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de
Trujillo
FACULTAD
DE INGENIERIA
Escuela Acadmico Profesional de Ingeniera Metalrgica
CURSO:
METALURGICA EXTRACTIVA II
DOCENTE:
ING. LUIS ALVARADO LOYOLA
ALUMNOS:
CICLO:
Trujillo Per
2015
Introduccin
BOF convertidor, fiabilidad y costes son vitales para el buen funcionamiento de las
plantas de acero en todo el mundo. En muchos sentidos, las tcnicas de fabricacin
de acero primaria eran desatendidas en favor de los procesos secundarios pero con
estos desarrollos logstica y la utilizacin flexible de los convertidores se hizo ms
crtica. La vida del convertidor vara de una planta a todo el mundo a partir de slo
unos cientos de calores 40.000 calores. Continuando con el exceso de capacidad y
los bajos precios de venta para el acero sigue existiendo una fuerza impulsora y una
motivacin para optimizar la vida, la disponibilidad y los costos de la produccin de
acero primaria.
Lnea para el suministro de un gas inerte (por parte inferior del tanque) tiene una estructura que
evita su obstruccin. Por lo tanto, la masa fundida puede proceder de gas continuamente suficiente
para proporcionar la agitacin deseada.
El flujo simulado es un multi-fase y tiene una temperatura alta, el flujo es turbulento.
Grid computacional fue generada en ANSYS ICEM CFD y consistieron en 500 mil. Las clulas.
Adems de los modelos de turbulencia y modelo de transferencia de calor tambin se utiliz
para simular el flujo con VOF superficie libre (fundido y escoria) y el modelo de partculas discretas
(Lagrange) para calcular las trayectorias de las burbujas de gas inertes. Modelado duracin de la
inyeccin de gas de proceso de 20 minutos en un clster de Linux, que incluye no menos de 10
computadoras, tomaron dos semanas. Costes computacionales eran grandes no relacionada con el
tamao de la rejilla de clculo, y la complejidad de los procesos simulados.
Para tener en cuenta los efectos adicionales, tales cambios arrastran burbujas (para su
crecimiento), UDF especiales usados (Funciones del Usuario Deflned, UDF).
Los resultantes datos de la investigacin han ayudado a mejorar el diseo de la boquilla para
aumentar la profundidad la penetracin del chorro y en consecuencia para mejorar el intercambio de
calor y mezcla del convertidor. A pesar de los relativamente pequeos problemas de cobertura de
derivados ahora los resultados fueron suficientes para hormign haciendo las secuencias esenciales
durante la fusin y la introduccin de medidas para optimizar. Por lo tanto, cada convertidor puede ser
adaptado a las necesidades individuales de los clientes.
Figura 1. Que muestra el comportamiento del carbono de la muestra y la concentracin del oxgeno disuelto en el acero el cual es medido por la
celda de oxgeno para el proceso convencional del BOF.
Tambin se analiz la relacin que existe entre la concentracin del oxgeno disuelto en el acero
respecto a la temperatura encontrndose muy poca correlacin como se aprecia en la figura 2.
Figura 2. Correlacin que existe entre la ppm de oxigeno respecto a la temperatura del acero lquido para el proceso normal, los valores de las
ppm son los emitidos por la celda de oxigeno.
De acuerdo a la poca correlacin que existe respecto a la temperatura, se opto por establecer como
mandatoria la relacin carbono oxigeno para lo cual se toma como punto de partida el resultado de
la muestra de acero liquido y cuyo valor es reportado por el espectro robotizado en un tiempo mximo
de 3 minutos desde que la muestra es tomada por el operador.
Posterior a la determinacin de la relacin carbono oxigeno para el proceso convencional actual del
BOF, se establecen la tabla de las ppm de oxigeno estimadas de acuerdo al contenido de carbono de
la muestra emitido por el espectro robotizado, tal como se muestra en la tabla I.
En esta tabla se establecen como limites de trabajo desde las 200 ppm hasta las 1300 ppm de
oxigeno disuelto en el acero, de acuerdo a la informacin estadstica de los 4 meses considerados
para esta evaluacin.
En la tabla de referencia se establecen primero rangos de medicin de cada 25 ppm y despus de las
750 ppm intervalos de 50 ppm, lo anterior con el fin de que los valores del contenido de carbono de la
muestra sean lo mas cercano posible de un valor a otro.
Tabla I
La informacin de las coladas en donde se trabaja a con la tabla y la celda de oxigeno se analiza
correlacionndose primeramente las ppm de oxigeno de la celda respecto al contenido de carbono
real de la muestra y el carbono que marca la misma celda.
De la grfica se puede afirmar que la relacin que existe entre las mediciones de carbono y oxigeno
de la celda se comportan mediante una lnea curva perfecta ya que su R 2es de 0.999, sin embargo la
relacin real entre las ppm de oxigeno de la celda respecto al contenido de carbono real de la muestra
es de 0.81 la R2.
En la figura 3 se muestra grficamente la relacin que existe entre los valores de ppm de la celda
respecto al contenido de carbono real y el de la celda de oxigeno.
Figura 3. Grfica que muestra la correlacin existente de las ppm de la celda de oxigeno respecto a los valores de carbono de la muestra de
acero analizada por el robot y el carbono de la celda.
Adems se evala la correlacin del carbono real de la muestra de acero respecto a las ppm
estimadas de la tabla y los valores de las ppm emitidas por la celda de oxigeno, es esta grafica se
observa que existen datos con valores en ppm de oxigeno que mide la celda y que no son
congruentes al contenido de carbono de la muestra de acero para un proceso normal en donde no se
tiene soplado por el fondo del horno resultando valores del producto carbono oxigeno de 0.0022.
En la figura 4 se muestra la correlacin existente, tomando como punto de partida el carbono real de
la muestra de acero respecto a las ppm de oxigeno estimadas de la tabla y las ppm medidas por la
celda de oxigeno.
Figura 4. Correlacin entre el contenido de carbono real de la muestra respecto a las mediciones de oxigeno de la celda y las estimadas por la
tabla, se muestran algunos datos de la celda que no van de acuerdo para el proceso normal de BOF.
Al evaluar los resultados de trabajar con la tabla se observa una dispersin del producto C*O de
0.0033 hasta 0.0035 por manejarse intervalos de 25 a 50 ppm, considerndose aceptable esta
dispersin y no detectndose ninguna anomala para la aplicacin de las tablas de desoxidacion en
donde se utiliza el carbocoque para predesoxidar el acero.
Al comparar los cumplimientos en la acertividad del aluminio esperado en el acero de la olla posterior
al vaciado con el uso de la celda se tenia un promedio de 81.5%, al trabajarse a la par con la celda y
tabla el cumplimiento bajo a un 79% y posteriormente al trabajar exclusivamente con la tabla de ppm
estimadas el cumplimiento subi a un 82.2%.
Durante el mes de julio que se hizo la evaluacin al trabajarse a la par con la utilizacin de las celdas
y las tablas de ppm estimadas se vaciaron un total de 645 cols., de las cuales en 145 se utiliza la
celda de medicin de oxigeno que equivale al 22.5 %, adems de las 645 cols. En 67 cols. Se resopla
y no se toma muestra esto equivale al 10.38% y de estas 67 cols. Solamente en 10 cols. Se utiliza la
celda como referencia (15%).
Por lo anterior tomando como referencia que en el 10% de las coladas no se tom como referencia las
condiciones de los elementos residuales del acero, el mximo cumplimiento que podramos esperar
sera del orden del 90%, del valor obtenido real 82.2% falta considerar que por el efecto del paso de
escoria del convertidor a la olla de acero se tiene la mayor prdida de aluminio la cual llega a ser
hasta de 100 kg.
En la Figura 5 se muestra el cumplimiento en el contenido de aluminio esperado en el acero de la olla posterior al vaciado del horno, al trabajar
simultneamente con el uso de la tabla y la celda de oxigeno.
El ahorro que se puede esperar por la sustitucin de la celda de oxigeno por la tabla de ppm
estimadas, para el proceso normal sera considerando el promedio de coladas vaciadas durante el
ao 2012 fue de 1425 por los 2 convertidores, significa un ahorro potencial anual de 713 cols.
Dejndose de consumir la celda de oxigeno cuyo costo es de 11.00 USD, utilizando solamente el
termopar convencional cuyo costo es de 1.10 USD, nos da un ahorro anual de $889,396.00 pesos.
Hay que considerar que la evaluacin anterior est basada para las condiciones actuales del proceso
normal y que si se llega a dar cualquier cambio significativo, como por ejem. Cambios en la prctica
de soplado, principalmente en la posicin de la altura de la lanza as como cambios en el diseo de la
misma se tendra que llevar a cabo una evaluacin similar para el ajuste correspondiente.
En la Figura 1 se aprecia la distribucin de la mezcla de grados que se fabrica en la acera BOF y CC.
Anteriormente, para la fabricacin de los grados de acero bajo carbono se tena estandarizada una
tabla general de desoxidacin en donde se establece la cantidad de carbocoque a utilizar para la
predesoxidacion (eliminacin parcial del oxigeno del acero), as como la cantidad de aluminio para
completar la desoxidacin total. La Tabla I muestra la tabla de referencia.
Sacos de
300
0.000
350
0.000
400
0.000
450
0.000
500
0.000
550
0.000
600
0.000
650
0.000
700
0.000
Ccoque
Kg. de Aluminio
Aceros sin Silicio
Incr. en
%C
750
0.000
800
299
0.000
850
308
0.000
900
282
0.000
950
291
0.000
1000
300
0.000
1050
309
0.000
1100
319
0.000
1150
293
0.000
1200
302
0.000
1250
311
0.000
1300
320
0.000
1350
330
0.000
Como se aprecia en esta tabla de desoxidacion, a partir de las 800 ppm de oxgeno que equivale
aproximadamente a un 0.043% de carbono, se utiliza el carbocoque para la predesoxidacion del
acero, considerando adems el que resulta de la incorporacin del ferromanganeso.
Para llegar a utilizar el carbn de la manera ms eficiente, una de las tareas principales fue
determinar la cantidad de carbono que se pierde durante el vaciado del convertidor a la olla de acero.
Para lograr esto, se evaluaron una serie de coladas vaciadas a diferentes contenidos de carbono
residual y considerando la aportacin de carbono del ferromanganeso. La Figura 2 muestra el carbono
perdido con respecto al carbono residual, y en la Figura 3 se aprecia la evolucin del carbono perdido
en forma de CO.
Figura 2. Determinacin del carbono perdido durante el vaciado del convertidor a la olla de acero
Posteriormente, la ecuacin obtenida se optimiza aplicndose hasta los del nivel del acero en la
olla, de acuerdo al siguiente esquema mostrado en la Figura 4.
Olla llena ( eliminacin parcial del oxgeno por el carbono residua olla Optimizacin predesoxidacion
con carbono residual y/o carbocoque
Figura 4. Esquema del llenado de la olla donde se muestran las diferentes etapas en la desoxidacion parcial del acero por el carbono en la olla.
Debido a que el carbono es el factor determinante para el balance de las entradas y salidas de
acuerdo al establecimiento de las diferentes practicas de desoxidacion, fue necesario agrupar los
grados de acero de acuerdo a su especificacin de carbono y manganeso, agrupndose en 3
diferentes grupos, tal como se muestra en la Figura 5. Para el grupo 1, se continuo con la aplicacin
de la practica comn mostrada en la Tabla I, desarrollndose otra tabla para cada uno de los grupos II
y III considerando que la cantidad agregada de ferromanganeso es similar.
Figura 5: Diagrama que muestra los criterios para la agrupacin de los grados de acero bajo carbono y manganeso
Durante el proceso de evaluacin se detecto que se presentan eventos con las celdas de oxigeno al
emitir resultados errneos, pero la mayor parte de ellos atribuidos a factores operativos como son:
tomas sobre la escoria y sobrecalentamiento de la lanza del celox. Por lo anterior se dio a la tarea de
desarrollar tablas para el proceso normal (sin soplo combinado), en donde se establece el contenido
de oxigeno tomando como referencia el contenido de carbno residual de acero analizado va
espectro robotizado en un tiempo promedio de 3 minutos.
La confiabilidad de estas tablas se muestra en la grfica de la Figura 6, comparndose contra el
equipo de medicin utilizado:
Figura 6. Comparacin tablas carbono-oxigeno contra la celda de oxigeno, periodo enero a abril 2013.
De la aplicacin de la ecuacin obtenida sobre la perdida del carbono durante el vaciado del
convertidor a la olla, se establece el contenido de carbono mximo para vaciar y el esperado en la olla
de acero, especificando en las nuevas tablas e incorporando el contenido de carbono residual
estimado en base a las ppm de oxigeno, tal como se muestra en la tabla II.
GUI/Equation editor
Optimizing tool
Equation Solver
Analyzing tool
Spreadsheet
Results
unit as well as a production line or a whole factory. Each process node has its own energy demand in
the form of electricity and/or heat demand. These demands depend on the amount of material
processed in the unit and may be described by linear or piecewise linear relations. The variations are
described in the system with boundary conditions, for instance, production capacity, limited availability
for various resources such as
Energy supply
node
Process
nodes
1
5
Production
demand node
Energy flow
Material flow
In connection with the multi-objective optimization, it is possible to find Pareto-optimal solutions [10].
A Pareto-optimal solution is a solution where no objective can be improved without another
deteriorating. The plot of the objective functions is called the Pareto front, an example of a Pareto front
is shown in Figure 5. As for the bi-objective optimization problem, the Pareto front curve represents all
the solutions from minimizing one objective with upper-level constraints bounded by the other
objective, and vice versa. This allows the decision maker to choose an acceptable trade-off between
the two goals by considering the different solutions along the Pareto front.
Coke oven
CHP
Rolling
Mill
BF
BOF
System I
CC
System II
System III
Table II. Base model constraints for the BF and the BOF.
Production
Pellet use
(t h_1)
(%)
BF
BOF
500
Scrap use
% C in product
% Si in product
Coal injection
(%)
(%)
(%)
(kg t_1 HM)
o20
4.5
0.21.0
160
0.05
0
0
Slag volume
Slag CaO/SiO2
Tap temperature
(1C)
165
1
1468
3.3
1675
Unit
Energy (GJ)
(ton)
(ton)
(ton)
(ton)
(GJ)
(ton)
(ton)
(ton)
(ton)
(1000 m3n)
(MWh)
28.05
27.21
1
3.6
0.0147
3.035
2.468
0.0565
0.44
0.477
Cost (USD)
90
230
250
50
5
60
10
10
10
25
50
No opt.
Objective value
CO2 emission
Energy
Min. CO2
Min. energy
Min. cost
(t t_1 LS)
(GJ t_1 LS)
(USD t_1 LS)
1.25
12.56
0.99
9.95
0.99
9.95
1.43
14.29
246
256
256
238
1425
1124
1124
1431
Scrap
HM quality
Coke1PCI
Fluxes
(t t_1 HM)
(% Si)
(kg t_1 HM)
(kg t_1 HM)
0
0.60
475
117
197
1.0
425
149
197
1.0
425
149
0
0.20
468
109
Slag volume
BOF
Pellets
Scrap
Oxygen
Fluxes
165
165
165
165
24
170
48
53
0
296
50
76
0
296
50
76
56
0
48
24
Slag volume
110
147
147
62
Min. CO2
Min. energy
Min. cost
Cost
BF
Pellets
BF system only
No opt.
Objective value
CO2 emission
Energy
(t t_1 HM)
(GJ t_1 HM)
(USD t_1 HM)
1.25
13.97
1.07
12.13
1.07
12.13
1.23
13.78
224
228
228
223
(t t_1 HM)
1425
1146
1146
1431
Scrap
HM quality
Coke1PCI
Fluxes
(t t_1 HM)
(% Si)
(t t_1 HM)
(kg t_1 HM)
0
0.60
475
117
197
0.20
412
132
197
0.20
412
132
0
0.20
468
109
Slag volume
165
165
165
165
Cost
BF
Pellets
Scrap offers effective means to lower the CO 2 emissions in the BFBOF system, however the previous
calculations have delivered inconsistent solutions on which combination of the BF and BOF practice
that is the most effective. Scrap is possible to charge to both the BF and the BOF processes.
Figure 7 shows the different scrap distributions between the two considered processes. Constant
quantities of scrap (50, 100, 150, 200 and 225 t h_1) have been added to the system and have been
allocated in different proportions to the BF and the BOF. The propagation of each of the filled lines in
the figure corresponds to the feasibility region of the defined system. The minimum CO 2 objective of
the system is 0.99 t t_1, which was given earlier in Table II. This corresponds to a singular point in the
diagram situated directly below the 200 t h _1 line. The minimum CO2 objective when there will be no
scrap charged to the system is 1.43 t t _1, corresponding to the singular point situated on the right upper
side of the diagram. The dotted line in Figure 7 represents the distribution that corresponds to the
minimum CO2 objective for different scrap addition levels to the system. It can be seen that the CO 2
emission is decreasing with adding more scraps to the system. When the scrap addition level is lower
tan
100 t h_1, the optimized solution will always choose to add scraps into the BOF in order to have a lower
CO2 emission. The minimum CO2 objective when 100 t h_1 (200 kg t_1 LS) of scrap is
the system is 1.20 t t_1,
available
to
which
corresponds
to the right end point
of the
100 t h_1
line.
When the addition level is above
100 t h_1, the scraps to system will be distributed between the BF and the BOF for the minimum CO 2
emission. Thus, when seeking a lower CO 2 emission by increase of the scrap additions, it is possible to
find an optimum distribution between scrap charging in the BF and the BOF for each scrap-charging
level.
Pareto front analysis
A Pareto-optimal solution is a solution where no objective can be improved without another deteriorating. The two objectives of Cost and CO 2 can be weighed versus each other as shown in Figure 8,
where the Pareto front defined by minimum cost at different CO 2 emission levels have been drawn with
a line between A1 and A2. The points A1 and A2 represent the solutions Min CO 2 and Min Cost from the
optimization of the BFBOF system. A simplistic description of the conditions A1 and A2 is that the use
of scrap is maximized in A1 and the use of iron ore pellets is maximized in A2. There are several
breakpoints for the Pareto front illustrated in Figure 8, which relates to the
1.45 BF
BOF
1.40
50 t/h (10%)
1.35
t CO2 / t LS
1.30
100 t/h (20%)
1.25
1.20
150 t/h
(30%)
1.15
1.10
200 t/h
(40%)
1.05
1.00
0.95 0
10
20
30
40
50
60
90
100
260
A1
255
250
245
240
a
235
0.90
(0.99) 1.00
b
1.10
1.20
c
1.30
A2
1.40
(1.43)
1.50
Reference
casebusiness
as scenario,
usual (BAU):
consistent assumptions.
In this
no This scenario is a projection based on a series of
measures (internal or external) were taken to reduce CO 2 emissions at the steel plant. The driving
force in the model is the projected production during time steps.
Case 1ETS simulation: In this simulation, the
EU ETS is used to fill up the emission gaps. The model was bounded by the CO 2 emissions
allowance, i.e. the steel plant needs to buy the excess emission via the emissionstrading mar-ket within the EU. An average carbon permit price of 29.6 US$ t _1 CO2
indicated in Hidalgo et al.s study [5] has been used in the model.
]
]
]
Case 2ETS and CDM optimization: In this scenario, the emission gap will be
filled up by either buying allowance permits via ETS or purchasing CERs via CDM.
The types of CDM projects in the study are recovery of BF gas, injection of natural
gas, pulverized coal injec-tion system for BF and waste gas recovery from BOF.
Case 3Optimization scenario: The optimized cost objective strives to decrease
the production
cost for the system to its minimum while satisfying the CO 2 emissions limitation,
and hence minimizing the CO2 reduction cost. Be-sides the EU ETS and CDM,
internal changes within the steel plant are included. The examples of internal
changes are coking coal mixing in the COP; different coal injection rates, BOF slag
charging and flue dust injection into the BF; HM/scrap rate and decreased iron ore
pellet charging into BOF; back pressure/con-densing operation in CHP, etc. The
model was set free to optimize among the different alter-natives.
The simulation results of CO2 emission are presented in Figure 9 indicating lower
predicated CO2 emission than the emission allowance allocated for the first 2 years in
the BKP period. However, the predicted CO2 emission will exceed the allocated
emission from the last year (2007) in the BKP period through the entire time step.
Figure 9 also shows the CO2 emission gaps during the different time steps and the
cost for CO2 emission reduction in the different cases. The abatement cost shown in
the figure is calculated
Table IV. Time steps used in the model and steel production forecast in the
studied system.
Time step
Year span
Production projection (%)
CO2 emission allowance (kt year_1)
BKP
KP
PKP
20052007
_107
20082012
108
20132020
108
_4000
_3800y (_4%)
Production forecast change is based on the production for the reference year with an
assumed increased production by 8% at the end of each period. For the year of 2007
in the BKP, the production forecast is assumed as a 7% increase compared with the
first 2 years. Note that the increased production is only a calculation scenario and not
a decided production plan.
_3600y (_10
Assumed emission levels for the KP (_4%) and the PKP (_10%) of the BKP level.
Figure 9. CO2 emission allowance, calculated CO2 emission (BAU scenario) and
abatement cost during different periods at the
studied system.
based on the assumed permit price from EU ETS and CDM, and the amount of CO 2
emission gap during different periods.
In case 1 (ETS simulation), the EU ETS is used to fill up the emission gaps. The steel
plant needs to buy the excess emission via the emission-trading market within the EU
with the price per unit allowance of 29.6US$ t_1-CO2.
In case 2 (ETS and CDM optimization), purchasing allowance permits via ETS or
CERs via CDM will fill the emissions gap. Compared with case 1, the abatement cost for
the different time steps decreases to 15.4 US$ t_1-CO2, on average.
In case 3 (optimization scenario), all possible alternatives are included in the model,
i.e. internal measures, ETS and CDM scenarios. The model was set free to optimize
among these different alternatives. The result from the optimization shows that through
internal changes, the calculated CO 2 emissions are reduced for all periods. Consequently,
the studied system will not make use of CDM and ETS during the first period (including
the year of 2007), when the CO 2 saved through the internal changes will be enough to fill
up the gap. However, from the KP period, the calculated CO 2 emissions will exceed the
emission allowance allocated if the plant only makes internal changes. Thus, other
measures are necessary. When further analyzing the modelling results, it was found out
that ETS will not be used to fill up the emission gap even for the last two periods; instead
the model will choose the alternatives from the CDM scenario due to its lower abatement
cost. The resulting abatement cost in case 3 is the lowest (9.8 US$ t _1-CO2 on average)
compared with the other two cases.
It should be pointed out that for the studied case, internal changes can play a major
role in reducing the abatement cost. When the internal changes are taken during the
whole BKP period, there will be no emission gap at all; instead there is an allowance
surplus, which can either be used to fill up future gap or bank them for the future trade.
Consequently, in the optimization case, the cost for CO 2 reduction is further lowered to
9.6 US$ t_1-CO2 during the period of the KP and to 13.6 US$ t _1-CO2 during the period of
the PKP.
Owing to the geographical situation it is necessary to extend the energy-saving methodologies compared with the situation at a normal integrated plant;
A holistic view is needed to economize the use of resources, and to evaluate and
incorporate new technologies and methods, in terms of a sustainable development.
As shown in Figure 10, the integrated steel plant in Luleaincludes coke ovens, an
ironmaking plant with one BF, a steelmaking plant with two BOFs, and a CC plant with
100% CC of slabs. The RM in Borlange includes both hot and cold rolling. Depending on
the customized products, the other process units such as pickling, annealing, aluzinkline
and galvline are included. Both the sites provide hot water to communities via district heat
system. Unlike the common integrated steel plant, in which some parts of process gases
generated during steelmaking is used in the RM, the excess process gases are
transported to a CHP plant for electricity production for both internal and external use.
The excess electricity is transmitted to the power grid. Thus, the RM is connected to the
steel plant to some extent as the electricity consumed at the RM is from the power grid.
Recently, a specific model for the RM has been created to analyse the energy system.
It will be very interesting to link this two-site model to analyse
Figure 10. Schematic diagram of steel and sheet production line at SSAB Tunnplat AB
the possibilities of reducing CO2 emission from an integrated point of view.
DISCUSSIONS
The optimization model developed for the CO 2 emission analysis for integrated
steelmaking can be used in different ways. The system boundary can be chosen
depending on interests of the research work; correspondingly, CO 2 emission can be
simulated for different process units, the whole steel plant or from a global point of view
(e.g. LCA).
The model used for analyzing scrap addition into the BF/BOF system shows that
different
technical solutions have been chosen to minimize CO 2 emission. When looking at the
combined system, it is more beneficial to allow higher coke consumption in the BF and
higher silicon content in HM in order to gain a higher scrap melting capacity in the BOF;
thus, lower CO2 emission will be achieved. However, if only looking at the BF optimization,
the solution will tend to a lower silicon content HM production and to keep a lower
consumption instead. It can be seen from this analysis that it is important to actually have
a systematic view in order to avoid a sub-optimal solution by just adding scrap, which will
make it possible to decrease CO2 emission by changing the raw materials in a clever way.
However, it should
be pointed out that the prerequisites for scrap charging in the processes are different, and
there are also a number of other factors to consider, among other things charging
technology, productivity effects, scrap availability and tramp element contamination.
The model can be used as an assistant tool to help the decision maker choose an
acceptable trade-off between two goals by considering the different solutions when
looking at the Pareto front. The use of the Pareto front for the BF/BOF system shows that
the solution range is quite extensive. This means that there is a wide range of possibilities
to operate the production system considering the trade-off between the two criterias cost
and CO2 emission. The choice of solution will, of course, vary, depending on the decision
makers preference. This approach supports the insight that optimization can be used as
a means to help the decision makers to make their decisions, especially for the future
emission trading.
With the extension of the model boundary, the optimization model was used to
investigate the opportunities of meeting the emission allowance with a lower cost for the
studied steel plant via carbon-trading schemes, in this case EU ETS and CDM. The
results show that compared with EU ETS, a lower CO 2 reduction cost could be achieved
by use of CERs generated from CDM projects. The internal changes within the plant will
also play an important role to help the studied steel plant to meet the emission-trading
allowance and the further emission reduction comments, indicating the importance of the
internal changes for the steel plant independent of carbon-trading schemes. Therefore,
internal abatement should be encouraged as they can further improve the efficiency and
promote the discovery of new technologies for creating a more sustainable energy supply
both from an economic and an environmental point of view. It should be pointed out that
the carbon prices from different trading schemes have been fluctuating. A sensitivity
analysis would show the influence of carbon prices on potential CO 2 emission reduction
options. However, the analysis shows that by using this kind of analysis it is possible to
evaluate different measures for CO 2 reduction and their effects on the whole operation
system. It should also be pointed out that this study is based on a Swedish steel plant as
a calculation example. However, the model developed can with little modification be used
in any similar steel plant within the EU countries and beyond.
As a specific integrated steel plant, it will be of great interest to investigate some
energy-saving potentials within SSAB Tunnplat AB. Considering the fact that these two
sites are located in two different geographical locations, it is impossible for the RM to
directly utilize process gases generated from the steel plant as an energy carrier.
However, it would be possible if some process gases, e.g. coke oven gas, could be
liquefied or transformed to other kinds of fuel. At the moment, at the steel plant there is
excess coke oven gas for potential energy use. Two recent reports have studied the
possibilities of coke oven gas liquification and methanol production from coke oven gas
[15,16]. As a fuel that could be transported by using the current existing traffic tools
between two sites, the possibility of substituting parts of fuels used at the RM, i.e. oil and
LPG, will increase, which is worth investigating in the future.
CONCLUSIONS
A model on CO2 emission reduction in integrated steelmaking is described in this paper. A
few application cases have also been presented. The main conclusions drawn in this
paper are as follows:
]
]
]
A PI method has been used to analyze CO2 emission for the steel industry with
considera-tion of the material and the energy system. This model has a friendly
interface, easy to be manipulated by non-programming persons and to make the
analysis.
The optimization model has the generality and flexibility to be extended to cover more
pro-cesses, and it can be used to analyze CO 2 emission for a small, large or global
integrated
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