Patent classifications
C07C45/002
PROCESS FOR PRODUCING BUTADIENE FROM ETHANOL WITH IN SITU REGENERATION OF THE CATALYST OF THE SECOND REACTION STEP
The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 2 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing a regeneration loop for the inert gas and at least one regeneration loop for the gas streams comprising oxygen.
PROCESS FOR PRODUCING BUTADIENE FROM ETHANOL WITH IN SITU REGENERATION OF THE CATALYST OF THE SECOND REACTION STEP
The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 2 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing a regeneration loop for the inert gas and at least one regeneration loop for the gas streams comprising oxygen.
Prevention of tissue ischemia and related methods
Provided herein are compositions for preventing, ameliorating, and/or reducing tissue ischemia and/or tissue damage due to ischemia, increasing blood vessel diameter, blood flow and tissue perfusion in the presence of vascular disease including peripheral vascular disease, atherosclerotic vascular disease, coronary artery disease, stroke and influencing other conditions, by suppressing CD47 and/or blocking TSP1 and/or CD47 activity or interaction. Influencing the interaction of CD47-TSP1 in blood vessels allows for control of blood vessel diameter and blood flow, and permits modification of blood pressure and cardiac function. Under conditions of decreased blood flow, for instance through injury or atherosclerosis, blocking TSP1-CD47 interaction allows blood vessels to dilate and increases blood flow, tissue perfusion and tissue survival.
Efficient Catalytic Greenhouse Gas-Free Hydrogen and Aldehyde Formation from Alcohols
Catalytic preparation of hydrogen and aldehyde(s) from alcohols, including bioalcohols, without production of carbon monoxide or carbon dioxide.
Efficient Catalytic Greenhouse Gas-Free Hydrogen and Aldehyde Formation from Alcohols
Catalytic preparation of hydrogen and aldehyde(s) from alcohols, including bioalcohols, without production of carbon monoxide or carbon dioxide.
METHOD FOR THE PRODUCTION OF BUTADIENE AND HYDROGEN FROM ETHANOL IN TWO LOW-WATER AND LOW-ENERGY-CONSUMPTION REACTION STEPS
The invention concerns a process for the production of butadiene from an ethanol feed comprising at least 80% by weight of ethanol, comprising at least one step A) for the conversion of ethanol into acetaldehyde A), a step B) for converting an ethanol/acetaldehyde mixture into butadiene, a step C1) for hydrogen treatment, a step D1) for butadiene extraction, a first butadiene purification step D2), a subsequent butadiene purification step D3), an effluent treatment step E1), a step E2) for eliminating impurities and brown oils and a step F) for scrubbing with water.
METHOD FOR THE PRODUCTION OF BUTADIENE AND HYDROGEN FROM ETHANOL IN TWO LOW-WATER AND LOW-ENERGY-CONSUMPTION REACTION STEPS
The invention concerns a process for the production of butadiene from an ethanol feed comprising at least 80% by weight of ethanol, comprising at least one step A) for the conversion of ethanol into acetaldehyde A), a step B) for converting an ethanol/acetaldehyde mixture into butadiene, a step C1) for hydrogen treatment, a step D1) for butadiene extraction, a first butadiene purification step D2), a subsequent butadiene purification step D3), an effluent treatment step E1), a step E2) for eliminating impurities and brown oils and a step F) for scrubbing with water.
METHOD FOR PRODUCING BUTADIENE FROM ETHANOL WITH OPTIMISED IN SITU REGENERATION OF THE CATALYST OF THE SECOND REACTION STEP
The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 4 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing three regeneration loops.
METHOD FOR PRODUCING BUTADIENE FROM ETHANOL WITH OPTIMISED IN SITU REGENERATION OF THE CATALYST OF THE SECOND REACTION STEP
The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 4 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing three regeneration loops.
Use of ruthenium complexes for preparing amides, polypeptides and cyclic dipeptides
A process for preparing amides by reacting a primary amine and a primary alcohol in the presence of a Ruthenium complex to generate the amide and molecular hydrogen. Primary amines are directly acylated by equimolar amounts of alcohols to produce amides and molecular hydrogen (the only byproduct) in high yields and high turnover numbers. Also disclosed are processes for hydrogenation of amides to alcohols and amines; hydrogenation of organic carbonates to alcohols; hydrogenation of carbamates or urea derivatives to alcohols and amines; amidation of esters; acylation of alcohols using esters; coupling of alcohols with water and a base to form carboxylic acids; dehydrogenation of beta-amino alcohols to form pyrazines and cyclic dipeptides; and dehydrogenation of secondary alcohols to ketones. These reactions are catalyzed by a Ruthenium complex which is based on a dearomatized PNN-type ligand of formula A1 or precursors thereof of formulae A2 or A3.