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Inventor:
Correia; Yves
Address:
Chateau-Arnoux, FR
No. of patents:
22
Patents:




Patent Number Title Of Patent Date Issued
5972827 Catalytic oxychlorination of hydrocarbons to produce chlorocarbons October 26, 1999
Hydrocarbons, e.g., ethylene, are steady-state catalytically oxychlorinated into chlorocarbons, e.g., 1,2-dichloroethane, by fluidizing a fluidizable charge by directing a gaseous feedstream containing a hydrocarbon therethrough and therein oxychlorinating such hydrocarbon, the gaseous
5705720 Continuous process for cracking 1,2-dichloroethane January 6, 1998
A thermal process for cracking 1,2-dichloroethane to form vinyl chloride comprising heating 1,2-dichloroethane in a reaction zone at a temperature between 300.degree. and 650.degree. C. under an absolute pressure between 1 and 40 bars; said heating being conducted in the presence of
5637781 Process for the alcoholysis of carbon tetrachloride June 10, 1997
The invention relates to a process for the alcoholysis of carbon tetrachloride which consists in simultaneously sending, on the one hand, carbon tetrachloride and, on the other hand, an alcohol ROH, over a catalytic composition, characterized in that the said catalytic composition co
5488190 Prepartion of vinyl chloride by ultrapyrolysis of 1,2-dichloroethane January 30, 1996
Vinyl chloride monomer is selectively prepared by intimately contacting, in the absence of steam, a feedstream of 1,2-dichloroethane with a flow of fluid or solid particulates heated to such elevated temperature and for such minim period of time, e.g., 0.010 to 0.5 second, as to flash tr
5475135 Catalyst for the dehalogenation of .alpha.-halogenated carboxylic acids December 12, 1995
The invention relates to a catalyst comprising a rare metal of Group VIII of the Periodic Table of Elements which has been deposited on an inert support and which has been used to dehalogenate .alpha.-halogenated carboxylic acids in the presence of hydrogen, and a rare metal of Group
5466650 Catalyst for the dehalogenation of alphahalogenated carboxylic acids and its use for purifying m November 14, 1995
The invention relates to a catalyst formed of an active charcoal support in the form of particles or of cylinders having a diameter from 0.3 to 1.5 mm and a length of 0.3 to 5 mm or spheres having a diameter from 0.3 to 2 mm, the said particles being loaded with a precious metal from gro
5466650 Catalyst for the dehalogenation of alphahalogenated carboxylic acids and its use for purifying m November 14, 1995
The invention relates to a catalyst formed of an active charcoal support in the form of particles or of cylinders having a diameter from 0.3 to 1.5 mm and a length of 0.3 to 5 mm or spheres having a diameter from 0.3 to 2 mm, the said particles being loaded with a precious metal from gro
5414116 Catalyst for the dehalogenation of alphahalogenated carboxylic acids and its use for purifying m May 9, 1995
The invention relates to a catalyst formed of an active charcoal support in the form of particles or of cylinders having a diameter from 0.3 to 1.5 mm and a length of 0.3 to 5 mm or spheres having a diameter from 0.3 to 2 mm, the said particles being loaded with a precious metal from gro
5401876 Synthesis of chloroacetic acids March 28, 1995
Chloroacetic acids and essentially pure hydrochloric acid are prepared by chlorinating acetic acid in the presence of a catalytically effective amount of acetic anhydride, acetyl chloride, or admixture thereof, whereby byproducing a gaseous stream of crude hydrochloric acid, contacting s
5399796 Purification of 1,1-dichloro-1-fluoroethane March 21, 1995
This invention relates to a process for the purification of 1,1-dichloro-1-fluorethane.To remove unsaturated impurities such as 1,1-dichloroethylene and dichloracetylene the crude 1,1-dichloro-1-fluoroethane is subjected to the action of chlorine and/or of a hydracid. This treatment is c
5356850 Catalyst for the dehalogenation of .alpha.-halogenated carboxylic acids October 18, 1994
The invention relates to a catalyst comprising a rare metal of Group VIII of the Periodic Table of Elements which has been deposited on an inert support and which has been used to dehalogenate .alpha.-halogenated carboxylic acids in the presence of hydrogen, and a rare metal of Group
5326918 Purification of 1,1-dichloro-1-fluoroethane July 5, 1994
This invention relates to a process to remove the unsaturated impurities (in particular vinylidene chloride) present in a crude 1,1-dichloro-1-fluoroethane. This process comprises subjecting the product to be purified, in the liquid phase, in the presence of oxygen, to an irradiation
5278122 Catalyst for dehalogenation of alpha-halogenated carboxylic acids/esters January 11, 1994
The alpha-halogenated carboxylic acids/esters are dehalogenated by reaction with hydrogen in the presence of a catalytically effective amount of (i) a Group VIII precious metal catalyst and (ii) either sulfur or a sulfur compound, or (iii) a novel precious metal/sulfur solid phase cataly
5243111 Catalytic oxychlorination of hydrocarbons to produce chlorocarbons September 7, 1993
Hydrocarbons, e.g., ethylene, are steady-state catalytically oxychlorinated into chlorocarbons, e.g., 1,2-dichloroethane, by fluidizing a fluidizable charge by directing a gaseous feedstream containing a hydrocarbon therethrough and therein oxychlorinating such hydrocarbon, the gaseous
5227549 Synthesis of 1,2-dichloroethane by CCl.sub.4 oxychlorination of ethylene July 13, 1993
A major amount of 1,2-dichloroethane (D12) and lesser amounts of trichloroethane and tetrachloroethane are prepared by contacting carbon tetrachloride, ethylene and oxygen (or an oxygen-containing gas, notably air) with an oxychlorination catalyst at a temperature sufficient to produ
5191118 Catalytic dehalogenation of alpha-halogenated carboxylic acids/esters March 2, 1993
The alpha-halogenated carboxylic acids/esters are dehalogenated by reaction with hydrogen in the presence of a catalytically effective amount of (i) a Group VIII precious metal catalyst and (ii) either sulfur or a sulfur compound, or (iii) a novel precious metal/sulfur solid phase cataly
5116799 Oxychlorination of hydrocarbons May 26, 1992
Chlorinated hydrocarbons, e.g., 1,2-dichloroethane, are prepared by heterogeneously oxychlorinating a hydrocarbon with an oxygen-containing gas and gaseous hydrochloric acid in a fluidized bed containing admixture of (i) a catalytically effective amount of an oxychlorination catalyst,
5097081 Hydrodechlorination of higher chloromethanes March 17, 1992
The highly chlorinated methanes, e.g., carbon tetrachloride, are improvedly dechlorinated by reacting same with hydrogen in the presence of oxygen or an oxygen-containing gas, e.g., air, and a catalytically effective amount of a metal of the copper or precious metal Groups of the Periodi
5053567 Oxychlorination of hydrocarbons October 1, 1991
Chlorinated hydrocarbons, e.g., 1,2-dichloroethane, are prepared by heterogenously oxychlorinating a hydrocarbon with an oxygen-containing gas and gaseous hydrochloric acid in a fluidized bed containing admixture of (i) a catalytically effective amount of an oxychlorination catalyst, (ii
4954231 Functional chlorofluoro compounds and their preparation September 4, 1990
The subject of the invention is functional chlorofluoro compounds of general formula: ##STR1## in which R.sub.F denotes a perfluoroalkyl radical, n is equal to 0 or 1, X denotes a chlorine or fluorine atom or a trichloromethyl or trifluoromethyl radical, and Y denotes a chlorine
4301092 Preparation of oxalyl chloride November 17, 1981
Oxalyl chloride is prepared by (i) first esterifying ethylene glycol with trichloroacetyl chloride, (ii) next photochemically chlorinating the ester which results from the step (i), i.e., ethylene glycol bis-trichloroacetate, and (iii) then decomposing the tetrachloroethylene glycol
4172957 Production of monochloroacetyl chloride and monochloroacetic acid by hydration of trichloroethyl October 30, 1979
Continuous process for the production of monochloroacetyl chloride accompanied, if the need should arise, by monochloroacetic acid, from trichloroethylene and/or 1,1,1,2-tetrachloroethane by reaction for hydration of trichloroethylene and/or 1,1,1,2-tetrachloroethane under pressure o


 
 
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