CN102190322A - Method for removing sodium from red mud generated in aluminum oxide industry - Google Patents

Method for removing sodium from red mud generated in aluminum oxide industry Download PDF

Info

Publication number
CN102190322A
CN102190322A CN2010101217563A CN201010121756A CN102190322A CN 102190322 A CN102190322 A CN 102190322A CN 2010101217563 A CN2010101217563 A CN 2010101217563A CN 201010121756 A CN201010121756 A CN 201010121756A CN 102190322 A CN102190322 A CN 102190322A
Authority
CN
China
Prior art keywords
red mud
sodium
ammonium chloride
aluminum oxide
chloride
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN2010101217563A
Other languages
Chinese (zh)
Other versions
CN102190322B (en
Inventor
王云山
杨刚
张金平
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.)
Institute of Process Engineering of CAS
Original Assignee
Institute of Process Engineering of CAS
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 Institute of Process Engineering of CAS filed Critical Institute of Process Engineering of CAS
Priority to CN2010101217563A priority Critical patent/CN102190322B/en
Publication of CN102190322A publication Critical patent/CN102190322A/en
Application granted granted Critical
Publication of CN102190322B publication Critical patent/CN102190322B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • 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
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/91Use of waste materials as fillers for mortars or concrete

Abstract

The invention relates to a method for removing sodium from red mud generated in aluminum oxide industry, particularly a method in which strong acid ammonium salt (ammonium chloride) is used to substitute a strong acid (hydrochloric acid) for removing sodium from red mud generated in aluminum oxide industry. In the invention aiming to treat high-base red mud generated in aluminum oxide industry, strong basicity of the red mud is used to decompose ammonium chloride and release ammonia gas, and sodium element, calcium element, magnesium element and the like in the red mud are converted into soluble chlorides so as to separate from a final residue of the red mud; sodium element and magnesium element in the final residue meet the requirement of a cement additive, thereby utilizing the red mud and eliminating environmental pollution; under the action of ammonia gas released and decomposed from ammonium chloride and added carbon dioxide, magnesium and calcium chlorides generate magnesium hydroxide precipitate and calcium carbonate precipitate, and sodium chloride is converted into low-solubility sodium bicarbonate; after being separated from ammonium chloride, the low-solubility sodium bicarbonate is causticized to return to aluminum oxide production process to be recycled, thus immobilizing carbon dioxide and circularly regenerating ammonium chloride.

Description

Remove the method for sodium in the red mud of aluminum oxide industry output
Technical field
The present invention relates to remove the method for sodium in the red mud of aluminum oxide industry output, particularly utilize strong acid ammonium salt (ammonium chloride) to replace strong acid (hydrochloric acid) to remove the method for sodium in the red mud of aluminum oxide industry output.
Technical background
Red mud is the iron content solid slag of discharging in the aluminum oxide smelting process, and along with the decline of aluminum oxide aluminium industrial expansion and ore grade, red mud amount is more and more big, about 2,000 ten thousand tons of the red mud of the annual discharging of China at present.No matter be to adopt Bayer process, sintering process or integrated process, alkali content higher (generally being higher than 2.5%) in the red mud, because of its sodium content exceeds standard, its utilization ratio is lower, red mud takes off sodium and make, and turns waste into wealth to change into social concern into reality.A large amount of red muds are stacked at open storage, not only take valuable land resources, cause environmental pollution, a kind of especially wasting of resources.How to effectively utilize red mud, making it to turn waste into wealth becomes the social concern of a reality, also becomes the interested research topic of numerous researchers.
Since nineteen seventies,, carried out many-sided research both at home and abroad, occurred successively that wet method is taken off sodium, pyrogenic process takes off methods such as sodium, bacterium leaching, membrane technique and selective flocculation for reducing the red mud alkalinity.Pyrogenic process expense height, it is low to take off the sodium rate, and operational condition also is restricted, if only for reducing alkali number in the red mud, generally should not adopt pyrogenic process; No matter be Bayer process red mud or red mud from sintering process, wet method is taken off sodium and is all comprised alkali stripping method, acid leaching process, salt lixiviation process etc.No matter adopt which kind of method, purpose all is to make red mud after dealkalize, and the gained filter cake becomes low alkali red mud (Na 2O<1%), the raw material that can be used as manufacture of cement.
Lime dealkalize method is the more a kind of method of using in the present alkali stripping method, is about to the sodium oxide (Na in the red mud 2O) with lime (Ca (OH) 2) displacement, reaction equation is shown in (1) formula: Na 2OAl 2O 31.7SiO 2XH 2O+Ca (OH) 2→ CaOAl 2O 31.7SiO 2XH 2O+Na 2O (1)
Lime dealkalize method exist the quantity of slag big, take off problems such as the sodium rate is low, cost height.
Pickling process mainly is to adopt concentrated acid to leach red mud to realize its comprehensive utilization, and leaching agent is sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, hydrofluoric acid and sulfurous gas etc., and the key of this method is the residue after how rationally utilizing leach liquor and leaching.There is the shortcoming that operating environment is poor, waste liquid amount big and be difficult to handle again in pickling process.
The salt lixiviation process mainly is meant and adopts some inorganic salt solution or its acidic solution to make leaching agent, with sodium oxide and other useful component in the dissolving red mud.External priority is carried out persulfuric acid iron, Tai-Ace S 150, calcium sulfate waste liquid, is reached sulfuric acid mixing ammonium sulfate leaching etc.It is higher that the salt method is taken off the sodium rate, but red mud slurry strainability is poor.
Summary of the invention
The method that the purpose of this invention is to provide sodium in a kind of red mud that removes the aluminum oxide industry output particularly utilizes strong acid ammonium salt (ammonium chloride) to replace strong acid (hydrochloric acid) to remove the method for sodium in the red mud of aluminum oxide industry output.
The method of sodium is meant that the high-alkali red mud with the aluminum oxide industry output is a process object in the red mud that removes the aluminum oxide industry output of the present invention, utilize the strong basicity of red mud that ammonium chloride is decomposed and discharge ammonia, make elements such as sodium element, calcium constituent and magnesium in the red mud form soluble chloride simultaneously and separate with the red mud finishing slag; Sodium element in the finishing slag and magnesium element content satisfy the cement additire requirement, make red mud utilized, and eliminate environmental pollution; The ammonia that utilizes ammonium chloride to decompose to discharge and the carbonic acid gas of interpolation, make magnesium and calcium muriate form magnesium hydrate precipitate and precipitation of calcium carbonate, sodium-chlor changes into the low solubility sodium bicarbonate to be separated with ammonium chloride after causticization is returned the aluminum oxide production process recycle, both fixed carbonic acid gas, and made ammonium chloride be able to cyclic regeneration again.
The method of sodium comprises that mainly the ammonium chloride pressurization leaches, filters operation stepss such as (solid-liquid separation), washing, precipitation and ammonium chloride reprocessing cycle in the red mud that removes the aluminum oxide industry output of the present invention:
A. at first the red mud of the aluminum oxide industry output behind the pulverizing and jevigating is mixed with ammonium chloride solution that (wherein the two ratio is formed according to different red muds and decided, make integral molar quantity theoretical excessive 20%~50% of the metal oxide of magnesium elements, calcium constituent, sodium element, ferro element and aluminium element in the relative red mud of ammonium chloride, the mass concentration of ammonium chloride solution is preferably 20~40%); In temperature is preferred reaction about 3~5 hours under 130~170 ℃, airtight, agitation condition; In reaction process, when temperature is higher than 100 ℃,, will produce pressure in the reactor because ammonium chloride decomposes the generation of water vapour when discharging ammonia and system and reaching vapor liquid equilibrium, so raise with temperature, pressure increases thereupon, therefore claims the pressurization leaching; Because intermittent discharge ammonia (wherein water entrainment steam) will make the pressure in the reactor produce fluctuation in the reaction process, along with the discharge of ammonia, react continuous forward and will carry out, and emit ammonia, till ammonium chloride no longer decomposes in system; The pressure that produces under above-mentioned temperature of reaction is 0.3~0.8MPa; By making the magnesium elements in the red mud, metal oxide of calcium constituent and sodium element (sodium element in the red mud mainly exists with sodium hydroxide and yellow soda ash form) and ammonium chloride reaction, obtain containing the magnesium chloride of ammonium chloride, the metal chloride mixing solutions of calcium chloride and sodium-chlor is (because of ferric oxide in the red mud and aluminum oxide are intermediate oxide (existing acidity, alkalescence is arranged) again, therefore also can consume ammonium chloride as alkaline metal oxide, just since in the end reaction system pH about 4.0, the iron(ic) chloride of generation and aluminum chloride can take place hydrolysis become ironic hydroxide and aluminium hydroxide stay slag mutually in), (element that contains in the red mud finishing slag mainly is an iron for ammonium chloride decomposition and the ammonia that contains water vapour that discharges and red mud finishing slag, aluminium and silicon etc.); The ammonia that contains water vapour that obtains is obtained ammoniacal liquor after condensation;
B. the magnesium chloride that contains ammonium chloride that step a is obtained after filtering, the metal chloride mixing solutions of calcium chloride and sodium-chlor reacts (all relative described magnesium chloride that contains ammonium chloride of ammoniacal liquor and carbonic acid gas with ammoniacal liquor and carbonic acid gas (extracting in the stack gas or other approach acquisition) that step a obtains, the integral molar quantity of the metal chloride of calcium chloride and sodium-chlor theoretical excessive about 20~30%), obtain magnesium hydroxide and precipitation of calcium carbonate, sodium-chlor is transformed into sodium bicarbonate simultaneously, and utilize the lower characteristics of the solubleness of sodium bicarbonate in ammonium chloride solution, sodium bicarbonate is separated with ammonium chloride solution;
C. the ammonium chloride solution that step b is obtained returns step a, recycles;
D. can send the cement mill to make raw material after the red mud finishing slag that step a is obtained after filtering washes with water uses.
Step a can be expressed by equation (1)~(6):
CaO+2NH 4Cl→CaCl 2+2NH 3↑+H 2O (1)
MgO+2NH 4Cl→MgCl 2+2NH 3↑+H 2O (2)
NaOH+NH 4Cl→NaCl+NH 3↑+H 2O (3)
Na 2CO 3+2NH 4Cl→2NaCl+2NH 3↑+CO 2↑+H 2O (4)
Fe 2O 3+6NH 4Cl→2FeCl 3+6NH 3↑+3H 2O (5)
Al 2O 3+6NH 4Cl→2AlCl 3+6NH 3↑+3H 2O (6)
Wherein iron(ic) chloride and aluminum chloride generation hydrolysis reaction are as follows:
FeCl 3→Fe 3++3Cl - H 2O→H ++OH - Fe 3++3OH -→Fe(OH) 3
AlCl 3→Al 3++3Cl - H 2O→H ++OH - Al 3++3OH -→Al(OH) 3
Step b can be expressed by equation (7)~(9):
MgCl 2+2NH 3+2H 2O→2NH 4Cl+Mg(OH) 2↓ (7)
CaCl 2+2NH 3+CO 2+H 2O→2NH 4Cl+CaCO 3↓ (8)
NaCl+NH 3+CO 2+H 2O→NH 4Cl+NaHCO 3↓ (9)
The red mud of described aluminum oxide industry output is meant the iron content solid slag that produces in the aluminum oxide production process, no matter is to adopt Bayer process, sintering process or integrated process, because of its sodium content exceeds standard, and makes its utilization ratio lower.Red mud method for removing Na of the present invention can be turned waste into wealth.
The present invention is a conversion medium with strong acid ammonium salt ammonium chloride, realizes removing of sodium in the red mud, and calcium and magnesium can stabilizing carbon dioxides, and sodium and magnesium index satisfy the cement additire requirement in the red mud finishing slag.
The present invention is not because of there being the adding of strong acid, and the requirement of equipment material is greatly reduced, and technical process is comparatively simple, and sodium decreasing ratio height, red mud finishing slag after taking off sodium can be made cement, eliminates environmental pollution.
The present invention utilizes ammonium chloride to replace the hydrochloric acid pressurization to leach sodium in the red mud that removes the aluminum oxide industry output.More than 130 ℃, utilize the strong basicity of red mud that ammonium chloride is decomposed and discharge ammonia, make elements such as sodium, calcium and magnesium in the red mud form soluble chloride simultaneously and separate with the red mud finishing slag; Sodium in the finishing slag and magnesium elements get content and satisfy the cement additire requirement, make red mud utilized, and eliminate environmental pollution; The ammonia that utilizes ammonium chloride to decompose to discharge and the carbonic acid gas of interpolation, make the muriate of elements such as calcium, magnesium and sodium form magnesium hydroxide and precipitation of calcium carbonate, sodium-chlor changes into sodium bicarbonate to be separated with ammonium chloride after causticization is returned the aluminum oxide production process recycle, both carbon dioxide fixation can be played, the ammonium chloride cyclic regeneration can be made again.Experimental results show that the sodium in the red mud that utilizes ammonium chloride to remove the aluminum oxide industry output is practical, sodium decreasing ratio height in the finishing slag, sodium oxide content<0.7%, therefore content of magnesia<0.5% can be used as cement raw material and is able to resource utilization; Because of there not being the adding of strong acid, equipment material requires to reduce, and technical process is comparatively simple; Finishing slag system cement has been realized the red mud resource utilization, has eliminated environmental pollution.The present invention provides novel method for the resource utilization of a large amount of red muds of aluminum oxide industry output.It is a new method that removes sodium in the aluminum oxide industry output red mud.
The present invention is further illustrated below in conjunction with drawings and Examples.
Description of drawings
Fig. 1. aluminum oxide industry output red mud of the present invention takes off the process flow diagram of sodium.
Fig. 2. the synoptic diagram of the sodium equipment therefor in the red mud that removes the aluminum oxide industry output is leached in the pressurization of the inventive method ammonium chloride.
Reference numeral
1. collector 2. condensers 3. gas bombs 4. air intake valves
5. charging valve 6. bleeder valves 7. electrically heated pressure reaction stills 8. stirring arms
9. tensimeter 10. magnetic stirrers 11. thermopairs 12. program temperature controllers
Embodiment
Embodiment 1.
See also Fig. 2, this device leaches the main reaction device synoptic diagram of the sodium in the red mud that removes the aluminum oxide industry output for ammonium chloride pressurizes, and major parts is that electrically heated pressure reaction still 7 (make by stainless steel, useful volume 2L, kettle cover is detachable, by bolted, airtight can the highest withstand voltage 10MPa).
Tensimeter 9 is installed to show the still internal pressure on the kettle cover outside of described electrically heated pressure reaction still 7; Thermopair 11 at the bottom of the described electrically heated pressure reaction still of insertion of the described electrically heated stress reaction temperature in the kettle of one control, the program temperature controller 12 that is communicated with power supply with described electrically heated pressure reaction still outward is connected; Inner bottom part central authorities at described electrically heated pressure reaction still are provided with stirring arm 8, and described stirring arm is connected with the magnetic stirrer 10 of top, described electrically heated stress reaction kettle cover outside, and are controlled the rotating speed of stirring arm by magnetic stirrer; One gas bomb 3 is connected with the pipeline that has air intake valve 4 that inserts described electrically heated pressure reaction still inside, on the pipeline that has air intake valve 4, be connected with the pipeline that has charging valve 5, one the other end that inserts the pipeline that has bleeder valve 6 of described electrically heated pressure reaction still inside is connected with condenser 2, and condenser 2 is connected with collector 1 by pipeline.
Material is added by the detachable kettle cover of described electrically heated pressure reaction still 7, and uses bolted, and is airtight; Connect power supply, open outer described program temperature controller 12 switches of described electrically heated pressure reaction still, setting program, heating together with power supply; Open described magnetic stirrer 10 switches of top, described electrically heated stress reaction kettle cover outside, adjust the rotating speed of the central described stirring arm 8 that is provided with of inner bottom part of described electrically heated pressure reaction still, stir material in the described electrically heated pressure reaction still; The outer described tensimeter of installing 9 of described electrically heated stress reaction kettle cover shows the still internal pressure, and described program temperature controller 12 shows temperature in the kettle, and by described thermopair 11 controlled temperature; Described gas bomb 3 (experiment is the nitrogen steel cylinder) provides pressure (greater than the still internal pressure), to go in the still from the hydraulic pressure of described feed valve 5 through described intake valve 4, gas is discharged in still via described bleeder valve 6, after described condenser 2 coolings, is collected by described collector 1.
Above-mentioned equipment therefor is a kind of selection, does not have uniqueness and exclusiveness, also can adopt other similar devices to realize the present invention.
The red mud that provides with Gongyi, Henan alumina producer is as raw material, and its chemical constitution is as shown in table 1.
The chemical constitution of aluminum oxide industry output red mud is adopted in table 1, experiment
Element Na Ca Mg Fe Al Si K O Other Add up to
Wt% 6.16 6.85 0.29 15.27 10.53 12.77 0.024 33.91 14.196 100
Oxide compound Na 2O CaO MgO Fe 2O 3 Al 2O 3 SiO 2 K 2O - Other Add up to
Wt% 8.30 9.59 0.48 21.81 19.89 27.37 0.029 - 12.531 100
The method core that the present invention removes sodium in the red mud of aluminum oxide industry output is an ammonium chloride pressurization leaching process, comprises supporting processes such as filtration, precipitation, washing in addition, and technical process sees also Fig. 1, and the ammonium chloride pressurization is leached used reaction unit as above.
Take by weighing the 100g red mud and (cross 100 mesh sieves behind the pulverizing and jevigating, form as shown in table 1) and 182g ammonium chloride, and measure the 425ml deionized water with the dissolving ammonium chloride of being got, the mass concentration that obtains ammonium chloride solution is 30% (the ammonium chloride consumption is with respect to theoretical excessive 20% of the integral molar quantity of the metal oxide of the magnesium elements in the red mud, calcium constituent, sodium element, ferro element and aluminium element at this moment).Above-mentioned whole materials are added in the described electrically heated pressure reaction still 7, airtight, temperature programming is carried out in control by described thermopair 11 and described program temperature controller 12, making the temperature in the described electrically heated pressure reaction still is 130 ℃, the mixing speed of controlling described stirring arm 8 by described magnetic stirrer 10 is 300rpm, carry out the ammonium chloride pressurization (along with temperature in the kettle raises, ammonium chloride decomposes, to there be ammonia and water vapour to exist in the system, thereby the gas-liquid-solid phase reaction that leaches generation pressure), reaction times is 4 hours, make the magnesium elements in the red mud, the metal oxide of calcium constituent and sodium element and ammonium chloride react, and obtain containing the magnesium chloride of ammonium chloride, the metal chloride mixing solutions of calcium chloride and sodium-chlor, ammoniacal liquor and red mud finishing slag.After 130 ℃ of the temperature of reaction that reaches setting, be interrupted the rare gas element (system initially has residual air) of discharging in the reaction system by described blow-off valve 6, carbonic acid gas, ammonia and water vapor, and by described condenser 2 condensations, collect ammoniacal liquor and recording volume by described collector 1, (this pressure changes with the still internal pressure to provide pressure by described nitrogen gas steel cylinder 3 simultaneously, a little higher than still internal pressure, purpose is to overcome the still internal pressure and hydraulic pressure is gone in the still, to keep liquid-solid ratio in the still), control by described air intake valve 4 and described charging valve 5 adds entry, the water equivalent that the water yield of this adding is taken out of when discharging via bleeder valve 6 with ammonia is with the maintenance system liquid-solid ratio.After reaching 4 hours time of setting reaction, stop heating, be cooled to below 100 ℃ and normal pressure (by described tensimeter 9 indications), stop to stir, open the capping of described electrically heated pressure reaction still 7, discharging, filter while hot, and (dry back is 85.7g to add the red mud finishing slag of gained behind the clear water washing and filtering, can send the cement mill to make raw material uses), the ammoniacal liquor and the carbonic acid gas that in pH is 4.3 filtered liquid, add simultaneously system recoveries, (all relative described magnesium chloride that contains ammonium chloride of ammoniacal liquor with carbonic acid gas, the integral molar quantity of the metal chloride of calcium chloride and sodium-chlor theoretical excessive 20~30%) make magnesium chloride in the system and calcium chloride form magnesium hydrate precipitate and precipitation of calcium carbonate, sodium-chlor change into low solubility sodium bicarbonate and with can remove calcining system soda ash after ammonium chloride separates, the ammonium chloride solution that generates in the precipitation process returns ammonium chloride pressurization leaching process and recycles.
The result that embodiment 1 handles the 100g red mud is: magnesium hydroxide and precipitation of calcium carbonate be 15.3g altogether, the about 85.7g of red mud finishing slag amount, its sodium element content<0.5% (sodium oxide content<0.7%), magnesium element content<0.2% (content of magnesia<0.5%), satisfy the cement additire requirement, can be used as the system cement raw material.
Embodiment 2
Adopting the method and apparatus of embodiment 1, is that different reaction conditionss is:
Material proportion: take by weighing 100g red mud (cross 100 mesh sieves behind the pulverizing and jevigating, form as shown in table 1), take by weighing 210g ammonium chloride, measure deionized water 490ml.
Experiment condition: in 170 ℃ of temperature of reaction, the relative red mud of ammonium chloride the mass concentration theoretical excessive 50%, ammonium chloride solution of the integral molar quantity of the metal oxide of magnesium elements, calcium constituent, sodium element, ferro element and aluminium element be 30%, mixing speed 300rpm, in 4 hours reaction times, all the other operations are identical with embodiment 1.
Experimental result: filtering filtrate pH is 4.1, and filtering the dry back of filter cake (red mud finishing slag) is 86.3g.
The result that embodiment 2 handles the 100g red mud is: magnesium hydroxide and precipitation of calcium carbonate be 15g altogether, the about 86.3g of red mud finishing slag amount, its sodium element content<0.5% (sodium oxide content<0.7%), magnesium element content<0.2% (content of magnesia<0.5%), satisfy the cement additire requirement, can be used as the system cement raw material.

Claims (4)

1. the method for sodium in the red mud that removes the aluminum oxide industry output is characterized in that this method may further comprise the steps:
A. at first the red mud of the aluminum oxide industry output behind the pulverizing and jevigating is mixed with ammonium chloride solution, and make the metal oxide of magnesium elements, calcium constituent, sodium element, ferro element and aluminium element in the relative red mud of ammonium chloride integral molar quantity theoretical excessive 20%~50%; Under temperature is 130~170 ℃, airtight, agitation condition, react, and to make the pressure that produces under above-mentioned temperature of reaction be 0.3~0.8MPa; Metal oxide and ammonium chloride reaction by making magnesium elements, calcium constituent and sodium element in the red mud obtain containing the metal chloride mixing solutions of magnesium chloride, calcium chloride and the sodium-chlor of ammonium chloride, the ammonia that contains water vapour and red mud finishing slag; The ammonia that contains water vapour that obtains is obtained ammoniacal liquor after condensation;
B. the ammoniacal liquor and the carbon dioxide reaction that obtain of the metal chloride mixing solutions of the magnesium chloride that contains ammonium chloride, calcium chloride and the sodium-chlor that step a is obtained after filtering and step a, obtain magnesium hydroxide and precipitation of calcium carbonate, sodium-chlor is transformed into sodium bicarbonate simultaneously, and utilize the lower characteristics of the solubleness of sodium bicarbonate in ammonium chloride solution, sodium bicarbonate is separated with ammonium chloride solution; Wherein, theoretical excessive 20~30% of the integral molar quantity of the metal chloride of all relative described magnesium chloride, calcium chloride and the sodium-chlor that contains ammonium chloride of ammoniacal liquor with carbonic acid gas;
C. the ammonium chloride solution that step b is obtained returns step a, recycles.
2. the method for sodium in the red mud that removes the aluminum oxide industry output according to claim 1 is characterized in that: send the cement mill to make raw material after the red mud finishing slag that step a is obtained after filtering washes with water and use.
3. the method for sodium in the red mud that removes the aluminum oxide industry output according to claim 1, it is characterized in that: the mass concentration of the described ammonium chloride solution of step a is 20~40%.
4. the method for sodium in the red mud that removes the aluminum oxide industry output according to claim 1 is characterized in that: the time of reaction is 3~5 hours to the described air tight condition of step a down.
CN2010101217563A 2010-03-10 2010-03-10 Method for removing sodium from red mud generated in aluminum oxide industry Expired - Fee Related CN102190322B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010101217563A CN102190322B (en) 2010-03-10 2010-03-10 Method for removing sodium from red mud generated in aluminum oxide industry

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010101217563A CN102190322B (en) 2010-03-10 2010-03-10 Method for removing sodium from red mud generated in aluminum oxide industry

Publications (2)

Publication Number Publication Date
CN102190322A true CN102190322A (en) 2011-09-21
CN102190322B CN102190322B (en) 2013-02-27

Family

ID=44599322

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010101217563A Expired - Fee Related CN102190322B (en) 2010-03-10 2010-03-10 Method for removing sodium from red mud generated in aluminum oxide industry

Country Status (1)

Country Link
CN (1) CN102190322B (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102491620A (en) * 2011-12-06 2012-06-13 中国铝业股份有限公司 Method for separating red mud component
CN110540225A (en) * 2019-09-17 2019-12-06 昆明理工大学 recycling treatment process for red mud roasted by waste mushroom sticks
CN111960451A (en) * 2020-09-02 2020-11-20 陶予敏 Process for producing soda ash, alumina and blended cement by utilizing red mud
CN112479230A (en) * 2020-12-16 2021-03-12 中原工学院 Carbon fixation method for high-alkalinity alumina red mud
CN113005285A (en) * 2021-02-26 2021-06-22 青岛核盛智能环保设备有限公司 Process for producing brown corundum by using red mud
CN113044868A (en) * 2021-04-25 2021-06-29 青岛核盛智能环保设备有限公司 Red mud hydrogen reduced iron secondary heat molten salt iron, scandium, gallium, aluminum, titanium and silicon decomposition process
CN113929107A (en) * 2021-10-18 2022-01-14 北京科技大学 Method and equipment for solidifying sodium element in red mud by virtue of supergravity
WO2024074144A1 (en) * 2022-10-08 2024-04-11 淄博益海环保科技有限公司 Resource comprehensive utilization process for solid waste of red mud, fly ash, steel slag and coal gangue

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN86104039A (en) * 1986-06-17 1987-12-30 郑州铝厂 Produce the red mud separating technique in the alumina process
JP2006045053A (en) * 2004-07-05 2006-02-16 Showa Denko Kk Method for manufacturing aluminum salt solution, aluminum salt solution, aluminum salt, purifying facility using aluminum salt solution, and article manufactured using aluminum salt solution

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN86104039A (en) * 1986-06-17 1987-12-30 郑州铝厂 Produce the red mud separating technique in the alumina process
JP2006045053A (en) * 2004-07-05 2006-02-16 Showa Denko Kk Method for manufacturing aluminum salt solution, aluminum salt solution, aluminum salt, purifying facility using aluminum salt solution, and article manufactured using aluminum salt solution

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
张振: "利用氯化镁降低赤泥中碱含量的研究", 《化学工程师》 *
梅贤功等: "国外氧化铝赤泥脱钠的进展", 《轻金属》 *
马淑花等: "赤泥中氧化钠和氧化铝的回收", 《矿产综合利用》 *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102491620A (en) * 2011-12-06 2012-06-13 中国铝业股份有限公司 Method for separating red mud component
CN110540225A (en) * 2019-09-17 2019-12-06 昆明理工大学 recycling treatment process for red mud roasted by waste mushroom sticks
CN111960451A (en) * 2020-09-02 2020-11-20 陶予敏 Process for producing soda ash, alumina and blended cement by utilizing red mud
CN112479230A (en) * 2020-12-16 2021-03-12 中原工学院 Carbon fixation method for high-alkalinity alumina red mud
CN113005285A (en) * 2021-02-26 2021-06-22 青岛核盛智能环保设备有限公司 Process for producing brown corundum by using red mud
CN113044868A (en) * 2021-04-25 2021-06-29 青岛核盛智能环保设备有限公司 Red mud hydrogen reduced iron secondary heat molten salt iron, scandium, gallium, aluminum, titanium and silicon decomposition process
CN113929107A (en) * 2021-10-18 2022-01-14 北京科技大学 Method and equipment for solidifying sodium element in red mud by virtue of supergravity
CN113929107B (en) * 2021-10-18 2022-05-03 北京科技大学 Method and equipment for solidifying sodium element in red mud by virtue of supergravity
WO2024074144A1 (en) * 2022-10-08 2024-04-11 淄博益海环保科技有限公司 Resource comprehensive utilization process for solid waste of red mud, fly ash, steel slag and coal gangue

Also Published As

Publication number Publication date
CN102190322B (en) 2013-02-27

Similar Documents

Publication Publication Date Title
CN102190322B (en) Method for removing sodium from red mud generated in aluminum oxide industry
CN106830030B (en) A kind of method using the safe and efficient production sandy alumina of aluminium ash
CN102351226B (en) Method for producing aluminum oxide from fly ash
CN104520237B (en) The method for handling flying dust
CN100542961C (en) A kind of technology of processing bauxite to produce hydroted alumina with sodium hydroxide molten salt growth method
CN104386720B (en) Method for acid-alkali combined extraction of alumina from high-silicon aluminum-containing mineral raw material
CN103030160B (en) Method for recycling alumina and sodium oxide from bayer process red mud
CN102191374B (en) Method for recycling traditional chromium residue
CN104445313B (en) Method for extracting aluminum oxide from fly ash by acid-base combination
CN102897810B (en) Method for producing aluminum oxide by using fly ash
CN102476820B (en) Method for extracting alumina from coal ash through wet process
CN103276218B (en) Method for recycling vanadium from vanadium-containing electrolysis aluminum slag ash
CN101863500A (en) Method for producing alumina with aluminum-containing metallurgical material
CN111498820A (en) Process for simultaneously preparing high-quality calcium sulfate whiskers from phosphorus concentrate enriched by medium-low-grade phosphate ore or phosphorus tailings
CN102502733A (en) Method for treating gibbsite by using high-concentration alkali liquor under normal pressure
CN102965506B (en) Method for removing aluminum from rare earth solution by benzoate precipitation method
CN108946772A (en) A method of pure Lithium Carbonate is prepared by lithium ore
Zhang et al. A novel indirect wollastonite carbonation route for CO2 sequestration
CN103318960A (en) Separation method for completion liquid of caustic soda liquid-phase oxidation of chromite
CN104445310A (en) Novel process for treating middle-low bauxite in complete wet method alkali system
CN103351014A (en) Method for extraction and preparation of alumina from coal ash
CN101760638B (en) Method for recovering magnesium from magnesium sulfate solution
CN111777087A (en) System and method for producing alumina from coal gangue
CN115353139B (en) Preparation method of high-purity calcium carbonate
CN103738989B (en) A kind of middle-low bauxite produces the method for aluminum oxide

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20130227

Termination date: 20170310