CN114890803A - Preparation method of high-temperature oxide melt containing superoxide radical - Google Patents

Preparation method of high-temperature oxide melt containing superoxide radical Download PDF

Info

Publication number
CN114890803A
CN114890803A CN202210619484.2A CN202210619484A CN114890803A CN 114890803 A CN114890803 A CN 114890803A CN 202210619484 A CN202210619484 A CN 202210619484A CN 114890803 A CN114890803 A CN 114890803A
Authority
CN
China
Prior art keywords
temperature oxide
oxide melt
mol
temperature
crucible
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
CN202210619484.2A
Other languages
Chinese (zh)
Inventor
黄奥
彭越芳
李昇昊
顾华志
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wuhan University of Science and Engineering WUSE
Original Assignee
Wuhan University of Science and Engineering WUSE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wuhan University of Science and Engineering WUSE filed Critical Wuhan University of Science and Engineering WUSE
Priority to CN202210619484.2A priority Critical patent/CN114890803A/en
Publication of CN114890803A publication Critical patent/CN114890803A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/66Monolithic refractories or refractory mortars, including those whether or not containing clay
    • 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
    • C04B35/057Shaped 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 calcium oxide
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B9/00General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
    • C22B9/10General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals with refining or fluxing agents; Use of materials therefor, e.g. slagging or scorifying agents
    • C22B9/106General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals with refining or fluxing agents; Use of materials therefor, e.g. slagging or scorifying agents the refining being obtained by intimately mixing the molten metal with a molten salt or slag
    • 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
    • C04B2235/3206Magnesium oxides 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
    • C04B2235/3217Aluminum 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
    • C04B2235/327Iron 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
    • C04B2235/50Constituents 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
    • C04B2235/65Aspects 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
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Compounds Of Iron (AREA)
  • Glass Compositions (AREA)

Abstract

The invention discloses a preparation method of a high-temperature oxide melt containing superoxide radicals, which is characterized by comprising the following steps: according to CaO: 30 to 60 wt% of Al 2 O 3 :20~35wt%,MgO:0~15wt%,SiO 2 :8~15wt%,Fe 2 O 3 : 0-10 wt% of the components, uniformly mixing by using a mixing and grinding method, putting the mixture into a crucible, putting the crucible into a high-temperature furnace in air or argon atmosphere, heating to 1500-1700 ℃ to melt the mixture, and keeping the temperature to obtain a high-temperature oxide melt containing rich superoxide radicals; by changing CaO, MgO and Fe 2 O 3 The content of the superoxide radical can be regulated to 1.007 × 10 ‑5 mol/g to 9.078X 10 ‑5 In the mol/g range. The high-temperature oxide melt has high reactivity and high solubilityFast impurity desorption and high molten steel purifying capacity.

Description

Preparation method of high-temperature oxide melt containing superoxide radical
Technical Field
The invention belongs to the technical field of high-temperature melts, and particularly relates to a preparation method of a high-temperature oxide melt containing superoxide radicals.
Background
The high-temperature oxide melt is widely used in the fields of metallurgy and building materials, such as cement and glass synthesis, 3D ceramic printing, geology and the like. Such asIn the ferrous metallurgy industry, CaO-Al is generally adopted 2 O 3 -SiO 2 The system melt plays a role in absorbing impurities and purifying molten steel. The metallurgical properties of the oxide melt are closely related to its structure. At present, there are four main slag structure theories or hypotheses, which are a molecular structure theory, an ionic structure theory, an ion-molecule coexistence theory and a polymer theory, respectively. In none of these structural theories, the existence of free radicals is mentioned, and the free radicals (including singlet oxygen, superoxide radical, hydroxyl radical, etc.) widely exist in the research of organic chemistry such as photocatalysis, biomaterials, and medicinal chemistry, and have important influence on the reaction activity. Therefore, the exploration of the high-temperature oxide melt containing the free radicals and the regulation and control method thereof are urgently needed, which have important significance for the production of high-quality clean steel and provide reference for geological research and other related fields.
Disclosure of Invention
The invention provides a preparation method of a high-temperature oxide melt containing superoxide radicals, which is characterized in that CaO, MgO and Fe2O in high-temperature oxide components are subjected to reaction 3 The content of the superoxide radical can be adjusted and controlled by adjusting the content of the superoxide radical, the specific technical scheme is as follows,
according to CaO: 30 to 60 wt% of Al 2 O 3 :20~35wt%,MgO:0~15wt%,SiO 2 :8~15 wt%,Fe 2 O 3 : 0-10 wt% of a mixture is formed, and the mixture is uniformly mixed by using a mixing and grinding method; and putting the mixture into a crucible, putting the crucible into a high-temperature furnace in an air or argon atmosphere, heating to 1500-1700 ℃ to melt the mixture, and preserving the temperature to form a high-temperature oxide melt containing the superoxide radical. By varying the CaO, MgO or Fe in the mixture 2 O 3 The mass fraction of (a) regulates the content of superoxide radicals in the high-temperature oxide melt. The content of superoxide radical in the high-temperature oxide melt is 1.007 × 10 -5 mol/g to 9.078X 10 -5 mol/g。
Further, the content of superoxide radical in the above high-temperature oxide melt was 1.007X 10 by varying the CaO mass fraction within a range of 50 to 60 wt% -5 mol/g to 9.078X 10 -5 mol/g。
Further, the content of superoxide radical in the high-temperature oxide melt was 1.746X 10 by varying the MgO mass fraction in the range of 0 to 13 wt% -5 mol/g to 3.87X 10 -5 mol/g。
Further, Fe is changed within the range of 0 to 10 wt% 2 O 3 The content of superoxide radical in the high-temperature oxide melt is 1.648 multiplied by 10 -5 To 3.864 × 10 -5 mol/g。
Further, Al in the above mixture 2 O 3 、SiO 2 CaO, MgO or Fe 2 O 3 The purity is more than or equal to 98wt percent and the granularity is less than or equal to 88 mu m.
Further, CaCO is used as the CaO 3
Further, the mixing and grinding method is planetary ball milling, vibration milling, air flow milling, hammer milling or wet milling.
Further, the crucible is a platinum crucible, a graphite crucible, a corundum crucible or a magnesium oxide crucible.
Compared with the prior art, the invention has the following beneficial effects:
the invention is to CaO, MgO and Fe in the high-temperature oxide component 2 O 3 The content of the oxygen radicals can be regulated and controlled by regulating the content of the oxygen radicals, and the high-temperature oxide melt prepared by the method has the advantages of high reaction activity, high speed of dissolving and absorbing impurities, strong molten steel purifying capacity and the like.
The oxide melt structure in the invention forms a plurality of complexes at high temperature, and simultaneously, the temperature and CaO, MgO and Fe are regulated and controlled 2 O 3 The content of the free oxygen can be regulated and controlled to release different contents of free oxygen, the two lone pair electrons in the original parallel spins of the free oxygen in the melt are opposite in spins under the high-temperature thermal activation, a plurality of singlet oxygen are generated in the oxide melt, and the singlet oxygen can capture electrons of ionic groups in the melt (such as [ SiO ] 4 ] 4- ,[Si 2 O 7 ] 6- ,[Si 2 O 6 ] 4- ,[Si 2 O 5 ] 2- ,[AlO 4 ] 5- Al-O-Si, ferritetrahedron, octahedronSi-O-Si, Ca-O, Mg-O), are converted to superoxide radicals, all provoking multiple local reaction perturbations within the system. At the same time, the superoxide radical will lose electrons and convert into singlet oxygen, the singlet oxygen and superoxide radical are converted into each other, and the formula of the autocatalysis reaction is
Figure BDA0003669560950000031
(wherein A is the above-mentioned ionic group), the activity of the oxide melt can be greatly improved by the nonlinear reaction of singlet oxygen and superoxide radical, so that the high-temperature oxide melt has the advantages of high reaction activity, fast inclusion dissolution and absorption, strong molten steel purification capability and the like.
Detailed Description
The invention will be further described with reference to specific embodiments:
firstly, according to CaO: 30 to 60 wt% of Al 2 O 3 :20~35wt%,MgO:0~15wt%,SiO 2 : 8~15wt%,Fe 2 O 3 : 0-1 Owt% of Al in the mixture 2 O 3 、 SiO 2 CaO, MgO or Fe 2 O 3 The purity is more than or equal to 98wt percent and the granularity is less than or equal to 88 mu m. And uniformly mixing the mixture by using a mixing and grinding method, wherein the mixing and grinding method is planetary ball milling, vibration milling, jet milling, hammer milling or wet milling.
The mixture is then placed in a crucible, which may be selected from a platinum crucible, a graphite crucible, a corundum crucible, or a magnesium oxide crucible. Then the crucible is put into a high temperature furnace with air or argon atmosphere, and the temperature is raised to 1500 ℃ to 1700 ℃ to melt and preserve the temperature, so as to form a high temperature oxide melt containing superoxide radicals.
By varying the content of CaO, MgO or Fe in the above mixture 2 O 3 The content of the superoxide radical in the high-temperature oxide melt is regulated and controlled by the mass fraction, the content of the superoxide radical is detected by using an electron spin spectrometer (ESR), the quenching mode is that the quenching slag is poured on a copper plate for circulating water cooling for quenching, the quenching rate is 200-400 ℃/s, and the content of the superoxide radical in the high-temperature oxide melt is measured and obtained1.007×10 -5 mol/g to 9.078X 10 -5 mol/g. The CaO mass fraction is changed within the range of 50-60 wt%, and the content of superoxide radical in the high-temperature oxide melt is 1.007 x 10 -5 mol/g to 9.078X 10 -5 mol/g. Changing MgO mass fraction in the range of 0-13 wt%, the content of superoxide radical in the high temperature oxide melt is 1.746 × 10 -5 mol/g to 3.87X 10 -5 mol/g. Varying Fe in the range of 0-10 wt% 2 O 3 The mass fraction of the superoxide radical in the high-temperature oxide melt is 1.648 multiplied by 10 -5 To 3.864 × 10 -5 mol/g。
Example 1
In this example, according to Al 2 O 3 :34~36wt%,SiO 2 : 11-15 wt%, CaO: mixing 50-60 wt% of the raw materials by a ball milling method, putting the mixture into a graphite crucible, putting the graphite crucible into a high-temperature furnace in an argon atmosphere, heating to 1500 ℃ to melt the mixture, and keeping the temperature to obtain a high-temperature oxide melt containing superoxide radicals;
in this example, the content of the high temperature oxide melt containing a superoxide radical was changed from 1.007X 10 by changing the content of CaO therein from 50 to 60 wt% -5 mol/g to 4.92X 10 -5 mol/g。
Example 2
In this example, according to Al 2 O 3 :34~36wt%,SiO 2 : 8-11 wt%, CaO: mixing 30-50 wt% of the raw materials by a ball milling method, putting the mixture into a platinum crucible, putting the platinum crucible into a high-temperature furnace in an argon atmosphere, heating to 1600 ℃, melting and preserving heat to obtain a high-temperature oxide melt containing rich superoxide radicals; the content of the superoxide radical in the active carbon can be regulated from 2.68X 10 by changing the content of CaO in the active carbon from 50 to 60wt percent -5 mol/g to 9.078X 10 - 5 mol/g。
Example 3
In this example, the ratio of MgO: 1 to 5 wt% of Al 2 O 3 :34~30wt%,SiO 2 : 12-14 wt%, CaO: 50-53 wt%, mixing by ball milling method,putting the mixture into a graphite crucible, putting the graphite crucible into a high-temperature furnace, heating to 1600 ℃ to melt the mixture and preserving the temperature to obtain a high-temperature oxide melt containing rich superoxide radicals;
in this example, the superoxide radical decreased gradually from 2.048X 10 by changing the MgO content therein from 1 to 5 wt% -5 mol/g to 1.746X 10 -5 mol/g。
Example 4
In this example, the ratio of MgO: 5 to 8 wt% of Al 2 O 3 :30~27wt%,SiO 2 : 12-14 wt%, CaO: mixing 51-53 wt% by ball milling method, placing the mixture into a graphite crucible, placing into a high temperature furnace in argon atmosphere, heating to 1600 deg.C for melting and maintaining the temperature, changing MgO content from 5-8 wt%, increasing content of superoxide radical generated from high temperature oxide melt from 1.746 × 10 -5 mol/g to 3.158X 10 -5 mol/g。
Example 5
In this example, the ratio of MgO: 8 to 10 wt% of Al 2 O 3 :27~25wt%,SiO 2 : 12-14 wt%, CaO: mixing 51-53 wt% by using a ball milling method, putting the mixture into a graphite crucible, placing the graphite crucible into a high-temperature furnace, heating to 1600 ℃, melting and preserving heat. The content of MgO is changed from 8 to 10 wt%, and the content of superoxide radical generated by high-temperature oxide melt is reduced from 3.158 × 10 -5 mol/g to 2.704X 10 -5 mol/g。
Example 6
This example is carried out according to MgO: 10 to 15 wt% of Al 2 O 3 :25~20wt%,SiO 2 : 12-14 wt%, CaO: mixing 51-53 wt% by using a ball milling method, placing the mixture into a graphite crucible, placing the graphite crucible into a high-temperature furnace in an argon atmosphere, heating to 1700 ℃ to melt the mixture, and keeping the temperature. The content of MgO is changed from 10 to 15 wt%, and the content of superoxide radical generated by high-temperature oxide melt is increased from 2.704X 10 -5 mol/g to 3.87X 10 -5 mol/g。
Example 7
This example is carried out according to MgO: 1 to 15 wt% of Al 2 O 3 :35~30wt%,SiO 2 : 11-13 wt%, CaO: mixing 45-52 wt% of the raw materials by a ball milling method, putting the mixture into a platinum crucible, putting the platinum crucible into a high-temperature furnace, heating to 1600 ℃, melting and preserving heat. The content of MgO is changed from 1 to 15 wt%, and the content of superoxide radical generated by high-temperature oxide melt is increased and stabilized from 2.078X 10 -5 mol/g to 3.146X 10 -5 mol/g。
Example 8
This example is in accordance with Fe 2 O 3 :1~10wt%,Al 2 O 3 :22~35wt%,SiO 2 : 12-13 wt%, CaO: 52 wt%, ball milling to mix, placing the mixture into a platinum crucible, placing the platinum crucible into a high temperature furnace, heating to 1600 ℃ to melt and keeping the temperature. Change of Fe therein 2 O 3 From 1 to 10 wt.%, the content of superoxide radicals generated by the high-temperature oxide melt is increased from 1.648X 10 -5 mol/g to 3.864 × 10 -5 mol/g。
Example 9
This example is carried out according to MgO: 1 to 5 wt% of Fe 2 O 3 :5wt%,Al 2 O 3 :30wt%,SiO 2 : 12 wt%, CaO: mixing the components in a proportion of 48 wt% by a ball milling method, putting the mixture into a corundum crucible, putting the corundum crucible into a high-temperature furnace, heating to 1600 ℃, melting and preserving heat. The content of MgO in the high-temperature oxide melt is changed from 1 to 5 wt%, and the content of superoxide radical generated by the high-temperature oxide melt is increased from 2.686 multiplied by 10 -5 mol/g to 3.586X 10 -5 mol/g。
Example 10
This example is performed according to the following MgO: 8 wt% of Fe 2 O 3 :1~5wt%,Al 2 O 3 :28wt%,SiO 2 : 12 wt%, CaO: mixing the components in a proportion of 46 wt% by using a ball milling method, putting the mixture into a platinum crucible, putting the platinum crucible into a high-temperature furnace, heating to 1600 ℃, melting and preserving heat. Change of Fe therein 2 O 3 Of (1) containsThe amount is from 1 to 5 wt%, and the content of superoxide radical generated by high-temperature oxide melt is increased from 2.738 × 10 -5 mol/g to 3.078X 10 -5 mol/g。
Example 11
This example is carried out according to MgO: 8 wt% of Fe 2 O 3 :1~5wt%,Al 2 O 3 :28wt%,SiO 2 : 12 wt%, CaO: mixing the components in a proportion of 46 wt% by using a ball milling method, putting the mixture into a graphite crucible, placing the graphite crucible into a high-temperature furnace, heating to 1700 ℃ to melt the mixture, and keeping the temperature. Change of Fe therein 2 O 3 From 1 to 5 wt.%, the content of superoxide radicals generated by the high-temperature oxide melt is increased from 1.543 x 10 -5 mol/g to 3.994X 10 -5 mol/g。
Table 1 example 12-example 18 process conditions
Figure BDA0003669560950000071
As shown in Table 1, examples 12 to 18 further modified MgO and Fe 2 O 3 、Al 2 O 3 、 SiO 2 And CaO in different proportions, mixing by a ball milling method, putting the mixture into a graphite crucible, and placing the graphite crucible into a high-temperature furnace for processing at high temperature to obtain the content determination condition of the superoxide radical generated by the high-temperature oxide melt. Therefore, the technical scheme of the invention can obtain the high-temperature oxide melt containing the superoxide radical and adjust CaO, MgO or Fe 2 O 3 The content changes the content of the superoxide radical, regulates the reaction activity of the high-temperature oxide melt, and the like.
The above description is only a preferred embodiment of the present invention, and is not intended to limit the scope of the present invention, and all modifications and equivalents of the present invention, which are made by the present specification and directly/indirectly applied to other related technical fields within the spirit of the present invention are included in the scope of the present invention.

Claims (10)

1. A method for preparing a high-temperature oxide melt containing superoxide radicals is characterized by comprising the following steps:
according to CaO: 30 to 60 wt% of Al 2 O 3 :20~35wt%,MgO:0~15wt%,SiO 2 :8~15wt%,Fe 2 O 3 : 0-10 wt% of a mixture is formed, and the mixture is uniformly mixed by using a mixing and grinding method;
and putting the mixture into a crucible, putting the crucible into a high-temperature furnace in an air or argon atmosphere, heating to 1500-1700 ℃ to melt the mixture, and preserving the temperature to form a high-temperature oxide melt containing the superoxide radical.
2. The method of claim 1, wherein the mixture is modified by changing CaO, MgO, or Fe 2 O 3 The mass fraction of (a) regulates the content of superoxide radicals in the high-temperature oxide melt.
3. The method for preparing a high-temperature oxide melt containing superoxide radicals according to claim 2, wherein the content of superoxide radicals in the high-temperature oxide melt is 1.007 x 10 -5 mol/g to 9.078X 10 -5 mol/g。
4. The method for producing a high-temperature oxide melt containing a superoxide radical according to claim 3, wherein the mass fraction of CaO is changed within a range of 50 to 60 wt%, and the content of the superoxide radical in the high-temperature oxide melt is 1.007 x 10 - 5 mol/g to 9.078X 10 -5 mol/g。
5. The method for preparing a high-temperature oxide melt containing superoxide radicals according to claim 3, wherein the MgO mass fraction is changed in the range of 0 to 15 wt%, and the content of superoxide radicals in the high-temperature oxide melt is 1.746 x 10 - 5 mol/g to 3.87X 10 -5 mol/g。
6. According to the rightThe method for preparing a high-temperature oxide melt containing superoxide radicals as claimed in claim 3, wherein Fe is changed within the range of 1-10 wt% 2 O 3 The mass fraction of the superoxide radical in the high-temperature oxide melt is 1.648 multiplied by 10 -5 To 3.864 × 10 -5 mol/g。
7. The method of claim 1, wherein the Al in the mixture is selected from the group consisting of Al, and combinations thereof 2 O 3 、SiO 2 CaO, MgO or Fe 2 O 3 The purity is more than or equal to 98wt percent and the granularity is less than or equal to 88 mu m.
8. The method as claimed in claim 1, wherein CaO is CaCO 3
9. The method for preparing a high-temperature oxide melt containing superoxide radicals as claimed in claim 1, wherein: the mixing and grinding method is planetary ball milling, vibration milling, air flow milling, hammer milling or wet milling.
10. The method for preparing a high-temperature oxide melt containing superoxide radicals as claimed in claim 1, wherein: the crucible is a platinum crucible, a graphite crucible, a corundum crucible or a magnesium oxide crucible.
CN202210619484.2A 2022-05-30 2022-05-30 Preparation method of high-temperature oxide melt containing superoxide radical Pending CN114890803A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202210619484.2A CN114890803A (en) 2022-05-30 2022-05-30 Preparation method of high-temperature oxide melt containing superoxide radical

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202210619484.2A CN114890803A (en) 2022-05-30 2022-05-30 Preparation method of high-temperature oxide melt containing superoxide radical

Publications (1)

Publication Number Publication Date
CN114890803A true CN114890803A (en) 2022-08-12

Family

ID=82726101

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202210619484.2A Pending CN114890803A (en) 2022-05-30 2022-05-30 Preparation method of high-temperature oxide melt containing superoxide radical

Country Status (1)

Country Link
CN (1) CN114890803A (en)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1504280A (en) * 1975-05-02 1978-03-15 Stein Refractories Methods of reducing inclusions in castings
AU2657977A (en) * 1976-07-13 1979-01-04 Kloeckner Werke Ag Refining of steel free of non-metallic inclusions after deoxidation and desulphurisation
DE19752243A1 (en) * 1997-11-26 1999-07-29 Paul Loerke Cement production with reduced grinding energy costs and increased grinding mill and kiln throughput
JP2014091057A (en) * 2012-10-31 2014-05-19 Sekisui Chem Co Ltd Manufacturing method of gas barrier film
CN112555111A (en) * 2020-12-07 2021-03-26 武汉科技大学 Method for converting chemical energy into mechanical energy at high temperature
CN112595715A (en) * 2020-12-07 2021-04-02 武汉科技大学 High-temperature slag structure characterization method
CN112697826A (en) * 2020-12-07 2021-04-23 武汉科技大学 CaO-Al2O3Method for measuring free radicals of oxide-containing melt
CN112697839A (en) * 2020-12-07 2021-04-23 武汉科技大学 Method for measuring free radicals of high-temperature oxide melt
US20210183271A1 (en) * 2019-12-11 2021-06-17 Wuhan University Of Science And Technology Method for simulating intraplate volcanism

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1504280A (en) * 1975-05-02 1978-03-15 Stein Refractories Methods of reducing inclusions in castings
AU2657977A (en) * 1976-07-13 1979-01-04 Kloeckner Werke Ag Refining of steel free of non-metallic inclusions after deoxidation and desulphurisation
DE19752243A1 (en) * 1997-11-26 1999-07-29 Paul Loerke Cement production with reduced grinding energy costs and increased grinding mill and kiln throughput
JP2014091057A (en) * 2012-10-31 2014-05-19 Sekisui Chem Co Ltd Manufacturing method of gas barrier film
US20210183271A1 (en) * 2019-12-11 2021-06-17 Wuhan University Of Science And Technology Method for simulating intraplate volcanism
CN112555111A (en) * 2020-12-07 2021-03-26 武汉科技大学 Method for converting chemical energy into mechanical energy at high temperature
CN112595715A (en) * 2020-12-07 2021-04-02 武汉科技大学 High-temperature slag structure characterization method
CN112697826A (en) * 2020-12-07 2021-04-23 武汉科技大学 CaO-Al2O3Method for measuring free radicals of oxide-containing melt
CN112697839A (en) * 2020-12-07 2021-04-23 武汉科技大学 Method for measuring free radicals of high-temperature oxide melt

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
LI, SHENGHAO等: "Corrosion resistance and anti-reaction mechanism of Al2O3-based refractory ceramic under weak static magnetic field", pages 2869 - 2877 *
PENG, YUEFANG等: "Radical reaction-induced Turing pattern corrosion of alumina refractory ceramics with CaO-Al2O3-SiO2-MgO slags", pages 166 - 172 *
罗莉萍等: "炼钢生产", 29 February 2016, 冶金工业出版社, pages: 121 *
赵烁等: "低碳低合金钢中CaO-Al2O3-SiO2-MgO系夹杂物熔化温度的控制", pages 3121 - 3128 *
赵贵州等: "熔融钢渣调质制备高酸度系数矿物棉", pages 145 *
赵鸿波等: "镁铝比对高炉低铝渣系流动性能及热稳定性影响规律", pages 14 *
陈欣雨等: "电熔镁砂在CaO–Al2O3–SiO2熔渣中的溶解行为", pages 610 - 618 *
韩吟文等: "《地球化学》", 31 July 2003, 地质出版社, pages: 269 *

Similar Documents

Publication Publication Date Title
CN105130190B (en) Using granite mine tailing as devitrified glass of main material production and preparation method thereof
Sun et al. Low-temperature synthesis and sintering of γ-Y 2 Si 2 O 7
CN101456575B (en) Method for preparing calcium-hexaluminate ceramic powder by calcium slag
CN106316134B (en) A kind of diopside and feldspar principal crystalline phase devitrified glass and preparation method thereof
CN113943159A (en) Preparation method of boron carbide composite ceramic
CN103420614A (en) Method for preparing thick-film dielectric glass powder
CN109369026B (en) Method for producing yellow phosphorus and preparing high-calcium complex phase glass ceramics simultaneously by electric furnace method
CN114890803A (en) Preparation method of high-temperature oxide melt containing superoxide radical
CN101665363B (en) Additive for silicon nitride sintered bodies
CN108546131B (en) Preparation method of silicon nitride porous ceramic
CN101323893A (en) Technological process for removing fine occluded foreignsubstance in molten steel
CN110451806B (en) Uniform crystallization control method of glass ceramic
CN113213968B (en) Micron-sized metastable phase epsilon-Fe 2 O 3 Preparation method of (1)
CN111847403B (en) Preparation method of aluminum nitride powder
CN105110646B (en) A kind of devitrified glass containing pyroxferroite crystalline phase and preparation method thereof
CN1598008A (en) Surface additive for sintering mine of iron smelting by furnace
CN106865550B (en) Calcium carbide with phosphogypsum as main material and preparation method thereof
CN114315382B (en) Magnesia-alumina spinel prepared by electric melting of hydrated magnesia-alumina bricks and preparation method thereof
CN108409144A (en) A kind of preparation method of low-temperature sintering type cinder microcrystalline glass material
CN114394820B (en) Magnesia-alumina spinel sintered by waste magnesia-alumina brick powder and preparation method thereof
CN114890430B (en) Preparation method of tetragonal petalite powder
CN113957269B (en) Can stabilize beta-C in magnesium slag 2 S magnesium smelting pellet and magnesium smelting method
CN113755045B (en) Infrared radiation coating and preparation method thereof
CN111362275B (en) Preparation method of lithium borate
CN108558412B (en) Preparation method of porous silicon nitride ceramic material

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