CN114524667A - High-stability low-cost preparation process for artificially synthesized mullite - Google Patents

High-stability low-cost preparation process for artificially synthesized mullite Download PDF

Info

Publication number
CN114524667A
CN114524667A CN202111651101.1A CN202111651101A CN114524667A CN 114524667 A CN114524667 A CN 114524667A CN 202111651101 A CN202111651101 A CN 202111651101A CN 114524667 A CN114524667 A CN 114524667A
Authority
CN
China
Prior art keywords
raw material
steps
following
mullite
raw materials
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.)
Pending
Application number
CN202111651101.1A
Other languages
Chinese (zh)
Inventor
华志高
曹超
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.)
Jiangsu Xinshi High Temperature Material Co ltd
Original Assignee
Jiangsu Xinshi High Temperature Material Co ltd
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 Jiangsu Xinshi High Temperature Material Co ltd filed Critical Jiangsu Xinshi High Temperature Material Co ltd
Priority to CN202111651101.1A priority Critical patent/CN114524667A/en
Publication of CN114524667A publication Critical patent/CN114524667A/en
Pending legal-status Critical Current

Links

Images

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
    • C04B35/16Shaped 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 silicates other than clay
    • C04B35/18Shaped 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 silicates other than clay rich in aluminium oxide
    • C04B35/185Mullite 3Al2O3-2SiO2
    • 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
    • C04B35/6303Inorganic additives
    • 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
    • C04B35/64Burning or sintering processes
    • 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
    • C04B35/653Processes involving a melting step
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B15/00Other processes for the manufacture of iron from iron compounds
    • C21B15/02Metallothermic processes, e.g. thermit reduction
    • 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
    • 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
    • C04B2235/327Iron group oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3272Iron oxides or oxide forming salts thereof, e.g. hematite, magnetite
    • 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
    • C04B2235/34Non-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
    • C04B2235/40Metallic constituents or additives not added as binding phase
    • C04B2235/402Aluminium
    • 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
    • C04B2235/656Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Metallurgy (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)

Abstract

The invention discloses a high-stability low-cost preparation process for artificially synthesized mullite, which belongs to the technical field of mullite, and comprises the following steps: the method comprises the following steps of firstly, preparing raw materials in advance, wherein the raw materials comprise a raw material A, a raw material B and a raw material C, carrying out primary crushing, screening and airing on all the raw materials, secondly, proportioning and mixing ferric oxide and aluminum simple substances in the raw material A, carrying out alumina proportion adjustment on high bauxite and kaolin contained in the raw material B, and drying and crushing. The method has the advantages that the aluminothermic reaction generated by combining the elemental aluminum and the ferric oxide can realize the preliminary hot melting of various raw materials, the heating energy consumption ratio is saved in the subsequent sintering process of the kiln, the production energy consumption ratio for producing the mullite can be reduced, a large amount of waste gas cannot be generated, the actual environmental protection performance is higher, and the proportion of various raw materials to the aluminum oxide is utilized.

Description

High-stability low-cost preparation process for artificially synthesized mullite
Technical Field
The invention relates to the technical field of mullite, in particular to a high-stability low-cost preparation process for artificially synthesized mullite.
Background
Mullite refers to a series of minerals composed of aluminosilicate and is generally called, it is worth mentioning that a SiO2-Al2O3 system is the most important binary system in ceramics, more than ten different phase diagrams are published in succession from a first mullite phase diagram published in 1909, the focus of controversy is whether mesophase mullite is a stable compound or an unstable compound, and later problems are unified, the components of the mullite are not fixed, and the alumina content of the mullite fluctuates between 72% and 78%.
The existing mullite production usually needs to adopt high-purity electric melting, common electric melting, all-natural sintering and light burning, a large amount of waste gas and waste are generated in the actual production process, the actual environmental protection effect is poor, in the subsequent recording process, the production cost is found to be high, the energy consumption mainly concentrated in the heating stage is high, a large amount of time is spent, the raw materials are wasted in primary heating, and the quality of a finished product is not stable.
Disclosure of Invention
The invention aims to provide a preparation process for artificially synthesizing mullite with high stability and low cost. According to the high-stability low-cost preparation process for artificially synthesized mullite, disclosed by the invention, the aluminothermic reaction generated by combining the elemental aluminum and the ferric oxide can realize the primary hot melting of various raw materials, the energy consumption ratio of heating is saved in the subsequent sintering process of a kiln, the heat preservation is well carried out, the production energy consumption ratio of the produced mullite can be reduced, a large amount of waste gas cannot be generated, the actual environmental protection performance is higher, and the stable finished product quality can be realized by utilizing the proportion of various raw materials to the aluminum oxide.
In order to achieve the above effects, the present invention provides the following technical solutions: a high-stability low-cost preparation process for artificially synthesized mullite comprises the following steps:
the method comprises the steps of firstly, preparing raw materials in advance, wherein the raw materials comprise a raw material A, a raw material B and a raw material C, and performing primary crushing, screening and airing on all the raw materials.
And step two, proportioning and mixing ferric oxide and the simple substance aluminum in the raw material A, adjusting the alumina proportion of the high-alumina bauxite and kaolin contained in the raw material B, drying and crushing.
And step three, the raw material C comprises silicon dioxide, calcium hexaluminate and calcium oxide, is subjected to wet grinding by a ball mill, and is dried and broken up.
And step four, firstly, placing the raw material A into the reaction kettle, igniting the raw material A by using magnesium powder, then, putting sufficient raw material B into the reaction kettle, removing liquid molten iron, and then, putting the raw material C into the reaction kettle.
And fifthly, firing by using a kiln at 1450-1800 ℃, and cooling to obtain a finished product.
Further, the method comprises the following steps: according to the operation steps in the first step, the raw materials A, B and C need to be humidified in advance before being prepared, and the humidity is kept at 15%.
Further, the method comprises the following steps: according to the operation steps in the second step, the molar mass ratio of the ferric oxide to the simple substance aluminum is 2: 1-1.25.
Further, the method comprises the following steps: according to the operation steps in the second step, the alumina content of the high bauxite and the kaolin is not less than 45%.
Further, the method comprises the following steps: according to the operating procedure in step three, the ratio of silica, calcium hexaluminate and calcium oxide is 5: 1: 2. further, the method comprises the following steps: according to the operation steps in the third step, the water content of the dried and scattered raw material C is lower than 1%. Further, the method comprises the following steps: according to the operation steps in the fourth step, the water content of the dried raw material C is lower than 1%. Further, the method comprises the following steps: and (4) according to the operation steps in the fourth step, liquid molten iron is removed, the inclined reaction kettle is adopted, so that the molten iron flows out, and the residual molten iron is oxidized to generate iron oxide when the temperature is reduced and the C raw material is waited.
Further, the method comprises the following steps: according to the operation steps in the fifth step, the firing time of the kiln is controlled to be 5-12 hours, the heating temperature is increased by 100 ℃ every ten minutes in the first 1 hour.
Further, the method comprises the following steps: and cooling according to the operation steps in the fifth step, wherein the temperature needs to be reduced to 780 ℃ for 1 hour.
The invention provides a high-stability low-cost preparation process for artificially synthesized mullite, which has the following beneficial effects:
the high-stability low-cost preparation process for artificially synthesized mullite can realize preliminary hot melting of various raw materials by combining aluminothermic reaction generated by the elemental aluminum and the ferric oxide, saves the energy consumption ratio of heating in the subsequent sintering process of a kiln, well preserves heat, can reduce the production energy consumption ratio of the produced mullite, does not generate a large amount of waste gas, has higher actual environmental protection performance, and can realize stable finished product quality by utilizing the proportion of various raw materials to aluminum oxide.
Drawings
FIG. 1 is a schematic diagram of the present invention.
Detailed Description
The invention provides a technical scheme that: referring to fig. 1, a process for preparing synthetic mullite with high stability and low cost includes the following steps:
the method comprises the steps of firstly, preparing raw materials in advance, wherein the raw materials comprise a raw material A, a raw material B and a raw material C, and performing primary crushing, screening and airing on all the raw materials.
And step two, proportioning and mixing ferric oxide and the simple substance aluminum in the raw material A, adjusting the alumina proportion of the high-alumina bauxite and kaolin contained in the raw material B, drying and crushing.
And step three, the raw material C comprises silicon dioxide, calcium hexaluminate and calcium oxide, is subjected to wet grinding by a ball mill, and is dried and broken up.
And step four, firstly, placing the raw material A into the reaction kettle, igniting the raw material A by using magnesium powder, then, putting sufficient raw material B into the reaction kettle, removing liquid molten iron, and then, putting the raw material C into the reaction kettle.
And fifthly, firing by using a kiln at 1450-1800 ℃, and cooling to obtain a finished product.
Specifically, the method comprises the following steps: according to the operation steps in the first step, the raw materials A, B and C need to be humidified in advance before being prepared, and the humidity is kept at 15%.
Specifically, the method comprises the following steps: according to the operation steps in the second step, the molar mass ratio of the ferric oxide to the simple substance aluminum is 2: 1-1.25.
Specifically, the method comprises the following steps: according to the operation steps in the second step, the alumina content of the high bauxite and the kaolin is not less than 45%.
Specifically, the method comprises the following steps: according to the operating procedure in step three, the ratio of silica, calcium hexaluminate and calcium oxide is 5: 1: 2.
specifically, the method comprises the following steps: according to the operation steps in the third step, the water content of the dried and scattered raw material C is lower than 1 percent
Specifically, the method comprises the following steps: according to the operation steps in the fourth step, the water content of the dried raw material C is lower than 1%.
Specifically, the method comprises the following steps: and (4) according to the operation steps in the fourth step, liquid molten iron is removed, the inclined reaction kettle is adopted, so that the molten iron flows out, and the residual molten iron is oxidized to generate iron oxide when the temperature is reduced and the C raw material is waited.
Specifically, the method comprises the following steps: according to the operation steps in the fifth step, the firing time of the kiln is controlled to be 5-12 hours, the heating temperature is increased by 100 ℃ every ten minutes in the first 1 hour.
Specifically, the method comprises the following steps: and cooling according to the operation steps in the fifth step, wherein the temperature needs to be reduced to 780 ℃ for 1 hour. The methods of the examples were carried out for detection analysis,
and compared with the prior art, the following data are obtained:
production cost Environmental protection performance Energy consumption ratio
Examples Is lower than Is higher than Is lower than
Prior Art Is higher than Is lower than Is higher than
According to the table data, when the embodiment is implemented, the high-stability low-cost preparation process for the artificially synthesized mullite is adopted, the high-stability low-cost preparation process for the artificially synthesized mullite can realize the preliminary hot melting of various raw materials by combining the aluminothermic reaction generated by the simple substance aluminum and the ferric oxide, saves the energy consumption ratio of heating in the subsequent sintering process of the kiln, well preserves the heat, can reduce the production energy consumption ratio of the mullite, does not generate a large amount of waste gas, has higher actual environmental protection performance, and can realize stable finished product quality by utilizing the proportion of the various raw materials to the aluminum oxide. The invention provides a high-stability low-cost preparation process of artificially synthesized mullite, which comprises the following steps:
the method comprises the following steps of firstly, preparing raw materials in advance, wherein the raw materials comprise a raw material A, a raw material B and a raw material C, performing primary crushing, screening and airing on all the raw materials, humidifying the raw materials A, B and C in advance before preparation, keeping the humidity at 15%, secondly, proportioning and mixing ferric oxide and an aluminum simple substance in the raw material A, adjusting the alumina proportion of high bauxite and kaolin contained in the raw material B, drying and crushing, and performing molar mass proportioning of the ferric oxide and the aluminum simple substance to be 2: 1-1.25, the content of alumina in the high-alumina bauxite and kaolin is not less than 45%, in the third step, the raw material C contains silica, calcium hexaluminate and calcium oxide, wet grinding is carried out by adopting a ball mill, then air drying and scattering are carried out, and the proportion of the silica, the calcium hexaluminate and the calcium oxide is 5: 1: 2, the water content of the C material after being dried and scattered is lower than 1%, step four, firstly, the A material is placed in the reaction kettle, the A material is ignited by utilizing magnesium powder, the principle of thermit reaction is that a redox reaction of aluminum simple substance is carried out under the condition of high temperature, the strong reducibility of aluminum is reflected, because the enthalpy of formation (-1645kJ/mol) of aluminum oxide is extremely low, huge heat can be emitted by the reaction, even the generated metal can appear in a molten state, on the other hand, the reaction emits large amount of heat to melt aluminum, the reaction speed is extremely high in the liquid phase, a great amount of heat can be emitted in a short time, the intensity of the thermit reaction is determined by the oxidability of metal ions, according to estimation, 500 g of thermit (the components are iron oxide and aluminum) can be burnt out in 30 seconds, at this moment, a sufficient amount of the B material is put into the reaction kettle, liquid molten iron is removed, and putting the C raw material into a reaction kettle, wherein the water content of the dried C raw material is lower than 1%, removing liquid molten iron, inclining the reaction kettle to enable the molten iron to flow out, and oxidizing the residual molten iron to generate ferric oxide when the temperature of the residual molten iron is reduced to wait for the C raw material, wherein the sintering temperature is 1450-1800 ℃, a finished product can be prepared after cooling, the sintering time of the kiln is controlled for 5-12 hours, the heating temperature is increased by 100 ℃ every ten minutes for 1 hour, cooling is carried out until the temperature is reduced to 780 ℃, and the cooling lasts for 1 hour, wherein the actual main components of the finished product are 68-73% of aluminum oxide, less than or equal to 1.0% of ferric oxide and 22-25% of silicon oxide.
Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.

Claims (10)

1. The preparation process of artificially synthesized mullite with high stability and low cost is characterized by comprising the following steps:
s1, preparing raw materials in advance, wherein the raw materials comprise a raw material A, a raw material B and a raw material C, and performing primary crushing, screening and airing on all the raw materials;
s2, proportioning and mixing ferric oxide and aluminum simple substance in the raw material A, adjusting the alumina proportion of high bauxite and kaolin contained in the raw material B, drying and crushing;
s3, grinding the raw material C containing silicon dioxide, calcium hexaluminate and calcium oxide by a ball mill in a wet method, and then airing and scattering;
s4, firstly, placing the raw material A into a reaction kettle, igniting the raw material A by using magnesium powder, then, putting sufficient raw material B into the reaction kettle, removing liquid molten iron, and then, putting the raw material C into the reaction kettle;
and S5, firing by using a kiln at 1450-1800 ℃, and cooling to obtain the finished product.
2. The process for preparing artificial mullite according to claim 1, which comprises the following steps: according to the operation procedure in S1, the raw materials a, B and C need to be humidified in advance before being prepared, and the humidity is maintained at 15%.
3. The process for preparing artificial mullite according to claim 2, which comprises the following steps: according to the operation step in S2, the molar mass ratio of the ferric oxide to the aluminum simple substance is 2: 1-1.25.
4. The process for preparing artificial mullite according to claim 3, which comprises the following steps: according to the operation procedure in S2, the alumina content of the high bauxite and the kaolin is not less than 45%.
5. The process for preparing artificial mullite according to claim 4, which comprises the following steps: according to the operating procedure in S3, the ratio of silica, calcium hexaluminate and calcium oxide is 5: 1: 2.
6. the process for preparing artificial mullite according to claim 5, which comprises the following steps: according to the operation step in S3, the water content of the dried and scattered raw material C is lower than 1%.
7. The process for preparing artificial mullite according to claim 6, which comprises the following steps: according to the operation step in S4, the moisture content of the dried raw material C is lower than 1%.
8. The process for preparing artificial mullite according to claim 7, which comprises the following steps: according to the operation step in the S4, liquid molten iron is removed, the reaction kettle is inclined, so that the molten iron flows out, and the residual molten iron is oxidized to generate iron oxide when the temperature is reduced and the residual molten iron is waiting for the raw material C.
9. The process for preparing artificial mullite according to claim 8, which comprises the following steps: according to the operation steps in the S5, the firing time of the kiln is controlled to be 5-12 hours, the heating temperature is increased by 100 ℃ every ten minutes in the first 1 hour.
10. The process for preparing artificial mullite according to claim 9, which comprises the following steps: according to the operation step in S5, the cooling needs to be carried out at 780 ℃ for 1 hour.
CN202111651101.1A 2021-12-30 2021-12-30 High-stability low-cost preparation process for artificially synthesized mullite Pending CN114524667A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202111651101.1A CN114524667A (en) 2021-12-30 2021-12-30 High-stability low-cost preparation process for artificially synthesized mullite

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202111651101.1A CN114524667A (en) 2021-12-30 2021-12-30 High-stability low-cost preparation process for artificially synthesized mullite

Publications (1)

Publication Number Publication Date
CN114524667A true CN114524667A (en) 2022-05-24

Family

ID=81621175

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202111651101.1A Pending CN114524667A (en) 2021-12-30 2021-12-30 High-stability low-cost preparation process for artificially synthesized mullite

Country Status (1)

Country Link
CN (1) CN114524667A (en)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB716265A (en) * 1951-06-13 1954-09-29 Babcock & Wilcox Co Mullite refractories
CN1312237A (en) * 2001-02-16 2001-09-12 张世平 Artificial mullite synthesizing process
CN101805197A (en) * 2010-04-22 2010-08-18 上海海事大学 Production method of corundum-mullite-zirconia
CN101905969A (en) * 2010-09-06 2010-12-08 山西高科耐火材料股份有限公司 Bauxite-based low-creep mullite product
CN103408297A (en) * 2013-08-26 2013-11-27 武汉科技大学 Calcium hexaluminate-mullite composite material and preparation method thereof
CN106220190A (en) * 2015-11-12 2016-12-14 中国科学院过程工程研究所 A kind of method utilizing aluminous fly-ash to prepare mullite
CN106431370A (en) * 2016-09-09 2017-02-22 武汉科技大学 Mullite raw material adopting alumina-chrome slag as main ingredient and preparation method thereof
CN112430756A (en) * 2020-10-13 2021-03-02 中色(宁夏)东方集团有限公司 Niobium-iron alloy production method

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB716265A (en) * 1951-06-13 1954-09-29 Babcock & Wilcox Co Mullite refractories
CN1312237A (en) * 2001-02-16 2001-09-12 张世平 Artificial mullite synthesizing process
CN101805197A (en) * 2010-04-22 2010-08-18 上海海事大学 Production method of corundum-mullite-zirconia
CN101905969A (en) * 2010-09-06 2010-12-08 山西高科耐火材料股份有限公司 Bauxite-based low-creep mullite product
CN103408297A (en) * 2013-08-26 2013-11-27 武汉科技大学 Calcium hexaluminate-mullite composite material and preparation method thereof
CN106220190A (en) * 2015-11-12 2016-12-14 中国科学院过程工程研究所 A kind of method utilizing aluminous fly-ash to prepare mullite
CN106431370A (en) * 2016-09-09 2017-02-22 武汉科技大学 Mullite raw material adopting alumina-chrome slag as main ingredient and preparation method thereof
CN112430756A (en) * 2020-10-13 2021-03-02 中色(宁夏)东方集团有限公司 Niobium-iron alloy production method

Similar Documents

Publication Publication Date Title
CN105540627A (en) Preparation method for clinker of alumina produced by sintering process
US20120160135A1 (en) Process for the Manufacture of Synthetic Pozzolan
CN102839249B (en) Method for producing iron fine powder by directly reducing high-iron red mud with rotary hearth furnace
CN107216127A (en) Dehua pearl white porcelain and its preparation technology
CN108178516A (en) A kind of preparation and application of ceramic color glaze
CN108892478B (en) Low-temperature porcelain and preparation method thereof
CN110028091A (en) A kind of Bayer process red mud production aluminium oxide wet laid furnishes dry sintering technique
CN114524667A (en) High-stability low-cost preparation process for artificially synthesized mullite
CN109095904A (en) A kind of low temperature fast firing Dali stone ceramic tile and preparation method thereof
CN109265001A (en) Ice-crack-like glaze, ice-crack-like glaze ceramic and production method
CN110331021B (en) Method for improving combustion heat efficiency of straw biomass charcoal
CN107162563A (en) It is a kind of unleaded nontoxic from releasing glaze ceramic ware for daily use
US3341289A (en) Production of ortho phosphoric acid
CN103819174A (en) Sintered ceramsite adopting tailings generated during germanium extraction of lignite as main raw material and preparation method of sintered ceramsite
CN102199040B (en) Novel sink head brick and its processing technology
CN109133651A (en) It is a kind of by mentioning the devitrified glass that titanium slag is prepared containing chlorine
CN115231580A (en) Method for preparing forsterite and magnesite by sintering fine granular magnesite flotation tailings
CN108285271A (en) A kind of method that original position vapour deposition process fires the red glaze of imitative an ancient unit of weight
CN113277838A (en) One-time sintering alumina ceramic glazing method and product
CN106747297A (en) Red stoneware tea kettle and preparation method thereof
CN105925747A (en) High-performance slag collecting agent
JP2864165B2 (en) Shaped charcoal and coffee bean roasting method using the shaped charcoal
CN109231961A (en) A kind of resistance to deformation is rapidly fired to fine earthenware blank and its preparation and application method
CN109336431A (en) Make the producing cement from phosphor sulfuric acid new method of anti-agglomerant using calcium oxide as intermediate sulphur
CN115557526B (en) Energy-saving method for cerium oxide tunnel kiln

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
RJ01 Rejection of invention patent application after publication

Application publication date: 20220524

RJ01 Rejection of invention patent application after publication