Patent classifications
C07C253/00
PROCESS FOR PURIFYING AMINOCAPRONITRILE
A process for converting caprolactam to aminocapronitrile (ACN), the process comprising contacting a caprolactam feed stream with ammonia to produce a first crude product stream; separating the first crude product stream to produce an intermediate product stream comprising ACN and caprolactam recovery stream; and purifying the intermediate product stream to produce a purified product stream comprising greater than 95 wt % aminocapronitrile.
PROCESS FOR CATALYST REGENERATION
A process for regenerating a deactivated catalyst, the process comprising contacting a deactivated aluminosilicate zeolite catalyst comprising a nitrogen-containing contaminant with an oxidant to provide a regenerated catalyst comprising less than 0.5% contaminant and a regeneration by-product stream comprising nitrogen.
PROCESS FOR CATALYST REGENERATION
A process for regenerating a deactivated catalyst, the process comprising contacting a deactivated aluminosilicate zeolite catalyst comprising a nitrogen-containing contaminant with an oxidant to provide a regenerated catalyst comprising less than 0.5% contaminant and a regeneration by-product stream comprising nitrogen.
Process for preparing cyanoacetates
This invention relates to a process for producing cyanoacetates involving contacting a salt of an alkyl, alkenyl, alkynyl or aryl formyl acetate with a hydroxyl amine acid under appropriate conditions and for a time sufficient to yield a cyanoacetate.
Process for preparing cyanoacetates
This invention relates to a process for producing cyanoacetates involving contacting a salt of an alkyl, alkenyl, alkynyl or aryl formyl acetate with a hydroxyl amine acid under appropriate conditions and for a time sufficient to yield a cyanoacetate.
Process for the production of 2-[4-(cyclopropanecarbonyl)phenyl]-2-methyl-propanenitrile
A new process for the production of 2-[4-(cyclopropanecarbonyl)phenyl]-2-methyl-propanenitrile is described. This compound can be used for the production of drugs, such as Fexofenadine.
Hydrogen storage system by catalytic dehydrogenation of amines
The current disclosure is directed to a hydrogen-storage system that employs catalytic dehydrogenation of low-molecular-weight amines in a hydrogen reactor. The hydrogen-storage system comprises aliphatic amines and di-amines as organic carriers that store hydrogen covalently, a hydrogen reactor that releases and separates hydrogen gas from the carrier, and metal or metal-oxide catalysts that promote a dehydrogenation reaction to release hydrogen. In certain implementations, a metal or metal-oxide catalyst may be carried on high-surface-area support materials, such as gamma-alumina and metal-organic-framework materials, to enhance catalytic properties. The hydrogen reactor may be a packed-bed reactor, a monolith reactor, or a flow-through hydrogen-membrane reactor. In one implementation, the flow-through hydrogen-membrane reactor comprises an inlet through which the organic hydrogen carrier flows into the reactor, a hydrogen-separation membrane selectively permeable to hydrogen, a recirulation outlet for removing unspent organic carrier, and a hydrogen outlet for releasing hydrogen and reaction byproducts. The spent organic carrier are collected and hydrogenated to regenerate the original fuel.
Hydrogen storage system by catalytic dehydrogenation of amines
The current disclosure is directed to a hydrogen-storage system that employs catalytic dehydrogenation of low-molecular-weight amines in a hydrogen reactor. The hydrogen-storage system comprises aliphatic amines and di-amines as organic carriers that store hydrogen covalently, a hydrogen reactor that releases and separates hydrogen gas from the carrier, and metal or metal-oxide catalysts that promote a dehydrogenation reaction to release hydrogen. In certain implementations, a metal or metal-oxide catalyst may be carried on high-surface-area support materials, such as gamma-alumina and metal-organic-framework materials, to enhance catalytic properties. The hydrogen reactor may be a packed-bed reactor, a monolith reactor, or a flow-through hydrogen-membrane reactor. In one implementation, the flow-through hydrogen-membrane reactor comprises an inlet through which the organic hydrogen carrier flows into the reactor, a hydrogen-separation membrane selectively permeable to hydrogen, a recirulation outlet for removing unspent organic carrier, and a hydrogen outlet for releasing hydrogen and reaction byproducts. The spent organic carrier are collected and hydrogenated to regenerate the original fuel.
Hydrogen storage system by catalytic dehydrogenation of amines
The current disclosure is directed to a hydrogen-storage system that employs catalytic dehydrogenation of low-molecular-weight amines in a hydrogen reactor. The hydrogen-storage system comprises aliphatic amines and di-amines as organic carriers that store hydrogen covalently, a hydrogen reactor that releases and separates hydrogen gas from the carrier, and metal or metal-oxide catalysts that promote a dehydrogenation reaction to release hydrogen. In certain implementations, a metal or metal-oxide catalyst may be carried on high-surface-area support materials, such as gamma-alumina and metal-organic-framework materials, to enhance catalytic properties. The hydrogen reactor may be a packed-bed reactor, a monolith reactor, or a flow-through hydrogen-membrane reactor. In one implementation, the flow-through hydrogen-membrane reactor comprises an inlet through which the organic hydrogen carrier flows into the reactor, a hydrogen-separation membrane selectively permeable to hydrogen, a recirulation outlet for removing unspent organic carrier, and a hydrogen outlet for releasing hydrogen and reaction byproducts. The spent organic carrier are collected and hydrogenated to regenerate the original fuel.
Heterogeneous metal-free catalyst
The inventive concepts disclosed and/or claimed herein relate generally to catalysts and, more particularly, but not by way of limitation, to a heterogeneous, metal-free hydrogenation catalyst containing frustrated Lewis pairs. In one non-limiting embodiment, the heterogeneous, metal-free catalyst comprises hexagonal boron nitride (h-BN) having frustrated Lewis pairs therein.