CN105936508A - Method for extracting silica from ore slag - Google Patents

Method for extracting silica from ore slag Download PDF

Info

Publication number
CN105936508A
CN105936508A CN201610381980.3A CN201610381980A CN105936508A CN 105936508 A CN105936508 A CN 105936508A CN 201610381980 A CN201610381980 A CN 201610381980A CN 105936508 A CN105936508 A CN 105936508A
Authority
CN
China
Prior art keywords
filtrate
time
silicon dioxide
slag
filter cake
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
CN201610381980.3A
Other languages
Chinese (zh)
Inventor
徐国友
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.)
Wangjiang Jinfeng Mineral Product Science And Technology Co Ltd
Original Assignee
Wangjiang Jinfeng Mineral Product Science And Technology 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 Wangjiang Jinfeng Mineral Product Science And Technology Co Ltd filed Critical Wangjiang Jinfeng Mineral Product Science And Technology Co Ltd
Priority to CN201610381980.3A priority Critical patent/CN105936508A/en
Publication of CN105936508A publication Critical patent/CN105936508A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00Silicon; Compounds thereof
    • C01B33/113Silicon oxides; Hydrates thereof
    • C01B33/12Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/80Compositional purity

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Silicon Compounds (AREA)

Abstract

The invention discloses a method for extracting silica from ore slag. The method comprises the following steps: 1, introducing oxygen to the ore slag, sequentially carrying out primary roasting, secondary roasting and tertiary roasting, and cooling the three-roasted ore slag to obtain a material a; 2, fusing the material a and sodium carbonate, and carrying out water quenching to obtain fine articles; 3, carrying out wet grinding on the fine particles to form a thick slurry, carrying out multi-step alkali dissolving, and filtering the obtained solution to obtain a filtrate which is a material b; 4, introducing carbon dioxide to the material b, and filtering the material b to obtain a filtrate which is a material c; 5, adding ethyl acetate to the material c in a dropwise manner, adding a sulfuric acid solution, centrifuging the obtained solution, taking the obtained filtrate, washing the filtrate with distilled water, drying the washed material in a drying box, and cooling the dried material at room temperature to obtain silica. The purity of the obtained silica reaches 98% or above.

Description

A kind of method extracting silicon dioxide in slag
Technical field
The present invention relates to a kind of extracting method, a kind of method particularly relating to extract silicon dioxide in slag.
Background technology
Ore residue after ore dressing or smelting is referred to as slag, containing units such as abundant aluminum and silicon in slag Element, and silicon dioxide is had many uses general, is mainly used in glass processed, waterglass, pottery, enamel, fire proofed wood Material, aerogel blanket, ferrosilicon, molding sand, elemental silicon, cement etc., the huge market demand, hence with slag In element silicon to extract silicon dioxide be the problem that at present technology needs solution badly.
Summary of the invention
For solving technical problem present in background technology, the present invention proposes to extract silicon dioxide in a kind of slag Method, technological process is simple to operation, low cost, and the silica purity that obtains is high, the efficiency of extraction Good.
The method extracting silicon dioxide in a kind of slag that the present invention proposes, comprises the steps:
S1, slag is put in reactor, in reactor, is then passed through oxygen, carries out a roasting successively, After baking and three roastings, be cooled to room temperature and obtain material a;
S2, material a is mixed homogeneously with sodium carbonate after put in stove and melt, obtain molten mass, then By molten mass shrend, obtain fine grained material;
S3, the fine grained material wet grinding obtained by S2 become thick slurry, dilute, be filtrated to get first-time filtrate and Secondary filter cake;Taking a filter cake sodium hydroxide solution A to dissolve, then heat concentration, baking is dried to obtain dry Powder, by dry mash water dissolution, is filtrated to get secondary filtrate and secondary filter cake;Then secondary filter cake is used Sodium hydroxide solution B dissolves, and filters, obtains three filtrates and three filter cakes;By first-time filtrate, secondary filter Liquid and three filtrates merge, and dilute with water filters, takes filtrate and obtain material b;
S4, in material b, it is passed through carbon dioxide, takes filtrate after filtration and obtain material c;
S5, ethyl acetate is added drop-wise in material c, does not stop stirring during dropping, be subsequently adding sulphuric acid Solution, centrifugation takes filtrate, then uses distilled water wash filtrate, and the material after washing is placed on drying baker In be dried, be cooled to room temperature and obtain silicon dioxide.
Preferably, in S1, the temperature of a roasting is 280-350 DEG C, and the time of a roasting is 1-3h; The temperature of after baking is 500-550 DEG C, and the time of after baking is 2-4h;The temperature of three roastings is 600-650 DEG C, the time of three roastings is 0.5-1.5h.
Preferably, in S2, melt putting in stove after material a and sodium carbonate mix homogeneously, melted temperature Degree is for 1150-1350 DEG C, and the melting time is 30-40min, obtains the molten mass of 1050-1150 DEG C, then will Molten mass shrend, obtains fine grained material.
Preferably, in S2, the weight ratio of material a and sodium carbonate is 1:1.2-1.8.
Preferably, in S2, the particle diameter of fine grained material is 1-5mm.
Preferably, in S3, the fine grained material wet grinding obtained by S2 becomes thick slurry, dilutes, is filtrated to get one Secondary filtrate and a filter cake;Take a filter cake sodium hydroxide solution A in 70-80 DEG C of dissolving, then heat dense Contracting, bakees and is dried to obtain dry mash, by dry mash water dissolution, be filtrated to get secondary filtrate and secondary filter cake; Then by secondary filter cake with sodium hydroxide solution B in 65-85 DEG C of dissolving, filter, obtain three filtrates and three times Filter cake;First-time filtrate, secondary filtrate and three filtrates are merged, dilute with water, filter, take filtrate and obtain Material b.
Preferably, in S3, the concentration of sodium hydroxide solution A is 45-55wt%;Sodium hydroxide solution B's is dense Degree is 65-75wt%.
Preferably, in S4, in material b, it is passed through carbon dioxide, reduces filtrate pH to 5.2-6.3, Take filtrate after filtration and obtain material c.
Preferably, in S5, the mass ratio of ethyl acetate, material c and sulfuric acid solution is 5-15:2-8:3-9.
Preferably, in S5, the concentration of sulfuric acid solution is 28-32wt%.
Preferably, in S5, the time of washing is 20-50min.
Preferably, in S5, the temperature being dried is 80-120 DEG C, and the time being dried is 1-5h.
In the present invention, in S1, the oxygen being passed through is as the calcined gas of carbon removing step, as those skilled in the art Routine techniques means, therefore the consumption of oxygen does not limits in the present invention.
In S3, the carbon dioxide being passed through regulates gas as acidity, as the conventional skill of those skilled in the art Art means, its consumption does not limits, therefore the consumption of carbon dioxide does not limits in the present invention.
In the present invention, with slag as major ingredient, first slag is carried out a point benefit calcining, removes the carbon in slag, By adding sodium carbonate fusion after making carbon fully remove, it is to allow the SiO in slag2And Al2O3With Na2CO3 Reaction transforms into solvable Na2O·SiO2And Na2O·Al2O3, separate with other compositions in slag, soda Na newly-generated when alkali melts2O·Al2O3·2SiO2It is easy to be decomposed by NaOH, discharges Na2O·Al2O3With Na2O·SiO2。Na2O·Al2O3Meet water can part hydrolyze, produce Al (OH)3With NaOH;Na2O·Fe2O3 Meet water all to hydrolyze, produce Fe (OH)3With NaOH.It is dissolved in water by wet grinding and to the underflow material after wet grinding, Na2O·Al2O3And Na2O·Fe2O3NaOH and Na that hydrolysis produces2O·Al2O3·2SiO2Reaction, part Na2O·Al2O3·2SiO2It is decomposed into Na2O·Al2O3And Na2O·SiO2It is dissolved in water and enters solution.Cross After filter, the Na of dissolving2O·Al2O3And Na2O·SiO2With comprise unreacted Na2O·Al2O3·2SiO2Solid And Fe (OH)3, part Al (OH)3Impurity solid separate in advance.Filter cake after wet grinding, dissolving adds Caustic soda NaOH solution baking are dried to dry mash, and NaOH is by filter cake in its effect Na2O·Al2O3·2SiO2All it is decomposed into Na2O·Al2O3And Na2O·SiO2.Meanwhile, the Al in filter cake (OH)3 With Fe (OH)3Also Na is again changed into2O·Al2O3And Na2O·Fe2O3。SiO2At Na2O·Al2O3In solution Stabilizing dissolved degree the lowest, excess SiO2Meeting and Na2O·Al2O3Generate Na2O·Al2O3·2SiO2Precipitation, Make Al2O3With SiO2Extraction ratio reduce, Na2O alkaline consumption increases.After dry powder dissolves, Na2O·Al2O3And Na2O·SiO2 It is fully dissolved in water, part Na2O·Al2O3Hydrolyze, produce Al (OH)3With NaOH;Na2O·Fe2O3Entirely Portion hydrolyzes, and produces Fe (OH)3With NaOH.The NaOH that hydrolysis produces can strengthen again SiO further2In the solution Molten stability of solution.Solution after being dissolved by dry powder filters and separates, except impurity in filter cake, and also part Al(OH)3.Dissolve the filter cake after dry powder dissolves with soda bath, make the Al (OH) in filter cake3React with NaOH Change into Na2O·Al2O3Dissolve and enter solution and magazins' layout.Filtrate CO after dilution hydrolysis2Gas pressurized Carry out carbonating process, neutralize NaOH, reduce the pH value of solution, make remaining Na in solution2O·Al2O3 Almost all hydrolysis becomes Al (OH)3Precipitation.Isolate Al (OH)3After, solution becomes Na2CO3And NaHSiO3 Mixed solution.Continue Na2CO3And NaHSiO3Mixed solution CO2Gas pressurized carries out carbonating process, fall The pH value of low solution, makes NaHSiO in solution3Almost all hydrolysis becomes H2SiO3Precipitation.Isolate H2SiO3 After, solution becomes dilute Na2CO3Solution.The technological process of the present invention is simple to operation, low cost, two obtained Silicon oxide purity is high, and the purity of silicon dioxide has reached more than 98%.
Accompanying drawing explanation
Fig. 1 is the schematic flow sheet of the method extracting silicon dioxide in a kind of slag that the present invention proposes.
Detailed description of the invention
Below in conjunction with specific embodiment, the present invention is described in detail, it should be appreciated that embodiment is served only for The bright present invention rather than be used for limiting the invention, any made on the basis of the present invention amendment, Equivalents etc. are the most within the scope of the present invention.
As it is shown in figure 1, a kind of slag that Fig. 1 is the present invention to be proposed extracts the flow process of the method for silicon dioxide Schematic diagram.
With reference to Fig. 1, the method extracting silicon dioxide in a kind of slag that the present invention proposes, comprise the steps:
S1, slag is put in reactor, in reactor, is then passed through oxygen, carries out a roasting successively, After baking and three roastings, be cooled to room temperature and obtain material a;
S2, material a is mixed homogeneously with sodium carbonate after put in stove and melt, obtain molten mass, then By molten mass shrend, obtain fine grained material;
S3, the fine grained material wet grinding obtained by S2 become thick slurry, dilute, be filtrated to get first-time filtrate and Secondary filter cake;Taking a filter cake sodium hydroxide solution A to dissolve, then heat concentration, baking is dried to obtain dry Powder, by dry mash water dissolution, is filtrated to get secondary filtrate and secondary filter cake;Then secondary filter cake is used Sodium hydroxide solution B dissolves, and filters, obtains three filtrates and three filter cakes;By first-time filtrate, secondary filter Liquid and three filtrates merge, and dilute with water filters, takes filtrate and obtain material b;
S4, in material b, it is passed through carbon dioxide, takes filtrate after filtration and obtain material c;
S5, ethyl acetate is added drop-wise in material c, does not stop stirring during dropping, be subsequently adding sulphuric acid Solution, centrifugation takes filtrate, then uses distilled water wash filtrate, and the material after washing is placed on drying baker In be dried, be cooled to room temperature and obtain silicon dioxide.
Embodiment 1
The method extracting silicon dioxide in a kind of slag that the present invention proposes, comprises the steps:
S1, slag is put in reactor, in reactor, be then passed through oxygen, carry out a roasting, one The temperature of secondary roasting is 315 DEG C, and the time of a roasting is 2h, and a roasting continues to be passed through oxygen after terminating, Carrying out after baking, the temperature of after baking is 525 DEG C, and the time of after baking is 3h, and after baking is tied Continuing after bundle to be passed through oxygen, carry out three roastings, the temperature of three roastings is 625 DEG C, the time of three roastings For 1h, it is cooled to room temperature and obtains material a;
S2, melt putting in stove after 1 part of material a and 1.5 parts of sodium carbonate mix homogeneously by weight, Melt temperature is 1200 DEG C, and the melting time is 35min, obtains the molten mass of 1100 DEG C, then by molten mass Shrend, obtains the fine grained material that particle diameter is 3mm;
S3, the fine grained material wet grinding obtained by S2 become thick slurry, dilute, be filtrated to get first-time filtrate and Secondary filter cake;Take filter cake concentration be the sodium hydroxide solution A of 50wt% in 75 DEG C of dissolvings, then heat Concentrate, bakee and be dried to obtain dry mash, by dry mash water dissolution, be filtrated to get secondary filtrate and secondary filter Cake;Then by sodium hydroxide solution B that secondary filter cake concentration is 70wt% in 75 DEG C of dissolvings, filter, To three filtrates and three filter cakes;First-time filtrate, secondary filtrate and three filtrates are merged, dilute with water, Filter, take filtrate and obtain material b;
S4, in material b, it is passed through carbon dioxide, reduces filtrate pH to 5.75, take filtrate after filtration and obtain To material c;
S5, by weight 10 parts of ethyl acetate are added drop-wise in 5 parts of material c, do not stop during dropping to stir Mixing, being subsequently adding 6 parts of concentration is the sulfuric acid solution of 30wt, and centrifugation takes filtrate, then with distillation washing Washing filtrate, wash time is 35min, is placed in drying baker by the material after washing and is dried, and baking temperature is 100 DEG C, drying time is 3h, is cooled to room temperature and obtains silicon dioxide.
Embodiment 2
The method extracting silicon dioxide in a kind of slag that the present invention proposes, comprises the steps:
S1, slag is put in reactor, in reactor, be then passed through oxygen, carry out a roasting, one The temperature of secondary roasting is 280 DEG C, and the time of a roasting is 3h, and a roasting continues to be passed through oxygen after terminating, Carrying out after baking, the temperature of after baking is 500 DEG C, and the time of after baking is 4h, and after baking is tied Continuing after bundle to be passed through oxygen, carry out three roastings, the temperature of three roastings is 600 DEG C, the time of three roastings For 1.5h, it is cooled to room temperature and obtains material a;
S2, melt putting in stove after 1 part of material a and 1.2 parts of sodium carbonate mix homogeneously by weight, Melt temperature is 1350 DEG C, and the melting time is 30min, obtains the molten mass of 1150 DEG C, then by molten mass Shrend, obtains the fine grained material that particle diameter is 1mm;
S3, the fine grained material wet grinding obtained by S2 become thick slurry, dilute, be filtrated to get first-time filtrate and Secondary filter cake;Take filter cake concentration be the sodium hydroxide solution A of 45wt% in 80 DEG C of dissolvings, then heat Concentrate, bakee and be dried to obtain dry mash, by dry mash water dissolution, be filtrated to get secondary filtrate and secondary filter Cake;Then by sodium hydroxide solution B that secondary filter cake concentration is 65wt% in 85 DEG C of dissolvings, filter, To three filtrates and three filter cakes;First-time filtrate, secondary filtrate and three filtrates are merged, dilute with water, Filter, take filtrate and obtain material b;
S4, in material b, it is passed through carbon dioxide, reduces filtrate pH to 5.2, take filtrate after filtration and obtain To material c;
S5, by weight 5 parts of ethyl acetate are added drop-wise in 8 parts of material c, do not stop during dropping to stir Mixing, being subsequently adding 3 parts of concentration is the sulfuric acid solution of 28wt%, and centrifugation takes filtrate, then uses distilled water Wash filtrate, the time of washing is 20min, is placed in drying baker by the material after washing and is dried, the temperature being dried Degree is 120 DEG C, and the time being dried is 1h, is cooled to room temperature and obtains silicon dioxide.
Embodiment 3
The method extracting silicon dioxide in a kind of slag that the present invention proposes, comprises the steps:
S1, slag is put in reactor, in reactor, be then passed through oxygen, carry out a roasting, one The temperature of secondary roasting is 350 DEG C, and the time of a roasting is 1h, and a roasting continues to be passed through oxygen after terminating, Carrying out after baking, the temperature of after baking is 550 DEG C, and the time of after baking is 2h, and after baking is tied Continuing after bundle to be passed through oxygen, carry out three roastings, the temperature of three roastings is 650 DEG C, the time of three roastings For 0.5h, it is cooled to room temperature and obtains material a;
S2, melt putting in stove after 1 part of material a and 1.8 parts of sodium carbonate mix homogeneously by weight, Melt temperature is 1150 DEG C, and the melting time is 40min, obtains the molten mass of 1050 DEG C, then by molten mass Shrend, obtains the fine grained material that particle diameter is 5mm;
S3, the fine grained material wet grinding obtained by S2 become thick slurry, dilute, be filtrated to get first-time filtrate and Secondary filter cake;Take filter cake concentration be the sodium hydroxide solution A of 45wt% in 80 DEG C of dissolvings, then heat Concentrate, bakee and be dried to obtain dry mash, by dry mash water dissolution, be filtrated to get secondary filtrate and secondary filter Cake;Then by sodium hydroxide solution B that secondary filter cake concentration is 65wt% in 85 DEG C of dissolvings, filter, To three filtrates and three filter cakes;First-time filtrate, secondary filtrate and three filtrates are merged, dilute with water, Filter, take filtrate and obtain material b;
S4, in material b, it is passed through carbon dioxide, reduces filtrate pH to 6.3, take filtrate after filtration and obtain To material c;
S5, by weight 15 parts of ethyl acetate are added drop-wise in 2 parts of material c, do not stop during dropping to stir Mixing, being subsequently adding 9 parts of concentration is the sulfuric acid solution of 32wt%, and centrifugation takes filtrate, then uses distilled water Wash filtrate, the time of washing is 50min, is placed in drying baker by the material after washing and is dried, the temperature being dried Degree is 80 DEG C, and the time being dried is 5h, is cooled to room temperature and obtains silicon dioxide.
Embodiment 4
The method extracting silicon dioxide in a kind of slag that the present invention proposes, comprises the steps:
S1, slag is put in reactor, in reactor, be then passed through oxygen, carry out a roasting, one The temperature of secondary roasting is 300 DEG C, and the time of a roasting is 2.5h, and a roasting continues to be passed through oxygen after terminating, Carrying out after baking, the temperature of after baking is 510 DEG C, and the time of after baking is 3.5h, and after baking is tied Continuing after bundle to be passed through oxygen, carry out three roastings, the temperature of three roastings is 610 DEG C, the time of three roastings For 1.2h, it is cooled to room temperature and obtains material a;
S2, melt putting in stove after 1 part of material a and 1.3 parts of sodium carbonate mix homogeneously by weight, Melt temperature is 1300 DEG C, and the melting time is 32min, obtains the molten mass of 1120 DEG C, then by molten mass Shrend, obtains the fine grained material that particle diameter is 2mm;
S3, the fine grained material wet grinding obtained by S2 become thick slurry, dilute, be filtrated to get first-time filtrate and Secondary filter cake;Take filter cake concentration be the sodium hydroxide solution A of 48wt% in 78 DEG C of dissolvings, then heat Concentrate, bakee and be dried to obtain dry mash, by dry mash water dissolution, be filtrated to get secondary filtrate and secondary filter Cake;Then by sodium hydroxide solution B that secondary filter cake concentration is 68wt% in 82 DEG C of dissolvings, filter, To three filtrates and three filter cakes;First-time filtrate, secondary filtrate and three filtrates are merged, dilute with water, Filter, take filtrate and obtain material b;
S4, in material b, it is passed through carbon dioxide, reduces filtrate pH to 5.5, take filtrate after filtration and obtain To material c;
S5, by weight 8 parts of ethyl acetate are added drop-wise in 6 parts of material c, do not stop during dropping to stir Mixing, being subsequently adding 4 parts of concentration is the sulfuric acid solution of 29wt%, and centrifugation takes filtrate, then uses distilled water Wash filtrate, the time of washing is 25min, is placed in drying baker by the material after washing and is dried, the temperature being dried Degree is 115 DEG C, and the time being dried is 2h, is cooled to room temperature and obtains silicon dioxide.
Embodiment 5
The method extracting silicon dioxide in a kind of slag that the present invention proposes, comprises the steps:
S1, slag is put in reactor, in reactor, be then passed through oxygen, carry out a roasting, one The temperature of secondary roasting is 330 DEG C, and the time of a roasting is 1.5h, and a roasting continues to be passed through oxygen after terminating, Carrying out after baking, the temperature of after baking is 540 DEG C, and the time of after baking is 2.5h, and after baking is tied Continuing after bundle to be passed through oxygen, carry out three roastings, the temperature of three roastings is 640 DEG C, the time of three roastings For 0.8h, it is cooled to room temperature and obtains material a;
S2, melt putting in stove after 1 part of material a and 1.7 parts of sodium carbonate mix homogeneously by weight, Melt temperature is 1200 DEG C, and the melting time is 38min, obtains the molten mass of 1080 DEG C, then by molten mass Shrend, obtains the fine grained material that particle diameter is 4mm;
S3, the fine grained material wet grinding obtained by S2 become thick slurry, dilute, be filtrated to get first-time filtrate and Secondary filter cake;Take filter cake concentration be the sodium hydroxide solution A of 48wt% in 78 DEG C of dissolvings, then heat Concentrate, bakee and be dried to obtain dry mash, by dry mash water dissolution, be filtrated to get secondary filtrate and secondary filter Cake;Then by sodium hydroxide solution B that secondary filter cake concentration is 68wt% in 82 DEG C of dissolvings, filter, To three filtrates and three filter cakes;First-time filtrate, secondary filtrate and three filtrates are merged, dilute with water, Filter, take filtrate and obtain material b;
S4, in material b, it is passed through carbon dioxide, reduces filtrate pH to 5.5, take filtrate after filtration and obtain To material c;
S5, by weight 14 parts of ethyl acetate are added drop-wise in 3 parts of material c, do not stop during dropping to stir Mixing, being subsequently adding 8 parts of concentration is the sulfuric acid solution of 31wt%, and centrifugation takes filtrate, then uses distilled water Wash filtrate, the time of washing is 45min, is placed in drying baker by the material after washing and is dried, the temperature being dried Degree is 85 DEG C, and the time being dried is 4h, is cooled to room temperature and obtains silicon dioxide.
The above, the only present invention preferably detailed description of the invention, but protection scope of the present invention not office Being limited to this, any those familiar with the art is in the technical scope that the invention discloses, according to this The technical scheme of invention and inventive concept thereof in addition equivalent or change, all should contain the protection in the present invention Within the scope of.

Claims (10)

1. the method extracting silicon dioxide in a slag, it is characterised in that comprise the steps:
S1, slag is put in reactor, in reactor, is then passed through oxygen, carries out a roasting successively, After baking and three roastings, be cooled to room temperature and obtain material a;
S2, material a is mixed homogeneously with sodium carbonate after put in stove and melt, obtain molten mass, then By molten mass shrend, obtain fine grained material;
S3, the fine grained material wet grinding obtained by S2 become thick slurry, dilute, be filtrated to get first-time filtrate and Secondary filter cake;Taking a filter cake sodium hydroxide solution A to dissolve, then heat concentration, baking is dried to obtain dry Powder, by dry mash water dissolution, is filtrated to get secondary filtrate and secondary filter cake;Then secondary filter cake is used Sodium hydroxide solution B dissolves, and filters, obtains three filtrates and three filter cakes;By first-time filtrate, secondary filter Liquid and three filtrates merge, and dilute with water filters, takes filtrate and obtain material b;
S4, in material b, it is passed through carbon dioxide, takes filtrate after filtration and obtain material c;
S5, ethyl acetate is added drop-wise in material c, does not stop stirring during dropping, be subsequently adding sulphuric acid Solution, centrifugation takes filtrate, then uses distilled water wash filtrate, and the material after washing is placed on drying baker In be dried, be cooled to room temperature and obtain silicon dioxide.
The method extracting silicon dioxide in slag the most according to claim 1, it is characterised in that S1 In, the temperature of a roasting is 280-350 DEG C, and the time of a roasting is 1-3h;The temperature of after baking For 500-550 DEG C, the time of after baking is 2-4h;The temperature of three roastings is 600-650 DEG C, three times The time of roasting is 0.5-1.5h.
The method extracting silicon dioxide in slag the most according to claim 1 and 2, it is characterised in that In S2, melting putting in stove after material a and sodium carbonate mix homogeneously, melt temperature is 1150-1350 DEG C, the melting time is 30-40min, obtains the molten mass of 1050-1150 DEG C, then will be melted Body shrend, obtains fine grained material;
Preferably, in S2, the weight ratio of material a and sodium carbonate is 1:1.2-1.8;
Preferably, in S2, the particle diameter of fine grained material is 1-5mm.
4., according to the method extracting silicon dioxide in the slag described in any one of claim 1-3, its feature exists In, in S3, the fine grained material wet grinding obtained by S2 becomes thick slurry, dilutes, is filtrated to get first-time filtrate With a filter cake;Take a filter cake sodium hydroxide solution A in 70-80 DEG C of dissolving, then heat concentration, Baking is dried to obtain dry mash, by dry mash water dissolution, is filtrated to get secondary filtrate and secondary filter cake;So After by secondary filter cake with sodium hydroxide solution B in 65-85 DEG C of dissolving, filter, obtain three filtrates and three times Filter cake;First-time filtrate, secondary filtrate and three filtrates are merged, dilute with water, filter, take filtrate and obtain Material b.
The method extracting silicon dioxide in slag the most according to claim 4, it is characterised in that S3 In, the concentration of sodium hydroxide solution A is 45-55wt%;The concentration of sodium hydroxide solution B is 65-75wt%.
6., according to the method extracting silicon dioxide in a kind of slag described in any one of claim 1-5, it is special Levy and be, in S4, in material b, be passed through carbon dioxide, reduce filtrate pH to 5.2-6.3, filter After take filtrate and obtain material c.
7., according to the method extracting silicon dioxide in a kind of slag described in any one of claim 1-6, it is special Levying and be, in S5, the mass ratio of ethyl acetate, material c and sulfuric acid solution is 5-15:2-8:3-9.
8., according to the method extracting silicon dioxide in a kind of slag described in any one of claim 1-7, it is special Levying and be, in S5, the concentration of sulfuric acid solution is 28-32wt%.
9., according to the method extracting silicon dioxide in a kind of slag described in any one of claim 1-8, it is special Levying and be, in S5, the time of washing is 20-50min.
10. according to the method extracting silicon dioxide in a kind of slag described in any one of claim 1-9, its Being characterised by, in S5, the temperature being dried is 80-120 DEG C, and the time being dried is 1-5h.
CN201610381980.3A 2016-06-01 2016-06-01 Method for extracting silica from ore slag Pending CN105936508A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610381980.3A CN105936508A (en) 2016-06-01 2016-06-01 Method for extracting silica from ore slag

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610381980.3A CN105936508A (en) 2016-06-01 2016-06-01 Method for extracting silica from ore slag

Publications (1)

Publication Number Publication Date
CN105936508A true CN105936508A (en) 2016-09-14

Family

ID=57151639

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610381980.3A Pending CN105936508A (en) 2016-06-01 2016-06-01 Method for extracting silica from ore slag

Country Status (1)

Country Link
CN (1) CN105936508A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101172633A (en) * 2007-10-11 2008-05-07 刘成长 Technique for producing hydroted alumina and silicic acid with high-silicon low-aluminium mineral raw material
CN102534190A (en) * 2012-01-20 2012-07-04 彭武星 Three-section type heating and roasting method for refining vanadium pentoxide

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101172633A (en) * 2007-10-11 2008-05-07 刘成长 Technique for producing hydroted alumina and silicic acid with high-silicon low-aluminium mineral raw material
CN102534190A (en) * 2012-01-20 2012-07-04 彭武星 Three-section type heating and roasting method for refining vanadium pentoxide

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
秦晓东等: "高比表面积超细二氧化硅粉体的制备", 《石油大学学报(自然科学版)》 *

Similar Documents

Publication Publication Date Title
CN103397213B (en) Method for decomposing and extracting Baotou rare earth ore through mixed alkali roasting process
CN103194603B (en) Preparation method of high-purity vanadium pentoxide
CN102531056B (en) Method for cleaner production of sodium vanadate and sodium chromate by pressure leaching of vanadium slag
AU2012395690B2 (en) Method for preparing soda-lime-silica glass basic formula and method for extracting aluminum from fly ash for co-production of glass
CN102071321B (en) Method for extracting vanadium and chromium from vanadium-containing steel slag by high-alkalinity potassium hydroxide
CN107098365B (en) A method of extracting lithium carbonate from lepidolite ore
CN103757425A (en) Cleaning process for producing sodium vanadate and sodium chromate alkali solution by high chromium vanadium slag
CN110042225A (en) A kind of roasting of lepidolite ore sodium sulphate and leaching method
CN101306928B (en) Pre- desiliconizing method from fly ash or slag
CN102897810A (en) Method for producing aluminum oxide by using fly ash
CN105502426B (en) The method that silica prepares waterglass in chrysotile tailing is extracted with highly basic roasting method
CN103738972B (en) A kind of residue of aluminum-extracted pulverized fuel ash prepares the method for silicon powder
CN108178171A (en) A kind of method that lithium carbonate is produced from lepidolite
CN115216645A (en) Method for extracting lithium from electrolytic aluminum waste slag by mixed salt calcination method
CN102815728A (en) Method for preparing nano-sized magnesium hydroxide and nano-silica by utilization of boron mud
CN105060326B (en) The technique that AZS solid wastes prepare sodium metaaluminate
CN103819086B (en) Method for preparing basic formula of soda-lime silicate glass and method for extracting aluminum from fly ash and co-producing glass
CN113860343A (en) Comprehensive utilization method of red mud and bauxite
CN101607721A (en) Utilize olivine tailing mine to prepare the method for high purity magnesium hydroxide and hexa-magnesium silicate
CN109022772A (en) A kind of method that lepidolite ore is leached in sulfuric acid curing
CN109384244B (en) Process method for purifying silica micropowder by using industrial silica fume oxidation
CN101397604B (en) Dense alkali liquid leaching pre-desiliconisation method for bauxite
CN105936508A (en) Method for extracting silica from ore slag
CN107416869A (en) A kind of production line that lithium carbonate is extracted from lepidolite ore
CN108275720A (en) A kind of method that zirconium oxychloride white residue takes off zirconium

Legal Events

Date Code Title Description
C06 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
RJ01 Rejection of invention patent application after publication

Application publication date: 20160914