A chemical reaction is catalyzed in an organic solvent using a water soluble N-heterocyclic carbene homogeneous catalyst to form a reaction mixture. An aqueous phase in the reaction mixture. A solvent in which the catalyst is insoluble is added to the reaction mixture, causing the catalyst to migrate to the aqueous phase to form a catalyst-laden aqueous phase. The catalyst is extracted from the catalyst-laden aqueous phase.

A chemical reaction is catalyzed in an organic solvent using a water soluble N-heterocyclic carbene homogeneous catalyst to form a reaction mixture. An aqueous phase in the reaction mixture. A solvent in which the catalyst is insoluble is added to the reaction mixture, causing the catalyst to migrate to the aqueous phase to form a catalyst-laden aqueous phase. The catalyst is extracted from the catalyst-laden aqueous phase.

The present disclosure describes a non-destructive process for removing metals, metal ions and metal oxides present in alumina-based materials without destroying alumina, allowing the regeneration of alumina-based catalysts. Known conventional procedures and/or methods for removing metals, metal ions and metal oxides present in alumina-based materials use some inorganic acid or its mixtures to carry out digestion, which modifies the properties of alumina and those of any other element contained in the material, destroying alumina and preventing its reuse. The present disclosure is characterized by using an extracting agent that sequesters metals, metal ions and/or metal oxides present in alumina-based materials without modifying their properties. The employed extracting agent is an alcohol. The non-destructive process introduced in the present invention reaches metal (M) removal rates of at least 42% when using a continuous flow reactor and of at least 27% when a batch reactor is employed.

The present disclosure describes a non-destructive process for removing metals, metal ions and metal oxides present in alumina-based materials without destroying alumina, allowing the regeneration of alumina-based catalysts. Known conventional procedures and/or methods for removing metals, metal ions and metal oxides present in alumina-based materials use some inorganic acid or its mixtures to carry out digestion, which modifies the properties of alumina and those of any other element contained in the material, destroying alumina and preventing its reuse. The present disclosure is characterized by using an extracting agent that sequesters metals, metal ions and/or metal oxides present in alumina-based materials without modifying their properties. The employed extracting agent is an alcohol. The non-destructive process introduced in the present invention reaches metal (M) removal rates of at least 42% when using a continuous flow reactor and of at least 27% when a batch reactor is employed.

Disclosed herein are methods to rejuvenate a deactivated hydroformylation catalyst solution wherein the solution comprises rhodium, polydentate phosphine ligands, and polydentate phosphine ligand degradation products. In one embodiment, such methods comprise adding a peroxide to the deactivated hydroformylation catalyst solution.

Disclosed herein are methods to rejuvenate a deactivated hydroformylation catalyst solution wherein the solution comprises rhodium, polydentate phosphine ligands, and polydentate phosphine ligand degradation products. In one embodiment, such methods comprise adding a peroxide to the deactivated hydroformylation catalyst solution.

A process for the production of methyl acetate by carbonylating dimethyl ether with carbon monoxide at a temperature of 250 to 350 C. in the presence of a zeolite catalyst and hydrogen such that the molar ratio of hydrogen to carbon monoxide is at least 1, and one or more compounds containing a hydroxyl functional group and in the absence of any added methyl acetate.

A process for the production of methyl acetate by carbonylating dimethyl ether with carbon monoxide at a temperature of 250 to 350 C. in the presence of a zeolite catalyst and hydrogen such that the molar ratio of hydrogen to carbon monoxide is at least 1, and one or more compounds containing a hydroxyl functional group and in the absence of any added methyl acetate.

A method for producing a dicyclopentadiene-modified phenolic resin. The method including reusing a fluorine-based ion-exchange resin as a catalyst in a reaction between a phenol and a dicyclopentadiene, the fluorine-based ion-exchange resin having been used as a catalyst when a phenol and a dicyclopentadiene are allowed to react with each other to produce a first dicyclopentadiene-modified phenolic resin. In the method, the fluorine-based ion-exchange resin is washed with an organic solvent. The dicyclopentadiene-modified phenolic resin obtained by the method has a stable quality, has a high purity, and is inexpensive.

The present disclosure relates to a method for regenerating a waste organic zinc catalyst by performing surface modification using a dicarboxylic acid and a zinc compound. When using the method for regenerating an organic zinc catalyst according to the present disclosure, the organic zinc catalyst can be regenerated using a convenient method which modifies the dicarboxylic acid and the zinc compound in an alternately repeated manner.