Heat Balance
Heat Balance
Heat Balance
Email address:
ayush.bhattacharya2015@gmail.com (A. Bhattacharya)
*
Corresponding author
Received: August 29, 2017; Accepted: September 11, 2017; Published: October 10, 2017
Abstract: In this study a static heat energy balance analysis has been carried out for an iron blast furnace. The objective of this
work is to provide a mathematical calculation model of the heat distributions for the various components of the blast furnace. The
model presented, is also indicative to the amount of excess fuel being charged. To prepare a proper heat balance, the first step is
to attain a proper mass balance calculation. To do so, each input and output materials has been analysed, and the respective
elemental compositions have been calculated. All major components and reactions of a blast furnace have been included in the
study. Each calculation has been done with sufficient details, to allow estimation of heat requirements, according to the working
conditions of a blast furnace.
Keywords: Blast Furnace, Heat Energy Balance, Blast Furnace Reactions, Blast Furnace Efficiency
bricks, which is used to convert iron oxide into pig iron. The again reacts with excess C, to produce CO gas. This hot gas
blast furnace is an example of a counter current reactor where then moves upwards in the furnace reducing the iron oxides
solids descend and gasses ascend. The fuel (coke, coal, nut and the other input materials. Other than reduction by CO gas
coke) and other raw materials (iron ore, sinter, dunite, (Indirect Reduction), other reducing processes are reduction
dolomite, quartzite) are weighed, and charged into the furnace by C (Direct Reduction) and reduction by H₂. Dunite,
from the top. dolomite and quartzite are slag producing agents, which
Coke is a mixture of coals, crushed and then heated to produce slag along with iron ore impurities such as alumina
remove most of the volatile matter. Coke has higher calorific and silica, and help in the removal of elements like sulphur
values due to the presence of more carbon content. Nut coke is and phosphorus. The raw materials require around 6 to 8 hours
smaller in size and has a lesser calorific value than coke. Sinter to descend to the bottom of the furnace, as the final products:
is produced by agglomerating iron ore fines with other plant hot metal and slag. The hot metal and slag flow out of the blast
wastages, having some iron percentages, such as screened furnace through the tapping hole. The hot metal flows through
sinter fines, flue dust and sludge from the blast furnace, and the runner and is collected in the ladles. The slag having a
scales from mills. Limestone and dolomite are added to lesser density than that of the hot metal, separates out from the
maintain the required basicity of sinter. Coke fines are used in hot metal, as the slag runner is placed in a different direction.
the coke oven plant, to heat the iron ore fines along with the The slag is granulated by sprinkling water over it and later sent
flux material, to form lumps of sinter. The iron ore is found in to cement factories, where it used as a raw material. During
mainly two forms, Hematite (Fe₂O₃) and Magnetite (Fe₃O₄). reactions, various other gases are produced at various levels
Air is collected from the atmosphere and heated to 1200°C inside the furnace. These gases leave the furnace and is known
with the help of giant hot blast stoves. From the stoves the hot as Blast Furnace Gas (BF Gas). The BF gas carries small
combustion air is given sufficient oxygen enrichment, and particulate matter (dust), which are removed by passing the
supplied into the furnace at high pressure, through the tuyeres, gas through the Dust Catcher and then the Gas Cleaning Plant
as hot blast. The coke descends to the bottom of the furnace (GCP). The BF Gas carries significant amount of energy, and
and is ignited by the hot combustion air blast. The coke reacts after removal of dust, is reused in various areas of the plant.
to produce CO₂ and heat, raising temperatures of the The dust collected in the Dust Catcher and GCP is used as a
combustion region to around 1900°C. The wustite ore, having raw material for sinter. Figure 1 shows a schematic diagram of
a high melting point, melts in this region. The CO₂ produced a blast furnace plant.
All data for the study has been taken from the month of each batch, on arrival. These fuel analysis values have been
April 2017. A heat energy flow diagram is shown in Figure 2 taken for the fuel used in the month of April, 2017.
for a demonstration of the calculations. (-) sign indicates Quantity of Coke Consumed= 381 Kg/THM
components which release heat, whereas (+) sign indicates Calorific Value of Coke= 7020 Kcal/Kg
heat absorbing components. Quantity of Coal Consumed= 130 Kg/THM
Hot Metal Production in April 2017= 48411 Tons Calorific Value of Coal= 5605 Kcal/Kg
Quantity of Nut Coke Consumed= 19 Kg/THM
3.1. Fuel Analysis Calorific Value of Nut Coke= 6850 Kcal/Kg
The calorific values of coke, coal and nut coke are tested for
Energy Generated from Coke Combustion (A1) = 381 Kg/THM * 7020 Kcal/Kg
= 2674620 Kcal/THM
Energy Generated from Coal Combustion (A2) = 130 Kg/THM * 5605 Kcal/Kg
= 728650 Kcal/THM
Energy Generated from Nut Coke Combustion (A3) = 19 Kg/THM * 6850 Kcal/Kg
= 130150 Kcal/THM
Total Energy Generated from Fuel Input = A1+ A2+ A3
= 3533420 Kcal/THM (-)
3.2. Combustion Air or Hot Blast Analysis
Element H₂O O₂ N₂
m³/THM 53 272 916
Moles/THM 2362 12143 40911
Latent Heat of H₂O (Liquid → Gas) (B1) = 42.5 Kg/THM * 540 Kcal/Kg
= 22950 Kcal/THM
Sensible Heat of H₂O (298K → 1473K) (B2) = 2362 moles/THM * 11.14 Kcal/moles
= 26313 Kcal/THM
Sensible Heat of O₂ (B3) = 12143 moles/THM* 9.37 Kcal/moles
= 113780 Kcal/THM
Sensible Heat of N₂ (B4) = 40911 moles/THM * 8.93 Kcal/moles
= 365335 Kcal/THM
Total Heat of all combustion air constituents = B1 + B2 + B3 + B4
= 528378 Kcal/THM (-)
3.3. Composition Analysis
For simplicity in calculations, it has been assumed the input iron ore to be only in the form of Hematite (Fe₂O₃). The
percentage compositions of the various input materials are studied using XRF analysis, which is carried out for every batch of
input materials, on arrival. The values are of that input materials, used in the month of April 2017. Only the percentage
composition of the elements, taken into consideration for this study, has been shown.
3.3.2. Sinter
Total Quantity Used= 53101 Tons
The sinter composition analysis results is shown in Table 3.
Element Fe₂O₃ FeO SiO₂ CaO MgO P₂O₅ MnO TiO₂ Al₂O₃
% 66.28 10.23 3.57 11 2.26 0.037 0.35 0.16 2.65
Kg/THM 707.04 113.11 40.08 112.14 28.8 1.86 3.27 1.76 29.72
Moles/THM 4419 1571 668 2002.5 720 13.09 46 22 291.42
3.3.3. Dunite
Total Quantity Used= 1232 Tons
Moisture Content = 2.5% = 31 Tons = 0.64 Kg/THM =35.35 moles/THM
International Journal of Mineral Processing and Extractive Metallurgy 2017; 2(5): 57-67 61
3.3.4. Dolomite
Total Quantity Used= 324 Tons
Moisture Content= 0%
The dolomite composition analysis results is shown in Table 5.
3.3.5. Quartzite
Total Quantity Used= 238 Tons
Moisture Content= 2.5% = 6 Tons = 6.83 Moles/THM
Dry Weight= 232 Tons
The quartzite composition analysis results is shown in Table 6.
3.3.6. Coke
Total Quantity Used= 18445 Tons
Moisture Content= 221 Tons =1.2% =4.57 Kg/THM =254 moles/THM
Dry Weight= 18224 Tons
The coke and coke ash composition analysis results are shown in Table 7 and Table 8 respectively.
3.3.7. Coal
Total Quantity Used= 6301 Tons
Moisture Content= 8% = 504 Tons= 10.41 Kg/THM = 578.38 moles/THM
The coal and coal ash composition analysis results are shown in Table 9 and Table 10 respectively.
Element Si Mn P Ti C
% 0.61 0.42 0.162 0.065 4.42
Kg/THM 6.1 4.2 1.62 0.65 44.2
Moles/THM 218 76.36 52.26 13.54 3684
3.4.1. Silicon
Quantity of Si in Hot Metal= 218 moles/THM
Sensible Heat of Si in Hot Metal (C1) = 218 moles/THM * 21 Kcal/moles
= 4578 Kcal/moles
Heat of Solution of Si (C2) = 218 moles/THM * - 28.5 Kcal/mole
= - 6213 Kcal/mole
3.4.2. Manganese
Quantity of Mn in Hot Metal = 76.36 moles/THM
Sensible Heat of Mn in Hot Metal (C3) = 76.36 moles/THM * 17.89 Kcal/mole
= 1366.08 Kcal/THM
Heat of Solution of Mn (C4) = 76.36 moles/THM * 1.2 Kcal/mole
= 91.63 Kcal/THM
3.4.3. Phosphorus
Quantity of P in Hot Metal = 52.26 moles/THM
= 26.13 moles/THM {2P→P₂}
Sensible Heat of P in Hot Metal (C5) = 26.13 moles/THM * 46.266 Kcal/mole
= 1209 Kcal/THM
Heat of Solution of P (C6) = 26.13 moles/THM * - 29.2 Kcal/mole
= - 763 Kcal/mole
3.4.4. Titanium
Quantity of Ti in Hot Metal = 13.54 moles/THM
Sensible Heat of Ti in Hot Metal (C7) = 13.54 moles/THM * 11.38 Kcal/mole
= 154.08 Kcal/THM
International Journal of Mineral Processing and Extractive Metallurgy 2017; 2(5): 57-67 63
Element CO CO₂ O₂ N₂ H₂
% 23.74 20.09 0.71 53.41 2.05
m³/THM 404 342 12 909 35
Moles/THM 18024 15257 536 40580 1564
The slag calculation is done taking reference from [1]. The values of [1] are selected, as the slag composition data is similar to that
produced in the blast furnace, taken in the study.
Heat produced during slag formation= 362.2 Kg/THM * 140 Kcal/Kg-slag
= 50708 Kcal/THM (-)
Sensible Heat of Blast Furnace Slag= 362.2 * [(1561℃ * 0.2741 Kcal/Kg℃) – (25°C * 0.185 Kcal/Kg℃)]
= 153299 Kcal/THM (+)
3.11. Reactions
Table 18 shows the elements entering into the blast furnace for reactions, after excluding dust losses, carbon in hot metal and FeO in
slag. The mentioned elements have been excluded in beforehand for more accuracy in results. The amounts excluded are taken from
the respective composition sheets.
Table 18. Elements Entering the Blast Furnace for Reactions after Excluding Dust Losses, Carbon in Hot Metal and FeO in Slag.
The enthalpies of reactions, as shown in Table 19, are calculated according to the temperature in which the reaction takes place, by
applying Kirchoff’s equation (1).
(∆HReaction)T2 = (∆HReaction)T1 + [∑ (∆HT2 - ∆HT1)Products - ∑ (∆HT2 - ∆HT1)Reactants] (1)
66 Ayush Bhattacharya and Sadhasivam Muthusamy: Static Heat Energy Balance
Mathematical Model for an Iron Blast Furnace
where, T2 is the temperature at which the reaction takes place and T1 is the standard temperature of 298K. Figure 3 shows the different
temperature zones in a blast furnace.
The CO produced, for the reduction of ores, is produced by the combustion of fuels at 1700 K.
2C(s) (23214) + O₂(g) (11607) → 2CO(g) (23214)
The values in brackets is the number of moles of the substance undergoing reaction according to the mass balance shown in
Table 18.
After performing various calculations, the reduction percentages are taken to be 60% Indirect Type (CO) Reduction, 35%
Direct Type (C) and 5% reduction by Hydrogen (H₂), as this yields the most accurate results, as shown in Table 19. These
percentages vary according to the operating conditions of the furnace. The percentages can be estimated by taking into
consideration the BF Gas analysis.
Reactions (Value in brackets indicate number of moles) Temperature (K) ∆H Reaction (Kcal/mole) Total ∆H (Kcal)
C(s) (2677) + H₂O(g) (2677) → CO(g) (2677) + H₂(g) (2677) 1700 +32.1 +85931.7
3Fe₂O₃(s) (4574) + CO(g) (1525) → 2Fe₃O₄(s) (3049) + CO₂(g) (1525) 1000 -12.47 -19012.59
Fe₃O₄(s) (3049) + CO(g) (3049) → 3FeO(s) (9147) + CO₂(g) (3049) 1200 +4.585 +13979.66
FeO(s) (9147 + 921 = 10068) + CO(g) (10068) → Fe(s) (10068) +CO₂(g) (10068) 1200 -3.85 -38761.8
3Fe₂O₃(s) (2668) + C(s) (889) → 2Fe₃O₄(s) (1179) + CO(g) (889) 1400 +26.95 +23967.53
Fe₃O₄(s) (1179) + C(s) (1179) → 3FeO(s) (3537) + CO(g) (1179) 1400 +44.43 +52383
FeO(s) (3537 + 537 = 4074) + C(s) (4074) → Fe(s) (4074) +CO(g) (4074) 1700 +27.48 +111953.5
3Fe₂O₃(s) (381) + H₂(g) (127) → 2Fe₃O₄(s) (254) + H₂O(g) (127) 1200 -46 -5842
Fe₃O₄(s) (254) + H₂(g) (254) → 3FeO(s) (762) + H₂O(g) (254) 1200 +12.45 +3162.3
FeO(s) (762 + 76 = 838) + H₂(g) (838) → Fe(s) (838) + H₂O(g) (838) 1300 +3.73 +3126
CaCO₃(s) (31)→ CaO(s) (31) + CO₂(g) (31) 1200 +39.42 +1222.02
MgCO₃(s) (162) → MgO(s) (162) + CO₂(g) (162) 700 +27 +4374
P₂O₅(s) (26) + 5C(s) (130) → 2P(s) (52) + 5CO(g) (130) 1700 +206 +5356
TiO₂(s) (13) + 2C(s) (26) → Ti(s) (13) + 2CO(g) (26) 1700 +129.36 +1681.68
MnO(s) (76) + C(s) (76) → Mn(s) (76) + CO(g) (76) 1700 +69.33 +5269.08
SiO₂(s) (218) +2C(s) (436) → Si(s) (218) + 2CO(g) (436) 1700 +158.89 +34638.02
CO(g) (1219) + H₂O(g) (1219) → CO₂(g) (1219) + H₂(g) (1219) 1000 -8.33 -20350.19
C(s) (910) + CO₂(g) (910) → 2CO(s) (1820) --------------------------------- (X) 1300 +40.05 +36445.5
Fe(s) (16780) → Fe(l) (16780) 1800 +3.56 +59737
∑ Summation of Enthalpies +359261
Reaction X is the mass balancing equation to balance the Moles produced in the BF according to calculations:
excess C supplied (excess fuel). CO = 18660; CO₂ = 15144
International Journal of Mineral Processing and Extractive Metallurgy 2017; 2(5): 57-67 67
But the moles leaving the furnace in BF Gas: output component, taken in the study, would help to alter the
CO = 18024; CO₂ = 15257 quantity of supply of any component, for improving the
Difference in moles of CO =18660 – 18024 =636 (Excess) efficiency. From the above calculations, one can account for
Difference in moles of CO₂=15144 – 15257 =113 (Less) approximately 73% of the heat supplied [Table 20]. This result
This difference in the number of moles can be explained is in accordance with the literature of heat energy balance for a
due to the other reactions taking place inside the furnace. It blast furnace [3-5]. The remaining 27% can be explained as
can be said that 113 moles of CO are reducing some other other heat losses taking place in the tuyere region [9-10],
oxides (other than those taken in this study) to produce 113 conduction, convection, radiation etc.
moles of CO₂. Hence CO₂ balance will then be achieved.
Excess CO (523) may be due to the following reasons: 1.
Furnace having a lesser percentage of direct reduction (<35%). References
2. Excess fuel supply (From reaction X)
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