CA2649969A1 - Method for agglomeration - Google Patents
Method for agglomeration Download PDFInfo
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- CA2649969A1 CA2649969A1 CA002649969A CA2649969A CA2649969A1 CA 2649969 A1 CA2649969 A1 CA 2649969A1 CA 002649969 A CA002649969 A CA 002649969A CA 2649969 A CA2649969 A CA 2649969A CA 2649969 A1 CA2649969 A1 CA 2649969A1
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- Canada
- Prior art keywords
- agglomeration
- acid
- ore material
- ore
- solution
- 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.)
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- 238000005054 agglomeration Methods 0.000 title claims abstract description 46
- 230000002776 aggregation Effects 0.000 title claims abstract description 46
- 238000000034 method Methods 0.000 title claims abstract description 37
- 239000002253 acid Substances 0.000 claims abstract description 60
- 239000000463 material Substances 0.000 claims abstract description 44
- 238000005325 percolation Methods 0.000 claims description 19
- 239000011230 binding agent Substances 0.000 claims description 15
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 9
- 235000011149 sulphuric acid Nutrition 0.000 claims description 9
- 229910001710 laterite Inorganic materials 0.000 claims description 7
- 239000011504 laterite Substances 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 239000001117 sulphuric acid Substances 0.000 claims description 6
- 241001417517 Scatophagidae Species 0.000 description 15
- 238000002386 leaching Methods 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000002245 particle Substances 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 239000004927 clay Substances 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229920006322 acrylamide copolymer Polymers 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910001919 chlorite Inorganic materials 0.000 description 1
- 229910052619 chlorite group Inorganic materials 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000009852 extractive metallurgy Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 229910052598 goethite Inorganic materials 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000011019 hematite Substances 0.000 description 1
- 229910052595 hematite Inorganic materials 0.000 description 1
- AEIXRCIKZIZYPM-UHFFFAOYSA-M hydroxy(oxo)iron Chemical compound [O][Fe]O AEIXRCIKZIZYPM-UHFFFAOYSA-M 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910000273 nontronite Inorganic materials 0.000 description 1
- 239000011022 opal Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000010878 waste rock Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/24—Binding; Briquetting ; Granulating
- C22B1/242—Binding; Briquetting ; Granulating with binders
- C22B1/243—Binding; Briquetting ; Granulating with binders inorganic
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B23/00—Obtaining nickel or cobalt
- C22B23/005—Preliminary treatment of ores, e.g. by roasting or by the Krupp-Renn process
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B23/00—Obtaining nickel or cobalt
- C22B23/04—Obtaining nickel or cobalt by wet processes
- C22B23/0407—Leaching processes
- C22B23/0415—Leaching processes with acids or salt solutions except ammonium salts solutions
- C22B23/043—Sulfurated acids or salts thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
A method for agglomeration (10) characterised by the method steps of: i) adjusting the moisture content of an ore material to be agglomerated to a predetermined level, ii) passing the ore material to an agglomeration circuit (20); and iii) adding an acid containing agglomerating solution to the ore material in the agglomeration circuit to provide an agglomerated ore material, whereby the acid concentration of the agglomerating solution does not exceed about 100g/L.
Description
"Method for Agglomeration"
Field of the Invention The present invention relates to a method for agglomeration. More particularly, the present invention is intended to produce agglomerates of an ore to be leached using a dilute acid solution. The method of the present invention has particular application in the agglomeration of nickel laterite ores prior to heap leaching.
Background Art Agglomeration is an ore treatment method that has been used extensively in the mining industry to improve the ore's leaching characteristics. Agglomeration typically involves the binding of finer particles, including clays, to larger particles.
This improves the percolation of leach solutions through the ore material and prevents migration of those finer particles. Additionally, this ensures that the target metal values contained in the fine materials are available to the leaching solution.
A variety of methods for agglomeration have been practised over the years, the simplest method involving the use of water to form the agglomerated particles.
Water is popular from an economic viewpoint, but its use is highly dependent on the ore characteristics. Ores with particularly high clay and/or fines content may not necessarily respond as well to water agglomeration.
For this reason binding agents became very popular, and the use of such agents has been adopted quite extensively. However, binding agents, such as cement, are generally only used in alkaline leaching conditions as many of these binding agents are not stable in low pH conditions.
Strong or concentrated acid has been a popular choice for agglomerating when binding agents are not suitable. In particular, the general trend is that the more concentrated the acid the more advantageous the results, although the use of concentrated acid is generally limited by economic factors. The advantages of concentrated acid are known to be that heat is generated by the exothermic reaction of the acid and the small amount of moisture present in the ore, resulting in better break-down of the ore minerals and exposing the target metal values.
Concentrated acid also helps to form better agglomerates by breaking down bulk non-valuable minerals in the ore, for example silicates, particularly in laterites, such that upon re-precipitation and curing, a relatively strong agglomerate can be formed.
One of the main problems with using concentrated acid solutions in agglomeration, is that agglomerates can become friable, resulting in blockages in the heap once particles begin to break away. Further, the use of concentrated acid can also promote dissolution of unwanted impurities.
Further, agglomeration of ores prior to exposure to extractive metallurgical processes has most commonly been practised on a limited range of ore types.
Most commonly these ore types include those bearing precious metals, such as gold and silver, and some limited base metals, particularly copper bearing ores.
Nickel laterite or oxide ores have not been studied in particular detail with regard to heap leaching and present a number of particular difficulties, many of which are related directly to what is a generally high clay content.
The present invention disclosed herein relates to the use of a dilute acid solution for agglomeration with surprising results. The disadvantages of using water or strong or concentrated acid appear to be overcome, without sacrificing structural integrity of the agglomerates, whilst percolation rates and extraction levels are improved.
The preceding discussion of the background art is intended to facilitate an understanding of the present invention only. 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.
Field of the Invention The present invention relates to a method for agglomeration. More particularly, the present invention is intended to produce agglomerates of an ore to be leached using a dilute acid solution. The method of the present invention has particular application in the agglomeration of nickel laterite ores prior to heap leaching.
Background Art Agglomeration is an ore treatment method that has been used extensively in the mining industry to improve the ore's leaching characteristics. Agglomeration typically involves the binding of finer particles, including clays, to larger particles.
This improves the percolation of leach solutions through the ore material and prevents migration of those finer particles. Additionally, this ensures that the target metal values contained in the fine materials are available to the leaching solution.
A variety of methods for agglomeration have been practised over the years, the simplest method involving the use of water to form the agglomerated particles.
Water is popular from an economic viewpoint, but its use is highly dependent on the ore characteristics. Ores with particularly high clay and/or fines content may not necessarily respond as well to water agglomeration.
For this reason binding agents became very popular, and the use of such agents has been adopted quite extensively. However, binding agents, such as cement, are generally only used in alkaline leaching conditions as many of these binding agents are not stable in low pH conditions.
Strong or concentrated acid has been a popular choice for agglomerating when binding agents are not suitable. In particular, the general trend is that the more concentrated the acid the more advantageous the results, although the use of concentrated acid is generally limited by economic factors. The advantages of concentrated acid are known to be that heat is generated by the exothermic reaction of the acid and the small amount of moisture present in the ore, resulting in better break-down of the ore minerals and exposing the target metal values.
Concentrated acid also helps to form better agglomerates by breaking down bulk non-valuable minerals in the ore, for example silicates, particularly in laterites, such that upon re-precipitation and curing, a relatively strong agglomerate can be formed.
One of the main problems with using concentrated acid solutions in agglomeration, is that agglomerates can become friable, resulting in blockages in the heap once particles begin to break away. Further, the use of concentrated acid can also promote dissolution of unwanted impurities.
Further, agglomeration of ores prior to exposure to extractive metallurgical processes has most commonly been practised on a limited range of ore types.
Most commonly these ore types include those bearing precious metals, such as gold and silver, and some limited base metals, particularly copper bearing ores.
Nickel laterite or oxide ores have not been studied in particular detail with regard to heap leaching and present a number of particular difficulties, many of which are related directly to what is a generally high clay content.
The present invention disclosed herein relates to the use of a dilute acid solution for agglomeration with surprising results. The disadvantages of using water or strong or concentrated acid appear to be overcome, without sacrificing structural integrity of the agglomerates, whilst percolation rates and extraction levels are improved.
The preceding discussion of the background art is intended to facilitate an understanding of the present invention only. 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 "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.
Throughout the specification, the term "atmospheric" when used with reference to leaching is to be understood to refer to any one of a heap, vat, dump, thin-layer or in-situ leach, unless the context requires otherwise.
Throughout the specification, the terms "ore" and "ore material" are understood to refer to any one of ore, ore reject material, concentrate, waste rock or mill scats material.
The term "agglomerate" is to be understood to refer to agglomerated ore material.
Throughout the specification, the term "curing" is understood to be the period of time occurring between agglomeration and subsequent application of leaching solution.
Disclosure of the Invention In accordance with the present invention there is provided a method for agglomeration comprising the method steps of:
i) adjusting the moisture content of an ore material to be agglomerated to a predetermined level, ii) passing the ore material to an agglomeration circuit; and iii) adding an acid containing agglomerating solution to the ore material in the agglomeration circuit to provide an agglomerated ore material, whereby the acid concentration of the agglomerating solution does not exceed about 100g/L.
Throughout the specification, the term "atmospheric" when used with reference to leaching is to be understood to refer to any one of a heap, vat, dump, thin-layer or in-situ leach, unless the context requires otherwise.
Throughout the specification, the terms "ore" and "ore material" are understood to refer to any one of ore, ore reject material, concentrate, waste rock or mill scats material.
The term "agglomerate" is to be understood to refer to agglomerated ore material.
Throughout the specification, the term "curing" is understood to be the period of time occurring between agglomeration and subsequent application of leaching solution.
Disclosure of the Invention In accordance with the present invention there is provided a method for agglomeration comprising the method steps of:
i) adjusting the moisture content of an ore material to be agglomerated to a predetermined level, ii) passing the ore material to an agglomeration circuit; and iii) adding an acid containing agglomerating solution to the ore material in the agglomeration circuit to provide an agglomerated ore material, whereby the acid concentration of the agglomerating solution does not exceed about 100g/L.
Preferably, the acid concentration of the agglomerating solution does not exceed about 50g/L.
Still preferably, the acid in the agglomerating solution is sulphuric acid.
The moisture content of the ore material prior to agglomeration preferably falls within the range of about 5% and 30%.
Still preferably, the moisture content of the ore material prior to agglomeration falls within the range of about 15% and 25%.
The agglomeration circuit may comprise one or more drum or rotary disc agglomerators.
The agglomerating solution of step iii) still preferably comprises a pregnant leach solution (PLS) from an existing atmosphe(c or pressure leach circuit.
Preferably, the agglomeration of step iii) is achieved by adding a maximum of about 100 kg of acid per tonne of ore material.
Still preferably, the agglomeration of step iii) is achieved by adding a total amount of acid which falls within the range of about 5 and 50 kg of acid per tonne of ore.
Preferably, a binding agent is applied to the ore material in the agglomeration circuit.
Still preferably, the binding agent may comprise any known binding agent, for example a polymeric binder.
Preferably, the agglomerated ore material is allowed to cure for a period not exceeding 21 days.
Still preferably, the acid in the agglomerating solution is sulphuric acid.
The moisture content of the ore material prior to agglomeration preferably falls within the range of about 5% and 30%.
Still preferably, the moisture content of the ore material prior to agglomeration falls within the range of about 15% and 25%.
The agglomeration circuit may comprise one or more drum or rotary disc agglomerators.
The agglomerating solution of step iii) still preferably comprises a pregnant leach solution (PLS) from an existing atmosphe(c or pressure leach circuit.
Preferably, the agglomeration of step iii) is achieved by adding a maximum of about 100 kg of acid per tonne of ore material.
Still preferably, the agglomeration of step iii) is achieved by adding a total amount of acid which falls within the range of about 5 and 50 kg of acid per tonne of ore.
Preferably, a binding agent is applied to the ore material in the agglomeration circuit.
Still preferably, the binding agent may comprise any known binding agent, for example a polymeric binder.
Preferably, the agglomerated ore material is allowed to cure for a period not exceeding 21 days.
Still preferably, the curing time of the agglomerated ore material does not exceed 7 days.
Still more preferably, the curing time of the agglomerated ore material falls within the range of about 5 to 7 days.
The method for agglomeration of the present invention preferably provides for a percolation rate of leach solution through either a column or heap of greater than about 2,000 Um2/hr. Still preferably, the percolation rate is between about 2,000 and 45,000 Um2/hr.
Brief Description of the Drawings The present invention will now be described, by way of example only, with reference to an embodiment thereof and the accompanying drawing, in which;
Figure 1 is a diagrammatic representation of a method for agglomeration in accordance with the present invention;
Figure 2 is a graphical representation of size distribution date for whole ore and "scats" used in Example 1; and Figure 3 is a graphical representation of Kappes test results showing acidity versus percolation or "drain down" rate.
Best Mode(s) for Carrying Out the Invention In Figure 1 there is shown a method for agglomeration 10 in accordance with the present invention.
A nickel laterite ore 12 is subjected to a preparation step 14 during which the moisture content is adjusted to within about 5% and 30%, for example 15% and 25%. This moisture content may be achieved by air drying the ore in a heap 16, or by adding water 18 to the ore, as required.
Still more preferably, the curing time of the agglomerated ore material falls within the range of about 5 to 7 days.
The method for agglomeration of the present invention preferably provides for a percolation rate of leach solution through either a column or heap of greater than about 2,000 Um2/hr. Still preferably, the percolation rate is between about 2,000 and 45,000 Um2/hr.
Brief Description of the Drawings The present invention will now be described, by way of example only, with reference to an embodiment thereof and the accompanying drawing, in which;
Figure 1 is a diagrammatic representation of a method for agglomeration in accordance with the present invention;
Figure 2 is a graphical representation of size distribution date for whole ore and "scats" used in Example 1; and Figure 3 is a graphical representation of Kappes test results showing acidity versus percolation or "drain down" rate.
Best Mode(s) for Carrying Out the Invention In Figure 1 there is shown a method for agglomeration 10 in accordance with the present invention.
A nickel laterite ore 12 is subjected to a preparation step 14 during which the moisture content is adjusted to within about 5% and 30%, for example 15% and 25%. This moisture content may be achieved by air drying the ore in a heap 16, or by adding water 18 to the ore, as required.
The ore 12 is then passed to an agglomeration circuit 20 where an acid containing agglomerating solution 22 containing between about 5 and 100g/L of sulphuric acid, for example 45 g/L H2SO4, and a known binding agent 24, is added, and the ore 12 agglomerated to provide an agglomerated ore material 26.
The agglomerated ore material 26 may then be cured for a period of time. The curing time should not exceed 21 days as the stability of the agglomerated ore material 26 begins to deteriorate after this time. The balance between the stability of the agglomerated ore material 26 and permeability and extraction is maximised when the curing time falls within the range of 5 and 7 days.
The agglomeration circuit 20 may comprise one ore more drum or rotary disc agglomerators.
It is envisaged that the acid containing agglomerating solution 22 may comprise a dilute sulphuric acid solution, or a leach solution exiting an atmospheric or pressure leach circuit, or a mixture of both, such that the acid concentration falls within the range of about 5 to 100 kg acid per tonne of ore, for example between about 5 and 50 kg acid per tonne of ore.
It is further envisaged that the known binding agent may be provided in the form of a polymeric binder. For example, the non-ionic high molecular weight polyacrylamide copolymer Hi-Tex 82200T'" and the cationic high molecular weight acrylamide copolymer OPTIMER AA182HT"" are two that may be utilised.
It is still further envisaged that the acid in the agglomerating solution may also comprise any one of nitric acid and hydrochloric acid.
The present invention is further illustrated by way of the following non-limiting example:
The agglomerated ore material 26 may then be cured for a period of time. The curing time should not exceed 21 days as the stability of the agglomerated ore material 26 begins to deteriorate after this time. The balance between the stability of the agglomerated ore material 26 and permeability and extraction is maximised when the curing time falls within the range of 5 and 7 days.
The agglomeration circuit 20 may comprise one ore more drum or rotary disc agglomerators.
It is envisaged that the acid containing agglomerating solution 22 may comprise a dilute sulphuric acid solution, or a leach solution exiting an atmospheric or pressure leach circuit, or a mixture of both, such that the acid concentration falls within the range of about 5 to 100 kg acid per tonne of ore, for example between about 5 and 50 kg acid per tonne of ore.
It is further envisaged that the known binding agent may be provided in the form of a polymeric binder. For example, the non-ionic high molecular weight polyacrylamide copolymer Hi-Tex 82200T'" and the cationic high molecular weight acrylamide copolymer OPTIMER AA182HT"" are two that may be utilised.
It is still further envisaged that the acid in the agglomerating solution may also comprise any one of nitric acid and hydrochloric acid.
The present invention is further illustrated by way of the following non-limiting example:
Percolation testing, using a standard Kappes test procedure, was employed to measure the quality of the agglomerates produced using the method for agglomeration of the present invention.
Nickel laterite ore "scats" have been utilised in this example. The term "scats" is used to refer to the coarse fraction of the ore resulting from beneficiation of the nickel laterite ore. The scats contain both ore and gangue minerals that require additional processing to liberate the mineral. Mineralogical testing of the scats used indicate that the scats are 60% to 70% nontronite clay, 5% to 10% quartz, 5% to 10% goethite, 5% to 10% hematite, <5% kaolin, <5% opal, <5% chlorite, and less than 1 % asbolane and bauxite.
Size distribution data for several sources of scats or whole ore are shown in Figure 2. Agglomerates were formed using the method of the present invention as described above, without binder and without curing. Specifically, agglomeration was carried out in a 20 L drum held securely in a portable cement mixer. 5 to 6 kg of 'as received' ore was loaded into the drum, mixed and a small amount of water or acid solution added to suppress dust generation. Some samples, noted below, were previously air dried. The required amount of concentrated acid (99% H2SO4) or dilute acid (45 g/L) was then added and the agglomerates formed continually assessed. All amounts of water and acid added were recorded. The agglomeration tests are summarised in Table 1 below:
Table 1 Ore Type Agglomer- Dry % Acid Water Liquid Acid %
ation Ore Moist- Added Added to Solid Load- Moist-solution (kg) ure (g) (g) Ratio ing ure (vol/wt) (kg/t) (caic) Low-grade Dilute acid 29.87 9.5 371 11,186 0.38 12 27 Saprolitic Whole Ore Concentrated 29.87 9.5 4,492 9,597 0.40 150 24 acid Scats 1 Dilute acid 2765 7.8 20.4 677 0.25 7.4 20 Concentrated 2765 7.8 275.4 486 0.23 100 15 acid Scats 2 Dilute acid 2763 7.9 28.4 853 0.31 10.3 24 Concentrated 2763 7.9 277.2 746 0.32 100 21 acid Scats 3 Dilute acid 2713 9.5* 18.9 694 0.26 7.0 20 Concentrated 2713 9.5" 273.0 623 0.28 101 21 acid The Kappes percolation test involves filling a leaching column (0.1 m diameter and 0.6m height) with agglomerates and measuring the initial ore height.
The column is tapped with a rubber mallet over its length so that the agglomerates are settled. The new height is then measured in order to determine the "slump"
of the ore.
The column is then filled from the bottom with leaching solution containing sulphuric acid such that the solution covers all of the ore. The column then stands for 48 hours before the height of the agglomerates is measured again.
The percolation rate is then measured by opening the bottom drain valve, drained for an initial period of 5 seconds, then taking a timed sample of solution, measuring the quantity of solution discharged and calculating a flow rate in L/hr/m2.
In order for the test to pass, a flow rate of at least 10,000 L/hr/m2 and a slump of less than 10% must be achieved.
The Kappes percolation test results of the nickel laterite ore materials are shown in Table 2 below.
Nickel laterite ore "scats" have been utilised in this example. The term "scats" is used to refer to the coarse fraction of the ore resulting from beneficiation of the nickel laterite ore. The scats contain both ore and gangue minerals that require additional processing to liberate the mineral. Mineralogical testing of the scats used indicate that the scats are 60% to 70% nontronite clay, 5% to 10% quartz, 5% to 10% goethite, 5% to 10% hematite, <5% kaolin, <5% opal, <5% chlorite, and less than 1 % asbolane and bauxite.
Size distribution data for several sources of scats or whole ore are shown in Figure 2. Agglomerates were formed using the method of the present invention as described above, without binder and without curing. Specifically, agglomeration was carried out in a 20 L drum held securely in a portable cement mixer. 5 to 6 kg of 'as received' ore was loaded into the drum, mixed and a small amount of water or acid solution added to suppress dust generation. Some samples, noted below, were previously air dried. The required amount of concentrated acid (99% H2SO4) or dilute acid (45 g/L) was then added and the agglomerates formed continually assessed. All amounts of water and acid added were recorded. The agglomeration tests are summarised in Table 1 below:
Table 1 Ore Type Agglomer- Dry % Acid Water Liquid Acid %
ation Ore Moist- Added Added to Solid Load- Moist-solution (kg) ure (g) (g) Ratio ing ure (vol/wt) (kg/t) (caic) Low-grade Dilute acid 29.87 9.5 371 11,186 0.38 12 27 Saprolitic Whole Ore Concentrated 29.87 9.5 4,492 9,597 0.40 150 24 acid Scats 1 Dilute acid 2765 7.8 20.4 677 0.25 7.4 20 Concentrated 2765 7.8 275.4 486 0.23 100 15 acid Scats 2 Dilute acid 2763 7.9 28.4 853 0.31 10.3 24 Concentrated 2763 7.9 277.2 746 0.32 100 21 acid Scats 3 Dilute acid 2713 9.5* 18.9 694 0.26 7.0 20 Concentrated 2713 9.5" 273.0 623 0.28 101 21 acid The Kappes percolation test involves filling a leaching column (0.1 m diameter and 0.6m height) with agglomerates and measuring the initial ore height.
The column is tapped with a rubber mallet over its length so that the agglomerates are settled. The new height is then measured in order to determine the "slump"
of the ore.
The column is then filled from the bottom with leaching solution containing sulphuric acid such that the solution covers all of the ore. The column then stands for 48 hours before the height of the agglomerates is measured again.
The percolation rate is then measured by opening the bottom drain valve, drained for an initial period of 5 seconds, then taking a timed sample of solution, measuring the quantity of solution discharged and calculating a flow rate in L/hr/m2.
In order for the test to pass, a flow rate of at least 10,000 L/hr/m2 and a slump of less than 10% must be achieved.
The Kappes percolation test results of the nickel laterite ore materials are shown in Table 2 below.
Table 2 Ore Agglomeration Loose Bulk % Slump Percolation Material Solution Density Rate (L/hr/m2) (kg/m3) Low-grade Dilute acid 0.74 8.6 15,144 Saprolitic (12 kg/t) Whole Ore Concentrated 0.93 14.9 351 acid (150kg/t) Scats 1 Dilute acid 0.78 11.6 8,937 (7.4 kg/t) Concentrated 0.93 15.5 764 Acid (100 kg/t) Scats 2 Dilute acid 0.74 11.2 2,673 (10.3 kg/t) Concentrated 0.94 16.8 1,528 acid (100 kg/t) Scats 3 Dilute acid 0.74 10.6 2,903 (50 kg/t) Concentrated 0.83 12.5 2,292 acid (101 kg/t) Agglomerates produced with both 100 kg/t and 150 kg/t concentrated sulphuric acid had a tendency to break down during the flooding stage, resulting in a layer of fines at the top of the agglomerated material, which in turn, affected percolation.
As can be seen from the results in Table 2, agglomerating with dilute acid in comparison to concentrated acid resulted in the samples passing the Kappes test.
Further, the initial moisture content of the samples clearly alters the characteristics of the final agglomerates, affecting the percolation rates.
As can be seen from the results in Table 2, agglomerating with dilute acid in comparison to concentrated acid resulted in the samples passing the Kappes test.
Further, the initial moisture content of the samples clearly alters the characteristics of the final agglomerates, affecting the percolation rates.
Shown in Figure 3 are the results of additional Kappes testing, conducted as noted above, showing percolation rates versus acidity for a number of tests on scats in various sized columns as noted in the legend. Agglomerates were produced using a dilute acid of 100 g/L H2SO4. As will be noted, most effective percolation rates are shown to be obtained at about 50 kg/t acid to ore. The percolation rates obtained at this level were between about 15,000 and 45,000 L/m2/hr.
The ability to produce better agglomerates by controlling the moisture content of the ore material and the concentration of acid during agglomeration is shown to result in more stable agglomerates and better rates of percolation of leaching solution through the ore material. In turn, improved percolation rates lead to faster leaching kinetics and higher extractions.
Modifications and variations such as would be apparent to the skilled addressee are considered to fall within the scope of the present invention.
The ability to produce better agglomerates by controlling the moisture content of the ore material and the concentration of acid during agglomeration is shown to result in more stable agglomerates and better rates of percolation of leaching solution through the ore material. In turn, improved percolation rates lead to faster leaching kinetics and higher extractions.
Modifications and variations such as would be apparent to the skilled addressee are considered to fall within the scope of the present invention.
Claims (20)
1. A method for agglomeration characterised in that the method comprises the steps of:
(i) adjusting the moisture content of an ore material to be agglomerated to a predetermined level;
(ii) passing the ore material to an agglomeration circuit; and (iii) adding an acid containing agglomerating solution to the ore material in the agglomeration circuit to provide an agglomerated ore material, whereby the acid concentration of the agglomerating solution does not exceed about 100g/L.
(i) adjusting the moisture content of an ore material to be agglomerated to a predetermined level;
(ii) passing the ore material to an agglomeration circuit; and (iii) adding an acid containing agglomerating solution to the ore material in the agglomeration circuit to provide an agglomerated ore material, whereby the acid concentration of the agglomerating solution does not exceed about 100g/L.
2. A method according to claim 1, wherein the acid concentration of the agglomerating solution does not exceed about 50g/L.
3. A method according to claim 1 or 2, wherein the acid in the agglomerating solution is sulphuric acid.
4. A method according to any one of the preceding claims, wherein the moisture content of the ore material prior to agglomeration falls within the range of about 5% and 30%.
5. A method according to any one of the preceding claims, wherein the moisture content of the ore material prior to agglomeration falls within the range of about 15% and 25%.
6. A method according to any one of the preceding claims, wherein the agglomeration circuit may comprise one or more drum or rotary disc agglomerators.
7. A method according to any one of the preceding claims, wherein the agglomerating solution of step iii) comprises a pregnant leach solution (PLS) from an existing atmospheric or pressure leach circuit.
8. A method according to any one of the preceding claims, wherein the agglomeration of step iii) is achieved by adding a maximum of about 100 kg of acid per tonne of ore material.
9. A method according to any one of the preceding claims, wherein the agglomeration of step iii) is achieved by adding a total amount of acid which falls within the range of about 5 and 50 kg of acid per tonne of ore.
10. A method according to any one of the preceding claims, wherein the binding agent is applied to the ore material in the agglomeration circuit.
11. A method according to any one of the preceding claims, wherein the binding agent comprises a polymeric binder.
12. A method according to any one of the preceding claims, wherein a curing step is provided after the agglomeration circuit.
13. A method according to claim 12, wherein the curing time of the agglomerated ore material does not exceed 21 days.
14. A method according to claim 12 or 13, wherein the curing time of the agglomerated ore material does not exceed 7 days.
15. A method according to any one of claims 12 to 14, wherein, the curing time of the agglomerated ore material falls within the range of about 5 to 7 days.
16. A method according to any one of the preceding claims, wherein a percolation rate of leach solution through either a column or heap of greater than about 2,000 L/m2/hr is achieved.
17. A method according to any one of the preceding claims, wherein a percolation rate of between about 2,000 and 45,000 L/m2/hr is achieved.
18. A method according to any one of the preceding claims, wherein the ore material is a nickel laterite ore material.
19. A method for agglomeration substantially as hereinbefore described with reference to Figure 1.
20. A method for agglomeration substantially as hereinbefore described with reference to Example 1.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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AU2006903158A AU2006903158A0 (en) | 2006-06-12 | Method for Agglomeration | |
AU2006903158 | 2006-06-12 | ||
PCT/AU2007/000817 WO2007143779A1 (en) | 2006-06-12 | 2007-06-12 | Method for agglomeration |
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CA2649969A1 true CA2649969A1 (en) | 2007-12-21 |
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CA002649969A Abandoned CA2649969A1 (en) | 2006-06-12 | 2007-06-12 | Method for agglomeration |
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EP (1) | EP2035589B1 (en) |
AU (1) | AU2007260577B2 (en) |
BR (1) | BRPI0711527A2 (en) |
CA (1) | CA2649969A1 (en) |
WO (1) | WO2007143779A1 (en) |
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AU2010207893B2 (en) * | 2009-02-02 | 2015-12-03 | Cerro Matoso Sa | Method of agglomeration |
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DE2903971C2 (en) * | 1979-02-02 | 1982-10-21 | Th. Goldschmidt Ag, 4300 Essen | Process for the solidification of fly dust containing zinc oxide |
DE2919272A1 (en) * | 1979-05-12 | 1980-11-27 | Metallgesellschaft Ag | METHOD FOR BRIKETTING MATERIAL CONTAINING SPONGE IRON |
US6312500B1 (en) * | 2000-03-30 | 2001-11-06 | Bhp Minerals International Inc. | Heap leaching of nickel containing ore |
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2007
- 2007-06-12 AU AU2007260577A patent/AU2007260577B2/en not_active Ceased
- 2007-06-12 CA CA002649969A patent/CA2649969A1/en not_active Abandoned
- 2007-06-12 WO PCT/AU2007/000817 patent/WO2007143779A1/en active Application Filing
- 2007-06-12 BR BRPI0711527-0A patent/BRPI0711527A2/en not_active Application Discontinuation
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WO2007143779A1 (en) | 2007-12-21 |
AU2007260577B2 (en) | 2010-10-28 |
EP2035589A4 (en) | 2012-01-18 |
EP2035589B1 (en) | 2013-02-13 |
AU2007260577A1 (en) | 2007-12-21 |
BRPI0711527A2 (en) | 2011-11-01 |
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