Classifications

• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
  • C03C17/42—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating of an organic material and at least one non-metal coating
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
  • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B23/00—Re-forming shaped glass
  • C03B23/02—Re-forming glass sheets
  • C03B23/023—Re-forming glass sheets by bending
  • C03B23/03—Re-forming glass sheets by bending by press-bending between shaping moulds
  • C03B23/0307—Press-bending involving applying local or additional heating, cooling or insulating means
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B27/00—Tempering or quenching glass products
  • C03B27/012—Tempering or quenching glass products by heat treatment, e.g. for crystallisation; Heat treatment of glass products before tempering by cooling
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
  • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
  • C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
  • C03C17/3626—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer one layer at least containing a nitride, oxynitride, boronitride or carbonitride
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
  • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
  • C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
  • C03C17/3644—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the metal being silver
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
  • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
  • C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
  • C03C17/3657—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the multilayer coating having optical properties
  • C03C17/366—Low-emissivity or solar control coatings
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
  • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
  • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
  • C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
  • C03C17/3681—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the multilayer coating being used in glazing, e.g. windows or windscreens
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2218/00—Methods for coating glass
  • C03C2218/10—Deposition methods
  • C03C2218/11—Deposition methods from solutions or suspensions
  • C03C2218/116—Deposition methods from solutions or suspensions by spin-coating, centrifugation
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2218/00—Methods for coating glass
  • C03C2218/10—Deposition methods
  • C03C2218/15—Deposition methods from the vapour phase
  • C03C2218/154—Deposition methods from the vapour phase by sputtering
  • C03C2218/156—Deposition methods from the vapour phase by sputtering by magnetron sputtering
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2218/00—Methods for coating glass
  • C03C2218/30—Aspects of methods for coating glass not covered above
  • C03C2218/32—After-treatment
  • C03C2218/328—Partly or completely removing a coating
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2218/00—Methods for coating glass
  • C03C2218/30—Aspects of methods for coating glass not covered above
  • C03C2218/34—Masking
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2218/00—Methods for coating glass
  • C03C2218/30—Aspects of methods for coating glass not covered above
  • C03C2218/355—Temporary coating

Definitions

• the invention relates to glazing on which a physical vapor deposition process (PVD for Physical Vapor Deposition) has been deposited under vacuum, mainly cathode sputtering assisted by magnetron, chemical vapor deposition assisted by plasma (PECVD for Plasma Enhanced Chemical Vapor Deposition) or evaporation or a liquid deposition process, of one or more thin layers having a spatial structure on scales that can vary from several cm to less than 10pm.
• PVD Physical Vapor Deposition
• PECVD Plasma Enhanced Chemical Vapor Deposition
• evaporation or a liquid deposition process of one or more thin layers having a spatial structure on scales that can vary from several cm to less than 10pm.
• the products targeted are varied: silver layers (solar control, low-emissivity, electromagnetic shielding, heating), layers modifying the level of reflection in the visible (anti-reflection or mirror layers), transparent or non-transparent electrode layers, layers electrochromic, electroluminescent, anti-iridescence, anti-fouling, anti-scratch, magnetic, colored or absorbent layers to modify the transmittance in the visible for aesthetic purposes.
• the products concerned are in particular the stacks deposited by magnetron sputtering.
• glazing covered with a conductive layer ensuring an electrode role - for example for a heating function (eglass for building applications, windshield or lateral heating (e) for automotive or aeronautical applications) or can be used as an antenna to receive electromagnetic waves.
• a heating function eglass for building applications, windshield or lateral heating (e) for automotive or aeronautical applications
• e glass for building applications, windshield or lateral heating (e) for automotive or aeronautical applications
• a particular case concerns the microwave band around the GHz (100pm ⁇ l ⁇ 1 m) which finds applications for radio transmissions (GSM, Satellite, Radar ).
• GSM Global System for Satellite, Radar
• the possibility of structuring the layer on a scale lower than that of the wavelength gives access to the range of metamaterials where the electromagnetic transmission can be modulated.
• the highly conductive layer and without earthing causes significant attenuation of the high frequency electromagnetic waves and it is difficult to ensure the compromise between thermal control (above the reduction of temperature rise in a vehicle) and good reception of communication signals.
• the conventional attenuation on a windshield of a thermal control layer can be for example from -30 to -45dB approximately between 0.4 and 5 GHz.
• the thermal control function can be provided not by a thin conductive layer but not a polyvinyl butyral (PVB) interlayer or other containing nanoparticles of a conductive compound such as oxide indium doped with tin (ITO for indium tin oxide) for example.
• ITO oxide indium doped with tin
• the thermal control is ensured by absorption and no longer reflection of the energy part of the spectrum.
• This solution is only possible for solar control, and not very effective compared to the reflection solution and requires laminated glazing.
• the second solution consists in etching the silver layer after deposition so as to selectively remove the silver on strips which are sufficiently thin (100 ⁇ m) to be difficult to perceive by the eye and spaced apart from each other by a few mm depending on the wavelengths which we wish to favor the transmission.
• Complex patterns can be used for this full face application. Representatives of this technique are in particular documents W09954961 A1 and WO2014033007 A1.
• the heating efficiency of a conductive layer depends on its surface or surface resistance R sq or R n , on the voltage between the electrodes but also on the distance between the electrodes. For building applications, this dependence poses a problem because, with the same electrical source, an electrical resistance of the glazing is required for each size of the heating zone.
• One solution may consist in etching once more for example a base layer Ag so as to modulate its overall surface resistance to allow it to be compatible with the distance between electrodes and the desired surface heating power.
• a silver-based glazing can be functionalized in the form of an antenna provided that the electromagnetic decoupling of the layer with the frame of the car is ensured, for example. This is also done by engraving.
• the alternative selective etching methods mainly come from the microelectronics industry. Some use temporary layers, others consist of direct etching.
• photolithography uses temporary layers to serve as a mask for selective acid attacks.
• Photo lithography allows very fine engravings (45-90 nm today industrially) but remains limited to the size of the masks today limited by the size of the optics.
• the laser etching of the conductive layer is provided by a point etching laser which will sublimate the thin layer stack by scanning the beam. This operation has low productivity on large glazing units and requires significant investment with regard to the surfaces treated.
• the impact etching of ions or electrons has the same limitations as laser etching in terms of productivity.
• inkjet printing techniques are still limited for sizes greater than 10 m 2 at printing times greater than one minute.
• Screen printing may be preferred to other techniques when a resolution scale smaller than 50 ⁇ m is sought: this process in fact provides relatively poor edge qualities at these small scales.
• the object of the invention is therefore to provide functional glazing units which allow radio frequencies to pass.
• functional glazing here means antenna glazing, heating, with thermal control, or the like, glazing with or without electrically conductive layer (s), as well as all the other glazings mentioned above.
• Radiofrequencies are high frequency electromagnetic waves, around the GHz, and find applications in radio transmissions (GSM, satellite, radar ...), communication (for example 2G / 3G / 4G).
• the invention relates to a method of depositing on a glass substrate a layer or a stack of layers essentially mineral (s) functional (s), characterized in that it comprises the steps consisting in
• the crosslinking of the resin by laser makes it possible to harden it along an extremely fine line, with a width of the order of a few tens of microns or even less, generally between 5 and 100 ⁇ m.
• a width of the order of a few tens of microns or even less generally between 5 and 100 ⁇ m.
• heat treatment is not necessary, the line of organic resin and the layer or the magnetron stack which covers it can be eliminated only by wiping techniques, blowing gaseous, washing, etc.
• a heat treatment can also be carried out in this case, in particular with a view to giving the glass substrate improved mechanical properties.
• the technique according to the invention provides excellent quality of the substrate and especially of the edges of areas not coated with the organic coating and covered with the mineral layer (s) (sharpness, resolution).
• the method makes it possible to produce an essentially organic coating pattern on an industrial production line, on a large surface substrate.
• the reduced cycle time makes it possible to validate the industrially applicable character.
• the liquid precursor composition of a photosensitive resin is deposited using a Mayer bar, a film puller, a spinner, by immersion or the like;
• the liquid precursor composition of a photosensitive resin is of the type which can be used for photolithography, in particular in the field of microelectronics, and comprises an epoxy resin in a solvent such as cyclopentanone, a monomer and / or oligomer acrylate, epoxyacrylate, polyester acrylate , polyurethane acrylate, polyvinylpyrrolidone + EDTA composition, polyamide, polyvinylbutyral, positive photosensitive resin of diazonaphthoquinone-novolak type, any organic material crosslinkable under ultraviolet, infrared or visible radiation, alone or as a mixture of several of them;
• a solvent such as cyclopentanone, a monomer and / or oligomer acrylate, epoxyacrylate, polyester acrylate , polyurethane acrylate, polyvinylpyrrolidone + EDTA composition, polyamide, polyvinylbutyral, positive photosensitive resin of diazonaphthoquinon
• the liquid precursor composition of a photosensitive resin is deposited on the substrate in a thickness of between 1 and 40 ⁇ m; in the context of the invention, this can be considered to be approximately equivalent to the thickness of the solid resin after crosslinking; this thickness must be sufficient to guarantee the elimination of the magnetron layer or stack in accordance with sharp edges, sufficiently resolved;
• the pattern of crosslinked solid resin comprises lines of widths between 5 and 20 ⁇ m; below 5 pm, the loss of the electromagnetic wave signal is too great to achieve the aim of the invention; above 20 pm, especially from 30, the ablation line of the magnetron layer or stack begins to be visible, even with difficulty, depending on the light conditions, contrast;
• the coated substrate is immersed in a good solvent for the noncrosslinked liquid composition, then it is extracted therefrom, then good solvent is gently sprayed onto the substrate, then the surface of the substrate is washed by gently spraying a solvent such as isopropanol to remove the correct solvent and in the vicinity of the crosslinked solid resin pattern, then the substrate and the crosslinked solid resin pattern are dried with a flow of gas such as nitrogen or air;
• the layer or stack of layers essentially functional mineral (s) is formed by a physical vapor deposition (PVD for Physical Vapor Deposition) process under vacuum such as cathode sputtering, in particular assisted by magnetron, evaporation or chemical vapor deposition assisted by plasma (PECVD for Plasma Enhanced Chemical Vapor Deposition) or by liquid;
• PVD physical vapor deposition
• PECVD Plasma Enhanced Chemical Vapor Deposition
• the layer or stack of layers essentially functional mineral (s) consists of Ag, transparent conductive oxide (TCO) such as indium oxide doped with tin (ITO), oxide indium zinc doped (IZO), ZnO: AI, Ga, cadmium stannate, Al, Nb, Cu, Au, compound of Si and N such as Si 3 N 4 , dielectric stack afferent, alone or in combination of several of them ;
• TCO transparent conductive oxide
• ITO indium oxide doped with tin
• IZO oxide indium zinc do
• the thickness of the layer or the stack of essentially functional mineral (s) layers is at least ten times less than that of the crosslinked solid resin pattern, and is in particular at most equal to 300, preferably 200 and especially 150 nm; this eliminates the fraction covering the solid resin crosslinked along sharp edges, as already mentioned above.
• the glass can no longer be cut once tempered, it can be, in certain applications, for example building, stored then cut, demarcated, etc. before tempering.
• This glazing can be sold as such, mainly in this case with the pattern of crosslinked solid resin and the magnetron layer or stack, then removed by quenching in a transformer, in accordance with the process of the invention.
• the heat treatment is part of a thermal quenching of the glass substrate.
• the resin disappears by combustion and effectively eliminates the layer or stack of layers essentially mineral (s) functional (s), possibly conductive (s) at the locations of the resin patterns, which causes selective etching wanted.
• the heat treatment forms part of a bending of the glass substrate, in particular of a bending by pressing.
• a preliminary heat treatment causes the combustion of the resin, then any pulverulent residue of combustion of the resin as well as the fraction of the magnetron layer or stack covering the crosslinked resin pattern is eliminated by any suitable means. , before the pressing tools come into contact with the glass substrate.
• at least one essentially organic photosensitive resin sequence is deposited again - layer or stack of essentially functional mineral layer (s) (s).
• This deposition is preferably carried out before the heat treatment for the combustion of the essentially organic resin closest to the substrate, and a subsequent heat treatment will produce the combustion of several superimposed essentially organic resins as well as the subsequent elimination of several layers or stacks of essentially functional mineral layers covering them.
• essentially organic resin sequences - layer or stack of essentially mineral (s) functional layer (s) from the second sequence, after the heat treatment of combustion of the first essentially organic resin and wiping or elimination by gas blast of its organic residues and of the mineral residues covering them, also forms part of the invention.
• the glass substrate obtained by the process of the invention is also capable of being integrated into a laminated glazing or other laminated composite product, and / or into a multiple glazing.
• s essentially mineral
• s essentially mineral
• a uniform thickness of a composition is applied by spin-coating (spinner) liquid precursor of an organic photosensitive resin, sold by the company MicroChem Corp under the registered trademark MicroChem® SU-8 2015.
• This liquid composition contains in mass percentages:
• the substrate, the crosslinked solid resin pattern and the noncrosslinked liquid resin are placed for one minute in a bath of good solvent for the noncrosslinked resin. It is, as a percentage by mass,
• the substrate, the crosslinked solid resin pattern and the noncrosslinked liquid resin are then removed from the bath, then good solvent is gently sprayed using a pipette to complete the washing (removal) of the noncrosslinked liquid resin.
• the correct solvent is washed from the surface of the substrate and from the solid resin pattern crosslinked with isopropanol using a pipette.
• the substrate + the crosslinked solid resin pattern are dried with a flow of nitrogen.
• the lines of the crosslinked solid resin pattern are 30 +/- 2 ⁇ m wide, and 20 +/- 5 ⁇ m high.
• the crosslinked resin pattern is a 3 mm square mesh network (distance between the midpoints of two consecutive parallel lines).
• a stack of thin layers is deposited in a conforming manner by magnetron-assisted cathode sputtering on the glass + pattern of crosslinked solid resin.
• This stack of thin layers has the following constitution, in which the thicknesses are in nm: S1 3 N 4 20 / SnZnO 6 / ZnO 7 / NiCr 0.5 / Ag 9 / NiCr 0.5 / ZnO 5 / Si 3 N 4 40 / SnZnO 30 / ZnO 5 / NiCr 0.5 / Ag 14 / NiCr 0.5 / ZnO 5 / S13N4 28.
• the layers of ZnO are non-porous. This stack with thermal control function is hardenable.
• the glass substrate, the crosslinked solid resin pattern and the stack of mineral layers are tempered in a thermal annealing oven sold under the registered trademark Nabertherm® (model N41 / H), at 650 ° C for 10 minutes, in order to give the substrate and its stack of mineral layers their final mechanical properties. Tempering also partially removes the crosslinked solid resin pattern, thereby peeling off the mineral layers that cover it. Mechanical action should be taken to completely remove resin residue; for this purpose, this mechanical action is sufficient in the absence of the heat treatment because the lines of the pattern of crosslinked solid resin have a width less than 40 ⁇ m.
• the final product has the stack of thin layers described above, structured in a pattern corresponding to the negative of that produced with the resin.
• the transmission attenuation of the glazing of the invention comprising the magnetron stack except in a grid pattern of 3 mm X 3 mm, line width of 30 pm, is -9, respectively -19, respectively -25 dB.
• the transmission attenuation of the glazing of the invention is -9, respectively -19, respectively -25 dB.
• the transmission attenuation of the glazing of the invention is -9, respectively -19, respectively -25 dB.
• it is - 25, respectively -40, respectively -54 dB.
• the invention provides functional glazing with reduced attenuation of the transmission of waves of frequencies between 0.4 and 5 GHz.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Geochemistry & Mineralogy (AREA)
• Physics & Mathematics (AREA)
• Thermal Sciences (AREA)
• Laminated Bodies (AREA)
• Surface Treatment Of Glass (AREA)

Applications Claiming Priority (1)

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• 2018
  • 2018-11-14 CN CN201880099520.9A patent/CN112969671A/zh active Pending
  • 2018-11-14 CA CA3118348A patent/CA3118348A1/fr active Pending
  • 2018-11-14 JP JP2021523732A patent/JP7234358B2/ja active Active
  • 2018-11-14 WO PCT/FR2018/052836 patent/WO2020099729A1/fr unknown
  • 2018-11-14 BR BR112021008628-5A patent/BR112021008628A2/pt unknown
  • 2018-11-14 EP EP18821709.5A patent/EP3880621A1/de not_active Withdrawn
  • 2018-11-14 US US17/291,179 patent/US20220073424A1/en not_active Abandoned

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