Patent classifications
B01J27/138
Methods of making acrylic acid from lactic acid or its derivatives in liquid phase
Methods for making acrylic acid, acrylic acid derivatives, or mixtures thereof by contacting a feed stream containing lactic acid, lactic acid derivatives, or mixtures thereof with a molten salt catalyst comprising an ionic liquid (IL) and an acid in liquid phase are provided.
Methods of making acrylic acid from lactic acid or its derivatives in liquid phase
Methods for making acrylic acid, acrylic acid derivatives, or mixtures thereof by contacting a feed stream containing lactic acid, lactic acid derivatives, or mixtures thereof with a molten salt catalyst comprising an ionic liquid (IL) and an acid in liquid phase are provided.
CATALYSTS AND INTEGRATED PROCESSES FOR PRODUCING TRIFLUOROIODOMETHANE
The present disclosure provides a process for producing trifluoroiodomethane (CF.sub.3I). The process may include providing a vapor-phase reactant stream comprising trifluoroacetic acid and iodine and reacting the reactant stream in the presence of a catalyst to produce a product stream comprising the trifluoroiodomethane. The catalyst includes silicon carbide.
Catalysts and integrated processes for producing trifluoroiodomethane
The present disclosure provides a process for producing trifluoroiodomethane (CF.sub.3I). The process may include providing a vapor-phase reactant stream comprising trifluoroacetic acid and iodine and reacting the reactant stream in the presence of a catalyst to produce a product stream comprising the trifluoroiodomethane. The catalyst includes silicon carbide.
Process for catalytic oxidative dehydrogenation of ethane to ethylene in the presence of chlorine intermediates
A process for producing ethylene comprising: (a) reacting a reactant mixture in a reactor to yield a product mixture, wherein the reactor comprises a catalyst, wherein the reactant mixture comprises ethane, oxygen, and a chlorine intermediate precursor, wherein the product mixture comprises ethylene, unreacted ethane, carbon monoxide, and carbon dioxide, wherein the catalyst comprises a redox agent, an alkali metal, and a rare earth element; and (b) recovering at least a portion of the ethylene from the product mixture. The reacting in step (a) further comprises (i) contacting at least a portion of the chlorine intermediate precursor with the catalyst to form a chlorinated catalyst; (ii) allowing at least a portion of the chlorinated catalyst to generate a chlorine intermediate; and (iii) allowing at least a portion of the reactant mixture to react via the chlorine intermediate.
Synthesis of magnesium dichloride support for the AST off-line ZN catalyst with a plug flow reactor (PFR)
The various embodiments of the invention provide, a magnesium dichloride support and the magnesium titanium polymerization procatalyst made therefrom, and methods for making and using the same.
Synthesis of magnesium dichloride support for the AST off-line ZN catalyst with a plug flow reactor (PFR)
The various embodiments of the invention provide, a magnesium dichloride support and the magnesium titanium polymerization procatalyst made therefrom, and methods for making and using the same.
Catalysis of dehydrocoupling reactions between amines and silanes
A method for dehydrocoupling silanes and amines. The method comprises contacting: (a) an aliphatic amine; (b) a silane; and (c) a catalyst which is Z.sub.nX.sub.2, wherein X is alkyl, chloride, bromide, iodide, trifluoromethanesulfonate, bis(trifluoromethane)sulfonamide, tosylate, methanesulfonate or O.sub.3S(CF.sub.2)XCF.sub.3 wherein x is an integer from 1 to 10.
Catalysis of dehydrocoupling reactions between amines and silanes
A method for dehydrocoupling silanes and amines. The method comprises contacting: (a) an aliphatic amine; (b) a silane; and (c) a catalyst which is Z.sub.nX.sub.2, wherein X is alkyl, chloride, bromide, iodide, trifluoromethanesulfonate, bis(trifluoromethane)sulfonamide, tosylate, methanesulfonate or O.sub.3S(CF.sub.2)XCF.sub.3 wherein x is an integer from 1 to 10.
SYNTHESIS OF CANNABIGEROL
Multiple methods of synthesizing cannabigerol are presented. Combining olivetol with geraniol derivatives are provided. Cross-coupling methods of combing functionalized resorcinols are provided. Useful intermediates are formed during such cross-coupling steps.