ABSTRACT
Williams, M.C. and Meloy, T.P., 1983. Dynamic model of flotation cell banks -- circuit
analyses. Int. J. Miner. Process., 10: 141--160.
While all mineral industry flotation circuits are stable, they are sensitive to low-frequen-
cy perturbations in the feedrate. In both countercurrent and cocurrent circuits, the lead
cell is more sensitive to feed variations. The frequency response predicts the amount o f
extra cell capacity needed to handle the m a x i m u m feed due to a sinusoidal forcing func-
tion. Feedback loops are more significant than sump delays. The countercurrent 4 x 4
circuit floating quartz, with a 200-sec retention time, requires 75 minutes for the concen-
tration o f quartz in the input to the first cell to reach 95% o f its steady-state value. Coun-
tercurrent circuits were found superior to cocurrent circuits in all respects.
INTRODUCTION
(2) particle attached to a bubble in the pulp phase; (3) particle attached to a
bubble in the froth phase; and (4) free particle in the froth phase. Mika and
Fuerstenau (1969) assumed first-order kinetics; ideal mixing (spatially homo-
geneous phase); continuous flotation; quick mechanical removal of the froth,
eliminating the need to consider recycle phenomena; the existence of classes
of floatable material with constant and distinct Kj (flotation rates) tantamount
to the assumption of linearity; and finally, negligible solids' volume. Four
mass balances, one for each state, solved simultaneously yield the particle
densities within each state. Mika and Fuerstenau (1969) evaluated the intra-
cellular phenomenon occurring within single flotation cells. Concerning the
existence of delays between individual flotation cells in a bank, Mika and
Fuerstenau (1969) concluded that the resistance to pulp flow between cells
in contemporary flotation practice was "limitingly small" and, consequently,
did not develop the differential equations describing the hydraulic behavior
between flotation cells. Mika viewed flotation cells as being separated by a
marginal weir in contrast with Davis (1964) who limited the applicability of
dynamic models to pneumatic and batch flotation.
Gardener {1980) measured particle retention time with radioisotopes.
Thus, the concept of a retention time distribution arose. Without violating
the mass balance envelope around a flotation cell, an apparent volume could
be defined or empirically determined for each operating condition and flota-
tion equipment type. The apparent volume could be substituted for the actual
volume in any derivations involving mass balances.
In the literature, there is little or no information on feed rate oscillations
or delays in flotation circuits. Machinery-induced feed oscillation was noted in
Mining Engineering (1979), but no systematic investigation of sinusoidal in-
puts was found, nor was any quantitative treatment of intercellular delays.
TABLEI
MODEL
Assume a flotation cell floating a single mineral class,j, where the input
o f j t h class, Feedi, equals the sum of the underflow, Sj, float, Fj, and accumu-
lation, Tj :
Feedj = Sj + Fj + Tj (4a)
The input stream mass, Feed i for an increment of time, is the input flow-
rate, Q(t}, times the solids concentration of the input stream, Cij(t), times the
small time interval dt:
Feed i = Q(t)Cii(t)dt (4b)
The assumption of a perfectly mixed, homogeneous pulp makes the model
a lumped parameter model. This is tantamount to assuming the solids' con-
centration throughout the cell is the same during the interval dt. The under-
flow stream mass, $1, is the concentration in the cell during the interval,
Coj(t), times Q(t) times dr:
Sj = Coj(t)Q(t)dt (4c)
The accumulation term, Ti, is the mass of t h e ] t h class in the cell during the
interval dt, or the incremental change of the concentration in the cell times
the flotation cell's volume:
T i = d[ViCoi(t)] (4d)
The assumption of an apparent volume distribution, V/, is made. Ideally, the
retention time of all species should be identical, however, particle density
differences lead to increased residence time with increased density (Gardener,
1980).
146
The float term, Fi, is the product of the cell concentration, Coj(t), to the
first power (first order kinetics), dt, the apparent cell volume, Vj, and the
flotation rate constant Kj.
Fj = Coj(t)VjKjdt (4e)
Flotation rate distributions, Ki, are functions of size, mineralogy, shape,
etc., for a specific operating condition. As in the case of the Inoue and Imaizumi
(1966) and Mika and Fuerstenau (1969) models, the values of individual Kj
are assumed constant for a given species in the jth class and assumed indepen-
dent of total cell solids' concentration. Kj is a continuous function over all
the individual species in a mineral class. For example, in the flotation of galena
and quartz described by Davis (1964), quartz and galena are two, distinct
mineral classes. Within the classes are various species distinguished by size,
shape, degree of lockedness, density, etc.. The first-order kinetic assumption
restricts the feed to narrow particle size ranges as defined by Tomlinson and
Fleming (1963). Assuming quick removal of the froth eliminates the need to
consider any recycle phenomenon. Finally, the volume associated with the
solids is not considered, and thus assumed negligible.
Substituting eqs. 4b--e into eq. 4a, one obtains:
Q(t)Cij(t)dt = Q(t)Coi(t)dt + d[VjCo](t)] + VjKjCoj(t)dt (4f)
Assuming Q(t) = Q and dividing both sides of eq. 4f by Qdt:
Cij(t) = Coj(t) + d[Coj(t)] /Aj + KjCoj(t)/A j (5)
where ,4i is the inverse retention time distribution, Q/Vi. In eq. 5, at steady-
state, the accumulation term is zero, and Co1 and Cij are constant. Under
these conditions eq. 5 reduces to:
Cij = Coj + KjCoj/Aj (6)
Solving eq. 6 for Coj,
Coj = UjCi1 (7)
where,
Uj =Aj/(Aj + Kj) (7a)
Substituting eq. 7 into the float term of eq. 6, the float concentration, Pj, is:
Pj = RjCij (8)
where,
Rj =Kj/(Aj + Kj) (8a)
Equations 7a and 8a contain the steady-state transfer functions for the
float concentration, R], and underflow or cell concentration, Uj, of a single
flotation cell. At steady-state, a large Cij increases Pj for constant Kj and Aj.
Also, small Aj and large Kj result in a large Pj.
147
Q Q
o Q
¢~--J Cocurrent (coc) 3x3 F I
C o u n t e r c u r r e n t Ix 3 Cocurrent Ix 3
2-
Countercurrent 3x 1
_~ Seines, no feedback lx 3
Cocurrent 3x 1
In the mineral industries, where many, individual separation cells are used,
certain spatial arrangements of the cells into banks or circuits are c o m m o n .
Figures 1 and 2 illustrate seven possible flotation circuits. In these figures,
" Q " , represents make-up water whose addition occurs when a float is re-
wetted prior to refloating; " O " represents the location of a dewaterer unit
operation included when m any underflows o f flowrate " Q " are recycled,
dewatered and refloated, i.e., when the feed must be concentrated. Applying
the c o m p a c t circuit analysis techniques of Meloy (1983a, b) to the seven
circuit ty p es in Figs. 1 and 2, the steady-state or overall transient transfer
functions are obtained. The overall transient transfer functions for Pl(s),
the float c o n c e n t r a t i o n of the final cell in the p r o d u c t leg, for t he seven
designs with identical cells with initial concentrations zero, are:
COC, 4 X 4 circuit
COC, 4 X 1 circuit
Pi{s) = Rj(s)4Cii(s)/[1 - - R l ( s ) U j ( s ) -- Ri{s)2Ul(s ) -- Ri(s)3U/(s) ] (22)
COC, 1 X 4 circuit
Pj(s) = Ri(s)Cij(s)/[ 1 -- Rj(s)Uj(s ) -- Rj(s)Ul(s) 2 -- R](s)U/(s) 3] (23)
COC, 4 X 4 circuit
Pi(t) = 0 . 0 5 8 exp (--3.29t) -- 0 . 5 6 0 e x p (--0.10t)
+ 0.155 e x p ( - - 2 . 3 2 t sin 0 . 8 5 t ) + 0.001 exp (--2.32 cos 0 . 8 5 t )
+ 0.500 (25)
CC, 4 X 4 circuit
P j ( t ) = 0.186 e x p ( - - 1 . 2 3 5 t ) + 0 . 0 8 3 e x p ( - - 2 . 7 6 5 t )
- - 0.635 e x p (--0.15t) + 0.025 exp {--3.85t) + 0 . 5 0 0 (26)
CC, 4 X 1 circuit
Pj(t) = 0 . 1 9 8 -- 0.36 e x p (-<).38t) + 0 . 0 3 8 e x p (--3.62t)
+ 0 . 2 6 5 e x p (--1.39t) - - 0 . 1 4 1 e x p (--2.61t) (27)
CC, 1 X 4 circuit
P i ( t ) = [--1.53 e x p (--0.38t) -- 0.16 e x p ( - - 3 . 6 2 t ) + 0 . 0 5 9 e x p (--1.39t)
+ 0 . 0 3 2 e x p ( - - 2 . 6 1 0 + 1.60] -- 2 [ - - 0 . 5 8 5 e x p (--0.38t)
- - 0.061 e x p ( - - 3 . 6 2 t ) + 0 . 1 5 8 e x p (--1.39t) + 0.085 e x p (--2.61t)
+ 0.401] (28)
150
COC, 4 X 1 circuit
Pj(t) = --0.220 exp (--0.53t) + 0.112 exp (--3.0t) + 0.253 exp
[--2.23t sin (0.8t + 359°)] + 0.112 (29)
COC, 1 X 4 circuit
Pj(t) = --0.110 exp (--3t) -- 0.688 exp (--0.53t) + 0.146 exp
[--2.23t sin (0.80 + 317°}] + 0.920 (30)
FREQUENCY RESPONSE
DELAYS
The only fair comparison which can be made between circuits must be on
the basis of production of desirable species (yield and sharpness) for a given
feed. The total concentrations of all mineral species with rate constants Kj
must be summed (eq. 9). Meloy (1983a) has shown that for symmetrically
arranged heavy-media circuits, the steepness of the recovery versus particle
density curve increases with the number of additional units. The use of eq.
8a, the steady-state separation function, can serve in steady-state circuit
design and analysis. Circuit design and selection can also be based on many
features of dynamic responses such as response times which are obtained by
plotting concentration versus time.
16
14t
05
02
O0 I ~ t I
0 10 100 200
W ( r a d min ]
TABLE IIb
Oscillation of float of cell 1 for a retention time of three minutes with three different
flotation rates, Kj, at a function frequency W
TABLE IIc
Oscillation of sink of cell 1 for a retention time of three minutes with three different
flotation rates, Ki, at a function frequency W
TABLE IId
Oscillation of sink of cell 2 for a retention time of three minutes with three different
flotation rates, Kj, at a function frequency W
5C 8O
67 67
6C 60
4o ~ 4o
2O 2O
I I I 1(3 I l I 810 I t
O( 10 20 30 4 50 60 70 °o ~o 20 3'0 4'o 5'o 6o 7'0 ~'o
t (min) t (rain)
Fig. 4. Percentage of time versus steady-state reached by a 4 x 4 COC floating quartz with
a flotation rate of 0.005 sec-' and a retention time of 200 sec. Note 67% and 95% of
steady-state reached in 30 and 70 minutes, respectively.
Fig. 5. Percentage of steady-state reached by a 1 x 2 CC floating quartz with a flotation
rate of 0.005 sec-' and a retention time of 400 sec. versus time.
TABLE TIT
CC, 4 x 4, Kj = 0.3 min -1
, / / \'~ I \ ~/r
~o4o ~' \ , /
030 / /
o o, ;
0
O I 2 3 4 5 6 7 8 9 10 11 12
t (rain)
OB
•
/¢3
O
07
0.6
OE
~ 04 mJA
O ~n
02
01
0
0.01 0 0 2 Q03 0,04 0.05 0.06 0.07 0.08
K (sec -~)
DISCUSSION
tion, the first cell requires special consideration. To avoid the deleterious
effects of operating at high pulp densities in the first cell, such as floating of
gangue along with ore, the frequency response can be used to predict the ac-
tual expected maximum concentration due to oscillations and to estimate
the actual required flotation capacity necessary to insure effective operation.
The frequency response plots, Fig. 3, show that all cells in the flotation
bank are sensitive to very low frequency inputs. To handle a sinusoidal forc-
ing function with frequency 18 per hour, the 1 X 3 COC requires a 60% in-
crease in capacity. An oscillating feed forcing function could be created by
performing repetitive task influencing solids concentration every 4 minutes.
During start-up and shut<town of a mineral processing circuit, the time to
reach steady-state is long. For a 4 X 4 COC flotation bank with a residence
time of 4 minutes per cell it takes 1.5 hours to reach 95% of steady-state.
During start-up, a plant with six, mineral processing, feedback, unit opera-
tions in series, may take a day or more to reach 95% steady-state. The time
for the systems to reach steady-state is greater than the sum of the individual
subsystems to reach equilibrium.
Calculation of response times for a given mineral species provides a criteria
for distinguishing among flotation banks, especially where the plant process
is started and stopped daily. Grade and recovery are impaired during non-
steady-state. Transient responses also can be used directly in a first approxi-
mation to determine the range of operation required by control and sensing
equipment, such as assay and percent solids instrumentation.
Delays influenced both transient and frequency responses. The correct
approximation of the delay transfer function is important if the dynamic
model is to accurately describe the flotation separation circuits. Both tur-
bulent flow in pipes of a small length and sumps can accurately be approxi-
mated by well-mixed reactors, although detailed analysis may involve a more
accurate delay transfer function.
In the circuit responses to step function inputs shown in the model sec-
tion, there is a lower than anticipated number of eigenvalues in the solutions
of the symmetric forms. This occurs only if all the cells in the flotation cir-
cuit are identical. Fortunately, this assumption and the attendant simplifica-
tion expedite the dynamic analysis generalizations which are the focus of this
investigation.
While this analysis of flotation circuits deals with a pure mineral species,
flotation circuits operate on a number of mineral species simultaneously. The
effects are additive (eq. 9). Constructive and destructive interference occur
between the various responses in determining the total, undifferentiated
mass flowrates, but the concentration and location of a given mineral species
in any cell, at any time, may be determined. Because each species has its own
flotation rate, the solid's concentration fluctuation in a given cell is mitigated
by a variety of minerals in the float.
159
SUMMARY
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