EP1252115A1 - Kohlenstoffhaltiger feuerfester formkörper mit schutzbeschichtung - Google Patents

Kohlenstoffhaltiger feuerfester formkörper mit schutzbeschichtung

Info

Publication number
EP1252115A1
EP1252115A1 EP00969452A EP00969452A EP1252115A1 EP 1252115 A1 EP1252115 A1 EP 1252115A1 EP 00969452 A EP00969452 A EP 00969452A EP 00969452 A EP00969452 A EP 00969452A EP 1252115 A1 EP1252115 A1 EP 1252115A1
Authority
EP
European Patent Office
Prior art keywords
protective coating
article
carbon
oxide
article according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP00969452A
Other languages
English (en)
French (fr)
Inventor
Cécile DESVIGNES
Gilbert Brandy
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.)
Vesuvius Crucible Co
Original Assignee
Vesuvius Crucible Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Vesuvius Crucible Co filed Critical Vesuvius Crucible Co
Priority to EP00969452A priority Critical patent/EP1252115A1/de
Publication of EP1252115A1 publication Critical patent/EP1252115A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/02Frit compositions, i.e. in a powdered or comminuted form
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/14Glass frit mixtures having non-frit additions, e.g. opacifiers, colorants, mill-additions
    • 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
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/50Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials
    • C04B41/5022Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials with vitreous materials
    • 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
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/80After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
    • C04B41/81Coating or impregnation
    • C04B41/85Coating or impregnation with inorganic materials
    • C04B41/86Glazes; Cold glazes
    • 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
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/0087Uses not provided for elsewhere in C04B2111/00 for metallurgical applications
    • C04B2111/00879Non-ferrous metallurgy

Definitions

  • Carbon-containing refractory article having a protective coating Description.
  • the invention relates to a carbon-containing refractory article having a protective coating. More particularly, the invention describes a protective coating that reduces carbon oxidation. Description of the Prior Art
  • Refractory articles which are used in the continuous casting of steel, often comprise refractory oxides and a significant amount of elemental carbon. Carbon can improve the article's resistance to thermochemical and thermomechanical stresses when contacting molten steel.
  • SES sub-entry shrouds
  • transfer molten steel from a tundish to a mold and often comprise 5-40 wt.% graphite.
  • Carbon is susceptible to oxidation, which can seriously impair the performance of the refractory article. Elevated temperatures accelerate oxidation and can occur at least during the firing, preheating and casting operations. A carbon-containing article is often fired in a reducing, non-oxidizing atmosphere, so that oxidation cannot then occur. In contrast, a reducing atmosphere is impracticable in preheating and casting operations.
  • the article is often covered with a protective coating that is relatively impervious to oxygen.
  • Protective coatings can be formed from solids or liquids that fuse to form a protective, oxygen barrier. Importantly, the protective coating should "wet" and completely coat the article without defects or "pinholes".
  • Pinholes in a protective coating allow oxygen to contact and oxidize the carbon- containing refractory article.
  • carbon itself can act to inhibit wetting by a protective coating.
  • Coatings that are not designed for carbon-containing refractories also attempt to reduce pinholes and improve wetting.
  • U.S. Pat. No. 5,013,697 to Akhtar teaches a sealing glass for the semiconductor industry that uses up to 30 wt.% bismuth oxide to lower fusing temperatures below 400°C and improve the wettability of the glaze on ceramic substrates, especially metal coated ceramics.
  • a sealing glass bonds two ceramic surfaces together forming an hermetically sealed container that is resistant to breakage and destruction.
  • a lower fusing temperature reduces damage to the semiconductor.
  • Akhtar does not teach a protective coating for carbon-containing substrates, a reduction in pinholing, or use in high temperature applications.
  • EP-A-0252621 does describe a protective coating for a carbon-containing refractory article.
  • the coating comprises a solid, particulate glaze for an electric arc furnace graphite electrode.
  • the glaze comprises 20-40 wt.% of a graphite-wetting, fusible material, 35-70 wt.% of a refractory filler, and 10-25 wt.% of a metal or metalloid, which is oxidizable to a refractory oxide while the electrode is at an elevated temperature.
  • the graphite-wetting, fusible material is a boron compound or a boron- containing glass, such as a borosilicate glass.
  • the metal or metalloid is preferably aluminum, and is intended to react with any oxygen before the oxygen reaches the refractory article.
  • the solid particulate glaze is sprayed and fuses onto the hot electrode.
  • Similar solid compositions including alkali and boron oxides are also known from the document DE-A1-4216934. These compositions are trowelled, rammed or sprayed. Spraying, trowelling or ramming cannot easily and fastly coat complex geometries or cavities, including, for example, the bore of a pour tube.
  • Other protecting composition that also comprises boron oxide are disclosed in the USP 3,460,987.
  • compositions however cannot be used directly on a substrate that contains less than 5% of boron oxide and are therefore not useful for the most carbon containing refractory articles used in the glass or metal industry.
  • Applicant herein incorporates by reference U.S. Pat. No. 5,856,015 to Buchanan, which teaches a protective coating for carbon-containing articles.
  • the protective coating is an aqueous suspension comprising clay, glass frit, powders of aluminum, silicon or their alloys, and an inhibitor.
  • the frit is a borosilicate, borophosphate or phosphate glass having a softening point below 600°C.
  • the powders are described as anti-oxidants, which inhibit oxidation of carbon.
  • the inhibitor is described as decreasing the reactivity of the powder with water.
  • the inhibitor includes several acids and salts, and is preferably sodium triphosphate. Benefits claimed include improved storage life and promotion of a more even protective coating. Despite the addition of wetting aids and inhibitors, pinholing and the resultant oxidation can still occur on carbon-containing refractory articles, especially articles further comprising alumina, magnesia and zirconia. A need persists for a protective coating that reduces pinholing on a carbon-containing refractory article at high temperature and protects the article from oxidation during preheating and casting operations.
  • the present invention relates to a carbon-containing refractory article having a coating that protects the article from oxidation.
  • the article comprises a form of carbon, preferably graphite, and at least one other refractory component, such as, for example, an oxide, carbide or nitride.
  • the protective coating comprises silica, boron oxide, alumina and a wetting aid. Alternatively, calcia or magnesia may substitute for all or part of the alumina.
  • the carbon-containing refractory article is described as an article that contacts a stream of molten metal during casting, such as, for example, a shroud, nozzle, monoblock or stopper rod.
  • the article may be a crucible or other refractory article for containing or contacting molten metal.
  • the protective coating is described as particularly effective on difficult to wet refractory compositions, such as articles comprising magnesia and zirconia.
  • the wetting aid is described as reducing the surface energy of the protective coating at elevated temperature, thereby improving wetting and reducing pinholing and oxidation of the carbon-containing refractory.
  • the wetting aid is described as a metal oxide of metals selected from the group consisting of arsenic, antimony, bismuth, tin, vanadium and lead.
  • the metal oxide is bismuth oxide and is present at 10 wt.% or less.
  • the protective coating also comprises a flux, which improves fluidity of the protective coating.
  • the flux may be an oxide of an alkali metal, and preferably will be an oxide of lithium, sodium or potassium.
  • the invention relates to a carbon-containing refractory article having a protective coating.
  • the refractory article includes any article comprising carbon in an amount where oxidation of the carbon would have a significant impact on the article's performance.
  • the refractory article comprises 2-40 wt.% carbon and carbon is in the form of graphite.
  • Such articles are also frequently carbon-bonded and intended to directly contact molten metal.
  • the article will comprise at least one refractory component, such as, for example, a refractory oxide, carbide or nitride. The choice of such refractory components is known to one skilled in the art.
  • refractory articles examples include submerged entry nozzles, submerged entry shrouds, slide gate plates, stopper rods, graphite electrodes, crucibles and other components used in the steel and metallurgical industry.
  • a refractory article may also include "monoblock" articles, which are unitary pieces comprising a slide gate plate fixedly secured to a tube, such as a nozzle or shroud.
  • the protective coating includes a minor portion of a high temperature wetting aid, and a major portion comprising suitable oxides, such as silica, boron oxide and oxides of aluminum, calcium or magnesium.
  • suitable oxides such as silica, boron oxide and oxides of aluminum, calcium or magnesium.
  • the major portion of the present invention is substantially described in U.S. Pat. No. 5,856,015, the teaching of which Applicant hereby incorporates by reference.
  • the major portion is formed from particles of refractory oxides, particularly lead-free and barium-free glass comprising borosilicate, borophosphate or phosphate having a dilatometric softening point below 600°C.
  • the major portion has 40-80 wt.% silica, 5-20 wt.% boron oxide and 5-20 wt.% of at least one refractory oxide selected from the group consisting of alumina, calcia and magnesia. Additionally, the major portion may have up to 4 wt.% cobalt oxide. The major portion is commonly present in the protective coating up to about 99 wt.%.
  • the major portion may also contain an antioxidant that sacrificially oxidizes before elemental carbon in the refractory article.
  • the inclusion of an antioxidant may recommend the use of an inhibitor, which delays oxidation of the antioxidant.
  • the antioxidant and inhibitor may comprise up to about 30 wt.% of the major portion.
  • Suitable antioxidants include powders of a metal, metalloid, carbides, nitrides or combinations thereof.
  • the term "powder" includes both powder and flake materials.
  • the powder preferably has a particle size in the range from 1 to 250 ⁇ m, and most preferably from 10 to 50 ⁇ m. Larger particle sizes are preferred when a thicker protective coating is desired.
  • Common antioxidants include aluminum, magnesium, boron, calcium, silicon, and carbides of silicon, calcium, zirconium, boron, tantalum and titanium.
  • the high temperature wetting aid will improve the wetting of the protective coating on a carbon-containing refractory article at temperatures above around 300°C. Improved wetting reduces pinholing and increases the protective coating's ability to protect the article from oxidation. Without intending to be bound by this explanation, the wetting aid may decrease the surface energy of the protective coating, thereby improving wetting, reducing pinholing and the diffusion of oxygen to the carbon- containing refractory article.
  • the wetting aid comprises an oxide of a metal selected from the group consisting of arsenic, antimony, bismuth, tin, vanadium and lead. Bismuth oxide is particularly useful as a wetting aid. It will be appreciated that these metals may often be present both in their reduced state and as an oxide. Firing of the carbon-containing refractory article in a reducing atmosphere may contribute to the reduced metal being present. As is customary in the industry, the presence of the reduced metal is reported in weight percent as if it were an oxide.
  • a sufficient amount of wetting aid will be present to improve wetting and reduce pinholing.
  • An effective level depends on the particular conditions, such as, for example, the composition of the refractory article, the thickness of the protective coating, and the fusion temperature.
  • An upper limit exists where the amount of wetting aid impairs the barrier properties of the major portion and allows oxygen to diffuse though the coating to the carbon-containing refractory article.
  • the amount of wetting aid will be in the range from 0.5 to 10 wt.% of the protective coating.
  • the protective coating may also comprise a flux that decreases the viscosity of the protective coating at high temperatures. A lower viscosity increases fluidity and permits the protective coating to seal more easily minor imperfections in the coating.
  • the flux should not deleteriously react with the other components of the protective coating, especially the antioxidant.
  • the level of flux addition depends on the particular properties desired and may readily be determined by one skilled in the art. Oxides and fluorides of alkali metals, such as lithium, sodium and potassium, are especially useful fluxes. Fluxes are most effective in a range up to about 5 wt.%; although, up to about 20 wt.% may be used.
  • the protective coating may be applied to the refractory article by any suitable application method, including, for example, slip casting, immersion, dry or wet spraying, or cementing.
  • additives such as a liquid carrier and rheology modifiers may be needed.
  • the method will affect the type and amount additives required.
  • the wetting aid and major portion will be suspended in a liquid carrier.
  • a rheology modifier may be used to thicken and stabilize the suspension in the liquid carrier, thereby facilitating coating of the suspension onto the refractory article.
  • a liquid carrier will most commonly be water, but may be other suitable liquids, such as alcohols and other organic solvents.
  • liquid carrier A sufficient amount of liquid carrier will be needed to suspend the wetting aid, major portion, and rheology modifier so that the protective coating may be coated onto the refractory article.
  • the amount of liquid carrier and rheology modifier can be experimentally determined by combining with other components of the protective coating until the desired consistency is achieved.
  • a carbon-bonded stopper rod was made having a protective coating.
  • the body of the stopper rod was carbon-bonded and comprised alumina and at least 20 wt.% graphite.
  • the nose of the stopper rod comprised magnesia and at least 20 wt.% graphite.
  • the protective coating consisted essentially of the following composition:
  • the protective coating was applied to the stopper rod as an aqueous suspension and prior to heating the article in an oxidizing atmosphere in excess of 800°C.
  • the protective coating appeared to completely wet the stopper rod and no pinholes were observed.
  • the stopper rod with the protective coating was heated in air at 1100°C for a period of 90 minutes. No oxidation or decarburization was noted. In contrast, a stopper rod without the protective coating exhibited extensive oxidation and embrittled as the carbon-bonding deteriorated.
EP00969452A 1999-10-14 2000-10-05 Kohlenstoffhaltiger feuerfester formkörper mit schutzbeschichtung Withdrawn EP1252115A1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP00969452A EP1252115A1 (de) 1999-10-14 2000-10-05 Kohlenstoffhaltiger feuerfester formkörper mit schutzbeschichtung

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP99870209 1999-10-14
EP99870209 1999-10-14
EP00969452A EP1252115A1 (de) 1999-10-14 2000-10-05 Kohlenstoffhaltiger feuerfester formkörper mit schutzbeschichtung
PCT/EP2000/009859 WO2001027048A1 (en) 1999-10-14 2000-10-05 Carbon-containing refractory article having a protective coating

Publications (1)

Publication Number Publication Date
EP1252115A1 true EP1252115A1 (de) 2002-10-30

Family

ID=8243908

Family Applications (1)

Application Number Title Priority Date Filing Date
EP00969452A Withdrawn EP1252115A1 (de) 1999-10-14 2000-10-05 Kohlenstoffhaltiger feuerfester formkörper mit schutzbeschichtung

Country Status (10)

Country Link
EP (1) EP1252115A1 (de)
JP (1) JP2003511341A (de)
KR (1) KR20020042710A (de)
CN (1) CN1181000C (de)
AR (1) AR026000A1 (de)
AU (1) AU7916100A (de)
BR (1) BR0014661A (de)
MX (1) MXPA02003677A (de)
TW (1) TW538014B (de)
WO (1) WO2001027048A1 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005016846A1 (en) * 2003-08-12 2005-02-24 Ut-Battelle, Llc Alkali resistant refractories

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1300260C (zh) * 2004-01-13 2007-02-14 中南大学 碳/碳复合材料抗氧化涂层的前躯体
CN1899997B (zh) * 2006-06-23 2010-05-12 吉林大学 在金属载体上制备玻璃陶瓷涂层的方法
DE102009037540B4 (de) 2009-08-17 2013-02-28 Technische Universität Bergakademie Freiberg Gepresste, kohlenstoffgebundene Feuerfesterzeugnisse auf Aluminiumoxidbasis und Verfahren zu ihrer Herstellung
CN102674902B (zh) * 2012-05-15 2013-08-28 陕西科技大学 一种C-AlPO4-莫来石/玻璃层梯度复合抗氧化涂层的制备方法
CN107686355A (zh) * 2017-09-18 2018-02-13 佛山市高捷工业炉有限公司 高强度坩埚的制备方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1136503A (en) * 1965-01-27 1968-12-11 English Electric Co Ltd Processes for coating articles with glass-ceramic
US5013697A (en) * 1990-06-21 1991-05-07 Johnson Matthey Inc. Sealing glass compositions
DE4216934A1 (de) * 1992-05-22 1993-11-25 Fleischmann Adolf A Fa Feuerfeste Auskleidung, insbesondere für Industrieöfen
GB9326526D0 (en) * 1993-12-29 1994-03-02 Cookson Group Plc Glaze for refractory materials

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0127048A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005016846A1 (en) * 2003-08-12 2005-02-24 Ut-Battelle, Llc Alkali resistant refractories

Also Published As

Publication number Publication date
AR026000A1 (es) 2002-12-26
AU7916100A (en) 2001-04-23
MXPA02003677A (es) 2002-08-30
BR0014661A (pt) 2002-06-11
WO2001027048A1 (en) 2001-04-19
CN1181000C (zh) 2004-12-22
CN1378524A (zh) 2002-11-06
KR20020042710A (ko) 2002-06-05
JP2003511341A (ja) 2003-03-25
TW538014B (en) 2003-06-21

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