CN109400127B - Air-permeable material for ladle and preparation method thereof - Google Patents

Air-permeable material for ladle and preparation method thereof Download PDF

Info

Publication number
CN109400127B
CN109400127B CN201811267733.6A CN201811267733A CN109400127B CN 109400127 B CN109400127 B CN 109400127B CN 201811267733 A CN201811267733 A CN 201811267733A CN 109400127 B CN109400127 B CN 109400127B
Authority
CN
China
Prior art keywords
powder
less
content
granularity
ladle
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201811267733.6A
Other languages
Chinese (zh)
Other versions
CN109400127A (en
Inventor
王周福
熊鑫
刘浩
王玺堂
马妍
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.)
Wuhan University of Science and Engineering WUSE
Original Assignee
Wuhan University of Science and Engineering WUSE
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 Wuhan University of Science and Engineering WUSE filed Critical Wuhan University of Science and Engineering WUSE
Priority to CN201811267733.6A priority Critical patent/CN109400127B/en
Publication of CN109400127A publication Critical patent/CN109400127A/en
Application granted granted Critical
Publication of CN109400127B publication Critical patent/CN109400127B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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
    • 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
    • C04B35/10Shaped 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 aluminium oxide
    • C04B35/101Refractories from grain sized mixtures
    • C04B35/103Refractories from grain sized mixtures containing non-oxide refractory materials, e.g. carbon
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D41/00Casting melt-holding vessels, e.g. ladles, tundishes, cups or the like
    • B22D41/02Linings
    • 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
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/10Shaped 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 aluminium oxide
    • C04B35/101Refractories from grain sized mixtures
    • C04B35/1015Refractories from grain sized mixtures containing refractory metal compounds other than those covered by C04B35/103 - C04B35/106
    • 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
    • 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
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/62605Treating the starting powders individually or as mixtures
    • 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
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/0038Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by superficial sintering or bonding of particulate matter
    • C04B38/0041Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by superficial sintering or bonding of particulate matter the particulate matter having preselected particle sizes
    • 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
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/08Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by adding porous substances
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C7/00Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
    • C21C7/04Removing impurities by adding a treating agent
    • C21C7/064Dephosphorising; Desulfurising
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3205Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
    • C04B2235/3208Calcium oxide or oxide-forming salts thereof, e.g. lime
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3217Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
    • C04B2235/3218Aluminium (oxy)hydroxides, e.g. boehmite, gibbsite, alumina sol
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3217Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
    • C04B2235/3222Aluminates other than alumino-silicates, e.g. spinel (MgAl2O4)
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3231Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3232Titanium oxides or titanates, e.g. rutile or anatase
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3231Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3239Vanadium oxides, vanadates or oxide forming salts thereof, e.g. magnesium vanadate
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3284Zinc oxides, zincates, cadmium oxides, cadmiates, mercury oxides, mercurates or oxide forming salts thereof
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/34Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3418Silicon oxide, silicic acids, or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3817Carbides
    • C04B2235/3826Silicon carbides
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/40Metallic constituents or additives not added as binding phase
    • C04B2235/407Copper
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/42Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
    • C04B2235/422Carbon
    • C04B2235/425Graphite
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/42Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
    • C04B2235/428Silicon
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/44Metal salt constituents or additives chosen for the nature of the anions, e.g. hydrides or acetylacetonate
    • C04B2235/444Halide containing anions, e.g. bromide, iodate, chlorite
    • C04B2235/445Fluoride containing anions, e.g. fluosilicate
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/74Physical characteristics
    • C04B2235/77Density
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Mold Materials And Core Materials (AREA)
  • Porous Artificial Stone Or Porous Ceramic Products (AREA)

Abstract

The invention relates to a breathable material for a ladle and a preparation method thereof. The technical scheme is as follows: mixing fine corundum powder and alpha-Al2O3Mixing the micro powder, the fine quartz sand powder, the aluminum hydroxide, the aluminum fluoride, the additive, the foaming agent, the foam stabilizer, the water reducer and the calcium aluminate cement, adding water, stirring, forming, curing, drying, performing heat treatment at 1400-1600 ℃, crushing, and screening to obtain a granular material A and a granular material B with different granularities. And then mixing the thermosetting phenolic resin, the surfactant, the elemental silicon powder, the silicon carbide powder, the copper powder and the ammonium metavanadate, and uniformly stirring to obtain the modified resin. And then uniformly mixing the corundum particles, the particle material A, the particle material B, the crystalline flake graphite, the silicon carbide powder and the modified resin, pressing and forming, and carrying out heat treatment at 100-300 ℃ to obtain the breathable material for the ladle. The invention has low production cost, and the prepared air permeable material for the ladle has the characteristics of high-temperature rupture strength, stable air permeability, excellent anti-scouring performance and long service life.

Description

Air-permeable material for ladle and preparation method thereof
Technical Field
The invention belongs to the technical field of breathable materials. In particular to a breathable material for a ladle and a preparation method thereof.
Background
The molten iron pretreatment desulfurization process is an important metallurgical process flow for smelting low-sulfur or ultra-low-sulfur steel. Aiming at the problems of low slagging efficiency, large iron loss, more residual slag in molten iron and the like after molten iron desulfurization, the air brick is arranged on the side surface or the bottom surface of the molten iron ladle, gas is blown into the molten iron through the air brick to stir, a bare surface is formed on the liquid surface, and remarkable effects are achieved in the aspects of improving slag discharge and slag collection, improving the molten iron pretreatment process and the like.
The existing air permeable material comprises clay, corundum, spinel and the like, and the types of the air permeable material mainly comprise a dispersion type, a straight through hole type, a slit type and the like according to actual working conditions. In the actual use process, the breathable material mainly has the problems of unstable breathable performance, poor corrosion resistance, low high-temperature strength and the like.
In the prior art, the additive is introduced to promote the sintering of the breathable material and adjust the texture structure, so that the mechanical strength, the erosion resistance and the like of the breathable material are improved to a certain extent, but certain defects still exist in the aspects of the high-temperature strength, the breathable stability and the like of the breathable material.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and aims to provide the preparation method of the air permeable material for the ladle, which has low production cost, and the air permeable material for the ladle prepared by the method has the advantages of high-temperature rupture strength, stable air permeability, excellent anti-scouring performance and long service life.
In order to achieve the purpose, the technical scheme adopted by the invention comprises the following specific steps:
firstly, 40-60 wt% of corundum fine powder and 1-10 wt% of alpha-Al2O3Mixing micro powder, 30-50 wt% of quartz sand fine powder, 1-10 wt% of aluminum hydroxide, 1-10 wt% of aluminum fluoride, 1-5 wt% of additive, 1-5 wt% of foaming agent, 1-5 wt% of foam stabilizer, 0.1-1 wt% of water reducer and 1-5 wt% of calcium aluminate cement to obtain a mixture; and adding water accounting for 10-20 wt% of the mixture, uniformly stirring, casting, and curing for 10-20 hours to obtain a cured blank.
Secondly, drying the cured blank at 90-120 ℃ for 12-24 hours, and then carrying out heat treatment at 1400-1600 ℃ for 5-7 hours to obtain a pre-sintered material; and then crushing and screening the pre-sintered material to obtain a granular material A with the granularity of less than 0.25mm and a granular material B with the granularity of 0.25-1 mm.
And thirdly, mixing 40-60 wt% of thermosetting phenolic resin, 1-10 wt% of surfactant, 10-20 wt% of elemental silicon powder, 20-40 wt% of silicon carbide powder, 1-5 wt% of copper powder and 1-10 wt% of ammonium metavanadate, and uniformly stirring to obtain the modified resin.
And fourthly, mixing 50-70 wt% of corundum particles, 1-10 wt% of particle materials A, 10-30 wt% of particle materials B, 1-10 wt% of crystalline flake graphite, 1-5 wt% of silicon carbide powder and 1-10 wt% of modified resin, uniformly stirring, performing compression molding under the condition of 80-120 MPa, and performing heat treatment at 100-300 ℃ for 10-20 hours to obtain the breathable material for the ladle.
The corundum fine powder is plate-shaped corundum fine powder or Al of white corundum fine powder and corundum fine powder2O3The content is more than 99 wt%, and the granularity of the corundum fine powder is less than 0.088 mm.
The corundum particles are plate-shaped corundum particles or white corundum particles and Al of the corundum particles2O3The content is more than 99 wt%, and the granularity of the corundum particles is 1-3 mm.
The alpha-Al2O3Micronized Al2O3More than 99 wt% of alpha-Al2O3The granularity of the micro powder is less than 0.01 mm.
SiO of the quartz sand fine powder2The content is more than 99 wt%, and the granularity of the quartz sand fine powder is less than 0.088 mm.
Al (OH) of the aluminum hydroxide3The content is more than 99 wt%, and the granularity of the aluminum hydroxide is less than 0.045 mm.
The Si content of the elemental silicon powder is more than 99 wt%, and the granularity is less than 0.088 mm.
The SiC content of the silicon carbide powder is more than 97 wt%, and the granularity is less than 0.088 mm.
The Cu content of the copper powder is more than 99 wt%, and the particle size is less than 0.088 mm.
The content of C in the flake graphite is more than 97 wt%, and the granularity is less than 0.088 mm.
The additive is zinc oxide or titanium dioxide, the purity of the additive is more than 99 wt%, and the granularity of the additive is less than 0.088 mm.
AlF of said aluminum fluoride3The content is more than 99 wt%.
The foaming agent is sodium dodecyl benzene sulfonate or sodium dodecyl sulfate, and the purity of the foaming agent is more than 98 wt%.
The foam stabilizer is fatty alcohol-polyoxyethylene ether sodium sulfate or sodium carboxymethylcellulose.
The water reducing agent is sodium hexametaphosphate or sodium tripolyphosphate, and the purity of the water reducing agent is more than 98 wt%.
In the calcium aluminate cement: al (Al)2O3The content is more than 65 wt%; SiO 22The content is less than 0.5 wt%; fe2O3The content is less than 0.3 wt%.
The room temperature viscosity of the thermosetting phenolic resin is less than 10000 centipoises, and the moisture content is less than 15 wt%.
The surfactant is fatty acid methyl ester or propylene oxide.
The purity of the ammonium metavanadate is more than 99 wt%.
Due to the adoption of the technical scheme, compared with the prior art, the invention has the following positive effects:
(1) the invention utilizes additive, corundum, quartz sand, aluminum hydroxide and alpha-Al2O3The reactivity of different raw materials such as micro powder, foaming agent and the like under different temperature conditions, the prefabricated fine-grain structure granules mainly comprising corundum and mullite have the characteristics of multi-stage through hole structure and high strength. The invention utilizes the modified resin obtained after the thermosetting phenolic resin treatment to ensure that the simple substance silicon powder, the silicon carbide powder and the like are uniformly distributed among the corundum particles, the prefabricated particle material A and the prefabricated particle material B, and the organizational structure of the material is adjusted by combining with the heat treatment. Therefore, the prepared air permeable material for the ladle has higher normal-temperature rupture strength.
(2) The invention avoids the introduction of impurity phase due to the control of the high-temperature reaction process among the raw materials with different characteristics, and forms stable fine grain mosaic structures among the prefabricated granule A, the prefabricated granule B and the corundum granules, so that the prepared air-permeable material for the ladle has higher high-temperature rupture strength.
(3) According to the invention, through hole structures with different scales are formed among different raw material particles by utilizing the composite action of the raw materials such as the additive, the foaming agent, the thermosetting phenolic resin, the silicon carbide and the like at different stages and the particle size difference among different raw materials, so that the material is endowed with stable air permeability while the high mechanical strength is ensured.
(4) According to the structure and performance characteristics of the air-permeable material for the ladle, the preparation process is controlled step by step, so that the growth and occurrence states of crystal grains are regulated, the formation and communication states of pores are controlled, and the ingenious control on the structure and performance of the material is realized. In addition, the invention has wide raw material source and low production cost, and the prepared air permeable material for the ladle has stable performance.
The performance of the prepared air-permeable material for the ladle is detected as follows: the bulk density is 2.5-2.9 g/cm3The apparent porosity is 23-31%, the normal temperature flexural strength is more than 7MPa, and the high temperature (1400 ℃) flexural strength is more than 6 MPa.
Therefore, the invention has low production cost, and the prepared air permeable material for the ladle has the characteristics of high-temperature rupture strength, stable air permeability, excellent anti-scouring performance and long service life.
Detailed Description
The invention is further described with reference to specific embodiments, without limiting its scope.
In order to avoid repetition, the particle sizes of the raw materials related to the present embodiment are uniformly described as follows, and are not described in detail in the examples:
al of the corundum fine powder2O3The content is more than 99 wt%, and the granularity of the corundum fine powder is less than 0.088 mm.
Al of the corundum particles2O3The content is more than 99 wt%, and the granularity of the corundum particles is 1-3 mm.
The alpha-Al2O3Micronized Al2O3More than 99 wt% of alpha-Al2O3The granularity of the micro powder is less than 0.01 mm.
SiO of the quartz sand fine powder2The content is more than 99 wt%, and the granularity of the quartz sand fine powder is less than 0.088 mm.
Al (OH) of the aluminum hydroxide3The content is more than 99 wt%, and the granularity of the aluminum hydroxide is less than 0.045 mm.
The Si content of the elemental silicon powder is more than 99 wt%, and the granularity is less than 0.088 mm.
The SiC content of the silicon carbide powder is more than 97 wt%, and the granularity is less than 0.088 mm.
The Cu content of the copper powder is more than 99 wt%, and the particle size is less than 0.088 mm.
The content of C in the flake graphite is more than 97 wt%, and the granularity is less than 0.088 mm.
The purity of the additive is more than 99 wt%, and the particle size is less than 0.088 mm.
AlF of said aluminum fluoride3The content is more than 99 wt%.
The purity of the foaming agent is more than 98 wt%.
The purity of the water reducing agent is more than 98 wt%.
In the calcium aluminate cement: al (Al)2O3The content is more than 65 wt%; SiO 22The content is less than 0.5 wt%; fe2O3The content is less than 0.3 wt%.
The room temperature viscosity of the thermosetting phenolic resin is less than 10000 centipoises, and the moisture content is less than 15 wt%.
The purity of the ammonium metavanadate is more than 99 wt%.
Example 1
A permeable material for a ladle and a preparation method thereof. The preparation method in this example is:
firstly, 40-45 wt% of corundum fine powder and 1-10 wt% of alpha-Al2O3Mixing micro powder, 45-50 wt% of quartz sand fine powder, 1-10 wt% of aluminum hydroxide, 1-10 wt% of aluminum fluoride, 1-5 wt% of additive, 1-5 wt% of foaming agent, 1-5 wt% of foam stabilizer, 0.1-1 wt% of water reducer and 1-5 wt% of calcium aluminate cement to obtain a mixture; and adding water accounting for 10-15 wt% of the mixture, uniformly stirring, casting and molding, and curing for 15-20 hours to obtain a cured blank.
Secondly, drying the cured blank at the temperature of 90-110 ℃ for 12-16 hours, and then carrying out heat treatment at the temperature of 1500-1600 ℃ for 5-7 hours to obtain a pre-sintered material; and then crushing and screening the pre-sintered material to obtain a granular material A with the granularity of less than 0.25mm and a granular material B with the granularity of 0.25-1 mm.
And thirdly, mixing 40-45 wt% of thermosetting phenolic resin, 1-10 wt% of surfactant, 10-20 wt% of elemental silicon powder, 35-40 wt% of silicon carbide powder, 1-5 wt% of copper powder and 1-10 wt% of ammonium metavanadate, and uniformly stirring to obtain the modified resin.
And fourthly, mixing 50-55 wt% of corundum particles, 1-4 wt% of particle materials A, 25-30 wt% of particle materials B, 7-10 wt% of crystalline flake graphite, 3-5 wt% of silicon carbide powder and 1-4 wt% of modified resin, uniformly stirring, performing compression molding under the condition of 80-100 MPa, and performing heat treatment at 100-180 ℃ for 10-15 hours to obtain the breathable material for the ladle.
In this embodiment:
the corundum fine powder is plate-shaped corundum fine powder;
the corundum particles are plate-shaped corundum particles;
the additive is zinc oxide;
the foaming agent is sodium dodecyl benzene sulfonate;
the foam stabilizer is fatty alcohol-polyoxyethylene ether sodium sulfate;
the water reducing agent is sodium tripolyphosphate;
the surfactant is fatty acid methyl ester.
The performance of the permeable material for ladles prepared in this example was tested: the bulk density is 2.5-2.7g/cm3(ii) a The apparent porosity is 26-31%; the normal temperature rupture strength is more than 8 MPa; the high-temperature (1400 ℃) rupture strength is more than 7 MPa.
Example 2
A permeable material for a ladle and a preparation method thereof. The preparation method in this example is:
firstly, 45-50 wt% of corundum fine powder and 1-10 wt% of alpha-Al2O3The material comprises micro powder, 40-45 wt% of quartz sand fine powder, 1-10 wt% of aluminum hydroxide, 1-10 wt% of aluminum fluoride, 1-5 wt% of additives, 1-5 wt% of foaming agents, 1-5 wt% of foam stabilizers, 0.1-1 wt% of water reducing agents and 1-5 wt% of calcium aluminate cementMixing to obtain a mixture; and adding water accounting for 14-20 wt% of the mixture, uniformly stirring, casting, and curing for 10-16 hours to obtain a cured blank.
Secondly, drying the cured blank at 100-120 ℃ for 15-20 hours, and then carrying out heat treatment at 1400-1500 ℃ for 5-7 hours to obtain a pre-sintered material; and then crushing and screening the pre-sintered material to obtain a granular material A with the granularity of less than 0.25mm and a granular material B with the granularity of 0.25-1 mm.
And thirdly, mixing 45-50 wt% of thermosetting phenolic resin, 1-10 wt% of surfactant, 10-20 wt% of elemental silicon powder, 30-35 wt% of silicon carbide powder, 1-5 wt% of copper powder and 1-10 wt% of ammonium metavanadate, and uniformly stirring to obtain the modified resin.
And fourthly, mixing 55-60 wt% of corundum particles, 3-6 wt% of particle materials A, 20-25 wt% of particle materials B, 5-8 wt% of crystalline flake graphite, 1-3 wt% of silicon carbide powder and 7-10 wt% of modified resin, uniformly stirring, performing compression molding under the condition of 90-110 MPa, and performing heat treatment at the temperature of 200-300 ℃ for 14-20 hours to prepare the breathable material for the ladle.
In this embodiment:
the corundum fine powder is white corundum fine powder;
the corundum particles are white corundum particles;
the additive is titanium dioxide;
the foaming agent is sodium dodecyl sulfate;
the foam stabilizer is sodium carboxymethyl cellulose;
the water reducing agent is sodium hexametaphosphate;
the surfactant is propylene oxide.
The performance of the permeable material for ladles prepared in this example was tested: the bulk density is 2.5-2.8 g/cm3(ii) a The apparent porosity is 25-31%; the normal temperature rupture strength is more than 9 MPa; the high-temperature (1400 ℃) rupture strength is more than 7 MPa.
Example 3
A permeable material for a ladle and a preparation method thereof. The preparation method in this example is:
firstly, 50-55 wt% of corundum fine powder and 1-10 wt% of alpha-Al2O3Mixing micro powder, 35-40 wt% of quartz sand fine powder, 1-10 wt% of aluminum hydroxide, 1-10 wt% of aluminum fluoride, 1-5 wt% of additive, 1-5 wt% of foaming agent, 1-5 wt% of foam stabilizer, 0.1-1 wt% of water reducer and 1-5 wt% of calcium aluminate cement to obtain a mixture; and adding 15-18 wt% of water into the mixture, uniformly stirring, casting and molding, and curing for 12-17 hours to obtain a cured blank.
Secondly, drying the cured blank at the temperature of 90-110 ℃ for 18-24 hours, and then carrying out heat treatment at the temperature of 1450-1550 ℃ for 5-7 hours to obtain a pre-sintered material; and then crushing and screening the pre-sintered material to obtain a granular material A with the granularity of less than 0.25mm and a granular material B with the granularity of 0.25-1 mm.
And thirdly, mixing 50-55 wt% of thermosetting phenolic resin, 1-10 wt% of surfactant, 10-20 wt% of elemental silicon powder, 25-30 wt% of silicon carbide powder, 1-5 wt% of copper powder and 1-10 wt% of ammonium metavanadate, and uniformly stirring to obtain the modified resin.
And fourthly, mixing 60-65 wt% of corundum particles, 5-8 wt% of particle materials A, 15-20 wt% of particle materials B, 3-6 wt% of crystalline flake graphite, 2-4 wt% of silicon carbide powder and 5-8 wt% of modified resin, uniformly stirring, performing compression molding under the condition of 100-120 MPa, and performing heat treatment at the temperature of 150-250 ℃ for 10-15 hours to prepare the breathable material for the ladle.
In this embodiment:
the corundum fine powder is white corundum fine powder;
the corundum particles are white corundum particles;
the additive is zinc oxide;
the foaming agent is sodium dodecyl benzene sulfonate;
the foam stabilizer is fatty alcohol-polyoxyethylene ether sodium sulfate;
the water reducing agent is sodium tripolyphosphate;
the surfactant is fatty acid methyl ester.
The performance of the permeable material for ladles prepared in this example was tested: the bulk density is 2.7-2.9 g/cm3(ii) a The apparent porosity is 23-29%; the normal temperature rupture strength is more than 9 MPa; the high-temperature (1400 ℃) rupture strength is more than 10 MPa.
Example 4
A permeable material for a ladle and a preparation method thereof. The preparation method in this example is:
firstly, 55-60 wt% of corundum fine powder and 1-10 wt% of alpha-Al2O3Mixing micro powder, 30-35 wt% of quartz sand fine powder, 1-10 wt% of aluminum hydroxide, 1-10 wt% of aluminum fluoride, 1-5 wt% of additive, 1-5 wt% of foaming agent, 1-5 wt% of foam stabilizer, 0.1-1 wt% of water reducer and 1-5 wt% of calcium aluminate cement to obtain a mixture; and adding 15-18 wt% of water into the mixture, uniformly stirring, casting, and curing for 10-16 hours to obtain a cured blank.
Secondly, drying the cured blank at 100-120 ℃ for 15-20 hours, and then carrying out heat treatment at 1500-1600 ℃ for 5-7 hours to obtain a pre-sintered material; and then crushing and screening the pre-sintered material to obtain a granular material A with the granularity of less than 0.25mm and a granular material B with the granularity of 0.25-1 mm.
And thirdly, mixing 55-60 wt% of thermosetting phenolic resin, 1-10 wt% of surfactant, 10-20 wt% of elemental silicon powder, 20-25 wt% of silicon carbide powder, 1-5 wt% of copper powder and 1-10 wt% of ammonium metavanadate, and uniformly stirring to obtain the modified resin.
And fourthly, mixing 65-70 wt% of corundum particles, 7-10 wt% of particle materials A, 10-15 wt% of particle materials B, 1-4 wt% of crystalline flake graphite, 3-5 wt% of silicon carbide powder and 3-6 wt% of modified resin, uniformly stirring, performing compression molding under the condition of 90-110 MPa, and performing heat treatment at the temperature of 150-250 ℃ for 14-20 hours to obtain the breathable material for the ladle.
In this embodiment:
the corundum fine powder is plate-shaped corundum fine powder;
the corundum particles are plate-shaped corundum particles;
the additive is titanium dioxide;
the foaming agent is sodium dodecyl sulfate;
the foam stabilizer is sodium carboxymethyl cellulose;
the water reducing agent is sodium hexametaphosphate;
the surfactant is propylene oxide.
The performance of the permeable material for ladles prepared in this example was tested: the bulk density is 2.5-2.7g/cm3(ii) a The apparent porosity is 29-31%; the normal temperature rupture strength is more than 8 MPa; the high-temperature (1400 ℃) rupture strength is more than 7 MPa.
Compared with the prior art, the specific implementation mode has the following positive effects:
(1) the specific embodiment utilizes additives, corundum, quartz sand, aluminum hydroxide and alpha-Al2O3The reactivity of different raw materials such as micro powder, foaming agent and the like under different temperature conditions, the prefabricated fine-grain structure granules mainly comprising corundum and mullite have the characteristics of multi-stage through hole structure and high strength. In the embodiment, the modified resin obtained after the thermosetting phenolic resin is treated is used for ensuring that the elemental silicon powder, the silicon carbide powder and the like are uniformly distributed among the corundum particles, the prefabricated particle material A and the prefabricated particle material B, and the texture structure of the material is adjusted by combining heat treatment. Therefore, the prepared air permeable material for the ladle has higher normal-temperature rupture strength.
(2) According to the specific embodiment, the high-temperature reaction process among the raw materials with different characteristics is controlled, so that the introduction of an impurity phase is avoided, stable fine-grain mosaic structures are formed among the prefabricated granular material A, the prefabricated granular material B and the corundum particles, and the prepared breathable material for the ladle has high-temperature rupture strength.
(3) According to the specific embodiment, through hole structures with different scales are formed among different raw material particles by utilizing the composite action of the raw materials such as the additive, the foaming agent, the thermosetting phenolic resin, the silicon carbide and the like at different stages and the particle size difference among different raw materials, so that the high mechanical strength is ensured, and the material is endowed with stable air permeability.
(4) According to the structure and performance characteristics of the air-permeable material for the ladle, the preparation process is controlled step by step, so that the growth and occurrence states of crystal grains are adjusted, the formation and communication states of pores are controlled, and the ingenious control on the structure and performance of the material is realized. In addition, the specific embodiment has wide raw material sources and low production cost, and the prepared air permeable material for the ladle has stable performance.
The performance of the breathable material for the ladle prepared by the embodiment is detected as follows: the bulk density is 2.5-2.9 g/cm3The apparent porosity is 23-31%, the normal temperature flexural strength is more than 7MPa, and the high temperature (1400 ℃) flexural strength is more than 6 MPa.
Therefore, the production cost of the embodiment is low, and the prepared air permeable material for the ladle has the characteristics of high-temperature rupture strength, stable air permeability, excellent anti-scouring performance and long service life.

Claims (10)

1. A preparation method of the air permeable material for the ladle is characterized by comprising the following steps:
firstly, 40-60 wt% of corundum fine powder and 1-10 wt% of alpha-Al2O3Mixing micro powder, 30-50 wt% of quartz sand fine powder, 1-10 wt% of aluminum hydroxide, 1-10 wt% of aluminum fluoride, 1-5 wt% of additive, 1-5 wt% of foaming agent, 1-5 wt% of foam stabilizer, 0.1-1 wt% of water reducer and 1-5 wt% of calcium aluminate cement to obtain a mixture; adding water accounting for 10-20 wt% of the mixture, uniformly stirring, casting, and curing for 10-20 hours to obtain a cured blank;
secondly, drying the cured blank at 90-120 ℃ for 12-24 hours, and then carrying out heat treatment at 1400-1600 ℃ for 5-7 hours to obtain a pre-sintered material; then crushing and screening the pre-sintered material to obtain a granular material A with the granularity of less than 0.25mm and a granular material B with the granularity of 0.25-1 mm;
step three, mixing 40-60 wt% of thermosetting phenolic resin, 1-10 wt% of surfactant, 10-20 wt% of elemental silicon powder, 20-40 wt% of silicon carbide powder, 1-5 wt% of copper powder and 1-10 wt% of ammonium metavanadate, and uniformly stirring to obtain modified resin;
fourthly, mixing 50-70 wt% of corundum particles, 1-10 wt% of particle materials A, 10-30 wt% of particle materials B, 1-10 wt% of crystalline flake graphite, 1-5 wt% of silicon carbide powder and 1-10 wt% of modified resin, uniformly stirring, performing compression molding under the condition of 80-120 MPa, and performing heat treatment at the temperature of 100-300 ℃ for 10-20 hours to prepare the breathable material for the ladle;
the corundum fine powder is plate-shaped corundum fine powder or Al of white corundum fine powder and corundum fine powder2O3The content is more than 99 wt%, and the granularity of the corundum fine powder is less than 0.088 mm;
the corundum particles are plate-shaped corundum particles or white corundum particles and Al of the corundum particles2O3The content is more than 99 wt%, and the granularity of the corundum particles is 1-3 mm;
the alpha-Al2O3Micronized Al2O3More than 99 wt% of alpha-Al2O3The granularity of the micro powder is less than 0.01 mm;
SiO of the quartz sand fine powder2The content is more than 99 wt%, and the granularity of the quartz sand fine powder is less than 0.088 mm;
al (OH) of the aluminum hydroxide3The content is more than 99 wt%, and the granularity of the aluminum hydroxide is less than 0.045 mm;
the Si content of the elemental silicon powder is more than 99 wt%, and the granularity is less than 0.088 mm;
the SiC content of the silicon carbide powder is more than 97 wt%, and the granularity is less than 0.088 mm;
the Cu content of the copper powder is more than 99 wt%, and the granularity is less than 0.088 mm;
the content of C in the flake graphite is more than 97 wt%, and the granularity is less than 0.088 mm;
the additive is zinc oxide or titanium dioxide; the purity of the additive is more than 99 wt%, and the particle size is less than 0.088 mm.
2. The method for producing a permeable material for a ladle according to claim 1, characterized in thatCharacterised by AlF of the aluminium fluoride3The content is more than 99 wt%.
3. The method of claim 1, wherein the foaming agent is sodium dodecylbenzenesulfonate or sodium dodecylsulfate, and the purity of the foaming agent is greater than 98 wt%.
4. The method for preparing the air-permeable material for the foundry ladle according to claim 1, wherein the foam stabilizer is sodium fatty alcohol-polyoxyethylene ether sulfate or sodium carboxymethylcellulose.
5. The method for preparing the air-permeable material for the foundry ladle according to claim 1, characterized in that the water reducing agent is sodium hexametaphosphate or sodium tripolyphosphate, and the purity of the water reducing agent is more than 98 wt%.
6. The method for preparing the air-permeable material for the foundry ladle according to claim 1, wherein in the calcium aluminate cement: al (Al)2O3The content is more than 65 wt%; SiO 22The content is less than 0.5 wt%; fe2O3The content is less than 0.3 wt%.
7. The method of claim 1, wherein the thermosetting phenol resin has a room temperature viscosity of less than 10000 cps and a moisture content of less than 15 wt%.
8. The method according to claim 1, wherein the surfactant is fatty acid methyl ester or propylene oxide.
9. The method according to claim 1, wherein the purity of the ammonium metavanadate is greater than 99 wt%.
10. A ladle gas permeable material produced by the method for producing a ladle gas permeable material according to any one of claims 1 to 9.
CN201811267733.6A 2018-10-29 2018-10-29 Air-permeable material for ladle and preparation method thereof Active CN109400127B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811267733.6A CN109400127B (en) 2018-10-29 2018-10-29 Air-permeable material for ladle and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811267733.6A CN109400127B (en) 2018-10-29 2018-10-29 Air-permeable material for ladle and preparation method thereof

Publications (2)

Publication Number Publication Date
CN109400127A CN109400127A (en) 2019-03-01
CN109400127B true CN109400127B (en) 2021-12-17

Family

ID=65469482

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811267733.6A Active CN109400127B (en) 2018-10-29 2018-10-29 Air-permeable material for ladle and preparation method thereof

Country Status (1)

Country Link
CN (1) CN109400127B (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103242051A (en) * 2013-05-30 2013-08-14 武汉科技大学 Lightweight corundum-mullite castable and preparation method thereof
CN105859309A (en) * 2016-03-31 2016-08-17 武汉科技大学 Dispersive air brick and preparation method thereof
CN107311680A (en) * 2017-07-28 2017-11-03 武汉科技大学 A kind of lightweight corundum-mullite castable and preparation method thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101381241B (en) * 2008-10-16 2011-06-15 武汉科技大学 Porous breathable refractory materials for upper nozzle and production method thereof
CN105645979B (en) * 2016-01-15 2018-04-27 浙江自立高温科技有限公司 A kind of air brick of steel ladle and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103242051A (en) * 2013-05-30 2013-08-14 武汉科技大学 Lightweight corundum-mullite castable and preparation method thereof
CN105859309A (en) * 2016-03-31 2016-08-17 武汉科技大学 Dispersive air brick and preparation method thereof
CN107311680A (en) * 2017-07-28 2017-11-03 武汉科技大学 A kind of lightweight corundum-mullite castable and preparation method thereof

Also Published As

Publication number Publication date
CN109400127A (en) 2019-03-01

Similar Documents

Publication Publication Date Title
CN104801656A (en) Highly fire-resistant foundry sand for steel casting and preparation method of highly fire-resistant foundry sand
CN108751957B (en) Carbon-free high-purity aluminum-magnesium machine-pressed brick for refining steel ladle and preparation method thereof
CN104801655A (en) High-strength foundry casting sand and preparation method thereof
CN106830958B (en) Low-aluminum low-heat-conduction alkali-resistant castable
CN107382357A (en) A kind of ladle bottom blowing composite air bricks disperse material and preparation method thereof
CN109879661B (en) Tundish coating material and preparation method thereof
CN107805059A (en) A kind of Ladle Bottom brick cup and preparation method thereof
CN109320280B (en) Air-permeable material for converter and preparation method thereof
CN104261848A (en) Chrome-oxide-containing mullite brick and preparation method thereof
CN106045546A (en) Magnesium-based casting material and a preparation method thereof
CN109279906B (en) Magnesium castable and preparation method thereof
CN110040995B (en) Preparation method of high-temperature light tough mullite aggregate
CN109400188B (en) Anti-seepage castable for aluminum melting furnace and preparation method
CN109133987B (en) Corundum-spinel breathable material and preparation method thereof
CN103551489A (en) Foundry molding sand containing blast furnace slag
CN114477976A (en) Cementing material for steel ladle and preparation method thereof
CN109400127B (en) Air-permeable material for ladle and preparation method thereof
CN109336626B (en) Magnesium castable with forsterite as main raw material and preparation method thereof
CN105906355B (en) A kind of densification Calcium dialuminate grog refractory and preparation method thereof
CN109180160B (en) Magnesium breathable material for tundish and preparation method thereof
CN109400124B (en) Corundum breathable material and preparation method thereof
CN108706967A (en) A kind of forsterite brick and its production technology
CN109180207B (en) Refractory material for foundry ladle and preparation method thereof
CN109279846B (en) High-impermeability concrete and preparation method thereof
CN103204689B (en) Carbon-containing gunning mix for hot-state gunning mix of converter as well as preparation method and using method of carbon-containing gunning mix

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant