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AU2007260577B2 - Method for agglomeration - Google Patents

Method for agglomeration Download PDF

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Publication number
AU2007260577B2
AU2007260577B2 AU2007260577A AU2007260577A AU2007260577B2 AU 2007260577 B2 AU2007260577 B2 AU 2007260577B2 AU 2007260577 A AU2007260577 A AU 2007260577A AU 2007260577 A AU2007260577 A AU 2007260577A AU 2007260577 B2 AU2007260577 B2 AU 2007260577B2
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Australia
Prior art keywords
agglomeration
acid
ore material
ore
solution
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AU2007260577A
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AU2007260577A1 (en
Inventor
Michael Rodriguez
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Murrin Murrin Operations Pty Ltd
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Murrin Murrin Operations Pty Ltd
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Priority claimed from AU2006903158A external-priority patent/AU2006903158A0/en
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Priority to AU2007260577A priority Critical patent/AU2007260577B2/en
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    • 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
    • C22B1/243Binding; Briquetting ; Granulating with binders inorganic
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B23/00Obtaining nickel or cobalt
    • C22B23/005Preliminary treatment of ores, e.g. by roasting or by the Krupp-Renn process
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B23/00Obtaining nickel or cobalt
    • C22B23/04Obtaining nickel or cobalt by wet processes
    • C22B23/0407Leaching processes
    • C22B23/0415Leaching processes with acids or salt solutions except ammonium salts solutions
    • C22B23/043Sulfurated acids or salts thereof

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

WO 2007/143779 PCT/AU2007/000817 "Method for Aqglomeration" 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 5 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 10 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. 15 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 20 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 25 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 30 concentrated acid is generally limited by economic factors. The advantages of WO 2007/143779 PCT/AU2007/000817 -2 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 5 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 10 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 15 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 20 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 25 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 30 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.
WO 2007/143779 PCT/AU2007/000817 -3 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. 5 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. 10 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. 15 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 20 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, 25 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 30 material, whereby the acid concentration of the agglomerating solution does not exceed about 100g/L.
WO 2007/143779 PCT/AU2007/000817 -4 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. 5 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 10 within the range of about 15% and 25%. The agglomeration circuit may comprise one or more drum or rotary disc agglomerators. 15 The agglomerating solution of step iii) still preferably comprises a pregnant leach solution (PLS) from an existing atmospheric 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. 20 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 25 circuit. Still preferably, the binding agent may comprise any known binding agent, for example a polymeric binder. 30 Preferably, the agglomerated ore material is allowed to cure for a period not exceeding 21 days.
WO 2007/143779 PCT/AU2007/000817 -5 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 5 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 L/m 2 /hr. Still preferably, the percolation rate is between about 2,000 10 and 45,000 L/m 2 /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; 15 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 20 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 25 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.
WO 2007/143779 PCT/AU2007/000817 -6 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 H 2
SO
4 , and a known binding agent 24, is added, and the ore 12 agglomerated to provide an agglomerated ore material 26. 5 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. 10 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 15 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 82200TM and the cationic high molecular weight 20 acrylamide copolymer OPTIMER AA182H T M are two that may be utilized. 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: WO 2007/143779 PCT/AU2007/000817 -7 EXAMPLE 1 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. 5 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 10 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 15 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 20 samples, noted below, were previously air dried. The required amount of concentrated acid (99% H 2
SO
4 ) 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: 25 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 (vollwt) (kg/t) (calc) 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 WO 2007/143779 PCT/AU2007/000817 -8 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. 5 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 10 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, 15 measuring the quantity of solution discharged and calculating a flow rate in L/hr/m 2 . In order for the test to pass, a flow rate of at least 10,000 L/hr/m 2 and a slump of less than 10% must be achieved. 20 The Kappes percolation test results of the nickel laterite ore materials are shown in Table 2 below.
WO 2007/143779 PCT/AU2007/000817 -9 Table 2 Ore Agglomeration Loose Bulk % Slump Percolation Material Solution Density Rate (L/hr/m 2 ) (kg/m 3 ) Low-grade Dilute acid 0.74 8.6 15,144 Saprolitic (12 kg/t) Whole Ore Concentrated 0.93 14.9 351 acid (1 50kg/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 5 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 10 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.
WO 2007/143779 PCT/AU2007/000817 -10 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 H 2
SO
4 . As will be noted, most effective 5 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/m 2 /hr. The ability to produce better agglomerates by controlling the moisture content of 10 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 15 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.
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. WO 2007/143779 PCT/AU2007/000817 - 12
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/m 2 /hr is achieved. WO 2007/143779 PCT/AU2007/000817 -13
17. A method according to any one of the preceding claims, wherein a percolation rate of between about 2,000 and 45,000 L/m 2 /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.
AU2007260577A 2006-06-12 2007-06-12 Method for agglomeration Ceased AU2007260577B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2007260577A AU2007260577B2 (en) 2006-06-12 2007-06-12 Method for agglomeration

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
AU2006903158A AU2006903158A0 (en) 2006-06-12 Method for Agglomeration
AU2006903158 2006-06-12
AU2007260577A AU2007260577B2 (en) 2006-06-12 2007-06-12 Method for agglomeration
PCT/AU2007/000817 WO2007143779A1 (en) 2006-06-12 2007-06-12 Method for agglomeration

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AU2007260577A1 AU2007260577A1 (en) 2007-12-21
AU2007260577B2 true AU2007260577B2 (en) 2010-10-28

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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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Publication number Priority date Publication date Assignee Title
US20120174713A1 (en) 2009-02-02 2012-07-12 Nelson Mora Method of Agglomeration

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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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EP2035589A1 (en) 2009-03-18
EP2035589A4 (en) 2012-01-18
AU2007260577A1 (en) 2007-12-21
CA2649969A1 (en) 2007-12-21
BRPI0711527A2 (en) 2011-11-01
EP2035589B1 (en) 2013-02-13
WO2007143779A1 (en) 2007-12-21

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