![]() COMPOSITION BASED ON HYDROCHLOROFLUOROOLEFIN AND MINERAL OIL
专利摘要:
The invention relates to the use of a composition comprising at least one hydrochlorofluoroolefin, at least one mineral oil and air, the air being in a mass proportion of less than 1% relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air, wherein the composition is subjected to a maximum temperature of change of state greater than or equal to about 100 ° C. 公开号:FR3070982A1 申请号:FR1758429 申请日:2017-09-12 公开日:2019-03-15 发明作者:Wissam Rached;Pascale KINDLER 申请人:Arkema France SA; IPC主号:
专利说明:
COMPOSITION BASED ON HYDROCHLOROFLUOROOLEFIN AND MINERAL OIL FIELD OF THE INVENTION The present invention relates to compositions comprising a hydrochlorofluoroolefin, a mineral oil and air, which are stable and suitable for use as heat transfer compositions. TECHNICAL BACKGROUND Hydrochlorofluoroolefins are products with a low global warming potential (GWP). For example, trans-1-chloro- 3,3,3-trifluoropropene (HCFO-1233zd) has very favorable thermodynamic and thermophysical properties for use as a heat transfer fluid in cooling, air conditioning and air conditioning applications (in particular in centrifugal compressors), electricity production (in particular using organic Rankine cycles) and high temperature heat pumps. In air conditioning applications, the pressure of the HCFO-1233zdE in the evaporator is often lower than atmospheric pressure, which favors the infiltration of air, and in particular oxygen, into the installation. In heat pumps, air infiltration can occur when the system is stopped. There can also be air infiltration in any installation using a heat transfer fluid during filling or maintenance of said installation. The presence of air mixed with HCFO1233zdE promotes the isomerization reaction of HCFO-1233zdE and therefore the formation of the HCFO-1233zdZ (cis-1-chloro-3,3,3-trifluoropropene) isomer. This cis isomer has thermodynamic properties very different from those of HCFO-1233zdE, which has a negative impact on the performance of installations. In order to prevent the isomerization of HCFO-1233zdE to HCFO-1233zdZ, stabilizers can be added to HCFO-1233zdE. For example, document FR 3033791 describes the use of an alkene compound, in particular 2-methylbut-2-ene and 3-methylbut-1-ene, to prevent the isomerization of trans-1-chloro-3 , 3,3-trifluoropropene to cis-1chloro-3,3,3-trifluoropropene. In the industrial field, the most widely used refrigeration machines are based on evaporative cooling of a liquid refrigerant. After vaporization, the fluid is compressed then condensed and finally expanded to complete the cycle. The refrigeration compressors used can be of the reciprocating, scroll, centrifugal or screw type. In general, the internal lubrication of compressors is essential to reduce wear and warming of moving parts, improve their sealing and protect them against corrosion. As a lubricant, a mineral oil can be used, which is less expensive than oxygenated oils such as polyol esters. Document US 8,454,853 describes the miscibility of 1-chloro-3,3,3trifluoropropene with mineral oils and the use of the corresponding mixtures as refrigerant compositions. In refrigeration systems, the oil is in direct contact with the refrigerant (for example hydrochlorofluoroolefin) at the compressor and throughout the installation. The refrigerant / oil combination must be stable regardless of the thermal stresses in the installation, as well as in the presence of impurities, infiltrated air and humidity. The oil must provide lubrication for the compressor bearings regardless of the conditions of use of the compressor. In this regard, the viscosity of the refrigerant / oil mixture is an indicator of lubrication performance. The refrigerant dissolves in the oil and lowers its viscosity. Thus, to select an oil, measurements of solubility and viscosity on the oil / refrigerant pair are carried out to determine the variation in viscosity of the mixture according to the conditions of use. These measurements allow you to choose the optimal oil viscosity grade to use based on operating temperatures. However, if during the operation of the installation, there is degradation of the compounds and formation of new products, the solubility and viscosity measurements are no longer valid. The oil may then lose its role of lubrication. Thus, if there is isomerization or decomposition of the refrigerant or oil, the performance of the installation may be degraded, as well as that of the lubricant due to the variation of the viscosity outside the predefined ranges. For example, oil degradation and the formation of small particles as a result are harmful to the compressor. There is therefore a real need to provide a low GWP coolant / lubricant oil mixture, economical and stable over time, in particular stable at high temperatures. SUMMARY OF THE INVENTION The invention relates firstly to a composition comprising at least one hydrochlorofluoroolefin, at least one mineral oil and air, the air being in a mass proportion of less than 1% relative to the mass of the mixture of the at least hydrochlorofluoroolefin and air. According to one embodiment, the composition does not comprise a stabilizer. According to one embodiment, the composition essentially consists, and preferably consists, of at least one hydrochlorofluoroolefin, at least one mineral oil and air, the air being in a mass proportion of 0% excluded to 1% excluded by relative to the mass of the mixture of at least one hydrochlorofluoroolefin and air. According to one embodiment, the mass proportion of air in the composition is from 0.05% to 1% excluded, preferably from 0.1% to 1% excluded, even more preferably from 0.2% to 1% excluded , relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air. According to one embodiment, the mass proportion of air in the composition is from 0% excluded to 0.6% inclusive, preferably from 0% excluded to 0.4% inclusive, relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air. According to one embodiment, the mass proportion of air in the composition is from 0.05% inclusive to 0.4% inclusive, preferably from 0.1% inclusive to 0.4% inclusive, relative to the mass of the mixture of at least one hydrochlorofluoroolefin and air. According to one embodiment, the at least one hydrochlorofluoroolefin is chosen from 1-chloro-3,3,3-trifluoropropene, in particular trans-1chloro-3,3,3-trifluoropropene, 2-chloro-3, 3,3-trifluoropropene, 3,3,3,2tetrafluorochloro-1-propene, a dichlorotrifluoropropene or a combination thereof. According to one embodiment, the at least one hydrochlorofluoroolefin is 1-chloro-3,3,3-trifluoropropene. According to one embodiment, the 1-chloro-3,3,3-trifluoropropene is in trans form in a mass proportion greater than or equal to 90%, preferably greater than or equal to 95%, more particularly preferably greater than or equal at 98%, even more preferably greater than or equal to 99%, even more preferably greater than or equal to 99.5%, or even greater than or equal to 99.9%, relative to the total mass of 1-chloro -3,3,3-trifluoropropene. According to one embodiment, the mineral oil is in a mass proportion of 2% to 70% relative to the total mass of the composition. The invention also relates to the use for the heat transfer of a composition as described above in which the composition is subjected to at least one change of state at an average temperature greater than or equal to about 100 ° C. According to one embodiment, the composition is subjected to at least one change of state at an average temperature of from approximately 100 ° C. to approximately 200 ° C. According to one embodiment, the invention relates to a use as described above in a vapor compression system or in a machine for producing mechanical or electrical energy and preferably for producing electricity. According to one embodiment, the vapor compression system is an air conditioning system, a refrigeration system, a freezing system, or a heat pump system. The invention also relates to an installation comprising a circuit containing a composition as described above as a heat transfer composition. According to one embodiment, the installation is chosen from mobile or stationary installations for heating by heat pump, air conditioning, refrigeration, freezing and machines for producing mechanical or electrical energy, preferably for producing electricity. The invention also relates to a method of heating or cooling a fluid or a body by means of a vapor compression system containing a heat transfer composition, said method successively comprising evaporating the composition of heat transfer, compression of the heat transfer composition, condensation of the heat composition and expansion of the heat transfer composition, wherein the heat transfer composition is a composition as described above. The invention also relates to a method for producing mechanical or electrical energy, and preferably for producing electricity by means of a machine comprising a circuit containing a heat transfer composition, said method successively comprising evaporating the heat transfer composition, the expansion of the heat transfer composition in a turbine for generating mechanical or electrical energy, and preferably electricity, the condensation of the heat transfer composition and the compression of the heat transfer composition, wherein the heat transfer composition is a composition as described. The present invention makes it possible to meet the need expressed above. It more particularly provides compositions comprising a hydrochlorofluoroolefin, a mineral oil and air having good thermal stability, including at temperatures between 100 ° C and 200 ° C, and over a significant period. This is accomplished thanks both to the use of a mineral oil which reduces or even prevents the degradation, and in particular the isomerization, of hydrochlorofluoroolefin, and to the presence of air in a range of specific mass proportion making it possible to limit or even prevent the degradation of mineral oil. According to certain particular embodiments, the invention also has one or preferably several of the advantageous characteristics listed below: - The compositions according to the invention can be stored and used without adding stabilizer; - They are less complex and therefore expensive to produce than the compositions containing an oxygenated synthetic oil; - they can be used in existing installations already operating with mineral oil as a lubricant. DESCRIPTION OF EMBODIMENTS OF THE INVENTION The invention is now described in more detail and without limitation in the description which follows. In the context of the invention, "HCFO-1233zd" refers to 1-chloro- 3,3,3-trifluoropropene, regardless of whether it is the cis or trans form. The terms "HCFO-1233zdZ" and "HCFO-1233zdE" refer to the cis- and trans- forms of 1-chloro-3,3,3-trifluoropropene, respectively. The term “HCFO-1233zd” therefore covers HCFO-1233zdZ, HCFO-1233zdE, and all mixtures of the two isomeric forms in all proportions. Unless otherwise stated, throughout the application, the proportions of compounds indicated are given in percentages by mass. Unless otherwise indicated, throughout the request, the range limits are included in said range. hydrochlorofluoroolefin The invention uses at least one hydrochlorofluoroolefin. By "hydrochlorofluoroolefin" is meant an unsaturated hydrocarbon compound substituted by one or more chlorine atoms and by one or more fluorine atoms, knowing that at least one hydrogen atom is not substituted. Advantageously, the hydrochlorofluoroolefin is 1-chloro-3,3,3trifluoropropene, 2-chloro-3,3,3-trifluoropropene, 3,3,3,2tetrafluorochloro-1-propene, a dichlorotrifluoropropene or a combination of those -this. Preferably, the hydrochlorofluoroolefin is 1-chloro-3,3,3trifluoropropene. When the hydrochlorofluoroolefin is 1-chloro-3,3,3trifluoropropene, it may be trans-1-chloro-3,3,3-trifluoropropene, cis1-chloro-3,3,3-trifluoropropene or d 'a mixture of these. According to an advantageous embodiment, the hydrochlorofluoroolefin is 1-chloro-3,3,3-trifluoropropene, the latter being in trans form in a mass proportion greater than or equal to 90%, preferably greater than or equal to 95%, more particularly preferably greater than or equal to 98%, even more preferably greater than or equal to 99%, even more preferably greater than or equal to 99.5%, or even greater than or equal to 99.9%, relative to the total mass of 1-chloro-3,3,3trifluoropropene (i.e. relative to the sum of trans-1-chloro-3,3,3trifluoropropene and cis-1-chloro-3,3 , 3-trifluoropropene). Mineral oil The invention also uses mineral oil. Preferably, this mineral oil is a by-product from the refining of petroleum. Mineral oils can include paraffins (i.e. linear or branched saturated hydrocarbons), naphthenes (i.e. cyclic paraffins), aromatics (i.e. cyclic unsaturated hydrocarbons containing one or more rings characterized by double bonds alternating with single bonds) and non-hydrocarbon compounds. These mineral oil compounds are not necessarily present in the oil in the free state. It is common for a paraffinic chain to be attached to a naphthenic or aromatic structure. Likewise, a naphthenic ring to which a paraffinic chain is attached can in turn be attached to an aromatic structure. Because of these properties, a mineral oil is often described by an analysis of the types of carbon. In this analysis, the number of carbon atoms in the paraffin chains, naphthenic structures and aromatic rings is determined and represented as a percentage of the total. Thus, the percentage of carbon atoms having a paraffinic configuration% Cp, includes not only the free paraffins but also the paraffinic chains attached to the naphthenic or aromatic rings. Similarly, the percentage of carbon atoms in naphthenic structures% C / v includes the carbon atoms of free naphthenes as well as those of naphthenic rings attached to aromatic rings, and% Ca represents the carbon of aromatic rings. Carbon analysis describes a lubricant (or oil) in its basic structure and predicts a number of physical properties of the lubricant. The traditional classification of mineral oils as paraffinic or naphthenic oils refers to the number of paraffinic or naphthenic molecules in the oil. Paraffinic oils contain a higher proportion of paraffin wax, and thus have a higher viscosity index and pour point than naphthenic oils. According to an advantageous embodiment, the mineral oils used in the invention have an average kinematic viscosity ranging from 1 to 1000 cSt (centistokes) at 40 ° C, preferably from 10 to 300 cSt, measured according to standard ISO 3104. The ISO standard 3448 establishes a classification system for industrial liquid lubricants according to their viscosity. According to a particular embodiment, the mineral oil is a naphthenic oil, with% Cpde preferably less than 50%. Advantageously, the naphthenic cycles of the naphthenic fraction of the oil are mainly naphthenic cycles in C5 to C7. compositions The invention relates to a composition comprising at least one hydrochlorofluoroolefin, at least one mineral oil and air. According to the invention, the air is present in the composition in a mass proportion of 0% excluded to 1% excluded relative to the mass of the mixture of at least one hydrochlorofluoroolefin and air. This proportion of air means the composition in use, i.e. for example in the circuit in which it circulates. In certain embodiments, only one hydrochlorofluoroolefin is present in the composition, preferably as described above. Thus, preferably, the composition comprises only HCFO-1233zd (predominantly in trans form, as described above) as hydrochlorofluoroolefin (with the possible exception of other hydrochlorofluoroolefins present as impurities in a total mass content less than or equal at 1%, or at 0.5%, or at 0.1%, relative to the total of the composition). Alternatively mixtures of different hydrochlorofluoroolefins can be used in the composition. Advantageously, the composition according to the invention does not contain any stabilizer other than mineral oil. The term “stabilizer” means any compound making it possible to limit or eliminate the degradation of one of the constituents of the composition, in particular hydrochlorofluoroolefin or mineral oil, for example limiting or eliminating the isomerization of the hydrochlorofluoroolefin. According to one embodiment, the composition essentially consists of at least one hydrochlorofluoroolefin, at least one mineral oil and air in a mass proportion of 0% excluded to 1% excluded relative to the mass of the mixture of at least hydrochlorofluoroolefin and air. According to another embodiment, the composition consists of at least one hydrochlorofluoroolefin, at least one mineral oil and air in a mass proportion of 0% excluded to 1% excluded relative to the mass of the mixture of at least hydrochlorofluoroolefin and air. According to certain advantageous embodiments, the air in the composition is in a proportion by mass, relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air, from 0.05% to 1% excluded, of preferably from 0.1% to 1% excluded, even more preferably from 0.2% to 1% excluded. According to other advantageous embodiments, the air in the composition is in a proportion by mass, relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air, from 0% excluded to 0.6% inclusive, in particular from 0% excluded to 0.4% inclusive, in particular from 0.05% inclusive to 0.4% inclusive, and preferably from 0.1% inclusive to 0.4% inclusive. In other embodiments, the air is present in the composition, in a proportion by mass of 0% excluded to 0.05% inclusive, or from 0.05% included to 0.1% inclusive, or from 0, 1% inclusive at 0.15% inclusive, or 0.15% inclusive at 0.2% inclusive, or 0.2% inclusive at 0.25% inclusive, or 0.25% inclusive at 0.3% included, or from 0.3% included to 0.35% included, or from 0.35% included to 0.4% included, or from 0.4% included to 0.45% included, or by 0.45% included at 0.5% included, or from 0.5% included at 0.55% included, or from 0.55% included at 0.6% included, or from 0.6% included to 0.7% included, or 0.7% inclusive to 0.8% inclusive, or 0.8% inclusive to 0.9% inclusive, or 0.9% inclusive to 1% excluded, based on the mass of the mixture of at least one hydrochlorofluoroolefin and air. The mass proportion of air is determined by gas chromatography. The measurement of the mass proportion of air of a composition circulating in a functioning installation can be carried out by taking a sample of the gaseous phase of the composition in the installation, then analyzing the sample by gas chromatography. According to one embodiment, in the composition, the mineral oil is in a mass proportion of 2% to 70% relative to the total mass of the composition. According to other embodiments, the mineral oil is in a mass proportion of 1 to 5%, or from 5 to 10%, or from 10 to 15%, or from 15 to 20%, or from 20 to 25% , or 25 to 30%, or 30 to 35%, or 35 to%, or 40 to 45%, or 45 to 50%, or 50 to 55%, or 55 to 60%, 60 to 65%, 65 to 70%, 70 to 75%, 75 to 80%, or 80 to 85%, or 85 to 90%, or 90 to 95%, or 95 to 99% , relative to the total mass of the composition. The mass proportion of the hydrochlorofluoroolefin (s) can be from 1 to 5%, or from 5 to 10%, or from 10 to 15%, or from 15 to 20%, or from 20 to 25%, or from 25 to 30% , or from 30 to 35%, or from 35 to 40%, or from 40 to 45%, or from 45 to 50%, or from 50 to 55%, or from 55 to 60%, or from 60 to 65%, or from 65 to 70%, or from 70 to 75%, or from 75 to 80%, or from 80 to 85%, or from 85 to 90%, or from 90 to 95%, or from 95 to 99%, by relative to the total of the composition. In embodiments, the composition also comprises at least one additive, preferably chosen from nanoparticles, surfactants, tracer agents, fluorescent agents, odorous agents and solubilizing agents. According to a particular embodiment, the composition essentially consists, preferably consists, of at least one hydrochlorofluoroolefin, at least one mineral oil, air and one or more additives chosen from nanoparticles, surfactants, tracer agents, agents fluorescent, odorous agents and solubilizing agents, the air being in a mass proportion of 0% excluded to 1% excluded relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air. As nanoparticles, it is possible in particular to use carbon nanoparticles, metal oxides, preferably copper or aluminum oxides, titanium dioxide T1O2, alumina AI2O3, molybdenum disulphide SO2 or combinations thereof. As tracer agents (capable of being detected), mention may be made of deuterated or non-deuterated hydrofluorocarbons, deuterated hydrocarbons, perfluorocarbons, fluoroethers, brominated compounds, iodized compounds, alcohols, aldehydes, ketones, nitrous oxide and combinations thereof. The tracer is different from the hydrochlorofluoroolefin (s) of the invention. As solubilizers, mention may be made of hydrocarbons, dimethyl ether, polyoxyalkylene ethers, amides, ketones, nitriles, chlorocarbons, esters, lactones, aryl ethers, fluoroethers and 1.1 , 1-trifluoroalcanes. The solubilizing agent is different from the hydrochlorofluoroolefin (s) of the invention. As fluorescers, there may be mentioned naphthalimides, perylenes, coumarins, anthracenes, phenanthracenes, xanthenes, thioxanthenes, naphthoxanhtenes, fluoresceins and derivatives thereof. As odorants, mention may be made of alkylacrylates, allylacrylates, acrylic acids, acrylesters, alkyl ethers, alkyl esters, alkynes, aldehydes, thiols, thioethers, disulfides, allylisothiocyanates, alkanoic acids , amines, norbornenes, norbornene derivatives, cyclohexene, heterocyclic aromatic compounds, ascaridole, 10-methoxy (methyl) -phenol and combinations thereof. uses An object of the invention is the use for the heat transfer of a composition as described above in which the composition is subjected to at least one change of state at an average temperature greater than or equal to 100 ° C. , preferably at an average temperature of about 100 ° C to about 200 ° C. According to particular embodiments, the composition is subjected to at least one change of state at an average temperature of approximately 100 ° C to approximately 110 ° C, or approximately 110 ° C to approximately 120 ° C, or d '' approximately 120 ° C to approximately 130 ° C, or approximately 130 ° C to approximately 140 ° C, or approximately 140 ° C to approximately 150 ° C, or approximately 150 ° C to approximately 160 ° C, or from about 160 ° C to about 170 ° C, or from about 170 ° C to about 180 ° C, or from about 180 ° C to about 200 ° C. By “change of state” is meant either a condensation, that is to say the passage of the composition from the gaseous state to the liquid state, or an evaporation, that is to say the passage of the composition from liquid to gaseous state. "Average temperature of change of state" means the temperature of change of state if this temperature is constant or, if the temperature of change of state is not constant, the arithmetic mean of the temperature at the start of the change of state and the temperature at the end of the change of state. According to one embodiment, the composition is used in a vapor compression system. The present invention also relates to a heat transfer method based on the use of an installation comprising a vapor compression system which contains the composition of the invention as a heat transfer composition. The heat transfer process can be a process of heating or cooling a fluid or a body. By "heat transfer composition" is meant a composition comprising a heat transfer fluid and optionally one or more additives which are not heat transfer compounds for the intended application. By “heat transfer fluid”, is meant a fluid capable of absorbing heat by evaporating at low temperature and low pressure and rejecting heat by condensing at high temperature and high pressure, in a circuit of vapor compression. Generally, a heat transfer fluid may comprise a single, two, three or more of three heat transfer compounds. By "heat transfer compound" is meant a compound capable of absorbing heat by evaporating at low temperature and low pressure and rejecting heat by condensing at high temperature and high pressure, in a circuit of vapor compression. According to one embodiment, the vapor compression system is: - an air conditioning system; or - a refrigeration system; or - a freezing system; or - a heat pump system. According to another embodiment, the composition is used in a machine for producing mechanical or electrical energy. The composition of the invention can thus be used in a process for the production of mechanical work or electricity, in particular in accordance with an organic Rankine cycle. It has been found that the higher the average temperature of change of state to which the composition is subjected, the lower the maximum threshold for the quantity of air acceptable. Thus, it is advisable to further limit the presence of air in the composition when the average temperature of at least one change of state of the composition during its use is relatively high. Installations and processes The subject of the invention is also a heat transfer installation comprising a circuit containing a composition as described above as a heat transfer composition. The circuit comprising the heat transfer composition is for example a vapor compression circuit. According to one embodiment, this installation is chosen from mobile or stationary refrigeration, heating (heat pump), air conditioning and freezing installations, and mechanical or electrical energy production machines. It can notably be a heat pump installation, in which case the fluid or body that is heated (generally air and possibly one or more products, objects or organisms) is located in a room or a vehicle interior (for mobile installation). According to a preferred embodiment, it is an air conditioning installation, in which case the fluid or body that is cooled (generally air and possibly one or more products, objects or organisms) is located in a room or vehicle interior (for mobile installation). It may be a refrigeration installation or a freezing installation (or cryogenic installation), in which case the fluid or body which is cooled generally comprises air and one or more products, objects or organisms. , located in a room or container. The invention also relates to a method of heating or cooling a fluid or a body by means of a vapor compression system containing a heat transfer composition as described above, said method comprising successively evaporating the heat transfer composition, compressing the heat transfer composition, condensing the heat transfer composition and relaxing the heat transfer composition. A subject of the invention is also a method for producing mechanical work, or preferably for producing electricity, by means of a machine comprising a circuit which contains a heat transfer composition as described above, said method successively comprising the evaporation of the heat transfer composition, the expansion of the heat transfer composition in a turbine making it possible to generate mechanical or electrical energy, and preferably electricity, the condensation of the composition heat transfer and compression of the heat transfer composition. The vapor compression circuit containing a heat transfer composition includes at least one evaporator, compressor, condenser and expander, as well as lines for transporting heat transfer fluid therebetween. The evaporator and the condenser include a heat exchanger allowing heat exchange between the heat transfer composition and another fluid or body. As a compressor, it is possible in particular to use a centrifugal compressor with one or more stages or a centrifugal mini-compressor. Rotary, piston or screw compressors can also be used. The compressor can be driven by an electric motor or by a gas turbine (for example powered by vehicle exhaust gases, for mobile applications) or by gear. A centrifugal compressor is characterized in that it uses rotary elements to radially accelerate the heat transfer composition; it typically comprises at least one rotor and one diffuser housed in an enclosure. The heat transfer composition is introduced into the center of the rotor and flows towards the periphery of the rotor undergoing acceleration. Thus, on the one hand the static pressure increases in the rotor, and especially on the other hand, at the level of the diffuser, the speed is converted into an increase in the static pressure. Each rotor / diffuser assembly constitutes a stage of the compressor. Centrifugal compressors can have from 1 to 12 stages, depending on the desired final pressure and the volume of fluid to be treated. The compression ratio is defined as being the ratio of the absolute pressure of the heat transfer composition at the outlet to the absolute pressure of said composition at the inlet. The rotation speed for large centrifugal compressors ranges from 3000 to 7000 revolutions per minute. Small centrifugal compressors (or centrifugal mini-compressors) generally operate at a rotational speed ranging from 40,000 to 70,000 revolutions per minute and have a small rotor (generally less than 0.15 m). A multi-stage rotor can be used to improve the efficiency of the compressor and limit the energy cost (compared to a single-stage rotor). For a two-stage system, the output of the first stage of the rotor feeds the inlet of the second rotor. The two rotors can be mounted on a single axis. Each stage can provide a fluid compression ratio of approximately 4 to 1, that is, the absolute outlet pressure can be approximately four times the absolute suction pressure. Examples of two-stage centrifugal compressors, in particular for automotive applications, are described in documents US 5,065,990 and US 5,363,674. The centrifugal compressor can be driven by an electric motor or by a gas turbine (for example powered by vehicle exhaust gases, for mobile applications) or by gear. The installation may include a coupling of the regulator with a turbine to generate electricity (Rankine cycle). The installation may also optionally include at least one heat transfer fluid circuit used to transmit heat (with or without change of state) between the circuit of the heat transfer composition and the fluid or body to be heated or cooled. The installation can also optionally include two (or more) vapor compression circuits, containing identical or distinct heat transfer compositions. For example, the vapor compression circuits can be coupled together. The vapor compression circuit operates according to a conventional vapor compression cycle. The cycle includes changing the state of the heat transfer composition from a liquid phase (or two-phase liquid / vapor) to a vapor phase at a relatively low pressure, then compressing the composition in the vapor phase to a relatively high pressure, the change of state (condensation) of the heat transfer composition from the vapor phase to the liquid phase at a relatively high pressure, and the reduction in pressure to start the cycle again. In the case of a cooling process, heat from the fluid or from the body which is cooled (directly or indirectly, via a heat transfer fluid) is absorbed by the heat transfer composition, upon evaporation of the latter, and at a relatively low temperature compared to the environment. The cooling methods include the methods of air conditioning (with mobile installations, for example in vehicles, or stationary), refrigeration and freezing or cryogenics. In the case of a heating process, heat is transferred (directly or indirectly, via a heat transfer fluid) from the heat transfer composition, during the condensation thereof, to the fluid or to the body that the it is heated to a relatively high temperature compared to the environment. The installation for carrying out the heat transfer is called in this case "heat pump". It is possible to use any type of heat exchanger for implementing the heat transfer compositions according to the invention, and in particular co-current heat exchangers or, preferably, counter heat exchangers -current. According to a preferred embodiment, the invention provides that the cooling and heating methods, and the corresponding installations, include a counter-current heat exchanger, either in the condenser or in the evaporator. In fact, the heat transfer compositions according to the invention are particularly effective with counter-current heat exchangers. Preferably, both the evaporator and the condenser include a counter-current heat exchanger. According to the invention, the term “counter-current heat exchanger” means a heat exchanger in which heat is exchanged between a first fluid and a second fluid, the first fluid at the inlet of the exchanger exchanging heat with the second fluid at the outlet of the exchanger, and the first fluid at the outlet of the exchanger exchanging heat with the second fluid at the inlet of the exchanger. For example, counter-current heat exchangers include devices in which the flow of the first fluid and the flow of the second fluid are in opposite directions, or almost opposite. Exchangers operating in cross-current mode with counter-current tendency are also included among the counter-current heat exchangers within the meaning of the present application. In "low temperature refrigeration" processes, the inlet temperature of the heat transfer composition to the evaporator is preferably from -45 ° C to -15 ° C, especially from -40 ° C to -20 ° C, more particularly preferably from -35 ° C to -25 ° C and for example around -30 ° C; and the temperature at the start of the condensation of the heat transfer composition in the condenser is preferably from 25 ° C to 80 ° C, especially from 30 ° C to 60 ° C, more particularly from 35 ° C to 55 ° C and for example around 40 ° C. In "moderate temperature cooling" processes, the inlet temperature of the heat transfer composition to the evaporator is preferably from -20 ° C to 10 ° C, especially from -15 ° C to 5 ° C , more particularly preferably from -10 ° C to 0 ° C and for example around -5 ° C; and the temperature at the start of the condensation of the heat transfer composition in the condenser is preferably from 25 ° C to 80 ° C, especially from 30 ° C to 60 ° C, more particularly from 35 ° C to 55 ° C and for example around 50 ° C. These methods can be refrigeration or air conditioning methods. In "moderate temperature heating" processes, the inlet temperature of the heat transfer composition to the evaporator is preferably from -20 ° C to 10 ° C, especially from -15 ° C to 5 ° C , more particularly preferably from -10 ° C to 0 ° C and for example around -5 ° C; and the temperature at the start of the condensation of the heat transfer composition in the condenser is preferably from 25 ° C to 80 ° C, especially from 30 ° C to 60 ° C, more particularly from 35 ° C to 55 ° C and for example around 50 ° C. In "high temperature heating" methods, the inlet temperature of the heat transfer composition to the evaporator is preferably from -20 ° C to 90 ° C, in particular from 10 ° C to 90 ° C, more particularly preferably from 50 ° C to 90 ° C and for example about 80 ° C; and the temperature at the start of the condensation of the heat transfer composition in the condenser is preferably from 70 ° C to 160 ° C, in particular from 90 ° C to 150 ° C, more particularly from 110 ° C to 140 ° C and for example around 135 ° C. The compositions according to the invention are particularly advantageous in refrigerated transport. It is considered as "refrigerated transport" any movement of perishable products under refrigerated space. Food or pharmaceutical products represent an important part of perishable products. Refrigerated transport can be carried out by truck, rail or boat, possibly using multi-platform containers which can be adapted as well on trucks, rails or boats. In refrigerated transport, the temperature of the refrigerated spaces is between -30 ° C and 16 ° C. The refrigerant charge in transport by truck, rail or multi-platform containers varies between 4 kg and 8 kg of refrigerant. Installations in boats can contain between 100 and 500 kg of refrigerant. The most widely used refrigerant to date for this application is R404A. The operating temperatures of the refrigeration installations depend on the refrigeration temperature requirements and the external climatic conditions. The same refrigeration installation must be able to cover a wide range of temperatures between -30 ° C and 16 ° C and operate in both cold and hot climates. The most restrictive condition in evaporation temperature is -30 ° C. EXAMPLES The following examples illustrate the invention without limiting it. Example 1 The thermal stability of different compositions has been tested. These thermal stability tests are carried out according to the ASHRAE 97-2007 standard entitled "Sealed glass tube method to test the chemical stability of materials for use within refrigerant Systems". The compositions were prepared as follows. All tubes are loaded under vacuum with the following quantities: g of Suniso 3GS oil and 2 g of HCFO-1233zdE. Air is added at the end according to the following compositions, in percentage by mass relative to the mixture HCFO-1233zdE and air. Composition No. 1 2 3 air (% by mass) 0.2 0.4 1 Immediately after their preparation, the compositions exhibit a coloration which corresponds to the original oil color. The various compositions were left for 14 days at 180 ° C. Then a color analysis by spectrocolorimetry of the compositions according to the Gardner color scale was carried out, according to standard ISO 4630: 2015. The intensity of the color observed is proportional to the degradation of the oil. Indeed, this degradation also causes the formation of black particles with a mass percentage of air greater than or equal to 1%. The results are summarized in the table below: Composition No. 1 2 3 air (% by mass) 0.2 0.4 1 Color according to Gardner's color scale Dark yellow Orange Brown Gardner scale: • Gardner 1: very pale yellow; • Gardner 2 to 5: pale yellow; • Gardner 6 to 10: dark yellow; • Gardner 11 to 14: orange; • Gardner 15 to 17: very dark orange / light brown; • Gardner 18: brown. It is noted that during use at 180 ° C., the compositions comprising HCFO-1233zd, mineral oil and 0.2 or 0.4% by mass of air are stable, the degradation of the oil being low. On the other hand, when the mass percentage of air is greater than or equal to 1%, the oil degrades relatively significantly at a temperature of 180 ° C.
权利要求:
Claims (13) [1" id="c-fr-0001] 1. Use for the heat transfer of a composition comprising at least one hydrochlorofluoroolefin, at least one mineral oil and air, the air being in a mass proportion of less than 1% relative to the mass of the mixture of l at least one hydrochlorofluoroolefin and air, in which the composition is subjected to at least one change of state at an average temperature greater than or equal to about 100 ° C. [2" id="c-fr-0002] 2. Use according to claim 1, wherein the composition is subjected to at least one change of state at an average temperature of from about 100 ° C to about 200 ° C. [3" id="c-fr-0003] 3. Use according to claim 1 or 2, wherein the composition does not comprise a stabilizer. [4" id="c-fr-0004] 4. Use according to one of claims 1 to 3, wherein the composition consists essentially, and preferably consists, of at least one hydrochlorofluoroolefin, at least one mineral oil and air, the air being in a mass proportion from 0% excluded to 1% excluded relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air. [5" id="c-fr-0005] 5. Use according to one of claims 1 to 4, in which the mass proportion of air in the composition is from 0.05% to 1% excluded, preferably from 0.1% to 1% excluded, even more preferably from 0.2% to 1% excluded, relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air. [6" id="c-fr-0006] 6. Use according to one of claims 1 to 4, in which the mass proportion of air in the composition is from 0% excluded to 0.6% inclusive, preferably from 0% excluded to 0.4% inclusive with respect to to the mass of the mixture of at least one hydrochlorofluoroolefin and air. [7" id="c-fr-0007] 7. Use according to one of claims 1 to 6, in which the mass proportion of air in the composition is from 0.05% inclusive to 0.4% inclusive, preferably from 0.1% inclusive to 0.4 % included relative to the mass of the mixture of the at least one hydrochlorofluoroolefin and air. [8" id="c-fr-0008] 8. Use according to one of claims 1 to 7, in which the at least one hydrochlorofluoroolefin is chosen from 1-chloro- 3,3,3-trifluoropropene, in particular trans-1-chloro-3,3,3trifluoropropene, 2-chloro-3,3,3-trifluoropropene, 3,3,3,2tetrafluorochloro-1-propene, a dichlorotrifluoropropene or a combination thereof. [9" id="c-fr-0009] 9. Use according to one of claims 1 to 8, wherein the at least one hydrochlorofluoroolefin is 1-chloro-3,3,3trifluoropropene. [10" id="c-fr-0010] 10. Use according to claim 9, in which the 1-chloro-3,3,3trifluoropropene is in trans form in a mass proportion greater than or equal to 90%, preferably greater than or equal to 95%, more particularly preferably greater or equal to 98%, even more preferably greater than or equal to 99%, even more preferably greater than or equal to 99.5%, or even greater than or equal to 99.9%, relative to the total mass of 1 chloro-3,3,3-trifluoropropene. [11" id="c-fr-0011] 11. Use according to one of claims 1 to 10, in which the mineral oil is in a mass proportion of 2% to 70% relative to the total mass of the composition. [12" id="c-fr-0012] 12. Use according to one of claims 1 to 11, in a vapor compression system or in a machine for producing mechanical or electrical energy and preferably for producing electricity. [13" id="c-fr-0013] 13. Use according to claim 12, wherein the vapor compression system is an air conditioning system, a refrigeration system, a freezing system, or a heat pump system.
类似技术:
公开号 | 公开日 | 专利标题 FR3070982B1|2019-08-30|COMPOSITION BASED ON HYDROCHLOROFLUOROOLEFIN AND MINERAL OIL EP3044278B1|2020-07-29|Heat transfer fluids comprising difluoromethane, pentafluoroethane, tetrafluoropropene and optionally propane WO2018134528A1|2018-07-26|Composition comprising 2,3,3,3-tetrafluoropropene WO2018134530A1|2018-07-26|Composition comprising 2,3,3,3-tetrafluoropropene FR3057271A1|2018-04-13|USE OF TETRAFLUOROPROPENE COMPOSITIONS EP3516007B1|2022-01-05|Composition comprising 1-chloro-3,3,3-trifluoropropene EP3523389B1|2022-03-16|Tetrafluoropropene-based azeotropic compositions EP1664234A2|2006-06-07|Hydrofluorocarbon-based composition and use thereof CA2844478C|2019-01-08|Tetrafluoropropene-based supercritical heat-transfer fluids FR3067035A1|2018-12-07|TRIFLUOROETHYLENE COMPOSITIONS AND USES THEREOF FR3077822A1|2019-08-16|HEAT TRANSFER COMPOSITIONS IN REPLACEMENT OF R-134A FR3077773A1|2019-08-16|METHOD FOR HEATING AND / OR AIR CONDITIONING A VEHICLE EP3592821A1|2020-01-15|Quasi-azeotropic composition comprising 2,3,3,3-tetrafluoropropene and trans-1,3,3,3-tetrafluoropropene EP3601468B1|2021-10-20|Tetrafluoropropene-based composition WO2019243704A1|2019-12-26|Stabilisation of 1,1,1,4,4,4-hexafluorobut-2-ene FR2988729A1|2013-10-04|COMPOSITIONS OF 2,4,4,4-TETRAFLUOROBUT-1-ENE AND 1-METHOXYHEPTAFLUOROPROPANE
同族专利:
公开号 | 公开日 CN111133076A|2020-05-08| EP3681968A1|2020-07-22| FR3070982B1|2019-08-30| WO2019053355A1|2019-03-21| US11053420B2|2021-07-06| JP2020533432A|2020-11-19| US20200216734A1|2020-07-09|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US8454853B2|2008-03-07|2013-06-04|Arkema Inc.|Halogenated alkene heat transfer composition with improved oil return| US20140070129A1|2011-05-19|2014-03-13|Arkema Inc.|Non-flammable compositions of chloro-trifluoropropene| JPH076707B2|1986-03-27|1995-01-30|三菱重工業株式会社|Heat pump device| US5065990A|1986-12-15|1991-11-19|Susan M. Durfee|Vise jaw accessory system for attaching and releasing vise accessories while maintaining positional accuracy of the accessories| JPH03168566A|1989-11-28|1991-07-22|Toshiba Corp|Operation of refrigeration cycle device| JPH04110388A|1990-08-31|1992-04-10|Daikin Ind Ltd|Fluid for heat transfer| JPH06272978A|1993-03-18|1994-09-27|Toshiba Corp|Air conditioner| US5363674A|1993-05-04|1994-11-15|Ecoair Corp.|Zero superheat refrigeration compression system| US6023002A|1998-01-26|2000-02-08|3M Innovative Properties Company|Process for preparing hydrofluoroethers| DE10056606A1|2000-11-15|2002-05-23|Solvay Fluor & Derivate|Mixtures of 1,1,1,3,3-pentafluoropropane with one or more partially fluorinated hydrocarbons as refrigerants or heat-transfer fluids, especially in high-temperature heat pumps| US9181410B2|2002-10-25|2015-11-10|Honeywell International Inc.|Systems for efficient heating and/or cooling and having low climate change impact| US9499729B2|2006-06-26|2016-11-22|Honeywell International Inc.|Compositions and methods containing fluorine substituted olefins| TR201908011T4|2002-10-25|2019-06-21|Honeywell Int Inc|Compositions containing fluorine-substituted olefins.| US20110037016A1|2003-10-27|2011-02-17|Honeywell International Inc.|Fluoropropene compounds and compositions and methods using same| US9085504B2|2002-10-25|2015-07-21|Honeywell International Inc.|Solvent compositions containing fluorine substituted olefins and methods and systems using same| US20150231527A1|2003-10-27|2015-08-20|Honeywell International Inc.|Monochlorotrifluoropropene compounds and compositions and methods using same| US20050096246A1|2003-11-04|2005-05-05|Johnson Robert C.|Solvent compositions containing chlorofluoroolefins| MX2007007457A|2004-12-21|2007-08-20|Honeywell Int Inc|Stabilized iodocarbon compositions.| US20060266976A1|2005-05-27|2006-11-30|Minor Barbara H|Compositions comprising bromofluoro-olefins and uses thereof| TWI657070B|2005-06-24|2019-04-21|美商哈尼威爾國際公司|Compositions containing fluorine substituted olefins and uses thereof| KR101477485B1|2007-06-27|2014-12-30|알케마 인코포레이티드|Stabilized hydrochlorofluoroolefins and hydrofluoroolefins| US7795480B2|2007-07-25|2010-09-14|Honeywell International Inc.|Method for producing 2-chloro-3,3,3,-trifluoropropene | US20090095014A1|2007-10-12|2009-04-16|Andrew Sun|Working fluid of a blend of 1,1,1,2-tetrafluoroethane, 1,1,1,2,3,3,3-heptafluoropropane, and 1,1,1,3,3,3-hexafluoropropane and method and apparatus for using| JP5788789B2|2008-05-12|2015-10-07|アーケマ・インコーポレイテッド|Composition of hydrochlorofluoroolefins| US9340758B2|2008-05-12|2016-05-17|Arkema Inc.|Compositions of hydrochlorofluoroolefins| FR2932492B1|2008-06-11|2010-07-30|Arkema France|COMPOSITIONS BASED ON HYDROFLUOROOLEFINS| FR2932493B1|2008-06-11|2010-07-30|Arkema France|COMPOSITIONS BASED ON HYDROFLUOROOLEFINS| FR2936806B1|2008-10-08|2012-08-31|Arkema France|REFRIGERANT FLUID| FR2937328B1|2008-10-16|2010-11-12|Arkema France|HEAT TRANSFER METHOD| US9150768B2|2008-10-28|2015-10-06|Honeywell International Inc.|Azeotrope-like compositions comprising 1-chloro-3,3,3-trifluoropropene| US20170080773A1|2008-11-03|2017-03-23|Arkema France|Vehicle Heating and/or Air Conditioning Method| FR2937906B1|2008-11-03|2010-11-19|Arkema France|METHOD FOR HEATING AND / OR AIR CONDITIONING A VEHICLE| FR2938550B1|2008-11-20|2010-11-12|Arkema France|COMPOSITION COMPRISING 2,3,3,3-TETRAFLUOROPROPENE METHOD FOR HEATING AND / OR AIR CONDITIONING A VEHICLE| FR2938551B1|2008-11-20|2010-11-12|Arkema France|METHOD FOR HEATING AND / OR AIR CONDITIONING A VEHICLE| US8217208B2|2008-12-12|2012-07-10|Honeywell International, Inc.|Isomerization of 1-chloro-3,3,3-trifluoropropene| FR2942237B1|2009-02-13|2013-01-04|Arkema France|METHOD FOR HEATING AND / OR AIR CONDITIONING A VEHICLE| FR2948678B1|2009-07-28|2011-10-14|Arkema France|HEAT TRANSFER METHOD| FR2948679B1|2009-07-28|2011-08-19|Arkema France|HEAT TRANSFER METHOD| MX2012002900A|2009-09-09|2012-06-25|Honeywell Int Inc|Monochlorotrifluoropropene compounds and compositions and methods using same.| US10035938B2|2009-09-11|2018-07-31|Arkema France|Heat transfer fluid replacing R-134a| FR2950069B1|2009-09-11|2011-11-25|Arkema France|USE OF TERNARY COMPOSITIONS| FR2950067B1|2009-09-11|2011-10-28|Arkema France|HEAT TRANSFER FLUID IN REPLACEMENT OF R-410A| FR2950070B1|2009-09-11|2011-10-28|Arkema France|TERNARY COMPOSITIONS FOR HIGH CAPACITY REFRIGERATION| FR2950066B1|2009-09-11|2011-10-28|Arkema France|LOW AND MEDIUM TEMPERATURE REFRIGERATION| FR2950071B1|2009-09-11|2012-02-03|Arkema France|TERNARY COMPOSITIONS FOR LOW CAPACITY REFRIGERATION| FR2950068B1|2009-09-11|2012-05-18|Arkema France|HEAT TRANSFER METHOD| FR2950065B1|2009-09-11|2012-02-03|Arkema France|BINARY REFRIGERANT FLUID| US8323524B2|2009-10-01|2012-12-04|3M Innovative Properties Company|Apparatus including hydrofluoroether with high temperature stability and uses thereof| EP2501666B1|2009-11-16|2018-06-13|Arkema Inc.|Method to purify and stabilize chloroolefins| FR2954342B1|2009-12-18|2012-03-16|Arkema France|HEAT TRANSFER FLUIDS WITH REDUCED FLAMMABILITY| US20150252240A1|2010-01-25|2015-09-10|Arkema Inc.|Heat transfer composition of oxygenated lubricant with hydrofluoroolefin and hydrochlorofluoroolefin refigerants| FR2962130B1|2010-06-30|2012-07-20|Arkema France|COMPOSITION BASED ON 2,3,3,3-TETRAFLUOROPROPENE| FR2962442B1|2010-07-09|2016-02-26|Arkema France|STABLE 2,3,3,3-TETRAFLUOROPROPENE COMPOSITION| FR2964975B1|2010-09-20|2012-08-24|Arkema France|COMPOSITION BASED ON 2,3,3,3-TETRAFLUOROPROPENE| US8734671B2|2010-11-19|2014-05-27|Honeywell International Inc.|Azeotrope-like compositions comprising 1-chloro-3,3,3-trifluoropropene| EP3543311A1|2010-11-25|2019-09-25|Arkema France|Use of compositions of chloro-trifluoropropene and hexafluorobutene| FR2971512B1|2011-02-10|2013-01-18|Arkema France|BINARY COMPOSITIONS OF 2,3,3,3-TETRAFLUOROPROPENE AND AMMONIA| FR2974812B1|2011-05-04|2014-08-08|Arkema France|HEAT TRANSFER COMPOSITIONS HAVING IMPROVED MISCIBILITY WITH LUBRICATING OIL| FR2986007B1|2012-01-25|2015-01-23|Arkema France|HEAT TRANSFER COMPOSITIONS HAVING IMPROVED MISCIBILITY WITH LUBRICATING OIL| FR2986236B1|2012-01-26|2014-01-10|Arkema France|HEAT TRANSFER COMPOSITIONS HAVING IMPROVED MISCIBILITY WITH LUBRICATING OIL| FR3000093B1|2012-12-26|2015-07-17|Arkema France|AZEOTROPIC OR QUASI-AZEOTROPIC COMPOSITION OF CHLOROMETHANE| FR3000096B1|2012-12-26|2015-02-20|Arkema France|COMPOSITION COMPRISING 2,3,3,3-TETRAFLUOROPROPENE| FR3000095B1|2012-12-26|2015-02-20|Arkema France|COMPOSITION COMPRISING 2,3,3,3-TETRAFLUOROPROPENE AND 1,2-DIFLUOROETHYLENE| BR112015022450B1|2013-03-13|2021-04-27|Arkema Inc.|PROCESSES FOR PURIFICATION AND STABILIZATION OF HALOOLEFINS, COMPOSITION OF PURIFIED HALOOLEFIN, COOLING SYSTEM, AIR CONDITIONING OR HEAT PUMP, POLYMERIC COMPOSITION, TRANSFORMABLE IN FOAM, PULVERIZABLE PROCESSION, PROCESSING, PROCESSING, PROCESSING, PROCESSING, PROCESSING, PROCESSING, PROCESSING, PROCESSING A REGION TO PREVENT FIRE OR EXPLOSION AND SOLUTION| US8859829B2|2013-03-14|2014-10-14|Honeywell International Inc.|Stabilizer and inhibitor for chloropropenes, such as tetrachloropropene 1,1,2,3-tetrachloropropene , used in the manufacture of 2,3,3,3-tetrafluoropropene | FR3003565B1|2013-03-20|2018-06-29|Arkema France|COMPOSITION COMPRISING HF AND 2,3,3,3-TETRAFLUOROPROPENE| FR3008419B1|2013-07-11|2015-07-17|Arkema France|2,3,3,3-TETRAFLUOROPROPENE-BASED COMPOSITIONS HAVING IMPROVED MISCIBILITY| CN104449580B|2013-09-24|2018-01-26|中化蓝天集团有限公司|A kind of composition containing HFC 161 and stabilizer| FR3033791B1|2015-03-18|2017-04-14|Arkema France|STABILIZATION OF 1-CHLORO-3,3,3-TRIFLUOROPROPENE| US10767305B2|2016-05-02|2020-09-08|Koninklijke Philips N.V.|Steam iron with thermal bridge arrangement| FR3056222B1|2016-09-19|2020-01-10|Arkema France|COMPOSITION BASED ON 1-CHLORO-3,3,3-TRIFLUOROPROPENE| FR3057271B1|2016-10-10|2020-01-17|Arkema France|USE OF TETRAFLUOROPROPENE COMPOSITIONS| FR3061906B1|2017-01-19|2019-03-15|Arkema France|COMPOSITION COMPRISING 2,3,3,3-TETRAFLUOROPROPENE| FR3061905B1|2017-01-19|2019-05-17|Arkema France|COMPOSITION COMPRISING 2,3,3,3-TETRAFLUOROPROPENE| FR3067035B1|2017-06-02|2020-10-30|Arkema France|COMPOSITIONS BASED ON TRIFLUOROETHYLENE, AND THEIR USES| FR3070982B1|2017-09-12|2019-08-30|Arkema France|COMPOSITION BASED ON HYDROCHLOROFLUOROOLEFIN AND MINERAL OIL| FR3077572B1|2018-02-05|2021-10-08|Arkema France|TERNARY AZEOTROPIC OR QUASI-AZEOTROPIC COMPOSITION COMPRISING HF, 2,3,3,3-TETRAFLUOROPROPENE AND 1,1,1,2,2, -PENTAFLUOROPROPANE.| FR3077822B1|2018-02-15|2020-07-24|Arkema France|REPLACEMENT HEAT TRANSFER COMPOSITIONS FOR R-134A|FR2936806B1|2008-10-08|2012-08-31|Arkema France|REFRIGERANT FLUID| FR2937328B1|2008-10-16|2010-11-12|Arkema France|HEAT TRANSFER METHOD| US20170080773A1|2008-11-03|2017-03-23|Arkema France|Vehicle Heating and/or Air Conditioning Method| FR2950065B1|2009-09-11|2012-02-03|Arkema France|BINARY REFRIGERANT FLUID| FR3057271B1|2016-10-10|2020-01-17|Arkema France|USE OF TETRAFLUOROPROPENE COMPOSITIONS| FR3070982B1|2017-09-12|2019-08-30|Arkema France|COMPOSITION BASED ON HYDROCHLOROFLUOROOLEFIN AND MINERAL OIL| FR3077572B1|2018-02-05|2021-10-08|Arkema France|TERNARY AZEOTROPIC OR QUASI-AZEOTROPIC COMPOSITION COMPRISING HF, 2,3,3,3-TETRAFLUOROPROPENE AND 1,1,1,2,2, -PENTAFLUOROPROPANE.|
法律状态:
2019-03-15| PLSC| Search report ready|Effective date: 20190315 | 2019-08-15| PLFP| Fee payment|Year of fee payment: 3 | 2020-08-12| PLFP| Fee payment|Year of fee payment: 4 | 2021-08-12| PLFP| Fee payment|Year of fee payment: 5 |
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申请号 | 申请日 | 专利标题 FR1758429A|FR3070982B1|2017-09-12|2017-09-12|COMPOSITION BASED ON HYDROCHLOROFLUOROOLEFIN AND MINERAL OIL| FR1758429|2017-09-12|FR1758429A| FR3070982B1|2017-09-12|2017-09-12|COMPOSITION BASED ON HYDROCHLOROFLUOROOLEFIN AND MINERAL OIL| EP18795700.6A| EP3681968A1|2017-09-12|2018-09-07|Composition on the basis of hydrochlorofluoroolefin and mineral oil| PCT/FR2018/052188| WO2019053355A1|2017-09-12|2018-09-07|Composition on the basis of hydrochlorofluoroolefin and mineral oil| CN201880059287.1A| CN111133076A|2017-09-12|2018-09-07|Composition based on hydrochlorofluoroolefins and mineral oil| US16/641,024| US11053420B2|2017-09-12|2018-09-07|Composition on the basis of hydrochlorofluoroolefin and mineral oil| JP2020511444A| JP2020533432A|2017-09-12|2018-09-07|Composition based on hydrochlorofluoroolefin and mineral oil| 相关专利
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