WO2015083069A1

WO2015083069A1 - Process for dewatering mineral tailings by the treatment of these tailings with a solution comprising at least one polymer and at least one salt

Info

Publication number: WO2015083069A1
Application number: PCT/IB2014/066507
Authority: WO
Inventors: Stephen Adkins
Original assignee: Basf Se; Basf (China) Company Limited
Priority date: 2013-12-03
Filing date: 2014-12-02
Publication date: 2015-06-11
Also published as: CA2930003A1

Abstract

The present invention relates to a process of dewatering a suspension comprising particulate solids dispersed in an aqueous liquid, said particulate solids comprises clay and mineral parti- cles of size below 50 µm, which process comprises the steps of, (a) Addition of at least one polymer and of at least one salt solution to the suspension; and (b) Dewatering the polymer treated suspension of step (a).

Description

Process for dewatering Mineral Tailings by the treatment of these tailings with a solution comprising at least one polymer and at least one salt

Description

The present invention relates to the treatment of mineral material, especially waste mineral slurries. The invention is particularly suitable for the disposal of tailings and other waste material resulting from mining and mineral processing operations. The invention is particularly suitable for the treatment of oil sand tailings and especially mature fine tailings (MFT) derived from oil sand tailings.

Processes of treating mineral ores or oil sands in order to extract mineral values or in the case of oil sands to extract hydrocarbons will normally result in waste material. Often the waste material consists of an aqueous slurry or sludge comprising particulate mineral material, for instance clay, shale, sand, grit, oil sand tailings, metal oxides etc. admixed with water.

In some cases the waste material such as mine tailings can be conveniently disposed of in an underground mine to form backfill. Generally backfill waste comprises a high proportion of coarse large sized particles together with other smaller sized particles and is pumped into the mine as slurry where it is allowed to dewater leaving the sedimented solids in place. It is common practice to use flocculants to assist this process by flocculating the fine material to increase the rate of sedimentation. However, in this instance, the coarse material will normally sediment at a faster rate than the flocculated fines, resulting in a heterogeneous deposit of coarse and fine solids.

For other applications it may not be possible to dispose of the waste in a mine. In these instances, it is common practice to dispose of this material by pumping the aqueous slurry to lagoons, heaps or stacks and allowing it to dewater gradually through the actions of sedimentation, drainage and evaporation.

For example in oil sands processing, the ore is processed to recover the hydrocarbon fraction, and the remainder, including both process material and the gangue, constitutes the tailings that are to be disposed of. In oil sands processing, the main process material is water, and the gangue is mostly sand with some silt and clay. Physically, the tailings consist of a solid part (sand tailings) and a more or less fluid part (sludge). The most satisfactory place to dispose of these tailings is, of course, in the existing excavated hole in the ground. It turns out, however, that the sand tailings alone from the one cubic foot of ore occupy just about one cubic foot. The amount of sludge is variable, depending on ore quality and process conditions, but average about 0.3 cubic feet. The tailings simply will not fit back into the hole in the ground.

There is a great deal of environmental pressure to minimise the allocation of new land for disposal purposes and to more effectively use the existing waste areas. One method is to load multiple layers of waste onto an area to thus form higher stacks of waste. However, this pre- sents a difficulty of ensuring that the waste material can only flow over the surface of previously rigidified waste within acceptable boundaries, is allowed to rigidify to form a stack, and that the waste is sufficiently consolidated to support multiple layers of rigidified material, without the risk of collapse or slip. Thus the requirements for providing a waste material with the right sort of characteristics for stacking is altogether different from those required for other forms of disposal, such as back-filling within a relatively enclosed area.

In a typical mineral or oil sands processing operation, waste solids are separated from solids that contain mineral values in an aqueous process. The aqueous suspension of waste solids often contains clays and other minerals, and is usually referred to as tailings. These solids are often concentrated by a flocculation process in a thickener to give a higher density underflow and to recover some of the process water. It is usual to pump the underflow to a surface holding area, often referred to as a tailings pit or dam or more usually a tailings pond in the case of oil sands. Once deposited at this surface holding area, water will continue to be released from the aqueous suspension resulting in further concentration of the solids over a period of time. Once a sufficient volume of water has been collected this is usually pumped back to the mineral or oil sands processing plant.

The tailings pond or dam is often of limited size in order to minimise the impact on the environ- ment. In addition, providing larger tailings ponds can be expensive due to the high costs of earth moving and the building of containment walls. These ponds tend to have a gently sloping bottom which allows any water released from the solids to collect in one area and which can then be pumped back to the plant. A problem that frequently occurs is when fine particles of solids are carried away with the run-off water, thus contaminating the water and having a detrimental impact on subsequent uses of the water.

In many mineral and oil sands processing operations, for instance a mineral sands beneficiation process, it is also common to produce a second waste stream comprising of mainly coarse (> 0.1 mm) mineral particles. It is particularly desirable to dispose of the coarse and fine waste particles as a homogeneous mixture as this improves both the mechanical properties of the de- watered solids, greatly reducing the time and the cost eventually required to rehabilitate the land. However, this is not usually possible because even if the coarse waste material is thoroughly mixed into the aqueous suspension of fine waste material prior to deposition in the disposal area, the coarse material will settle much faster than the fine material resulting in banding within the dewatered solids. Furthermore, when the quantity of coarse material to fine material is relatively high, the rapid sedimentation of the coarse material may produce excessive beach angles which promote the run off of aqueous waste containing high proportions of fine particles, further contaminating the recovered water. As a result, it is often necessary to treat the coarse and fine waste streams separately, and recombine these materials by mechanically re-working, once the dewatering process is complete.

Generally oil sands tailings ponds are located within close proximity of the oil sands mining and extraction operations in order to facilitate pipeline transportation, discharging and management of the tailings. A tailings pond may be contained within a retaining structure which may be referred to as a dyke structure. A suitable dyke structure may generally be constructed by placing the sand fraction of the tailings within cells or on beaches. Tailings streams initially discharged into the ponds may have relatively low densities and solids contents, for instance around 0.5 to 10% by weight.

In an oil sands tailings pond, the process water, unrecovered hydrocarbons and minerals settle naturally to form different strata. The upper stratum can be predominantly water that maybe recycled as process water to the extraction process. The lower stratum can contain settled re- sidual hydrocarbon and minerals which are predominantly fines. It is usual to refer to this lower stratum as "mature fine tailings" (MFT). It is known that mature fine tailings consolidate extremely slowly and may take many hundreds of years to settle into a consolidated solid mass. Consequently mature fine tailings and the ponds containing them are a major challenge to tailings management and the mining industry.

The composition of mature fine tailings tends to be highly variable. The upper part of the stratum may have a mineral content of about 10% by weight but at the bottom of the stratum the mineral content may be as high as 50% by weight. The variation in the solids content is believed to be as a result of the slow settling of the solids and consolidation occurring over time. The average mineral content of the M FT tends to be of about 30% by weight.

The MFT generally comprises a mixture of sand, fines and clay. Generally the sand may referred to siliceous particles of a size greater than 44 μιτι and may be present in the MFT in an amount of up to 15% by weight. The remainder of the mineral content of the MFT tends to be made up of a mixture of clay and fines. Generally the fines refer to mineral particles no greater than 44 μιτι. The clay may be any material traditionally referred to as clays by virtue of its mineralogy and will generally have a particle size of below 2 μιτι. Typically the clays tend to be water swelling clays, such as montmorillonites. The clay content may be up to 75% by weight of the solids.

Additional variations in the composition of M FT maybe as a result of the residual hydrocarbon which may be dispersed in the mineral or may segregate into mat layers of hydrocarbon. The MFT in a pond not only has a wide variation of compositions distributed from top to bottom of the pond but there may also be pockets of different compositions at random locations through- out the pond.

In addition, aqueous suspensions waste solids from mining and mineral processing operations including mining tailings, such as MFT, held in ponds of holding areas may also contain coarse debris. The type and composition of this coarse debris depends on the origin of the suspension. In the case of MFT the coarse debris tends to be of different sizes, shapes and chemical compositions. For instance, MFT may include coarse debris such as biomass, such as wood or other plant material; petrified matter; solids having a density low enough to float at or near the surface of the pond; glass; plastic; metal; bitumen globules; or mats. The coarse debris found other mining tailings may include similar debris as in the case of MFT, with the exception of bitumen materials and may also include other debris materials such as lumps of ore or other masses depending on the geology of the ore mine, the ore extraction processing technique, or the location of the tailings pond.

It is known that aqueous suspensions and mining tailings, such as MFT, may be dewatered and solidified through the action of chemical treatments. A typical chemical treatment employs the addition of chemical flocculating agents to bring about flocculation and be so formed flocculated suspensions can be subjected to dewatering.

It is well known to concentrate these oil sand tailings in a thickener to give a higher density underflow and to recover some of the process water as mentioned above.

For example, Xu.Y et al, Mining Engineering, November 2003, pages 33 to 39 describe the ad- dition of anionic flocculants to the oil sand tailings in the thickener before disposal.

The underflow can be disposed of and/or subjected to further drying for subsequent disposal in an oil sand tailings stacking area. In the Bayer process for recovery of alumina from bauxite, the bauxite is digested in an aqueous alkaline liquor to form sodium aluminate which is separated from the insoluble residue. This residue consists of both sand, and fine particles of mainly ferric oxide. The aqueous suspension of the latter is known as red mud. After the primary separation of the sodium aluminate solution from the insoluble residue, the sand (coarse waste) is separated from the red mud. The supernatant liquor is further processed to recover aluminate. The red mud is then washed in a plurality of sequential washing stages, in which the red mud is contacted by a wash liquor and is then flocculated by addition of a flocculating agent. After the final wash stage the red mud slurry is thickened as much as possible and then disposed of. Thickening in the context of this specification means that the solids content of the red mud is increased. The final thickening stage may comprise settlement of flocculated slurry only, or sometimes, includes a filtration step. Alternatively or additionally, the mud may be subjected to prolonged settlement in a lagoon. In any case, this final thickening stage is limited by the requirement to pump the thickened aqueous suspension to the disposal area.

The mud can be disposed of and/or subjected to further drying for subsequent disposal on a mud stacking area. To be suitable for mud stacking the mud should have a high solids content and, when stacked, should not flow but should be relatively rigid in order that the stacking angle should be as high as possible so that the stack takes up as little area as possible for a given volume. The requirement for high solids content conflicts with the requirement for the material to remain pumpable as a fluid, so that even though it may be possible to produce a mud having the desired high solids content for stacking, this may render the mud unpumpable. The sand fraction removed from the residue is also washed and transferred to the disposal area for separate dewatering and disposal.

EP-A-388108 describes adding a water-absorbent, water-insoluble polymer to a material com- prising an aqueous liquid with dispersed particulate solids, such as red mud, prior to pumping and then pumping the material, allowing the material to stand and then allowing it to rigidify and become a stackable solid. The polymer absorbs the aqueous liquid of the slurry which aids the binding of the particulate solids and thus solidification of the material. However this process has the disadvantage that it requires high doses of absorbent polymer in order to achieve adequate solidification. In order to achieve a sufficiently rigidified material it is often necessary to use doses as high as 10 to 20 kilograms per tonne of mud. Although the use of water swellable absorbent polymer to rigidify the material may appear to give an apparent increase in solids, the aqueous liquid is in fact held within the absorbent polymer. This presents the disadvantage that as the aqueous liquid has not actually been removed from the rigidified material and under cer- tain conditions the aqueous liquid could be desorbed subsequently and this could risk re- fluidisation of the waste material, with the inevitable risk of destabilising the stack.

WO-A-96/05146 describes a process of stacking aqueous slurry of particulate solids which comprises admixing an emulsion of a water-soluble polymer dispersed in a continuous oil phase with the slurry. Preference is given to diluting the emulsion polymer with a diluent, and which is preferably in a hydrocarbon liquid or gas and which will not invert the emulsion. Therefore it is a requirement of the process that the polymer is not added in to the slurry as an aqueous solution.

WO-A-0192167 describes a process where a material comprising a suspension of particulate solids is pumped as a fluid and then allowed to stand and rigidify. The rigidification is achieved by introducing into the suspension particles of a water soluble polymer which has an intrinsic viscosity of at least 3 dl/g. This treatment enables the material to retain its fluidity as being pumped, but upon standing causes the material to rigidify. This process has the benefit that the concentrated solids can be easily stacked, which minimises the area of land required for disposal. The process also has the advantage over the use of cross linked water absorbent polymers in that water from the suspension is released rather than being absorbed and retained by the polymer. The importance of using particles of water soluble polymer is emphasised and it is stated that the use of aqueous solutions of the dissolved polymer would be ineffective. Very efficient release of water and convenient storage of the waste solids is achieved by this process, especially when applied to a red mud underflow from the Bayer alumina process.

WO2004/060819 describes a process in which material comprising an aqueous liquid with dispersed particulate solids is transferred as a fluid to a deposition area, then allowed to stand and rigidify, and in which rigidification is improved whilst retaining the fluidity of the material during transfer, by combining with the material an effective rigidifying amount of an aqueous solution of a water-soluble polymer. Also described is a process in which dewatering of the particulate solids is achieved. Canadian patent application 2512324 describes a process for the rigidification of a suspension which is or comprises oil sand tailings. The process involves transferring the suspension as a fluid to a deposition area in which an effective rigidifying amount of an aqueous solution of a water-soluble polymer is combined with the suspension during transfer and then allowing the so treated suspension to stand and rigidify. The rigidification is improved whilst retaining the fluidity of the material during transfer. The process was particularly suited to the treatment of tailings as they are produced from the oil sands processing operation.

WO 01/05712 A1 discloses a process for treating an aqueous suspension of suspended solids by adding a concentrated polymer solution and a dilute polymer solution. This process is conducted to treat mineral tailings in general, tailings comprising very small particles like oil sand tailings, especially M FT, are not mentioned.

However, suspensions which contain a very high proportion of fine solids and clays, such as MFT, are particularly difficult to dewater and generally require very high doses of chemical treatment aids.

It is further known in the art that polymers that are used in processes for dewatering of mineral comprising slurries shall desirably have a high molecular weight, because generally the higher the molecular weight of these polymers is, the better the dewatering effect is. A problem that arises with the use of high molecular weight polymers is that the viscosity of solutions comprising these high molecular weight polymers is high, handling and effective mixing of these solutions with the mineral slurry is compromised. Therefore it is an objective of the present invention to achieve a more efficient process for de- watering a suspension containing high levels of fine solids and clays, especially MFT derived from oil sand tailings. In particular it would be desirable if such a process required reduced total amounts of chemical treatment aids. Moreover, it would be desirable for the process of removing water or dewatering process is a rigidification process. Further, a process for dewatering a solid containing suspension is desired in which the suspension is treated in a way that its viscosity is decreased to improve the removal of water and facilitate transportation. A further object of the process according to the present invention is to provide a process for dewatering a suspension comprising minerals wherein polymers are used that have high molecular weights, preferably without the drawback of handling solutions having high viscosity and/or applying high energy to the suspension to be treated.

According to the present invention we provide a process of dewatering a suspension comprising particulate solids dispersed in an aqueous liquid, said particulate solids comprises clay and mineral particles of size below 50 μιτι, which process comprises the steps of,

(a) Addition of a solution comprising at least one polymer and at least one salt to the suspension; and (b) Dewatering the polymer treated suspension of step (a).

The process brings about significant improvements in removing water from the suspension using lower levels of treatment chemicals than previously possible and improved rigidification

By mineral particles of particle size below 50 μιτι, we mean solid mineral particles that are not water swelling clays that may generally be referred to as fines. Often these mineral particles may be referred to as silt. Usually these mineral particles have a size of no greater than 44 μιτι. Typically they will have a size between 2 μιτι and 44 μιτι, although their size may be smaller. The mineral origin of the particles often will be silica and/or quartz and/or feldspar.

The mineral particles may typically be present in the suspension in an amount of at least 10% by weight of the mineral content. Often the particles may be present in amount of at least 15% by weight, more often of at least 20% by weight of the solids content. In some cases the solids content of the suspension may be made up of 50 or 60% by weight.

The clay may be any material traditionally referred to as clays by virtue of its mineralogy and will tend to have a particle size of below 2 μιτι. Generally the clays may tend to be a mixture of clays. Typically the clay component may comprise kaolinite; illite; chlorite; montmorillonites; kao- linite-smectite mixtures; illite-smectite mixtures. The clay content of the suspension would usually be at least 20% by weight of the solids and may be up to 75% by weight of the solids.

Without being limited by theory the inventors believe that suspensions which contain a high proportion of very small sized mineral particles and clay particles, especially where they have been held in tailings ponds over a considerable time, even many years, such as oil sands derived MFT, exhibit three-dimensional particle network structure based on the clays. These network structures are believed to include clay-clay intra-particle networks and clay-inter-particle network structures which incorporate the fine mineral particles. The inventors believe that these network structures comprise clay particles linked to each other and network structures where clay particles and the fine particles are linked together by clay particles. Further, it is believed that this network structure is responsible for retaining more water than in suspensions of equivalent solids. Furthermore, it is considered that the electrostatic forces within the clay inter-particle structure may be responsible for the difficulty in achieving adequate water release with conventional doses of chemical treatment aids.

Unexpectedly, the inventors discovered that applying a solution comprising at least one polymer and at least one salt provides a polymer treated suspension which is significantly more conducive to releasing water by chemical treatment. The inventors believe that the use of a polymer solution that further comprises at least one salt lowers the viscosity of this solution and the con- tacting of the mineral particles and the at least one polymer is improved. Without being bound to any theory the inventors believe that in the presence of at least one salt the polymer is present in a so called coiled form, whereas, after addition of the solution comprising the at least one polymer and the at least one salt, the polymers uncoils again and binds to the mineral particles, due to the decreased concentration of the at least one salt in the mixture of solution of the at least one polymer and the at least one salt and the aqueous slurry comprising minerals. The uncoiling process takes some time, for example some seconds to minutes or even hours, depending on the concentration and amount of polymer and salt that are used. Therefore, the mix- ing of mineral particles and coiled polymers can be done efficiently before the polymers uncoil again and bind to the mineral particles.

Preferably, the suspension comprises mature fine tailings derived from oil sands tailings. The process of the present invention involves addition of a solution comprising at least one polymer and at least one salt.

The addition of a solution comprising at least one polymer and at least one salt facilitates the removal of water in the dewatering step.

The dewatering of the polymer treated suspension according to step (b) may employ any known dewatering method. For instance the dewatering step may involve sedimentation of the polymer treated suspension to produce settled sediment. Such a process may be carried out in a vessel for example a gravimetric thickener or in a settlement pond. Alternatively the dewatering pro- cess may involve pressure dewatering, for example using a filter press, a belt press or a centrifuge.

Preferably the dewatering process is a process of rigidification of the solids in the suspension and the dewatering step is part of the rigidification process. Thus in a preferred form of the in- vention the polymer treated suspension is transferred as a fluid to a deposition area, then allowed to stand and rigidifying, in which the solution comprising at least one polymer and at least one salt is added to the suspension during the transfer of the suspension.

Rigidification is a term that refers to a networked structure of particulate solids. Compared with settling or sedimentation, rigidification is faster, produces more recovered water and results in a chemically bonded tailings that occupy a smaller surface area, which is more quickly

rehabilitated. Rigidified tailings are also less likely to spread laterally after deposition enabling more efficient land use; and would more rapidly form a solid structure in the form of a beach or stack; and have a greater yield stress when deposited, with increased uniformity or homogenity of coarse and fine particles. Further by reason of its heaped geometry as a beach or stack such rigidified material would result in downward compression forces, driving water out of the stack and more rapid release of water, with better clarity.

Preferably, the solution comprising at least one polymer and at least one salt is added to the suspension in the form of an aqueous solution.

The addition of the solution comprising at least one polymer and at least salt, preferably as aqueous solution, allows the suspension to retain sufficient fluidity during transfer and then once the material is allowed to stand it will form a solid mass strong enough to support subsequent layers of rigidified material. We have unexpectedly found that the addition of a solution comprising the at least one polymer and at least one salt, preferably as aqueous solution, to the suspension does not cause instant rigidification or substantially any settling of the solids prior to standing. A possible explanation of the effect, without being bound to any theory, can be found above.

The solution comprising at least one polymer and at least one salt may be metered directly into the suspension comprising minerals.

According to a preferred embodiment of the present invention the solution that is added is provided by addition of the at least one polymer to a solution, preferably an aqueous solution, of the at least one salt. The present invention therefore preferably relates to the process according to the present invention in which the solution that is added is provided by addition of the at least one polymer to a solution, preferably an aqueous solution, of the at least one salt.

The, preferably aqueous, solution comprising at least one polymer and at least one salt prefera- bly comprises the at least one polymer in an amount of from 0.05 to 99% by weight, more preferably 0.1 to 10% by weight, most preferably 0.5 to 2.0 % by weight, in each case based on the, preferably aqueous, solution.

The, preferably aqueous, solution comprising at least one polymer and at least one salt com- prises at least one salt preferably in an amount of from 0.01 to 99% by weight, more preferably 0.1 to 30% by weight, most preferably 1 to 10% by weight or more than 10% by weight to 15% by weight, i. e. 1 to 15% by weight, in each case based on the, preferably aqueous, solution.

A, preferably aqueous, solution comprising at least one polymer and the at least one salt com- prises at least one polymer in an amount of 0.05 to 99% by weight, more preferably 0.1 to 10% by weight, most preferably 5 to 2.0% by weight, and at least one salt in an amount of 0.01 to 99% by weight, more preferably 0.1 to 30% by weight, most preferably 1 .0 to 10% by weight or more than 10% by weight to 15% by weight, i. e. 1 to 15% by weight, in each case in respect of the, preferably aqueous, solution.

According to the present invention, the sum of all components present in the mixtures, for example the at least one polymer, the at least one salt and solvent, preferably water, add up to 100% by weight. Suitable doses of polymer range from 10 grams to 10,000 grams per tonne of material solids. Generally the appropriate dose can vary according to the particular material and material solids content. Preferred doses are in the range 30 to 3,000 grams per tonne, while more preferred doses are in the range of from 60 to 2,700 grams per tonne, in each case in respect of the sum of all polymers and in different solutions. In some instances better results may be obtained when the suspension, particular the oil sands derived MFT, is relatively concentrated and homogenous. It may also be desirable to combine the addition of at least one polymer and at least one salt solution with other additives. For in- stance the flow properties of the material through a conduit may be facilitated by including a dispersant. Typically where a dispersant is included it would be included in conventional amounts. However, we have found that surprisingly the presence of dispersants or other additives does not impair the rigidification of the material on standing. It may also be desirable to pre-treat the material with either an inorganic or organic coagulant to pre-coagulate the fine ma- terial to aid its retention in the rigidified solids.

Thus in the present invention the solution comprising at least one polymer and at least one salt , preferably an aqueous solution, is added directly to the aforementioned suspension. The solution may comprise only or partially water-soluble polymers. Thus the solution may comprise a blend of cross-linked polymer and water soluble polymer, provided sufficient of the polymer is in solution or behaves as though it is in solution to bring about rigidification on standing.

According to the present invention the solution that is added in step (a) comprises at least one polymer for example one, two, three, four etc. polymers, more preferably one polymer. Accord- ing to the present invention the solution that is added in step (a) comprises at least one salt, for example one, two, three, four etc., more preferably one salt. The at least one polymer according to the present invention, may comprise a physical blend of swellable polymer and soluble polymer or alternatively a lightly cross-linked polymer for instance as described in EP202780. Although the at least one polymer may comprise some cross-linked polymer it is preferred to the present invention that a significant amount of water soluble polymer is present. When the at least one polymer comprises some swellable polymer it is desirable that at least 80% of the polymer is water-soluble.

Preferably the at least one polymer is wholly or at least substantially water soluble. The water soluble polymer may be branched by the presence of branching agent, for instance as described in WO-A-9829604, for instance in claim 12, or alternatively the water soluble polymer is Preferably the at least one polymer is of moderate to high molecular weight.

The at least one polymer preferably has an intrinsic viscosity of at least 3 dl/g, more preferably at least 5 dl/g, most preferably at least 6 dl/g. The at least one polymer has an intrinsic viscosity of up to 25 dl/g or 35 dl/g or even higher. Preferably the polymer will have an intrinsic viscosity in the range of 6 dl/g to 28dl/g, more preferably 1 1 dl/g or 12 dl/g to 18 dl/g or 26dl/g.

Intrinsic viscosity of polymers may be determined by preparing an aqueous solution of the pol- ymer (0.5 to 1 % w/w) based on the active content of the polymer. 2 g of this 0.5 to 1 % w/w polymer solution is diluted to 100 ml in a volumetric flask with 50 ml of 2M sodium chloride solution that is buffered to pH 7.0 (using 1 .56 g sodium dihydrogen phosphate and 32.26 g disodium hydrogen phosphate per litre of deionised water) and the whole is diluted to the 100 ml mark with deionised water. The intrinsic viscosity of the polymers is measured using a Number 1 suspended level viscometer at 25 ^°C in 1 M buffered salt solution.

The at least one polymer may be a natural polymer, for instance polysaccharides such as starch, guar gum or dextran, or a semi-natural polymer such as carboxymethyl cellulose or hy- droxyethyl cellulose. Preferably the at least one polymer is synthetic and preferably it is formed from an ethylenically unsaturated water-soluble monomer or blend of monomers.

The at least one polymer may be cationic, non-ionic, amphoteric, or anionic, preferably anionic or non-ionic, particularly preferably anionic.

Therefore, the present invention preferably relates to the process according to the present invention, whereinthe at least one polymer is anionic, cationic or non-ionic, preferably anionic or non-ionic, particularly preferably anionic.

The at least one polymer may be formed from any suitable water-soluble monomers. Typically the water soluble monomers have solubility in water of at least 5 g/100 ml at 25 °C. Particularly preferred anionic polymers are formed from monomers selected from ethylenically unsaturated carboxylic acid and sulphonic acid monomers, preferably selected from (meth) acrylic acid, allyl sulphonic acid and 2-acrylamido-2-methyl propane sulphonic acid (ATBS), and their salts, optionally in combination with non-ionic co-monomers, preferably selected from (meth) acrylamide, hydroxy alkyl esters of (meth) acrylic acid and N-vinyl pyrrolidone.

Preferred non-ionic polymers are formed from ethylenically unsaturated monomers selected from (meth) acrylamide, hydroxy alkyl esters of (meth) acrylic acid and N-vinyl pyrrolidone.

Preferred cationic polymers are formed from ethylenically unsaturated monomers selected from dimethyl amino ethyl (meth) acrylate - methyl chloride, (DMAEA.MeCI) quat, diallyl dimethyl ammonium chloride (DADMAC), trimethyl amino propyl (meth) acrylamide chloride (ATPAC) optionally in combination with non-ionic co-monomers, preferably selected from (meth) acrylamide, hydroxy alkyl esters of (meth) acrylic acid and N-vinyl pyrrolidone.

In some instances, it has been found advantageous to separately add combinations of polymer types. Thus an aqueous solution of an anionic, cationic and/or non-ionic polymer may be added to the above mentioned material as at least one polymer.

In the invention, the at least one polymer may be formed by any suitable polymerisation process. The polymers may be prepared for instance as gel polymers by solution polymerisation, water-in-oil suspension polymerisation or by water-in-oil emulsion polymerisation. When prepar- ing gel polymers by solution polymerisation the initiators are generally introduced into the monomer solution. Optionally a thermal initiator system may be included. Typically a thermal initiator would include any suitable initiator compound that releases radicals at an elevated temperature, for instance azo compounds, such as azo-bis-isobutyronitrile. The temperature during polymerisation should rise to at least 70 °C but preferably below 95 °C. Alternatively polymerisation may be effected by irradiation (ultra violet light, microwave energy, heat etc.) optionally also using suitable radiation initiators. Once the polymerisation is complete and the polymer gel has been allowed to cool sufficiently the gel can be processed in a standard way by first commuting the gel into smaller pieces, drying to the substantially dehydrated polymer followed by grinding to a powder. Alternatively polymer gels may be supplied in the form of polymer gels, for instance as neutron type gel polymer logs.

Such polymer gels may be prepared by suitable polymerisation techniques as described above, for instance by irradiation. The gels may be chopped to an appropriate size as required and then on application mixed with the material as partially hydrated water soluble polymer particles.

The polymers may be produced as beads by suspension polymerisation or as a water-in-oil emulsion or dispersion by water-in-oil emulsion polymerisation, for example according to a process defined by EP-A-150933, EP-A-102760 or EP-A126528. Alternatively the polymers may be provided as dispersion in an aqueous medium. This may for instance be a dispersion of polymer particles of at least 20 microns in an aqueous medium containing an equilibrating agent as given in EP-A-170394. This may for example also include aqueous dispersions of polymer particles prepared by the polymerisation of aqueous monomers in the presence of an aqueous medium containing dissolved low IV polymers such as polydial- lyldimethyl ammonium chloride and optionally other dissolved materials for instance electrolyte and/or multi-hydroxy compounds e. g. polyalkylene glycols, as given in WO-A-9831749 or WO- A-9831748.

The, preferably aqueous, solution comprising at least one polymer and at least one salt is pref- erably obtained by dissolving the at least one polymer in a, preferably aqueous, solution of at least one salt. Generally solid particulate polymer, for instance in the form of powder or beads, is dispersed in preferably water and allowed to dissolve with agitation. This may be achieved using conventional make up equipment. Desirably, the polymer solution can be prepared using the Auto Jet Wet (trademark) supplied by BASF. Alternatively, the polymer may be supplied in the form of a reverse phase emulsion or dispersion which can then be inverted into preferably water.

According to the present invention a solution comprising at least one salt is understood as at least one, preferably aqueous, solution comprising one or more inorganic or organic salt(s). In general, the one or more salt(s) that is present in the solution according to the present invention can be selected from any naturally occurring or synthetically prepared salts. The salts in general comprise at least one kind of anion and at least one kind of cation, wherein the stoichi- ometry within the salt depends on the negative valency of the at least one anion and on the pos- itive valency of the at least one cation. According to the present invention the at least one salt is at least partially dissociated in the solvent, preferably in water, wherein the cations are preferably present in hydrated form. Examples of anions that may be present in the at least one salt are selected from the group of inorganic anions like chloride, nitrate, bromide, iodide, carbonate, phosphate, sulphate and mixtures thereof.

Examples of cations that may be present in the at least one salt are selected from the group of inorganic cations like lithium, sodium, potassium, rubidium, caesium, francium, beryllium, magnesium, strontium, barium, radium, aluminium and mixtures thereof.

According to the embodiment of the present invention that the at least polymer is based on 2- acrylamido-2-methyl propane sulphonic acid (ATBS), the cations that may be present in the at least one salt are selected from the group of inorganic cations like lithium, sodium, potassium, rubidium, caesium, francium, beryllium, calcium, magnesium, strontium, barium, radium, aluminium and mixtures thereof.

A key feature of the present invention is that a solution comprising at least one polymer and at least one salt, but no, preferably essentially no, precipitated cation-polymer-complex is present in the solution that is added in step (a) of the process according to the present invention. Minor amounts of precipitates, for example less than 1 % by weight, based on the whole solution, are acceptable according to the present invention. The concentration of the at least one salt that is present in the at least one solution according to the present invention is preferably adjusted to a value that the, preferably aqueous, solution comprising the at least one polymer and the at least one salt has a viscosity that allows an improved contact of the at least one polymer and the mineral particles. According to the present invention, the concentration of the at least one salt depends on the valency of the at least one cation and the at least one anion that are present.

Preferably, the at least one solution that is used according to the present invention comprises the at least one salt in an amount of 0.001 to 43 mol/l, more preferably 0.01 to 10 mol/l, most preferably 0.25 to 2.5 mol/l.

For example, a salt comprising sodium as one or single cation may be present in the solution in an amount that at least 50 ppm, more preferably at least 1000 ppm, sodium-cations Na⁺ are present. This amount reduces the viscosity of the solution that is used according to the present invention, preferably a solution comprising an anionic polymer, particularly advantageously.

According to another example, a salt comprising magnesium as one or single cation may be present in the solution in an amount that at least 50 ppm, more preferably 50 to 500 ppm, mag- nesium-cations Mg²⁺ are present. This amount reduces the viscosity of the solution that is used according to the present invention, preferably a solution comprising an anionic polymer, particularly advantageously. According to another example, preferably in the case that the at least polymer is based on 2- acrylamido-2-methyl propane sulphonic acid (ATBS), a salt comprising calcium as one or single cation may be present in the solution in an amount that at least 5 ppm calcium-cations Ca²⁺ are present. This amount reduces the viscosity of the solution that is used according to the present invention, preferably a solution comprising an anionic polymer, particularly advantageously.

Particularly preferably the cations and anions as mentioned above are added in amounts that the viscosity of the solution of the at least one polymer is decreased by at least 20%, more preferably by at least 75%. According to a particularly preferred embodiment of the present invention the at least one solution that is used in the process according to the present invention is based on saline water. Saline water is known to the skilled artisan. In general "saline water" is understood as a term for water that contains a significant concentration of dissolved salts, in particular NaCI. The concentration is usually expressed in parts per million (ppm) of salt.

Saline water in general contains significant amounts of dissolved salts. The concentration is the amount (by weight) of salt in water, as expressed in "parts per million" (ppm). If water has a concentration of 10,000 ppm of dissolved salts, then one percent by weight of the water comes from dissolved salts.

According to the present invention, saline water is classified according to the United States Geological Survey in three categories. Slightly saline water contains 1 ,000 to 3,000 ppm, moderately saline water contains 3,000 to 10,000 ppm and highly saline water contains 10,000 to 35,000 ppm of salt. Seawater has a salinity of about 35,000 ppm, equivalent to 35 g/L.

According to preferred embodiments of the present invention slightly saline water, moderately saline water or highly saline water, in each case as defined above, is used as the basis of the solution comprising at least one polymer and at least one salt. According to a preferred embodiment the aqueous composition comprising the at least one polymer and the at least one salt solution may be formed by introducing a solution of at least one polymer into a flowing stream of a solution of the at least one salt. A suitable and effective rigidifying amount of the at least one polymer, being present in the solution comprising the at least one polymer at least one salt, preferably as aqueous solution, can be mixed with the suspension prior to a pumping stage. In this way the polymer can be distributed throughout the suspension. Alternatively, the solution can be introduced and mixed with the suspension during a pumping stage or subsequently. The most effective point of addition will depend upon the substrate and the distance from the preferably present kinetic energy stage to the deposition area. If the conduit is relatively short it may be advantageous to dose the solution close to where the modified, preferably sheared, suspen- sion flows from the preferably used kinetic energy device. On the other hand, where the deposition area is significantly remote from preferably used the kinetic energy device in may be desirable to introduce the solution closer to the outlet. In some instances in may be convenient to introduce the solution into the preferably modified, preferably sheared, suspension as it exits the outlet.

One of the positive effects of the present invention is that by the resultant polymer solution viscosity reduction resulting from the presence of salt in the make up water, an improved dispersion/mixing of the polymer through the slurry is obtained. Furthermore, when the polymer solution is applied to the aqueous mineral slurry, a reduction in the overall saline environment, permits the polymer to uncoil, so enhancing its effective performance. Due to the reduction in polymer solution viscosity brought about by the inclusion of salts according to the present invention, it is possible to effectively apply polymers of high Intrinsic Viscosity, of for example more than 30 dl/g, preferably 31 to 50 dl/g.

Preferably the suspension treated with the solution comprising at least one polymer and at least one salt will be pumped as a fluid to an outlet at the deposition area and the so treated suspension is allowed to flow over the surface of rigidified material. The suspension is allowed to stand and rigidify and therefore forming a stack of rigidified material. This process may be repeated several times to form a stack that comprises several layers of rigidified solids of the suspension. The formation of stacks of rigidified material has the advantage that less area is required for disposal.

The rheological characteristics of the suspension treated with the solution comprising at least one polymer and at least one salt as it flows through the conduit to the deposition area is important, since any significant reduction in flow characteristics could seriously impair the efficiency of the process. It is important that there is no significant settling of the solids as this could result in a blockage, which may mean that the plant has to be closed to allow the blockage to be cleared. In addition it is important that there is no significant reduction in flow characteristics, since this could drastically impair the pumpability on the suspension. Such a deleterious effect could result in significantly increased energy costs as pumping becomes harder and the likelihood of increased wear on the pumping equipment.

The rheological characteristics of the suspension as it rigidifies is important, since once the suspension treated with the solution comprising at least one polymer and at least one salt is allowed to stand it is important that flow is minimised and that solidification of the suspension proceeds rapidly. If the suspension is too fluid then it will not form an effective stack and there is also a risk that it will contaminate water released from the suspension. It is also necessary that the rigidified material is sufficiently strong to remain intact, but must be compressable, and with- stand the weight of subsequent layers of rigidified suspension being applied to it.

Preferably the process of the invention will achieve heaped disposal geometry and will co- immobilise the fine and any coarse fractions of the solids in the suspension and also allowing any released water to have a higher driving force to separate it from the suspension by virtue of hydraulic gravity drainage. The heaped geometry appears to give a higher downward compaction pressure on underlying solids which seems to be responsible for enhancing the rate of de- watering. We find that this geometry results in a higher volume of waste per surface area, which is both environmentally and economically beneficial.

A preferred feature of the present invention is the release of aqueous liquor that often occurs during the rigidification step. Thus in a preferred form of the invention the suspension is de- watered during rigidification to release liquor containing significantly less solids. The liquor can then be returned to the process thus reducing the volume of imported water required and there- fore it is important that the liquor is clear and substantially free of contaminants, especially migrating particulate fines. Suitably the liquor may for instance be recycled to the mining operation, for instance oil sands operation, from which the suspension originates. Alternatively, the liquor can be recycled to the spirals or other processes within the same plant. Furthermore clarifying polymers may optionally be added after the thickener to the underflow but before disposal by rigidification. This may enhance the clarity of the water released from the rigidifying stack.

The clarifying polymers are typically low molecular weight, polymers. For the purposes of the invention low molecular weight means an average molecular weight ranging from about 10,000 to about 1 ,000,000 g/mol. For example, anionic polymers in the range of about 10,000 to about 500,000 g/mol may be used.

These can be anionic, non-ionic or cationic. They can be synthetic or naturally derived, e.g. from starch, gums or cellulose, e.g. carboxymethyl cellulose. Preferably they are anionic, e.g. a homopolymer of sodium acrylate, or as a copolymer with acrylamide, or hydrolysed polyacrylo- nitrile or hydrolysed acrylamide.

The amount of clarifying polymer will be determined by the composition of the oil sands tailings but generally about 5 to about 500 g/tonne of dry solids. For example the amount of clarifying polymer may be about 5 g to about 100 g/tonne of dry solids.

The clarifying polymer may be added as a solution and may be added in any suitable concentration. It may be desirable to employ a relatively concentrated solution, for instance up to 10% or more based on weight of polymer in order to minimise the amount of water introduced into the material. The clarifying polymer solution can be added at a relatively dilute concentration, for instance as low as 0.01 % by weight of polymer. Typically the clarifying polymer solution will normally be used at a concentration between 0.05 and 5% by weight of polymer. Preferably the polymer concentration will be the range 0.1 % to 2 or 3%. More preferably the concentration will range from 0.25% to about 1 or 1.5%.

The clarifying polymer may be added before, simultaneously, or after the rigidifying amount of the water-soluble polymer added according to the present invention. According to a further preferred embodiment, the present invention relates to a process according to the present invention in which step (a) is conducted by selecting the salt solution and the conditions in a way that the at least one polymer precipitates, contacting the precipitated poly- mer with the particulate solids, adding at least one second salt solution which is selected in a way that the at least one polymer will at least partially be dissolved again, and subjecting this mixture to step (b).

The present invention therefore preferably relates to the process according to the present inven- tion in which step (a) is conducted by selecting the salt solution and the conditions in a way that the at least one polymer precipitates, contacting the precipitated polymer with the particulate solids, adding at least one second salt solution which is selected in a way that the at least one polymer will at least partially be dissolved again, and subjecting this mixture to step (b). Further preferred the present invention relates to a process according to the present invention in which before, during or after step (a) kinetic energy is applied to the suspension

The inventors believe that the action of the kinetic energy on the suspension directly interacts with the clay-clay intra-particle network structures and the clay inter-particle network structures. In fact it is believed that the kinetic energy will at least partially breakdown these network structures.

By kinetic energy we mean that suspension is subjected to some energy which is or induces motion within the suspension. In one form the kinetic energy may be ultrasonic energy. General- ly it is expected that the application of ultrasonic energy will induce vibrations which will at least partially break down the network structures. Other forms of kinetic energy may be alternative means for inducing vibrations.

Kinetic energy may be applied before, during and/or after the addition of the solution comprising at least one polymer and at least one salt according to step (a) of the process according to the present invention. Preferably, kinetic energy is applied before step (a) of the process according to the present invention. According to this preferred embodiment, a modified, preferably sheared, suspension is introduced into step (a) of the process according to the present invention.

An advantage of the present invention over the prior art is that the addition of a solution comprising at least one polymer and at least one salt makes it possible that the amount of energy that is to be applied in the process can be lowered due to the lower viscosity caused by the, preferably high molecular weight, polymer. If kinetic energy is applied after the addition of the solution according to step (a) of the process according to the present invention, the amount of energy can therefore be lower than the amount that is necessary without the addition of the solution. One particularly suitable form of kinetic energy is shearing.

The shearing may be carried out in a shearing vessel before being transferred to the next step of the process. Alternatively, the shearing may be carried out in line as the suspension is being transferred.

Any conventional shearing device may be employed as such devices are very well known in the industry and also described in the literature. Industrial scale shear devices, for instance shear mixing devices or shear pumps are available from a variety of manufacturers, for instance IKA which manufactures Ultra Turrax high shear devices, for instance the devices in the Ultra Turrax UTL 2000 range; Fluko-high shear mixers; Silverson high shear mixers, for instance Ultramix mixers or In-line mixers; Euromixers; Greaves; Admix Inc which manufactures Rotosolver high shear devices; Charles Ross and Son Company which manufactures Ross high shear mixers; Robbins Myers which manufactures Greerco high shear mixers; Powershear Mixers.

Suitable shearing devices generally have moving elements: such as rotating components, for instance impellers; kneeding components; or moving plates. The mixing pumps may also contain static elements such as baffles or plates, for instance containing orifices. The moving elements will tend to move quite rapidly in order to generate shear. In general this will depend up- on the mode of action within the shearing chamber and the size of the volume that is being sheared. This may be for instance at least 5 cycles per second (5 s ¹), preferably at least 6 cycles per second (6 s ¹), more preferably at least 7 cycles per second (7 s ¹), most preferably at least 8 cycles per second (8 s ¹), even more preferably 9 cycles per second (9 s ¹), and usually at least 10 cycles per second (10 s ¹), suitably at least 20 cycles per second (20 s ¹). Typically this may be up to 170 s ¹, up to 200 s ¹ or up to 300 s ¹ or more.

When the suspension, for instance oil sands derived MFT, is subjected to shearing, the period of shearing may be referred to as the residence time. The residence time in the shearing device may be, for instance at least 1 second. Often it will be at least 5 seconds and sometimes at least 10 seconds. It may be up to 30 seconds or more or it may be up to 15 seconds or up to 20 seconds. In some situations it may be at least 20 seconds, for instance at least 1 min and often may be several hours, for instance up 10 hours or more. Suitably the residence time may be at least 5 min, suitably at least 10 min and often at least 30 min. In many cases it may be at least one hour. In some cases the residence time may be up to 8 hours but desirably less than this.

The shearing device may even be a milling device. Milling devices include colloid mills, cone mills and rotor mills etc. In general milling devices tend to have moving elements, for instance cones, screens or plates containing gaps, grooves, slots or orifices which move against other static elements. The moving elements may move instance by rotation. These devices tend to generate a high level of shear stress on liquids and other materials passing through them. The moving elements tend to combine high-speed with a very small shear gap which produces intense friction on the material being processed. The friction and shear that result is commonly referred to as wet milling. In one form the milling device may contain a rotor and a stator which are both cone shaped and may have one or more stages of fine grooves, gaps, slots or orifices. This stator can be adjusted to obtain the desired gap setting between the rotor and stator. The grooves, gaps, slots or orifices may change direction in each stage to increased turbulence. The moving elements will tend to move quite rapidly in order to generate sufficient shear. This may be for instance at least 5 cycles per second (5 s ¹), preferably at least 6 cycles per second

(6 s ¹), more preferably at least 7 cycles per second (7 s ¹), most preferably at least 8 cycles per second (8 s ¹), even more preferably 9 cycles per second (9 s ¹), and usually at least 10 cycles per second (10 s ¹), suitably at least 20 cycles per second (20 s ¹). Typically this may be up to 170 s-¹, up to 200 s-¹ or up to 300 s ¹ or more.

Alternatively the suspension may be passed through a static mixer or other static elements which bring about a shearing action, for instance baffles in a pipeline or alternatively a constriction in a pipeline. The inventors have noted that during the application of kinetic energy, for instance by shearing of the suspension, in particular the oil sands derived M FT, a notable reduction in viscosity of the suspension can occur. The inventors considered that this may be as a result of the clay-clay intra-particle network structures and clay inter-particle network structures being broken down and releasing water previously entrained within these networks. It is thought that this availability of the water may bring about a reduction in viscosity. Typically viscosity may be measured by an instrument called a controlled stress rheometer, such as Brookfield RS. Viscosity may be measured at 25 °C.

Generally the viscosity of the modified (for instance sheared) suspension would often be below 90% of the viscosity of the suspension prior to the application of kinetic energy, such as the shearing stage. Preferably the viscosity of the modified suspension, for instance sheared suspension, is no more than 80% of the viscosity of the suspension before the application of kinetic energy, such as shearing and more preferably no more than 70%. More preferably still the modified suspension, for instance sheared suspension, viscosity will be up to 60% and in particular less than 50% of the suspension before the application of kinetic energy, for instance un- sheared suspension. In some cases the viscosity of the modified suspension, for instance sheared suspension, may be as little as 0.001 % of the suspension before the application of kinetic energy, for instance shearing, or even below. Often the modified suspension, for instance sheared suspension, will be at least 0.05% or 0.1 % of the suspension before the application of kinetic energy, for instance un-sheared suspension. In many cases the modified suspension, for instance sheared suspension will be at least 1 %, at least 5% or at least 10% of the suspension before the application of kinetic energy, for instance un-sheared suspension.

Generally the change in viscosity from the suspension before the application of kinetic energy to the modified suspension tends to increase as the clay content of the suspension increases.

The present invention also includes a test method for evaluating suspensions which contain fine mineral particles and clay, especially mature fine tailings derived from oil sands tailings. A further aspect of the invention defines a method of testing a suspension which comprises particulate solids dispersed in an aqueous liquid, said particulate solids comprise clay and mineral particles of size below 50 μιτι, which method comprises the steps of,

(a) Addition of a solution comprising at least one polymer and of at least one salt to the suspension;

(b) Transferring the polymer treated suspension onto a mesh; and

(c) Measuring the water drained through the mesh and measuring the angle formed between the base of the solids retained on the mesh and a line drawn between the perimeter of the solids at the highest point in the center of the solids. The suspension may be in accordance with the suspension already defined herein. Preferably the suspension comprises mature fine tailings (MFT) that have been derived from oil sands tailings.

General and preferred embodiments in respect of at least one polymer, the at least one salt, the solution and ways of addition, preferably according to the preferred embodiment of the addition step (a), are outlined above.

Preferably, the present invention relates to the method according to the present invention in which before, during or after step (a) kinetic energy is applied to the suspension. According to a further preferred embodiment, the present invention relates to the method according to the present invention in which the kinetic energy is shearing.

By kinetic energy we mean that suspension is subjected some energy which is or induces motion within the suspension. In one form the kinetic energy may be ultrasonic energy. Generally it is expected that the application of ultrasonic energy will induce vibrations which will at least partially break down the network structures. Other forms of kinetic energy may be alternative means for inducing vibrations.

General and preferred embodiments of the application of kinetic energy, in particular shearing, are outlined above.

The present invention preferably relates to the method according to the present invention in which the kinetic energy is shearing and the modified suspension is a sheared suspension. The shearing may be carried out by any suitable shearing devices that may be employed in a laboratory. Typically such shearing devices may be domestic or laboratory shearing devices, such as those manufactured by Silverson or Moulinex. One particularly suitable shearing device comprises a flat paddle impeller. Suitably a sample of the suspension, desirably MFT, may be placed into a beaker or other convenient receptacle, suitably having a circular cross-section. The shearing member of the shearing device should then be inserted into the suspension. When the shearing device comprises a flat paddle impeller it is preferred that the length of the paddle fits substantially across the diam- eter of the beaker or receptacle. By this we mean that there may be up to 1 , 2, or 3 mm clearance between the wall of the beaker or receptacle and the ends of the flat paddle.

Desirably the sample should be sheared by operating the shearing device at a rate of at least 200 rpm, preferably at least 300 rpm and more preferably at least 400 rpm, especially at the 450 rpm. There is no upper limit to the rate of shearing but generally this would tend to depend on the type of shearing device and this would tend not to be greater 10,000 rpm or 20,000 rpm. In the case of the shearing device with the flat paddle impeller the upper rate of shearing may be no more than 1000 rpm and usually less than this. A desirable rate of shearing when using the flat paddle impeller may be in the range of between 200 and 800 rpm, preferably between 300 and 700 rpm, more preferably between 400 and 600 rpm, especially between 450 and 550 rpm.

The duration of the shearing will tend to be at least 1 or 2 seconds and usually at least 5 seconds and in some cases at least 30 seconds or at least 1 min. The period of shearing may be longer than this, for instance up to 30 min or more. Generally the period of shearing would be up to 20 min.

Typically the, preferably aqueous, solution comprising at least one polymer and the at least one salt will normally have a concentration as mentioned above. Following the addition of the solution to the preferably modified, more preferably sheared, suspension, it may be desirable to as- sist the polymer treated suspension to be integrated throughout the solids of the suspension. This may be achieved by stirring. Alternatively the polymer treated suspension may be transferred to a sealed container and inverted several times, for instance between 2 and 10 inversions, suitably between 3 and 5 inversions. The mesh onto which the polymer treated suspension is applied maybe any suitable mesh which allows water to drain through it and retain the solids on top of it. The mesh may be part of a sieve. The mesh may be made from metal or other material such as plastic.

The test method is useful for determining which polymer products and which salt solutions are likely to be most effective for the treatment of the suspension. The method should also be useful in determining the optimal doses of polymers, molecular weights of polymers, amount and kind of salt solutions.

The present invention further relates to the use of a combination of at least one polymer and of at least one salt, preferably in solution, for dewatering a suspension comprising particulate solids dispersed in an aqueous liquid, said particulate solids comprises clay and mineral particles of size below 50 μιτι. Details and preferred embodiments of the solution comprising at least one polymer and at least one salt, of the suspension comprising particulate solids dispersed in an aqueous liquid, said particulate solids comprises clay and mineral particles of size below 50 μιτι, apply according to the above mentioned process and method.

Figures:

Figure 1 shows the Net Water Release [% by weight] (y-axis) in relation to polymer conditioning time [seconds]. The continuous line relates to the experiment, wherein no Na⁺-cations are pre- sent in the solution (Control Test), the dashed line relates to the experiment, wherein 40 g/l (gpl) Na⁺-cations are present in the solution, and the line comprising lines and points relates to the experiment, wherein 80 to 100 g/l (gpl) Na⁺-cations are present in the solution.

Figure 2 shows the Stump Angle [°] (y-axis) in relation to polymer conditioning time [seconds]. The continuous line relates to the experiment, wherein no Na⁺-cations are present in the solution (Control Test), the dashed line relates to the experiment, wherein 40 g/l (gpl) Na⁺-cations are present in the solution, and the line comprising lines and points relates to the experiment, wherein 80 to 100 g/l (gpl) Na⁺-cations are present in the solution. Examples:

Water release experiments and the Acquisition of Stump Angles have been conducted according to the following: The polymer used in the test work was Rheomax^®9010, being a Sodium acrylate/acrylamide copolymer. The slurry that is used in the experiments is a synthetic slurry comprising Super Fine Sand in an amount of 36% by weight, Silica (Slit) in an amount of 60% by weight and Hectalite in an amount of 4% by weight. The standard ETD test method, as endorsed by the Advanced Mineral Processing Group

(APMG), was used for all tests. For all experiments, mixing speed applied to the slurry during and after polymer addition was 80 rpm. The amount of Rheomax^® 9010 was 134 g/t in all experiments. The concentration of polymer in the solution was 0.5% by weight in all experiments. NaCI was used as salt. A solution comprising Rheomax^® 9010 and NaCI was used to the treat the slurry comprising particulate solids.

Performance demonstrated 1. Effective water release of the polymer treated slurry

The presence of 40g/l NaCI in the polymer solution produced an improved water release than the Control test. Further increase in the polymer solution salinity, 80 and 100 g/l further improved the optimum water release for a given polymer dose. 2. Slump angle of polymer treated slurry

The presence of 40 g/l NaCI in the polymer solution significantly reduced the slump angle (yield stress) of the treated slurry. Increasing the level of NaCI within the polymer solution to between 80 and 10Ogpl further reduces the slump angle of the treated slurry for a given polymer condi- tioning time.

In combination, the presence of NaCI in the polymer solution creates an improved water release from the treated slurry and at the same time reduces the associated slump angle (yield stress) resulting in both improved tailings consolidation and reduced pumping energies (back pres- sures)

Claims

A process of dewatering a suspension comprising particulate solids dispersed in an aqueous liquid, said particulate solids comprises clay and mineral particles of size below 50 μιτι, which process comprises the steps of,

(a) Addition of a solution comprising at least one polymer and at least one salt to the suspension; and

(b) Dewatering the polymer treated suspension of step (a).

A process according to claim 1 in which the suspension comprises mature fine tailings derived from oil sands tailings.

A process according to any preceding claims in which the suspension that is to be de- watered is transferred as a fluid to a deposition area, then allowed to stand and rigidify, in which the solution comprising at least one polymer and at least one salt is added to the suspension during transfer of the suspension.

A process according to any preceding claims in which before, during or after step (a) kinetic energy is applied to the suspension.

A process according to claim 4 in which the kinetic energy is shearing.

A process according to any of the preceding claims in which the solution of the at least one polymer and at least one salt is provided by adding the at least polymer to a solution of at least one salt.

A process according to any preceding claim in which the at least one polymer is anionic, cationic or non-ionic, preferably anionic or non-ionic, particularly preferably anionic.

A method of testing a suspension which comprises particulate solids dispersed in an aqueous liquid, said particulate solids comprise clay and mineral particles of size below 50 μιτι, which method comprises the steps of,

Addition of a solution comprising at least one polymer and at least one salt to the suspension;

Transferring the polymer treated suspension onto a mesh; and

Measuring the water drained through the mesh and measuring the angle formed be tween the base of the solids retained on the mesh and a line drawn between the pe rimeter of the solids at the highest point in the center of the solids.

9. A method according to claim 8 in which the suspension comprises mature fine tailings derived from oil sands tailings.

A method according to claim 8 or claim 9 in which before, during or after step (a) kinetic energy is applied to the suspension.

1 1 . A method according to claim 10 in which the kinetic energy is shearing.

A method according to any preceding claims in which the solution of the at least one polymer and at least one salt is provided by adding the at least polymer to a solution of at least one salt.

The use of a combination of at least one polymer and of at least one salt, preferably in solution, for dewatering a suspension comprising particulate solids dispersed in an aqueous liquid, said particulate solids comprises clay and mineral particles of size below 50 μιτι.