CN107662935A - A kind of method that aluminum oxide and silicic acid are extracted from flyash - Google Patents

A kind of method that aluminum oxide and silicic acid are extracted from flyash Download PDF

Info

Publication number
CN107662935A
CN107662935A CN201711076688.1A CN201711076688A CN107662935A CN 107662935 A CN107662935 A CN 107662935A CN 201711076688 A CN201711076688 A CN 201711076688A CN 107662935 A CN107662935 A CN 107662935A
Authority
CN
China
Prior art keywords
flyash
aluminum oxide
solution
filtrate
silicic acid
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
CN201711076688.1A
Other languages
Chinese (zh)
Inventor
洪伟
张渤
�田�浩
张春田
张冀平
程红兵
吴舒
任宇红
孙敬
曹光
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.)
People's Republic Of China Qinhuangdao Entry-Exit Inspection And Quarantine Bureau Coal Inspection Technique Center
Original Assignee
People's Republic Of China Qinhuangdao Entry-Exit Inspection And Quarantine Bureau Coal Inspection Technique Center
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 People's Republic Of China Qinhuangdao Entry-Exit Inspection And Quarantine Bureau Coal Inspection Technique Center filed Critical People's Republic Of China Qinhuangdao Entry-Exit Inspection And Quarantine Bureau Coal Inspection Technique Center
Priority to CN201711076688.1A priority Critical patent/CN107662935A/en
Publication of CN107662935A publication Critical patent/CN107662935A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F7/00Compounds of aluminium
    • C01F7/02Aluminium oxide; Aluminium hydroxide; Aluminates
    • C01F7/04Preparation of alkali metal aluminates; Aluminium oxide or hydroxide therefrom
    • C01F7/08Preparation of alkali metal aluminates; Aluminium oxide or hydroxide therefrom by treating aluminous minerals with sodium carbonate, e.g. sinter processes
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)
  • Silicon Compounds (AREA)

Abstract

The invention discloses a kind of method that aluminum oxide and silicic acid are extracted from flyash, flyash and soda ash are mixed into stove, react 40min at a temperature of 1300 DEG C, fine grained material of the obtained molten mass with cold water water quenching into 1mm~5mm;By the wet-milling of fine grained material into thick slurry, dilution, it is heated to 70 DEG C and is filtered in 2h, multiple times of filtration again after worrying too much, and the filtrate of multiple times of filtration is merged into dilution and hydrolyzes and uses CO2Gas pressurized carries out carbonating processing, obtains Al (OH)3Precipitation and the 4th filtrate;Aluminium hydroxide is calcined to obtain aluminum oxide;CO is used to the 4th filtrate2Gas pressurized carries out carbonating processing, reduces the pH value of solution, makes NaHSiO in solution3Almost all hydrolysis turns into H2SiO3Precipitation, isolates H2SiO3Afterwards, solution turns into dilute Na2CO3Solution.Simple efficient extraction extraction aluminum oxide and silicic acid, and recycle soda ash.

Description

A kind of method that aluminum oxide and silicic acid are extracted from flyash
Technical field
The present invention relates to a kind of method that aluminum oxide and silicic acid are extracted from flyash.
Background technology
Flyash, is the fine ash that catching is got off from the flue gas after coal combustion, and flyash is the main of coal-burning power plant's discharge Solid waste.The main oxides of power plants flyash form:SiO2, Al2O3, FeO, Fe2O3, CaO, TiO2 etc.. With the development of power industry, the flyash discharge capacity of coal-burning power plant increases year by year, turns into the larger industry of the current discharge capacity in China One of waste residue.Substantial amounts of flyash is untreated, will produce airborne dust, pollutes air;River can be caused to silt up if being discharged into water system, And toxic chemical substance therein can also damage to human body and biology.
Therefore how to extract beneficial compound from flyash turns into urgent problem to be solved.
The content of the invention
In order to solve the above-mentioned technical problem, it is an object of the invention to provide one kind to extract aluminum oxide and silicic acid from flyash Method.
In order to solve the above technical problems, the present invention adopts the following technical scheme that:
A kind of method that aluminum oxide and silicic acid are extracted from flyash, comprises the following steps:
Flyash and soda ash are mixed into stove, react 40min at a temperature of 1300 DEG C, the cold water water quenching of obtained molten mass Into 1mm~5mm fine grained material;
By the wet-milling of fine grained material into thick slurry, dilution, it is heated to 70 DEG C and is filtered in 2h, obtain a filter cake; Concentration is reheated after one time filter cake is dissolved with concentrated caustic, bakees drying, obtains dry powder;By the dissolving of obtained dry mash, filtering, two are obtained Secondary filter cake, secondary filter cake are dissolved with concentrated caustic, filtered again, obtain filter cake three times;
The filtrate of 3 filterings is merged into dilution hydrolysis and uses CO2Gas pressurized carries out carbonating processing, neutralizes NaOH, The pH value of solution is reduced, obtains Al (OH)3Precipitation and the 4th filtrate;
Aluminium hydroxide is calcined to obtain aluminum oxide;
4th filtrate is Na2CO 3And NaHSiO3Mixed solution, continue to mixed solution CO2Gas pressurized is entered The processing of row carbonating, reduces the pH value of solution, makes NaHSiO in solution3Almost all hydrolysis turns into H2SiO3Precipitation, is isolated H2SiO3Afterwards, solution turns into dilute Na2CO3Solution.
Further, the mass ratio of flyash and soda ash is 1 ︰ 1.2~1.3.
Further, by dilute Na2CO3After appropriate concentration, continue to use CO2Pressurization carries out carbonating and handles to obtain NaHCO3It is brilliant Body, to NaHCO3Crystal is dried processing and obtains soda ash Na2CO3Circulate and melt process for soda ash alkali and make raw material.
Compared with prior art, advantageous effects of the invention:Its extraction process is simple, can efficiently utilize soda ash Purged with from flyash and take out aluminium hydroxide and silicic acid, and Na can be obtained from final product2CO3Solution is pure to recycle Alkali.
Embodiment
A kind of method that aluminum oxide and silicic acid are extracted from flyash, comprises the following steps:
Flyash and soda ash are mixed into stove for 1 ︰ 1.2~1.3 in mass ratio, 40min is reacted at a temperature of 1300 DEG C, so Fine grained material by obtained molten mass with cold water water quenching into 1mm~5mm afterwards;
By the wet-milling of fine grained material into thick slurry, dilution, it is heated to 70 DEG C and is filtered in 2h, obtain a filter cake; Concentration is reheated after one time filter cake is dissolved with concentrated caustic, bakees drying, obtains dry powder;By the dissolving of obtained dry mash, filtering, two are obtained Secondary filter cake, secondary filter cake are dissolved with concentrated caustic, filtered again, obtain filter cake three times;
The filtrate of 3 filterings is merged into dilution hydrolysis and uses CO2Gas pressurized carries out carbonating processing, neutralizes NaOH, The pH value of solution is reduced, obtains Al (OH)3Precipitation and the 4th filtrate;
Aluminium hydroxide is calcined to obtain aluminum oxide;
4th filtrate is Na2CO 3And NaHSiO3Mixed solution, continue to mixed solution CO2Gas pressurized is entered The processing of row carbonating, reduces the pH value of solution, makes NaHSiO in solution3Almost all hydrolysis turns into H2SiO3Precipitation, is isolated H2SiO3Afterwards, solution turns into dilute Na2CO3Solution.
By dilute Na2CO3After appropriate concentration, continue to use CO2Pressurization carries out carbonating and handles to obtain NaHCO3Crystal, to NaHCO3 Crystal is dried processing and obtains soda ash Na2CO3Circulate and melt process for soda ash alkali and make raw material.
Embodiment described above is only that the preferred embodiment of the present invention is described, and not the scope of the present invention is carried out Limit, on the premise of design spirit of the present invention is not departed from, those of ordinary skill in the art make to technical scheme Various modifications and improvement, all should fall into claims of the present invention determination protection domain in.

Claims (3)

  1. A kind of 1. method that aluminum oxide and silicic acid are extracted from flyash, it is characterised in that comprise the following steps:
    Flyash and soda ash are mixed into stove, react 40min at a temperature of 1300 DEG C, obtained molten mass with cold water water quenching into 1mm~5mm fine grained material;
    By the wet-milling of fine grained material into thick slurry, dilution, it is heated to 70 DEG C and is filtered in 2h, obtain a filter cake;Once Filter cake reheats concentration, bakees drying after being dissolved with concentrated caustic, obtain dry powder;By the dissolving of obtained dry mash, filtering, secondary filter is obtained Cake, secondary filter cake are dissolved with concentrated caustic, filtered again, obtain filter cake three times;
    The filtrate of 3 filterings is merged into dilution hydrolysis and uses CO2Gas pressurized carries out carbonating processing, neutralizes NaOH, reduces molten The pH value of liquid, obtain Al (OH)3Precipitation and the 4th filtrate;
    Aluminium hydroxide is calcined to obtain aluminum oxide;
    4th filtrate is Na2CO3And NaHSiO3Mixed solution, continue to mixed solution CO2Gas pressurized is carbonated Processing, reduces the pH value of solution, makes NaHSiO in solution3Almost all hydrolysis turns into H2SiO3Precipitation, isolates H2SiO3Afterwards, it is molten Liquid turns into dilute Na2CO3Solution.
  2. 2. the method according to claim 1 that aluminum oxide and silicic acid are extracted from flyash, it is characterised in that:Flyash with The mass ratio of soda ash is 1 ︰ 1.2~1.3.
  3. 3. the method according to claim 1 that aluminum oxide and silicic acid are extracted from flyash, it is characterised in that:Will be dilute Na2CO3After appropriate concentration, continue to use CO2Pressurization carries out carbonating and handles to obtain NaHCO3Crystal, to NaHCO3Crystal is dried Processing obtains soda ash Na2CO3Circulate and melt process for soda ash alkali and make raw material.
CN201711076688.1A 2017-11-06 2017-11-06 A kind of method that aluminum oxide and silicic acid are extracted from flyash Pending CN107662935A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711076688.1A CN107662935A (en) 2017-11-06 2017-11-06 A kind of method that aluminum oxide and silicic acid are extracted from flyash

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711076688.1A CN107662935A (en) 2017-11-06 2017-11-06 A kind of method that aluminum oxide and silicic acid are extracted from flyash

Publications (1)

Publication Number Publication Date
CN107662935A true CN107662935A (en) 2018-02-06

Family

ID=61145027

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711076688.1A Pending CN107662935A (en) 2017-11-06 2017-11-06 A kind of method that aluminum oxide and silicic acid are extracted from flyash

Country Status (1)

Country Link
CN (1) CN107662935A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101172634A (en) * 2007-10-11 2008-05-07 刘成长 Technique for producing hydroted alumina and silicic acid with coal ash
CN101857253A (en) * 2009-04-09 2010-10-13 刘庆玲 Process for producing aluminium hydroxide, silicic acid and sodium carbonate by utilizing fly ash

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101172634A (en) * 2007-10-11 2008-05-07 刘成长 Technique for producing hydroted alumina and silicic acid with coal ash
CN101857253A (en) * 2009-04-09 2010-10-13 刘庆玲 Process for producing aluminium hydroxide, silicic acid and sodium carbonate by utilizing fly ash

Similar Documents

Publication Publication Date Title
CN1330562C (en) Process of industrialize for waste acid concentrition recovering used in titanium white production by sulfuric acid method
CN102897810B (en) Method for producing aluminum oxide by using fly ash
CN102627305A (en) Method using alkaline process to extract alumina in coal ash
CN110395757B (en) Method for removing alkali metal and alkaline earth metal impurities in acid-process alumina
CN110407249A (en) A kind of method that discarded honeycomb type denitrification catalyst prepares titanium dioxide
CN105347785A (en) Titanium-based ceramic taking waste vanadium-titanium denitration catalyst as raw material and preparation method thereof
CN103738972B (en) A kind of residue of aluminum-extracted pulverized fuel ash prepares the method for silicon powder
CN103818969B (en) Red iron oxide and preparation method thereof
CN101306928B (en) Pre- desiliconizing method from fly ash or slag
CN103214013A (en) Preparation method of high-purity alumina powder
CN102815728A (en) Method for preparing nano-sized magnesium hydroxide and nano-silica by utilization of boron mud
CN101302021A (en) Method for extracting aluminum oxide from fly ash
CN102229455A (en) Process for processing chromate-containing waste water
CN105502426A (en) Method for preparing water glass through extracting silicon oxide from chrysotile tailings by strong-base roasting method
CN103449483A (en) Impurity removing method in process of preparing alumina from fly ash by utilizing acid method
CN107662935A (en) A kind of method that aluminum oxide and silicic acid are extracted from flyash
CN105668597B (en) The method of flyash soda acid combined extracting aluminium base product and silica-based products
CN1940097A (en) Extraction of chromium from mud containing chromium by sodium-salt calcination
CN110540223A (en) method for simultaneously extracting aluminum oxide from two aluminum-containing waste residues of fly ash and red mud
CN107573978A (en) Chemical method prepares the removing system and method for acid-soluble mineral in ultra-clean coal
CN104478001A (en) Method for producing iron oxide yellow from acidic waste water in titanium dioxide industry
CN102092732A (en) Method for preparing water glass and precipitated silica from treatment waste residues of sulfuric acid residues
CN108147454B (en) method for treating dilute waste acid byproduct in acid preparation from sulfur concentrate sand
CN207646156U (en) Chemical method prepares the removing system of acid-soluble mineral in ultra-clean coal
CN103754905A (en) Process for combined production of alumina as well as active calcium silicate and cement from gangue

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: 20180206

RJ01 Rejection of invention patent application after publication