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Mass and Heat Balances Grinding PDF
Mass and Heat Balances Grinding PDF
TABLE OF CONTENTS
1.1 INTRODUCTION....................................................................................................... 3
1.2 MASS BALANCE ....................................................................................................... 4
1.2.1 The General System ................................................................................................ 4
1.2.2 Total Mass Balance ................................................................................................ 5
1.2.3 Partial Balances ..................................................................................................... 7
1.3 GAS BALANCES ........................................................................................................ 9
1.3.1 General Theory....................................................................................................... 9
1.3.2 Measurement and Calculation of Gas Flows ....................................................... 10
1.3.3 Determination of Gas Flows ................................................................................ 16
1.3.4 False Air Calculation ........................................................................................... 27
1.4 HEAT BALANCE ..................................................................................................... 33
1.4.1 Introduction .......................................................................................................... 33
1.4.2 Heat Balance for the Mill System ......................................................................... 33
1.5 CONCLUSION.......................................................................................................... 34
1.6 APPENDIX I .............................................................................................................. 35
1.7 APPENDIX II ............................................................................................................ 37
1.8 APPENDIX III........................................................................................................... 39
1.9 APPENDIX IV ........................................................................................................... 42
1.1 INTRODUCTION
The mill installation is supplied with materials, gas flow and heat energy. The mass, gas and
heat balances for the mill system should be in equilibrium.
There are various reasons for which it is of interest to know the mass and heat balance. These
are:
In this module the significance of mass and heat balance and relevant factors identified for
calculating mass and heat balances will be described. The subjects will be covered in the
following order:
Mass Balance
Gas Balance
Heat Balance
The major part of planning the production, control of the quality and control of the process is
based on mass balances. The mass balances can be calculated as total balances or partial
balances. All of them can be divided in non-equilibrated and equilibrated balances (See
Figure1). This section will deal with the following aspects of mass balance:
The general system of the mass flow is shown on Figure 2. The total quantity of material A(t)
in the system, which has CjA(t) concentration of component "j", is a sum of the different
material flows In(t), which have different concentration of common component "j". The output
of the system consist of different flows Ok(t), which have different concentration of component
"j".
N K
dA t
I t Q
n 1
n
k 1
k
dt
There are two principal cases of the above mentioned equation:
The first one is very complicated, and is normally limited to considerations on large time
horizons, f. ex. daily, weekly, and monthly balance of the production, contents of stocks, etc.
The second case is less complex, and the equation is reduced to:
N K
I t Q
n 1
n
k 1
k
This mass balance can represent output from mills, kilns, crushers etc. at a stabilised
production. Figure3 shows the raw mill system, where the mill is fed with lime-stone, marl and
sand, and supplied with drying air. Mill output consists of raw mix and humid air. A typical
example is shown on the "Raw Mill Production Summary" (see Figure 4).
Quantity [tons]
Dry limestone 874,2
Dry marl 134,5
Dry sand 51,0
Raw meal production 1.059,7
Partial Balances
Component balances
Molecular balances
t O k t C kO, j t dA t
N K
I n t C I
n, j
n 1 k 1 dt
The component balances can also be divided in non-equilibrated and equilibrated systems. The
non-equilibrated component balance requires a large amount of information f. ex. process
control on filling of pre-homogenising stores, where a fixed quality is required. In cases where
the flows and concentrations do not vary in relation to time (equilibrated component balances),
the general equation is reduced to:
I t C t O t C t
N K
I O
n n, j k k, j
n 1 k 1
This equation is used for programming and proportioning purposes (assuming that the quality
of the raw materials is known) such as raw material proportioning, proportioning of stockpiles,
programming of quarry work and control of the dosage of gypsum to the cement mill.
There are no chemical reactions; therefore, this is a component balance, whereby the general
rule is valid:
INPUT = OUTPUT
INPUT
I t C
n 1
n
I
n , SO 3
t
0 ,5 46 ,1
86 h
6 th 6 0 2 0
t t t
h h
100 100
0 , 43 2 , 77 0 0 3, 20
OUTPUT
O k t C k , SO 3 t 100
K
3, 20
h 3, 20
t
k 1 100
Grasim Industries 8 FLSmidth 2009, all rights reserved
Mass and Heat Balances
The molecular balances are very difficult to handle, taking into consideration that chemical
reactions take place in the system. The same is the case for non equilibrated molecular
balances, where no chemical changes occur.
General Theory.
Measurement and calculation of gas flow.
Determination of gas flow.
False Air Calculation.
The major part of the process which takes place during the burning of cement clinker involve
gases, for example:
b) Heating
In the cement industry, heating takes place by combustion during which hot
gases are formed and heat content exchanged with a solid phase.
c) Cooling
In the cement industry, two main types of cooling takes place; one is cooling by
gases and the other is cooling by evaporation of water.
d) Transport
In various types of equipment, air or gases are used to transport powdery
materials e.g. air slides, screw pumps, Flux pumps, air lifts etc.
As it was mentioned in section 3.1, there are various reasons for which it is of interest to know
the gas flows which circulate between the different systems. The gas balances are formed on
the basis of total balance in the system. During the process, it is possible that certain
FLSmidth 2009, all rights reserved 9 Grasim Industries
Mass and Heat Balances
compounds change phases in such a manner that part of the solid material in the system leaves
in the form of gases. The reasons for that are chemical reactions such as decarbonisation or
physical-chemical reactions such as evaporation. Sometimes it is possible to separate the
balance of water/vapour from the gas balance. In this way three balances are developed on basis
of the total balance:
Based on the three balances, one balance of solids may be calculated. This balance comprises
the balance of dry solids and the part of the moisture balance for the water or moisture which
has not evaporated. In the same manner it is possible to calculate the total gas balance, i.e. the
balance of dry gases plus the part of the moisture balance that comprises the vapour, i.e. the
water evaporated during the process.
The total gas balance in the system contains several unknown variables. These variables must
be determined on the basis of specific measurements. In order to determine the total balance,
the following specific measurements are performed:
Gas analyzer.
Determination of the dew point temperature.
The most appropriate measurements depend on the particular situation and should be decided in
each actual case.
In cement factories, there is a great need to find out the different air and gas flows through
mills, kilns, coolers and filters.
To determine these flows several measurements and calculations exist, and they will be
presented as follows:
Chemical composition
Physical conditions.
As a point of reference for the physical conditions used: 0oC and an atmospheric pressure of
10333 mm WG (pressure at sea level). The specific gravity, ρot, of a dry gas under these
conditions, is calculated on the basis of the volumetric percentages of its content of CO 2, O2,
CO and N2:
If the physical conditions are different from the reference conditions (10333 mm WG, 0oC), the
following formula is used to find the specific gravity of the actual condition.
273 b p
t ot
273 t 10333
kg
m3
where t is the actual temperature, measured in oC, p is the relative pressure (in duct), b is the
barometric pressure which depends on the altitude h, in m, above sea level, and which is
calculated as:
10000
Barometric pressure b ( mmWG)
9000
8000
7000
6000
0 1000 2000 3000 4000
Altitude h (meter)
In this way, it is possible to calculate the specific gravity of any dry gas, on condition that its
chemical composition, temperature and barometric pressure are known.
The dew point is an important value because a decrease in the gas temperature to a value
below dew point will cause condensation of the water vapour and may result in problems
during operation.
The dry bulb temperature refers to the intensity of the heat content of substance as measured
with a common thermometer in degrees.
The wet bulb temperature is a method for determining the amount of moisture in air or gases.
This is accomplished by using a standard, common thermometer with a wick or a sock on the
sensing element (bulb). With the wick wet with clean water the thermometer is inserted into the
gas stream or whirled through the air to create air movement over the bulb and wick. The
resulting cooling effect from the evaporation process lowers the thermometer reading. The
temperature will drop corresponding to the rate of evaporation, which will be determined by the
amount of moisture in the air or gas stream. The more moisture there is present in the air, the
slower will the rate of evaporation be, thus resulting in higher wet bulb reading.
The dew point temperature is defined as the temperature at which air is 100% saturated with
moisture and the moisture begins to condense out of the air. When air or gas steam is cooled it
becomes denser and, therefore, can hold less moisture. When the air is cooled to the
temperature at which it cannot hold any more moisture, it is 100% saturated, and this represents
the dew point temperature. The relation is shown graphically in Figure 7 (Dew Point
Temperature).
It should be pointed out that in lowering the temperature of the air until the dew point is
reached, the moisture content of the air does not change. However, each change in the
temperature changes the percentage of humidity in the air, since the ratio of moisture in the air
to the amount of moisture the air can hold changes with the temperature.
Humidity is a term used to describe the presence of moisture in the air. The amount of
moisture that the air will hold depends upon its temperature. The warm air will hold more
moisture than the cold air.
Relative humidity refers to the amount of moisture in a given volume of air compared to the
amount of moisture the air would hold if completely saturated at the temperature at which the
comparison is being made. The relative humidity is expressed in percentage.
Absolute humidity is the ratio between the amount of water and gases expressed as kg H2O
per kg gas. If the units are moles, then the ratio expresses the absolute molar humidity. In most
cases the molar ratio is more convenient to use, due to the fact that it is easy to make
conversions between molar and volume ratios on basis of the ideal gas laws.
Determination of the absolute humidity may be done graphically by using Figure 8 (Water
Vapour in Air and Gases). The graph shows the ratio between water and dry gas amount wo and
the ratio between the water and wet gas amount y = wo/(1+ wo).
0,8 0,8
0,6 0,6
0,5 0,5
0,4 0,4
0,3 0,3
0,2 0,2
0,1 0,1
0,0 0,0
10 20 30 40 50 60 70 80 90 100
Dew point temperature (degC)
a) Measure the temperature of the dry and the wet thermometers on the chosen gas and
water vapour mixture.
b) Look up the figure "Dew Point Temperature". The dew point is then found at the co-
ordinates given by the wet and dry thermometer temperatures, respectively. The
value of the dew point temperature is determined by interpolation between the curves
ranging from 0 to 80oC.
c) When the dew point has been determined as described in points a) and b) proceed to
Figure 8. Water Vapour in Air and Gases. Select the dew point temperature on the
abscissa and follow the corresponding vertical line to the interpolated curve for %
CO2 (as determined by Orsat analysis). Then follow a horizontal line from the
intercept to the ordinate axis, where the absolute humidity in kg vapour per kg dry gas
can be read.
If it is required to determine the molar humidity, then the above value should be
converted to a volume ratio at the required conditions by using the corresponding
water and gas densities.
d) Knowing the absolute humidity of the gas wo, it is possible to calculate the specific
gravity of the moist gas, - i.e. dry gas + water vapour, according to the following
formula:
1 wo
o
1 w
kg
Nm 3
moist gasses
o
ot 0,8
Examples of calculating gas humidity are available in Appendix I of this module.
Evaporation of water (transformation from liquid into steam) can happen not only when the
water is boiled at 100 °C. The evaporation heat for the water heated up to 100 °C is 539
kcal/kg, Since the heat, used for heating the water to 100 °C, is 100 kcal ( specific heat 1
kcal/kg), the total heat consumption will be 639 kcal/kg. Knowing the specific heat for the
steam between 0 °C and 100 °C, it is possible to calculate the evaporation heat at the
temperature lower than 100 °C (see figure 9). If we assume that the average specific heat of the
steam is 0.44 kcal/kg, the evaporation heat at 0 °C will be:
Evaporation of water
700
630,2
595 639
600
500
Heat content (kcal/kg)
400
300
200
100
100
80
0
0 10 20 30 40 50 60 70 80 90 100
Temperature (degC)
In this lesson, the methods A and B are treated, while C is treated separately.
The measuring point is very important for the reliability of the measurement when D is the
diameter of a duct. There should not be curves, dampers or other obstructions in a distance of
minimum 5 x D before and 2 x D after the measuring point. If possible, a point with small dust
load and maximum distance to cyclones, separator and fans should be chosen.
The total pressure, p, is the sum of the dynamic pressure, pd, and the static pressure, ps.
p = pd + ps
With the Pitot tube all three types of pressure can be measured by connecting simple
manometers to the Pitot tube in the following way:
p: manometer connected to +
ps: manometer connected to -
pd : manometer connected to + and -
p dm
pd
n
Knowing the dynamic pressure it is possible to calculate the air velocity in the duct, v, as:
v 4,43
f * p dm
m sec
t
where f is dynamic pressure correction and ρ is the specific gravity of the gas.
f = 1 for normal Pitot tube, f = 0,7 for S-type (normally marked on the tube) – see figures 10a
and 10b)
Knowing the air velocity the air or gas flow in the duct can be calculated as:
Q1 3600 D 2 v t kg
4 hour
If it is necessary to find the flow in m 3 or Nm3 the following relations can be used:
Q Q1 t
1
m3
hour
Q 0 Q1 o
1
Nm 3
hour
In the duct from R1S11 to the bottom of the separator, Pitot tube measurements have been
carried our as follows:
Data:
Duct diameter = 2000 mm.
pd(a) pd(b)
0,97 D 1 2 mm WG
0,90 D 12 18 mm WG
0,81 D 85 75 mm WG
0,68 D 120 115 mm WG
0,32 D 125 120 mm WG
0,19 D 70 80 mm WG
0,10 D 20 15 mm WG
0,03 D 2 2 mm WG
Calculate the air flow rate in m3/s, m3/min, Nm3/min and kg/min.
The gas density is: ρt = 1,05 kg/m3 (ρo at 0oC and 1 atm)
ρo = 1,30 kg/Nm3
Q 2,0 2 27,02 84,9 m s 5093 m min
3 3
4
t 1,05
Q0 Q 5093 4113 Nm min
3
0 1,30
- +
pd
+ -
pd
Figure 10b. S-type Pitot tube is used, if the gas stream is dust filled
Fan Characteristics
To determine the air flow in a system by means of fan characteristics the following rules and
procedures should be used:
Rule No. 1:
Fan characteristics are valid only at the conditions given together with the curves (fan
revolutions, temperature, pressure and specific gravity).
Rule No. 2:
Because of rule No. 1, it is necessary to distinguish between diagram and actual values:
1) Calculate the specific gravity of the gas/air at actual conditions, using the
equation:
273 b p
t o
273 t 10333
kg
m3
2) Based on the actual power consumption of the fan, PA, the diagram value can
be calculated as:
n
3
PA1 PA 1 1
n t
3) With PA1 calculated, use the fan characteristics to find Q1 and Pt1.
4) To transform Q1 and Pt1 to actual values use the following formulas:
Q Q1
n
m3
s
n1
2
n
Pt Pt1 t mbar
n1 1
pt is the total pressure at the pressure side minus the total pressure at the suction side, or the
static pressure at the pressure side minus the static pressure at the suction side, providing that
the dynamic pressure is the same on both sides.
n1
Q v1 Q v
n
2
n
p t1 p t 1
n
3
n
PA1 PA 1
n
d1
Q v1 Q v
d
2
d
pt1 pt 1
d
3
d
PA1 PA 1
d
Q v1 Q v
pt1 pt 1
t
PA1 PA 1
t
Specific gravity calculation at changed temperature and atmospheric pressure: (see Figure
14)
273 t PA
1 t
273 t1 PA1
The following symbols are used for all calculations:
When considering the air flow participating in the overall clinker burning process, which are
schematically represented in Fig 15, an important factor must always be taken into
consideration. This factor is the so-called false air (also known as parasite, in-leaking or
infiltrating air). False air enters through badly closed openings, e.g. mill inlet seal, inspection
doors, dampers, etc.
This in-leakage should at all times be kept at a minimum, since it cuts down the efficiency of
the system fan. The cold false air may also cause an undesirable temperature drop to below the
dew point which may cause condensation and eventually result in corrosion problems. The
extra volume of air which the system fan has to transport requires extra power to drive this fan.
It can be calculated that a false air quantity of 40 % may result in an extra power consumption
consumption of the system fan of about 40 %, which is a significant inefficiency of the system.
It is thus of importance at all times to maintain an effective sealing of all unnecessary openings.
The quantity of false air is usually determined on the basis of O2 or CO2 analyses by using the
Orsat apparatus at any two given points in the system. False air is usually expressed in per cent
of unmixed gases at the inlet measuring point. In the calculations, atmospheric air is reckoned
to contain 0 % CO2 and 21 % O2. In the calculations the term "gas" signifies the unmixed gases
and the term "mixture" signifies the mixture of gases and false air.
At the measuring point I is found:
QI O2, I
100
Nm 3
O2
At the measuring point II is found:
A calculation of the false air which infiltrates the system between points I and II can then be
determined according to:
Where:
Q1 O 2 , I
0,21 Q II Q I
O 2 , II 100 100 %
Q II
from which:
21 O 2 , I
Q II Q I Nm 3
21 O 2 , II
If the air or gas quantities are unknown, the percentage of false air may simply be calculated on
the basis of the oxygen contents:
O 2 , II O 2 , I
False air 100 %
21 O 2 , II
Example
In the raw mill circuit shown in Figure 16, measurements of CO2 and O2 were carried out by
Orsat analysis. The quantity of false air in the raw mill circuit is calculated according to the
equation in Figure 17.
Position A to B:
29,0 27,4
CO 2 100 5,84 %
27,4 0,0
4,75 4,33
O2 100 2,58%
21 4,75
Average 4,2 %
Position B to C:
27,4 18,9
CO 2 100 44,97 %
18,9 0,0
8,93 4,75
O2 100 34,63 %
21 8,93
Average 39 ,8 %
Position C to D:
18,9 16,8
CO 2 100 12,50 %
16,8 0,0
9,97 8,93
O2 100 9,43 %
21 9,97
Average 10 ,97 %
Position A to D:
29,0 16,8
CO2 100 72,62 %
16,8 0
9,97 4,33
O2 100 51,13 %
21 9,97
Average 61 ,88 %
Too much false air at the system inlet lowers the temperature.
False air increases the total air quantities, and thereby the load on the fan.
1.4.1 Introduction
Now and then it is useful to establish a total material- and heat (energy) balance of the mill
system. This is a rather elaborated calculation, however, it gives one of the most complete
description of the operating system.
If we consider the mill as the system, it becomes basically a question of determining the heat
content flowing into and out of the system. Apart from electrical power input all major energy
exchanges are directly related to the heat transfer.
NOTE:
The accumulated energy - i.e. the energy used to create new surface - is negligible
according to the low efficiency of the grinding process (less than 1 %).
To establish the heat balance an arbitrary standard condition of 0oC and 760 mm Hg are
normally used. Still it is common to calculate in kcal/h. The system may consist of any subpart
of the total mill system. Figure 18 shows a mill system with typical input and output
components.
1.4.2.1 Input
Material to the mill will be the heat content of the total dry feed. For close circuit the separator
is normally not included, i.e. the return has to be considered as feed. Heat content of raw
materials, clinker and other components ( e.g. gypsum) can be found from tables.
Air to the mill is an atmospheric air for the cement mill. For the raw mills it will often be solely
kiln gases, or a mixture of kiln gases and auxiliary heat generator air. Coal mills use of
atmospheric air or kiln gases will depend on the used system ( non-inert atmospheric air, inert
kiln gases ). In the calculation a consideration of false air amount entering the system should be
made.
The water calculation should include moisture in the feed components and water injected into
the mill (cement mills). The power supplied to the mill should be converted to kcal/h : 1 kWh =
860 kcal.
1.4.2.2 Output
The material can always be calculated by a simple mass balance.
The air will contain a total air out of the system ( together with the false air).
The water will include heat consumption of the residual moisture in the material and
evaporated water as vapour.
The heat losses are mainly surface losses from the mill shell, and depend on the surface
temperature. Normally the surface loss for the ball mill is calculated as 600 kcal/h·m2.
Examples of heat balance calculations are attached to this Module in Appendix IV.
1.5 CONCLUSION
Correct balances of mass, heat and gases in a ball mill grinding system are of considerable
importance. Balances that are not properly checked and maintained can cause malfunctioning
of the grinding system and also cause excessive power consumption. In this module problems
of mass and heat calculations have been introduced and the proper solutions given. It is
recommended to train additionally with problem solving by using the CBT pertaining to the
module.
1.6 APPENDIX I
Determination of ρot
Orsat-analyses
CO2 11,66 %
O2 6,52 %
CO 0,04 %
N2 81,78 %
Specific gravities
O2 = 1,4289 kg/Nm3
CO = 1,250 kg/Nm3
N2 = 1,251 kg/Nm3
Nm 3 CO 2 kg CO 2
CO 2 0,1166 3
1,9643 3
0,2290 kg Nm3 gas
Nm gas Nm CO 2
Nm 3 O 2 kg O 2
O2 0,0652 1, 4289 0, 0932 kg
Nm 3
gas
Nm 3 gas Nm 3 O 2
Nm 3 CO kg CO
CO 0,0004 3
1, 250 3
0,0005 kg Nm 3 gas
Nm gas Nm CO
Nm 3 N 2 kg N 2
N2 0,8178 3
1, 251 3
1,0231 kg Nm 3 gas
Nm gas Nm N 2
Determination of ρo
1
Volume of 1,000 kg dry gas 0,743 Nm3
1,3458
0 , 068
Volume of 0,068 kg vapour 0,85 Nm3
0 ,8
1, 068
Specific gravity of the moist gas, ρ0 1,290 kg/Nm3
0 ,828
Determination of ρ
b ps
t o
273
273 t dry 10333
kg
m3
1.7 APPENDIX II
In the duct from R1S11 to the bottom of the separator (see Figure 19), Pitot tube measurements
have been carried out as follows:
Data:
pd(a) pd(b)
0,97 D 1 2 mm WG
0,90 D 12 18 mm WG
0,81 D 85 75 mm WG
0,68 D 120 115 mm WG
0,32 D 125 120 mm WG
0,19 D 70 80 mm WG
0,10 D 20 15 mm WG
0,03 D 2 2 mm WG
Calculate the air flow rate in m3/s, m3/min, Nm3/min and kg/min.
Q 2,0 2 27,02 84,9 m s 5093 m min
3 3
4
t 1, 05
Q0 Q 5093 4113 Nm 3
0
min
1,30
Q m Q t 5093 1,05 5347 kg min
pd pd
1,00 1,41
3,46 424
9,22 8,66
10,95 10,72
11,18 10,95
8,37 8,94
4,47 3,87
1,41 1,41
50,06 50,20
pd 6,22 6,28
Average p d 6 , 26
p d 39 ,3 mm WG
t 1, 05 kg
m3
39 ,3
v 4, 43
1,05
27 ,1 m s
Grasim Industries 38 FLSmidth 2009, all rights reserved
Mass and Heat Balances
PA = 230 kW
t = 89oC
p = -20 mbar = -204 mm WG
b = 10072 mm WG
Use the performance curve for the fan to determine the quantity of air transported in:
a) Nm3/s
b) m3/s
c) kg/s
The fan motor is replaced with a new motor with the speed: n = 1050 rpm.
Calculate the quantity of air transported with the same data as above in:
d) Nm3/s
e) m3/s
f) kg/s
75 0 ,96 kg
m3
1 75 0,96 kg m3
273 75
0 0,96 kg
Nm3
1,22 kg Nm3
273
1 0,96
PA1 PA 230 251 kW
t 0,88
a) Qv Qv1 25,5 m3
s
b) Qv 0,88 25,5 kg
s 22,4 kg s
22 , 4 kg s
c)
Qv kg
18 ,4 Nm 3
s
1,22 Nm 3
n 1050 RPM
n 1 970 RPM
n
Q v Q v1
n1
24 ,3 kg s
d)
Qv 19 ,9 Nm 3
s
1, 22 kg Nm 3
1050
e)
Qv 25,5 27,6 m
s
970
1.9 APPENDIX IV
HEAT BALANCE CALCULATIONS
Case 1
An open-circuit cement mill with two grinding compartments has the following characteristics:
Operational data:
Production 85 tph
o
Feed temperature (clinker + gypsum) 170 C
o
Material temperature, outlet C1 108 C
o
Material temperature, outlet C2 122 C
o
Air temperature, mill inlet 25 C
o
Air temperature, outlet C1 108 C
o
Air temperature, outlet C2 122 C
o
Water temperature (injected water) 18 C
Airflow at mill inlet 20000 kg/h
a) Use a heat balance for the first compartment to calculate the amount of water that must be
injected to maintain 108o in the outlet.
b) Use a heat balance for the second compartment to calculate total amount of water that must
be injected to maintain 122oC in the outlet.
c) Calculate the total airflow in the mill outlet (airflow at inlet + vapour) in kg/h, Nm3/h and
m3/h at 122oC.
d) Calculate the air velocity in the free area above the ball charge at the mill outlet (q = 30%).
e) Calculate the total amount of vapour in the airflow in kg vapour/kg dry air, and find the
expected dew point and wet temperature in the mill outlet (Figures 3.7 and 3.8)
Case 2
For a TIRAX coal mill, 32 x 4,5 + 2,8, the following operational data are given:
a) Based on a heat balance for the coal mill operating at above conditions find the necessary
amount of gases for drying, in kg/h and m3/h.
b) The hot gas duct between the grate cooler and the coal mill inlet has a diameter of 1 m.
Calculate the air velocity in this duct.
Case 3
We will now treat a closed-circuit raw mill installation, as shown in the following diagram:
a) With a circulation factor of 2,0 calculate the maximum water % which can be dried in this
mill. False air is 0%.
b) Will the drying capacity increase with a circulation factor of 3,0?
c) What will the drying capacity be with 25% false air in the mill?
Circulation factor = 2,0 and the same amount of kiln gases.