FURTHER DEVELOPMENTS IN THE CONTROL OF LEVEL IN … · 2010. 9. 23. · Moys and Finch (1988a,...

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FURTHER DEVELOPMENTS IN THE CONTROL OF LEVEL IN FLOTATION COLUMNS M H MOYS DEPARTMENT OF CHEMICAL ENGINEERING UNIVERSITY OF THE WITWATERSRAND

Transcript of FURTHER DEVELOPMENTS IN THE CONTROL OF LEVEL IN … · 2010. 9. 23. · Moys and Finch (1988a,...

  • FURTHER DEVELOPMENTS IN THE CONTROL OF LEVEL IN FLOTATION COLUMNS

    M H MOYS

    DEPARTMENT OF CHEMICAL ENGINEERING UNIVERSITY OF THE WITWATERSRAND

  • Further Developments in the Control of Level

    Abstract

    in Flotation Columns

    M. H. Moys,

    Consultant in Column Flotation,

    Multotec Cyclones (Pty) Ltd.

    and

    Department of Chemical Engineering

    University of the Witwatersrand

    Johannesburg

    Interface level in flotation columns is generally measured with the

    aid of a pressure-sensitive instrument ego a differential pressure

    cell or Metritape. The use of this type of measurement is critisised,

    and other methods which are claimed to give more accurate measures of

    interface level are discussed. The paper focusses on the development

    of methods based on the measurement of conductivity across the froth-

    -slurry interface. These are generally sabotaged by variations in the

    conductivity of the feed slurry, particularly when the pH of the

    slurry is being controlled, ego in sulphide flotation. Methods of

    improving the accuracy and reliability of this technique are devel-

    oped. The result is a level control scheme which successfully rejects

    large disturbances in plant operation (including a 5:1 change in

    slurry conductivity) while controlling level to an accuracy of ± 4cm.

    1. Introduction

    For effective operation of a flotation column the level must be

    controlled near a pre-specified level Lset ' so that the froth height

    h f is (a) not so low that the significant mixing that occurs in the

    froth phase results in a loss in grade, Hnd (b) not too high, n~stll

    ting both in an excessive residence time of bubbles in the froth phase

    and a loss of residence time in the pulp phase (both of whi~h effects

    result in a loss of recovery). Yianatos et. al. (1987) recommend a

    froth height of approximately 1 m. Current methods for measuring

    interface level L are reviewed below, and research work aimed at

    developing a reliable method of measuring L using conductivity

    measurements is described.

  • Level Control in Column Flotation Moys Page 2

    2. Review of methods for measuring interface level

    The method most widely used is that based on a measurement of hydro-

    static pressure P at a distance between 1,5 and 2 m below the overflow

    lip. P is however not an accurate indicator of interface level because

    it is a strong function of other variables, such as slurry density,

    hold-up of liquid in the froth, bubble loading, etc. Moys and Finch

    (l988a) showed that errors in L exceeding 0,5 m are easily possible

    when high gas rates, small bubbles and high bubble loadings occur,

    particularly when the flotable mineral is dense, e.g. pyrite or

    galena. Moys and Finch (1989) measured an error of 0,4 m in galena

    flotation in a limited test programme at the Polaris Mine, N.W.T.,

    Canada and the variation of level with pneumatic pressure measurement

    in pyrite testwork in South Africa is shown in Figure 1. This lack of

    precision means that frequent checks on level must be made by the

    operator in situations where a sight window on the side of the column

    exists; in the absence of a sight window the poor performance of the

    measurement cannot be checked, so the operator is forced to set the

    froth depth at a conservatively high level to avoid disaster, thereby

    incurring losses associated with unnecessarily deep froths most of the

    time.

    Several papers have reported the use of Metritape, a patented device

    which consists of a wire coil wound round a contact strip and insula-

    ted from the slurry by a flexible, corrosion-resistant sheath. A strip

    of Metritape 2m long is inserted in the top of the column. The design

    is such that the wire does not make contact with the contact strip

    until the pressure in the fluid outside the tape exceeds l50mm water.

    This is sufficient to collapse the sheath and wire coil so that

    contact is made. The resistance of the wire which is not in contact

    with the contact strip is measured and provides and accurate (± 1 cm) measure of the level at which the first contact is made. ~~ile Metri-

    tape is widely used for the measurement of fluid level in tanks, its

    use in colu~n flotation must be seriously questioned, since it

    provides a measure of the depth in the column at which the pressure is

    150 mm of water above atmospheric pressure. This can only provide

    relatively accurate measurements of interface level for columns where

    the pressure at the interface level is less than this critical value -

    a condition which can only occur for froths which are lightly laden,

    have little interstitial fluid and/or where froth height is low. The

    measurement is in addition subject to all the disadvantages of dip

    cells discussed above.

    Accurate measurement of interface level relies on the measurement of

    intensive properties of the fluids near the interface (such as densi-

    ty, temperature or conductivity) rather than an extensive property

    such as pneumatic pressure which is a function of the total mass of

  • Level Control in Column Flotation Moys Page 3

    material obove the measurement point. Some of these are discussed

    below.

    Techniques based on the measurement of the position of a float at the

    interface (this is essentially a density technique and is used

    successfully

    the density

    with conventional flotation) cannot be relied upon since

    of the froth near the froth-slurry interface varies over

    too wide a range. It is not generally possible to select the density

    of the float which will apply to all possible conditions.

    Moys and Finch (1988a, 1988b and 1989) have reported the use of

    measurements of temperature profile across the froth-slurry interface.

    The technique relies on the existence of a significant and reliable

    temperature differential between the wash water and the feed slurry.

    Provided that the column is operated under positive bias conditions

    (i.e. with wash water flowing downwards through the froth phase, so

    that the froth phase temperature is close to the wash water tempera-

    ture) there is a sharp change in temperature at the interface.

    Measurements obtained in an industrial galena cleaner are shown in

    Figure 2 (Moys and Finch, 1989). Detection of the level at which this

    change occurs provides an estimate of interface level accurate to

    ± 7 cm. The method suffers the disadvantage of requiring intelligent analysis of 10-15 temperature measurements, so will be expensive.

    Significant other advantages (see Moys and Finch, 1989) to be obtained

    from such measurements (such as online measurements of froth washing

    efficiency) may make this technique an attractive option, particularly

    in an environment where computer control resources are already avail-

    able.

    The use of conductivity

    is reliable, simple to

    discussed initial work

    measurements may provide a measurement which

    implement and cheap. Moys and Finch (1988a)

    in this area, using the conductivity sensor

    arrangements shown in Figures 3 and 4. The first involves the use of

    two paralllel, vertical probes which provide a fairly linear correla-

    tion between level and conductivity. The second involves measurement

    of conductivity between two probes, one above and one below the inter-

    face. The correlation is non-linear but the simplicity of the design

    (the two probes can be mounted on a vertical rod passing through the

    froth phase) makes the exploitation of this approach attractive.

    Multotec Cyclones (Pty) Ltd (a South African supplier of flotation

    columns) have used this method successfully on pilot column tests at a

    local fluorspar mine, and it has also been used in coal column flota-

    tion tests (sponsored by the National Energy Council) at the Universi-

    ty of the Witwatersrand. The conductivity signal is connected to a PID

    controller with a conductivity setpoint which keeps the interface just

    below the lower edge of the upper conductivity probe. Level was

  • Level Control in Column Flotation Moys Page 4

    controlled to an accuracy of ± 1 cm.

    While the method worked well in the above applications it failed when

    applied to pyrite flotation, because the conductivity of the slurry

    varied widely as a result of the necessity to control the pH of the

    slurry at a setpoint of 3,8 pH units. Small variations in pH resulted

    in large variations in conductivity, so it was impossible to select a

    reliable setpoint for the conductivity (i.e. level) controller. It was

    necessary in this situation to revert to the use of pneumatic measure-

    ments for level control. The data given in Figure 1 was collected

    during this experimental programme: clearly a more reliable estimate

    of interface level is required.

    We decided to invetigate further the use of conductivity measurements.

    It was evident that

    the variations in

    scheme is described

    a control scheme was required which would adapt to

    slurry conductivity. The development of such a

    below.

    3. Theoretical Developments

    3.1 The variation of conductivity across the interface.

    This is discussed by Moys and Finch (1988a) in some detail; the

    salient points are summarised here.

    The conductivity of a gas-liquid dispersion typical of column flota-

    tion froths (Yianatos, et al, 1985) is given by

    - 0,432 kl,fr

    \vhere kl fr , respectively

    and

    of €l,fr are

    the liquid

    the conductivity and fractional holdup

    between the bubbles in the froth phase.

    Typically ~l,fr is leGs than 0,4 at the base of the froth and drops rapidly to approximately 0,2 at the top of the froth phase. kfr 1 , will be similar to the conductivity of the slurry ksl at the base of

    the froth but in columns where washing of the froth phase by the wash

    water is efficient it will change rapidly towards the conductivity of

    the wash water.

    In the pulp phase the conductivity is given by

    k pulp 1,55 - 0,55€sl

    where slurry hold-up €sl is generally greater than 0,7. For kl fr ,

  • Level Control in Column Flotation Moys Page 5

    k sl ' €l,fr 0,4 and €sl 0,7 the ratio between froth and

    pulp conductivities is 0,48. In cases where ~ash < ksl this ratio will be decreased, giving ample variation in k across the interface,

    while if ~ash > ksl (e.g. this can occur in cases where the pH of wash water must be controlled) the variation of k across the interface

    will not provide a reliable basis for interface detection.

    3.2 A model for conductivity across the interface

    Conduction in fluids between two small probes a significant distance

    apart is a complex phenomenon. In an infinite uniform medium the

    conduction paths follow lines through the medium that constitute the

    lines of steepest descent in the voltage field set up between the two

    probes as shown in Figure 5(a) (please note that the diagrams in

    Figure 5 are not accurate; they were created for illustrative purposes

    only). While most of the current follows a relatively short, direct

    path between the probes, a significant proportion of it follows much

    longer paths. The conductivity between the two probes is a stong

    function of the specific conductivity of the liquid, the distance

    between the probes and the surface area and the geometrical arrange-

    ment of the probes. The very simple model that assumes that the

    current is conducted through two resistances set up by the froth and

    the pulp provides the following model (formulated in terms of resis-

    tances; see Figure 5(b»:

    R tot +

    where R is resistance per cm, L

    Zbot are the probe positions.

    between Rtot (=l/ktot ) and L.

    distance from the top probe, as

    is the interface level and Ztop and This implies a linear relationship

    This is true only for L some

    shown in Figure 4. A more comprehen-

    sive model must account for the geometrical design of the sensors and

    must in particular account for the different conduction paths followed

    by the current when the interface level is rising past the probe

    faces. This is illustrated in Figures 5(c) and (d), where the presence

    of an interface at the top probe introduces a distortion in the paths

    followed by the current between the probes.

    3.3 The measurement of conductivity

    Relatively cheap conductivity meters rely on the (simplified) circuit

    diagram shown in Figure 6. A high-frequency alternating voltage E is

    applied to a range resistor RR connected in series with the conducti-

    vity sensor (which has a resistance Rk ). The voltage drop VR across

    RR is easily related to Rk :

  • Level Control in Column Flotation Moys Page 6

    In th~ conductivity meters we used, this voltage was converted into a

    4-20 mA signal i k corresponding to a two-decade range on k (=l/Rk )

    and a 0-100% guage output p as follows:

    i k (mA)

    k (0- 1 )

    p(l)

    Thus the meter

    the relationship

    change in p or

    4

    RR/10

    0

    12

    RR 50

    20

    10RR

    100

    output is strongly and non-linearly related to k;

    is such that a 10% change in k results in a large

    i k , relatively independent of the value of k. This

    means that the signal is sensitive to changes in k over a twodecade

    range of k, something which could not be achieved with a linear

    instrument. The design of this instrument lends itself ideally to the

    purpose of this investigation as will be revealed below at the appro-

    priate dramatic moment!

    4. Equipment

    Experiments were performed in a square (12 cm x 12 cm) perspex labora-tory column 1,8 m tall. The pilot plant is illustrated in Figure 7. Two sources of feed material were available (water only; one source

    was dosed with HCl to raise its conductivity substantially above that

    in the other source, which was ordinary tap water). Turbine meters

    provided measurements of these flowrates. Wash water dosed with

    Dowfroth 250 was added at the top of the column. Gas was added through

    a canvas sparger; both wash water and gas rate were measured using

    rotameters. Two LTH DCM-l conductivity meters and an analog PID

    controller were available. All measurements were interfaced to an

    IBM-compatible PC which was programmed to display, print and store all data collected.

    5. Experimental Results and Discussion

    The objective of the work was to develop a level control method which

    would adapt to changes in feed conductivity. Several approaches were

    investigated.

    5.1 Setpoint obtained from measurement of pulp conductivity.

    2 Conductivity sensors were used. Each sensor consisted of 2 brass

    strips 1 cm long clamped around a 6 mm diameter perspex rod 30 cm

  • Level Control in Column Flotation Moys Page 7

    apart. The second conductivity meter was connected to a sensor approx-

    imately a,6m below the level sensor. This was used to obtain a

    measurement of pulp conductivity which was then passed through a vari-

    able resistor to obtain a remote setpoint for the level controller. It /

    was found that there was excessive interference between the two

    conductivity meters; this was reduced by making sure that the top

    probe of the bottom sensor and the bottom probe of the top sensor were

    connected to the earth connection of their respective meters, and

    finally overcome by increasing the size of these probes with a wire

    grid that spanned the crossectional area of the col~~n. This ensured

    that no current could bypass these probes and travel between the two

    non-earth probes of the sensors. Secondly it was found that matching

    the sensors (both in terms of the large scale geometry of the sensor

    design and in terms of the size of the probes used) was critical to

    the performance of the control system. This arrangement was used

    successfully to control level for a wide range of operating variables

    (feedrate, gas rate and wash water rate) but failed when large changes

    (e.g. 3:1) in feed conductivity were imposed.

    5.2 Use of a modified single conductivity meter

    The problems found in 5.1 above were probably caused by the need to

    use two conductivity meters plus associated sensors which interfered

    with each other and were difficult to match accurately for the whole

    range of conductivities used in the these tests. An examination of the

    circuit diagram for the meters led to a dramatically simplified solu-

    tion to the problem. This consisted of using the resistance across the

    second probe discussed above (used for measuring the pulp conductivi-

    ty) as the range resistor for the first conductivity meter, as shown

    in Figure 8. The governing equation for this meter then becomes

    where 'Y

    This arrangement eliminates problems associated with both unmatched

    sensors and unmatched meters and obviously simplifies the whole

    control system.

    One of the existing sensors was modified to provide the sensor shown

    in Figure 9. This contained only three probe surfaces, with the

    centre probe being used to provide the VR signal rather than the more

    general probe illustrated in Figure 8. Existing terminal connections

    on the conductivity meter.were used. The measurement was now a 4-20 mA signal denoted iq (to distinguish it from i k ) which was recorded as

    a variable q (0-100% of span). This signal was connected to the

    controller which was given a manual setpoint qsP = 15-20% as shown

    in Figures 10 and 11 below.

  • Level Control in Column Flotation Moys Page 8

    To characterise the measurement the signal q was recorded as the

    interface was allowed to drop over the full height spanned by the

    level sensor. The variation of interface level L with q (and 1) is shown in Figure 9. Clearly the sensor design was not symmetrical with

    respect to the middle probe surface; if this had been the case, then

    we would have obtained q - 50% when the sensor was completely submer-

    ged (L> 50 cm.), because in this case we would have had equal conduc-tivities (1 - 1) between the two probe pairs. No adjustments were made

    so that the necessity for probe matching could be assessed.

    The

    in

    ability

    the face

    of this arrangement to provide adequate control of level

    of operating changes is shown in Figure 10. Clearly

    changes in the gas superficial

    disturbances than changes in

    control scheme controlled level

    4 cm.

    velocity J G provide much more serious

    the wash water J W. Nevertheless the near 38 cm with maximum deviations of

    The effect of a setpoint change and a major disturbance in feed

    conductivity is shown in Figure 11. The setpoint response overshoots

    slightly but is nevertheless completely satisfactory. The conductivity

    disturbance produces very little effect on the level, in spite of the

    fact that conductivity changed by a factor of approximately 5:l!

    Extensive tests of various combinations of these disturbances showed

    that the control scheme was able to control level successfully in the

    face of disturbances which are generally much larger than those to be

    encountered during normal operation of flotation columns.

    The main problem that needs a solution before a rugged industrial

    instrument becomes available is the selection of materials of

    construction for the probe which will resist the corrosive environment

    found in different applications while maintaining a repeatable

    response over long periods of time. Reliability is more important than

    accuracy where level control is concerned, and the differential

    pressure cell is a tough competitor.

    6. Summary and Conlusions

    Various methods for level measurement have been reviewed. The work-

    horse of industry, the differential pressure cell is reliable but

    inaccurate. An instrument based on the measurement of conductivity has

    been developed which can provide accurate control of level under a

    wide range of operating conditions and changes in feed conductivity.

    The method must now be tested in an industrial environment to provide

    an instrument which will eliminate the need for the frequent operator

    attention which is typical of existing techniques.

  • Level Control in Column Flotation Moys Page 9

    7, Acknowledgements

    This work has been funded by a grant from the Chamber of Mines Block

    Grant made available in 1988, and by Mu1totec Cyclones (Pty) Ltd. The

    assistance provided by Mr G Gloag in setting up the experimental

    equipment and running the experiments is gratefully acknowledged.

    8. References

    Moys, M.H. and Finch, J.A., 1988a. The Measurement and Control of

    Level in Flotation Columns. Presented at the Int. Symp. on COlU~l

    Flotation, SME Annual Meeting, Phoenix, Arizona, January 1988.

    Moys, M.H. and Finch, J.A., 1988b. Developments in the Control of

    Flotation Columns. Int. J. Hiner. Process., 23 : 265-278.

    Moys, M.H and Finch, J.A., 1989. The use of Temperature Measurement in

    the Analysis and Control of Flotation Columns. Presented at the "Role

    of the Practical Metallurgist" Symposium, Mine Metallurgical Managers

    . Association of South Africa, Johannesburg, June 1989.

    Yianatos, J.B., Finch, J.A. and Laplante, A.R., 1987. The Cleaning

    Action in Column Flotation Froths, Trans. I.H.H., 96: C199-C205

    Yianatos, J.B., Laplante, A.R. and Finch, J.A., 1985. Estimation of

    Local Hold-up in the Bubbling and Froth Zones of a Gas-liquid Column,

    Chem. Eng. Sci., vol 40, no la, pp 1965-1968.

  • BO

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    L-___________________________ ~ __ ~ __

    460 470 4BO A90 500 510

    PRESSURE READING (mV)

    Figure 1. Variation of true interface level with pneumatic pressure

    signal.

    145

    E ~ -'

    v > .. --'

    i \

    Frolh Surface \-----~----

    \ \ \ \

    \

    \ ~

    "-'2 '-.

    \ \

    \

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    \ 20 '\

    \ \

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    Tesl No. 36

    J G = 1.6 J w =0.12 J F =0.64 J o = 0.08

    (I) O.L-_______ . ______________ ~L__

    Frolh Surface \,\\\---\~------

    \\ \ \ \ \ \\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \

    \ \ \ \ \ \ ~ '{io

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    +

    +* ...

    ... + ... ... ...

    ...

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    Figure 2. Measurement of interface level by analysis of temperature

    measurements obtained from probes located at the positions indicated

    in the Figure.

  • E

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    -J

    ~

  • MULTOTEC CYCLONES. COLUMN FLOTATION

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    O--~--l

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    FIgure 6. Simplified circuit for a conductivity meter.

    LEV EL PROBE

    Figure 7. Pilot flotation test ri' g.

  • Level ~ Probe ~

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    MULTOTEC CYCLONES. COLUMN FLOTATION

    r~ecorder

    or Cornputor

    v voltage to Current Conversion

    --1::r-----'--fO se i" a to rI E (Volts AC)

    Figure 8. Conductivity cicuit adapted for the measurement of

    conductivity across the interface relative to slurry conductivity.

    60

    w co 0

    E 50 0: D... ~ -1 -1 W W > > w W -1 -1

    40 w ~ 0 Lt :> f= 0: 0 W - - - => l- Q ~ 30 z

    0 0

    20

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    METER OUTPUT (('0) 0,2 0,3 0.4 0,5

    CONDUCTIVITY RATIO, ll=kLIkSf

    Figure 9. Variation of relative conductivity with interface level.

  • rr u c

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    Coni roller Output

    --'------"-- - _____ -LJ, ____ L __ L ________ ~ 800 900 1000

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    Figure 10. Level control subject to disturbances 1.n gas rate and WilSI! water rate.

    ;;g ~

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