CN102674477A - Method for co-production of superfine ferroferric oxide and aluminum oxide by red mud of Bayer process - Google Patents

Method for co-production of superfine ferroferric oxide and aluminum oxide by red mud of Bayer process Download PDF

Info

Publication number
CN102674477A
CN102674477A CN2012101645156A CN201210164515A CN102674477A CN 102674477 A CN102674477 A CN 102674477A CN 2012101645156 A CN2012101645156 A CN 2012101645156A CN 201210164515 A CN201210164515 A CN 201210164515A CN 102674477 A CN102674477 A CN 102674477A
Authority
CN
China
Prior art keywords
red mud
bayer process
water lotion
obtains
washing
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
CN2012101645156A
Other languages
Chinese (zh)
Inventor
党晓娥
兰新哲
刘成鹏
董缘
淮敏超
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Xian University of Architecture and Technology
Original Assignee
Xian University of Architecture and Technology
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 Xian University of Architecture and Technology filed Critical Xian University of Architecture and Technology
Priority to CN2012101645156A priority Critical patent/CN102674477A/en
Publication of CN102674477A publication Critical patent/CN102674477A/en
Pending legal-status Critical Current

Links

Abstract

The invention discloses a method for co-production of superfine ferroferric oxide and aluminum oxide by red mud of the Bayer process, comprising the following steps of: adding wet red mud after being dried and hydrochloric acid into a reactor to stir and filter, obtaining filter liquid 1 containing iron ions and aluminum ions; adding Na2SO3 and polyethylene glycol to the filter liquid 1, and then using NaOH to regulate the pH (Potential Of Hydrogen) of leaching liquid to 11.5-12.5; obtaining Fe3O4 deposition and filter liquid 3; washing Fe3O4 deposition by water and absolute ethyl alcohol, drying the deposition, and obtaining pure Fe3O4; after adding polyethylene glycol to the filter liquid 3, using hydrochloric acid to regulate the pH in order to enable the aluminum ions deposit in an aluminum hydroxide manner, and obtaining aluminum hydroxide deposition; and washing the aluminum hydroxide deposition by water and absolute ethyl alcohol, drying and calcining the deposition, and then obtaining Al2O3. The preparation method disclosed by the invention is suitable for various Bayer process red mud with different components, so that environment pollution and land occupation problem caused by the red mud of Bayer process can be solved, waste is changed into treasure, and simultaneously, alence component iron and aluminum in the red mud are used to prepare magnetic ferroferric oxide and aluminum oxide so as to improve the comprehensive utilization value of the red mud of the Bayer process.

Description

Bayer process red mud co-production of ultrafine Z 250, method of alumina
Technical field
The present invention relates to a kind of method of comprehensive utilization of Bayer process red mud, belong to the comprehensive utilization of environmental protection and industrial residue, be specifically related to a kind of Bayer process red mud co-production of ultrafine Z 250, method of alumina.
Background technology
Bayer process red mud is the solid waste of discharging in the alumina producing Bayer process process, because of its appearance color is gained the name with redness of the skin or complexion earth is similar.Red mud belongs to the highly basic waste residue, is a kind of serious alkaline pollution source, and one ton of aluminum oxide of every production approximately produces 0.8-1.5 ton red mud.China is alumina producing big country, produces 2,378 ten thousand tons in aluminum oxide in 2009, and nearly 3,000 ten thousand tons of the red mud that produces.China's red mud comprehensive utilization ratio is merely 4% at present, and the accumulation volume of cargo in storage reaches 200,000,000 tons.Along with the growth year by year of China's aluminum oxide output and the reduction gradually of bauxite grade, the contracts amount of red mud also will constantly increase, and expect 2015, and red mud accumulative total volume of cargo in storage will reach 3.5 hundred million tons.
The mineral composition of Bayer process red mud is comparatively complicated; And different and different with the raw ore mineral composition with leaching condition, staple has the hydrated alumina of rhombohedral iron ore (or pyrrhosiderite etc.), hydrated aluminum silicate (sodalite, kankrinite), calcium aluminosilicate hydrate, quartz, calcium titanate and a small amount of not stripping etc.Because the Bayer process red mud iron content is high; Corrosion-resistant is difficult to directly be used for building material industry, and Bayer process red mud basicity is high, output is big; Traditional store up, fill out processing mode such as sea and will water body, atmosphere, the soil of periphery be polluted, had a strong impact on the Sustainable development of aluminium industry.Therefore, the comprehensive recovery of Bayer process red mud has become the important topic that China's aluminum oxide industry is realized recycling economy and Sustainable development with utilization.
At present, the comprehensive utilization main path of Bayer process red mud has three aspects: (1) comprehensive treating process is used to produce the pig iron, aluminum oxide and cement, and this some countries that are utilized in of red mud have reached the pilot-plant test stage.(2) produce material of construction and stupalith, at the existing industrial practice of states such as Germany and Hungary.(3) replace bentonite to be used for the briquetting of blast furnace ironmaking raw material.These three kinds are utilized approach basically all is the application of traditional field, and the secondary valence value is low.Therefore; From the utilization of resources, prevent and remedy pollution, protect land resources and economic benefit aspect to take all factors into consideration, the best mode that addresses this problem is to be that raw material production aluminium, iron series higher pair is worth fine chemical product and extracts yttrium wherein with the red mud.
Summary of the invention
The object of the present invention is to provide a kind of Bayer process red mud co-production of ultrafine Z 250, method of alumina; The present invention is the ultra-fine Z 250 of feedstock production, ultra-fine alumina with the waste red mud residues; This method has made full use of the principal element of the iron in the red mud, aluminium, silicon, reduces the harm of red mud to environment to greatest extent.
For realizing the foregoing invention purpose, the present invention takes following technical scheme:
Bayer process red mud co-production of ultrafine Z 250, method of alumina may further comprise the steps:
1) lixiviate: behind the red mud drying that will wet, be 1g:3-5mL, dried red mud and 8-10 mol hydrochloric acid added in the reactor drum stir, and be heated to 80-100 ℃, be incubated 1-2 hour according to red mud weight and hydrochloric acid volume ratio;
2) filter: filtered while hot obtains containing iron ion, aluminum ions filtrating 1 and a residue;
3) ultra-fine Fe 3O 4Preparation:
After the iron concentration of adjustment filtrating 1 was 0.25mol/L, the iron concentration mol ratio was that the concentration of 1:1-1.5 is the reductive agent Na of 0.5mol/L in adding and the solution 2SO 3Solution and solution quality 15-20% surfactant polyethylene, pH of leaching solution is regulated to 11.5-12.5 with the NaOH of 2mol/L in the back, at 70-90 ℃ of stirring reaction 0.5-1.0 hour after-filtration, obtains Fe 3O 4The deposition and filtrate 3, Fe 3O 4Deposition obtains pure Fe through washing, organic solvent absolute ethanol washing after drying 3O 4, obtain water lotion 4 and organic solvent washing liquid 5 simultaneously;
4) ultra-fine Al 2O 3Preparation:
After in filtrating 3, adding the surfactant polyethylene of its quality 2-4%; Regulate its pH value with the hydrochloric acid of 2mol/L again; Aluminum ion is wherein precipitated with the white lake form; Obtain aluminum hydroxide precipitation and post precipitation liquid 6, aluminum hydroxide precipitation obtains Al through washing, organic solvent absolute ethanol washing, drying, calcining 2O 3, obtain water lotion 7 and organic solvent washing liquid 8 simultaneously.
Said step 2) a residue obtains washings 2 with the hot wash of 1-3 times of volume 80-100 ℃ of its quality; Regulate the acidity continued of washings 2 and return the lixiviate of step 1) process.
The processing of a residue of said step 1), active SiO in residue 2Content greater than 25% o'clock, soak SiO through alkali 2The preparation WHITE CARBON BLACK, the secondary residue that obtains is as titanium content during greater than 6g/t, recyclable TiO wherein 2
Described water lotion 4, post precipitation liquid 6 and water lotion 7 are regulated the acidity continued and are returned the lixiviate of step 1) process; Sodium-chlor enrichment in water lotion 4, post precipitation liquid 6 and water lotion 7 is to 20g/L; Water lotion 4, post precipitation liquid 6 and water lotion 7 are concentrated preparation sodium-chlor, and the solution behind the preparation sodium-chlor gets into step 1) process lixiviate or treating part discharging after adjusting pH with hydrochloric acid.
Described organic solvent washing liquid 5 and 8 mixes back preparation absolute ethyl alcohol, and the absolute ethyl alcohol that obtains is applied to Fe again 3O 4, Al 2O 3Washing process.
Described drying all adopts microwave drying.
Preparing method of the present invention adapts to the Bayer process red mud of various heterogeneities; Environmental pollution and land occupation problem that Bayer process red mud causes have been solved on the one hand; Turn waste into wealth on the other hand, utilize valuable constituent iron, aluminium, preparation magnetic ferroferric oxide, aluminum oxide in the red mud, improved the comprehensive utilization value of Bayer process red mud; And level of residue is few, the solution reusable edible.
The extraction yield of iron of the present invention, aluminium, recovery height obtain the high-quality Z 250 easily, and can combine with existing sophisticated preparation aluminum oxide, silicon oxide technology, for the comprehensive utilization new model that realizes red mud provides gordian technique.
At the ultra-fine Fe of preparation 3O 4, Al 2O 3In the process, tensio-active agent adopts polyoxyethylene glycol, but the amount that the two preparation process adds is distinguished Fe to some extent 3O 4The preparation process adds the 15-20% tensio-active agent, and tensio-active agent plays dispersion agent and protectant effect (preventing to generate red oxide of iron), and Al 2O 3Add the tensio-active agent of 2-4% in the preparation process, tensio-active agent only plays dispersion agent.Used organic solvent is an absolute ethyl alcohol during washing.
Embodiment
The red mud that the present invention adopts mainly consists of rhombohedral iron ore content 10%, pyrrhosiderite content 23%, gipsite content 17%, quartz content 36%, illite content 6%, Na through the X diffraction analysis 6(Al 6Si 6O 24) 2NaFxH 2O content 7%, other composition are 1%.
Embodiment 1:
1) lixiviate: behind the red mud drying that will wet, be 1g:5mL, dried red mud and 10 mol hydrochloric acid added in the reactor drum stir, and be heated to 80 ℃, be incubated 1 hour according to red mud weight and hydrochloric acid volume ratio;
2) filter: filtered while hot obtains containing iron ion, aluminum ions filtrating 1 and a residue;
A residue account for 70% through X diffraction analysis result for quartz, illite accounts for 3%, anatase octahedrite accounts for 1%, diasporite accounts for 7%, pyrrhosiderite and limonite account for 4%, diopside accounts for 2%, amorphous phase accounts for 10%.The content of rhombohedral iron ore and pyrrhosiderite drops to 4% by 33% in the red mud after acidleach, and most of rhombohedral iron ore and pyrrhosiderite are dissolved in the acid, and anatase octahedrite obtains enrichment in red mud s.t. process simultaneously, and content reaches 1%.
Residue obtains washings 2 with the hot wash of 100 ℃ of the volumes of 3 times of its quality; Regulate the acidity continued of washings 2 and return the lixiviate of step 1) process;
3) ultra-fine Fe 3O 4Preparation:
After the iron concentration of adjustment filtrating 1 was 0.25mol/L, the iron concentration mol ratio was that the concentration of 1:1 is the reductive agent Na of 0.5mol/L in adding and the solution 2SO 3Solution and solution quality 20% surfactant polyethylene, pH of leaching solution to 11.5 is regulated with the NaOH of 2mol/L in the back, at 0.5 hour after-filtration of 90 ℃ of stirring reactions, obtains Fe 3O 4The deposition and filtrate 3, Fe 3O 4Deposition obtains pure Fe with microwave drying behind washing, organic solvent absolute ethanol washing 3O 4, obtaining the pure Z 250 of particle diameter 1.78um, it is higher that this method obtains Fe 3 O purity, obtains water lotion 4 and organic solvent washing liquid 5 simultaneously;
4) ultra-fine Al 2O 3Preparation:
After in filtrating 3, adding the surfactant polyethylene of its quality 3%; Regulate its pH value with the hydrochloric acid of 2mol/L again; Aluminum ion is wherein precipitated with the white lake form; Obtain aluminum hydroxide precipitation and post precipitation liquid 6, aluminum hydroxide precipitation obtains the Al of particle diameter 6.4um through washing, organic solvent absolute ethanol washing, microwave drying, calcining 2O 3, obtain water lotion 7 and organic solvent washing liquid 8 simultaneously.
Wherein water lotion 4, post precipitation liquid 6 and water lotion 7 are regulated the acidity continued and are returned the lixiviate of step 1) process; Sodium-chlor enrichment in water lotion 4, post precipitation liquid 6 and water lotion 7 is to 20g/L; To water lotion 4, post precipitation liquid 6 and the water lotion 7 concentrated sodium-chlor that prepare, the lixiviate of entering step 1) process was perhaps arranged the processing back after the solution behind the preparation sodium-chlor was adjusted pH with hydrochloric acid.
Wherein organic solvent washing liquid 5 and 8 mixes back preparation absolute ethyl alcohol, and the absolute ethyl alcohol that obtains is applied to Fe again 3O 4, Al 2O 3Washing process.
Active SiO in the residue 2Content greater than 25% o'clock, soak SiO through alkali 2Preparation WHITE CARBON BLACK, the secondary residue that obtains are worked as titanium content and are reclaimed TiO wherein greater than 6g/t 2
Embodiment 2:
1) lixiviate: behind the red mud drying that will wet, be 1g:3mL, dried red mud and 9 mol hydrochloric acid added in the reactor drum stir, and be heated to 100 ℃, be incubated 2 hours according to red mud weight and hydrochloric acid volume ratio;
2) filter: filtered while hot obtains containing iron ion, aluminum ions filtrating 1 and a residue;
A residue is used 90 ℃ the hot wash of 1 times of its quality, obtains washings 2; Regulate the acidity continued of washings 2 and return the lixiviate of step 1) process;
3) ultra-fine Fe 3O 4Preparation:
After the iron concentration of adjustment filtrating 1 was 0.25mol/L, the iron concentration mol ratio was that the concentration of 1:1.3 is the reductive agent Na of 0.5mol/L in adding and the solution 2SO 3Solution and solution quality 15% surfactant polyethylene,
PH of leaching solution to 12 is regulated with the NaOH of 2mol/L in the back, at 1 hour after-filtration of 70 ℃ of stirring reactions, obtains Fe 3O 4The deposition and filtrate 3, Fe 3O 4Deposition obtains pure Fe with microwave drying behind washing, organic solvent absolute ethanol washing 3O 4, obtain water lotion 4 and organic solvent washing liquid 5 simultaneously;
4) ultra-fine Al 2O 3Preparation:
After in filtrating 3, adding the surfactant polyethylene of its quality 2%; Regulate its pH value with the hydrochloric acid of 2mol/L again; Aluminum ion is wherein precipitated with the white lake form; Obtain aluminum hydroxide precipitation and post precipitation liquid 6, aluminum hydroxide precipitation obtains Al through washing, organic solvent absolute ethanol washing, microwave drying, calcining 2O 3, obtain water lotion 7 and organic solvent washing liquid 8 simultaneously.
Wherein water lotion 4, post precipitation liquid 6 and water lotion 7 are regulated the acidity continued and are returned the lixiviate of step 1) process; Sodium-chlor enrichment in water lotion 4, post precipitation liquid 6 and water lotion 7 is to 20g/L; Water lotion 4, post precipitation liquid 6 and water lotion 7 are concentrated preparation sodium-chlor, and the solution behind the preparation sodium-chlor gets into the lixiviate of step 1) process after adjusting pH with hydrochloric acid.
Wherein organic solvent washing liquid 5 and 8 mixes back preparation absolute ethyl alcohol, and the absolute ethyl alcohol that obtains is applied to Fe again 3O 4, Al 2O 3Washing process.
Active SiO in the residue 2Content greater than 25% o'clock, soak SiO through alkali 2Preparation WHITE CARBON BLACK, the secondary residue that obtains are worked as titanium content and are reclaimed TiO wherein greater than 6g/t 2
Embodiment 3:
1) lixiviate: behind the red mud drying that will wet, be 1g:4mL, dried red mud and 8 mol hydrochloric acid added in the reactor drum stir, and be heated to 90 ℃, be incubated 1.5 hours according to red mud weight and hydrochloric acid volume ratio;
2) filter: filtered while hot obtains containing iron ion, aluminum ions filtrating 1 and a residue;
A residue is used 80 ℃ the hot wash of 2 times of its quality, obtains washings 2; Regulate the acidity continued of washings 2 and return the lixiviate of step 1) process;
3) ultra-fine Fe 3O 4Preparation:
After the iron concentration of adjustment filtrating 1 was 0.25mol/L, the iron concentration mol ratio was that the concentration of 1:1.5 is the reductive agent Na of 0.5mol/L in adding and the solution 2SO 3Solution and solution quality 18% surfactant polyethylene,
PH of leaching solution to 12.5 is regulated with the NaOH of 2mol/L in the back, at 1 hour after-filtration of 80 ℃ of stirring reactions, obtains Fe 3O 4The deposition and filtrate 3, Fe 3O 4Deposition obtains pure Fe with microwave drying behind washing, organic solvent absolute ethanol washing 3O 4, obtain water lotion 4 and organic solvent washing liquid 5 simultaneously;
4) ultra-fine Al 2O 3Preparation:
After in filtrating 3, adding the surfactant polyethylene of its quality 4%; Regulate its pH value with the hydrochloric acid of 2mol/L again; Aluminum ion is wherein precipitated with the white lake form; Obtain aluminum hydroxide precipitation and post precipitation liquid 6, aluminum hydroxide precipitation obtains Al through washing, organic solvent absolute ethanol washing, microwave drying, calcining 2O 3, obtain water lotion 7 and organic solvent washing liquid 8 simultaneously.
Wherein water lotion 4, post precipitation liquid 6 and water lotion 7 are regulated the acidity continued and are returned the lixiviate of step 1) process; Sodium-chlor enrichment in water lotion 4, post precipitation liquid 6 and water lotion 7 is to 20g/L; Water lotion 4, post precipitation liquid 6 and water lotion 7 are concentrated preparation sodium-chlor, and the solution behind the preparation sodium-chlor gets into the lixiviate of step 1) process after adjusting pH with hydrochloric acid.
Wherein organic solvent washing liquid 5 and 8 mixes back preparation absolute ethyl alcohol, and the absolute ethyl alcohol that obtains is applied to Fe again 3O 4, Al 2O 3Washing process.
Active SiO in the residue 2Content greater than 25% o'clock, soak SiO through alkali 2Preparation WHITE CARBON BLACK, the secondary residue that obtains are worked as titanium content and are reclaimed TiO wherein greater than 6g/t 2

Claims (6)

1. Bayer process red mud co-production of ultrafine Z 250, method of alumina is characterized in that may further comprise the steps:
1) lixiviate: behind the red mud drying that will wet, be 1g:3-5mL, dried red mud and 8-10 mol hydrochloric acid added in the reactor drum stir, and be heated to 80-100 ℃, be incubated 1-2 hour according to red mud weight and hydrochloric acid volume ratio;
2) filter: filtered while hot obtains containing iron ion, aluminum ions filtrating 1 and a residue;
3) ultra-fine Fe 3O 4Preparation:
After the iron concentration of adjustment filtrating 1 was 0.25mol/L, the iron concentration mol ratio was that the concentration of 1:1-1.5 is the reductive agent Na of 0.5mol/L in adding and the solution 2SO 3Solution and solution quality 15-20% surfactant polyethylene, pH of leaching solution is regulated to 11.5-12.5 with the NaOH of 2mol/L in the back, at 70-90 ℃ of stirring reaction 0.5-1.0 hour after-filtration, obtains Fe 3O 4The deposition and filtrate 3, Fe 3O 4Deposition obtains pure Fe through washing, organic solvent absolute ethanol washing after drying 3O 4, obtain water lotion 4 and organic solvent washing liquid 5 simultaneously;
4) ultra-fine Al 2O 3Preparation:
After in filtrating 3, adding the surfactant polyethylene of its quality 2-4%; Regulate its pH value with the hydrochloric acid of 2mol/L again; Aluminum ion is wherein precipitated with the white lake form; Obtain aluminum hydroxide precipitation and post precipitation liquid 6, aluminum hydroxide precipitation obtains Al through washing, organic solvent absolute ethanol washing, drying, calcining 2O 3, obtain water lotion 7 and organic solvent washing liquid 8 simultaneously.
2. Bayer process red mud co-production of ultrafine Z 250 according to claim 1, method of alumina is characterized in that: a residue said step 2) obtains washings 2 with the hot wash of 1-3 times of volume 80-100 ℃ of its quality; Regulate the acidity continued of washings 2 and return the lixiviate of step 1) process.
3. Bayer process red mud co-production of ultrafine Z 250 according to claim 1, method of alumina is characterized in that: the processing of a residue of said step 1), active SiO in residue 2Content greater than 25% o'clock, soak SiO through alkali 2The preparation WHITE CARBON BLACK, the secondary residue that obtains is as titanium content during greater than 6g/t, recyclable TiO wherein 2
4. Bayer process red mud co-production of ultrafine Z 250 according to claim 1, method of alumina; It is characterized in that: described water lotion 4, post precipitation liquid 6 and water lotion 7 are regulated the acidity continued and are returned the lixiviate of step 1) process; Sodium-chlor enrichment in water lotion 4, post precipitation liquid 6 and water lotion 7 is to 20g/L; Water lotion 4, post precipitation liquid 6 and water lotion 7 are concentrated preparation sodium-chlor, and the solution behind the preparation sodium-chlor gets into step 1) process lixiviate or treating part discharging after adjusting pH with hydrochloric acid.
5. Bayer process red mud co-production of ultrafine Z 250 according to claim 1, method of alumina is characterized in that: described organic solvent washing liquid 5 and 8 mixes back preparation absolute ethyl alcohol, and the absolute ethyl alcohol that obtains is applied to Fe again 3O 4, Al 2O 3Washing process.
6. Bayer process red mud co-production of ultrafine Z 250 according to claim 1, method of alumina, it is characterized in that: described drying all adopts microwave drying.
CN2012101645156A 2012-05-24 2012-05-24 Method for co-production of superfine ferroferric oxide and aluminum oxide by red mud of Bayer process Pending CN102674477A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2012101645156A CN102674477A (en) 2012-05-24 2012-05-24 Method for co-production of superfine ferroferric oxide and aluminum oxide by red mud of Bayer process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2012101645156A CN102674477A (en) 2012-05-24 2012-05-24 Method for co-production of superfine ferroferric oxide and aluminum oxide by red mud of Bayer process

Publications (1)

Publication Number Publication Date
CN102674477A true CN102674477A (en) 2012-09-19

Family

ID=46807121

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2012101645156A Pending CN102674477A (en) 2012-05-24 2012-05-24 Method for co-production of superfine ferroferric oxide and aluminum oxide by red mud of Bayer process

Country Status (1)

Country Link
CN (1) CN102674477A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105366971A (en) * 2014-08-29 2016-03-02 北新集团建材股份有限公司 Method for preparing radiation protection board
CN105439520A (en) * 2014-08-29 2016-03-30 北新集团建材股份有限公司 Method for producing radiation resisting plates
CN105801077A (en) * 2016-02-17 2016-07-27 中国科学院地球化学研究所 Preparation method of red mud/carbon-based magnetic composite material
CN106115794A (en) * 2016-06-15 2016-11-16 天津市国润永泰环保科技有限公司 A kind of method using industrial waste acid and red soil resource to produce ferroferric oxide magnetic powder
CN106315687A (en) * 2016-08-03 2017-01-11 安徽八化工股份有限公司 Method for preparing Fe3O4 from wastewater in chlorobenzene production
CN107475520A (en) * 2017-08-11 2017-12-15 中国科学院过程工程研究所 The separating technology of iron aluminium in a kind of red mud
CN108866318A (en) * 2018-07-02 2018-11-23 深圳市中金环保科技有限公司 A method of low-cost high-efficiency separates iron compound from red mud
CN109987641A (en) * 2017-12-30 2019-07-09 天津友发钢管集团股份有限公司 A kind of method that red soil prepares iron oxide black
CN110055400A (en) * 2019-06-04 2019-07-26 长沙资生环保科技有限公司 A kind of technique that step-by-step reduction realizes red mud higher value application
CN110156029A (en) * 2019-04-28 2019-08-23 于拴全 Red mud Chemical Physics integrated conduct method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002090605A1 (en) * 2001-05-03 2002-11-14 Goldendale Aluminum Company Acid digestion process for treating alumina-bearing ores to recover metal values therefrom
CN101830516A (en) * 2010-05-18 2010-09-15 浙江大学 Method for preparing nano ferroferric oxide particles
CN102344171A (en) * 2010-07-30 2012-02-08 孙建之 New method for resource comprehensive utilization of red mud and fly ash

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002090605A1 (en) * 2001-05-03 2002-11-14 Goldendale Aluminum Company Acid digestion process for treating alumina-bearing ores to recover metal values therefrom
CN101830516A (en) * 2010-05-18 2010-09-15 浙江大学 Method for preparing nano ferroferric oxide particles
CN102344171A (en) * 2010-07-30 2012-02-08 孙建之 New method for resource comprehensive utilization of red mud and fly ash

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
《无机盐工业》 20101231 姚万军等 "拜耳法赤泥综合利用研究现状" 第9-11页 1-6 第42卷, 第12期 *
《材料与冶金学报》 20100331 鲁桂林等 "赤泥中氧化铝和氧化铁的浸出" 第31-34、67页 1-6 第9卷, 第1期 *
姚万军等: ""拜耳法赤泥综合利用研究现状"", 《无机盐工业》, vol. 42, no. 12, 31 December 2010 (2010-12-31), pages 9 - 11 *
鲁桂林等: ""赤泥中氧化铝和氧化铁的浸出"", 《材料与冶金学报》, vol. 9, no. 1, 31 March 2010 (2010-03-31) *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105439520B (en) * 2014-08-29 2017-09-29 北新集团建材股份有限公司 A kind of method for preparing radiation-proof plate
CN105439520A (en) * 2014-08-29 2016-03-30 北新集团建材股份有限公司 Method for producing radiation resisting plates
CN105366971A (en) * 2014-08-29 2016-03-02 北新集团建材股份有限公司 Method for preparing radiation protection board
CN105366971B (en) * 2014-08-29 2017-09-29 北新集团建材股份有限公司 A kind of method for preparing radiation-proof plate
CN105801077A (en) * 2016-02-17 2016-07-27 中国科学院地球化学研究所 Preparation method of red mud/carbon-based magnetic composite material
CN106115794A (en) * 2016-06-15 2016-11-16 天津市国润永泰环保科技有限公司 A kind of method using industrial waste acid and red soil resource to produce ferroferric oxide magnetic powder
CN106115794B (en) * 2016-06-15 2018-03-02 天津市国润永泰环保科技有限公司 A kind of method that ferroferric oxide magnetic powder is produced using industrial waste acid and red soil recycling
CN106315687A (en) * 2016-08-03 2017-01-11 安徽八化工股份有限公司 Method for preparing Fe3O4 from wastewater in chlorobenzene production
CN106315687B (en) * 2016-08-03 2018-10-09 安徽八一化工股份有限公司 A kind of waste water with chlorobenzene production prepares Fe3O4Method
CN107475520A (en) * 2017-08-11 2017-12-15 中国科学院过程工程研究所 The separating technology of iron aluminium in a kind of red mud
CN109987641A (en) * 2017-12-30 2019-07-09 天津友发钢管集团股份有限公司 A kind of method that red soil prepares iron oxide black
CN108866318A (en) * 2018-07-02 2018-11-23 深圳市中金环保科技有限公司 A method of low-cost high-efficiency separates iron compound from red mud
CN110156029A (en) * 2019-04-28 2019-08-23 于拴全 Red mud Chemical Physics integrated conduct method
CN110055400A (en) * 2019-06-04 2019-07-26 长沙资生环保科技有限公司 A kind of technique that step-by-step reduction realizes red mud higher value application

Similar Documents

Publication Publication Date Title
CN102674477A (en) Method for co-production of superfine ferroferric oxide and aluminum oxide by red mud of Bayer process
CN103103361B (en) Method for preparing rare earth oxide from rare earth polishing powder waste
CN106319218A (en) Method for recovering rare earth, aluminum and silicon from rare earth-containing aluminum and silicon wastes
CN102586610B (en) Cleaner production process for synchronously extracting vanadium and aluminum from aluminothermic vanadium iron slag
CN104711424B (en) A kind of method of recovering rare earth and aluminium in removal of impurities slag from weathered superficial leaching rare-earth ore leachate
CN102417978B (en) Method for enriching titanium in coal gangue
CN104495899A (en) Method for synergic resource utilization of acetylene sludge and coal ash
CN101418379B (en) Method for extracting nickel and cobalt by enclosed leaching nickel oxide mine
CN102876896B (en) Method for recovering vanadium by decomposing vanadium extraction tailings by using sodium hydroxide solution
CN104556097A (en) Method for preparing hydrotalcite-like compounds and zeolites by using blast furnace slag
CN103193213A (en) Method for comprehensively utilizing low-grade phosphate ores
CN102432071A (en) Method for integrally utilizing high-iron-content bauxite
CN103121700A (en) Method for preparing ultrafine alumina and coproducing and white carbon black by utilizing coal series kaolin
CN106319227A (en) Comprehensive utilization method for acid leaching slag of neodymium iron boron waste
CN105585039A (en) Method for efficient and fast desilication of bauxite
CN103408050B (en) Method of efficient extraction of aluminum, iron, and titanium in coal gangue
CN102249274A (en) Method for producing aluminum oxide with alumyte
CN102115828B (en) Method for preparing iron and aluminum and coproducing sodium sulfate from red mud produced by bayer process
CN104232944B (en) Process for comprehensively recycling indium from ammonia leaching residues and co-producing zinc oxide
CN102557091A (en) Method for subsequent treatment of aluminum sulfate generated in technical process of extracting alumina from fly ash
CN105238924A (en) Method for extracting aluminum and iron from high-iron diasporic bauxite
CN101298639B (en) Comprehensive utilization process of malachite ore
CN110896643B (en) Method for producing zinc-containing compound or zinc oxide from zinc-containing raw ore through intermediate step of calcium zincate synthesis
CN100506734C (en) Method for removing brucite powder chromophore impurity
CN102115209B (en) Method for producing ferrous nitrate and barium sulfate by using waste acid obtained by producing titanium white by sulfuric acid method

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20120919