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6
a
“HOLDERBANK”
Cement Seminar
Process Technology .....
F
‘Aspects of Raw
Material HomogenizationTABLE OF CONTENTS
4.1
4.
4.
PPeeees
INTRODUCTION AND DEFINITIONS
INTERPRETATION OF THE STANDARD DEVIATION
CHARACTERIZATION OF CHEMICAL FLUCTUATIONS
HOMOGENIZATION
Blending
Mode?
Homogenizing efficiency of blenders
Examples
Mixing
Mode?
2 Homogenizing efficiency of mixers
3 Examples
Homogenizing elements
Definition of fluctuations
Comment on the homogenizing elements
DETERMINATION OF CHEMICAL FLUCTUATIONS
Investigation of chemical fluctuations in the quarry
Chemical fluctuations after the preblending bed
Chemical fluctuations after the homogenizing silo
LITERATURE
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25SUMMARY
Raw material prehomogenization became a most essential part in modern
plants. As daily practice. demonstrates, chemical fluctuations often
influence kiln operation considerably by coating and ring formation as
well as encrustation and clogging problems. As a consequence not only
the operation is hampered but also the life time of the lining is
shortened.
The homogenizing efficiency is normally expressed by
Sa
Se
However a better value to judge a homogenizing element with regard to
effectiveness is the standard deviation (sp) of the homogenized mate~
rial. The standard deviation is only applicable if the samples are
statistically independent which can be verified by the correlation
function,
e
Homogenization is achieved by two procedures, by "blending" or
"mixing". Blending means that two or more material streams or layers
are combined whereas mixing signifies the homogenization of several
materials by agitation. By both methods good homogenizing efficiencies
are achievable. However a limit is given by the length of chemical
fluctuations that can be homogenized.
During the whole raw material preparation process the following homo-
genizing elements can be me
= selective quarrying
~ preblending bed
~ raw material proportioning
= grinding
~ raw meal or slurry homogenization
To select and dimension these homogenizing elements correctly, the
determination of the chemical fluctuations is of utmost importance. On
existing plants the chemical fluctuations are relatively easily de-
tected whereas on plants in projection they have to be estimated with
the aid of the drill hole prospection of the raw material deposit.
If the efficiency of the homogenizing elements has to be judged the
chemical fluctuations after each element must be determined.1. INTRODUCTION AND DEFINITIONS
As the daily practice demonstrates, chemical fluctuations in the raw
mix have a considerable influence on kiln operation e.g. coating and
ring formation as well as encrustation and clogging problems.
Therefore the degree of homogeneity directly influences the life time
of the refractory lining. Homogenization of the raw materials and the
raw mix is, thus of utmost importance.
Homogenizing efficiency
normally expressed by
Sa
ers
where
Sq = Standard deviation of the unhomogenized raw material
S = Standard deviation of the homogenized raw material
Standard deviation : s
x => = mean value
X, = single observations (samples)
n= number of observations (samples)Other_measures of variability
- The variance is the mean, square deviation of single observations from
‘the mean, expressed as s°.
- The coefficient of variation is a relative measure of the variability
- The range is the difference between the largest and the smallest value
R* ax ~ %nin
Problems with the homogenizing efficiency €
Since the homogenizing efficiency is a function of sq and sq, the
factor e can be low although the preblending bed or the homogenizing
silo works satisfactorily, i.e. the fluctuations s of the homogenized
material are within the tolerable limit. This is the case if the
original fluctuations sq are small. If, contrarily, sq is very large,
the fluctuation s@ can be unacceptably high although the homogenizing
efficiency factor is large and within the specifications.
Due to this ambiguity of the factor e, it is better to specify the
desired maximum value for the standard deviation s@ of the homogenized
material.
2. INTERPRETATION OF THE STANDARD DEVIATION
Practice has shown that in most cases the single observations follow a
"Normal Distribution" or a “Gaussian Distribution".
The "Normal Distribution" is determined by the mean and the standard
deviation shown in Fig. 1.Fig. 1 : "Normal Distribution"
For the normal distribution about 68.3 % of the observations are expected
in the interval x +/- 1s, about 95.5 % in the interval x +/- 2s and
99.7 % in the interval x +/- 3s.
If the distribution is not "normal", the standard deviation allows no
direct interpretation. Therefore other criterias to interpret the
variability are demanded (e.g. the range).
The following Fig. 2 illustrates another presentation of the standard
deviation, a plot related to time.CONCENTRATION
SMcLE OBSERVATIONS x
i as
z at/\ og
1h
1 2s
h
j t
| | |
Xm
at at at Te QUANT
wat
Fig. 2 : Chemical values and standard deviation versus time
Note : Normally the range of +/- 2s (about 95 % of all observations) is
taken into consideration, that means a confidence interval of 95 %
corresponding to +/- 2s.
um_number_of samples taken
To arrive at a meaningful sufficiently accurate standard deviation a
minimum number of 30 better 50 samples is required.
Estimation of s
A rough approximation of the standard deviation is achieved by taking
(Xaax 7 *min)
whereby single observations which are far out of the range are not
considered,3. CHARACTERIZATION OF CHEMICAL FLUCTUATIONS
A global feature to express the chemical fluctuations in a raw material
composition is the “standard deviation" as indicated in the previous
chapter.
However, the standard deviation gives no indication about the time
behaviour, i.e. the frequency and amplitude of the fluctuations. Fur-
thermore it is only applicable for statistically independent samples.
Interpretation of statistical independency
The samples of a series are statistically independent (uncorrelated)
if, in the average, a subsequent sample is at the opposite side of the
mean value. Contrarily, statistically dependent (correlated) means
that, in the average, a subsequent sample always lays at the same side
of the mean value. A mathematical description of this phenomena is
given by the correlation function.
The preassumption of statistically independent samples is only valid
for raw material samples located in the quarry sufficiently apart of
each other. The chemical difference of subsequent raw material samples
is reduced with decreasing distance between the samples and from a
certain point the latter become statistically dependent.
4 CONCENTRATION
Fig. 3 : Type of chemical fluctuationsThe correlation function
The correlation function indicates the statistical dependency of the
single samples in a series. It is calculated in the following way:
pic
Poaty= say | ES (45 = 8) je 8)
. =r
So bse a .
where:
k = parameter for the number of a, indicating the distance related to
time or material quantity between single samples
parameter indicating single samples
number of samples
&
5
distance or material quantity between single samples
DP cwetD
CORRELATION TERM T
Fig. 4 : Correlation function
Interpretation:
kat =0 full correlation (1)
kat >0 correlation (dependency) is valid
kat 2T statistically independent-10-
4, HOMOGENIZATION
Homogenization is achieved by two procedures:
- By “blending” where two or more material components are combined. The
materials are fed alternately or time delayed in a conmon system and
reclaimed simultaneously afterwards.
- By_“mixing" where two or more different material components are fed
Yna common system and agitated such as to achieve one homogeneous
component . :
4.1 Blending
4.1.1 Model
The following model idea describes the principle of "blending".
ALTERNATIVELY int
Fig. 5
Blending" mode1
Model description
The portions at . ii, (where m,, is the average input mass flow) are
entering the system subsequently Succeeding in time intervals 47 from
compartment 1 to k. Due to the different material levels in the
compartments the simultaneous extraction effects a time delayed combine-
ment of single material portions at .-ue
4.1.2 Homogenizing efficiency of blenders
Due to the special filling procedure of the individual silos and assum-
‘ing a sufficiently large aT it can be expected that the raw materials
extracted from each silo are statistically independent (uncorrelated).
Therefore the blending efficiency approaches the factor
1
es
Ver
If the material components to be blended are statistically dependent
(correlated), the blending efficiency can be much below above value.
4.1.3 Examples
"Blending" at the quarry
From two or more quarry faces the materials are fed simultaneously to
the crusher (selective quarrying).
"Blending" in a prehomogenizing bed
The raw material is stacked in several layers into the bed and re-
claimed in a way that all layers are simultaneously cut, i.e. “pre-
blended".-12-
"Blending" of the raw mix by proportioning
comRECTINE
OU
are A 0
OS oes
7 *
Bad MATERIAL
COMPONENT &
ANALYSIS
INTEGRATION
ADJUSTMENT
mie,
Fig. 6 : Raw mix proportioning
Note : The final raw mix is prepared by proportioning single raw
material components. This procedure effects the combinement of the
single material components, and thus "blending" resp. dampening of
their original chemical fluctuations is achieved. OF course by wrong
adjustments of the components, also very large errors (additional
fluctuations) can be introduced into the raw mix.-13-
Blending" of raw meal
Raw meal simultaneously extracted from parallel bins which have been
filled subsequently (time delayed) as shown on the model (usual solu-
tion before the large raw meal homogenizing silos were known).
"Blending" of slurry
Extracting from several parallel slurry tanks and feeding into a common
storage basin.
"Blending" of coal
(If no special preblending bed is provided).
Stacking the coal in longitudinal rows and reclaiming it from the front
with wheel loaders.
4.2 Mixing
4.2.1 Model
The following model idea describes the principle of mixing which is
done by agitation.
AGITATING
measunna |
Power 2
“WiGW COMPONENT A
“Low? COMPONENT 8
eAsuRING,
power
Fig. 7 : Mixing unitModel _description
-4-
It is assumed that two components (A) and (B) are fed in a mixer so
that they first are completely separated. By agitating, the components
are homogenized (Fig. 7).
4.2.2 Homogenizing efficiency of mixers
The homogenizing efficiency is shown by the plots below (Fig. 8 and 9)
where the measuring points
analyzed.
24
8 |
A@AGITATING TIME
Fig. 8 : Analyses of measuring
point 1
and 2 are periodically sampled and
APAGITATING TIME
Fig. 9 : Analyses of measuring
point 2-15-
Similar measurements on several systems have confirmed that above plots
follow the so-called "ideal blender" curve which is mathematically
described as follows:
Fig. 10 : “Ideal blender" curve
where : T= Characteristic agitation time
The mixer shall be agitated approx. 5 times (T) so as to achieve the
optimum homogenizing efficiency.
Comment
Mixing units are operated either batchwise or continuously. In both
cases mixers provide very good honogentzing effetenctes ase figures
above) .
However chemical fluctuations larger than the batch volume (in case of
batchwise operation) or the mean retention time, i.e. Y , v = volume
of the mixer, ¥ = volume flow, (in case of continuous operation) are
not homogenized and pass the mixer undampened.- 16 -
In case of continuous mixing it has to be assured that the mean
retention time is larger than the required characteristic agitiation
time T.
The mixing should also not be made too long since after a certain
mixing period the mix starts segregating again.
Fig. 11 illustrates the mixing behaviour between batch and continuous
operation.
CONCENTRATION
BATCH WISE MIXING
1 i
| CONTINUOUS MIXING
i i}
{ j
| !
Fig. 11 : Batchwise - continuous mixing4.2.3 Examples
oro
Homogenizing Element
Homogenization
Homogenizing Silo
Batch Type Continuous
Ry |
Slurry Tank resp. Basin
MillPra
4.3 Homogenizing elements
Homogenization takes place during the whole raw material preparation
process. It starts already in the quarry where blending occurs by
combining different components at the crusher feed and ends at the bin
feed where raw meal from several silos is extracted.
During the total process the following homogenizing elements can be met.
Homogenizing element
Homogenizing procedure
Type of homogenized
fluctuations
Selective quarrying | Blending Longterm to middleterm
fluctuations
Preblending Blending MNiddleterm to longterm
fluctuations
Proportioning Blending Longterm to middleterm
fluctuations
Grinding Mixing Shortterm fluctuations
Homogenizing Mixing / blending Shortterm to middle-
term fluctuations
4.3.1 Definition of fluctuations
The type of fluctuation as generally outlined in chapter 3, Fig. 3, can
be refined more specifically in time relation as follows:
Short term fluctuations
Middle term fluctuations
Long term fluctuations
fl min, h
; 1-5 days
5-7 days.-19-
4.3.2 Comment _on the homogenizing elements
Selective quarrying
If the quarry operation is well organized in a integrated preblending
bed concept and the raw material components are located not too far
away, premixing of certain material qualities by alternate crusher feed
can reduce long and middle term fluctuations to hourly or dayly
Fluctuations.
Preblending
Depending on the size of the preblending bed, fluctuations within the
range of 5 - 7 days (preblending bed capacity) are normally blended.
Proportioning
Nore component preblending bed concepts incorporate the raw material
qualities separated in two or more preblending beds. By proportioning
the single components to the final raw mix already blended, fluctua~
tions within pile capacity (approximately one week) or even exceeding
pile capacity can be combined (it means blended), As previously men-
tioned also very large errors (additional fluctuations) by wrong adjust-
ments can be introduced into the raw mix.
Grinding
If grinding is considered as a mixing element it holds true only for
short time fluctuations which are related to the retention time on
material particles passing through the mill.
Homogenizing silo
In the continuous homogenizing silo fluctuations of few hours depending
on the inactive volume of the silo, are mixed which is equal to the
retention time of material passing through the silo. Whereby in the
batch type homogenizing silo the certain batches are first mixed and
combined afterwards in the succeeding storage silo. There, fluctuations
amounting up to days are blended.-20-
5. DETERMINATION OF CHEMICAL FLUCTUATIONS
The determination of the chemical raw material fluctuations is manda-
tory in order to select the appropriate homogenizing elements and to
dimension them correctly. Furthermore it allows to judge their homo-
genizing efficiency.
Chemical fluctuations are detected by taking samples. The required
sample number depends on the quantity and the homogeneity of the
material to be sampled. The required number of samples rises with
increasing inhomogeneity of the raw material. With an increasing number
of samples also the sampling reliability improves. To be representa-
tive, the sample must be collected in an appropriate quantity depending
on the maximum grain size. The relation between maximum grain size and
necessary sample quantity is given in Fig. 17 as guide line.
Please note that the error of analysis has to be deducted in the
following way:
2
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adwes K b= b
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— .
—&
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f { 8
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‘Ov
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—l- t p re ‘oot
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(um) zis upeu6 wn xeua7
5.1 Investigation of chemical fluctuations in the quarry
On existing plants the chemical fluctuations of the quarried material
are detected by hourly samples taken after the crusher e.g. on a belt
transfer point. In order to get a representative sample, the whole
cross section of the transport belt ought to be sampled. Another, less
accurate method is to sample the dust of the blast drill holes.
On plants in projection the chemical fluctuations of the future quarry
must be determined WIth the aid of the drill hole prospection which 1s
executed to assess the future raw material deposit. The chemical
analyses of all drill hole cores are taken to calculate the standard
deviation. If the drill holes cover the total deposit area, sufficient-
ly accurate results can be expected for the overall chemical flucuta-
tions of the quarry. The absolute accuracy is only dependent on the
number of realized drill holes and the homogeneity of the deposit.
However, in the raw material preparation process not the whole quarry
Fluctuations are relevant but only the fluctuations within one blast
approximately or within the raw material quantity of one preblending
bed. Usually the raw material deposit shows some stratification so that
the chemical fluctuations are not equal in all three directions, i.e.
horizontally (length and width) and vertically. Thus, with the applic
tion of a certain quarrying method, the chemical fluctuations within
one blast are reduced as compared to the overall quarry fluctuations.
In order to assess this reduction, the chemical fluctuations in each
direction shall be calculated. Form these calculations the standard
deviation of an individual blast must be estimated.
5.2 . Chemical fluctuations after the preblending bed
The sample procedure after the preblending bed takes place in the
following way (Fig. 18).= 23
SPOT SAMPLES
CONVEYOR BELT
RECLAIMING
CUMULATINE SAMPLE.
SPoT SAMPLES
Fig. 18 : Sampling of the preblending bed
In order to judge the fluctuations at the exit of the preblending bed
the different cross sectional slices of the pile have to be compared.
It is that within one slice approximately 6 to 9 spot samples have to
be taken from which one cumulative sample is made. The samples can be
taken from the exit belt leaving the preblending bed on an equal
distance with a quantity per spot sample of about 10 kilograms. The
cumulative sample has to be prepared and respresentatively divided down
to 8 to 10 kilograms from which the analysis in the laboratory is made
representing then the concentration value of one cross sectional area.
In this described way 60 to 80 cumulative samples distributed over the
whole stock pile must be taken. Each sample must represent approximate-
ly the same stockpile mass.
From all cumulative samples the mean value and standard deviation is
calculated.- 24 -
Note : An achievable homogenizing efficiency of the preblending bed
obtained by the above sampling procedures (under the circumstance of
normal raw material qualities) amounts to
Sa
Sp
However, not the homogenizing efficiency e is important. But to judge
the effectiveness of the preblending bed, the most interesting value
represents Sq which is in normal case expected to be below 1 % CaC0,.
e- = 5-6
5.3 Chemical fluctuations after the homogenizing silo
To assure an appropriate representativity of the sample the following
considerations are essential:
- The sampling location is preferably on a meal discharge point where
the total material flow is accessible, if necessary by taking some
subsamples in short time intervals, which afterwards are combined to
one “spot sample".
- The samples themselves should be spot samples or “spot samples" as
described above, evenly distributed over the total sampling period.
= Period for continuous homogenizing silo:
one sample = 48 samples)
24h (e.g. every 30 min,
- Period for batch homogenizing silo: should contain 3 batches e.g. 3
time 8 h = 24 h again every 30 min. one sample = 48 samples).
- The sampling quantity per spot sample amounts to approx. 1 kg which
then is homogenized and divided.Bros
LITERATURE
qa)
(2)
(3)
(4)
(5)
(6)
(7)
J. Zulauf
Design of blending installations
TC-Report VA 72/4364/E
A. W. Gerstel and E. Luttekes
Homogenisieren in Mischbetten
2KG 1/1973
W. Gerstel
Homogenisierung von Schiittgut in Mischbetten
2KG 8/1980
R. Hasler
Vergleichmassigung im Mischbett
Tc-Report VA 75/4481/D
R. Hasler, K. VOlImin
Stand der Mischbett-Technik in der Zementindustrie
2KG 12/1975
R. Hasler, G. Lingford
Investigation on blending and homogenizing systems
TC-Reports VA 81/48099/E, VA 81/4810/E
R. Hasler
Vorhomogenisieren und Zwischenlagern von gebrochenen Rohmate-
rialien mittels Mischbett