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Processes of preparing, purifying, or recovering unsaturated compound

Subclass of:

570 - Organic compounds -- part of the class 532-570 series

570000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

570101000 - HALOGEN CONTAINING

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Class / Patent application numberDescriptionNumber of patent applications / Date published
570216000 Processes of preparing, purifying, or recovering unsaturated compound 56
20120215041PROCESS FOR CIS-1-CHLORO-3,3,3-TRIFLUOROPROPENE - Disclosed is a process for making one isomer of CF08-23-2012
20150031925Process For Producing Chlorinated Hydrocarbons - The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of ferric chloride and a polyvalent antimony compound that includes a pentavalent antimony compound.01-29-2015
570217000 From carbon source other than hydrocarbon, halocarbon, or halohydrocarbon 2
20100105969METHOD OF PRODUCING IODIZING AGENT, AND METHOD OF PRODUCING AROMATIC IODINE COMPOUND - A method of the present invention, for producing an iodizing agent, includes the step of electrolyzing iodine molecules in a solution by using an acid as a supporting electrolyte. This realizes (i) a method of producing an iodine cation suitable for use as an iodizing agent that does not require a sophisticated separation operation after iodizing reaction is completed, and (ii) an electrolyte used in the method. Further, a method of the present invention, for producing an aromatic iodine compound, includes the step of causing an iodizing agent, and an aromatic compound whose nucleus has one or more substituent groups and two or more hydrogen atoms, to react with each other under the presence of a certain ether compound. This realizes such a method of producing an aromatic iodine compound that position selectivity in iodizing reaction of an aromatic compound is improved.04-29-2010
20140275657METHOD FOR PRODUCING CHLOROHYDROCARBON HAVING CONJUGATED DOUBLE BONDS - Provided is a method for producing a chlorohydrocarbon having conjugated double bonds by stereoselectively chlorinating an alcohol having conjugated double bonds. More specifically, provided is a method for producing a chlorohydrocarbon having conjugated double bonds, the method including a step of chlorinating an alcohol having conjugated double bonds with a chlorinating agent in a solvent in the presence of a base and in the absence of metal salt for chlorination of the alcohol, and the alcohol being represented by the formula (1):09-18-2014
570219000 Plural diverse reactions in separate zones 8
20090216055METHODS OF MAKING CHLORINATED HYDROCARBONS - Methods for the manufacture of 1,1,1,2,3-pentachloropropane from 1,1,1,3-tetrachloropropane and chlorine are disclosed. Improved methods are provided for the manufacture of 1,1,2,3-tetrachloropropene from 1,1,1,2,3-pentachloropropane. Methods are also disclosed for the manufacture of 1,1,2,3-tetrachloropropene from 1,1,1,3-tetrachloropropane and chlorine and for the manufacture of 1,1,2,3-tetrachloropropene from carbon tetrachloride ethylene, and chlorine.08-27-2009
20140235906PROCESS TO MAKE 1,1,2,3-TETRACHLOROPROPENE FROM 1,1,3-TRICHLOROPROPENE AND/OR 3,3,3- TRICHLOROPROPENE - Disclosed is a process for the synthesis of 1,1,2,3-tetrachloropropene (HCC-1230xa) using 1,1,3-trichloropropene (HCC-1240za) and/or 3,3,3-trichloropropene (HCC-1240zf) and Cl08-21-2014
20150025282Process to make 1,1,2,3-Tetrachloropropene - Disclosed is a process for the synthesis of 1,1,2,3-tetrachloropropene (HCC-1230xa) using 1,1,3-trichloropropene (HCC-1240za) and/or 3,3,3-trichloropropene (HCC-1240zf) and Cl01-22-2015
570220000 Dehalogenation or dehydrohalogenation with halogenation in separate zones 5
20100036180METHOD OF OBTAINING 1,2-DICHLOROETHANE BY DIRECT CHLORINATION WITH A STEP OF SEPARATION FROM THE CATALYST BY DIRECT EVAPORATION, AND FACILITY FOR THE IMPLEMENTATION THEREOF - The present invention relates to a method of producing liquid 1,2-dichloroethane (DCE), obtained by low-temperature direct chlorination of ethylene, in the presence of a Lewis acid-type catalyst, that makes it possible to obtain, after separation of the catalyst, DCE of sufficient purity to give, via cracking, vinyl chloride monomer (VCM); characterized in that it comprises a step of dechlorination (02-11-2010
20120035402METHODS OF MAKING CHLORINATED HYDROCARBONS - Methods for the manufacture of 1,1,1,2,3-pentachloropropane from 1,1,1,3-tetrachloropropane and chlorine are disclosed. Improved methods are provided for the manufacture of 1,1,2,3-tetrachloropropene from 1,1,1,2,3-pentachloropropane. Methods are also disclosed for the manufacture of 1,1,2,3-tetrachloropropene from 1,1,1,3-tetrachloropropane and chlorine and for the manufacture of 1,1,2,3-tetrachloropropene from carbon tetrachloride, ethylene, and chlorine.02-09-2012
20130190541CATALYST SYSTEM, COMPRISING CATALYST PELLETS AND DILUENT BEADS WITH PREDEFINED DIMENSIONS AND PHYSICOCHEMICAL PROPERTIES - A catalyst system for use in oxychlorination, the catalyst system comprising catalyst pellets comprising a catalyst carried on a substrate the pellets having length x, breadth y and depth z, intrinsic density P and bulk density p and diluent beads having length x±25%, breadth y±25% and depth z±25%, intrinsic density≧P+25% and a bulk density p ±25%.07-25-2013
20140221705SYNTHESIS OF 1,1,2,3-TETRACHLOROPROPENE - The present invention provides an improved process for producing 1,1,2,3-tetrachloropropene. By using a first reactive distillation column for HCC-250fb dehydrochlorination, and a second reactive distillation column for HCC-240db dehydrochlorination/HCC-1230xf isomerization, the 1,1,2,3-tetrachloropropene manufacturing process can be greatly simplified, resulting in reduced equipment use, energy use, as well as increased productivity.08-07-2014
570221000 Acetylene reactant 1
20140058142PRODUCTION OF VINYL CHLORIDE FROM A METHANE CONVERSION PROCESS - Methods and systems are provided for converting methane in a feed stream to acetylene. The method includes processing the acetylene to form a hydrocarbon stream having vinyl chloride. The hydrocarbon stream is introduced into a supersonic reactor and pyrolyzed to convert at least a portion of the methane to acetylene. The reactor effluent stream is be treated to convert acetylene to other hydrocarbon processes. The method according to certain aspects includes controlling the level of carbon monoxide in the hydrocarbon stream to limit downstream side reactions in the downstream processing units.02-27-2014
570224000 Oxyhalogenation 8
20090082602Method of Operating a Distillation column for Purifying 1, 2-Dichloroethane and for Coupled Sodium Hydroxide Solution Evaporative Concentration - Process for operating a distillation column for the removal of water and lower-boiling components than 1,2-dichloroethane from 1,2-dichloroethane in which at least part of the heat from condensation of the aqueous vapours from the distillation column is used to concentrate caustic soda solution by evaporation; furthermore, at least part of the 1,2-dichloroethane formed when chlorine and ethylene react in a direct chlorination unit is used to heat said distillation column and can subsequently also be used as a heat transfer fluid to concentrate caustic soda solution by evaporation.03-26-2009
20100087691Swing Reactor and Process for Oxychlorination - A reactor with swing feeds is provided for oxychlorination. This reactor comprises multiple inlets with controls capable of introducing feed streams sequentially to the reactor. In one configuration, a feed stream comprises a paraffin or olefin hydrocarbon such as methane or ethylene, and a second feed stream comprises oxygen and hydrogen chloride. By segregating these feeds, combustion reactions can be minimized and yields of chlorinated components increased.04-08-2010
20100152505CATALYSTS FOR OXYCHLORINATION OF ETHYLENE TO 1.2-DICHLOROETHANE - Catalysts for the oxychlorination of ethylene to 1.2-dichloroethane, in form of hollow granules having definite geometrical configuration and pore volume distribution with at least 20% of the total volume formed of macropores wherein the diameter of the pores at the maximum of the macropore distribution curve is higher than 800 nm and up to 1500 nm.06-17-2010
20100160697CATALYSTS FOR FIXED BED OXYCHLORINATION OF ETHYLENE TO 1.2-DICHLOROETHANE - Catalyst for the fixed bed oxychlorination of ethylene to 1.2-dichloroethane in form of hollow cylindrical granules having total pore volume from 0.4 to 0.55 ml/g prevailingly formed of micro and mesopores having diameter between 7 and 50 nm, wherein the mesopores constitute the major component, and the macropores having diameter of more than 50 nm up to 10.000 nm being present by 15-35%.06-24-2010
570225000 Liquid medium or inorganic melt utilized 4
20080207965Process For The Manufacture Of 1,2-Dichloroethane - Process for the manufacture of 1,2-dichloroethane starting with a hydrocarbon source according to which: a) the hydrocarbon source is subjected to a first cracking step, namely a pyrolysis step performed in a cracking oven, thus producing a mixture of cracking products; b) the said mixture of cracking products is subjected to a succession of treatment steps ending with a drying step which makes it possible to obtain a mixture of products containing ethylene and other constituents; c) the said mixture of products containing ethylene derived from step b) is separated into at least one fraction containing ethylene and into a heavy fraction; d) the fraction(s) containing the ethylene is (are) conveyed to a chlorination reactor and/or to an oxychlorination reactor, in which reactors most of the ethylene present is converted to 1,2 -dichloroethane; e) the 1,2-dichloroethane obtained is separated from the streams of products derived from the chlorination and oxychlorination reactors; the process being characterized in that a step for hydrogenating the acetylene is carried out upstream of the drying step ending the succession of treatment steps constituting step b) and/or on at least one of the fractions containing ethylene after separation during step c).08-28-2008
20080207966Process For The Manufacture Of 1,2-Dichloroethane - Process for the manufacture of 1,2-dichloroethane starting with a hydrocarbon source according to which: a) the hydrocarbon source is subjected to cracking which produces a mixture of products containing ethylene and other constituents; b) the mixture of products containing ethylene is conveyed to at least one storage reservoir; c) a chlorination reactor and/or an oxychlorination reactor is (are) supplied with the previously stored mixture of products containing ethylene, in which reactors most of the ethylene present is converted to 1,2-dichloroethane; d) the 1,2-dichloroethane obtained is separated from the streams of products derived from the chlorination and oxychlorination reactors.08-28-2008
20080207967Process For The Manufacture Of 1,2-Dichloroethane - Process for the manufacture of 1,2-dichloroethane starting with a hydrocarbon source according to which: a) the hydrocarbon source is subjected to cracking which produces a mixture of products containing ethylene and other constituents; b) the said mixture of products is separated into at least one fraction containing ethylene and into a heavy fraction (fraction C); c) the fraction or fractions containing ethylene are conveyed to a chlorination reactor and/or to an oxychlorination reactor, in which reactors most of the ethylene present is converted to 1,2-dichloroethane; d) the 1,2-dichloroethane obtained is separated from the streams of products derived from the chlorination and oxychlorination reactors and it is conveyed to the pyrolysis oven; and e) the fraction C is conveyed to cracking or to the oven for pyrolysis of 1,2-dichloroethane as fuel.08-28-2008
20090054708Catalytic Oxychlorination - Catalyst compositions for use in oxychlorination reactions, in particular the oxychlorination of ethylene, are disclosed. The catalyst compositions are in the form of particles suitable for use in fluid bed reactors, in particular baffled fluid bed reactors.02-26-2009
570226000 Dehydrohalogenation 23
20110230683Process and apparatus for producing ethylenically unsaturated halogenated hydrocarbons - Process and apparatus for producing ethylenically unsaturated halogenated hydrocarbons09-22-2011
20110230684PROCESS AND APPARATUS FOR PRODUCING EHTYLENICALLY UNSATURATED HALOGENATED HYDROCARBONS - The invention relates to a process and an apparatus for product-conserving thermal dissociation of halogenated aliphatic hydrocarbons, preferably for thermal dissociation of 1,2-dichloroethane to vinyl chloride. This uses chemical dissociation promoters and/or physical measures which initiate the dissociation reaction. The initiation of the dissociation reaction, with the same conversion, lowers the temperature level in the reaction mixture and the temperature of the dissociation gas on exit from the dissociation furnace. The amount and the exit temperature of the flue gas from the radiation zone of the dissociation furnace likewise decrease at the same time. It order to be able to implement the product-conserving mode of operation in the radiation zone of the dissociation furnace and simultaneously to maintain the function of the convection zone, the heat input to the dissociation furnace is divided such that a portion of the heat introduced by underfiring is introduced by burners in the radiation zone, and the other portion of the heat supplied by underfiring is introduced by burners arranged at the exit of the flue gas from the radiation zone.09-22-2011
20110237848PROCESS AND APPARATUS FOR PRODUCING ETHYLENICALLY UNSATURATED HALOGENATED HYDROCARBONS - The invention is directed to a process and to an apparatus for saving fuel in furnaces for thermal dissociation of halogenated aliphatic hydrocarbons, especially of 1,2-dichloroethane, using chemical dissociation promoters or physical measures which initiate the dissociation reaction.09-29-2011
20120116133METHOD FOR PREPARING OLEFIN FLUORINE COMPOUNDS - The invention relates to a method for preparing olefin fluorine compounds. Specifically, the invention relates to a method for producing a (hydro)fluoroolefin compound, including: (i) in an agitated reactor provided with at least one reactant inlet and at least one outlet, contacting, with potassium hydroxide in an aqueous reaction medium, at least one compound containing three to six carbon atoms, at least two fluorine atoms, and at least one hydrogen atom, with the proviso that at least one hydrogen atom and one fluorine atom are located on adjacent carbon atoms, so as produce the (hydro)fluoroolefin compound, separated in a gaseous state from the reaction medium and from potassium fluoride; (ii) in an aqueous medium, contacvting the potassium fluoride formed in step (i) with calcium hydroxide in a second reactor so as to produce potassium hydroxide and to precipitate calcium fluoride; (iii) separating the calcium fluoride precipitated in step (ii) from the reaction medium; and (iv) optionally recirculating the reaction medium after optionally recirculating the reaction medium after optionally adjusting the concentration of potassium hydroxide in step (i), characterized in that potassium hydroxide, with regard to the reaction medium of step (ii), is between 10 and 35 wt % of the weight of the water/potassium hydroxide mixture of the medium.05-10-2012
20120289751PROCESS FOR PREPARING 1,1,2,3-TETRACHLOROPROPENE - The present invention provides a process for preparing 1,1,2,3-tetrachloropropene, including heating 1,1,1,2,3-pentachloropropane in a gas phase in the absence of a catalyst to carry out a dehydrochlorination reaction. According to the process of the present invention, 1,1,2,3-tetrachloropropene (HCC-1230xa) can be efficiently produced by a simple and economically advantageous method that is suitable for industrial-scale production.11-15-2012
20140081055PROCESS FOR THE PRODUCTION OF CHLORINATED PROPENES - Processes for the production of chlorinated propenes are provided. The present processes make use of 1,2-dichloropropane, a by-product in the production of chlorohydrin, as a low cost starting material, alone or in combination with 1,2,3-trichloropropane. The present processes can also generate anhydrous HCl as a byproduct that can be removed from the process and used as a feedstock for other processes, providing further time and cost savings. Finally, the processes are advantageously conducted in the liquid phase, thereby presenting additional savings as compared to conventional, gas phase processes.03-20-2014
570227000 Catalyst utilized 16
20080242902Composition For the Vapor Phase Dehydrohalogenation of 1,1,2-Trihaloethane To 1,1-Dihaloethylene and Methods For Preparing and Using Such Composition - Described are compositions adapted to catalyze the vapor phase dehydrohalogenation of 1,1,2-trihaloethane to 1,1-dihaloethylene, e.g., 1,1,2-trichloroethane to vinylidene chloride. These materials include activated carbon and at least one benzimidazole-containing material defined herein as including benzimidazole, a derivative thereof, a salt thereof or mixtures thereof. Also described are methods for producing and using these catalytic compositions.10-02-2008
20090030249PROCESSES FOR PREPARING 1,1,2,3-TETRACHLOROPROPENE - Provided is a continuous process for preparing 1,1,2,3-tetrachloro-1-propene having the steps of catalytically dehydrochlorinating CH01-29-2009
20090118555INTEGRATED HFC TRANS-1234ZE MANUFACTURE PROCESS - An integrated process for the manufacture of HFO trans-1,3,3,3-tetrafluoropropene (HFO trans-1234ze) by first catalytically dehydrofluorinating 1,1,1,3,3-pentafluoropropane to thereby produce a mixture of cis-1,3,3,3-tetrafluoropropene, trans-1,3,3,3-tetrafluoropropene and hydrogen fluoride. Then optionally recovering hydrogen fluoride, catalytically isomerizing cis-1234ze into trans-1234ze, and recovering trans-1,3,3,3-tetrafluoropropene.05-07-2009
20090312586HYDROGENATION OF MULTI-BROMINATED ALKANES - Methods and systems for the hydrogenation of multi-brominated alkanes are provided herein. An embodiment of the present invention comprises a method, the method comprising: reacting at least hydrogen and multi-brominated alkanes in the presence of a catalyst to form a hydrogenated stream comprising brominated alkanes having fewer bromine substituents than the multi-brominated alkanes reacted with the hydrogen. Embodiments of the method further may comprise forming brominated alkanes. Embodiments of the method further may comprising forming product hydrocarbons from brominated alkanes.12-17-2009
20120142980SYNTHESIS OF 1,1,3-TRICHLORO-1-PROPENE - Disclosed is a process for the dehydrochlorination of 1,1,1,3-tetrachloropropane comprising contacting 1,1,1,3,tetrachloropropane in the vapor phase in a reaction zone with a catalyst comprising iron, to produce a product mixture comprising 1,1,3-trichloro-1-propene; and recovering said 1,1,3-trichloro-1-propene from the product mixture produced. Also disclosed is a process for the dehydrochlorination of 1,1,1,3-tetrachloropropane comprising heating 1,1,1,3-tetrachloropropane in the liquid phase to produce a mixture comprising 1,1,3-trichloro-1-propene, cooling said mixture, separating hydrogen chloride from said mixture and recovering 1,1,3-trichloro-1-propene.06-07-2012
20120142981METHOD FOR PRODUCING 1,1,3-TRICHLORO-1-PROPENE - A production method of 1,1,3-trichloro-1-propene comprising the following steps A and B;06-07-2012
20130012743METHODS OF MAKING CHLORINATED HYDROCARBONS - Methods for the manufacture of 1,1,1,2,3-pentachloropropane from 1,1,1,3-tetrachloropropane and chlorine are disclosed. Improved methods are provided for the manufacture of 1,1,2,3-tetrachloropropene from 1,1,1,2,3-pentachloropropane. Methods are also disclosed for the manufacture of 1,1,2,3-tetrachloropropene from 1,1,1,3-tetrachloropropane and chlorine and for the manufacture of 1,1,2,3-tetrachloropropene from carbon tetrachloride, ethylene, and chlorine.01-10-2013
20130165705METHOD FOR PRODUCING A CHLORINATED HYDROCARBON HAVING 3 CARBON ATOMS - A method of producing a chlorinated hydrocarbon having 3 carbon atoms, comprising a conversion step for converting a chloropropane represented by the following formula (1) into a chloropropane represented by the following formula (2) by reacting it with chlorine in the presence of anhydrous aluminum chloride.06-27-2013
20130204052CATALYST FOR PREPARING VINYL CHLORIDE, METHODS OF PREPARATION AND APPLICATION THEREOF - The present invention discloses a catalyst used in preparing vinyl chloride, its method of preparation, and its applications. Said catalyst used in making vinyl chloride comprises activated carbon as a support, a barium compound and a phosphorus compound supported thereon. The barium compound accounts for 0.2% to 20% of the total mass of the catalyst and the phosphorus compound accounts for 0% to 10% of the total mass of the catalyst based on the mass percentage. A water-soluble barium compound, a water-soluble phosphorus compound, an aqueous polymer monomer, and water are mixed to form a solution or emulsion A. The activated carbon is added into the solution or emulsion A. The activated carbon is removed from water after impregnation, spin-dried, and then the monomers are polymerized. The activated carbon, after polymerization step, is heated to remove water and to decompose and carbonize the polymer. The catalyst after carbonization was activated to obtain a catalyst used in making vinyl chloride.08-08-2013
20140235907METHODS FOR THE DEHYDROCHLORINATION OF 1,1,1,3-TETRACHLOROPROPANE TO 1,1,3-TRICHLOROPROPENE - This invention relates to a method to improve 1,1,3-trichloropropene selectivity in HCC-250fb (1,1,1,3-tetrachloropropane) dehydrochlorination. In normal practice, FeCl08-21-2014
20140275658METHOD TO REDUCE THE FORMATION OF HIGH BOILING COMPOUNDS DURING THE DEHYDROCHLORINATION OF 1,1,1,3-TETRACHLOROPROPANE - This invention relates to a method to improve 1,1,3-trichloropropene (HCC-1240za) and/or 3,3,3-trichloropropene (HCC-1240zf) selectivity in the dehydrochlorination of 1,1,1,3-tetrachloropropane (HCC-250fb). In normal practice, FeCl09-18-2014
20140275659METHOD TO IMPROVE 1,1,3-TRICHLOROPROPENE AND/OR 3,3,3-TRICHLOROPROPENE SELECTIVITY DURING THE DEHYDROCHLORINATION OF 1,1,1,3-TETRACHLOROPROPANE - This invention relates to a method to improve 1,1,3-trichloropropene (HCC-1240za) and/or 3,3,3-trichloropropene (HCC-1240zf) selectivity in the dehydrochlorination of 1,1,1,3-tetrachloropropane (HCC-250fb). In normal practice, FeCl09-18-2014
20150126786PROCESS FOR PREPARING A C3-C7 (HYDRO) FLUOROALKENE BY DEHYDROHALOGENATION - The invention provides a process for preparing a C05-07-2015
20150344387PROCESS FOR THE PRODUCTION OF CHLORINATED PROPENES - Processes for the production of chlorinated propenes are provided. The present processes make use of 1,2-dichloropropane, a by-product in the production of chlorohydrin, as a low cost starting material. 1,1,1,2,2-pentachloropropane produced by the process is subjected to catalytic dehydrochlorination and build-up of the same within the process is avoided.12-03-2015
20150353451METHODS OF MAKING CHLORINATED HYDROCARBONS - Methods for the manufacture of 1,1,1,2,3-pentachloropropane from 1,1,1,3-tetrachloropropane and chlorine are disclosed. Improved methods are provided for the manufacture of 1,1,2,3-tetrachloropropene from 1,1,1,2,3-pentachloropropane. Methods are also disclosed for the manufacture of 1,1,2,3-tetrachloropropene from 1,1,1,3-tetrachloropropane and chlorine and for the manufacture of 1,1,2,3-tetrachloropropene from carbon tetrachloride, ethylene, and chlorine.12-10-2015
20160002127PROCESS FOR THE PRODUCTION OF CHLORINATED PROPANES - Processes for the production of chlorinated propanes are provided. The processes comprise catalyzing the chlorination of 1,1,1,3-tetrachloropropane with aluminum chloride, either alone or in combination with ferric chloride. Low intensity conditions are appropriate for the process, e.g., temperatures of from ambient to 100° C. and pressures of from ambient to 200 psig may be used. Even though low intensity conditions are used, the aluminum chloride provides at least 1.5 times greater the conversion rate and/or productivity of 1,1,1,3-tetrachloropropane as compared to ferric chloride when used as a single catalyst under similar processing conditions.01-07-2016
570229000 Including chemical reaction with by-product hydrogen halide 1
20160176790PROCESS FOR THE DEHYDROCHLORINATION OF CHLORINATED HYDROCARBONS06-23-2016
570230000 Dehalogenation or dehydrogenation 6
20100041927PROCESS AND APPARATUS FOR PRODUCTION OF VINYL CHLORIDE MONOMER - Process and apparatus to form vinyl chloride monomer from ethylene dichloride in a cracking furnace, including a firebox chamber having a thermal protective layer disposed on refractory walls and/or process tubes disposed within the chamber, a quencher to form vinyl chloride monomer, and fractionator separate products. The thermal protective layer which contains an inorganic adhesive for metal/alloy tubes or colloidal silica and/or colloidal alumina for refractory walls or ceramic tubes, a filler, and one or more emissivity agents.02-18-2010
20140206911Process For Producing Chlorinated Hydrocarbons - The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of ferric chloride and a polyvalent antimony compound that includes a pentavalent antimony compound.07-24-2014
20140371494PROCESS FOR THE PRODUCTION OF CHLORINATED PROPANES AND PROPENES - Processes for the production of chlorinated propanes and propenes are provided. The present processes comprise catalyzing at least one chlorination step with one or more regios elective catalysts that provide a regioselectivity to one chloropropane of at least 5:1 relative to other chloropropanes.12-18-2014
20150045591Processes for Producing Chlorinated Hydrocarbons and Methods for Recovering Polyvalent Antimony Catalysts Therefrom - The preparation of chlorinated hydrocarbons, such as pentachloropropanes, such as 1,1,1,2,3-pentachloropropane, from tetrachloropropanes, such as 1,1,1,3-tetrachloropropane, in the presence of a polyvalent antimony compound that includes a pentavalent antimony compound, such as antimony pentachloride, is described. Also described are methods for preparing optionally chlorinated alkenes, such as, tetrachloropropenes, from chlorinated alkanes, such as pentachloropropanes, in the presence of polyvalent antimony compound that includes a pentavalent antimony compound, as well as methods for recovering polyvalent antimony compounds from such processes.02-12-2015
20150376094METHODS FOR RECOVERING CHLORINATED HYDROCARBONS - Processes for isolating 1,1,1,2,3-pentachloropropane from a crude product stream containing the 1,1,1,2,3-pentachloropropane and ferric chloride. The processes may include deep distillation of the crude, treatment of the crude with a reagent that deactivates the ferric chloride followed by distillation on the deactivated crude stream, aqueous washing of the crude product stream to remove ferric chloride followed by distillation on the deactivated crude stream. Other embodiments simultaneously prepare 1,1,2,3-tetrachloroprene and 1,1,1,2,3-pentachloroprane.12-31-2015
20160251283Processes for Producing Chlorinated Hydrocarbons and Methods for Recovering Polyvalent Antimony Catalysts Therefrom09-01-2016
570231000 Addition reaction of free halogen or hydrogen halide to carbon to carbon unsaturation 1
570232000 To triple bond 1
570233000 To acetylene 1
20100063333Catalytic Hydrochlorination System and Process for Manufacturing Vinyl Chloride from Acetylene and Hydrogen Chloride in the Presence of this Catalytic System - Catalytic hydrochlorination system comprising at least one amine hydrochloride and at least one group VIII metal compound chosen from the group composed of mixtures of a platinum (IV) compound with tin (II) chloride, mixtures of a platinum (II) compound with triphenylphosphine oxide and mixtures of a palladium (II) compound with triphenylphosphine. This catalytic system is suitable for preparing vinyl chloride by reaction of acetylene with hydrogen chloride.03-11-2010
570236000 Isomerization 1
20110218370PROCESS FOR THE MANUFACTURE OF HYDROCHLOROFLUOROOLEFINS - The present invention provides a process for the manufacture of trans 1-chloro-3,3,3-trifluoropropene (E-09-08-2011
570237000 Increasing the number of carbon atoms in the compound 2
20140088329PROCESS FOR THE PRODUCTION OF CHLORINATED AND/OR FLUORINATED PROPENES - Processes for the production of chlorinated and/or fluonnated propenes provide good product yield with advantageous impurity profiles in the crude product. Advantageously, the processes may be conducted at lower temperatures than 600° C., or less than 500° C., so that energy savings are provided, and/or at higher pressures so that high throughputs may also be realized. The use of catalysts or initiators may provide additional enhancements to conversion rates and selectivity, as may adjustments to the molar ratio of the reactants.03-27-2014
20160009615PROCESS FOR THE PRODUCTION OF CHLORINATED PROPENES01-14-2016
570238000 Purification or recovery 3
20140275660METHOD FOR MITIGATING HCL GENERATION DURING 1,1,2,3-TETRACHLOROPROPENE PURIFICATION - This invention is directed to a method for mitigating HCl generation during 1230xa purification, which comprises the steps of; (a) adding a chelating agent into 1230xa crude, and (b) conducting the 1230xa purification in the presence of said chelating agent at a quantity sufficient to reduce or prevent 1230xa decomposition. Examples of chelating agent include tributyl phosphate (TBP), tripropyl phosphate (TPP), and triethyl phosphate (TEP). The concentration of chelating agent in 1230xa crude can range from 0.001 to 20 wt %, preferably from 0.01 to 10 wt %, and more preferably from 0.1 to 5 wt %.09-18-2014
20150353452METHOD FOR HEAT RECOVERY IN VINYL CHLORIDE MONOMER STRUCTURES OR IN THE STRUCTURE COMPOSITE DICHLOROETHANE/VINYL CHLORIDE, AND DEVICE SUITABLE FOR SAME - Energy savings in an integrated DCE/VCM plant, optionally also containing a PVC plant, is accomplished by using at least part of the vapor from a DEC quenching column to supply heat to an HCl column. The DCE plant has a high boiler column operating at superatmospheric pressure, and heat is removed from an overhead stream and used to supply heat to other portions of the process.12-10-2015
570239000 Including contact with solid agent 1
20120226081METHOD TO PURIFY AND STABILIZE CHLOROOLEFINS - The present invention is directed towards a method of purification of chloroolefins having 3 carbons and to a method to provide stable compositions of chloroolefins having 3 carbons. The chloroolefins are purified via the use of a solid absorbents for the removal of decomposition product such as phosgene and/or phosgene precursory from the reaction of the chloroolefins with oxygen. The chloroolefins stabilized against an increase of the phosgene level via the addition of inhibitors to the chloroolefins.09-06-2012

Patent applications in all subclasses Processes of preparing, purifying, or recovering unsaturated compound

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