CN108129136A - Copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof - Google Patents

Copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof Download PDF

Info

Publication number
CN108129136A
CN108129136A CN201810008918.9A CN201810008918A CN108129136A CN 108129136 A CN108129136 A CN 108129136A CN 201810008918 A CN201810008918 A CN 201810008918A CN 108129136 A CN108129136 A CN 108129136A
Authority
CN
China
Prior art keywords
forsterite
fine powder
magnesia
carbon composite
copper converter
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.)
Granted
Application number
CN201810008918.9A
Other languages
Chinese (zh)
Other versions
CN108129136B (en
Inventor
徐义彪
李亚伟
桑绍柏
王庆虎
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
Wuhan University of Science and Technology WHUST
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 CN201810008918.9A priority Critical patent/CN108129136B/en
Publication of CN108129136A publication Critical patent/CN108129136A/en
Application granted granted Critical
Publication of CN108129136B publication Critical patent/CN108129136B/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
    • C04B35/03Shaped 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 magnesium oxide, calcium oxide or oxide mixtures derived from dolomite
    • C04B35/04Shaped 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 magnesium oxide, calcium oxide or oxide mixtures derived from dolomite based on magnesium oxide
    • C04B35/043Refractories from grain sized 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
    • 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
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632Organic additives
    • C04B35/634Polymers
    • C04B35/63448Polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B35/63472Condensation polymers of aldehydes or ketones
    • C04B35/63476Phenol-formaldehyde condensation polymers
    • 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
    • C04B2235/3244Zirconium oxides, zirconates, hafnium oxides, hafnates, 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
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3262Manganese oxides, manganates, rhenium oxides or oxide-forming salts thereof, e.g. MnO
    • 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
    • C04B2235/3427Silicates other than clay, e.g. water glass
    • C04B2235/3436Alkaline earth metal silicates, e.g. barium silicate
    • C04B2235/3445Magnesium silicates, e.g. forsterite
    • 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
    • C04B2235/349Clays, e.g. bentonites, smectites such as montmorillonite, vermiculites or kaolines, e.g. illite, talc or sepiolite
    • 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
    • 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
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3817Carbides
    • C04B2235/3839Refractory metal carbides
    • C04B2235/3843Titanium 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
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3852Nitrides, e.g. oxynitrides, carbonitrides, oxycarbonitrides, lithium nitride, magnesium nitride
    • C04B2235/3856Carbonitrides, e.g. titanium carbonitride, zirconium carbonitride
    • 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
    • C04B2235/3852Nitrides, e.g. oxynitrides, carbonitrides, oxycarbonitrides, lithium nitride, magnesium nitride
    • C04B2235/3873Silicon nitrides, e.g. silicon carbonitride, silicon oxynitride
    • 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
    • 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
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5427Particle size related information expressed by the size of the particles or aggregates thereof millimeter or submillimeter sized, i.e. larger than 0,1 mm
    • 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
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5436Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
    • 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
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5454Particle size related information expressed by the size of the particles or aggregates thereof nanometer sized, i.e. below 100 nm
    • 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
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/658Atmosphere during thermal treatment
    • 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
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/658Atmosphere during thermal treatment
    • C04B2235/6587Influencing the atmosphere by vaporising a solid material, e.g. by using a burying of sacrificial powder
    • 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
    • C04B2235/9607Thermal properties, e.g. thermal expansion coefficient
    • 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
    • C04B2235/9669Resistance against chemicals, e.g. against molten glass or molten salts
    • C04B2235/9676Resistance against chemicals, e.g. against molten glass or molten salts against molten metals such as steel or aluminium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

The present invention relates to a kind of copper converter lower part magnesia forsterite carbon composites and preparation method thereof.Its technical solution is:First with the fused magnesite particle of 35~55wt%, the forsterite particle of 10~30wt%, the caustic-calcined magnesite fine powder of 6~16wt%, the pyrophillite fine powder of 5~15wt%, the amorphous graphite micro mist of 3~7wt%, 3~7wt% Si2N2O/SiC/TiC/TiCN/C composite granules, the simple substance silica fine powder of 1~3wt%, the titanium aluminum carbide fine powder of 2~5wt% and 2~5wt% manganese monoxide fine powder be raw material, the cobalt improved phenolic resin of the zirconia sol of the additional 2~5wt% of raw material and 3~5wt% again, it stirs evenly, molding, it is dry;2~8h is kept the temperature under conditions of carbon atmosphere and 1200~1400 DEG C is buried to get copper converter lower part magnesia forsterite carbon composite.The made product of the present invention has the characteristics that environmental-friendly, microporosity is high, thermal shock resistance is good and anti-ice copper slag penetration erosion performance is excellent.

Description

Copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof
Technical field
The invention belongs to copper converter carbon containing refractory fields.It is aoxidized more particularly to a kind of copper converter lower part Magnesium-forsterite-carbon composite and preparation method thereof.
Background technology
Copper converter is important smelting equipment during the blowing refinement of the matte.In converting process, drum in the matte into converter Enter air, FeS is preferentially oxidized to FeO and enters slag with additional quartz reaction;Subsequent Cu2S is obtained by aoxidizing desulfuration More than 98% content is known a little about.
At present, copper converter inner lining material generally uses magnesite-chrome brick, although solubility of the brick in slag is relatively low, magnesium Chrome brick is difficult to be sintered, and structure is more loose, and apparent porosity is high and aperture is larger.In copper converter lower part, inner lining material is direct and oozes The very strong matte contact of permeability;And since partial pressure of oxygen is relatively low, ferro element is mainly very strong with permeability and aggressivity in slag FeO forms exist.Long-time service process finds that matte and slag can be penetrated into along the stomata of copper converter lower part magnesite-chrome brick It inside brick body, and reacts with material component, changes the prototype structure of refractory material, form metamorphic layer.Due to metamorphic layer Structure and performance differ greatly with former brick layer, part refractory material is caused to be detached with brick body, peeling is formed, causes copper converter It is seriously damaged with magnesite-chrome brick lower part.
In addition, there may be the six of very strong carcinogenesis for the chromium ion during being stacked after using and using in magnesite-chrome brick Valency chromium certainly will largely be would seriously pollute the environment using magnesite-chrome brick, threaten the health of humans and animals.
Invention content
The present invention is directed to overcome prior art defect, it is therefore an objective to which offer one kind is environmental-friendly, microporosity is high, thermal shock resistance Good and excellent anti-ice copper-slag penetration erosion performance copper converter lower part magnesia-forsterite-carbon composite and its Preparation method.
To achieve the above object, the technical solution adopted in the present invention is:First with the fused magnesite particle of 35~55wt%, The forsterite particle of 10~30wt%, the caustic-calcined magnesite fine powder of 6~16wt%, the pyrophillite fine powder of 5~15wt%, 3~ The amorphous graphite micro mist of 7wt%, the Si of 3~7wt%2N2O/SiC/TiC/TiCN/C composite granules, the elemental silicon of 1~3wt% are thin The manganese monoxide fine powder of powder, the titanium aluminum carbide fine powder of 2~5wt% and 2~5wt% is raw material, then the additional raw material 2~ The zirconia sol of 5wt% and the cobalt improved phenolic resin of 3~5wt%, stir evenly, and are molded, dry.Then carbon atmosphere is being buried With 1200~1400 DEG C under conditions of heat preservation 2~8h to get copper converter lower part magnesia-forsterite-carbon composite.
The SiO of the pyrophillite fine powder275 μm of content ﹥ 70wt%, grain size ﹤.
5 μm of C content the ﹥ 80wt%, grain size ﹤ of the amorphous graphite micro mist.
The Si2N2The preparation method of O/SiC/TiC/TiCN/C composite granules is:By pyrophillite fine powder, titanium oxide fine powder With coke fines (3~5) in mass ratio: mix to get mixture at 1: 1;The phenolic aldehyde of 8~10wt% is added in the mixture Spheric granules is made with comminutor in resin;The spheric granules is put into saggar, then the saggar is placed in electric furnace, stove Interior maintenance nitrogen atmosphere, atmosphere pressures are 0.01~0.03MPa, and temperature is 1350~1550 DEG C, keeps the temperature 2~4h, natural cooling To room temperature;It is broken, granularity is finely ground to less than 0.075mm to get Si2N2O/SiC/TiC/TiCN/C composite granules.
The content of MgO ﹥ 97wt% of the fused magnesite particle, grain size are 0.1~5mm.
The content of MgO ﹥ 45wt% of the forsterite particle, grain size are 0.1~3mm.
45 μm of content of MgO the ﹥ 97wt%, grain size ﹤ of the caustic-calcined magnesite fine powder.
45 μm of Si contents the ﹥ 97wt%, grain size ﹤ of the simple substance silica fine powder.
The Ti of the titanium aluminum carbide fine powder3AlC245 μm of content ﹥ 97wt%, grain size ﹤.
45 μm of MnO contents the ﹥ 97wt%, grain size ﹤ of the manganese monoxide fine powder.
The ZrO of the zirconia sol2Content is 20~40wt%, and grain size is 20~70nm.
The Co contents of the cobalt improved phenolic resin are 0.08~0.6wt%, carbon yield ﹥ 40wt%.
Due to the adoption of the above technical scheme, the present invention has following good effect compared with prior art:
Copper converter lower part prepared by the present invention is Trend of Chrome-free material with magnesia-forsterite-carbon composite, will not Environment is polluted, potential threat will not be caused to the health of humans and animals, it is environmental-friendly.
In sintering process of the present invention, pyrophillite fine powder decompose generation silica and aluminium oxide active it is very high, can compared with Reacting generation forsterite and spinelle, manganese monoxide with the caustic-calcined magnesite fine powder added in material under low temperature can be dissolved into In magnesia, forsterite and spinel crystal lattice, promote mass transfer and densifying materials.It buries under carbon atmosphere, cobalt improved phenolic aldehyde tree Lysisin situ is generated carbon nanotube by fat, and elemental silicon, nitrogen and carbon monoxide interaction can generate silicon carbide whisker and nitrogen Silica whisker.The carbon nanotube of above-mentioned reaction generation and different types of whisker are distributed in material matrix, can effectively be blocked Material internal stomata reduces the apparent porosity and aperture size of material, significantly improves copper converter lower part magnesia-magnesium olive Anti-ice copper-slag penetration performance of olive stone-carbon composite.
Copper converter lower part prepared by the present invention manganese monoxide added in magnesia-forsterite-carbon composite It is solid-solution in magnesia, forsterite lattice, is conducive to improve the chemical stability of magnesia and forsterite in slag.It corroded Cheng Zhong, the titanium aluminum carbide added in material are aoxidized, and fine and close metatitanic acid aluminium layer, and the titanium formed will be formed in situ in material surface Sour aluminium layer and the spinelle of generation can absorb the FeO in slag, increase the viscosity of slag, significantly improve copper converter The slag-resistant permeance property of lower part magnesia-forsterite-carbon composite.
Copper converter lower part prepared by the present invention silicon carbide whisker generated in magnesia-forsterite-carbon composite Must and solubility of the silicon oxynitride whisker in slag it is very low, and it is non-oxide to dissolve these high-melting-points in erosion process in slag Viscosity can greatly improve after object, effectively slow down slag and the infiltration of material is corroded.The amorphous graphite that is added in material and Si2N2O/SiC/TiC/TiCN/C composite granules can effectively improve the contact angle between material and matte-slag, make material not by Matte-slag wetting significantly improves anti-ice copper-slag of copper converter lower part magnesia-forsterite-carbon composite Permeate erosion performance.
Copper converter lower part prepared by the present invention is molten with zirconium oxide is introduced in magnesia-forsterite-carbon composite The tiny zirconium oxide of generation can be decomposed in glue heat treatment process to be dispersed in material matrix, improve the thermal shock resistance of material Energy.Carbon nanotube, silicon carbide whisker and the silicon oxynitride whisker of reaction generation are scattered in inside in material, can generate extraction, The energy dissipation mechanisms such as crack deflection and bridging play increasing to copper converter lower part with magnesia-forsterite-carbon composite Strong toughening effect.
The apparent porosity of copper converter lower part magnesia-forsterite-carbon composite prepared by the present invention for 7~ 13%, average pore size is 0.5~3.0 μm, thermal shock resistance at 1100 DEG C 5 residual strength conservation rates of water cooling for 86~ 96%, 10000~12000h is corroded in the infiltration that can effectively keep out matte-slag.
Therefore, the magnesia-forsterite-carbon composite of the copper converter lower part prepared by the present invention has environment friend Well, the characteristics of microporosity is high, thermal shock resistance is good and anti-ice copper-slag penetration erosion performance is excellent
Specific embodiment
The invention will be further described With reference to embodiment, not to the limitation of its protection domain:
It is first that the material Unify legislation involved by present embodiment is as follows to avoid repeating, in specific embodiment not It repeats again:
The SiO of the pyrophillite fine powder275 μm of content ﹥ 70wt%, grain size ﹤.
5 μm of C content the ﹥ 80wt%, grain size ﹤ of the amorphous graphite micro mist.
The Si2N2The preparation method of O/SiC/TiC/TiCN/C composite granules is:By pyrophillite fine powder, titanium oxide fine powder With coke fines (3~5) in mass ratio: mix to get mixture at 1: 1;The phenolic aldehyde of 8~10wt% is added in the mixture Spheric granules is made with comminutor in resin;The spheric granules is put into saggar, then the saggar is placed in electric furnace, stove Interior maintenance nitrogen atmosphere, atmosphere pressures are 0.01~0.03MPa, and temperature is 1350~1550 DEG C, keeps the temperature 2~4h, natural cooling To room temperature;It is broken, granularity is finely ground to less than 0.075mm to get Si2N2O/SiC/TiC/TiCN/C composite granules.
The content of MgO ﹥ 97wt% of the fused magnesite particle, grain size are 0.1~5mm.
The content of MgO ﹥ 45wt% of the forsterite particle, grain size are 0.1~3mm.
45 μm of content of MgO the ﹥ 97wt%, grain size ﹤ of the caustic-calcined magnesite fine powder.
45 μm of Si contents the ﹥ 97wt%, grain size ﹤ of the simple substance silica fine powder.
The Ti of the titanium aluminum carbide fine powder3AlC245 μm of content ﹥ 97wt%, grain size ﹤.
45 μm of MnO contents the ﹥ 97wt%, grain size ﹤ of the manganese monoxide fine powder.
The ZrO of the zirconia sol2Content is 20~40wt%, and grain size is 20~70nm.
The Co contents of the cobalt improved phenolic resin are 0.08~0.6wt%, carbon yield ﹥ 40wt%.
Embodiment 1
A kind of copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof.It is characterized in that
First with the fused magnesite particle of 35~45wt%, the forsterite particle of 20~30wt%, 6~10wt% it is light-burned Magnesia powder, the pyrophillite fine powder of 11~15wt%, the amorphous graphite micro mist of 3~5wt%, 5~7wt% Si2N2O/SiC/ TiC/TiCN/C composite granules, the simple substance silica fine powder of 1~3wt%, the titanium aluminum carbide fine powder of 2~5wt% and 2~5wt% one Manganese oxide fine powder is raw material, then the cobalt improved phenolic aldehyde tree of the zirconia sol of the additional 2~5wt% of raw material and 3~5wt% Fat stirs evenly, and is molded, dry.Then 2~5h is kept the temperature under conditions of carbon atmosphere and 1200~1250 DEG C is buried to get copper metallurgy Converter lower part magnesia-forsterite-carbon composite.
Copper converter lower part magnesia-forsterite-carbon composite prepared by the present embodiment 1:Apparent porosity is 7 ~10%;Average pore size is 0.5~1.5 μm;Thermal shock resistance at 1100 DEG C 5 residual strength conservation rates of water cooling for 86~ 90%;10000~11500h is corroded in the infiltration that slag can effectively be kept out.
Embodiment 2
A kind of copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof.It is characterized in that first With the fused magnesite particle of 38~48wt%, the forsterite particle of 17~27wt%, the caustic-calcined magnesite fine powder of 8~12wt%, 9 The pyrophillite fine powder of~13wt%, the amorphous graphite micro mist of 4~6wt%, 4~6wt% Si2N2O/SiC/TiC/TiCN/C is answered Close powder, the simple substance silica fine powder of 1~3wt%, the titanium aluminum carbide fine powder of 2~5wt% and 2~5wt% manganese monoxide fine powder be Raw material, then the cobalt improved phenolic resin of the zirconia sol of the additional 2~5wt% of raw material and 3~5wt%, stir evenly, into Type, it is dry.Then 3~6h is kept the temperature under conditions of carbon atmosphere and 1240~1290 DEG C is buried to aoxidize to get copper converter lower part Magnesium-forsterite-carbon composite.
Copper converter lower part magnesia-forsterite-carbon composite prepared by the present embodiment 2:Apparent porosity is 8 ~11%;Average pore size is 1.1~2.1 μm;Thermal shock resistance at 1100 DEG C 5 residual strength conservation rates of water cooling for 88~ 92%;11400~11900h is corroded in the infiltration that slag can effectively be kept out.
Embodiment 3:
A kind of copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof.It is characterized in that first With the fused magnesite particle of 41~51wt%, the forsterite particle of 14~24wt%, 10~14wt% caustic-calcined magnesite fine powder, The pyrophillite fine powder of 7~11wt%, the amorphous graphite micro mist of 5~7wt%, 3~5wt% Si2N2O/SiC/TiC/TiCN/C is answered Close powder, the simple substance silica fine powder of 1~3wt%, the titanium aluminum carbide fine powder of 2~5wt% and 2~5wt% manganese monoxide fine powder be Raw material, then the cobalt improved phenolic resin of the zirconia sol of the additional 2~5wt% of raw material and 3~5wt%, stir evenly, into Type, it is dry.Then 4~7h is kept the temperature under conditions of carbon atmosphere and 1280~1330 DEG C is buried to aoxidize to get copper converter lower part Magnesium-forsterite-carbon composite.
Copper converter lower part magnesia-forsterite-carbon composite prepared by the present embodiment 3:Apparent porosity is 9 ~12%;Average pore size is 1.7~2.7 μm;Thermal shock resistance at 1100 DEG C 5 residual strength conservation rates of water cooling for 90~ 94%;11500~12000h is corroded in the infiltration that slag can effectively be kept out.
Embodiment 4
A kind of copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof.It is characterized in that first With the fused magnesite particle of 44~54wt%, the forsterite particle of 11~21wt%, 12~16wt% caustic-calcined magnesite fine powder, The pyrophillite fine powder of 5~9wt%, the amorphous graphite micro mist of 3~5wt%, 5~7wt% Si2N2O/SiC/TiC/TiCN/C is answered Close powder, the simple substance silica fine powder of 1~3wt%, the titanium aluminum carbide fine powder of 2~5wt% and 2~5wt% manganese monoxide fine powder be Raw material, then the cobalt improved phenolic resin of the zirconia sol of the additional 2~5wt% of raw material and 3~5wt%, stir evenly, into Type, it is dry.Then 5~8h is kept the temperature under conditions of carbon atmosphere and 1320~1370 DEG C is buried to aoxidize to get copper converter lower part Magnesium-forsterite-carbon composite.
Copper converter lower part magnesia-forsterite-carbon composite prepared by the present embodiment 4:Apparent porosity is 10~13%;Average pore size is 2.0~3.0 μm;Thermal shock resistance at 1100 DEG C 5 residual strength conservation rates of water cooling for 92~ 96%;11300~11800h is corroded in the infiltration that slag can effectively be kept out.
Embodiment 5
A kind of copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof.It is characterized in that first With the fused magnesite particle of 45~55wt%, the forsterite particle of 10~20wt%, the caustic-calcined magnesite fine powder of 9~13wt%, 8 The pyrophillite fine powder of~12wt%, the amorphous graphite micro mist of 4~6wt%, 4~6wt% Si2N2O/SiC/TiC/TiCN/C is answered Close powder, the simple substance silica fine powder of 1~3wt%, the titanium aluminum carbide fine powder of 2~5wt% and 2~5wt% manganese monoxide fine powder be Raw material, then the cobalt improved phenolic resin of the zirconia sol of the additional 2~5wt% of raw material and 3~5wt%, stir evenly, into Type, it is dry.Then 4~7h is kept the temperature under conditions of carbon atmosphere and 1350~1400 DEG C is buried to aoxidize to get copper converter lower part Magnesium-forsterite-carbon composite.
Copper converter lower part magnesia-forsterite-carbon composite prepared by the present embodiment 5:Apparent porosity is 8 ~11%;Average pore size is 1.3~2.3 μm;Thermal shock resistance at 1100 DEG C 5 residual strength conservation rates of water cooling for 90~ 94%;11200~11700h is corroded in the infiltration that slag can effectively be kept out.
Present embodiment has following good effect compared with prior art:
Copper converter lower part prepared by present embodiment is Trend of Chrome-free with magnesia-forsterite-carbon composite Material does not pollute the environment, and potential threat will not be caused to the health of humans and animals, environmental-friendly.
In present embodiment sintering process, pyrophillite fine powder decomposes the silica generated and aluminium oxide active is very high, Generation forsterite can be reacted with the caustic-calcined magnesite fine powder added in material at a lower temperature and spinelle, manganese monoxide can To be dissolved into magnesia, forsterite and spinel crystal lattice, promote mass transfer and densifying materials.It buries under carbon atmosphere, cobalt changes Property phenolic resin lysisin situ is generated into carbon nanotube, elemental silicon, nitrogen and carbon monoxide interaction can generate silicon carbide Whisker and silicon oxynitride whisker.The carbon nanotube of above-mentioned reaction generation and different types of whisker are distributed in material matrix, energy Effective plugging material internal porosity, reduces the apparent porosity and aperture size of material, significantly improves copper converter lower part oxygen Change anti-ice copper-slag penetration performance of magnesium-forsterite-carbon composite.
Copper converter lower part prepared by present embodiment is with adding in magnesia-forsterite-carbon composite Manganese monoxide is solid-solution in magnesia, forsterite lattice, is conducive to improve the chemical stabilization of magnesia and forsterite in slag Property.In erosion process, the titanium aluminum carbide added in material is aoxidized, and fine and close metatitanic acid aluminium layer will be formed in situ in material surface, And the metatitanic acid aluminium layer and the spinelle of generation formed can absorb the FeO in slag, increase the viscosity of slag, significantly improve Slag-resistant permeance property of the copper converter lower part with magnesia-forsterite-carbon composite.
Copper converter lower part prepared by present embodiment is with generating in magnesia-forsterite-carbon composite The solubility of silicon carbide whisker and silicon oxynitride whisker in slag is very low, and dissolves these Gao Rong in erosion process in slag Viscosity can greatly improve after point non-oxidized substance, effectively slow down slag and the infiltration of material is corroded.The earthy stone added in material Ink and Si2N2O/SiC/TiC/TiCN/C composite granules can effectively improve the contact angle between material and matte-slag, make material Do not soaked by matte-slag, significantly improve the anti-ice copper of copper converter lower part magnesia-forsterite-carbon composite- Slag penetration erosion performance.
Copper converter lower part prepared by present embodiment is introduced in magnesia-forsterite-carbon composite The tiny zirconium oxide of generation can be decomposed in zirconia sol heat treatment process to be dispersed in material matrix, improve material Thermal shock resistance.Carbon nanotube, silicon carbide whisker and the silicon oxynitride whisker of reaction generation are scattered in inside in material, can produce The energy dissipation mechanisms such as raw extraction, crack deflection and bridging, to copper converter lower part magnesia-forsterite-carbon composite wood Material plays the role of activeness and quietness.
Copper converter lower part magnesia-forsterite-carbon composite prepared by present embodiment:Apparent pore Rate is 7~13%;Average pore size is 0.5~3.0 μm;Thermal shock resistance 5 residual strength conservation rates of water cooling at 1100 DEG C are 86~96%;10000~12000h is corroded in the infiltration that matte-slag can effectively be kept out.
Therefore, the copper converter lower part prepared by present embodiment has with magnesia-forsterite-carbon composite There is the characteristics of environmental-friendly, microporosity is high, thermal shock resistance is good and anti-ice copper-slag penetration erosion performance is excellent.

Claims (10)

1. a kind of copper converter lower part preparation method of magnesia-forsterite-carbon composite, it is characterised in that first with 35 The fused magnesite particle of~55wt%, the forsterite particle of 10~30wt%, the caustic-calcined magnesite fine powder of 6~16wt%, 5~ The pyrophillite fine powder of 15wt%, the amorphous graphite micro mist of 3~7wt%, 3~7wt% Si2N2O/SiC/TiC/TiCN/C is compound Powder, the simple substance silica fine powder of 1~3wt%, the titanium aluminum carbide fine powder of 2~5wt% and 2~5wt% manganese monoxide fine powder be original Material, then the cobalt improved phenolic resin of the zirconia sol of the additional 2~5wt% of raw material and 3~5wt%, stir evenly, into Type, it is dry;Then 2~8h is kept the temperature under conditions of carbon atmosphere and 1200~1400 DEG C is buried to aoxidize to get copper converter lower part Magnesium-forsterite-carbon composite;
The SiO of the pyrophillite fine powder275 μm of content ﹥ 70wt%, grain size ﹤;
5 μm of C content the ﹥ 80wt%, grain size ﹤ of the amorphous graphite micro mist;
The Si2N2The preparation method of O/SiC/TiC/TiCN/C composite granules is:By pyrophillite fine powder, titanium oxide fine powder and coke Charcoal fine powder (3~5) in mass ratio: 1: 1 mixing is to get mixture;The phenolic aldehyde tree of 8~10wt% is added in the mixture Spheric granules is made with comminutor in fat;The spheric granules is put into saggar, then the saggar is placed in electric furnace, in stove Nitrogen atmosphere is maintained, atmosphere pressures are 0.01~0.03MPa, and temperature is 1350~1550 DEG C, keeps the temperature 2~4h, naturally cools to Room temperature;It is broken, granularity is finely ground to less than 0.075mm to get Si2N2O/SiC/TiC/TiCN/C composite granules.
2. the copper converter lower part according to claim 1 preparation method of magnesia-forsterite-carbon composite, It is characterized in that the content of MgO ﹥ 97wt% of the fused magnesite particle, grain size is 0.1~5mm.
3. the copper converter lower part according to claim 1 preparation method of magnesia-forsterite-carbon composite, It is characterized in that the content of MgO ﹥ 45wt% of the forsterite particle, grain size is 0.1~3mm.
4. the copper converter lower part according to claim 1 preparation method of magnesia-forsterite-carbon composite, It is characterized in that 45 μm of content of MgO the ﹥ 97wt%, grain size ﹤ of the caustic-calcined magnesite fine powder.
5. the copper converter lower part according to claim 1 preparation method of magnesia-forsterite-carbon composite, It is characterized in that 45 μm of Si contents the ﹥ 97wt%, grain size ﹤ of the simple substance silica fine powder.
6. the copper converter lower part according to claim 1 preparation method of magnesia-forsterite-carbon composite, It is characterized in that the Ti of the titanium aluminum carbide fine powder3AlC245 μm of content ﹥ 97wt%, grain size ﹤.
7. the copper converter lower part according to claim 1 preparation method of magnesia-forsterite-carbon composite, It is characterized in that 45 μm of MnO contents the ﹥ 97wt%, grain size ﹤ of the manganese monoxide fine powder.
8. the copper converter lower part according to claim 1 preparation method of magnesia-forsterite-carbon composite, It is characterized in that the ZrO of the zirconia sol2Content is 20~40wt%, and grain size is 20~70nm.
9. the copper converter lower part according to claim 1 preparation method of magnesia-forsterite-carbon composite, It is characterized in that the Co contents of the cobalt improved phenolic resin are 0.08~0.6wt%, carbon yield ﹥ 40wt%.
10. a kind of copper converter lower part magnesia-forsterite-carbon composite, it is characterised in that under the copper converter Portion is according to the copper converter lower part described in any one of claim 1~9 with magnesia-forsterite-carbon composite With the magnesia-forsterite of the copper converter lower part prepared by the preparation method of magnesia-forsterite-carbon composite- Carbon composite.
CN201810008918.9A 2018-01-04 2018-01-04 Magnesium oxide-forsterite-carbon composite material for lower part of copper smelting converter and preparation method thereof Active CN108129136B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810008918.9A CN108129136B (en) 2018-01-04 2018-01-04 Magnesium oxide-forsterite-carbon composite material for lower part of copper smelting converter and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810008918.9A CN108129136B (en) 2018-01-04 2018-01-04 Magnesium oxide-forsterite-carbon composite material for lower part of copper smelting converter and preparation method thereof

Publications (2)

Publication Number Publication Date
CN108129136A true CN108129136A (en) 2018-06-08
CN108129136B CN108129136B (en) 2020-10-30

Family

ID=62399352

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810008918.9A Active CN108129136B (en) 2018-01-04 2018-01-04 Magnesium oxide-forsterite-carbon composite material for lower part of copper smelting converter and preparation method thereof

Country Status (1)

Country Link
CN (1) CN108129136B (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108821785A (en) * 2018-06-27 2018-11-16 武汉钢铁有限公司 A kind of coating against binding slags for hot-rolling heating furnace water beam heat preservation lining
CN108840667A (en) * 2018-07-30 2018-11-20 合肥铭佑高温技术有限公司 A kind of preparation method of the high temperature resistant tundish dry material modified based on pyrophillite
CN110451994A (en) * 2019-08-01 2019-11-15 辽宁科技大学 A kind of casting material prefabricated part of magnesia firing of magnesium aluminate spinel whisker reinforcement
CN110540434A (en) * 2019-09-06 2019-12-06 辽宁科技大学 Preparation method of zirconia sol reinforced magnesium aluminate spinel porous ceramic
CN111704472A (en) * 2020-06-22 2020-09-25 湖南立达高新材料有限公司 Additive for anhydrous stemming and preparation method thereof
CN112778015A (en) * 2021-01-08 2021-05-11 武汉科技大学 Lightweight periclase-spinel-carbon refractory material and preparation method thereof
CN114620997A (en) * 2022-04-14 2022-06-14 郑州振东科技有限公司 Method for improving performance of low-carbon magnesia carbon brick
CN115259839A (en) * 2022-07-25 2022-11-01 中冶武汉冶金建筑研究院有限公司 Integral refractory castable for preheating section side wall of belt type roasting machine and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1944346A (en) * 2006-10-19 2007-04-11 武汉科技大学 Titanium nitride magnesia carbon brick containing carbon and its preparing method
CN101148362A (en) * 2007-09-03 2008-03-26 武汉科技大学 Forsterite-carbon refractory brick and preparation method thereof
CN102584282A (en) * 2012-01-19 2012-07-18 北京炜润达冶金材料有限公司 Thermal-state mending material taking forsterite as raw material for converters and preparation method thereof
CN105777151A (en) * 2016-02-23 2016-07-20 鞍山市奥鞍耐火材料有限责任公司 Magnesium aluminate spinel refractory material containing manganese and preparing method thereof
CN106631053A (en) * 2016-09-29 2017-05-10 武汉科技大学 Refractory material for steel tapping hole of converter and preparation method for refractory material

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1944346A (en) * 2006-10-19 2007-04-11 武汉科技大学 Titanium nitride magnesia carbon brick containing carbon and its preparing method
CN101148362A (en) * 2007-09-03 2008-03-26 武汉科技大学 Forsterite-carbon refractory brick and preparation method thereof
CN102584282A (en) * 2012-01-19 2012-07-18 北京炜润达冶金材料有限公司 Thermal-state mending material taking forsterite as raw material for converters and preparation method thereof
CN105777151A (en) * 2016-02-23 2016-07-20 鞍山市奥鞍耐火材料有限责任公司 Magnesium aluminate spinel refractory material containing manganese and preparing method thereof
CN106631053A (en) * 2016-09-29 2017-05-10 武汉科技大学 Refractory material for steel tapping hole of converter and preparation method for refractory material

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
赵雷: ""氧化钴溶胶复合酚醛树脂的热解碳结构变化",赵雷,《功能高分子学报》,第25卷,第1期,第58-61页", 《功能高分子学报》 *
陈希来: ""熔盐介质中制备Ti(C,N)及不同添加剂对炭砖性能的影响",陈希来,《中国优秀硕士学位论文全文数据库 工程科技Ⅰ辑》,第 02 期,第B023-7页", 《中国优秀硕士学位论文全文数据库 工程科技Ⅰ辑》 *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108821785B (en) * 2018-06-27 2021-03-16 武汉钢铁有限公司 Slag adhesion preventing coating for hot rolling heating furnace water beam heat insulation lining
CN108821785A (en) * 2018-06-27 2018-11-16 武汉钢铁有限公司 A kind of coating against binding slags for hot-rolling heating furnace water beam heat preservation lining
CN108840667A (en) * 2018-07-30 2018-11-20 合肥铭佑高温技术有限公司 A kind of preparation method of the high temperature resistant tundish dry material modified based on pyrophillite
CN110451994A (en) * 2019-08-01 2019-11-15 辽宁科技大学 A kind of casting material prefabricated part of magnesia firing of magnesium aluminate spinel whisker reinforcement
CN110451994B (en) * 2019-08-01 2022-08-16 辽宁科技大学 Magnesium-based sintered castable prefabricated member reinforced by magnesium aluminate spinel whiskers
CN110540434A (en) * 2019-09-06 2019-12-06 辽宁科技大学 Preparation method of zirconia sol reinforced magnesium aluminate spinel porous ceramic
CN111704472A (en) * 2020-06-22 2020-09-25 湖南立达高新材料有限公司 Additive for anhydrous stemming and preparation method thereof
CN111704472B (en) * 2020-06-22 2022-08-16 湖南立达高新材料有限公司 Additive for anhydrous stemming and preparation method thereof
CN112778015A (en) * 2021-01-08 2021-05-11 武汉科技大学 Lightweight periclase-spinel-carbon refractory material and preparation method thereof
CN112778015B (en) * 2021-01-08 2022-06-14 武汉科技大学 Lightweight periclase-spinel-carbon refractory material and preparation method thereof
CN114620997A (en) * 2022-04-14 2022-06-14 郑州振东科技有限公司 Method for improving performance of low-carbon magnesia carbon brick
CN114620997B (en) * 2022-04-14 2023-03-24 郑州振东科技有限公司 Method for improving performance of low-carbon magnesia carbon brick
CN115259839A (en) * 2022-07-25 2022-11-01 中冶武汉冶金建筑研究院有限公司 Integral refractory castable for preheating section side wall of belt type roasting machine and preparation method thereof
CN115259839B (en) * 2022-07-25 2023-03-21 中冶武汉冶金建筑研究院有限公司 Integral refractory castable for preheating section side wall of belt type roasting machine and preparation method thereof

Also Published As

Publication number Publication date
CN108129136B (en) 2020-10-30

Similar Documents

Publication Publication Date Title
CN108129136A (en) Copper converter lower part magnesia-forsterite-carbon composite and preparation method thereof
CN100560538C (en) A kind of ZrO that contains 2Magnesia carbon brick and preparation method thereof
CN107473756B (en) Multipurpose low-dimensional carbon-containing ceramic/carbon composite material and production method thereof
CN106187225B (en) A kind of anti-erosion magnesia carbon brick and preparation method thereof
CN102603343B (en) Fireproof material of furnace bottom of blast furnace hearth and preparation method of fireproof material
CN105622121B (en) Low-carbon magnesia-alumina-carbon brick of Ceramic bond and preparation method thereof under a kind of high temperature
CN105367092A (en) Spray coating capable of preventing slag adhesion
CN104003738B (en) Smelting separation furnace lining material and preparation method thereof
CN105152666B (en) A kind of AlON combinations aluminum-carbon refractory material and preparation method thereof
CN102070339B (en) Modified carbon raw material for carbon-containing refractory material and preparation method thereof
CN113999027A (en) Corundum-mullite castable for zinc oxide rotary kiln and preparation method thereof
CN108101561A (en) A kind of stainless steel smelting pouring materialfor steel ladle and preparation method thereof
CN110218080A (en) Nitridation in situ generates silicon nitride magnesium combination magnesia-carbon refractory material and preparation method thereof
CN1968551A (en) Treatment process and device for protective layer for reducing consumption of graphite electrode
CN108083775A (en) Copper converter top magnesia-composite material of silicon carbide and preparation method thereof
CN108164274A (en) A kind of calcium Zr refractory material and preparation method thereof
UA109330C2 (en) REFRACTORY MATERIAL FOR THE INTERNAL LINING OF THE BURNING OVEN, WHICH IS OBTAINED BY PARTIAL GRAPHITIZATION OF THE MIXTURE CONTAINING C AND Si
CN108002854B (en) High-thermal-conductivity high-corrosion-resistance electrically calcined coal-based carbon brick and preparation method thereof
JPS6141862B2 (en)
JP4791761B2 (en) Carbon-containing refractories
CN112745138B (en) Whisker-reinforced lightweight aluminum-zirconium-carbon refractory material and preparation method thereof
CN106631150B (en) A kind of high voltage isolator insulation column and preparation method thereof
CN102424592B (en) Zirconia slide plate and preparation method thereof
EP0116194A1 (en) A carbon-containing refractory
Bagherabadi et al. Synthesis of dehydrated magnesium borate powders and the effect on the properties of MgO-C refractories

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