EP3769329A2 - Utilisation du 1-chloro-2,3,3,3-tetrafluoropropene pour l'isolation ou l'extinction d'arcs electriques - Google Patents
Utilisation du 1-chloro-2,3,3,3-tetrafluoropropene pour l'isolation ou l'extinction d'arcs electriquesInfo
- Publication number
- EP3769329A2 EP3769329A2 EP19742415.3A EP19742415A EP3769329A2 EP 3769329 A2 EP3769329 A2 EP 3769329A2 EP 19742415 A EP19742415 A EP 19742415A EP 3769329 A2 EP3769329 A2 EP 3769329A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- gas
- tetrafluoropropene
- chloro
- mol
- electrical
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- GDPWRLVSJWKGPJ-UHFFFAOYSA-N 1-chloro-2,3,3,3-tetrafluoroprop-1-ene Chemical compound ClC=C(F)C(F)(F)F GDPWRLVSJWKGPJ-UHFFFAOYSA-N 0.000 title claims abstract description 40
- 239000007789 gas Substances 0.000 claims description 98
- 150000001875 compounds Chemical class 0.000 claims description 34
- 239000000203 mixture Substances 0.000 claims description 29
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- 239000003085 diluting agent Substances 0.000 claims description 16
- 229910052799 carbon Inorganic materials 0.000 claims description 15
- IYRWEQXVUNLMAY-UHFFFAOYSA-N fluoroketone group Chemical group FC(=O)F IYRWEQXVUNLMAY-UHFFFAOYSA-N 0.000 claims description 11
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 238000010891 electric arc Methods 0.000 claims description 7
- 238000002955 isolation Methods 0.000 claims description 6
- 230000008033 biological extinction Effects 0.000 claims description 4
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 claims description 4
- 230000005611 electricity Effects 0.000 claims description 2
- 229910018503 SF6 Inorganic materials 0.000 description 17
- SFZCNBIFKDRMGX-UHFFFAOYSA-N sulfur hexafluoride Chemical compound FS(F)(F)(F)(F)F SFZCNBIFKDRMGX-UHFFFAOYSA-N 0.000 description 17
- 229960000909 sulfur hexafluoride Drugs 0.000 description 17
- 238000010292 electrical insulation Methods 0.000 description 13
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 10
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 description 8
- CDOOAUSHHFGWSA-OWOJBTEDSA-N (e)-1,3,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C\C(F)(F)F CDOOAUSHHFGWSA-OWOJBTEDSA-N 0.000 description 7
- 238000009413 insulation Methods 0.000 description 7
- 229910002092 carbon dioxide Inorganic materials 0.000 description 5
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- DMUPYMORYHFFCT-UPHRSURJSA-N (z)-1,2,3,3,3-pentafluoroprop-1-ene Chemical compound F\C=C(/F)C(F)(F)F DMUPYMORYHFFCT-UPHRSURJSA-N 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 239000012159 carrier gas Substances 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000001307 helium Substances 0.000 description 2
- 229910052734 helium Inorganic materials 0.000 description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000001272 nitrous oxide Substances 0.000 description 2
- 150000002924 oxiranes Chemical class 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- YFMFNYKEUDLDTL-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)C(F)(F)F YFMFNYKEUDLDTL-UHFFFAOYSA-N 0.000 description 1
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 1
- NLOLSXYRJFEOTA-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluorobut-2-ene Chemical compound FC(F)(F)C=CC(F)(F)F NLOLSXYRJFEOTA-UHFFFAOYSA-N 0.000 description 1
- SXKNYNUXUHCUHX-UHFFFAOYSA-N 1,1,2,3,3,4-hexafluorobut-1-ene Chemical class FCC(F)(F)C(F)=C(F)F SXKNYNUXUHCUHX-UHFFFAOYSA-N 0.000 description 1
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 description 1
- AASDJASZOZGYMM-UHFFFAOYSA-N 2,3,3,3-tetrafluoro-2-(trifluoromethyl)propanenitrile Chemical compound FC(F)(F)C(F)(C#N)C(F)(F)F AASDJASZOZGYMM-UHFFFAOYSA-N 0.000 description 1
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229920001774 Perfluoroether Polymers 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 231100000219 mutagenic Toxicity 0.000 description 1
- 230000003505 mutagenic effect Effects 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 231100001260 reprotoxic Toxicity 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- VPAYJEUHKVESSD-UHFFFAOYSA-N trifluoroiodomethane Chemical compound FC(F)(F)I VPAYJEUHKVESSD-UHFFFAOYSA-N 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 238000010200 validation analysis Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01H—ELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
- H01H33/00—High-tension or heavy-current switches with arc-extinguishing or arc-preventing means
- H01H33/02—Details
- H01H33/04—Means for extinguishing or preventing arc between current-carrying parts
- H01H33/22—Selection of fluids for arc-extinguishing
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/56—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances gases
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F27/00—Details of transformers or inductances, in general
- H01F27/28—Coils; Windings; Conductive connections
- H01F27/32—Insulating of coils, windings, or parts thereof
- H01F27/321—Insulating of coils, windings, or parts thereof using a fluid for insulating purposes only
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01H—ELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
- H01H33/00—High-tension or heavy-current switches with arc-extinguishing or arc-preventing means
- H01H33/60—Switches wherein the means for extinguishing or preventing the arc do not include separate means for obtaining or increasing flow of arc-extinguishing fluid
- H01H33/64—Switches wherein the means for extinguishing or preventing the arc do not include separate means for obtaining or increasing flow of arc-extinguishing fluid wherein the break is in gas
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02B—BOARDS, SUBSTATIONS OR SWITCHING ARRANGEMENTS FOR THE SUPPLY OR DISTRIBUTION OF ELECTRIC POWER
- H02B13/00—Arrangement of switchgear in which switches are enclosed in, or structurally associated with, a casing, e.g. cubicle
- H02B13/02—Arrangement of switchgear in which switches are enclosed in, or structurally associated with, a casing, e.g. cubicle with metal casing
- H02B13/035—Gas-insulated switchgear
- H02B13/055—Features relating to the gas
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01H—ELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
- H01H33/00—High-tension or heavy-current switches with arc-extinguishing or arc-preventing means
- H01H33/02—Details
- H01H33/53—Cases; Reservoirs, tanks, piping or valves, for arc-extinguishing fluid; Accessories therefor, e.g. safety arrangements, pressure relief devices
- H01H33/56—Gas reservoirs
- H01H2033/566—Avoiding the use of SF6
Definitions
- the present invention relates to a gas used for the electrical insulation or extinguishing of electric arcs, as well as electrical appliances provided with an enclosure containing this gas.
- the electrical insulation and, where appropriate, the extinction of electric arcs are typically provided by a gas that is confined within an enclosure of these devices.
- a gas that is confined within an enclosure of these devices.
- the most commonly used gas is sulfur hexafluoride (SFe): this gas has a relatively high dielectric strength, good thermal conductivity and low dielectric losses. It is chemically inert and non-toxic to humans and animals and, after being dissociated by an electric arc, it recombines quickly and almost completely. In addition, it is nonflammable and its price is still moderate today.
- SFe has the major disadvantage of having a global warming potential (GWP) of 22,800 (relative to CO2 over 100 years) and a residence time in the atmosphere of 3,200 years, which places it among the gases with strong greenhouse effect.
- GWP global warming potential
- Hybrid systems have been proposed which combine gas insulation with solid insulation (EP 1724802). This, however, increases the volume of electrical appliances compared to that allowed by SFe insulation; and the cut in the oil or vacuum requires a redesign of the equipment.
- Perfluorocarbons generally have interesting dielectric strength properties, but their GWP is typically in a range of 5,000 to 10,000.
- SFe and other gases such as nitrogen or nitrogen dioxide are used to limit the impact of SFe on the environment: see, for example, WO 2009/049144. Nevertheless, because of the strong SFe GWP, the GWP of these mixtures remains very high.
- a mixture of SFe and nitrogen in a volume ratio of 10/90 has a dielectric strength in alternating voltage (50 Hz) equal to 59% of that of SFe but its GWP is of the order of 8 000 to 8 650.
- Such mixtures can not therefore be used as a low environmental impact gas.
- the document FR 2955970 proposes the use of fluoroketones in the gaseous state for electrical insulation.
- the fluoroketones can be combined with a carrier gas or dilution gas (for example nitrogen, air, nitrous oxide, carbon dioxide, oxygen, helium, etc.).
- Document FR 2975818 proposes a mixture of octofluorobutan-2-one and carrier gas as isolation medium.
- the document FR 2983341 proposes the use of polyfluorinated oxiranes as electric insulation gas and / or electric arc extinguishing.
- Document FR 2986102 proposes the use of a combination of polyfluorinated oxirane and hydrofluoroolefin as electrical insulation gas.
- the hydrofluoroolefins mentioned are 1, 3,3,3-tetrafluoropropene (HFO-1234ze), 2,3,3,3-tetrafluoropropene (HFO-1234yf) and 1,2,3,3,3-pentafluoropropene (HFO -1225ye).
- WO 2012/160158 proposes the use of a mixture of decafluoro-2-methylbutan-3-one and a carrier gas as an electrical insulating gas.
- the document WO 2013/004796 proposes the use of a gas based on hydrofluoroolefin as an electrical insulation gas.
- the hydrofluoroolefins more particularly proposed are 1, 3,3,3-tetrafluoropropene
- HFO-1234ze 2,3,3,3-tetrafluoropropene
- HFO-1234yf 2,3,3,3-tetrafluoropropene
- the document WO 2013/041695 proposes the use of a mixture of hydrofluoroolefin and of fluoroketone as electrical insulation gas.
- the hydrofluoroolefins more particularly proposed are the
- HFO-1234yf 1,2,3,3,3-pentafluoropropene
- HFO-1225ye 1,2,3,3,3-pentafluoropropene
- the document WO 2013/136015 proposes the use of a mixture of hydrofluoroolefin and hydrofluorocarbon as electrical insulation gas.
- the hydrofluoroolefins more particularly proposed are the
- Hydrofluorocarbons more particularly proposed are the
- WO 2017/037360 proposes the use of hexafluorobutenes as gas for electrical insulation and / or extinction of electric arcs.
- the invention firstly relates to the use of a gas as an electrical insulation medium and / or electric arc extinguishing, wherein the gas comprises 1-chloro-2,3,3,3-tetrafluoropropene .
- 1-chloro-2,3,3,3-tetrafluoropropene comprises more than 80 mol% 1-chloro-2,3,3,3-tetrafluoropropene in Z-form, preferably more than 90 mol% of 1-chloro-2,3,3,3-tetrafluoropropene in Z form, more preferably more than 95 mol% of 1-chloro-2,3,3,3-tetrafluoropropene in Z form and more preferably more than 99 mol% of 1-chloro-2,3,3,3-tetrafluoropropene in Z form.
- the gas is used as an electrical isolation and / or arc extinguishing medium in a medium voltage substation electrical apparatus.
- the gas contains from 10 to 100 mol% of 1-chloro-2,3,3,3-tetrafluoropropene, preferably from 15 to 75 mol% and more particularly from 19 to 45 mol%. .
- the gas also comprises a diluent, preferably selected from air, nitrogen, methane, oxygen, carbon dioxide or a mixture thereof; and preferably the gas is a binary mixture of 1-chloro-2,3,3,3-tetrafluoropropene and a diluent.
- a diluent preferably selected from air, nitrogen, methane, oxygen, carbon dioxide or a mixture thereof; and preferably the gas is a binary mixture of 1-chloro-2,3,3,3-tetrafluoropropene and a diluent.
- the gas further comprises a halogenated compound, preferably a fluorinated compound, further preferably selected from fluoroketones, hydrofluoroolefins, hydrochlorofluoroolefins and combinations thereof.
- a halogenated compound preferably a fluorinated compound, further preferably selected from fluoroketones, hydrofluoroolefins, hydrochlorofluoroolefins and combinations thereof.
- the gas is used in a temperature range whose lower limit is from -30 to 30 ° C, preferably from -20 to 25 ° C, more preferably from -15 to 20 ° C. preferably from -10 to 10 ° C.
- the gas consists essentially, and preferably, of 1-chloro-2,3,3,3-tetrafluoropropene.
- the gas is used in a temperature range whose lower bound is greater than or equal to 10 ° C, or 11 ° C, or 12 ° C, or 13 ° C, or 14 ° C. ° C, or at 15 ° C to 16 ° C, or at 18 ° C, or at 20 ° C.
- the invention also relates to an electrical apparatus comprising a sealed enclosure in which there are electrical components as well as an electrical insulating gas and / or electric arc extinguishing, wherein the gas comprises 1-chloro-2, 3,3,3-tetrafluoropropene.
- 1-chloro-2,3,3,3-tetrafluoropropene comprises more than 80 mol% 1-chloro-2,3,3,3-tetrafluoropropene in Z-form, preferably more than 90 mol% of 1-chloro-2,3,3,3-tetrafluoropropene in Z form, more preferably more than 95 mol% of 1-chloro-2,3,3,3-tetrafluoropropene in Z form and more preferably more than 99 mol% of 1-chloro-2,3,3,3-tetrafluoropropene in Z form.
- the gas also comprises a diluent, preferably selected from air, nitrogen, methane, oxygen, carbon dioxide or a mixture thereof; and preferably the gas is a binary mixture of 1-chloro-2,3,3,3-tetrafluoropropene and a diluent.
- a diluent preferably selected from air, nitrogen, methane, oxygen, carbon dioxide or a mixture thereof; and preferably the gas is a binary mixture of 1-chloro-2,3,3,3-tetrafluoropropene and a diluent.
- the gas further comprises a halogenated compound, preferably a fluorinated compound, preferably further selected among fluoroketones, hydrofluoroolefins, hydrochlorofluoroolefins and combinations thereof.
- a fluorinated compound preferably further selected among fluoroketones, hydrofluoroolefins, hydrochlorofluoroolefins and combinations thereof.
- the gas consists essentially, and preferably, of 1-chloro-2,3,3,3-tetrafluoropropene.
- the electrical apparatus is a medium voltage electrical apparatus.
- the electrical apparatus is a high voltage electrical apparatus.
- the gas is at a pressure at 20 ° C of 0.1 to 1 MPa, preferably 0.1 to 0.5 MPa, and more preferably 0.12 to 0.15 MPa. .
- the apparatus is selected from a gas-insulated electrical transformer, a gas-insulated line for the transmission or distribution of electricity, and an electrical connection / disconnection apparatus.
- the present invention overcomes the disadvantages of the state of the art. More particularly, it provides electrical insulation and / or arc-extinguishing media having both low GWP and high dielectric strength.
- HCFO-1224yd 1-chloro-2,3,3,3-tetrafluoropropene-based media, commonly referred to as HCFO-1224yd, exhibit remarkable dielectric strength properties and that in admixture with inert compounds they provide effective electrical insulation even at relatively low temperatures.
- the invention relates to a gas used as an electrical isolation medium and / or electric arc extinguishing.
- the gas according to the invention comprises at least 1-chloro-2,3,3,3-tetrafluoropropene or HCFO-1224yd.
- HCFO-1224yd may be in E form, or Z form, or may be a mixture of both forms. Z form is preferred.
- the HCFO-1224yd comprises more than 50 mol% of the Z form, preferably more than 60 mol% of the Z form, preferably more than 70 mol% of the Z form, preferably more than 80 mol. % of the Z form, preferably more than 85 mole% of the Z form, preferably more than 90 mole%. of the Z form, preferably more than 95 mole% of the Z form, preferably more than 98 mole% of the Z form and more preferably more than 99 mole% of the Z form.
- HCFO-1224yd consists essentially or consists of H CFO-1224yd (Z).
- HCFO 1224yd (Z) is non-flammable.
- HCFO 1224yd (Z) has a very low level of toxicity.
- HCFO 1224yd (Z) is thermally stable and compatible with elastomers and plastics.
- the gas may also comprise additional compounds, in particular a diluent (or dilution gas, or buffer gas) and optionally one or more other halogenated compounds (especially fluorinated compounds).
- a diluent or dilution gas, or buffer gas
- other halogenated compounds especially fluorinated compounds
- the gas according to the invention consists essentially and preferably consists of HCFO-1224yd.
- the gas of the invention comprises (or optionally consists essentially of, or optionally consists of) a binary mixture of HCFO-1224yd and a diluent.
- the gas of the invention comprises (or optionally consists essentially of, or optionally consists of) a binary mixture of HCFO-1224yd and another halogenated compound.
- the gas of the invention comprises (or optionally consists essentially of, or optionally consists of) a mixture of HCFO-1224yd, another halogenated compound and a diluent.
- the diluent is an inert compound, which may be for example selected from air, nitrogen, methane, oxygen, nitrous oxide, helium and carbon dioxide. Mixtures of these are also possible.
- the halogenated compound is a hydrochlorofluoroolefin, a hydrofluoroolefin or a fluoroketone.
- the halogenated compound is a fluorinated compound, which is preferably selected from fluoroketones, fluoethers, fluoronitriles, fluorinated peroxides, fluoroamides and fluoroether oxides.
- Decafluoro-2-methylbutan-3-one is an example of a preferred halogenated compound.
- 2,3,3,3-Tetrafluoro-2- (trifluoromethyl) propanenitrile is an example of a preferred fluoronitrile compound.
- 1,1,1,4,4,4-Hexafluorobut-2-ene (E) is an example of a preferred hydrofluoroolefin compound.
- the gas according to the invention does not undergo condensation for the entire range of projected use temperature. It is also desired to use this gas at a sufficiently high pressure, in principle greater than 10 5 Pa. Under these conditions, the use of a diluent makes it possible to avoid reaching the saturation vapor pressure of HCFO-1224yd or other halogenated compounds that may be present throughout the range of the intended use temperature.
- a diluent is generally a compound having a boiling point lower than that of HCFO-1224yd and also having a lower electrical rigidity (at a reference temperature of, for example, 20 ° C).
- the absolute operating pressure of the gas according to the invention is preferably from 1 to 1.5 bar in medium voltage devices and from 4 to 7 bar in high voltage devices.
- medium voltage and “high voltage” are used herein in their usual acceptance that the term “medium voltage” refers to a voltage that is greater than 1000 volts AC and 1500 volts DC but that does not does not exceed 52000 volts AC and 75000 volts DC, while the term “high voltage” means a voltage that is strictly greater than 52000 volts AC and 75000 volts DC.
- Ptot represents the utilization pressure of the gas according to the invention
- Pi represents the partial pressure of HCFO-1224yd and other halogenated compounds
- PVSi represents the saturating vapor pressure of HCFO-1224yd and other halogenated compounds.
- the pressures are given at the filling temperature, in general about 20 ° C.
- the gas according to the invention can be used in a temperature range whose lower limit is: -30 to -25 ° C; or from -25 to -20 ° C; or from -20 to -15 ° C; or from -15 to -C ° C; or from -10 to -5 ° C; or from -5 to 0 ° C; or from 0 to 5 ° C; or from 5 to 10 ° C; or d at 10 to 15 ° C; or 15 to 20 ° C; or from 20 to 25 ° C; or 25 to 30 ° C.
- the gas may be used in a temperature range whose lower limit is -30 to 30 ° C, preferably -20 to 25 ° C, more preferably -15 to 20 ° C, and still preferably from -10 to 10 ° C.
- the gas according to the invention can be used in a temperature range whose upper limit is: 15 to 20 ° C; or from 20 to 25 ° C; or from 25 to 30 ° C; or from 30 to 35 ° C; or 35 to 40 ° C or 40 to 45 ° C; or 45 to 50 ° C.
- the gas may be used in a temperature range whose upper limit is 15 to 50 ° C, preferably 25 to 45 ° C, more preferably 20 to 40 ° C, and more preferably from 25 to 35 ° C.
- the temperature of use of the gas corresponds to the actual temperature of the gas during its use; it may vary during use, but remains between the lower bound and the upper bound defined above.
- the temperature of use is the temperature of the gas in the enclosure, which may vary over time depending in particular on climatic or environmental conditions.
- Embodiments in which a diluent gas is present generally allow to work in a temperature range whose lower limit is lower than in embodiments in which no diluent gas is present.
- the lower limit of the temperature range is preferably greater than or equal to 10 ° C, or at 11 ° C, or at 12 ° C, or at 13 ° C, or at 14 ° C, or at 15 ° C to 16 ° C, or at 18 ° C, or at 20 ° C.
- the gas according to the invention has a GWP of less than or equal to 20, more particularly less than or equal to 15 or to 10, or to 7, or to 5, or to 4, or to 3.
- GWP is defined in relation to carbon dioxide and compared to a duration of 100 years, according to the method indicated in "The scientific assessment of ozone depletion, 2002, report of the World Meteorological Association's Global Ozone Research and Monitoring Project".
- the (molar) proportion of HCFO-1224yd (and preferably HCFO-1224yd (Z)) in the gas may in some embodiments be 1 to 2%; or 2 to 3%; or 3-4%, or 4-5%; or from 5 to 6%; or 6-7%; or 7 to 8%; or from 8 to 9%; or from 9 to 10%; or from 10 to 12%; or from 12 to 14%; or from 14 to 16%; or from 16 to 18%; or 18 to 20%; or 20 to 22%; or 22 to 24%; or 24 to 26%; or from 26 to 28%; or from 28 to 30%; or from 30 to 35%; or 35 to 40%; or 40 to 45%; or 45 to 50%; or 50 to 55%; or 55 to 60%; or 60 to 70%; or 70 to 80%; or 80 to 90%; or 90 to 100%.
- the gas may contain from 10 to 100 mol. % of HCFO-1224yd, preferably from 15 to 75 mol% and more particularly from 19 to 45 mol%.
- the gas is used with a minimum temperature (lower limit of the temperature range of use) within the following ranges, in association with a proportion of HCFO-1224yd (and preferably HCFO-1224yd ( Z)) in the gas in the following ranges (in order to obtain maximum performance):
- the partial pressure of HCFO-1224yd in the gas at 20 ° C may in some embodiments be 0.002 to 0.004 MPa; or from 0.004 to 0.006 MPa; or from 0.006 to 0.008 MPa; or from 0.008 to 0.01 MPa; or from 0.01 to 0.012 MPa; or from 0.012 to 0.014 MPa; or from 0.014 to 0.016 MPa; or from 0.016 to 0.018 MPa; or from 0.018 to 0.02 MPa; or from 0.02 to 0.022 MPa; or from 0.022 to 0.024 MPa; or from 0.024 to 0.026 MPa; or from 0.026 to 0.028 MPa; or from 0.028 to 0.03 MPa; or from 0.03 to 0.032 MPa; or from 0.032 to 0.034 MPa; or from 0.034 to 0.036 MPa; or from 0.036 to 0.038 MPa; or from 0.04 to 0.045 MPa;
- the gas may have a pressure at 20 ° C of 0.1 to 1 MF3 ⁇ 4, preferably 0.1 to 0.5 MPa, and more preferably 0.12 to 0.15 MPa.
- the gas may have a pressure at 20 ° C of 0.1 to 0.15 MPa; or from 0.15 to 0.3 MPa; or 0.3 to 0.5 MPa; or from 0.5 to 0.7 MPa; or from 0.7 to 0.9 MPa; or from 0.9 to 1 MPa.
- the electrical appliances contain a relatively high amount of HCFO-1224yd (and possibly other halogenated and especially fluorinated gases), so that the dielectric, thermal and gas-off characteristics are sufficient over the normative or desired temperature range.
- a heating device in combination with an electrical appliance, said heating device being triggered according to the temperature of the gas mixture, its pressure or its density.
- a heating resistor ideally placed at the lowest point of the apparatus (point of convergence of the condensed liquids on the various parts inside the apparatus, by gravitation) can be used.
- Dielectric strength measurements are made at 20 ° C. and at 1.3 bar in a homogeneous field, with a distance between electrodes of 12 mm. The results are as follows, expressed as a percentage of the dielectric strength of the SFe reference gas:
- Fl CFO-1224yd (Z) Given its condensation temperature, Fl CFO-1224yd (Z) can be used in a pure state at a minimum temperature of 17 ° C, at a pressure of 1.14 bar, without condensation. Its dielectric strength value (with a distance between electrodes of 12 mm) is then the following, always with respect to SFe:
- each gas is considered independent of other gases in the same volume.
- the saturation pressure of HCFO-1224yd (Z) at -15 ° C is 0.29 bar
- the maximum number of moles in 1 m 3 of gas is 13.5 moles, if one wishes to avoid any condensation at this temperature.
- the HCFO-1224yd (Z) / inert mixture then comprises a molar composition of 25.3% of HCFO-1224yd (Z) and 74.7% of inert compound.
- the dielectric strength of the air is 54% of that of SFe at -15 ° C. and at 1.14 bar, the dielectric strength of the above binary mixture can be calculated under the same conditions:
- HCFO-1224yd (Z) at vapor saturation at the temperature of -15 ° C and the pressure of 1.14 bar is greater than that predicted by the ideal gas theory.
- HCFO-1224yd (Z) / inert binary compositions of interest may have a content of H CFO-1224yd (Z) greater than the values indicated above.
- the dielectric strength obtained may be greater than that calculated above.
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- Organic Insulating Materials (AREA)
- Gas-Insulated Switchgears (AREA)
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Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1852479A FR3079359B1 (fr) | 2018-03-22 | 2018-03-22 | Utilisation du 1-chloro-2,3,3,3-tetrafluoropropene pour l'isolation ou l'extinction d'arcs electriques |
| PCT/FR2019/050574 WO2019186017A2 (fr) | 2018-03-22 | 2019-03-14 | Utilisation du 1-chloro-2,3,3,3-tetrafluoropropene pour l'isolation ou l'extinction d'arcs electriques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP3769329A2 true EP3769329A2 (fr) | 2021-01-27 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19742415.3A Withdrawn EP3769329A2 (fr) | 2018-03-22 | 2019-03-14 | Utilisation du 1-chloro-2,3,3,3-tetrafluoropropene pour l'isolation ou l'extinction d'arcs electriques |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US11133139B2 (fr) |
| EP (1) | EP3769329A2 (fr) |
| FR (1) | FR3079359B1 (fr) |
| WO (1) | WO2019186017A2 (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20190035562A1 (en) * | 2017-05-26 | 2019-01-31 | Flash Power Capacitors, Llc | High energy density capacitor system and method |
| EP4235702A4 (fr) * | 2020-10-22 | 2024-07-24 | Agc Inc. | Équipement électrique |
| CN116635970A (zh) | 2020-12-16 | 2023-08-22 | Agc株式会社 | 电气设备、填充设备和储存设备 |
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| US9085721B2 (en) * | 2011-02-04 | 2015-07-21 | E I Du Pont De Nemours And Company | Azeotropic and azeotrope-like compositions involving certain haloolefins and uses thereof |
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| JP2002171624A (ja) | 2000-11-30 | 2002-06-14 | Mitsubishi Electric Corp | ガス封入形開閉装置 |
| US7250583B2 (en) | 2004-04-19 | 2007-07-31 | Abb Technology Ag | Gas-insulated switchgear device |
| JP4429205B2 (ja) | 2005-05-16 | 2010-03-10 | 三菱電機株式会社 | ガス絶縁機器 |
| US8287752B2 (en) | 2005-11-01 | 2012-10-16 | E I Du Pont De Nemours And Company | Fire extinguishing and fire suppression compositions comprising unsaturated fluorocarbons |
| US7736529B2 (en) | 2007-10-12 | 2010-06-15 | Honeywell International Inc | Azeotrope-like compositions containing sulfur hexafluoride and uses thereof |
| KR102884920B1 (ko) * | 2008-05-07 | 2025-11-12 | 더 케무어스 컴퍼니 에프씨, 엘엘씨 | 1,1,1,2,3-펜타플루오로프로판 또는 2,3,3,3-테트라플루오로프로펜을 포함하는 조성물 |
| US8163196B2 (en) * | 2008-10-28 | 2012-04-24 | Honeywell International Inc. | Azeotrope-like compositions comprising 1-chloro-3,3,3-trifluoropropene |
| US8871112B2 (en) * | 2008-11-19 | 2014-10-28 | E I Du Pont De Nemours And Company | Compositions comprising 2,3,3,3-tetrafluoropropene and hydrocarbons and uses thereof |
| BRPI0924862A2 (pt) | 2009-06-12 | 2016-08-23 | Abb Technology Ag | meio de isolação dielétrica |
| US20110144216A1 (en) | 2009-12-16 | 2011-06-16 | Honeywell International Inc. | Compositions and uses of cis-1,1,1,4,4,4-hexafluoro-2-butene |
| FR2954342B1 (fr) * | 2009-12-18 | 2012-03-16 | Arkema France | Fluides de transfert de chaleur a inflammabilite reduite |
| FR2955970B1 (fr) | 2010-02-02 | 2012-03-09 | Areva T & D Sas | Utilisation de fluorocetones a l'etat gazeux pour l'isolation electrique et/ou l'extinction d'arc electrique |
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| FR2965121B1 (fr) | 2010-09-22 | 2012-10-12 | Areva T & D Sas | Utilisation de melanges sf6/fluorocetone(s) pour l'isolation electrique et/ou l'extinction d'arc electrique |
| US9145480B2 (en) | 2010-10-28 | 2015-09-29 | Honeywell International Inc. | Mixtures containing 1,1,1,3,3,3-hexafluorobutene and 1-chloro-3,3,3-trifluoropropene |
| FR2968009B1 (fr) | 2010-11-25 | 2012-11-16 | Arkema France | Fluides frigorigenes contenant du (e)-1,1,1,4,4,4-hexafluorobut-2-ene |
| FR2975820B1 (fr) | 2011-05-24 | 2013-07-05 | Schneider Electric Ind Sas | Melange de decafluoro-2-methylbutan-3-one et d'un gaz vecteur comme milieu d'isolation electrique et/ou d'extinction des arcs electriques en moyenne tension |
| FR2975818B1 (fr) | 2011-05-24 | 2013-07-05 | Schneider Electric Ind Sas | Melange d'octofluorobutan-2-one et d'un gaz vecteur comme milieu d'isolation electrique et/ou d'extinction des arcs electriques en moyenne tension |
| FR2976289B1 (fr) * | 2011-06-07 | 2013-05-24 | Arkema France | Compositions binaires de 1,3,3,3-tetrafluoropropene et d'ammoniac |
| FR2977707B1 (fr) | 2011-07-05 | 2014-05-23 | Schneider Electric Ind Sas | Utilisation d'une hydrofluoroolefine comme milieu d'isolation et/ou d'extinction d'arc en moyenne tension et appareil electrique moyenne tension a isolation gazeuse le comprenant |
| FR2980628B1 (fr) | 2011-09-22 | 2014-07-25 | Schneider Electric Ind Sas | Melange d'hydrofluoroolefine et de fluorocetone pour l'utilisation comme milieu d'isolation et/ou d'extinction d'arc et appareil electrique moyenne tension a isolation gazeuse le comprenant |
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| US20150191576A1 (en) | 2012-08-01 | 2015-07-09 | E I Du Pont De Nemours And Company | Azeotropic and azeotrope-like compositions of e-1,3,4,4,4-pentafluoro-3-trifluoromethyl-1-butene and z-1,1,1,4,4,4-hexafluoro-2-butene and uses thereof |
| TW201414823A (zh) | 2012-09-19 | 2014-04-16 | Du Pont | 包含z-1,1,1,4,4,4-六氟-2-丁烯及2,2-二氯-1,1,1-三氟乙烷之組合物及其使用方法 |
| FR3000096B1 (fr) * | 2012-12-26 | 2015-02-20 | Arkema France | Composition comprenant du 2,3,3,3-tetrafluoropropene |
| FR3003569B1 (fr) * | 2013-03-20 | 2015-12-25 | Arkema France | Composition comprenant hf et 1,3,3,3-tetrafluoropropene |
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| FR3027154B1 (fr) | 2014-10-14 | 2016-11-25 | Arkema France | Gaz d'isolation ou d'extinction d'arcs electriques |
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-
2018
- 2018-03-22 FR FR1852479A patent/FR3079359B1/fr active Active
-
2019
- 2019-03-14 WO PCT/FR2019/050574 patent/WO2019186017A2/fr not_active Ceased
- 2019-03-14 US US16/959,765 patent/US11133139B2/en active Active
- 2019-03-14 EP EP19742415.3A patent/EP3769329A2/fr not_active Withdrawn
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9085721B2 (en) * | 2011-02-04 | 2015-07-21 | E I Du Pont De Nemours And Company | Azeotropic and azeotrope-like compositions involving certain haloolefins and uses thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| FR3079359B1 (fr) | 2020-10-09 |
| WO2019186017A3 (fr) | 2019-11-21 |
| FR3079359A1 (fr) | 2019-09-27 |
| WO2019186017A2 (fr) | 2019-10-03 |
| US11133139B2 (en) | 2021-09-28 |
| US20200365353A1 (en) | 2020-11-19 |
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