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Abstract
The collection zone recovery of a flotation column was modeled using a rectangular distribution function for the kinetic rate
constant and a tank in series model with different vessel sizes for the residence time distribution. It was demonstrated that an ana-
lytical expression can be obtained and that data from large industrial columns fits well, keeping the parsimony principle by using a
simple and practical solution. An example for the estimation of the maximum kinetic rate constant, useful for scale-up purposes, is
shown using data from industrial flotation columns.
2005 Elsevier Ltd. All rights reserved.
characteristics, machines and equipment involved, where the term (1 ekt) represents the mineral recov-
ery of a first order process with invariant kinetic con-
*
Corresponding author. Fax: +56 32 654478. stant k, as a time function. F(k) is the kinetic rate
E-mail address: juan.yianatos@usm.cl (J. Yianatos). constant distribution function for mineral species with
0892-6875/$ - see front matter 2005 Elsevier Ltd. All rights reserved.
doi:10.1016/j.mineng.2005.01.014
1374 J. Yianatos et al. / Minerals Engineering 18 (2005) 1373–1377
different flotation rates, and E(t) is the residence time process (Boutin and Tremblay, 1962) where the plug
distribution function for continuous processes with dif- flow with axial dispersion model was the most widely
ferent mixing characteristics. Thus, according to Eq. used by researchers (Sastry and Fuerstenau, 1970; Dob-
(2), the mineral recovery depends on the mixing level by and Finch, 1986; Laplante et al., 1988; Finch and
and the actual mean residence time that is related to Dobby, 1990; Luttrell et al., 1993; Tokoro and Okano,
the effective pulp volume in flotation equipments 2001). This kind of model suits the hydrodynamic
(Yianatos et al., 2003). Rearranging Eq. (2), yields behavior in pilot scale columns well, but the selection
Z Z of proper boundary conditions is difficult and the ana-
1 1
R lytical solution is commonly not possible. Therefore,
¼1 ekt F ðkÞEðtÞ dk dt: ð3Þ
R1 0 0 numerical solutions must be considered (Xu and Finch,
1991; Mavros, 1992).
Another shortcoming for the use of this model is that
2. Process modelling under axial dispersion conditions the dimensionless ves-
sel dispersion number must be lower than 0.2 (Leven-
The column flotation modelling distinguishes the col- spiel, 1966), however the literature reports vessel
lection and froth zones in order to calculate the overall dispersion numbers significantly higher (0.3–2.7) for
recovery RG, according to Finch and Dobby (1990), industrial columns (Laplante et al., 1988; Goodall and
OÕConnor, 1991; Yianatos and Bergh, 1992; Yianatos
RC RF et al., 2005).
RG ¼ ; ð4Þ
ð1 RC þ RC RF Þ On the other hand, with the help of radioactive tracer
where, RC represents the collection zone recovery and technology, it was shown that large size flotation col-
RF represents the froth zone recovery. umns perform closer to a perfect mixer. Plus a model
consisting of two small reactors (residence time sS) in
series with a larger one (residence time sL) gave the best
2.1. Collection zone model fit for a number of large size industrial columns, both
for liquid and solid (Yianatos et al., 2005). This model
The flotation model for the collection zone will be de- is represented by the following equation:
rived from Eq. (3), assuming a rectangular rate constant
t
distribution function F(k) and a tank in series model to t
t
sS
a e sS
þ a e sL
describe the mixing condition of industrial size columns. EðtÞ ¼ ; ð6Þ
ðsL sS Þ
2.1.1. Kinetic constant distribution F(k)
where
In flotation processes, it is common to observe miner-
als with different characteristics and sizes floating at dif- sL
a¼ ð7Þ
ferent rates. Thus, several models including normal, ðsL sS Þ
gamma or rectangular distributions have been used to
make the description of the flotation phenomena more and
flexible. t ¼ treal sP ð8Þ
In this study the rectangular distribution was used for
the kinetic constant distribution F(k) in order to keep with treal being the real time and sP the time delay of the
the parsimony principle in the sense of using the mini- model.
mum number of parameters. Thus, the model has only The conceptual diagram of the mixing model for the
one parameter, which corresponds to the maximum collection zone in large size industrial columns is pre-
kinetic constant kM sented in Fig. 1.
The integrals A and B in Eq. (10) have analytical solu- 3. Case example
tions and can be solved using the integration by parts
method (u dv = uv v du). The actual or effective mean residence time in an
industrial column can be calculated from Eq. (19), where
1 VEff is the effective pulp volume and Q the pulp flowrate
A¼ 1 a lnðk M sS þ 1Þ; ð11Þ
k M sS þ 1 V Eff
s¼ : ð19Þ
B ¼ a lnðk M sL þ 1Þ: ð12Þ Q
From plant experience, it was shown that the effective
Replacing Eqs. (11) and (12) in Eq. (10), the result is volume in industrial columns was around 77% of the
columns total volume VT (Yianatos et al., 2003). Thus,
RC 1 1 k M sL þ 1 the following relation will be considered for this
¼1 1 þ a ln :
R1 k M ðsL sS Þ k M sS þ 1 k M sS þ 1 purpose:
ð13Þ
V Eff ¼ 0:77 V T : ð20Þ
Eq. (13) is a new relation which allows for estimation of Also, the total residence time s is given by
the maximum kinetic rate constant from industrial col-
umn operating data. s ¼ sL þ 2 sS þ sP : ð21Þ
1376 J. Yianatos et al. / Minerals Engineering 18 (2005) 1373–1377
RC 4
w¼ ¼1
R1 3 kMs During these tests, the mineral quality was unstable
12 10 2ð5 k M s þ 6Þ and the global recovery was low, 40–50%, while the typ-
1 þ ln : ð24Þ ical recoveries were 60–70%. Difficulties were also ob-
kMs þ 1 9 k M s þ 12
served to keep the final concentrate grade near the
From Eq. (24) the effect of pulp residence time and max- target value, 30% copper, for a typical chalcopyrite
imum rate constant on the dimensionless mineral recov- ore. Thus, from Fig. 2, it can be observed that despite
ery is shown in Fig. 2. Here, the exponential nature of the column which was operated at relatively constant
the recovery can be seen, approaching R1 at larger res- pulp flowrate with a mean residence time of 12–
idence times and larger rates constants. 14 min, and despite changes in the manipulated vari-
Also, the experimental data from an industrial col- ables which were less than 15%, the overall recovery
umn of 2 · 6 · 13 m in size, operating at El Salvador and then the maximum kinetic rate constant varied
concentrator in Chile, are presented in Fig. 2 in white more significantly, i.e., kM values in the range 0.21–
circles. For this purpose, a maximum collection zone 0.39 min1 were found. This variation can be attributed
recovery R1 equal to 90% was assumed. to changes in mineralogy, feed grade, soluble copper
The operating conditions for the sampling points of a content and chemical conditioning, as well as the control
flotation column at El Salvador, with a total column system action trying to reach the final concentrate grade.
volume of 156 m3, are presented in Table 1.
4. Conclusions
1.0
τ=16 min The collection zone recovery of a flotation column
τ=14 min was modeled using a rectangular distribution function
τ=12 min for the rate constant and a tank in series model, consist-
Dimensionless recovery, ψ
0.9
Data ing of one large and two small size units, to account for
the residence time distribution. Thus, an analytical
0.8 expression relating to the dimensionless recovery
w = R/R1 and the dimensionless kinetic term kMs was
derived.
0.7
The column recovery can now be calculated in a more
flexible way considering the use of a rectangular rate
0.6 constant distribution while respecting the parsimony
principle, or the use of a minimum number of
parameters.
0.5 The model was applied to evaluate the kinetic rate
0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0
constant of an industrial column, and a range of kM val-
Maximum rate constant kM, 1/min ues 0.21–0.39 min1 was found. Work is now under
Fig. 2. Dimensionless recovery versus kinetic rate constant at different development to explore the use of this model for scale-
residence time. up purposes.
J. Yianatos et al. / Minerals Engineering 18 (2005) 1373–1377 1377