WO2001073142A1 - Agglomeration of alumina - Google Patents

Agglomeration of alumina Download PDF

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Publication number
WO2001073142A1
WO2001073142A1 PCT/AU2001/000214 AU0100214W WO0173142A1 WO 2001073142 A1 WO2001073142 A1 WO 2001073142A1 AU 0100214 W AU0100214 W AU 0100214W WO 0173142 A1 WO0173142 A1 WO 0173142A1
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Prior art keywords
alumina particles
slurry
alumina
particles
agglomerated
Prior art date
Application number
PCT/AU2001/000214
Other languages
French (fr)
Inventor
Barry James Robson
Ronald Gallagher
Original Assignee
Alcoa Of Australia Limited
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 Alcoa Of Australia Limited filed Critical Alcoa Of Australia Limited
Priority to AU37124/01A priority Critical patent/AU3712401A/en
Publication of WO2001073142A1 publication Critical patent/WO2001073142A1/en
Priority to US10/971,639 priority patent/US7449030B2/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B21/00Obtaining aluminium
    • C22B21/0038Obtaining aluminium by other processes
    • C22B21/0053Obtaining aluminium by other processes from other aluminium compounds
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F7/00Compounds of aluminium
    • C01F7/02Aluminium oxide; Aluminium hydroxide; Aluminates
    • C01F7/021After-treatment of oxides or hydroxides
    • C01F7/025Granulation or agglomeration
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B1/00Preliminary treatment of ores or scrap
    • C22B1/14Agglomerating; Briquetting; Binding; Granulating
    • C22B1/24Binding; Briquetting ; Granulating
    • C22B1/242Binding; Briquetting ; Granulating with binders
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/50Agglomerated particles
    • 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

Definitions

  • the present invention relates to a method for the agglomeration of particles of alumina, or particles containing a substantial portion of alumina.
  • alumina or alumina containing material have poor flow characteristics, creating difficulties in handling.
  • precipitated alumina tri- hydrate is filtered, dried and calcined. This yields high purity alumina with a narrow range of particle sizes.
  • a by-product of the calcination process comprises extremely fine particles of alumina, with an average size of less than 30 ⁇ m. This by-product is caught in the gas cleaning devices including multi- cyclones, electrostatic precipitators or bag-houses attached to the calcination device.
  • Such particles are commonly known as ESP dust.
  • ESP dust is difficult to reintroduce into the process stream, not being readily redigested in the highly caustic solution of the digestion phase.
  • agglomerate small particles of alumina such as ESP dust
  • coarser particles are of a size range suitable for use in aluminium smelting.
  • particles are agglomerated by spray drying using organic polymers as binders.
  • the agglomerates formed by these methods are typically weakly bonded and they are readily degraded when handled or transported.
  • alumina will be understood to encompass fully dehydrated alumina, fully hydrated alumina, partially hydrated alumina or a mixture of these forms.
  • alumina particles will be understood to include particles of an alumina containing material where the alumina content of said particles is at least about 30% by weight AI 2 O 3 .
  • agglomeration of alumina particles comprising the steps of:
  • the alumina particles are ground to a D 5 o of less than about 9 ⁇ m.
  • the alumina particles are ground to a D 50 of about 5 ⁇ m.
  • a quantity of water is added to the alumina particles to form a slurry, the slurry then being subjected to grinding.
  • the alumina particles are subjected to dry grinding before a quantity of water is added to form a slurry.
  • the slurry is of as high a density as possible.
  • the slurry comprises at least 50% solids.
  • the slurry comprises between about 40 and 60% solids.
  • the slurry may also contain a viscosity modifier.
  • the viscosity modifier may be one or more of acetic acid, citric acid or a polyacrylate viscosity modifier.
  • the viscosity modifier is acetic acid.
  • sufficient acetic acid is introduced such that the concentration of the acetic acid in the slurry is between about 0.2 and 1.5% by weight of the alumina particles.
  • the binding agent is a polymer form of a hydroxy salt of aluminium.
  • the binding agent is poly aluminium hydroxy chloride.
  • the concentration of the poly aluminium hydroxy chloride is less than 10% by weight relative to the alumina particles.
  • the concentration of the poly aluminium hydroxy chloride is approximately 5% by weight relative to the alumina particles.
  • the method of the present invention may comprise the additional step of:
  • the agglomerated particles are dehydroxylated by heating to approximately 300°C.
  • the agglomerated granules are calcined above 500°C.
  • agglomerated alumina particles produced by any one of the above-mentioned methods.
  • a quantity of water is added to paniculate alumina to form a slurry of a density between about 40 and 60% solids.
  • a viscosity modifier, in the form of acetic acid is added to the slurry such that the concentration of acetic acid in the slurry is between about 0.2 and 1.5% by weight of the alumina particles.
  • the slurry is then subjected to grinding such that the alumina particles are ground to a D 50 of less than 12 ⁇ m and preferably about 5 ⁇ m.
  • a quantity of binding agent in the form a hydroxy salt of aluminium such as poly aluminium hydroxy chloride is added to the slurry.
  • the poly aluminium hydroxy chloride is less than 10% by weight relative to the alumina particles.
  • the concentration of the poly aluminium hydroxy chloride is approximately 5% by weight relative to the alumina particles.
  • the mixture formed by the addition of the poly aluminium hydroxy chloride to the slurry is then spray dried to produce agglomerated granules.
  • the agglomerated granules may then be heated to in excess of approximately 300°C to effect dehydroxylation of such, or in excess of approximately above 500°C to effect calcination of such.
  • a slurry of water, poly aluminium hydroxy chloride (PAC) binder and the treated ESP dust was prepared to a solids density of approximately 50%.
  • the slurry was then spray dried to form micro agglomerates under the conditions set out in Table 2, below. Table 2
  • the product micro agglomerates are similar to the desired smelting grade alumina sizing.
  • micro agglomerates produced were tested for strength using an attrition test wherein 10 g of micro agglomerate was placed on the top screen in a stack on a RoTap, and the RoTap was activated for 5 minutes. A separate sample was placed on the RoTap for 20 minutes. The difference in particle size distribution was used as a comparative breakage test for the samples.
  • the results of the attrition tests conducted on agglomerates formed with 7% PAC appear in Table 4, below.
  • the method of the present invention is highly effective at agglomerating alumina particles into micro agglomerates of appropriate size and resistance to attrition to be readily incorporated into smelting grade alumina. This is achieved using levels of binder much lower than that utilised in the prior art, affording cost savings and industrial hygiene benefits.
  • a catalyst metal may be added to the slurry to produce a high surface area catalyst product on an alumina binder.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Geology (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Metallurgy (AREA)
  • Geochemistry & Mineralogy (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Abstract

A method for the agglomeration of alumina particles, the method comprising the steps of: grinding the alumina particles to a D50 of less than about 12 νm; adding a quantity of a binding agent; andspray drying the mixture so formed to produce agglomerated granules.

Description

"Agglomeration Of Alumina"
Field of the Invention
The present invention relates to a method for the agglomeration of particles of alumina, or particles containing a substantial portion of alumina.
Background Art
Small particles of alumina or alumina containing material have poor flow characteristics, creating difficulties in handling. In the Bayer process for the extraction of .alumina from alumina containing ores, precipitated alumina tri- hydrate is filtered, dried and calcined. This yields high purity alumina with a narrow range of particle sizes. However, a by-product of the calcination process comprises extremely fine particles of alumina, with an average size of less than 30 μm. This by-product is caught in the gas cleaning devices including multi- cyclones, electrostatic precipitators or bag-houses attached to the calcination device. Such particles are commonly known as ESP dust. In addition to being difficult to handle, ESP dust is difficult to reintroduce into the process stream, not being readily redigested in the highly caustic solution of the digestion phase.
Accordingly, it is desirable to be able to agglomerate small particles of alumina, such as ESP dust, to form coarser particles. Ideally, these coarser particles are of a size range suitable for use in aluminium smelting.
In the ceramics industry, particles are agglomerated by spray drying using organic polymers as binders. However, the agglomerates formed by these methods are typically weakly bonded and they are readily degraded when handled or transported.
In Australian Patent 664328, there is provided a method for agglomerating alumina particles with a binder comprising a polymer form of a hydroxy salt of aluminium. In a variant of the invention, activated alumina is used to reduce the quantities of the binding agent required. Where the polyhydroxy aluminium salt is used alone, concentrations of at least 10% of such are required to prevent collapse of the agglomerated granules on handling. Where the polyhydroxy aluminium salt is used in conjunction with activated alumina, binder concentrations of below 10% are possible. Indeed, by the addition of activated alumina, binder levels as low as 2.5% are able to produce sufficiently robust agglomerates.
However, the cost of the binding agent and that associated with the production of activated alumina have prevented the widespread application of this method. It is one object of the present invention to provide a method for the agglomeration of particles of alumina, or particles substantially comprising alumina, where the quantity of binder required is substantially reduced, and the need for activated alumina eliminated.
The preceding discussion of the background to the invention is intended to facilitate an understanding of the present invention. However, it should be appreciated that the discussion is not an acknowledgement or admission that any of the material referred to was part of the common general knowledge in Australia as at the priority date of the application.
Throughout the specification, unless the context requires otherwise, the word "alumina" will be understood to encompass fully dehydrated alumina, fully hydrated alumina, partially hydrated alumina or a mixture of these forms.
Throughout the specification, unless the context requires otherwise, the term "alumina particles" will be understood to include particles of an alumina containing material where the alumina content of said particles is at least about 30% by weight AI2O3.
Further, throughout the specification, unless the context requires otherwise, the word "comprise" or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers. Disclosure of the Invention
In accordance with the present invention, there is provided a method for the agglomeration of alumina particles, the method comprising the steps of:
grinding the alumina particles to a D50 of less than about 12μm;
adding a quantity of a binding agent; and
spray drying the mixture so formed to produce agglomerated granules.
Preferably, the alumina particles are ground to a D5o of less than about 9μm. In a highly preferred from of the invention, the alumina particles are ground to a D50 of about 5μm.
In one form of the invention, a quantity of water is added to the alumina particles to form a slurry, the slurry then being subjected to grinding.
In an alternate form of the invention, the alumina particles are subjected to dry grinding before a quantity of water is added to form a slurry.
Preferably, the slurry is of as high a density as possible. Preferably still, the slurry comprises at least 50% solids. Typically, the slurry comprises between about 40 and 60% solids.
The slurry may also contain a viscosity modifier. The viscosity modifier may be one or more of acetic acid, citric acid or a polyacrylate viscosity modifier. In a preferred form of the invention, the viscosity modifier is acetic acid. In a highly preferred form of the invention, sufficient acetic acid is introduced such that the concentration of the acetic acid in the slurry is between about 0.2 and 1.5% by weight of the alumina particles.
In one form of the invention, the binding agent is a polymer form of a hydroxy salt of aluminium. In a specific form of the invention, the binding agent is poly aluminium hydroxy chloride. Preferably, the concentration of the poly aluminium hydroxy chloride is less than 10% by weight relative to the alumina particles. Preferably still, the concentration of the poly aluminium hydroxy chloride is approximately 5% by weight relative to the alumina particles.
The method of the present invention may comprise the additional step of:
heating the agglomerated granules.
In one form of the invention, the agglomerated particles are dehydroxylated by heating to approximately 300°C. In an alternate form of the invention, the agglomerated granules are calcined above 500°C.
In accordance with the present invention there is further provided agglomerated alumina particles produced by any one of the above-mentioned methods.
Best Mode(s) for Carrying Out the Invention
The method of the present invention will subsequently be described, by way of example only, with reference to one embodiment thereof and several examples.
In the embodiment, a quantity of water is added to paniculate alumina to form a slurry of a density between about 40 and 60% solids. A viscosity modifier, in the form of acetic acid is added to the slurry such that the concentration of acetic acid in the slurry is between about 0.2 and 1.5% by weight of the alumina particles.
The slurry is then subjected to grinding such that the alumina particles are ground to a D50 of less than 12μm and preferably about 5μm.
A quantity of binding agent in the form a hydroxy salt of aluminium such as poly aluminium hydroxy chloride, is added to the slurry. The poly aluminium hydroxy chloride is less than 10% by weight relative to the alumina particles. Preferably the concentration of the poly aluminium hydroxy chloride is approximately 5% by weight relative to the alumina particles. The mixture formed by the addition of the poly aluminium hydroxy chloride to the slurry is then spray dried to produce agglomerated granules.
The agglomerated granules may then be heated to in excess of approximately 300°C to effect dehydroxylation of such, or in excess of approximately above 500°C to effect calcination of such.
The present invention will now be described by way of several examples. However, it must be appreciated that the following description of those examples is not to limit the generality of the above description of the invention.
Examples
ESP dust was collected and milled in a Hosokawa Alpine Jet Mill. The analysis of the treated ESP dust appears in Table 1 , below.
Table 1
Figure imgf000006_0001
A slurry of water, poly aluminium hydroxy chloride (PAC) binder and the treated ESP dust was prepared to a solids density of approximately 50%. The slurry was then spray dried to form micro agglomerates under the conditions set out in Table 2, below. Table 2
Figure imgf000007_0001
Six runs were conducted at different PAC addition levels. Agglomeration was noted in all cases. Particle size distribution analyses were conducted on the micro agglomerates. The particle size distribution (by screening) of the product is shown in Table 3, below.
Table 3
Figure imgf000007_0002
As can be seen, the product micro agglomerates are similar to the desired smelting grade alumina sizing.
The micro agglomerates produced were tested for strength using an attrition test wherein 10 g of micro agglomerate was placed on the top screen in a stack on a RoTap, and the RoTap was activated for 5 minutes. A separate sample was placed on the RoTap for 20 minutes. The difference in particle size distribution was used as a comparative breakage test for the samples. The results of the attrition tests conducted on agglomerates formed with 7% PAC appear in Table 4, below.
Table 4
Figure imgf000008_0001
The results of the attrition tests conducted on agglomerates formed with 5% PAC appear in Table 5, below.
Table 5
Figure imgf000008_0002
The results of the attrition tests conducted on agglomerates formed with 3% PAC appear in Table 6, below. Table 6
Figure imgf000009_0001
The results of the attrition tests conducted on agglomerates formed with 10% PAC appear in Table 7, below.
Table 7
Figure imgf000009_0002
The results of the attrition tests conducted on agglomerates formed with 4% PAC appear in Table 8, below. Table 8
Figure imgf000010_0001
The results of the attrition tests conducted on agglomerates formed with 2% PAC appear in Table 9, below.
Table 9
Figure imgf000010_0002
The results were compared to micro agglomerates formed using unground ESP and 10% PAC. The results of the attrition tests conducted on agglomerates formed with 10% PAC and unground ESP dust appear in Table 10, below. Table l O
Figure imgf000011_0001
The results were compared to the attrition behaviour of a typical smelting grade alumina. Results of the attrition tests conducted on a typical smelting grade alumina appear in Table 11 , below.
Table 11
Figure imgf000011_0002
The results demonstrate that before calcination, the products of mixes containing greater than 4% PAC binder have comparable resistance to the product of the unground ESP with 10% PAC binder. After heating to 600°C, there is more breakage of coarse particles at the 5% PAC level, and considerably more at the 4% PAC level. Most of this material goes into the 106 to 212 μm range and there is only a small increase in the smallest fraction measured. After heating to 900°C, there is much more breakage from the coarse fractions of the 4% PAC and 5% PAC samples than the product of the unground ESP. Again, most of this material goes into the 106 to 212 μm range and there is only a small increase in the smallest fraction measured.
From these results, it can be seen that the method of the present invention is highly effective at agglomerating alumina particles into micro agglomerates of appropriate size and resistance to attrition to be readily incorporated into smelting grade alumina. This is achieved using levels of binder much lower than that utilised in the prior art, affording cost savings and industrial hygiene benefits.
It is envisaged that a catalyst metal may be added to the slurry to produce a high surface area catalyst product on an alumina binder.
Modifications and variations such as would be apparent to the skilled addressee are considered to fall within the scope of the present invention.

Claims

The Claims Defining the Invention are as Follows
1. A method for the agglomeration of alumina particles, the method characterised by the steps of:
grinding the alumina particles to a D50 of less than about 12μm;
adding a quantity of a binding agent; and
spray drying the mixture so formed to produce agglomerated granules.
2. A method according to claim 1 characterised in that the alumina particles are ground to a D50 of less than about 9μm.
3. A method according to claim 1 or claim 2 characterised in that the alumina particles are ground to a D5o of about 5μm.
4. A method according to any one of the preceding claims characterised in that a quantity of water is added to the alumina particles to form a slurry, the slurry then being subjected to grinding.
5. A method according to any one of claims 1 to 4 characterised in that the alumina particles are subjected to dry grinding before a quantity of water is added to form a slurry.
6. A method according to any one of the preceding claims characterised in that the slurry is of a high density.
7. A method according to claim 6 characterised in that the slurry comprises between about 40 and 60% solids.
8. A method according to any one of the preceding claims characterised in that the slurry contains a viscosity modifier.
9. A method according to claim 8 characterised in that viscosity modifier comprises one or more of acetic acid, citric acid or a polyacrylate viscosity modifier.
10. A method according to claim 8 or 9 characterised in that the viscosity modifier is acetic acid.
11. A method according to claim 10 characterised in that sufficient acetic acid is introduced such that the concentration of the acetic acid in the slurry is between about 0.2 and 1.5% by weight of the alumina particles.
12. A method according to any one of the preceding claims characterised in that the binding agent is a polymer form of a hydroxy salt of aluminium.
13. A method according to claim 12 characterised in that the binding agent is poly aluminium hydroxy chloride.
14. A method according to claim 13 characterised in that the concentration of the poly aluminium hydroxy chloride is less than 10% by weight relative to the alumina particles.
15. A method according to claim 13 or 14 characterised in that the concentration of the poly aluminium hydroxy chloride is approximately 5% by weight relative to the alumina particles.
16. A method according to any one of the preceding claims characterised in that the method comprises the step of:
heating the agglomerated granules.
17. A method according to claim 16 characterised in that the agglomerated particles are dehydroxylated by heating to approximately 300°C.
18. A method according to claim 16 characterised in that the agglomerated granules are calcined above 500°C.
19. Agglomerated alumina particles produced by any one of the method of any one of claims 1 to 18
20. A method for the agglomeration of alumina particles substantially as described herein, with reference to any one of the Examples.
21. Agglomerated alumina particles substantially as described herein, with reference to any one of the Examples.
PCT/AU2001/000214 2000-03-28 2001-03-01 Agglomeration of alumina WO2001073142A1 (en)

Priority Applications (2)

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AU37124/01A AU3712401A (en) 2000-03-28 2001-03-01 Agglomeration of alumina
US10/971,639 US7449030B2 (en) 2001-03-01 2004-10-20 Agglomeration of alumina and binder therefor

Applications Claiming Priority (2)

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AUPQ6546 2000-03-28
AUPQ6546A AUPQ654600A0 (en) 2000-03-28 2000-03-28 Agglomeration of alumina

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150152268A1 (en) * 2012-07-02 2015-06-04 System S.P. A. Ceramic material for decoration and process for its preparation
CN107935138A (en) * 2017-11-22 2018-04-20 广东桑海环保有限公司 A kind of ionic control agent and its preparation method and application

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1295133A (en) * 1969-04-25 1972-11-01
US4579839A (en) * 1983-11-18 1986-04-01 Aluminum Company Of America Rehydration bondable alumina
WO1994014988A1 (en) * 1992-12-24 1994-07-07 Commonwealth Scientific And Industrial Research Organisation Agglomeration of alumina material

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1295133A (en) * 1969-04-25 1972-11-01
US4579839A (en) * 1983-11-18 1986-04-01 Aluminum Company Of America Rehydration bondable alumina
WO1994014988A1 (en) * 1992-12-24 1994-07-07 Commonwealth Scientific And Industrial Research Organisation Agglomeration of alumina material

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150152268A1 (en) * 2012-07-02 2015-06-04 System S.P. A. Ceramic material for decoration and process for its preparation
CN107935138A (en) * 2017-11-22 2018-04-20 广东桑海环保有限公司 A kind of ionic control agent and its preparation method and application

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