EP2904617B1 - Appareil contenant un gaz diélectrique d'isolation comprenant un composé organofluoré - Google Patents

Appareil contenant un gaz diélectrique d'isolation comprenant un composé organofluoré Download PDF

Info

Publication number
EP2904617B1
EP2904617B1 EP13774142.7A EP13774142A EP2904617B1 EP 2904617 B1 EP2904617 B1 EP 2904617B1 EP 13774142 A EP13774142 A EP 13774142A EP 2904617 B1 EP2904617 B1 EP 2904617B1
Authority
EP
European Patent Office
Prior art keywords
molecular sieve
desiccant
gas
organofluorine compound
insulation gas
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.)
Active
Application number
EP13774142.7A
Other languages
German (de)
English (en)
Other versions
EP2904617A1 (fr
Inventor
Thomas Alfred Paul
Navid Mahdizadeh
Patrick Stoller
Axel Kramer
Oliver Cossalter
Stephan Grob
Nitesh Ranjan
Javier Mantilla
Mathias-Dominic Buergler
Francia GALINDO-LOZANO
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hitachi Energy Ltd
Original Assignee
ABB Schweiz AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=53500978&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2904617(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by ABB Schweiz AG filed Critical ABB Schweiz AG
Priority to EP13774142.7A priority Critical patent/EP2904617B1/fr
Priority claimed from PCT/EP2013/070834 external-priority patent/WO2014053661A1/fr
Publication of EP2904617A1 publication Critical patent/EP2904617A1/fr
Application granted granted Critical
Publication of EP2904617B1 publication Critical patent/EP2904617B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/56Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances gases
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01HELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
    • H01H33/00High-tension or heavy-current switches with arc-extinguishing or arc-preventing means
    • H01H33/02Details
    • H01H33/53Cases; Reservoirs, tanks, piping or valves, for arc-extinguishing fluid; Accessories therefor, e.g. safety arrangements, pressure relief devices
    • H01H33/56Gas reservoirs
    • H01H2033/566Avoiding the use of SF6

Definitions

  • the present invention relates to an apparatus for the generation, the distribution and/or the usage of electrical energy, as well as to a method for operating such an apparatus, according to the preamble of the independent claims.
  • the term "distribution of electrical energy” can broadly encompass transmission or distribution of electrical energy on any voltage level.
  • Dielectric insulation media in liquid or gaseous state are conventionally applied for the insulation of an electrical component in a wide variety of apparatuses, such as for example switchgears, gas-insulated substations (GIS), gas-insulated lines (GIL), or transformers.
  • GIS gas-insulated substations
  • GIL gas-insulated lines
  • the electrical component is arranged in a gas-tight housing, which defines an insulating space, said insulation space comprising an insulation gas and separating the housing from the electrical component without letting electrical current to pass through.
  • the insulating gas further functions as an arc extinction gas.
  • WO-A-2010/142346 discloses a dielectric insulation medium comprising a fluoroketone having from 4 to 12 carbon atoms.
  • a dielectric insulation medium comprising a hydrofluoromonoether is disclosed in WO-A-2012/080222 .
  • Both groups of compounds have been shown to have high insulation capabilities, in particular a high dielectric strength, as well as high arc extinction capabilities. At the same time, they have a very low Global Warming Potential (GWP) and very low toxicity. The combination of these characteristics renders these organofluorine compounds highly suitable as a substitute for SF 6 (sulphur hexafluoride), which has commonly been used as a dielectric insulation medium, but which is known to have a high GWP.
  • GWP Global Warming Potential
  • FR 2 965 120 discloses a circuit breaker comprising a dielectric insulation gas and containing a fluoroketone, which is partially liquid and partially gaseous, and comprising means for absorbing molecular species which are formed after ionisation of the fluoroketone in an arc.
  • organofluorine compounds can be subject to decomposition.
  • the formation of decomposition products can also be due to partial discharge and can in particular occur when the moisture content in the insulation space is high.
  • the resulting decomposition products do not readily recombine, as it is possible for some decomposition products of SF 6 .
  • one decomposition product of the organofluorine compound is hydrogen fluoride (HF), which is highly corrosive and extremely toxic.
  • the decomposition products of the organofluorine compound shall, thus, be readily removed from the insulating space.
  • Removal of the decomposition products can theoretically be achieved by an adsorbent to which the decomposition product adsorbs and is bound permanently.
  • the presence of an adsorbent may lead to a decrease in the amount of organofluorine compound and, thus, to a decrease in the insulation and arc extinction performance of the insulation gas.
  • the problem of the present invention is, thus, to provide an apparatus using a dielectric insulation gas comprising an organofluorine compound, said apparatus allowing its insulating space to be kept essentially free from harmful decomposition products without negatively interfering with the insulation and arc extinction performance of the insulation gas.
  • the present invention relates to an apparatus for the generation, the distribution or the usage of electrical energy.
  • the apparatus comprises a housing enclosing an insulating space and an electrical component arranged in the insulating space.
  • the insulating space contains a dielectric insulation gas comprising an organofluorine compound A.
  • the apparatus further comprises a molecular sieve arranged such as to come into contact with the insulation gas.
  • the molecular sieve has an average pore size y greater than the molecular size of at least one decomposition product of the organofluorine compound A generated during operation of the apparatus, and the adsorption capability and/or absorption capability of the molecular sieve for the organofluorine compound A is lower than for the at least one decomposition product.
  • the present invention thus allows for selective removal of the decomposition product(s) from the insulation space, while leaving the organofluorine compound A unadsorbed and/or unabsorbed, and thus leaving the insulation and arc extinction capabilities of the insulation gas at least approximately unaffected or at least approximately not negatively affected.
  • adsorption capability shall encompass any adsorption processes, such as physisorption and/or chemisorption.
  • Physisorption can, in particular, be determined or be influenced by the relationship between the size of molecules of the dielectric medium and the pore size of the molecular sieve.
  • Chemisorption can, in particular, be determined or be influenced by chemical, typically reversal, interactions between molecules of the dielectric medium and the molecular sieve.
  • housing as used in the context of the present invention is to be understood broadly as any at least approximately closed system.
  • the term encompasses a plurality of chambers interconnected with each other.
  • housing encompasses a chamber, in which the electrical component is contained and which can be interconnected with a recycling system through which the dielectric insulation gas is removed, processed (e.g. cleaned) and reintroduced into the chamber.
  • Housing further comprises a chamber, in which the electrical component is contained and which can be interconnected with a pre-treatment chamber for pre-treating the dielectric insulation gas prior to introduction into the chamber.
  • the term "arranged such as to come into contact with the insulation gas” is to be understood broadly and encompasses both embodiments where there is a permanent contact of the molecular sieve with the insulation gas as well as embodiments in which there is only a temporary contact.
  • composition products relates to compounds comprising less atoms than organofluorine compound A from which they are generated and thus in most cases also having a molecular size which is substantially smaller than the molecular size of the organofluorine compound A.
  • the organofluorine compound A has a lower energy of adsorption (i.e. physical or chemical binding energy) and/or absorption (i.e. chemical binding energy) to the molecular sieve than the at least one decomposition product.
  • adsorption i.e. physical or chemical binding energy
  • absorption i.e. chemical binding energy
  • the forces acting between the adsorbed and/or absorbed compound and the molecular sieve in particular van der Waals forces, such as London dispersion forces, dipole-induced dipole, dipole-dipole and quadrupole interactions, as well covalent bonding forces
  • van der Waals forces such as London dispersion forces, dipole-induced dipole, dipole-dipole and quadrupole interactions, as well covalent bonding forces
  • the pore size of the molecular sieve can be chosen such that its adsorption capability and/or absorption capability for organofluorine compound A is lower than for the decomposition product. More particularly, the pore size is chosen small enough to keep organofluorine compound A out of the pores and thus to prevent adsorption and/or absorption to the pore surface.
  • the molecular sieve in embodiments has an average pore size y smaller than 15 ⁇ , preferably smaller than 13 ⁇ , more preferably smaller than 11 ⁇ , more preferably equal to or smaller than 9 ⁇ , preferably smaller than 7 ⁇ , more preferably smaller than 6 ⁇ and most preferably of about 5 ⁇ .
  • a fluoroketone having five carbon atoms or more does not enter a pore of a size of smaller than 9 ⁇ and therefore does not adsorb to such a pore surface and/or is not absorbed by such a pore surface.
  • the molecular sieve is at least temporarily charged with the organofluorine compound A, meaning that the content of organofluorine compound A in the molecular sieve is higher than its content in the dielectric insulation gas in equilibrium at operational conditions of the apparatus.
  • the organofluorine compound A is not kept from entering the pores of the molecular sieve, but on the contrary is forced into the molecular sieve, in particular by exposing the latter to a gas in which the partial pressure of the organofluorine compound A is higher than in the dielectric insulation gas present during operation of the apparatus.
  • the organofluorine compound A charging the molecular sieve is at least partially displaced by the at least one decomposition product adsorbing to the molecular sieve and/or being absorbed by the molecular sieve.
  • the molecular sieve according to this embodiment thus, functions simultaneously as a "reservoir” for the organofluorine compound A as well as a "sink” for the decomposition product.
  • the molecular sieve has an average pore y which is at least 2.7 ⁇ , preferably at least 2.8 ⁇ , more preferably at least 2.9 ⁇ , most preferably at least 3 ⁇ . It has been found that this pore size is sufficient for achieving good permeation of the at least one decomposition product and water into the molecular sieve and thus good adsorption on and/or absorption by the pore surface.
  • the removal of water is of high relevance, not only in view of a reduced formation of decomposition products, but also in view of preventing the solid components of the electrical apparatus, in particular the moveable parts, from corroding.
  • the molecular sieve is a zeolite, i.e. a microporous, aluminosilicate mineral that has undergone cation exchange to achieve a desired pore size.
  • Suitable zeolites include ZEOCHEM® molecular sieve 3A (having a pore size of 3 ⁇ ), 4A (having a pore size of 4 ⁇ ) and 5A (having a pore size of 5 A).
  • suitable zeolites can include e.g. ZEOCHEM® molecular sieve 13X (having a pore size of about 9 ⁇ ). This can improve the "reservoir" capacity e.g. for C5-fluoroketone while maintaining the adsorption capacity and/or absorption capacity for decomposition products, in particular when the molecular sieve is at least partly or even fully protected against water sorption by at least one desiccant being additionally present in the apparatus.
  • a larger pore size of 9 ⁇ or more, in particular up to 15 ⁇ , can also be useful when larger molecules than the C5-fluoroketone are comprised in the organofluorine compound A.
  • the apparatus further comprises at least one desiccant arranged such as to come into contact with the insulation gas.
  • This desiccant is different from the molecular sieve defined above.
  • the at least one desiccant is one which specifically adsorbs (or absorbs) water. More preferably, the at least one desiccant has a higher hydrophilicity than the molecular sieve, meaning that it has a higher tendency to bind water than the molecular sieve, and/or the at least one desiccant binds water irreversibly under normal operating conditions of the apparatus. In other words, the desiccant is more hygroscopic than the molecular sieve. Thus, the desiccant serves for protecting the molecular sieve from water or moisture.
  • the at least one desiccant is of a different type than a molecular sieve, i.e. the desiccant itself is not a molecular sieve.
  • the desiccant is not any of the group consisting of: aluminium, aluminium oxide, activated alumina, activated carbon, zeolite, and combinations thereof. These embodiments can apply to any aspect of the invention.
  • the at least one desiccant is selected from the group consisting of: calcium, calcium sulphate, in particular drierite, calcium carbonate, calcium hydride, calcium chloride, potassium carbonate, potassium hydroxide, copper(II) sulphate, calcium oxide, magnesium, magnesium oxide, magnesium sulphate, magnesium perchlorate, sodium, sodium sulphate, aluminium, lithium aluminium hydride, aluminium oxide, activated alumina, montmorrilonite, phosphorpentoxide, silica gel and a cellulose filter.
  • the at least one desiccant is selected from the group consisting of: calcium, calcium sulphate, in particular drierite, calcium carbonate, calcium hydride, calcium chloride, potassium carbonate, potassium hydroxide, copper(II) sulphate, calcium oxide, magnesium, magnesium oxide, magnesium sulphate, magnesium perchlorate, sodium, sodium sulphate, lithium aluminium hydride, montmorrilonite, phosphorpentoxide, silica gel and a cellulose filter.
  • calcium sulphate, magnesium sulphate and sodium sulphate are particularly preferred.
  • the present invention encompasses both embodiments in which only one desiccant is comprised in the apparatus as well as embodiments in which two or more desiccants (i.e. two or more different types of desiccants) are comprised.
  • the at least one desiccant and/or the molecular sieve (whichever is present, and in particular to which it may apply) is comprised in a region of the apparatus having a temperature lower than the average temperature present in the apparatus at operational conditions.
  • gas decomposition processes that might occur on the desiccant and/or on the molecular sieve due to surface catalysis can be significantly decelerated or avoided.
  • the desiccant and/or the molecular sieve can be comprised in a region to which cooling means, more particularly external cooling means, are attributed.
  • the desiccant and/or the molecular sieve is or are comprised in a region of the apparatus having a temperature less than 40 K (Kelvin) above ambient temperature, more preferably less than 20 K (Kelvin) above ambient temperature.
  • the desiccant and/or the molecular sieve (whichever is present, and in particular to which it may apply) is or are in powder form.
  • the desiccant and/or molecular sieve is or are designed to be at least essentially free, in particular free, of any binder in order to avoid potential issues regarding material compatibility inside the apparatus.
  • the binder provides unwanted adsorption sites for capturing water which is then available for unwanted reaction with the organofluorine compound, in particular C5-ketone or C5-fluoroketone (C5FK). Destruction of C5FK molecules could then ultimately degrade the dielectric strength of the insulation gas. Therefore, leaving out the binder material can be favourable.
  • the at least one desiccant and/or molecular sieve (whichever is present) is or are comprised in a permeable container, and/or is or are arranged on a carrier, thus allowing an intensive contact between the desiccant and/or the molecular sieve, respectively, with the insulation gas.
  • this permeable container or carrier can have the form of e.g. a tube, roll, fabric, lamella or honeycomb.
  • the at least one desiccant and/or molecular sieve is comprised in at least one permeable container, the cover of which is permeable at least for water and more particularly is a semipermeable membrane, which is selectively permeable for water.
  • the permeable container can e.g. form a sachet.
  • two or more permeable containers are arranged in a frame or holder in a manner spaced apart from each other. Due to the gaps formed between the permeable containers, and thus due to their freely exposed surface area, high gas permeation into the interior of the container and thus a good contact of the at least one desiccant and/or molecular sieve with the insulation gas can be achieved.
  • the permeable containers are arranged in a cuboid frame, and more particularly are arranged parallel to each other. If the permeable container is a sachet, it is typically lined by a fabric.
  • the permeable containers are flexible and are loosely arranged concentrically in a concentric holder.
  • the organofluorine compound A is selected from the group consisting of: fluoroethers, in particular hydrofluoromonoethers, fluoroketones and fluoroolefins, in particular hydrofluoroolefins, and mixtures thereof.
  • fluoroethers in particular hydrofluoromonoethers, fluoroketones and fluoroolefins, in particular hydrofluoroolefins, and mixtures thereof.
  • fluoroethers in particular hydrofluoromonoethers, fluoroketones and fluoroolefins, in particular hydrofluoroolefins, and mixtures thereof.
  • the invention encompasses both embodiments in which the dielectric insulation gas comprises either one of a fluoroether, in particular a hydrofluoromonoether, a fluoroketone and a fluoroolefin, in particular a hydrofluoroolefin, as well as embodiments in which it comprises a mixture of at least two of these compounds.
  • fluoroether encompasses both perfluoroethers, i.e. fully fluorinated ethers, and hydrofluoroethers, i.e. ethers that are only partially fluorinated.
  • the term further encompasses saturated compounds as well as unsaturated compounds, i.e. compounds including double and/or triple bonds.
  • the at least partially fluorinated alkyl chains attached to the oxygen atom of the fluoroether can be, independently of each other, linear or branched.
  • fluoroethers encompasses both non-cyclic and cyclic ethers.
  • the two alkyl chains attached to the oxygen atom can optionally form a ring.
  • the term encompasses fluorooxiranes.
  • the organofluorine compound A according to the present invention is a perfluorooxirane or a hydrofluorooxirane, more specifically a perfluorooxirane or hydrofluorooxirane comprising from three to fifteen carbon atoms.
  • the dielectric insulation gas comprises a hydrofluoromonoether containing at least three carbon atoms.
  • these hydrofluoromonoethers are chemically and thermally stable up to temperatures above 140°C. They are further non-toxic or have a low toxicity level. In addition, they are non-corrosive and non-explosive.
  • hydrofluoromonoether refers to a compound having one and only one ether group, said ether group linking two alkyl groups, which can be, independently from each other, linear or branched, and which can optionally form a ring.
  • the compound is thus in clear contrast to the compounds disclosed in e.g. US-B-7128133 , which relates to the use of compounds containing two ether groups, i.e. hydrofluorodiethers, in heat-transfer fluids.
  • hydrofluoromonoether as used herein is further to be understood such that the monoether is partially hydrogenated and partially fluorinated. It is further to be understood such that it may comprise a mixture of differently structured hydrofluoromonoethers.
  • structurally different shall broadly encompass any difference in sum formula or structural formula of the hydrofluoromonoether.
  • hydrofluoromonoethers containing at least three carbon atoms have been found to have a relatively high dielectric strength.
  • the ratio of the dielectric strength of the hydrofluoromonoethers according to the present invention to the dielectric strength of SF 6 is greater than about 0.4.
  • the GWP of the hydrofluoromonoethers is low.
  • the GWP is less than 1'000 over 100 years, more specifically less than 700 over 100 years.
  • hydrofluoromonoethers mentioned herein have a relatively low atmospheric lifetime and in addition are devoid of halogen atoms that play a role in the ozone destruction catalytic cycle, namely Cl, Br or I. Their ODP is zero, which is very favourable from an environmental perspective.
  • hydrofluoromonoether containing at least three carbon atoms and thus having a relatively high boiling point of more than -20°C is based on the finding that a higher boiling point of the hydrofluoromonoether generally goes along with a higher dielectric strength.
  • the hydrofluoromonoether contains exactly three or four or five or six carbon atoms, in particular exactly three or four carbon atoms, most preferably exactly three carbon atoms.
  • the hydrofluoromonoether is thus at least one compound selected from the group consisting of the compounds defined by the following structural formulae in which a part of the hydrogen atoms is substituted by a fluorine atom:
  • the ratio of the number of fluorine atoms to the total number of fluorine and hydrogen atoms, here briefly called "F-rate", of the hydrofluoromonoether is at least 5:8. It has been found that compounds falling within this definition are generally non-flammable and thus result in an insulation medium complying with highest safety requirements. Thus, safety requirements of the electrical insulator and the method of its production can readily be fulfilled by using a corresponding hydrofluoromonoether.
  • the ratio of the number of fluorine atoms to the number of carbon atoms ranges from 1.5:1 to 2:1.
  • Such compounds generally have a GWP of less than 1'000 over 100 years and are thus very environment-friendly. It is particularly preferred that the hydrofluoromonoether has a GWP of less than 700 over 100 years.
  • exactly one of c and f in the general structure (O) is 0.
  • the corresponding grouping of fluorines on one side of the ether linkage, with the other side remaining unsubstituted, is called "segregation". Segregation has been found to reduce the boiling point compared to unsegregated compounds of the same chain length. This feature is thus of particular interest, because compounds with longer chain lengths allowing for higher dielectric strength can be used without risk of liquefaction under operational conditions.
  • the hydrofluoromonoether is selected from the group consisting of pentafluoro-ethyl-methyl ether (CH 3 -O-CF 2 CF 3 ) and 2,2,2-trifluoroethyl-trifluoromethyl ether (CF 3 -O-CH 2 CF 3 ).
  • Pentafluoro-ethyl-methyl ether has a boiling point of +5.25°C and a GWP of 697 over 100 years, the F-rate being 0.625, while 2,2,2-trifluoroethyl-trifluoromethyl ether has a boiling point of +11°C and a GWP of 487 over 100 years, the F-rate being 0.75. They both have an ODP of 0 and are thus environmentally fully acceptable.
  • pentafluoro-ethyl-methyl ether has been found to be thermally stable at a temperature of 175°C for 30 days and therefore to be fully suitable for the operational conditions given in the apparatus. Since thermal stability studies of hydrofluoromonoethers of higher molecular weight have shown that ethers containing fully hydrogenated methyl or ethyl groups have a lower thermal stability compared to those having partially hydrogenated groups, it can be assumed that the thermal stability of 2,2,2-trifluoroethyl-trifluoromethyl ether is even higher.
  • hydrofluoromonoethers and in particular pentafluoro-ethyl-methyl ether as well as 2,2,2-trifluoroethyl-trifluoromethyl ether, have a lethal concentration LC 50 of higher than 10'000 ppm, rendering them suitable also from a toxicological point of view.
  • hydrofluoromonoethers mentioned have a higher dielectric strength than air.
  • pentafluoro-ethyl-methyl ether has a dielectric strength about 2.4 times higher than that of air at 1 bar.
  • the hydrofluoromonoethers mentioned are normally in the gaseous state at operational conditions.
  • a dielectric insulation medium in which every component is in the gaseous state at operational conditions of the apparatus can be achieved, which is advantageous.
  • the dielectric insulation gas comprises a fluoroketone containing from four to twelve carbon atoms.
  • fluoroketone as used in this application shall be interpreted broadly and shall encompass both perfluoroketones and hydrofluoroketones, and shall further encompass both saturated compounds and unsaturated compounds, i.e. compounds including double and/or triple bonds.
  • the at least partially fluorinated alkyl chain of the fluoroketones can be linear or branched.
  • the fluoroketone is a perfluoroketone.
  • the fluoroketone has a branched alkyl chain, in particular an at least partially fluorinated alkyl chain.
  • the fluoroketone is a fully saturated compound.
  • fluoroketones containing five or six carbon atoms have the advantage of a relatively low boiling point. Thus, problems which might go along with liquefaction can be avoided, even when the apparatus is used at low temperatures.
  • the fluoroketone is at least one compound selected from the group consisting of the compounds defined by the following structural formulae in which at least one hydrogen atom is substituted with a fluorine atom:
  • Fluoroketones containing five or more carbon atoms are further advantageous, because they are generally non-toxic with outstanding margins for human safety. This is in contrast to fluoroketones having less than four carbon atoms, such as hexafluoroacetone (or hexafluoropropanone), which are toxic and very reactive.
  • fluoroketones containing exactly five carbon atoms herein briefly named fluoroketones a
  • fluoroketones containing exactly six carbon atoms are thermally stable up to 500°C.
  • the fluoroketones in particular fluoroketones a), having a branched alkyl chain are preferred, because their boiling points are lower than the boiling points of the corresponding compounds (i.e. compounds with same molecular formula) having a straight alkyl chain.
  • the fluoroketone a) is a perfluoroketone, in particular has the molecular formula C 5 F 10 O, i.e. is fully saturated without double or triple bonds.
  • the fluoroketone a) may more preferably be selected from the group consisting of 1,1,1,3,4,4,4-heptafluoro-3-(trifluoromethyl)butan-2-one (also named decafluoro-2-methylbutan-3-one), 1,1,1,3,3,4,4,5,5,5-decafluoropentan-2-one, 1,1,1,2,2,4,4,5,5,5-decafluoropentan-3-one and octafluorocylcopentanone, and most preferably is 1,1,1,3,4,4,4-heptafluoro-3-(trifluoromethyl)butan-2-one.
  • C5-ketone 1,1,1,3,4,4,4-heptafluoro-3-(trifluoromethyl)butan-2-one, here briefly called "C5-ketone", with molecular formula CF 3 C(O)CF(CF 3 ) 2 or C 5 F 10 O, has been found to be particularly preferred for high and medium voltage insulation applications, because it has the advantages of high dielectric insulation performance, in particular in mixtures with a dielectric carrier gas, has very low GWP and has a low boiling point. It has an ODP of 0 and is practically non-toxic.
  • even higher insulation capabilities can be achieved by combining the mixture of different fluoroketone components.
  • a fluoroketone containing exactly five carbon atoms, as described above and here briefly called fluoroketone a), and a fluoroketone containing exactly six carbon atoms or exactly seven carbon atoms, here briefly named fluoroketone c) can favourably be part of the dielectric insulation at the same time.
  • an insulation medium can be achieved having more than one fluoroketone, each contributing by itself to the dielectric strength insulation medium.
  • the further fluoroketone c) is at least one compound selected from the group consisting of the compounds defined by the following structural formulae in which at least one hydrogen atom is substituted with a fluorine atom: and as well as any fluoroketone having exactly 6 carbon atoms, in which the at least partially fluorinated alkyl chain of the fluoroketone forms a ring, which is substituted by one or more alkyl groups (IIh); and/or is at least one compound selected from the group consisting of the compounds defined by the following structural formulae in which at least one hydrogen atom is substituted with a fluorine atom: and in particular dodecafluoro-cycloheptanone, as well as any fluoroketone having exactly 7 carbon atoms, in which the at least partially fluorinated alkyl chain of the fluoroketone forms a ring, which is substituted by one or more alkyl groups (IIIo).
  • the present invention also encompasses, in particular, each combination of any of the compounds according to structural formulae Ia to Id with any of the compounds according to structural formulae IIa to IIg and/or IIIa to IIIn.
  • the present invention encompasses each compound or each combination of compounds selected from the group consisting of the compounds according to structural formulae (Ia) to (Ii), (IIa) to (IIh), (IIIa) to (IIIo), and mixtures thereof.
  • fluoroketone c a fluoroketone containing exactly six carbon atoms (falling under the designation "fluoroketone c)" mentioned above) may be preferred; such a fluoroketone is non-toxic, with outstanding margins for human safety.
  • fluoroketone c alike fluoroketone a), is a perfluoroketone, and/or has a branched alkyl chain, in particular an at least partially fluorinated alkyl chain, and/or the fluoroketone c) contains fully saturated compounds.
  • the fluoroketone c) has the molecular formula C 6 F 12 O, i.e. is fully saturated without double or triple bonds.
  • the fluoroketone c) can be selected from the group consisting of 1,1,1,2,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pentan-3-one (also named dodecafluoro-2-methylpentan-3-one), 1,1,1,3,3,4,5,5,5-nonafluoro-4-(trifluoromethyl)pentan-2-one (also named dodecafluoro-4-methylpentan-2-one), 1,1,1,3,4,4,5,5,5-nonafluoro-3-(trifluoromethyl)pentan-2-one (also named dodecafluoro-3-methylpentan-2-one), 1,1,1,4,4,4-hexafluoro-3,3-bis-(trifluoromethyl)butan-2-one (also named dodecafluoro-3,3-(dimethyl)butan-2-one), dodecafluorohexan-2-one, dodecafluorohexan-3-one and deca
  • C6-ketone 1,1,1,2,4,4,5,5,5-Nonafluoro-4-(trifluoromethyl)pentan-3-one
  • C6-ketone with molecular formula C 2 F 5 C(O)CF(CF 3 ) 2
  • the organofluorine compound can also be a fluoroolefin, in particular a hydrofluoroolefin. More particularly, the fluoroolefin or hydrofluorolefin, respectively, contains exactly three carbon atoms.
  • the hydrofluoroolefin is, thus, selected from the group consisting of: 1,1,1,2-tetrafluoropropene (HFO-1234yf), 1,2,3,3-tetrafluoro-2-propene (HFO-1234yc), 1,1,3,3-tetrafluoro-2-propene (HFO-1234zc), 1,1,1,3-tetrafluoro-2-propene (HFO-1234ze), 1,1,2,3-tetrafluoro-2-propene (HFO-1234ye), 1,1,1,2,3-pentafluoropropene (HFO-1225ye), 1,1,2,3,3-pentafluoropropene (HFO-1225yc), 1,1,1,3,3-pentafluoropropene (HFO-1225zc), (Z)1,1,1,3-tetrafluoropropene (HFO-1234zeZ), (Z)1,1,2,3-tetrafluoro-2-
  • the dielectric insulation gas further comprises a carrier gas.
  • the dielectric insulation gas comprises the organofluorine compound, particularly a fluoroketone having exactly five carbon atoms, at a partial pressure corresponding to the vapour pressure of the organofluorine compound at the minimum operating temperature of the apparatus, with the remainder of the dielectric insulation gas being or comprising the carrier gas.
  • the organofluorine compound A particularly a fluoroketone having exactly five carbon atoms, is present in fully gaseous phase in the insulation space.
  • the carrier gas comprises an air component.
  • the carrier gas shall be selected from the group consisting of: oxygen (O 2 ), nitrogen (N 2 ), carbon dioxide (CO 2 ), and air.
  • the carrier gas can be a mixture of N 2 and O 2 , or the carrier gas can be a mixture of CO 2 and O 2 .
  • the carrier gas can also comprise a noble gas, and/or nitric oxide, and/or nitrogen dioxide.
  • the carrier comprises O 2 , since this allows to efficiently avoid or reduce the formation of harmful decomposition products.
  • the carrier gas comprises O 2
  • the partial pressure of O 2 is preferably at least about twice that of the partial pressure of the organofluorine compound.
  • the carrier gas can comprise CO 2 .
  • the technical effects on which the present invention is based namely the efficient removal of at least one decomposition product without interfering with the insulation and arc extinction performance of the organofluorine-compound-comprising dielectric insulation gas, are of particular relevance for an apparatus in which the housing encloses the insulation space in a gas-tight manner. It is further preferred that the apparatus is one in which the electrical component is a high voltage or medium voltage unit.
  • the apparatus in particular gas-insulated apparatus, relates to: a switchgear, in particular a gas-insulated metal (or otherwise)-encapsulated switchgear (GIS), or a part and/or component thereof.
  • the apparatus can be a bus bar, a bushing, a cable, a gas-insulated cable, a cable joint, a gas-insulated line (GIL), a transformer, a current transformer, a voltage transformer, a surge arrester, an earthing switch, a disconnector, a combined disconnector and earthing switch, a load-break switch, a circuit breaker, and/or any type of gas-insulated switch; high voltage apparatus, medium voltage apparatus, low voltage apparatus, direct-current apparatus, air-insulated insulator, gas-insulated metal-encapsulated insulator, sensors, capacitor, inductance, resistor, current limiter, high voltage switch, gas circuit breaker, vacuum circuit breaker, generator circuit breaker, medium voltage switch, ring main unit, recloser, sectionalizer, low voltage switch
  • the molecular sieve and optionally the desiccant can be arranged in a chamber (as part of the housing) in which the electrical component is contained, as well as in a recycling system and/or pre-treatment chamber (forming further parts of the housing).
  • the housing comprises a chamber in which the electrical component is contained and a recycling system comprising the molecular sieve and optionally the desiccant, e.g. the cellulose filters.
  • the desiccant is arranged in the recycling system, in particular in the chamber, such that the dielectric insulation gas in a first step comes into contact with the desiccant to reduce or eliminate moisture and only afterwards (or at least to a larger percentage or majority afterwards) in a second step comes into contact with the molecular sieve to reduce or eliminate decomposition products.
  • the recycling system is equipped with a compressor and a pump for pumping the dielectric insulation gas through at least one filter comprising the molecular sieve and optionally the desiccant. After that, the dried and cleaned dielectric insulation gas can be re-introduced into the chamber.
  • the humidity, density, pressure and/or content of decomposition product(s) are measured, e.g. by gas chromatography and/or infrared spectroscopy, and controlled by a respective (multi-) sensor system.
  • An electric apparatus of such embodiments is particularly preferred as it allows cleaning and/or drying of the dielectric insulation gas without evacuation of the insulation space.
  • the housing comprises a chamber, in which the electrical component is contained, and a recycling system comprising at least one of the molecular sieve and the desiccant (whichever is present), and the housing is equipped with a compressor and a pump for pumping the dielectric insulation gas through at least one filter comprising the at least one of the molecular sieve and the desiccant.
  • means for introducing carrier gas components adsorbing to and/or being absorbed by the molecular sieve and/or the desiccant (whichever is present) can be provided.
  • the means for introducing the carrier gas components are means for refilling after commissioning or during operation of the apparatus the carrier gas components adsorbing to and/or being absorbed by the molecular sieve and/or the desiccant.
  • the means for refilling may for example be implemented by or be in connection with the above-mentioned recycling system.
  • means for introducing CO 2 in particular means for refilling CO 2 during operation of the apparatus, can be provided for compensating the amount of CO 2 that is adsorbed and/or absorbed. This allows to reduce a pressure swing in the apparatus or to avoid a lock-out of the apparatus due to low pressure of the dielectric insulation gas present in the apparatus for generation, distribution and/or usage of electrical energy.
  • the present invention further relates to a method for operating an apparatus as described above, said method comprising a step of charging the molecular sieve with the organofluorine compound A, in particular comprising the step or steps of:
  • the organofluorine compound A charging the molecular sieve is at least partially displaced by the at least one decomposition product adsorbing to the molecular sieve and/or being absorbed by the molecular sieve.
  • the molecular sieve can be arranged in a temperature-controlled environment, in particular in a heatable environment, inside the housing, wherein a temperature of the molecular sieve is controlled such that a predeterminable amount of charged organofluorine compound A can be released at a predeterminable instant or occasion from the molecular sieve.
  • a temperature of the molecular sieve is controlled such that a predeterminable amount of charged organofluorine compound A can be released at a predeterminable instant or occasion from the molecular sieve.
  • This allows to regulate the amount of organofluorine compound A in the dielectric insulation gas, and/or to free the molecular sieve from at least a portion of the organofluorine compound A and thus to provide additional adsorption capacity in the molecular sieve to adsorb and/or absorb decomposition products.
  • the temperature control and, in particular, heating control of the molecular sieve enhances its performance and flexibility as a reservoir for the organofluorine compound A and as
  • the apparatus comprises temperature control means for controlling a temperature of the molecular sieve.
  • the apparatus comprises heating means for heating the molecular sieve.
  • the temperature control means or heating means are operable such that a predeterminable amount of charged organofluorine compound A is releasable from the molecular sieve at a predeterminable instant or occasion, in particular for regulating an amount of the organofluorine compound A in the dielectric insulation gas and/or for freeing the molecular sieve from at least a portion of the organofluorine compound A.
  • the present invention also relates to an apparatus for the generation, the distribution and/or the usage of electrical energy, in particular according to embodiments disclosed herein, with the apparatus comprising a housing enclosing an insulating space and an electrical component being arranged in the insulating space, wherein the insulating space contains a dielectric insulation gas comprising an organofluorine compound A, characterized in that the apparatus further comprises a desiccant arranged such as to come into contact with the insulation gas.
  • the at least one desiccant is selected from the group consisting of: calcium, calcium sulphate, in particular drierite, calcium carbonate, calcium hydride, calcium chloride, potassium carbonate, potassium hydroxide, copper(II) sulphate, calcium oxide, magnesium, magnesium oxide, magnesium sulphate, magnesium perchlorate, sodium, sodium sulphate, lithium aluminium hydride, montmorrilonite, phosphorpentoxide, silica gel and a cellulose filter.
  • This subject-matter is by itself suitable for solving the problem of the present invention. It has been found that the generation of toxic and corrosive decomposition products from the organofluorine compound A is generally due to the exposure of the compound to partial discharge and/or arcing in the presence of water. Thus, by reducing the water content using the desiccant, also the generation of these decomposition products is reduced. Furthermore, the reduction in the water content prevents the solid components of the electrical apparatus, in particular the moveable parts, from corroding, which further contributes to the safe operation of the apparatus.
  • the desiccant is not any of the group consisting of: aluminium, aluminium oxide, activated alumina, activated carbon, zeolite, and combinations thereof.
  • the above-mentioned specific desiccants of the further aspect of the invention can also be combined with a molecular sieve being different from the desiccant and of any type and pore size that is arranged such as to come into contact with the insulation gas.
  • a third aspect of the invention relates to an apparatus for the generation, the distribution and/or the usage of electrical energy, in particular as described above, said apparatus comprising a housing enclosing an insulating space and an electrical component arranged in the insulating space, said insulating space containing a dielectric insulation gas comprising an organofluorine compound A, wherein the apparatus further comprises at least one of a molecular sieve and a desiccant arranged such as to come into contact with the insulation gas, and that at least one of the at least one of the molecular sieve and the desiccant is or are in powder form.
  • the preferred features mentioned above for the subject matter comprising a molecular sieve or a desiccant without a molecular sieve likewise apply to the subject matter of the third aspect of molecular sieve and/or desiccant in powder form.
  • the molecular sieve can have an average pore size y greater than the molecular size of at least one decomposition product of the organofluorine compound A generated during operation of the apparatus, and the adsorption capability and/or absorption capability of the molecular sieve for the organofluorine compound A can be lower than for the at least one decomposition product.
  • the at least one desiccant can be selected from the group consisting of: calcium, calcium sulphate, in particular drierite, calcium carbonate, calcium hydride, calcium chloride, potassium carbonate, potassium hydroxide, copper(II) sulphate, calcium oxide, magnesium, magnesium oxide, magnesium sulphate, magnesium perchlorate, sodium, sodium sulphate, aluminium, lithium aluminium hydride, aluminium oxide, activated alumina, montmorrilonite, phosphorpentoxide, silica gel and a cellulose filter.
  • the at least one of a molecular sieve and a desiccant is not activated carbon.
  • This embodiment shows that it can be preferable to use a molecular sieve with a pore size smaller than 9 ⁇ , in particular when the organofluorine compound A is or comprises C5-fluoroketone.
  • a larger pore size equal to 9 ⁇ or larger can also be possible; an example can be, that an organofluorine compound A of a larger kinetic diameter than the C5-fluoroketone is used or that some adsorption and/or absorption of the organofluorine compound A, in particular C5-fluoroketone, to the molecular sieve is acceptable.
  • a desiccant is comprised in the apparatus/test device.
  • Two exemplary arrangements of at least one of the molecular sieve 1 and the desiccant 2 (whichever is present) are given in Fig. 2 and in Figs. 3a and 3b , respectively.
  • sachets 4a comprising the at least one of the molecular sieve 1 and the desiccant 2 in powder form are arranged in frame 6a, here for example a cuboid frame 6a.
  • the sachets 4a are arranged parallel to each other in a spaced-apart manner, such that between them a respective gap 8a is formed.
  • the sachets 4a are in the form of a sheet, the long sides of which corresponds more or less to the height and depth of the frame 6a. It is understood that any other form suitable for the respective purpose can be used.
  • the frame 6b is in cylindrical form and comprises an outermost hollow cylinder 10, in which two inner hollow cylinders 12, 14 are arranged concentrically, a middle hollow 12 cylinder and an innermost hollow cylinder 14.
  • a rod 16 is arranged coincidingly with the axis of the cylinders.
  • radial gaps 8b', 8b", 8b'", respectively, are formed.
  • a rolled sachet 4b', 4b", 4b' is arranged in a loose manner such that the surface of the sachets 4b', 4b", 4b"' is not in full contact with the surface of the respective cylinders 14, 12, 10 and thus comprises a freely exposed surface area.
  • the bottom end of the frame 6b can be closed, for example by an end plate 18, to safeguard that the at least one of the molecular sieve 1 and the desiccant 2 does not "fall out" of the gaps 8b', 8b", 8b'".
  • any number of cylinders 14, 12, 10 can be selected to provide respective inter-cylinder spaces or gaps 8b', 8b", 8b'" for receiving and holding the at least one of the molecular sieve 1 and the desiccant 2 (whichever is present) in containers 4b', 4b", 4b"', for example in sachets 4b', 4b", 4b"', and for providing insulation-gas-accessible surface areas of the at least one of the molecular sieve 1 and the desiccant 2.
  • the term "adsorbing” shall be understood broadly to encompass capturing or immobilizing molecules (as a whole or in dissociated form) on a surface of the sorbing agent (i.e. molecular sieve and/or desiccant) and can be done by any mechanism and in particular by physical or chemical binding the molecules to the sorbing agent.
  • the term "absorbing” shall be understood broadly to encompass capturing or immobilizing molecules (as a whole or in dissociated form) in the structure of the sorbing agent and can be done by any mechanism, and in particular by chemical binding the molecules (as a whole or in dissociated form) into the sorbing agent so that the absorbed molecules become part of the crystal structure of the sorbing agent.
  • a molecular sieve shall comprise also embodiments in which one molecular sieve or more than one molecular sieve is or are present.
  • the term “a molecular sieve” is thus to be understood as at least one molecular sieve.

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Organic Insulating Materials (AREA)

Claims (25)

  1. Appareil destiné à la production, la distribution et/ou l'utilisation d'énergie électrique, ledit appareil comprenant un boîtier renfermant un espace isolant et un composant électrique disposé dans l'espace isolant, ledit espace isolant contenant un gaz d'isolation diélectrique comprenant un composé organofluoré A, l'appareil comprenant en outre un tamis moléculaire (1) disposé de manière à venir en contact avec le gaz d'isolation, le tamis moléculaire (1) ayant une taille moyenne de pores y supérieure à la taille moléculaire d'au moins un produit de décomposition du composé organofluoré A généré pendant le fonctionnement de l'appareil, la capacité d'adsorption et/ou la capacité d'absorption du tamis moléculaire (1) pour le composé organofluoré A étant plus faible(s) que pour l'au moins un produit de décomposition, caractérisé en ce que l'appareil comprend en outre au moins un déshydratant (2) disposé de manière à venir en contact avec le gaz d'isolation et en ce que l'au moins un déshydratant (2) est différent du tamis moléculaire (1).
  2. Appareil selon la revendication 1, caractérisé en ce que le composé organofluoré A a une plus faible énergie d'adsorption et/ou d'absorption sur le tamis moléculaire (1) que l'au moins un produit de décomposition.
  3. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que le tamis moléculaire (2) a une taille moyenne de pores y inférieure à 15 Å, de préférence inférieure à 13 Å, mieux inférieure à 11 Å, mieux encore inférieure ou égale à 9 Å, mieux inférieure à 7 Å, mieux encore inférieure à 6 Å et idéalement d'environ 5 Å.
  4. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que le tamis moléculaire (1) est au moins temporairement chargé avec le composé organofluoré A, et/ou en ce que le tamis moléculaire (1) est une zéolithe.
  5. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que l'appareil comprend un moyen de contrôle de la température pour contrôler une température du tamis moléculaire (1), en particulier pour réguler une quantité du composé organofluoré A dans le gaz d'isolation diélectrique et/ou pour libérer le tamis moléculaire (1) d'au moins une partie du composé organofluoré A.
  6. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que le tamis moléculaire (1) a une taille moyenne de pores y qui est d'au moins 2,7 Å, de préférence au moins 2,8 Å, mieux encore au moins 2,9 Å, idéalement au moins 3 Å.
  7. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que l'au moins un déshydratant (2) est d'un type différent d'un tamis moléculaire (1), et/ou en ce que l'au moins un déshydratant (2) a une plus forte hydrophilie que le tamis moléculaire (1).
  8. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que l'au moins un déshydratant (2) est choisi dans le groupe constitué par : le calcium, le sulfate de calcium, en particulier la driérite, le carbonate de calcium, l'hydrure de calcium, le chlorure de calcium, le carbonate de potassium, l'hydroxyde de potassium, le sulfate de cuivre (II), l'oxyde de calcium, le magnésium, l'oxyde de magnésium, le sulfate de magnésium, le perchlorate de magnésium, le sodium, le sulfate de sodium, l'aluminium, l'hydrure de lithium et d'aluminium, l'oxyde d'aluminium, l'alumine activée, la montmorillonite, le pentoxyde de phosphore, le gel de silice et un filtre de cellulose.
  9. Appareil destiné à la production, la distribution et/ou l'utilisation d'énergie électrique, en particulier selon l'une quelconque des revendications précédentes, ledit appareil comprenant un boîtier renfermant un espace isolant et un composant électrique disposé dans l'espace isolant, ledit espace isolant contenant un gaz d'isolation diélectrique comprenant un composé organofluoré A, caractérisé en ce que l'appareil comprend en outre au moins un déshydratant (2) disposé de manière à venir en contact avec le gaz d'isolation, l'au moins un déshydratant (2) étant choisi dans le groupe constitué par le calcium, le sulfate de calcium, en particulier la driérite, le carbonate de calcium, l'hydrure de calcium, le chlorure de calcium, le carbonate de potassium, l'hydroxyde de potassium, le sulfate de cuivre (II), l'oxyde de calcium, le magnésium, l'oxyde de magnésium, le sulfate de magnésium, le perchlorate de magnésium, le sodium, le sulfate de sodium, l'hydrure de lithium et d'aluminium, la montmorillonite, le pentoxyde de phosphore, le gel de silice et un filtre de cellulose, l'appareil comprenant également un tamis moléculaire (1) différent de l'au moins un déshydratant (2) et disposé de manière à venir en contact avec le gaz d'isolation.
  10. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que le composé organofluoré A est choisi dans le groupe constitué par les fluoroéthers, en particulier les hydrofluoromonoéthers, les fluorocétones et les fluorooléfines, en particulier les hydrofluorooléfines, et les mélanges de ceux-ci.
  11. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que le gaz d'isolation diélectrique comprend un hydrofluoromonoéther contenant au moins trois atomes de carbone ; et/ou en ce que le gaz d'isolation diélectrique comprend une fluorocétone contenant de quatre à douze atomes de carbone, de préférence contenant exactement cinq atomes de carbone, ou exactement six atomes de carbone, ou un mélange de ceux-ci.
  12. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que le gaz d'isolation diélectrique comprend en outre un gaz vecteur, en particulier en ce que l'appareil comprend un moyen de rechargement, après la mise en service ou pendant le fonctionnement de l'appareil, des constituants du gaz vecteur s'adsorbant sur et/ou étant absorbés par au moins un des éléments suivants : le tamis moléculaire (1), l'au moins un déshydratant (2), et une combinaison de ceux-ci.
  13. Appareil selon la revendication 14, caractérisé en ce que le gaz vecteur comprend un constituant de l'air, en particulier choisi dans le groupe constitué par le dioxyde de carbone (CO2), l'oxygène (O2), l'azote (N2) et les mélanges de ceux-ci, et est de préférence l'air.
  14. Appareil selon la revendication 12 ou 13, caractérisé en ce que le gaz d'isolation diélectrique comprend le composé organofluoré à une pression partielle correspondant à la pression de vapeur du composé organofluoré à la température minimale de fonctionnement de l'appareil, le reste du gaz d'isolation diélectrique étant ou comprenant le gaz vecteur.
  15. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que le boîtier renferme l'espace d'isolation d'une manière étanche aux gaz ; et/ou en ce que le composant électrique est un appareil haute tension ou moyenne tension, ou est un composant haute tension ou moyenne tension.
  16. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que l'appareil est : un appareillage de commutation, en particulier un appareillage de commutation isolé au gaz (GIS), ou une partie et/ou un composant de celui-ci, une barre omnibus, une traversée, un câble, un câble isolé au gaz, une jonction de câbles, une ligne isolée au gaz (GIL), un transformateur, un transformateur de courant, un transformateur de tension, un parasurtenseur, un sectionneur de terre, un sectionneur, un sectionneur et sectionneur de terre combiné, un interrupteur à coupure en charge, un disjoncteur, et/ou n'importe quel type de commutateur isolé au gaz, un appareil haute tension, un appareil moyenne tension, un appareil basse tension, un appareil à courant continu, un isolateur isolé à l'air, un isolateur encapsulé dans du métal isolé au gaz, des capteurs, un condensateur, une bobine d'induction, une résistance, un limiteur de courant, un commutateur haute tension, un disjoncteur au gaz, un disjoncteur sous vide, un disjoncteur de générateur, un commutateur moyenne tension, une unité de réseau électrique bouclé, un disjoncteur à réenclenchement, un sectionnaliseur, un commutateur basse tension, un transformateur de distribution, un transformateur de puissance, un commutateur à prises de réglage, une traversée de transformateur, un dispositif semi-conducteur de puissance, un convertisseur de puissance, un poste convertisseur, un bâtiment convertisseur, un calculateur, et les composants et/ou les combinaisons de ces dispositifs.
  17. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que le boîtier comprend une chambre dans laquelle est contenu le composant électrique, et un système de recyclage comprenant au moins un élément parmi le tamis moléculaire (1) et le déshydratant (2), et en ce que le boîtier est équipé d'un compresseur et d'une pompe pour pomper le gaz d'isolation diélectrique à travers au moins un filtre comprenant l'au moins un élément parmi le tamis moléculaire (1) et le déshydratant (2).
  18. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que l'au moins un élément parmi le tamis moléculaire (1) et le déshydratant (2) est contenu dans une région de l'appareil ayant une température inférieure à la température moyenne présente dans l'appareil dans des conditions opérationnelles.
  19. Appareil destiné à la production, la distribution et/ou l'utilisation d'énergie électrique, en particulier selon l'une quelconque des revendications précédentes, ledit appareil comprenant un boîtier renfermant un espace isolant et un composant électrique disposé dans l'espace isolant, ledit espace isolant contenant un gaz d'isolation diélectrique comprenant un composé organofluoré A, caractérisé en ce que l'appareil comprend en outre au moins un élément parmi un tamis moléculaire (1) et un déshydratant (2) disposé de manière à venir en contact avec le gaz d'isolation, et en ce qu'au moins un élément parmi le tamis moléculaire (1) et le déshydratant (2) est sous forme de poudre, et en ce que l'au moins un élément parmi le tamis moléculaire (1) et le déshydratant (2) est une poudre sans liant.
  20. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que l'au moins un élément parmi le tamis moléculaire (1) et le déshydratant (2) est contenu dans un récipient perméable (4a, 4b', 4b", 4b"') et/ou est disposé sur un support, spécifiquement un récipient ou un support sous la forme d'un tube, d'un rouleau, d'un tissu, d'une lamelle ou d'un nid d'abeilles.
  21. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce que l'au moins un élément parmi le tamis moléculaire (1) et le déshydratant (2) est contenu dans au moins un récipient perméable (4a, 4b', 4b", 4b"') dont le couvercle est perméable au moins à l'eau, et de préférence dont le couvercle est une membrane semi-perméable qui est sélectivement perméable à l'eau.
  22. Appareil selon l'une quelconque des revendications précédentes, caractérisé en ce qu'au moins deux récipients perméables (4a, 4b', 4b", 4b"') sont disposés dans un cadre ou un support (6a, 6b) de manière espacée les uns des autres par des interstices (8a, 8b', 8b", 8b"').
  23. Procédé de fonctionnement d'un appareil destiné à la production, la distribution et/ou l'utilisation d'énergie électrique, en particulier selon l'une quelconque des revendications 1 à 8 précédentes, de la revendication 9 et des revendications 10 à 22 lorsqu'elles sont dépendantes de la revendication 9, caractérisé en ce que le procédé comprend une étape de chargement du tamis moléculaire (1) avec le composé organofluoré, comprenant l'étape ou les étapes consistant à :
    - exposer temporairement le tamis moléculaire (1) à un gaz dans lequel la pression partielle du composé organofluoré A est plus élevée que dans le gaz d'isolation diélectrique présent pendant le fonctionnement de l'appareil ; et/ou
    - refroidir le tamis moléculaire (1) jusqu'à une température inférieure à une température présente pendant le fonctionnement de l'appareil, et exposer le tamis moléculaire (1) refroidi à un gaz comprenant le composé organofluoré ; et/ou
    - mettre le tamis moléculaire (1) en contact avec un liquide comprenant le composé organofluoré,
    afin de charger le tamis moléculaire (1) avec le composé organofluoré A.
  24. Procédé selon la revendication 23, caractérisé en ce que pendant le fonctionnement de l'appareil, le composé organofluoré A chargeant le tamis moléculaire (1) est au moins partiellement déplacé par l'au moins un produit de décomposition s'adsorbant sur le tamis moléculaire (1) et/ou étant absorbé par le tamis moléculaire (1).
  25. Procédé selon l'une quelconque des revendications 23 et 24, caractérisé en ce que le tamis moléculaire (1) est contrôlé en température pour réguler une quantité du composé organofluoré A dans le gaz d'isolation diélectrique, et/ou pour libérer un espace dans le tamis moléculaire (1) pour adsorber et/ou absorber l'au moins un produit de décomposition.
EP13774142.7A 2012-10-05 2013-10-07 Appareil contenant un gaz diélectrique d'isolation comprenant un composé organofluoré Active EP2904617B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP13774142.7A EP2904617B1 (fr) 2012-10-05 2013-10-07 Appareil contenant un gaz diélectrique d'isolation comprenant un composé organofluoré

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EPPCT/EP2012/069733 2012-10-05
EP13774142.7A EP2904617B1 (fr) 2012-10-05 2013-10-07 Appareil contenant un gaz diélectrique d'isolation comprenant un composé organofluoré
PCT/EP2013/070834 WO2014053661A1 (fr) 2012-10-05 2013-10-07 Appareil contenant un gaz diélectrique d'isolation comprenant un composé organofluoré

Publications (2)

Publication Number Publication Date
EP2904617A1 EP2904617A1 (fr) 2015-08-12
EP2904617B1 true EP2904617B1 (fr) 2016-11-30

Family

ID=53500978

Family Applications (1)

Application Number Title Priority Date Filing Date
EP13774142.7A Active EP2904617B1 (fr) 2012-10-05 2013-10-07 Appareil contenant un gaz diélectrique d'isolation comprenant un composé organofluoré

Country Status (1)

Country Link
EP (1) EP2904617B1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2767732A1 (es) * 2018-12-18 2020-06-18 Ormazabal Corporate Tech A I E Sistema de aislamiento eléctrico de bajo impacto ambiental para aparamenta eléctrica de media y alta tensión
ES2781127A1 (es) * 2019-02-27 2020-08-28 Ormazabal Corporate Tech A I E Sistema de aislamiento eléctrico de bajo impacto ambiental para aparamenta eléctrica de media y alta tensión

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3546055B1 (fr) * 2018-03-28 2021-01-13 ABB Schweiz AG Procédé et système pour décomposer une fluorocétone en produits de décomposition jetables
EP3834914A1 (fr) * 2019-12-13 2021-06-16 General Electric Technology GmbH Utilisation d'un oxyde de métal de transition pour l'élimination de sous-produits fluorés à partir d'un gaz, dispositif et procédé de retrait de tels sous-produits
CN117941014A (zh) 2022-08-09 2024-04-26 日立能源有限公司 用于产生、传输和/或分配电能的电气设备

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4173690A (en) 1977-12-02 1979-11-06 Gould Inc. Method of producing electrical insulation foam
EP0885841A1 (fr) 1997-06-20 1998-12-23 Hitachi Engineering & Services Co., Ltd. Système et procédé epour rassembler et raffiner de SF6-gaz
EP1091182A2 (fr) 1999-10-01 2001-04-11 Kabushiki Kaisha Toshiba Dispositif pour la récupération de gaz
DE10356782A1 (de) 2003-12-02 2005-07-07 J. Rettenmaier & Söhne Gmbh + Co. Kg Verbessertes Verfahren zur Sprühtrocknung von Lösungen, Dispersionen, Emulsionen und Suspensionen
US20080135817A1 (en) 2006-12-12 2008-06-12 Honeywell International Inc. Gaseous dielectrics with low global warming potentials
JP2009285719A (ja) 2008-05-30 2009-12-10 Nippon Dennetsu Co Ltd フラックス塗布装置
WO2010142346A1 (fr) 2009-06-12 2010-12-16 Abb Technology Ag Milieu d'isolation diélectrique
FR2965120A1 (fr) 2010-09-22 2012-03-23 Areva T & D Sas Appareil de coupure d'un courant electrique de moyenne ou haute tension et son procede de fabrication
WO2012080222A1 (fr) 2010-12-14 2012-06-21 Abb Research Ltd Milieu d'isolation diélectrique
EP2676714A1 (fr) 2011-02-14 2013-12-25 Panasonic Corporation Corps de caisse d'isolation thermique

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4173690A (en) 1977-12-02 1979-11-06 Gould Inc. Method of producing electrical insulation foam
EP0885841A1 (fr) 1997-06-20 1998-12-23 Hitachi Engineering & Services Co., Ltd. Système et procédé epour rassembler et raffiner de SF6-gaz
EP1091182A2 (fr) 1999-10-01 2001-04-11 Kabushiki Kaisha Toshiba Dispositif pour la récupération de gaz
DE10356782A1 (de) 2003-12-02 2005-07-07 J. Rettenmaier & Söhne Gmbh + Co. Kg Verbessertes Verfahren zur Sprühtrocknung von Lösungen, Dispersionen, Emulsionen und Suspensionen
US20080135817A1 (en) 2006-12-12 2008-06-12 Honeywell International Inc. Gaseous dielectrics with low global warming potentials
JP2009285719A (ja) 2008-05-30 2009-12-10 Nippon Dennetsu Co Ltd フラックス塗布装置
WO2010142346A1 (fr) 2009-06-12 2010-12-16 Abb Technology Ag Milieu d'isolation diélectrique
FR2965120A1 (fr) 2010-09-22 2012-03-23 Areva T & D Sas Appareil de coupure d'un courant electrique de moyenne ou haute tension et son procede de fabrication
WO2012080222A1 (fr) 2010-12-14 2012-06-21 Abb Research Ltd Milieu d'isolation diélectrique
EP2676714A1 (fr) 2011-02-14 2013-12-25 Panasonic Corporation Corps de caisse d'isolation thermique

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
"F-200", BASF, 28 August 2017 (2017-08-28), XP055416240, Retrieved from the Internet <URL:https://www.standort-ludwigshafen.basf.de/group/corporate/site- ludwigshafen/de/brand/F_200>
"Hydrophilie", WIKIPEDIA, 18 December 2016 (2016-12-18), XP055416228, Retrieved from the Internet <URL:https://de.wikipedia.org/wiki/Hydrophilie>
"Montmorillonit", WIKIPEDIA, 27 August 2017 (2017-08-27), pages 5 von 6, XP055416265, Retrieved from the Internet <URL:https://de.wikipedia.org/wiki/Montmorillonit>
"Trocknungsmittel", MERCK, 28 August 2017 (2017-08-28), XP055295855, Retrieved from the Internet <URL:http://web.hs-merseburg.de/-ag- vt/ADS_Trocknungsmittel.pdf>

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2767732A1 (es) * 2018-12-18 2020-06-18 Ormazabal Corporate Tech A I E Sistema de aislamiento eléctrico de bajo impacto ambiental para aparamenta eléctrica de media y alta tensión
ES2781127A1 (es) * 2019-02-27 2020-08-28 Ormazabal Corporate Tech A I E Sistema de aislamiento eléctrico de bajo impacto ambiental para aparamenta eléctrica de media y alta tensión

Also Published As

Publication number Publication date
EP2904617A1 (fr) 2015-08-12

Similar Documents

Publication Publication Date Title
US9590397B2 (en) Apparatus containing a dielectric insulation gas comprising an organofluorine compound
US10522981B2 (en) Water and contamination absorber for C02 insulated electrical apparatus for the generation, transmission, distribution and/or usage of electrical energy
US20180005727A1 (en) Apparatus containing a dielectric insulation gas comprising an organofluorine compound
US20160043533A1 (en) Process For Providing A Contamination-Reducing Component To An Electrical Apparatus
EP2904617B1 (fr) Appareil contenant un gaz diélectrique d&#39;isolation comprenant un composé organofluoré
WO2014187940A1 (fr) Appareil électrique comprenant un composant de réduction de la contamination
EP3614401B1 (fr) Procédé de récupération d&#39;au moins une substance à partir d&#39;un milieu isolant d&#39;un appareil électrique pour la génération, la transmission, la distribution et/ou l&#39;utilisation d&#39;énergie électrique
JP2017503633A5 (fr)
EP3069421B1 (fr) Dispositif d&#39;absorption d&#39;eau et de contaminants pour appareil électrique isolé par co2 destiné à produire, transmettre, distribuer et/ou utiliser de l&#39;énergie électrique
CN109196600A (zh) 直链八氟丁烯在环境安全的介电绝缘或灭弧流体中作为介电化合物的用途
WO2018210938A1 (fr) Disjoncteur comprenant un matériau d&#39;ossature métallo-organique pour co-adsorption
CN113614854B (zh) 用于中压和高压电气开关设备的低环境影响的电气绝缘***
EP2989702A1 (fr) Procédé pour fournir un composant de réduction de contamination à un appareil électrique
JP7311803B2 (ja) 絶縁ガス用吸着剤、及びガス絶縁電力機器
EP4388562A1 (fr) Appareil électrique pour la génération, la transmission et/ou la distribution d&#39;énergie électrique
WO2015086067A1 (fr) Rupteur sous vide

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20150427

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAX Request for extension of the european patent (deleted)
GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20160603

RIC1 Information provided on ipc code assigned before grant

Ipc: H01B 3/56 20060101AFI20160524BHEP

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: ABB SCHWEIZ AG

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 850484

Country of ref document: AT

Kind code of ref document: T

Effective date: 20161215

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602013014814

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20161130

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 850484

Country of ref document: AT

Kind code of ref document: T

Effective date: 20161130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170301

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170228

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170330

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602013014814

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170228

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

26 Opposition filed

Opponent name: SIEMENS AKTIENGESELLSCHAFT

Effective date: 20170830

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 5

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

RIN2 Information on inventor provided after grant (corrected)

Inventor name: RANJAN, NITESH

Inventor name: GALINDO-LOZANO, FRANCIA

Inventor name: PAUL, THOMAS ALFRED

Inventor name: MAHDIZADEH, NAVID

Inventor name: MANTILLA, JAVIER

Inventor name: BUERGLER, MATHIAS-DOMINIC

Inventor name: STOLLER, PATRICK

Inventor name: GROB, STEPHAN

Inventor name: KRAMER, AXEL

Inventor name: COSSALTER, OLIVER

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20171007

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20171007

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20171031

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20171007

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20171031

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20171007

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 6

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20171007

PLCK Communication despatched that opposition was rejected

Free format text: ORIGINAL CODE: EPIDOSNREJ1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

RIN2 Information on inventor provided after grant (corrected)

Inventor name: KRAMER, AXEL

Inventor name: COSSALTER, OLIVER

Inventor name: RANJAN, NITESH

Inventor name: GROB, STEPHAN

Inventor name: MANTILLA, JAVIER

Inventor name: PAUL, THOMAS ALFRED

Inventor name: STOLLER, PATRICK

Inventor name: MAHDIZADEH, NAVID

Inventor name: GALINDO-LOZANO, FRANCIA

Inventor name: BUERGLER, MATHIAS-DOMINIC

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO

APBM Appeal reference recorded

Free format text: ORIGINAL CODE: EPIDOSNREFNO

APBP Date of receipt of notice of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA2O

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20131007

APBQ Date of receipt of statement of grounds of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA3O

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170330

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20161130

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602013014814

Country of ref document: DE

Owner name: HITACHI ENERGY SWITZERLAND AG, CH

Free format text: FORMER OWNER: ABB SCHWEIZ AG, BADEN, CH

Ref country code: DE

Ref legal event code: R082

Ref document number: 602013014814

Country of ref document: DE

Representative=s name: DENNEMEYER & ASSOCIATES S.A., DE

Ref country code: DE

Ref legal event code: R081

Ref document number: 602013014814

Country of ref document: DE

Owner name: ABB POWER GRIDS SWITZERLAND AG, CH

Free format text: FORMER OWNER: ABB SCHWEIZ AG, BADEN, CH

Ref country code: DE

Ref legal event code: R081

Ref document number: 602013014814

Country of ref document: DE

Owner name: HITACHI ENERGY LTD, CH

Free format text: FORMER OWNER: ABB SCHWEIZ AG, BADEN, CH

RAP2 Party data changed (patent owner data changed or rights of a patent transferred)

Owner name: ABB POWER GRIDS SWITZERLAND AG

RAP4 Party data changed (patent owner data changed or rights of a patent transferred)

Owner name: HITACHI ENERGY SWITZERLAND AG

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602013014814

Country of ref document: DE

Owner name: HITACHI ENERGY SWITZERLAND AG, CH

Free format text: FORMER OWNER: ABB POWER GRIDS SWITZERLAND AG, BADEN, CH

Ref country code: DE

Ref legal event code: R081

Ref document number: 602013014814

Country of ref document: DE

Owner name: HITACHI ENERGY LTD, CH

Free format text: FORMER OWNER: ABB POWER GRIDS SWITZERLAND AG, BADEN, CH

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230527

REG Reference to a national code

Ref country code: DE

Ref legal event code: R100

Ref document number: 602013014814

Country of ref document: DE

APBU Appeal procedure closed

Free format text: ORIGINAL CODE: EPIDOSNNOA9O

PLBN Opposition rejected

Free format text: ORIGINAL CODE: 0009273

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: OPPOSITION REJECTED

27O Opposition rejected

Effective date: 20230802

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20231025

Year of fee payment: 11

Ref country code: DE

Payment date: 20231020

Year of fee payment: 11

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602013014814

Country of ref document: DE

Representative=s name: DENNEMEYER & ASSOCIATES S.A., DE

Ref country code: DE

Ref legal event code: R081

Ref document number: 602013014814

Country of ref document: DE

Owner name: HITACHI ENERGY LTD, CH

Free format text: FORMER OWNER: HITACHI ENERGY SWITZERLAND AG, BADEN, CH