CN105692711A - Method for separating iron oxide from fly ash of pulverized coal furnace - Google Patents

Method for separating iron oxide from fly ash of pulverized coal furnace Download PDF

Info

Publication number
CN105692711A
CN105692711A CN201610066302.8A CN201610066302A CN105692711A CN 105692711 A CN105692711 A CN 105692711A CN 201610066302 A CN201610066302 A CN 201610066302A CN 105692711 A CN105692711 A CN 105692711A
Authority
CN
China
Prior art keywords
flyash
filter cake
solution
aluminum chlorhydrate
coal
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
CN201610066302.8A
Other languages
Chinese (zh)
Inventor
杨卓舒
张磊
邝清林
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.)
Zhuoda New Material Technology Group Co Ltd
Original Assignee
Zhuoda New Material Technology Group 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 Zhuoda New Material Technology Group Co Ltd filed Critical Zhuoda New Material Technology Group Co Ltd
Priority to CN201610066302.8A priority Critical patent/CN105692711A/en
Publication of CN105692711A publication Critical patent/CN105692711A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G49/00Compounds of iron
    • C01G49/02Oxides; Hydroxides
    • 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
    • C01F7/48Halides, with or without other cations besides aluminium
    • C01F7/56Chlorides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G49/00Compounds of iron
    • C01G49/02Oxides; Hydroxides
    • C01G49/08Ferroso-ferric oxide [Fe3O4]
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • C01P2004/61Micrometer sized, i.e. from 1-100 micrometer

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Compounds Of Iron (AREA)
  • Processing Of Solid Wastes (AREA)

Abstract

The invention provides a method for separating iron oxide from the fly ash of a pulverized coal furnace. In the method, through low-temperature hydrothermal reaction between hydrochloric acid and fly ash, all Fe2O3 and FeO and part of amorphous Al2O3 in the fly ash are dissolved out; and Fe2O3 and FeO are separated and extracted from the solution using glycerin to obtain high-purity iron oxide. The method provided by the invention imposes no special requirements on equipment, adopts low-temperature reaction and can efficiently separate and extract iron oxide from the fly ash; 90-96% of aluminum oxide and 98-100% of iron oxide in the fly ash can be dissolved out; and in the technical scheme provided by the invention, the fly ash resource is fully utilized, the preparation technology is simple, the production cost is low, and the method is suitable for large-scale production.

Description

A kind of separate the method for ferrum oxide in coal-powder boiler flyash
Technical field
The present invention relates to a kind of Ash Utilization Application way, separate the method for ferrum oxide in coal-powder boiler flyash in particular to a kind of。
Background technology
Coal fired power generation is one of commonly used power generation mode in countries in the world, and effective utilization of the coal-fired a large amount of flyash produced has become world subject。At present, China's electric power more than 70% is produced by coal fired power generation, and the yield about 30% of whole nation coal is used for generating electricity, and consequent flyash, if, with amount deficiency, not only occupies a large amount of soil, causes serious environmental pollution, be also the waste of a kind of resource。
From another angle, rich in many oxide in flyash, such as Al2O3, SiO2, Fe2O3, FeO, CaO, MgO, SO3, Na2O, K2O etc., additionally contain a small amount of rare earth element。These oxides separation and Extraction from flyash out and is prepared corresponding high value-added product, higher social economy's value can not only be produced, it is possible to alleviate the flyash harm to environment。
The comprehensive utilizating research of flyash, the particularly research of separation and Extraction aluminium oxide from flyash, from the forties in last century so far, many experts both domestic and external, scholar study at this and have carried out extensive work and proposed multiple separating and extracting process。But when extracting separation aluminium oxide, ferrum oxide is fallen as impurity treatment, not by Fe in flyash2O3With FeO recycling, cause the serious waste of resource。
And ferrum oxide is as a kind of inorganic pigment, it is widely used in the fields such as paint, rubber, plastic cosmetic, building ground material, accurate five metals instrument, optical glass, enamel, school supply and stationery, leather, magnetic alloy and high-grade alloy steel。
At present, Chinese scholars proposes certain methods for separation and Extraction ferrum oxide from flyash, such as: calcium oxide sintering process, soda lime sintering process etc., but these methods due to process conditions limit, the reason such as the ferrum oxide response rate is low, power consumption is big, production cost is high, bed drain purge is big, cause separation and Extraction ferrum oxide implementation result poor。
It is an object of the invention to utilize dilute hydrochloric acid to react with common coal-powder boiler flyash low-temperature hydrothermal, make Fe whole in flyash2O3, FeO and part amorphous state Al2O3Dissolution, recycling glycerol separate draw solution in Fe2O3, FeO, finally give the iron oxide product that purity is higher。
Summary of the invention
It is an object of the invention to provide and a kind of utilize the method for ferrum oxide in hydrochloric acid and glycerin extraction flyash under cryogenic。
Technical scheme provided by the invention includes utilizing hydrochloric acid to react with flyash low-temperature hydrothermal, makes Fe whole in flyash2O3, FeO and part amorphous state Al2O3Dissolution, the Fe in recycling glycerol separate draw solution2O3, FeO obtain highly purified ferrum oxide。Technical scheme processing technology provided by the invention is simple, reduce production cost, take full advantage of the resource of flyash, is suitable for large-scale production。
Realize the object of the invention technical scheme as follows:
A kind of separating the method for ferrum oxide in coal-powder boiler flyash, described preparation method comprises the steps:
1) magnetic bead in magnetic separation separation of fine coal ash;
2) acidleach: at 90 DEG C~100 DEG C, is the mixed in hydrochloric acid of 1%~6% by flyash with concentration in the ratio that solid-to-liquid ratio is 1:2~1:4 of flyash and hydrochloric acid, reacts 1~3h;
3) solid-liquid separation: after reactant is cooled to room temperature, sucking filtration, the filter cake water washing that solid-to-liquid ratio is 2:1~1:2 by flyash Yu water, obtain the solution of hydrochloric acid ferrum and aluminum chlorhydrate;
4) glycerin extraction aluminum chlorhydrate: by glycerol and step 3) in the volume ratio of the hydrochloric acid ferrum that obtains and aluminum chlorhydrate solution be that 1:1~2:1 prepares glycerol adding, after stirring 3~5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;
5) process aluminum sulfate filter cake: adding concentration by solid-to-liquid ratio 1:2~1:5 preparation of aluminum chlorhydrate filter cake with glycerine water solution is the glycerine water solution of 55%~70%, after stirring 10~30min, sucking filtration, then obtain aluminum chlorhydrate filter cake, and reclaim filtrate;This glycerine water solution washing procedure of repetitive operation 4~6 times, separates hydrochloric acid ferrum, the aluminum chlorhydrate filter cake that final iron-holder is extremely low to greatest extent, and reclaims filtrate;
6) ferrum oxide reclaims: add hydrogen peroxide with above-mentioned whole recovery filtrate volumes than for 1:1000~2:1000 preparation by hydrogen peroxide, and after standing 3~5min, dropping ammonia, to pH value of solution > 8, filters, obtains highly purified hydrated ferric oxide.。
Further, described flyash is following component by mass percentage:
Al2O3+SiO2+Fe2O3> 70%, CaO > 5%。
Further, described flyash following component by mass percentage: Al2O3, 29.87%;19.25%, 47.08%;Fe2O3, 7.01%;CaO, 6.98%;SO3, 1.2%;Loss on ignition, 7.68%。
Further, described step 1) in, carry out wet magnetic separation separation with wet type low-intensity (magnetic) separator;Described wet type low-intensity (magnetic) separator magnetic induction 0.2T, pan feeding speed 500mL/min, material concentration 8%, magnetic separation 3~5 times。
Further, described step 1) purpose of magnetic separation is to isolate magnetic bead, that isolates magnetic bead in flyash is mainly composed of Fe3O4。Because of Fe3O4Stable chemical nature, not easily react with strong acid and strong base, therefore for make the ferrum oxide in flyash be totally separated extraction, it is necessary to add magnetic separation step。
Further, the other method of described process aluminum sulfate filter cake includes: add water with water solid-to-liquid ratio 3:1~1:1 preparation by aluminum chlorhydrate filter cake, aluminum chlorhydrate is made to dissolve, again by the volume ratio of glycerol Yu solution be 3:1~12:1 prepare glycerol adding, after stirring 3~5min, sucking filtration, obtains aluminum chlorhydrate filter cake, and reclaims filtrate。
Further, described ferrum oxide reclaims other method and includes: in reclaiming dropping ammonia in filtrate, to pH value of solution > 10, filters, obtains highly purified hydrated ferric oxide.。
With immediate prior art ratio, technical scheme provided by the invention has following excellent effect:
1, technical scheme provided by the invention, the ferrum oxide in energy fully high efficiency extraction flyash。
2, technical scheme provided by the invention, utilizes the method treated coal ash of low-temp reaction, to equipment without particular/special requirement。
3, technical scheme provided by the invention, can by the alumina leaching 90%~96% in flyash, ferrum oxide dissolution 98%~100%。
4, technical scheme provided by the invention, flyash is after magnetic separation, and the response rate of magnetic bead reaches more than 85%, and magnetic bead particle diameter is at 20~30um;From flyash, reclaim magnetic bead less costly, except nonmagnetic portion iron content is relatively low in the flyash after magnetic bead, be more beneficial for integrated application;With magnetic bead in conjunction with HGMS technology process waste water, can by effective for the tp removal rate in waste water, efficiency is high, treating capacity is big。
5, technical scheme provided by the invention, has widened the scope of total utilization of PCA。
Detailed description of the invention
Further technical scheme is clearly and completely described below in conjunction with the embodiment of the present invention, it is clear that described embodiment is only a part of embodiment of the present invention, rather than whole embodiments。Based on the embodiment in the present invention, the every other embodiment that those of ordinary skill in the art obtain, broadly fall into the scope of protection of the invention。
Embodiment 1, flyash through 4 magnetic separation, then with 3% hydrochloric acid mix by solid-to-liquid ratio 1:3, and at 90 DEG C, react 3h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 1:1 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 1:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Mix with the ratio of 1:3 with the glycerine water solution that concentration is 70% in aluminum chlorhydrate filter cake, after stirring 15min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;This glycerine water solution washing procedure of repetitive operation 6 times, and reclaim filtrate;Hydrogen peroxide mixes by the volume ratio of 1:1000 with reclaiming filtrate, and after standing 5min, dropping ammonia, to pH value of solution > 8, filters, obtains hydrated ferric oxide.。
Embodiment 2, flyash through 3 magnetic separation, then with 5% hydrochloric acid mix by solid-to-liquid ratio 1:2, and at 80 DEG C, react 2h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 2:1 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 1:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 3min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Mix with the ratio of 1:5 with the glycerine water solution that concentration is 60% in aluminum chlorhydrate filter cake, after stirring 30min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;This glycerine water solution washing procedure of repetitive operation 4 times, and reclaim filtrate;Hydrogen peroxide mixes by the volume ratio of 1:1000 with reclaiming filtrate, and after standing 3min, dropping ammonia, to pH value of solution > 8, filters, obtains hydrated ferric oxide.。
Embodiment 3, flyash through 3 magnetic separation, then with 4% hydrochloric acid mix by solid-to-liquid ratio 1:4, and at 70 DEG C, react 1h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 2:1 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 2:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Mix with the ratio of 1:2 with the glycerine water solution that concentration is 60% in aluminum chlorhydrate filter cake, after stirring 10min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;This glycerine water solution washing procedure of repetitive operation 6 times, and reclaim filtrate;Hydrogen peroxide mixes by the volume ratio of 2:1000 with reclaiming filtrate, and after standing 3min, dropping ammonia, to pH value of solution > 8, filters, obtains hydrated ferric oxide.。
Embodiment 4, flyash through 5 magnetic separation, then with 1% hydrochloric acid mix by solid-to-liquid ratio 1:4, and at 70 DEG C, react 2h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 4:5 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 2:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Mix with the ratio of 1:4 with the glycerine water solution that concentration is 55% in aluminum chlorhydrate filter cake, after stirring 25min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;This glycerine water solution washing procedure of repetitive operation 5 times, and reclaim filtrate;Hydrogen peroxide mixes by the volume ratio of 1:1000 with reclaiming filtrate, and after standing 4min, dropping ammonia, to pH value of solution > 8, filters, obtains hydrated ferric oxide.。
Embodiment 5, flyash through 5 magnetic separation, then with 5% hydrochloric acid mix by solid-to-liquid ratio 1:3, and at 80 DEG C, react 3h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 2:1 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 2:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Mix with the ratio of 1:3 with the glycerine water solution that concentration is 65% in aluminum chlorhydrate filter cake, after stirring 20min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;This glycerine water solution washing procedure of repetitive operation 6 times, and reclaim filtrate;Dropping ammonia is in reclaiming in filtrate, to pH value of solution > 10, filters, obtains hydrated ferric oxide.。
Embodiment 6, flyash through 3 magnetic separation, then with 2% hydrochloric acid mix by solid-to-liquid ratio 1:2, and at 85 DEG C, react 2h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 2:1 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 1:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Mix with the ratio of 1:2 with the glycerine water solution that concentration is 60% in aluminum chlorhydrate filter cake, after stirring 10min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;This glycerine water solution washing procedure of repetitive operation 6 times, and reclaim filtrate;Dropping ammonia is in reclaiming in filtrate, to pH value of solution > 10, filters, obtains hydrated ferric oxide.。
Embodiment 7, flyash through 5 magnetic separation, then with 3% hydrochloric acid mix by solid-to-liquid ratio 1:3, and at 80 DEG C, react 3h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 2:1 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 1:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Add water with water solid-to-liquid ratio 3:1 preparation by aluminum chlorhydrate filter cake, make aluminum chlorhydrate dissolve, then be that 8:1 prepares glycerol adding by the volume ratio of glycerol Yu solution, after stirring 4min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Hydrogen peroxide mixes by the volume ratio of 1:1000 with reclaiming filtrate, and after standing 3~5min, dropping ammonia, to pH value of solution > 8, filters, obtains hydrated ferric oxide.。
Embodiment 8, flyash through 4 magnetic separation, then with 5% hydrochloric acid mix by solid-to-liquid ratio 1:4, and at 90 DEG C, react 2h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 1:2 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 2:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 4min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Add water with water solid-to-liquid ratio 1:1 preparation by aluminum chlorhydrate filter cake, make aluminum chlorhydrate dissolve, then be that 7:1 prepares glycerol adding by the volume ratio of glycerol Yu solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Hydrogen peroxide mixes by the volume ratio of 2:1000 with reclaiming filtrate, and after standing 5min, dropping ammonia, to pH value of solution > 8, filters, obtains hydrated ferric oxide.。
Embodiment 9, flyash through 5 magnetic separation, then with 6% hydrochloric acid mix by solid-to-liquid ratio 1:3, and at 90 DEG C, react 3h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 1:2 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 2:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Add water with water solid-to-liquid ratio 3:1 preparation by aluminum chlorhydrate filter cake, make aluminum chlorhydrate dissolve, then be that 12:1 prepares glycerol adding by the volume ratio of glycerol Yu solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Dropping ammonia is in reclaiming in filtrate, to pH value of solution > 10, filters, obtains hydrated ferric oxide.。
Embodiment 10, flyash through 4 magnetic separation, then with 4% hydrochloric acid mix by solid-to-liquid ratio 1:4, and at 75 DEG C, react 2h;Reaction end after sucking filtration obtains filter cake, and with the water washing that solid-to-liquid ratio is 1:2 of flyash Yu water, obtains the solution of hydrochloric acid ferrum and aluminum chlorhydrate after being cooled to room temperature;It is that 1:1 prepares glycerol adding by the volume ratio of glycerol with hydrochloric acid ferrum and aluminum chlorhydrate solution, after stirring 4min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Add water with water solid-to-liquid ratio 1:1 preparation by aluminum chlorhydrate filter cake, make aluminum chlorhydrate dissolve, then be that 7:1 prepares glycerol adding by the volume ratio of glycerol Yu solution, after stirring 5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;Dropping ammonia is in reclaiming in filtrate, to pH value of solution > 10, filters, obtains hydrated ferric oxide.。
Gained sample in above-described embodiment is carried out performance test respectively, obtains data as shown in table 1 below。
Table 1
Above example is only in order to illustrate that technical scheme is not intended to limit; those of ordinary skill in the field are to be understood that; the specific embodiment of the present invention can being modified with reference to above-described embodiment or equivalent replacement, these are all being applied within the claims awaited the reply without departing from any amendment or equivalent replacement of spirit and scope of the invention。

Claims (7)

1. one kind separates the method for ferrum oxide in coal-powder boiler flyash, it is characterised in that described preparation method comprises the steps:
1) magnetic bead in magnetic separation separation of fine coal ash;
2) acidleach: at 90 DEG C~100 DEG C, is the mixed in hydrochloric acid of 1%~6% by flyash with concentration in the ratio that solid-to-liquid ratio is 1:2~1:4 of flyash and hydrochloric acid, reacts 1~3h;
3) solid-liquid separation: after reactant is cooled to room temperature, sucking filtration, the filter cake water washing that solid-to-liquid ratio is 2:1~1:2 by flyash Yu water, obtain the solution of hydrochloric acid ferrum and aluminum chlorhydrate;
4) glycerin extraction aluminum chlorhydrate: glycerol and step 3) in the described solution that obtains mix by 1:1~2:1 volume ratio, after stirring 3~5min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;
5) aluminum sulfate filter cake is processed: mix with the ratio that solid-to-liquid ratio is 1:2~1:5 with the glycerine water solution that concentration is 55%~70% in aluminum chlorhydrate filter cake, after stirring 10~30min, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate;This glycerine water solution washing procedure of repetitive operation 4~6 times, and reclaim filtrate;
6) ferrum oxide reclaims: hydrogen peroxide mixes by the volume ratio of 1:1000~2:1000 with described recovery filtrate, and after standing 3~5min, dropping ammonia, to pH value of solution > 8, filters, obtains hydrated ferric oxide.。
2. as claimed in claim 1 a kind of separate the method for ferrum oxide in coal-powder boiler flyash, it is characterized in that, the other method of described process aluminum sulfate filter cake includes: add water with water solid-to-liquid ratio 3:1~1:1 preparation by aluminum chlorhydrate filter cake, aluminum chlorhydrate is made to dissolve, again by the volume ratio of glycerol Yu solution be 3:1~12:1 prepare glycerol adding, stirring 3~5min after, sucking filtration, obtain aluminum chlorhydrate filter cake, and reclaim filtrate。
3. as claimed in claim 1 a kind of separate the method for ferrum oxide in coal-powder boiler flyash, it is characterized in that, described ferrum oxide reclaims other method and includes: dropping ammonia is in described recovery filtrate, to pH value of solution > 10, filter, obtain hydrated ferric oxide.。
4. as claimed in claim 1 a kind of separate the method for ferrum oxide in coal-powder boiler flyash, it is characterised in that described flyash is following component by mass percentage:
Al2O3+SiO2+Fe2O3> 70%, CaO > 5%。
5. as claimed in claim 4 a kind of separate the method for ferrum oxide in coal-powder boiler flyash, it is characterised in that described flyash following component by mass percentage: Al2O3, 29.87%;19.25%, 47.08%;Fe2O3, 7.01%;CaO, 6.98%;SO3, 1.2%;Loss on ignition, 7.68%。
6. as claimed in claim 1 a kind of separate the method for ferrum oxide in coal-powder boiler flyash, it is characterised in that described step 1) in, carry out wet magnetic separation separation with wet type low-intensity (magnetic) separator。
7. as claimed in claim 6 a kind of separate the method for ferrum oxide in coal-powder boiler flyash, it is characterised in that described wet type low-intensity (magnetic) separator magnetic induction 0.2T, pan feeding speed 500mL/min, material concentration 8%, magnetic separation 3~5 times。
CN201610066302.8A 2016-01-29 2016-01-29 Method for separating iron oxide from fly ash of pulverized coal furnace Pending CN105692711A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610066302.8A CN105692711A (en) 2016-01-29 2016-01-29 Method for separating iron oxide from fly ash of pulverized coal furnace

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610066302.8A CN105692711A (en) 2016-01-29 2016-01-29 Method for separating iron oxide from fly ash of pulverized coal furnace

Publications (1)

Publication Number Publication Date
CN105692711A true CN105692711A (en) 2016-06-22

Family

ID=56229016

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610066302.8A Pending CN105692711A (en) 2016-01-29 2016-01-29 Method for separating iron oxide from fly ash of pulverized coal furnace

Country Status (1)

Country Link
CN (1) CN105692711A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6241721A (en) * 1985-08-19 1987-02-23 Nisshin Steel Co Ltd Method of recovering iron oxide
CN101870489A (en) * 2010-04-27 2010-10-27 中国神华能源股份有限公司 Method for producing superfine aluminium hydroxide and aluminium oxide by using flyash
CN102101689A (en) * 2010-12-23 2011-06-22 内蒙古昶泰资源循环再生利用科技开发有限责任公司 Technological method for producing high-purity low-iron aluminum sulfate by using coal ash and comprehensively utilizing coal ash
CN104445212A (en) * 2013-09-16 2015-03-25 贵阳铝镁设计研究院有限公司 Method for processing fly ash used for circulating fluidized bed

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6241721A (en) * 1985-08-19 1987-02-23 Nisshin Steel Co Ltd Method of recovering iron oxide
CN101870489A (en) * 2010-04-27 2010-10-27 中国神华能源股份有限公司 Method for producing superfine aluminium hydroxide and aluminium oxide by using flyash
CN102101689A (en) * 2010-12-23 2011-06-22 内蒙古昶泰资源循环再生利用科技开发有限责任公司 Technological method for producing high-purity low-iron aluminum sulfate by using coal ash and comprehensively utilizing coal ash
CN104445212A (en) * 2013-09-16 2015-03-25 贵阳铝镁设计研究院有限公司 Method for processing fly ash used for circulating fluidized bed

Similar Documents

Publication Publication Date Title
CN103397213B (en) Method for decomposing and extracting Baotou rare earth ore through mixed alkali roasting process
CN100584764C (en) Method for reclaiming ferric oxide from coal ash and coal gangue
CN106848472A (en) A kind of method that lithium is reclaimed in waste lithium iron phosphate battery
CN104495899A (en) Method for synergic resource utilization of acetylene sludge and coal ash
CN102897810B (en) Method for producing aluminum oxide by using fly ash
CN103738972B (en) A kind of residue of aluminum-extracted pulverized fuel ash prepares the method for silicon powder
CN103449483A (en) Impurity removing method in process of preparing alumina from fly ash by utilizing acid method
Long et al. Recovery of vanadium from alkaline leaching solution from roasted stone coal
CN105692709A (en) Method for separating iron oxide from fly ash of pulverized coal furnace
CN105776346A (en) Method for separating Fe2O3 in pulverized coal ash of pulverized coal furnace
CN105753063A (en) Method for separating ferric oxide in coal-powder boiler fly ash
CN105776345A (en) Method for separating Fe2O3 in pulverized coal ash of pulverized coal furnace
CN105776344A (en) Method for separating Fe2O3 in pulverized coal ash of circulating fluidized bed
CN105692711A (en) Method for separating iron oxide from fly ash of pulverized coal furnace
CN105692712A (en) Method for separating iron oxide from fly ash of pulverized coal furnace
CN105753065A (en) Method for separating ferric oxide in coal-powder boiler fly ash
CN105621492A (en) Method for separating iron oxide in coal ash of pulverized coal furnace
CN105621491A (en) Method for separating iron oxide in pulverized fuel ash in pulverized coal furnace
CN105753064A (en) Method for separating ferric oxide in coal-powder boiler fly ash
CN105621494A (en) Method for separating iron oxide in coal ash of pulverized coal furnace
CN105753061A (en) Method for separating ferric oxide in coal-powder boiler fly ash
CN105731546A (en) Method for separating ferric oxide in circulating fluidized bed coal ash
CN105692710A (en) Method for separating iron oxide from fly ash of pulverized coal furnace
CN105776343A (en) Method for separating Fe2O3 in pulverized coal ash of circulating fluidized bed
CN105692708A (en) Method for separating iron oxide from fly ash of circulating fluidized bed

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

Application publication date: 20160622

RJ01 Rejection of invention patent application after publication