AU561986B2 - Mineral separation - Google Patents

Mineral separation

Info

Publication number
AU561986B2
AU561986B2 AU28290/84A AU2829084A AU561986B2 AU 561986 B2 AU561986 B2 AU 561986B2 AU 28290/84 A AU28290/84 A AU 28290/84A AU 2829084 A AU2829084 A AU 2829084A AU 561986 B2 AU561986 B2 AU 561986B2
Authority
AU
Australia
Prior art keywords
agglomerates
solids
mineral
carbon source
hydrocarbon liquid
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.)
Expired
Application number
AU28290/84A
Other versions
AU2829084A (en
Inventor
Mark David Cadzow
Graham John Elkes
David E. Mainwaring
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BP PLC
Original Assignee
BP Australia Pty Ltd
BP PLC
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 BP Australia Pty Ltd, BP PLC filed Critical BP Australia Pty Ltd
Priority to AU28290/84A priority Critical patent/AU561986B2/en
Publication of AU2829084A publication Critical patent/AU2829084A/en
Application granted granted Critical
Publication of AU561986B2 publication Critical patent/AU561986B2/en
Anticipated expiration legal-status Critical
Expired legal-status Critical Current

Links

Description

AGGLOMERATES
This invention relates to separation of mineral material from ore bodies particularly where the mineral is present in low concentrations.
Proposals have been made to separate minerals by utilizing the lyophilic properties of certain minerals. U.S. patent 3,268,071 uses a liquid suspendant to separate two materials one of which is lyophilic to said liquid and the other being lyophobic. This technique, however, is difficult to initiate where the mineral which is sought to be recovered is present in low concentrations.
U.K. patent 161560 (1921) discloses an oil agglomeration of solids with a coal carrier. This specification is specific¬ ally concerned with concentration of iron fines in steel mills. There is no suggestion of how this technique can be adapted to recover minerals present in ore bodies in low concentrat¬ ions.
In Australian patents 450,549 and 475,788 the use of coal char has been proposed for mineral separation but these patents rely on the adsorbent properties of the coal char to adsorb ions from solution in contrast to the present invention which is concerned with minerals in solid mixtures.
It is an object of the present invention to improve the recovery of minerals present in low concentrations.
To this end the present invention provides a method of ' recovering a mineral having a lyophilic surface present in low concentration in a mixture of solids comprising grinding the mixture of solids forming a slurry of said solids either before or after said grinding step, adding thereto in a con¬ tacting zone a carbon source material and hydrocarbon liquid, mixing said slurry of solids, carbon source and hydrocarbon liquid in an agglomeration zone to form agglomerates contain¬ ing said lyophilic mineral carbon source material and hydro¬ carbon liquid, separating said agglomerates from the remaining slurry of solids and subsequently recycling said agglomerates to said contacting zone, the size of agglomerates in said con¬ tacting zone being below 500 microns and repeating the process until the concentration of lyophillic mineral in the separated
-" RE_ OMPI
^fa agglomerates has reached a desired level and then recovering, said mineral from said agglomerates.
Preferably the carbon source material is coal and the hydrocarbon liquid is an oil selected from kerosine, light gas oil or fuel oils. In most cases it is necessary to pre- treat the ores to condition them so that the surfaces of the minerals present are rendered either lyophilic or lyophobic. The minerals to which the present invention is partic¬ ularly applicable are gold present in its native form, copper present as chalcopyrite and other metallic, metallic sulphide or metallic oxide minerals present in low concentrations. Gold usually requires no pretreatment as its surface is lyo¬ philic. The other minerals normally require the addition of reagents to make their surfaces lyophillic. An important aspect of this invention is to increase the likelihood of contact between the coal/oil mix and the desired solid. By recycling agglomerates to the contacting zone it is possible to increase the concentration of the desired solid in the coal agglomerates. The number of recycling steps is not critical but depends on the desired level of mineral value recovery. However this is increased if the size of the agglom¬ erates after disintegration is below 500 microns as this increases the available surface contact and the likelihood of contact occurring is increased. In this invention the carbon source material, hydrocarbon liquid and ground solids are intimately mixed to increase surface contact in the contacting zone by using as the contact¬ ing zone a disintegration device selected from a rodmill, a shear scrubber, a pump/pipe loop or an in line mixer or other similar device. Further oil may be added in the agglomeration tank where the mixture is agitated. Residence time in the agglomeration zone may vary from 5 to 300 minutes and will depend in part on the desired size of the final agglomerates. A typical plant layout used according to this invention is shown in the drawing. The ore is crushed by any convent¬ ional grinding method in the crusher 1. At this point the ore is usually a slurry. A carbon source and some oil is then
OMPI added to the ore at point 2. This invention may be operated as a batch operation or continuously if the scale of operation makes a continuous operation feasible.
This mixture is then passed to a high shear scrubber 3 which is the selected contacting device for further condition¬ ing of the ore. It is in the scrubber 3 that disintegrated micro-agglomerates of oil and coal are formed and it is this conditioning which creates the maximum opportunity for contact between the lyophilic ore and the coal/oil agglomerates. After the scrubber 3 the mix is passed to the agglomer- ator 4 which is a stirred tank in which agitation of the mix occurs which encourages agglomerate growth. After the agglom¬ eration step the mix is passed to the separator 5. This may comprise a simple screen to separate out agglomerates from the slurry. Alternatively vacuum filtration or similar separ¬ ation means may be used. This process is operated with con¬ tinuous removal of gangue and may be operated with either con¬ tinuous or batch removal of agglomerates.
From the separator 5 the agglomerates are recycled through line 6 to the scrubber 3. Ho ogenizer 7 may be used to reduce the size of the recycled agglomerates before they enter the contacting zone. Batch or continuous removal of agglomerates containing mineral values can be made through line 9. Also from the separator 5 the gangue or remaining slurry is removed by line 8 to the tailings dispersal dam and water recovery plant 9. After the agglomerates have been recycled sufficiently to achieve' the desired mineral value level the mineral values may be separated from the agglomer¬ ates by pyro metallurgical techniques wherein the oil and coal are burnt away. However, other conventional separation tech¬ niques may be used.
An embodiment of this invention will now be described in relation to the recovery of gold and copper present as chal- copyrite. The ore is crushed and a carbon source (usually coal) and agglomerating oil are added. Any of the known oil agglomeration techniques can be adapted for use in this invent¬ ion. The spherical agglomerates formed by mixing can be
_ OMPI screened from the reject mineral matter. The majority of agglomerates are recycled to be further enriched. A small product offtake of agglomerates is taken at high mineral load¬ ing when operating in a continuous mode. The loss of carbon and oil in the product is made up by a small continuous addit¬ ion to the spherical agglomeration plant.
Example 1 - Gold
A representative sample of Wongawilli seam coal was ground so that 90% was less than 100 microns. The pulp was split into three equal parts and alluvial gold (-106 microns) was added to each sample. Agglomeration was then carried out as indicated above using Kerosine, light gas oil and fuel oil. A gold assay was carried out on the ashed agglomerates and reject mineral matter with the following results:
TABLE 1
Gold Recovery
Sample Oil Type Wt Gold Wt Gold Recovery Agglo Assay Mineral Assay % Ash(g) (g/t) Matter (g/t)
(g)
GOL 1.1 Kerosine 13.65 2960 13.04 12.2 99.51 GOL 1.2 LGO 12.45 2700 15.00 0.5 99.98 GOL 1.3 Fuel Oil 14.69 2220 12.10 32.4 98.80
These results show essentially complete recovery of gold into the agglomerates when using light gas oil for agglomer¬ ation.
Example 2 - Gold
Samples of a gold ore with grades between 120 and 0.5 g of gold tonne were treated with the process. Coal and light gas oil were used as the carbon carrier and the hydrocarbon oil respectively. Thirty minutes residence time in a rodmill was used to reduce the size of the recycled agglomerates and to promote contacting between the micro-agglomerates and the gold. A stirred tank was used as the agglomerating zone and a
OMH 30 minute residence time for agglomeration was allowed. The. agglomerates were recycled four times.
The results in the following Table show that after four recycles high recoveries of gold were achieved.
Grade of Ore Recovery of gold g of gold/tonne % by mass
120.5 97.2
23.3 98.6
5.2 93.5 2.5 88.0
0.6 60.0
Example 3 - .Gold
The system described in Example 2 was used to treat a sample of gold ore in which the agglomerates were recycled 20 times. The overall recovery of gold was 97.27. and the grade of the agglomerates at the end of the experiment was 1300 g of gold/tonne.
Example 4 - Copper (Chalcopyrite)
Experiments were carried out to form coal/chalcopyrite agglomerates and to use the agglomerates as recycle feed for a second agglomeration thus:
The agglomeration was carried out using the following proportions of chalcopyhrite/coal/quartz
Chalcopyrite 4.7% of solids
Quartz (as diluant) 75.3% of solids
Aerophine was used as a chalcopyrite promoter; pulp density for agglomeration was 107o.
Results of the agglomeration carried out are given in Table 2. TABLE 2
Chalcopyrite-Collection
Note: CHL 1.1 - Agglomeration with 25% light gas oil
CHL 1.2 - Agglomeration with 25% light gas oil, then agglomerates added to a standard charge except for coal and re-agglomerated with additional 5% light gas oil. The results show that high recoveries of copper into the agglomerates can be achieved and that the agglomerates can be recycled to collect further copper, again with high efficiency.
The main advantages seen for the technique are: (i) Agglomeration has the ability to give very high rec¬ overies of required minerals. The process operates in a way which is independent of feed particle size in the range of interest (less than 500 microns). In this respect, agglomeration is superior to other methods of collection, such as flotation, where particle size is a significant factor in collection efficiency. The invention allows these benefits of agglomeration to be obtained on low grade materials by successive load¬ ing and applies particularly to gold where concentrat¬ ions are less than 100 ppm. (ii) The coal/carbon used in the agglomeration can be used in some instances in further processing steps required (e.g. roasting a sulphide ore), (iii) Concentration by agglomeration could be carried out at a mine site and, because of the ease of handling of the spherical agglomerates, these could then be trans¬ ported to a centralised refining plant.
-fJRE
O PI

Claims (4)

THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS:
1. A method of recovering a mineral having a lyophilic surface present in low concentration in a mixture of solids comprising grinding the mixture of solids forming a slurry of said solids either before or after said grinding step, adding thereto in a contacting zone a carbon source material and a hydrocarbon liquid, mixing said slurry of solids, carbon source and hydrocarbon liquid in an agglomeration zone to form agglomerates containing said lyophilic mineral carbon source material and hydrocarbon liquid, separating said agglomerates from the remaining slurry of solids and subsequently recycling said agglomerates to said contacting zone,.the size of agglom¬ erates in said contacting zone being below 500 microns and repeating the process until the concentration of lyophilic mineral in the separated agglomerates has reached a desired level and then recovering said mineral from said agglomerates.
2. A method as claimed in claim 1 in which the carbon source material, hydrocarbon liquid and ground solids are intimately mixed to increase surface contact in the contacting zone by using as the contacting zone a disintegration device selected from a rodmill, a shear scrubber, a pump/pipe loop or an in-line mixer.
3. A method as claimed in claim 1 or 2 wherein further hydrocarbon liquid is added in the agglomeration zone.
4. A method as claimed in claim 1 wherein the carbon source material is coal.
ϊ
OMPI fay
AU28290/84A 1983-04-29 1984-04-26 Mineral separation Expired AU561986B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU28290/84A AU561986B2 (en) 1983-04-29 1984-04-26 Mineral separation

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AUPF912083 1983-04-29
AUPF9120 1983-04-29
AU28290/84A AU561986B2 (en) 1983-04-29 1984-04-26 Mineral separation

Publications (2)

Publication Number Publication Date
AU2829084A AU2829084A (en) 1984-11-19
AU561986B2 true AU561986B2 (en) 1987-05-21

Family

ID=25620626

Family Applications (1)

Application Number Title Priority Date Filing Date
AU28290/84A Expired AU561986B2 (en) 1983-04-29 1984-04-26 Mineral separation

Country Status (1)

Country Link
AU (1) AU561986B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU589291B2 (en) * 1986-08-21 1989-10-05 Charlton Mineral Associates Pty. Ltd. Mineral recovery process
AU593121B2 (en) * 1986-07-09 1990-02-01 British Petroleum Company Plc, The Separation process
AU600606B2 (en) * 1987-11-11 1990-08-16 Carbad Pty. Ltd. Recovery of lyophyllic mineral particles

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU593121B2 (en) * 1986-07-09 1990-02-01 British Petroleum Company Plc, The Separation process
AU589291B2 (en) * 1986-08-21 1989-10-05 Charlton Mineral Associates Pty. Ltd. Mineral recovery process
AU600606B2 (en) * 1987-11-11 1990-08-16 Carbad Pty. Ltd. Recovery of lyophyllic mineral particles

Also Published As

Publication number Publication date
AU2829084A (en) 1984-11-19

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