the oxidized carbon fiber with a polyamine compound to produce an amine modified carbon fiber; and reacting the amine modified carbon fiber with an organometallic macrocycle to produce the catalytic carbon fiber.
Catalytic carbon fiber contactor
A fiber bundle contactor may include: a flow path defined by a conduit; a catalytic carbon fiber bundle disposed in the conduit; and an inlet allowing fluid flow into the flow path. A method may include: introducing into vessel a hydrocarbon comprising mercaptan sulfur, an aqueous caustic solution, and an oxidizer; reacting at least a portion of the mercaptan sulfur and the aqueous caustic solution to produce a mercaptide; and reacting the mercaptide and the oxidizer in the presence of a catalytic carbon fiber bundle to produce a disulfide oil.