WO2014193549A1 - A KINETICALLY APPLIED GRADATED Zr-Al-C CERAMIC OR Ti-Al-C CERAMIC OR AMORPHOUS OR SEMI-AMORPHOUS STAINLESS STEEL WITH NUCLEAR GRADE ZIRCONIUM ALLOY METAL STRUCTURE - Google Patents

A KINETICALLY APPLIED GRADATED Zr-Al-C CERAMIC OR Ti-Al-C CERAMIC OR AMORPHOUS OR SEMI-AMORPHOUS STAINLESS STEEL WITH NUCLEAR GRADE ZIRCONIUM ALLOY METAL STRUCTURE Download PDF

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Publication number
WO2014193549A1
WO2014193549A1 PCT/US2014/033932 US2014033932W WO2014193549A1 WO 2014193549 A1 WO2014193549 A1 WO 2014193549A1 US 2014033932 W US2014033932 W US 2014033932W WO 2014193549 A1 WO2014193549 A1 WO 2014193549A1
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WIPO (PCT)
Prior art keywords
coating
coating composition
component
ceramic
cladding
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.)
Ceased
Application number
PCT/US2014/033932
Other languages
French (fr)
Inventor
Edward J. Lahoda
Jason P. Mazzoccoli
Peng Xu
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.)
Westinghouse Electric Co LLC
Westinghouse Electric Corp
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Westinghouse Electric Co LLC
Westinghouse Electric Corp
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.)
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Publication date
Application filed by Westinghouse Electric Co LLC, Westinghouse Electric Corp filed Critical Westinghouse Electric Co LLC
Priority to KR1020157036640A priority Critical patent/KR20160016900A/en
Priority to EP14804608.9A priority patent/EP3004420B1/en
Priority to CN201480025399.7A priority patent/CN105189820B/en
Priority to ES14804608T priority patent/ES2741832T3/en
Priority to JP2016516650A priority patent/JP6385015B2/en
Publication of WO2014193549A1 publication Critical patent/WO2014193549A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/10Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
    • C23C4/11Oxides
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    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/48Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zirconium or hafnium oxides, zirconates, zircon or hafnates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/62222Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products obtaining ceramic coatings
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C24/00Coating starting from inorganic powder
    • C23C24/02Coating starting from inorganic powder by application of pressure only
    • C23C24/04Impact or kinetic deposition of particles
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
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    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • C23C28/042Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material including a refractory ceramic layer, e.g. refractory metal oxides, ZrO2, rare earth oxides
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    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • C23C28/048Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material with layers graded in composition or physical properties
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/32Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer
    • C23C28/321Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer with at least one metal alloy layer
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/32Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer
    • C23C28/322Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer only coatings of metal elements only
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/32Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer
    • C23C28/324Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer with at least one metal matrix material layer comprising a mixture of at least two metals or metal phases or a metal-matrix material with hard embedded particles, e.g. WC-Me
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/34Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
    • C23C28/341Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one carbide layer
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/34Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
    • C23C28/345Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/34Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
    • C23C28/345Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer
    • C23C28/3455Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer with a refractory ceramic layer, e.g. refractory metal oxide, ZrO2, rare earth oxides or a thermal barrier system comprising at least one refractory oxide layer
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/36Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including layers graded in composition or physical properties
    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21CNUCLEAR REACTORS
    • G21C3/00Reactor fuel elements and their assemblies; Selection of substances for use as reactor fuel elements
    • G21C3/02Fuel elements
    • G21C3/04Constructional details
    • G21C3/06Casings; Jackets
    • G21C3/07Casings; Jackets characterised by their material, e.g. alloys
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin
    • Y02E30/30Nuclear fission reactors
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T50/00Aeronautics or air transport
    • Y02T50/60Efficient propulsion technologies, e.g. for aircraft

Definitions

  • This invention relates to coating compositions and methods of coating zirconium alloy nuclear fuel cladding to reduce oxidation corrosion of the cladding which is exposed to light water nuclear reactor under normal or accident conditions.
  • FIG. 1 shows a coated zirconium alloy cladding 10 in accordance with the prior art.
  • the zirconium alloy cladding 10 has an oxidation layer 12 resulting from the immediate oxidation of the substrate 10, and a further oxidation portion 14 added as the zirconium is exposed to air, water or other oxidizing media.
  • a coating layer 16 is applied to the oxidation portion 14.
  • the zirconium alloy cladding 10 is simply coated with the coating layer 16. Since the coating layer 16 is merely deposited on top of the oxidation layer 14, this process often results in the coating, peeling or spalling of the coating layer 16 when exposed to reactor conditions.
  • thermal and radiation induced stresses are typically introduced in any coating during operation that can cause the coating layer 16 to peel off the zirconium alloy cladding 10.
  • the zirconium alloy material of which the cladding is constructed is composed of zirconium (Zr) with up to about 2 wt. % of other metals, such as niobium (Nb), tin (Sn), iron (Fe), chromium (Cr) and mixtures thereof.
  • Zr zirconium
  • Such zirconium alloy cladding tubes are taught, for example, by Biancheria et al., Kapil, and Lahoda (see U.S. Patent Nos. 3,427,222; 5,075,075; and 7,139,360 respectively).
  • These fuel rods/cladding have an end cap at each end and a hold device such as a metal spring to keep the enclosed stack of nuclear fuel pellets in place.
  • Mazzoccoli et al. discloses a method of coating zirconium alloy cladding tubes with an adherent mass of oxidation resistant material, using high velocity thermal application for a Zr-Al-C ceramic or Ti-Al-C ceramic or an iron based alloy, Nanosteel or Zr-Al alloy.
  • a Zr-Al-C ceramic or Ti-Al-C ceramic or an iron based alloy, Nanosteel or Zr-Al alloy There are disadvantages associated with this method, such as the inability of the coating to adhere to the base Zr alloy during thermal cycles.
  • the above needs are met and objects accomplished by a method of depositing a coating composition onto an exterior surface of a zirconium alloy cladding of a light water nuclear reactor to form a coating which at least partially adheres to said exterior surface.
  • the method includes providing the zirconium alloy cladding which inherently has a zirconium oxide-containing layer at least partially formed on the exterior surface with an adherent coating of a graded composition.
  • the graded coating composition includes a first component and a second component.
  • the first component is selected from the group consisting of zirconium, zirconium oxide and mixtures thereof.
  • the second component is selected from the group consisting of Zr 2 AlC ceramic, Ti 2 AlC ceramic, Ti 3 AlC 2 ceramic, ⁇ 1 2 0 3, aluminum, zirconium silicide, amorphous and semi- amorphous alloyed stainless steel, and mixtures of Zr 2 AlC ceramic, Ti 2 AlC ceramic and Ti 3 AlC 2 ceramic.
  • the method further includes kinetically depositing the coating composition onto the exterior surface of the cladding to form the coating.
  • the coating has a gradient emanating from the surface of the cladding toward an exposed outer surface of the coating such that percent by weight of the first component decreases from the exterior surface of the cladding toward the exposed outer surface of the coating and percent by weight of the second component increases from the exterior surface of the cladding to the exposed outer surface of the coating, based on total weight of the coating composition.
  • the kinetic deposition of the coating composition can be conducted by employing a technique wherein a propellant is heated.
  • the kinetic deposition technique may be effective to at least partially penetrate the zirconium oxide-containing layer formed on the exterior surface of the cladding.
  • the coating may be applied by one or more passes of the kinetic deposition technique.
  • a first pass may include depositing the coating composition to form a first layer which includes from about 75% to about 100% by weight of the first component and from about 0% to about 25% by weight of the second component based on total weight of the coating composition.
  • a final pass may include depositing the coating composition to form the exposed outer surface which comprises from about 75% to about 100% by weight of the second component and from about 0% to about 25% by weight of the first component based on total weight of the coating composition.
  • a portion of the coating composition kinetically deposited adjacent to or near the exterior surface of the cladding mixes with the zirconium oxide-containing layer to form an integrated layer.
  • the zirconium alloy cladding is positioned in a light water nuclear reactor selected from the group consisting of a pressurized water reactor and a boiling water reactor.
  • the invention provides a coating composition for kinetic deposition on an exterior surface of a zirconium alloy cladding of a light water nuclear reactor to form a coating which at least partially adheres to said exterior surface.
  • the zirconium alloy cladding inherently has a zirconium oxide-containing layer at least partially formed on said exterior surface.
  • the coating composition includes a first component and a second component.
  • the first component is selected from the group consisting of zirconium, zirconium oxide, and mixtures thereof.
  • the second component is selected from the group consisting of Zr 2 AlC ceramic, Ti 2 AlC ceramic, Ti 3 AlC 2 ceramic, A1 2 0 3 , aluminum, zirconium silicide, amorphous or semi-amorphous alloyed stainless steel, and mixtures of Zr 2 AlC ceramic, Ti 2 AlC ceramic and Ti 3 AlC 2 ceramic.
  • the coating formed by the coating composition has a gradient emanating from the exterior surface of the cladding, which serves as the coating substrate, towards an exposed outer surface of the coating such that percent by weight of the first component decreases from the exterior surface of the cladding toward the exposed outer surface of the coating and percent by weight of the second component increases from the exterior surface of the cladding to the exposed outer surface of the coating, based on total weight percent of the coating composition.
  • FIG. 1 is a cross-section view of a coated zirconium alloy substrate in accordance with the prior art
  • FIG. 2 is a cross-section view of a coated zirconium alloy substrate in accordance with certain embodiments of the invention.
  • FIG. 3 is a block diagram of a method of applying a coating material employing a kinetic deposition technique in accordance with certain embodiments of the invention.
  • the invention provides a coating composition which includes a zirconium compound and a compound which protects the cladding surface from bulk oxidation.
  • the coating composition is deposited on an exterior surface of a zirconium alloy cladding, e.g., tube.
  • the deposition can be performed using various conventional techniques, such as a kinetic deposition technique (referred to as "cold spray").
  • the zirconium alloy cladding tube typically has a zirconium-oxide layer inherently formed on at least a portion of its exterior surface. Deposition of the coating composition results in a coating being formed on at least a portion of the exterior surface of the zirconium alloy cladding tube.
  • the zirconium alloy cladding is positioned in the core of a light water nuclear reactor, such as a pressurized water reactor (PWR) or a boiling water reactor (BWR).
  • a light water nuclear reactor such as a pressurized water reactor (PWR) or a boiling water reactor (BWR).
  • PWR pressurized water reactor
  • BWR boiling water reactor
  • the coating composition of the invention includes a first component and a second component.
  • the first component includes zirconium, zirconium oxide or mixtures thereof.
  • the second component includes Zr 2 AlC ceramic, Ti 2 AlC ceramic, Ti 3 AlC 2 ceramic, A1 2 0 3 , aluminum, zirconium silicide (ZrSi 2 ), amorphous or semi- amorphous alloyed stainless steel, or mixtures of Zr 2 AlC, Ti 2 AlC and Ti 3 AlC 2 .
  • ZrSi 2 zirconium silicide
  • Deposition of the coating composition of the invention results in a gradient coating or matrix that emanates from the exterior surface of the zirconium alloy cladding to an outer exposed surface of the coating.
  • This gradient coating is effective to eliminate bulk oxidation of the zirconium alloy cladding upon exposure to PWR or BWR conditions, e.g., coolant that circulates in the reactor core.
  • the gradient of the coating is such that the amount or weight percent (based on total weight of the coating composition) of each of the first and second components increases or decreases as the coating thickness emanates from the surface of the coating which is adjacent to or near the zirconium alloy cladding surface toward the exposed outer surface of the coating.
  • the amount of the first component decreases as the coating thickness emanates from the surface adjacent to or near the zirconium alloy cladding surface toward the exposed outer coating surface
  • the amount of the second component increases as the coating thickness emanates from the surface adjacent to or near the zirconium alloy cladding surface toward the exposed outer coating surface.
  • the decrease in the amount of the first component may correspond to the increase in the amount of the second component. For example, when the weight percent of the first component decreases from about 75% by weight at the surface of the coating adjacent to or near the cladding surface to about 10% by weight at the exposed outer surface, the weight percent of the second component
  • the weight percent of each of the first and second components may decrease and increase, respectively, such that the first component is present on the exposed outer surface of the coating in an amount of about 0%) by weight and the second component is present on the exposed outer surface of the coating in an amount of about 100% by weight.
  • the coating composition may be deposited onto the exterior surface of the zirconium alloy cladding to form the gradient coating by employing various coating techniques known in the art.
  • the coating composition is deposited using a conventional kinetic deposition technique which generally includes directing particulate material by a gas stream toward a substrate.
  • the coating composition is propelled by a propulsive gas stream toward the zirconium alloy cladding.
  • the first and second components of the coating composition may each be propelled separately or they may be propelled together, e.g., in a blend or mixture.
  • the coating composition may be propelled at room temperature or may be pre-heated to an elevated temperature, e.g., at or above the melting temperature of the first and second components.
  • this method of kinetic deposition is capable of at least partially disrupting the zirconium-oxide layer which is inherently formed on the zirconium alloy cladding such that the resulting coating is firmly bonded, e.g., atom-to-atom, to the cladding surface.
  • the gradient coating may be formed in several passes or in a single pass.
  • the first pass includes an excess amount of the first component. That is, the first component is present in greater than about 50% by weight based on total weight of the coating composition. In other embodiments, the first component in the first pass may be present in about 75% by weight or greater based on total weight of the coating composition. The remainder of the coating composition being composed of the second component.
  • the first pass includes about 100% by weight of the first component and about 0% by weight of the second component based on total weight of the coating composition. In each subsequent pass, the amount of the first component decreases and the amount of the second component increases. In certain embodiments, the amount by which the first component decreases is equal to the amount by which the second component increases.
  • a single pass technique is employed.
  • the amount (e.g., percent by weight) of each of the first and second components in the coating composition is continually varied to produce the gradient coating.
  • the kinetic deposition methodology of the invention produces an integrated gradient coating that is richer in the first component, e.g., the zirconium or zirconium oxide, in the portion of the coating that is closer to the substrate, e.g., zirconium alloy cladding, and richer in the second component, e.g., the oxidation resistant material, in the portion of the coating that is nearer the exposed surface of the coating.
  • the first component is present in excess (e.g., as compared to the second component) near the zirconium alloy cladding surface and the presence of the first component decreases throughout the coating thickness such that the exposed surface of the coating has an excess of the second component.
  • the gradient coating onto and into the surface, as the coating composition is chemically similar to the zirconium alloy cladding composition and, gradually changes the thermal expansion and radiation swelling characteristics to minimize thermal and radiation stresses during operation.
  • the gradient coating of the invention is created by kinetically depositing a first layer of the coating composition which includes from about 50% to about 100% or from greater than about 50% to about 100% or from about 75% to about 95% by weight of the first component, and from about 0% to about 50% or from about 0% to less than about 50% or from about 5% to about 25% by weight of the second component, based on total weight of the coating composition.
  • the first component is zirconium alloy.
  • additional layers of the coating composition may be deposited on the first layer. In certain embodiments, in each of the additional layers, the amount of the first component will successively decrease and the amount of the second component will successively increase.
  • the exposed outer surface of the coating is composed of an excess of the second component such that it retains the oxidation resistant behavior of the second component while a base is present (e.g., underlying layers) that is rich in zirconium, i.e., the first component.
  • the method of the invention is generally directed to depositing an oxidation resistant material into a zirconium oxide layer, such that the oxidation resistant material ultimately penetrates into the zirconium substrate resulting in strong adhesion, and the oxidation resistant material deposited on the exposed outer coating surface provides a dense oxidation resistant surface that protects the underlying substrate from the nuclear reactor environment.
  • FIG. 2 shows an integrated gradient coating deposited on a zirconium alloy substrate 10 in accordance with certain embodiments of the invention.
  • a coating layer 20 containing zirconium alloy e.g., the first component is applied to the zirconium alloy substrate 10.
  • the zirconium alloy substrate 10 includes an oxidation layer 12 thereon.
  • the coating layer 20 is adjacent to the oxidation layer 12.
  • Within the coating layer 20 is an integration layer 22. Without intending to be bound by any particular theory, it is believed that a portion of the coating layer 20 mixes together or integrates with a portion of the oxidation layer 12, to form the integration layer 22 adjacent to the oxidation layer 12, which may penetrate within the zirconium alloy substrate 10.
  • the zirconium (e.g., the first component) content of the coating layer 20 increases toward the zirconium alloy substrate 10 as shown by arrow 24 and the non- zirconium species (e.g., the second component) content increases toward the outside surface 26 as shown by arrow 28.
  • the gradient coating layer 20 is deposited and the integration layer 22 formed as a result of several passes of the kinetic deposition technique described herein. Each successive deposition increases in the non-zirconium alloy species, e.g., the second component, and decreases in zirconium alloy, e.g., the first component, content. In certain embodiments, a single pass deposition technique may be employed where the coating composition itself is altered in a continuous manner such that multiple passes are not required.
  • the thickness of the coating layer 20 may vary and in certain embodiments is less than or equal to about 100 micrometers thick, or more preferably from about 5 to about 100 micrometers thick, or from about 5 to about 50 micrometers thick.
  • the gradient coating of the invention provides numerous benefits over known corrosion resistant coatings.
  • known coatings may be applied on top of, e.g., overlay, the oxidation layer resulting in poor adhesion and failure.
  • the gradient coating provides oxidation resistant material directly into the oxidation layer which ultimately penetrates into the zirconium alloy cladding resulting in strong adhesion and a dense oxidation resistant surface that protects the underlying cladding from the reactor environment.
  • FIG. 3 shows a method of depositing a coating composition, e.g., the first and second components, in accordance with certain embodiments of this invention.
  • a zirconium alloy tube 30 is supplied.
  • a coating composition 32 is supplied to a Kinetic Cold Spray or Thermal Spray Deposition Process (KCS/TSDP) 34.
  • KCS/TSDP Kinetic Cold Spray or Thermal Spray Deposition Process
  • the KCS/TSDP provides or deposits the coating composition 32 to form a gradient coating 36.

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Abstract

A composition and method of kinetically depositing the composition to form a coating onto an exterior surface of a zirconium alloy cladding of a light water nuclear reactor which at least partially adheres to the exterior surface. The coating composition includes a first component and a second component. The first component is selected from the group consisting of zirconium, zirconium oxide and mixtures thereof. The second component is selected from the group consisting of Zr2AlC ceramic, Ti2AlC ceramic, Ti3AlC2 ceramic, A12O3, aluminum, zirconium silicide, amorphous and semi-amorphous alloyed stainless steel, and mixtures of Zr2AlC ceramic, Ti2AlC ceramic and Ti3AlC2 ceramic. The coating has a gradient emanating from the exterior surface of the cladding toward an exposed outer surface of the coating such that percent by weight of the first component decreases and the second component increases from the exterior surface of the cladding toward the exposed outer surface of the coating.

Description

A KINETICALLY APPLIED GRADATED Zr-Al-C CERAMIC OR Ti-Al-C CERAMIC OR AMORPHOUS OR SEMI-AMORPHOUS STAINLESS STEEL WITH NUCLEAR GRADE ZIRCONIUM ALLOY METAL STRUCTURE
CROSS REFERENCE TO RELATED APPLICATION
[0001] This application claims priority to U.S. Provisional Patent Application Serial No. 61/827,792 filed May 28, 2013, entitled "A Kinetically Applied Gradated Ti-Al-C Ceramic or Amorphous or Semi- Amorphous Stainless Steel With Nuclear Grade
Zirconium Alloy Metal Structure", and incorporated herein by reference.
BACKGROUND
1. Field
[0002] This invention relates to coating compositions and methods of coating zirconium alloy nuclear fuel cladding to reduce oxidation corrosion of the cladding which is exposed to light water nuclear reactor under normal or accident conditions.
2. Description of Related Art
[0003] The exposure of zirconium alloy cladding to the high temperature and pressure water environment in a nuclear reactor can result in corrosion (oxidation) of the cladding surface, and may ultimately lead to metal embrittlement. This weakening of the metal may adversely affect the performance, life -time, and safety margin of the nuclear fuel core. The inclusion of an oxidation resistant coating on the zirconium alloy cladding surface can in theory protect the zirconium alloy substrate from the reactor environment. However, there are problems associated with this solution. For example, achieving strong adherence of the coating to the zirconium alloy substrate is problematic due to a fine oxidation layer that inherently exists on top of the zirconium alloy cladding surface. FIG. 1 shows a coated zirconium alloy cladding 10 in accordance with the prior art. As shown in FIG. 1, the zirconium alloy cladding 10 has an oxidation layer 12 resulting from the immediate oxidation of the substrate 10, and a further oxidation portion 14 added as the zirconium is exposed to air, water or other oxidizing media. A coating layer 16 is applied to the oxidation portion 14. Thus, there are four distinct, separate layers that exist when the zirconium alloy cladding 10 is simply coated with the coating layer 16. Since the coating layer 16 is merely deposited on top of the oxidation layer 14, this process often results in the coating, peeling or spalling of the coating layer 16 when exposed to reactor conditions. In addition, thermal and radiation induced stresses are typically introduced in any coating during operation that can cause the coating layer 16 to peel off the zirconium alloy cladding 10.
[0004] The zirconium alloy material of which the cladding is constructed is composed of zirconium (Zr) with up to about 2 wt. % of other metals, such as niobium (Nb), tin (Sn), iron (Fe), chromium (Cr) and mixtures thereof. Such zirconium alloy cladding tubes are taught, for example, by Biancheria et al., Kapil, and Lahoda (see U.S. Patent Nos. 3,427,222; 5,075,075; and 7,139,360 respectively). These fuel rods/cladding have an end cap at each end and a hold device such as a metal spring to keep the enclosed stack of nuclear fuel pellets in place.
[0005] Various methods of coating nuclear fuel cladding tubes are known in the art. For example, such methods are taught by Knight et al., Bryan et al., Van Swam, and Lahoda et al. (see U.S. Patent Nos. 6,231,969; 5,171,520; 6,005,906 and 7,815,964; respectively).
[0006] Further, Mazzoccoli et al. (see U.S. Patent Application Serial No. 13/670,808 filed on 11/07/2012) discloses a method of coating zirconium alloy cladding tubes with an adherent mass of oxidation resistant material, using high velocity thermal application for a Zr-Al-C ceramic or Ti-Al-C ceramic or an iron based alloy, Nanosteel or Zr-Al alloy. There are disadvantages associated with this method, such as the inability of the coating to adhere to the base Zr alloy during thermal cycles.
[0007] Thus, there is a need in the art to develop a coating composition and method of depositing the composition to form a protective coating on a zirconium alloy cladding such that the coating sufficiently adheres to the cladding surface and is effective to reduce or prevent oxidation of the surface of the cladding due to its exposure to nuclear reactor coolant water. SUMMARY
[0008] In one aspect, the above needs are met and objects accomplished by a method of depositing a coating composition onto an exterior surface of a zirconium alloy cladding of a light water nuclear reactor to form a coating which at least partially adheres to said exterior surface. The method includes providing the zirconium alloy cladding which inherently has a zirconium oxide-containing layer at least partially formed on the exterior surface with an adherent coating of a graded composition. The graded coating composition includes a first component and a second component. The first component is selected from the group consisting of zirconium, zirconium oxide and mixtures thereof. The second component is selected from the group consisting of Zr2AlC ceramic, Ti2AlC ceramic, Ti3AlC2 ceramic, Α1203, aluminum, zirconium silicide, amorphous and semi- amorphous alloyed stainless steel, and mixtures of Zr2AlC ceramic, Ti2AlC ceramic and Ti3AlC2 ceramic. The method further includes kinetically depositing the coating composition onto the exterior surface of the cladding to form the coating. The coating has a gradient emanating from the surface of the cladding toward an exposed outer surface of the coating such that percent by weight of the first component decreases from the exterior surface of the cladding toward the exposed outer surface of the coating and percent by weight of the second component increases from the exterior surface of the cladding to the exposed outer surface of the coating, based on total weight of the coating composition.
[0009] The kinetic deposition of the coating composition can be conducted by employing a technique wherein a propellant is heated. The kinetic deposition technique may be effective to at least partially penetrate the zirconium oxide-containing layer formed on the exterior surface of the cladding. The coating may be applied by one or more passes of the kinetic deposition technique. A first pass may include depositing the coating composition to form a first layer which includes from about 75% to about 100% by weight of the first component and from about 0% to about 25% by weight of the second component based on total weight of the coating composition. A final pass may include depositing the coating composition to form the exposed outer surface which comprises from about 75% to about 100% by weight of the second component and from about 0% to about 25% by weight of the first component based on total weight of the coating composition.
[0010] In certain embodiments, a portion of the coating composition kinetically deposited adjacent to or near the exterior surface of the cladding mixes with the zirconium oxide-containing layer to form an integrated layer.
[0011] In certain embodiments, the zirconium alloy cladding is positioned in a light water nuclear reactor selected from the group consisting of a pressurized water reactor and a boiling water reactor.
[0012] In another aspect, the invention provides a coating composition for kinetic deposition on an exterior surface of a zirconium alloy cladding of a light water nuclear reactor to form a coating which at least partially adheres to said exterior surface. The zirconium alloy cladding inherently has a zirconium oxide-containing layer at least partially formed on said exterior surface. The coating composition includes a first component and a second component. The first component is selected from the group consisting of zirconium, zirconium oxide, and mixtures thereof. The second component is selected from the group consisting of Zr2AlC ceramic, Ti2AlC ceramic, Ti3AlC2 ceramic, A1203, aluminum, zirconium silicide, amorphous or semi-amorphous alloyed stainless steel, and mixtures of Zr2AlC ceramic, Ti2AlC ceramic and Ti3AlC2 ceramic. The coating formed by the coating composition has a gradient emanating from the exterior surface of the cladding, which serves as the coating substrate, towards an exposed outer surface of the coating such that percent by weight of the first component decreases from the exterior surface of the cladding toward the exposed outer surface of the coating and percent by weight of the second component increases from the exterior surface of the cladding to the exposed outer surface of the coating, based on total weight percent of the coating composition. BRIEF DESCRIPTION OF THE DRAWINGS
[0013] A further understanding of the invention can be gained from the following description of the preferred embodiments when read in conjunction with the
accompanying drawings in which:
[0014] FIG. 1 is a cross-section view of a coated zirconium alloy substrate in accordance with the prior art;
[0015] FIG. 2 is a cross-section view of a coated zirconium alloy substrate in accordance with certain embodiments of the invention; and
[0016] FIG. 3 is a block diagram of a method of applying a coating material employing a kinetic deposition technique in accordance with certain embodiments of the invention.
DESCRIPTION OF THE PREFERRED EMBODIMENT
[0017] The invention provides a coating composition which includes a zirconium compound and a compound which protects the cladding surface from bulk oxidation. The coating composition is deposited on an exterior surface of a zirconium alloy cladding, e.g., tube. The deposition can be performed using various conventional techniques, such as a kinetic deposition technique (referred to as "cold spray"). The zirconium alloy cladding tube typically has a zirconium-oxide layer inherently formed on at least a portion of its exterior surface. Deposition of the coating composition results in a coating being formed on at least a portion of the exterior surface of the zirconium alloy cladding tube.
[0018] The zirconium alloy cladding is positioned in the core of a light water nuclear reactor, such as a pressurized water reactor (PWR) or a boiling water reactor (BWR). Thus, the cladding is exposed to a high temperature and pressure water environment.
[0019] The coating composition of the invention includes a first component and a second component. The first component includes zirconium, zirconium oxide or mixtures thereof. The second component includes Zr2AlC ceramic, Ti2AlC ceramic, Ti3AlC2 ceramic, A1203, aluminum, zirconium silicide (ZrSi2), amorphous or semi- amorphous alloyed stainless steel, or mixtures of Zr2AlC, Ti2AlC and Ti3AlC2. [0020] Since the zirconium alloy cladding inherently has at least partially formed on its exterior surface a zirconium oxide-containing layer or film, the coating composition is actually deposited on and adhered to this zirconium oxide-containing layer. Deposition of the coating composition of the invention results in a gradient coating or matrix that emanates from the exterior surface of the zirconium alloy cladding to an outer exposed surface of the coating. This gradient coating is effective to eliminate bulk oxidation of the zirconium alloy cladding upon exposure to PWR or BWR conditions, e.g., coolant that circulates in the reactor core. The gradient of the coating is such that the amount or weight percent (based on total weight of the coating composition) of each of the first and second components increases or decreases as the coating thickness emanates from the surface of the coating which is adjacent to or near the zirconium alloy cladding surface toward the exposed outer surface of the coating. In certain embodiments, the amount of the first component decreases as the coating thickness emanates from the surface adjacent to or near the zirconium alloy cladding surface toward the exposed outer coating surface, and the amount of the second component increases as the coating thickness emanates from the surface adjacent to or near the zirconium alloy cladding surface toward the exposed outer coating surface. Further, the decrease in the amount of the first component may correspond to the increase in the amount of the second component. For example, when the weight percent of the first component decreases from about 75% by weight at the surface of the coating adjacent to or near the cladding surface to about 10% by weight at the exposed outer surface, the weight percent of the second component
correspondingly increases from about 25% by weight at the surface of the coating adjacent to or near the cladding surface to about 90%> by weight at the exposed outer surface of the coating. In certain embodiments, the weight percent of each of the first and second components may decrease and increase, respectively, such that the first component is present on the exposed outer surface of the coating in an amount of about 0%) by weight and the second component is present on the exposed outer surface of the coating in an amount of about 100% by weight.
[0021] The coating composition may be deposited onto the exterior surface of the zirconium alloy cladding to form the gradient coating by employing various coating techniques known in the art. In certain embodiments, the coating composition is deposited using a conventional kinetic deposition technique which generally includes directing particulate material by a gas stream toward a substrate. In accordance with the invention, typically, the coating composition is propelled by a propulsive gas stream toward the zirconium alloy cladding. The first and second components of the coating composition may each be propelled separately or they may be propelled together, e.g., in a blend or mixture. The coating composition may be propelled at room temperature or may be pre-heated to an elevated temperature, e.g., at or above the melting temperature of the first and second components. Without intending to be bound by any particular theory, it is believed that this method of kinetic deposition is capable of at least partially disrupting the zirconium-oxide layer which is inherently formed on the zirconium alloy cladding such that the resulting coating is firmly bonded, e.g., atom-to-atom, to the cladding surface.
[0022] The gradient coating may be formed in several passes or in a single pass. In certain embodiments wherein several passes are employed, the first pass includes an excess amount of the first component. That is, the first component is present in greater than about 50% by weight based on total weight of the coating composition. In other embodiments, the first component in the first pass may be present in about 75% by weight or greater based on total weight of the coating composition. The remainder of the coating composition being composed of the second component. In certain embodiments, the first pass includes about 100% by weight of the first component and about 0% by weight of the second component based on total weight of the coating composition. In each subsequent pass, the amount of the first component decreases and the amount of the second component increases. In certain embodiments, the amount by which the first component decreases is equal to the amount by which the second component increases.
[0023] In alternate embodiments, a single pass technique is employed. In these embodiments, the amount (e.g., percent by weight) of each of the first and second components in the coating composition is continually varied to produce the gradient coating. [0024] The kinetic deposition methodology of the invention produces an integrated gradient coating that is richer in the first component, e.g., the zirconium or zirconium oxide, in the portion of the coating that is closer to the substrate, e.g., zirconium alloy cladding, and richer in the second component, e.g., the oxidation resistant material, in the portion of the coating that is nearer the exposed surface of the coating. In certain embodiments in accordance with the invention, the first component is present in excess (e.g., as compared to the second component) near the zirconium alloy cladding surface and the presence of the first component decreases throughout the coating thickness such that the exposed surface of the coating has an excess of the second component. Without intending to be bound by any particular theory, it is believed that the increased presence of the first component adjacent to or near the cladding tube surface enhances
incorporation of the gradient coating onto and into the surface, as the coating composition is chemically similar to the zirconium alloy cladding composition and, gradually changes the thermal expansion and radiation swelling characteristics to minimize thermal and radiation stresses during operation.
[0025] In certain embodiments of the invention, the gradient coating of the invention is created by kinetically depositing a first layer of the coating composition which includes from about 50% to about 100% or from greater than about 50% to about 100% or from about 75% to about 95% by weight of the first component, and from about 0% to about 50% or from about 0% to less than about 50% or from about 5% to about 25% by weight of the second component, based on total weight of the coating composition. In certain embodiments, the first component is zirconium alloy. Subsequently, additional layers of the coating composition may be deposited on the first layer. In certain embodiments, in each of the additional layers, the amount of the first component will successively decrease and the amount of the second component will successively increase. As a result, the exposed outer surface of the coating is composed of an excess of the second component such that it retains the oxidation resistant behavior of the second component while a base is present (e.g., underlying layers) that is rich in zirconium, i.e., the first component. [0026] The method of the invention is generally directed to depositing an oxidation resistant material into a zirconium oxide layer, such that the oxidation resistant material ultimately penetrates into the zirconium substrate resulting in strong adhesion, and the oxidation resistant material deposited on the exposed outer coating surface provides a dense oxidation resistant surface that protects the underlying substrate from the nuclear reactor environment.
[0027] FIG. 2 shows an integrated gradient coating deposited on a zirconium alloy substrate 10 in accordance with certain embodiments of the invention. In FIG. 2, a coating layer 20 containing zirconium alloy, e.g., the first component is applied to the zirconium alloy substrate 10. The zirconium alloy substrate 10 includes an oxidation layer 12 thereon. The coating layer 20 is adjacent to the oxidation layer 12. Within the coating layer 20 is an integration layer 22. Without intending to be bound by any particular theory, it is believed that a portion of the coating layer 20 mixes together or integrates with a portion of the oxidation layer 12, to form the integration layer 22 adjacent to the oxidation layer 12, which may penetrate within the zirconium alloy substrate 10. The zirconium (e.g., the first component) content of the coating layer 20 increases toward the zirconium alloy substrate 10 as shown by arrow 24 and the non- zirconium species (e.g., the second component) content increases toward the outside surface 26 as shown by arrow 28.
[0028] Typically, the gradient coating layer 20 is deposited and the integration layer 22 formed as a result of several passes of the kinetic deposition technique described herein. Each successive deposition increases in the non-zirconium alloy species, e.g., the second component, and decreases in zirconium alloy, e.g., the first component, content. In certain embodiments, a single pass deposition technique may be employed where the coating composition itself is altered in a continuous manner such that multiple passes are not required. The thickness of the coating layer 20 may vary and in certain embodiments is less than or equal to about 100 micrometers thick, or more preferably from about 5 to about 100 micrometers thick, or from about 5 to about 50 micrometers thick.
[0029] The higher concentration of zirconium alloy, e.g., the first component, near the base of the coating layer 20, e.g., its presence in excess as compared to the second (non- zirconium) component, and its presence in general, reduces thermal stresses incorporated by the kinetic deposition technique and in operation, reduces thermal coefficient and radiation swelling mismatches between the corrosion resistant additive, e.g., the second component, and the zirconium alloy cladding, thus increasing the propensity of the coating layer 20 to adhere to the zirconium alloy cladding 10.
[0030] The gradient coating of the invention provides numerous benefits over known corrosion resistant coatings. For example, known coatings may be applied on top of, e.g., overlay, the oxidation layer resulting in poor adhesion and failure. In the invention as shown in FIG. 2, the gradient coating provides oxidation resistant material directly into the oxidation layer which ultimately penetrates into the zirconium alloy cladding resulting in strong adhesion and a dense oxidation resistant surface that protects the underlying cladding from the reactor environment.
[0031] FIG. 3 shows a method of depositing a coating composition, e.g., the first and second components, in accordance with certain embodiments of this invention. A zirconium alloy tube 30 is supplied. A coating composition 32 is supplied to a Kinetic Cold Spray or Thermal Spray Deposition Process (KCS/TSDP) 34. The KCS/TSDP provides or deposits the coating composition 32 to form a gradient coating 36.
[0032] While specific embodiments of the invention have been described in detail, it will be appreciated by those skilled in the art that various modifications and alternatives to those details could be developed in light of the overall teachings of the disclosure. Accordingly, the particular embodiments disclosed are meant to be illustrative only and not limiting as to the scope of the invention which is to be given the full breadth of the appended claims and any and all equivalents thereof.

Claims

What is claimed is:
1. A method of depositing a coating composition onto an exterior surface of a zirconium alloy cladding (10) to form a coating (20) which at least partially adheres to said exterior surface, comprising:
providing the zirconium alloy cladding (10) which inherently has a zirconium oxide-containing layer (12) at least partially formed on the exterior surface;
providing a coating composition, comprising:
a first component selected from the group consisting of zirconium, zirconium oxide, and mixtures thereof; and
a second component selected from the group consisting of Zr2AlC ceramic, Ti2AlC ceramic, Ti3AlC2 ceramic, A1203, aluminum, zirconium silicide, amorphous and semi-amorphous alloyed stainless steel, and mixtures of Zr2AlC ceramic, Ti2AlC ceramic and Ti3AlC2 ceramic; and
kinetically depositing (34) the coating composition onto the exterior surface of the cladding (10) to form a coating having a gradient (36) emanating from the exterior surface of the cladding (10) toward an exposed outer surface (26) of the coating such that percent by weight of the first component decreases from the exterior surface of the cladding (10) toward the exposed outer surface (26) of the coating and percent by weight of the second component increases from the exterior surface of the cladding (10) to the exposed outer surface (26) of the coating, based on total weight of the coating composition.
2. The method of claim 1, wherein the kinetically depositing (34) the coating composition is conducted by employing a propulsive gas or other propellant.
3. The method of claim 2, wherein the propulsive gas or other propellant is heated.
4. The method of claim 1, wherein the kinetically depositing (34) the coating composition is effective to at least partially penetrate the zirconium oxide-containing layer (12).
5. The method of claim 1, wherein the kinetically depositing (34) the coating composition includes one or more passes to form the coating.
6. The method of claim 5, wherein a first pass may include kinetically depositing (34) the coating composition to form a first layer which comprises from about 75% to about 100% by weight of the first component and from about 0% to about 25% by weight of the second component based on total weight of the coating composition.
7. The method of claim 5, wherein a final pass may include kinetically depositing (34) the coating composition to form the exposed outer surface (26) which comprises from about 75% to about 100% by weight of the second component and from about 0% to about 25% by weight of the first component based on total weight of the coating composition.
8. The method of claim 1, wherein a portion of the coating composition is kinetically deposited (34) adjacent to or near the exterior surface and mixes with the zirconium oxide-containing layer (12) to form an integrated layer (22).
9. The method of claim 1, wherein the zirconium alloy cladding (10) is positioned in a nuclear reactor selected from the group consisting of a pressurized water reactor and a boiling water reactor.
10. The method of claim 1, wherein the coating (20) is from about 5 to about 100 micrometers in thickness.
11. The method of claim 1 , wherein the coating (20) is from about 5 to about 50 micrometers in thickness.
12. A coating composition for kinetic deposition on an exterior surface of a zirconium alloy cladding (10) to form a coating (20) which at least partially adheres to said exterior surface, the zirconium alloy cladding (10) inherently having a zirconium oxide-containing layer (12) thereon, the coating composition comprises:
a first component selected from the group consisting of zirconium, zirconium oxide and mixtures thereof; and
a second component selected from the group consisting of Zr2AlC ceramic, Ti2AlC ceramic, Ti3AlC2 ceramic, A1203, aluminum, zirconium silicide, amorphous or semi-amorphous alloyed stainless steel, and mixtures of Zr2AlC ceramic, Ti2AlC ceramic and Ti3AlC2 ceramic,
wherein, the coating (20) formed by the coating composition has a gradient emanating from the exterior surface of the cladding (10) toward an exposed outer surface (26) of the coating (20) such that percent by weight of the first component decreases from the exterior surface of the cladding (10) toward the exposed outer surface (26) of the coating (20) and percent by weight of the second component increases from the exterior surface of the cladding (10) to the exposed outer surface (26) of the coating (20), based on total weight of the coating composition.
13. The coating composition of claim 12, wherein the coating (20) at least partially penetrates the zirconium oxide-containing layer (12).
14. The coating composition of claim 12, wherein the coating (20) is formed by one or more passes of a kinetic deposition technique (34).
15. The coating composition of claim 14, wherein a first pass may include kinetically depositing (34) the coating composition to form a first layer which comprises from about 75% to about 100% by weight of the first component and from about 0% to about 25% by weight of the second component based on total weight of the coating composition.
16. The coating composition of claim 14, wherein a final pass may include kinetically depositing (34) the coating composition to form the exposed outer surface (26) which comprises from about 75% to about 100% by weight of the second component and from about 0% to about 25% by weight of the first component based on total weight of the coating composition.
17. The coating composition of claim 12, wherein a portion of the coating composition mixes with the zirconium oxide-containing layer (12) to form an integrated layer (22).
18. The coating composition of claim 12, wherein the coating (20) is from about 5 to about 100 micrometers in thickness.
19. The coating composition of claim 12, wherein the coating (20) is from about 5 to about 50 micrometers in thickness.
PCT/US2014/033932 2013-05-28 2014-04-14 A KINETICALLY APPLIED GRADATED Zr-Al-C CERAMIC OR Ti-Al-C CERAMIC OR AMORPHOUS OR SEMI-AMORPHOUS STAINLESS STEEL WITH NUCLEAR GRADE ZIRCONIUM ALLOY METAL STRUCTURE Ceased WO2014193549A1 (en)

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EP14804608.9A EP3004420B1 (en) 2013-05-28 2014-04-14 A KINETICALLY APPLIED GRADATED Zr-Al-C CERAMIC OR Ti-Al-C CERAMIC OR AMORPHOUS OR SEMI-AMORPHOUS STAINLESS STEEL WITH NUCLEAR GRADE ZIRCONIUM ALLOY METAL STRUCTURE
CN201480025399.7A CN105189820B (en) 2013-05-28 2014-04-14 For Dynamic deposition with the application composition of the formation gradual change coating on zirconium alloy cladding
ES14804608T ES2741832T3 (en) 2013-05-28 2014-04-14 Amorphous or semi-morph stainless steel or Ti-Al-C ceramic or Zr-Al-C ceramic kinetically applied with nuclear quality zirconium alloy metal structure
JP2016516650A JP6385015B2 (en) 2013-05-28 2014-04-14 Dynamically deposited compositionally graded Zr-Al-C ceramic or Ti-Al-C ceramic or amorphous or quasi-amorphous stainless steel with nuclear grade zirconium alloy microstructure

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107805071A (en) * 2017-10-26 2018-03-16 西南交通大学 A kind of preparation method of the low glass wetting aluminium two/mullite composite ceramic of carbon of titanium three
KR20180031052A (en) * 2015-08-14 2018-03-27 웨스팅하우스 일렉트릭 컴퍼니 엘엘씨 Corrosion-resistant and abrasion-resistant coatings on zirconium alloy cladding
EP3438990A1 (en) * 2017-07-31 2019-02-06 Kabushiki Kaisha Toshiba Method of repairing fuel assembly, method of producing fuel assembly, and fuel assembly
WO2021044093A1 (en) * 2019-09-06 2021-03-11 Safran Coated part comprising a protective coating based on max phases
EP3933067A1 (en) * 2020-07-03 2022-01-05 Flender GmbH Coating, a component with a coating and method for producing a coating
US20220102017A1 (en) * 2019-01-14 2022-03-31 Westinghouse Electric Sweden Ab A cladding tube for a fuel rod for nuclear reactors

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10872701B2 (en) * 2016-06-10 2020-12-22 Westinghouse Electric Company Llc Zirconium-coated silicon carbide fuel cladding for accident tolerant fuel application
JP6517981B2 (en) * 2017-07-31 2019-05-22 株式会社東芝 Method of repairing fuel assembly, method of manufacturing fuel assembly
CN109207786B (en) * 2018-11-01 2020-08-07 西北工业大学 Zr3Al3C5-ZrAlxSiyMethod for preparing composite material
JP7242867B2 (en) * 2018-12-29 2023-03-20 昆明理工大学 Superalloy and its manufacturing method
CN110205567B (en) * 2019-06-18 2021-05-04 河海大学 A kind of iron-based amorphous/MAX phase composite material for piston ring and its preparation method and application
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CN112775428B (en) * 2020-12-25 2022-03-25 北京交通大学 Ti generated on the surface of a titanium substrate in situ2AlC ceramic layer and preparation method thereof
CN112921299B (en) * 2021-01-20 2022-03-25 哈尔滨工业大学 Preparation method of composite film on surface of zirconium cladding
CN116285468B (en) * 2023-03-09 2024-06-11 北京交通大学 A composite microwave absorbing coating of Al2O3 and Ti2AlC and a preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02194183A (en) * 1989-01-20 1990-07-31 Japan Atom Energy Res Inst Ceramic-coated zirconium alloy article and its production
EP0614195A1 (en) * 1993-03-02 1994-09-07 Westinghouse Electric Corporation Fret resistant fuel rod with zirconium oxide layer
US5412701A (en) * 1992-06-30 1995-05-02 Combustion Engineering, Inc. Internal fuel rod coating comprising metal silicate
JPH07120576A (en) * 1993-10-21 1995-05-12 Sumitomo Metal Ind Ltd High corrosion resistance zirconium alloy cladding tube
US7138183B2 (en) * 2004-01-13 2006-11-21 Central Research Institute Of Electric Power Industry Environmental barrier coating material and coating structure and ceramic structure using the same

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3427222A (en) 1965-10-15 1969-02-11 Westinghouse Electric Corp Nuclear fuel elements
JPS6166997A (en) 1984-09-11 1986-04-05 株式会社東芝 Purifier for reactor water of nuclear reactor
US5026517A (en) 1984-12-11 1991-06-25 Siemens Aktiengesellschaft Nuclear power plant with water or liquid sodium coolant and a metallic component contacting the coolant
JPS6271801A (en) 1985-09-26 1987-04-02 Toshiba Corp Standard sample for measuring thickness of oxide layer of zirconium-base alloy member
JPH02160550A (en) 1988-02-29 1990-06-20 Science & Tech Agency Manufacture of metal and ceramic laminated body
US5075075A (en) 1990-01-16 1991-12-24 Westinghouse Electric Corp. Nuclear reactor core having nuclear fuel and composite burnable absorber arranged for power peaking and moderator temperature coefficient control
US5434896A (en) 1990-09-04 1995-07-18 Combustion Engineering, Inc. Wear resistant coating for components of fuel assemblies and control assemblies, and method of enhancing wear resistance of fuel assembly and control assembly components using wear-resistant coating
US5171520A (en) 1990-09-04 1992-12-15 Combustion Engineering, Inc. Wear resistant coating for fuel cladding
US6005906A (en) 1996-06-12 1999-12-21 Siemens Power Corporation Corrosion and hydride resistant nuclear fuel rod
US6231969B1 (en) 1997-08-11 2001-05-15 Drexel University Corrosion, oxidation and/or wear-resistant coatings
CN1196810C (en) 2001-08-04 2005-04-13 山东科技大学机械电子工程学院 Method for depositing paint-coat of metal surface, especially for gradient paint-coat
CN1167824C (en) 2001-11-09 2004-09-22 中国科学院金属研究所 A method for preparing thermal barrier coating by explosive spraying
US7139360B2 (en) 2004-10-14 2006-11-21 Westinghouse Electric Co. Llc Use of boron or enriched boron 10 in UO2
US7815964B2 (en) 2007-03-29 2010-10-19 Westinghouse Electric Co Llc Method of applying a burnable poison onto the exterior of nuclear rod cladding
US20090022259A1 (en) 2007-07-20 2009-01-22 General Electric Company Fuel rod with wear-inhibiting coating
KR101405396B1 (en) 2012-06-25 2014-06-10 한국수력원자력 주식회사 Zirconium alloy with coating layer containing mixed layer formed on surface, and preparation method thereof
US8971476B2 (en) 2012-11-07 2015-03-03 Westinghouse Electric Company Llc Deposition of integrated protective material into zirconium cladding for nuclear reactors by high-velocity thermal application

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02194183A (en) * 1989-01-20 1990-07-31 Japan Atom Energy Res Inst Ceramic-coated zirconium alloy article and its production
US5412701A (en) * 1992-06-30 1995-05-02 Combustion Engineering, Inc. Internal fuel rod coating comprising metal silicate
EP0614195A1 (en) * 1993-03-02 1994-09-07 Westinghouse Electric Corporation Fret resistant fuel rod with zirconium oxide layer
JPH07120576A (en) * 1993-10-21 1995-05-12 Sumitomo Metal Ind Ltd High corrosion resistance zirconium alloy cladding tube
US7138183B2 (en) * 2004-01-13 2006-11-21 Central Research Institute Of Electric Power Industry Environmental barrier coating material and coating structure and ceramic structure using the same

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20180031052A (en) * 2015-08-14 2018-03-27 웨스팅하우스 일렉트릭 컴퍼니 엘엘씨 Corrosion-resistant and abrasion-resistant coatings on zirconium alloy cladding
CN108140434A (en) * 2015-08-14 2018-06-08 西屋电气有限责任公司 Corrosion and wear resistance coating on zirconium alloy cladding
EP3335220A4 (en) * 2015-08-14 2019-04-17 Westinghouse Electric Company Llc CORROSION AND WEAR RESISTANT COATING ON ZIRCONIUM ALLOY SHEATH
US10350856B2 (en) 2015-08-14 2019-07-16 Westinghouse Electric Company Llc Corrosion and wear resistant coating on zirconium alloy cladding
KR102573613B1 (en) 2015-08-14 2023-08-31 웨스팅하우스 일렉트릭 컴퍼니 엘엘씨 Corrosion-resistant and wear-resistant coating on zirconium alloy cladding
EP3438990A1 (en) * 2017-07-31 2019-02-06 Kabushiki Kaisha Toshiba Method of repairing fuel assembly, method of producing fuel assembly, and fuel assembly
CN107805071A (en) * 2017-10-26 2018-03-16 西南交通大学 A kind of preparation method of the low glass wetting aluminium two/mullite composite ceramic of carbon of titanium three
US20220102017A1 (en) * 2019-01-14 2022-03-31 Westinghouse Electric Sweden Ab A cladding tube for a fuel rod for nuclear reactors
WO2021044093A1 (en) * 2019-09-06 2021-03-11 Safran Coated part comprising a protective coating based on max phases
FR3100545A1 (en) * 2019-09-06 2021-03-12 Safran COATED PART INCLUDING A PROTECTIVE COATING BASED ON MAX PHASES
US12195857B2 (en) 2019-09-06 2025-01-14 Safran Coated part comprising a protective coating based on MAX phases
EP3933067A1 (en) * 2020-07-03 2022-01-05 Flender GmbH Coating, a component with a coating and method for producing a coating

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