Patent application number | Description | Published |
20140336424 | Method for Producing Trans-1-Chloro-3,3,3-Trifluoropropene - Provided is a method for producing trans-1-chloro-3,3,3-trifluoropropene usable as a raw material for a foaming agent for a hard polyurethane foam, a solvent, a cleaning agent, a cooling medium, a working fluid, a propellant, a fluorinated resin, etc., the method involving a step of bringing cis-1-chloro-3,3,3-trifluoropropene into contact with a catalyst, wherein the catalyst includes a fluorinated metal oxide or a metal fluoride each produced by applying a fluorination treatment to a metal oxide containing one kind or two or more kinds of metals and containing aluminum atoms that make up 50 at. % or more of metal atoms to thereby substitute some or all of oxygen atoms in the metal oxide with fluorine atom(s), wherein the fluorinated metal oxide or the metal fluoride is a compound produced through a drying treatment at 400 to 600° C. | 11-13-2014 |
20140357907 | Process for Producing 1,2-Dichloro-3,3,3-Trifluoropropene - Disclosed is a process for producing 1,2-dichloro-3,3,3-trifluoropropene, which is characterized by that 1-halogeno-3,3,3-trifluoropropene represented by the general formula [1]: | 12-04-2014 |
20150038749 | Process for Producing 2-Chloro-1,3,3,3-Tetrafluoropropene - Disclosed is a process for producing 2-chloro-1,3,3,3-tetrafluoropropene (1224), including a first step of separating 2,3-dichloro-1,1,1,3-tetrafluoropropane 234da) into erythro form and threo form, and a second step of bringing the separated erythro form or threo form in contact with a base to obtain 2-chloro-1,3,3,3-tetrafluoropropene (1224). The first step is a step of separating 234da by distillation to achieve a separation into a fraction containing mainly erythro form and a fraction containing mainly threo form. In the second step, 1224 cis form is obtained from the erythro form, and 1224 trans form is obtained from the threo form. By this process, it is possible to selectively and efficiently produce cis form or trans form of 2-chloro-1,3,3,3-tetrafluoropropene (1224). | 02-05-2015 |
20150080618 | Method for Producing CIS-1,3,3,3-Tetrafluoropropene - A production method of cis-1,3,3,3-tetrafluoropropene according to the present invention includes the steps of: subjecting 1,1,1,3,3-pentafluoropropane to dehydrofluorination to form a reaction mixture (A) containing cis-1,3,3,3-tetrafluoropropene, trans-1,3,3,3-tetrafluoropropene and unreacted 1,1,1,3,3-pentafluoropropane; distilling the reaction mixture (A) to separate the trans-1,3,3,3-tetrafluoropropene from the reaction mixture (A) and collect a reaction mixture (B) containing the cis-1,3,3,3-tetrafluoropropene and the 1,1,1,3,3-pentafluoropropane; and reacting the reaction mixture (B) with a base and thereby obtaining the cis-1,3,3,3-tetrafluoropropene from the reaction mixture (B). This production method enables efficient production of high-purity cis-1,3,3,3-tetrafluoropropene and thus has industrial advantages. | 03-19-2015 |
20150099907 | METHOD FOR PRODUCING 1-CHLORO-3,3,3-TRIFLUORO-1-PROPENE AND 1,3,3,3-TETRAFLUOROPROPENE - A method for producing a desired isomer of 1-chloro-3,3,3-trifluoro-1-propene or a desired isomer of 1,3,3,3-tetrafluoropropene at a high conversion ratio with no use of a solid catalyst is provided. Since no solid catalyst is used, a desired isomer of 1-chloro-3,3,3-trifluoro-1-propene and a desired isomer of 1,3,3,3-tetrafluoropropene can be stably obtained with no undesired possibility that the solid catalyst is deteriorated due to coking or the like caused as a result of long-time use thereof. | 04-09-2015 |
20150112103 | METHOD FOR PRODUCING CIS-1,3,3,3-TETRAFLUOROPROPENE - A method for producing 1234Z from 1234E while generation of 245fa as a byproduct is suppressed. The method for producing cis-1,3,3,3-tetrafluoropropene includes putting trans-1,3,3,3-tetrafluoropropene into contact with a catalyst. The trans-1,3,3,3-tetrafluoropropene is put into contact with the catalyst at a reaction temperature of higher than or equal to 200° C. and lower than or equal to 550° C. for a contact time of longer than or equal to 0.01 seconds and shorter than or equal to 500 seconds. | 04-23-2015 |
20150122461 | Medium for Boiling-Type Cooler and Method of Using Same - A working medium containing 2-methoxy-1,1,1,3,3,3-hexafluoropropane (HFE-356mmz) as a main component is disclosed. This working medium is a new working medium for a boiling-type cooler, which has a light burden on the environment such as the global warming potential, etc., is slightly flammable or flame retardant, has superior thermal and chemical stabilities, and a good compatibility with heat exchangers formed of various metal materials. This medium for the boiling-type cooler can be preferably used as a working medium for a cooler of a PCU (power control unit) of a car. | 05-07-2015 |
20150152749 | METHOD FOR CONVERTING THERMAL ENERGY INTO MECHANICAL ENERGY, ORGANIC RANKINE CYCLE DEVICE, AND METHOD FOR REPLACING WORKING FLUID - Provided is a method for converting thermal energy into mechanical energy by use of an organic rankine cycle system that accommodates a working fluid composition. The method includes sequentially performing: evaporating the working fluid composition; expanding the working fluid composition; condensing the working fluid composition; and transferring the working fluid composition, while raising a pressure thereof, by a pump. The working fluid composition contains cis-1,3,3,3-tetrafluoropropene at a ratio higher than or equal to 92.0% by mass and lower than or equal to 99.9% by mass and trans-1,3,3,3-tetrafluoropropene or 2,3,3,3-tetrafluoropropene at a ratio higher than or equal to 0.1% by mass and lower than or equal to 8.0% by mass; and has an evaporation temperature higher than or equal to 60° C. and lower than or equal to 150° C. | 06-04-2015 |