Numerical Study of The Gas Distribution in An Oxygen Blast Furnace. Part 1: Model Building and Basic Characteristics

You might also like

Download as pdf or txt
Download as pdf or txt
You are on page 1of 9

JOM, Vol. 67, No.

9, 2015
DOI: 10.1007/s11837-015-1529-y
Ó 2015 The Minerals, Metals & Materials Society

Numerical Study of the Gas Distribution in an Oxygen Blast


Furnace. Part 1: Model Building and Basic Characteristics

ZONGLIANG ZHANG,1 JIALE MENG,1 LEI GUO,1


and ZHANCHENG GUO1,2

1.—State Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing,
Haidian District, Beijing 100083, People’s Republic of China. 2.—e-mail: zcguo@metall.ustb.
edu.cn

Based on multifluid theory, transport phenomena theory, metallurgical reac-


tion kinetics, thermodynamics, and computational fluid dynamics, a multifluid
model for an oxygen blast furnace was established to evaluate the gas distri-
bution in a furnace. The uneven distribution of recycling gas in oxygen blast
furnaces was found to be a severe problem. This uneven distribution resulted
from injecting a large amount of recycling gas into the furnace shaft. Gas dis-
tribution substantially affects the energy and heat utilization of an oxygen blast
furnace. Therefore, the basic characteristics of the gas distribution in an oxygen
blast furnace are illustrated. The results show that in the top of the oxygen blast
furnace, the concentration differences of the CO and CO2 between the center
and edge reach 7.8% and 11.7%, respectively. The recycling gas from the shaft
tuyere only penetrates to two thirds the length of the radius.

transfer, mass transfer, and momentum transfer


INTRODUCTION
phenomena. Additionally, the internal processes are
Approximately two thirds of the global annual nearly unmeasurable because of the high tempera-
steel production utilizes a long blast furnace pro- ture and closed nature of ironmaking. Therefore,
cess. Therefore, blast furnaces play a significant role the blast furnace is considered to be the most com-
in the steel industry. However, this process involves plex reactor in the metallurgy field. To study the
high energy consumption, heavy environmental internal processes and phenomena of a blast fur-
pollution, and high CO2 emission, putting tremen- nace, numerous methods have been proposed, such
dous pressure on both the energy sector and the as a dissection investigation of blast furnaces4 and
environment. Furthermore, the energy-saving installing sensors in the inner wall of blast fur-
potential of traditional blast furnace technologies naces.5 However, a dissection investigation of blast
has reached a limit. Fortunately, oxygen blast fur- furnaces is expensive in terms of time and invest-
nace ironmaking1,2 can reduce more than 70% of the ment; sensors can only provide limited discrete
coke consumption, 11.1% of the energy consump- data, which is not sufficient for studying the com-
tion, and 59.6% of the CO2 emissions. This process prehensive internal phenomena. Among the meth-
can significantly improve the energy conservation ods, the mathematical models display unique
and reduce environmental pollution by transform- advantages, such as the multifluid model6,7 pro-
ing a traditional blast furnace. A variety of specific posed in the 1990s. These models can simulate
oxygen blast furnace processes have been proposed, temperature, velocities, concentration fields, and
among which the gasification furnace–full oxygen distributions of other parameters through mathe-
blast furnace (GF–FOBF) process3 (Fig. 1) displays matical calculations that are based on chemical
unique advantages because of the reforming and reactions, heat and mass transfers, and other com-
heating effects of the gasification furnace. The plex phenomena within the blast furnace. There-
gasification furnace provides safe, adequate, and fore, the situation inside the blast furnace can be
stable recycling gas. more visually understood. Moreover, many impor-
The ironmaking process involves many complex tant results derived from mathematical models have
chemical reactions and flow, phase change, heat been applied in the production process. Previously,

1936 (Published online July 8, 2015)


Numerical Study of the Gas Distribution in an Oxygen Blast Furnace Part 1: Model Building 1937
and Basic Characteristics

mathematical models have focused on traditional part, the influence of the design and operating
blast furnaces, and only a few models of oxygen parameters was investigated in Part 2 to further
blast furnaces have been reported. Oxygen blast optimize the gas distribution. The multifluid math-
furnaces such as the top-gas recycling blast furnace ematical model considered three phases: complex
in the ultra–low CO2 steelmaking (ULCOS) project chemical reactions, heat and momentum transfer,
in the European Union8 are currently in experi- and other processes. Therefore, this model is con-
mental and pilot-scale test stages. Additionally, sidered to be superior to most models that use two
limited numerical simulation studies are available phases and limited chemical reactions, ensuring the
concerning the internal phenomena of an oxygen validity of the results.
blast furnace.9,10 The gas distribution in an oxygen
blast furnace seriously affects its smooth operation, MODEL DESCRIPTION
energy consumption, and CO2 emissions because
Assumptions
the recycling gas carries a large amount of heat and
reducing gas. The distribution of this gas affects the To facilitate model building and numerical simu-
heat distribution in the blast furnace, which is sig- lation, the following was assumed:
nificant for energy conservation and environmental
1. Only gas, solid, and liquid phases were consid-
protection. However, no detailed descriptions are
ered; the fines in blast furnace were ignored.
available for the gas distribution in an oxygen blast
2. The coal injected into the blast furnace through
furnace or for the related influencing factors. In
the hearth tuyere was converted into substances
Part 1 of this study, the gas distribution in the
such as CO, CO2, and H2O under high temper-
oxygen blast furnace was studied with a multifluid
atures.
mathematical model, and the basic characteristics
3. Insignificant substances and reactions were
of the gas distribution in an oxygen blast furnace
ignored.
were summarized. Based on the findings of the first
4. The furnace top pressure was set to
1.2 9 105 Pa.
5. The cohesive zone was defined as the region in
which the solid temperature was 1373 K to
1673 K.
6. The blast furnace inner shape, tuyere positions,
and inner states were symmetrically dis-
tributed.

Phases and Reactions Involved in the Model


The substances in the blast furnace are divided into
three phases in the model.11,12 The phases and
substances involved in the model are shown in
Table I.
Table II shows the 12 chemical reactions and
three phase transitions in the model. In this model,
the indirect reduction reaction of iron ore is calcu-
lated using the unreacted core model.

Model Framework
The complexity of a blast furnace lies in the
chemical reactions and phase interactions, includ-
ing the heat and momentum exchanges among gas,
solid, and liquid phases. The material behavior in
the blast furnace follows three laws: conservations
of mass, conservation of momentum, and conserva-
Fig. 1. The schematic diagram of the GF–FOBF process. tion of energy. To facilitate computer programming,

Table I. Phases and substances involved in the model

Phases Substances
Gas CO, CO2, H2, H2O, N2, O2
Solid Fe2O3, Fe3O4, FewO, Fe, C, gangue(CaO, MgO, Al2O3, SiO2)
Liquid FewO, Fe, slag(CaO, MgO, Al2O3, SiO2)
1938 Zhang, Meng, L. Guo, and Z. Guo

Table II. Chemical reactions and phase transitions involved in the model

n Reactions Description
1 3Fe2O3(s) + CO(g) = 2Fe3O4(s) + CO2(g) CO indirect reduction reactions
2 w/(4w  3)Fe3O4(s) + CO(g) = 3/(4w  3)FewO(s) + CO2(g)
3 FewO(s) + CO(g) = wFe(s) + CO2(g)
4 3Fe2O3(s) + H2(g) = 2Fe3O4(s) + H2O(g) H2 indirect reduction reactions
5 w/(4w  3)Fe3O4(s) + H2(g) = 3/(4w  3)FewO(s) + H2O(g)
6 FewO(s) + H2(g) = wFe(s) + H2O(g)
7a FewO(l) + C(s) = wFe(l) + CO(absorbed on l) Direct reduction reactions
7b CO(absorbed on l) = CO(g)
8 C(s) + CO2(g) = 2CO(g) Boudouard reaction
9 C(s) + H2O(g) = CO(g) + H2(g) Water gas reaction
10 C(s) + 1/2O2(g) = CO(g) Incomplete combustion reaction
11 C(s) + O2(g) = CO2(g) Complete combustion reaction
12 CO(g) + H2O(g) = CO2(g) + H2(g) Vapor conversion reaction
13 Fe(s) = Fe(l) Melting phase change
14 FewO(s) = FewO(l)
15 Gangue(s) = Slag(l)

these conservation laws are represented in a unified where


form, as seen in Eq. 1. ll
b¼ (5)
@ðei qi wÞ ql ju~s  u~l jrh
þ divðei qi UwÞ ¼ divðei Cw gradwÞ þ Sw (1)
@t
where ei is the volume fraction of phase i in the blast el /s ds
furnace; qi is the fluid density of phase i, kg m3; U rh ¼ (6)
6es
is the velocity vector of phase, m s1; w is the uni-
versal variable of the conservation equation; Cw is ũi is the actual speed of phase i, m s1; us is the
the generalized diffusion coefficient; and Sw is the shape factor of the solid particle; CDgl is the gas–
generalized source term. Among these variables, w liquid interphase drag coefficient; ds is the solid
can represent u, v, w, H, and other solution vari- particle diameter, m; d1 is the droplet diameter, m;
ables. and ul is the droplet shape factor.
Similarly, the heat exchanges involved in the
Interphase Transfer of Momentum and Heat model include interactions among three phases. The
Because the phases and materials in the oxygen gas–solid, gas–liquid, and solid–liquid heat trans-
blast furnace model have been simplified, the fers can be calculated using Eqs. 7, 8, and 9, namely
interphase momentum exchanges involved in the the Ranz–Marshall equation,16 Mackey–Warner
model include interactions among three phases. The equation,17 and Eckert–Drake equation.18
gas–solid, gas–liquid, and solid–liquid interaction  
E_ gs ¼ Ags hgs Tg  Ts (7)
forces can be calculated using Eqs. 2, 3, and 4,
namely the Ergun equation,13 Richardson–Zaki
equation,14 and Kozeny–Carmen equation.15  
 2     2 E_ gl ¼ Agl hgl Tg  Tl (8)
lg 1  eg u~g  u~s qg 1  eg u~g  u~s
F~gs ¼ 150 þ 1:75
e2g d2s /2s eg ds /s
(2) E_ sl ¼ Asl hsl ðTl  Ts Þ (9)
where
 
3el ql    6eore 6ecoke
F~gl ¼ CDgl u~g  u~l  u~g  u~l (3) As ¼ fore þ fcoke (10)
4dl /l dore /ore dcoke /coke

q  
F~sl ¼ l ju~s  u~l j 5b þ 0:4b0:1 ðu~s  u~l Þ (4) Ags ¼ As  Asl (11)
rh
Numerical Study of the Gas Distribution in an Oxygen Blast Furnace Part 1: Model Building 1939
and Basic Characteristics

Fig. 3. Geometrical parameters and mesh distribution of the mod-


eled blast furnace.

1 1 1
¼ þ (17)
hsl hs hl
hij is the heat-transfer coefficient between phase i
Fig. 2. Solution procedures for the multifluid model. and phase j, W m2 K1; Weij is the Weber number
between phase i and j; hij is the contact angle be-
tween phase i and j, °; Frij is the Froude number
between phase i and j; and ks is the thermal con-
Asl ductivity of the solid phase, W m1 K1.
0:218
¼ 0:400Resl 0:0428
Wesl Fr0:0238
sl ð1 þ cos hsl Þ0:0235
As
Boundary Conditions and Solving Strategies
(12)
The boundary conditions of the three phases are
different, and the specific settings are described
! below. For the gas phase, the gas composition and
kg 1=3
hgs ¼ 2:0 þ 0:39Re1=2
gs Pr (13) temperature at the tuyere are set as the components
ds g
and temperature after reaction of pulverized coal
and oxygen. At the outlet of the top furnace, the gas
  flow is fully developed. The furnace wall allows the
h i Scg 2=3 gas phase to slide freely. For the solid phase, the
Agl hgl ¼ 4:18 eg qg u~g Cpg ðel u~l Þ0:35 Re0:37
gl composition and temperature of the solid phase at
Prg
the burden surface are set according to the actual
(14) production parameters. The outlet of the solid phase
was set at the bottom of the furnace wall, and the
 pffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi  solid phase flow is fully developed in the outlet. In
kl 2 Resl Prl
hl ¼ pffiffiffiffiffiffiffi pffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi (15) addition, the furnace wall and deadman produce
ds 1:55 Prl þ 3:09 0:372  0:15 Prl some friction to the solid phase flow. The total heat
loss of the furnace wall is allocated to the gas phase
and solid phase. The heat losses of the furnace wall
sffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi
in the gas and solid energy source terms are calcu-
ks Cps qs ju~l  u~s j lated using Eq. 18. The furnace wall is a freely
hs ¼ 2 (16)
pds sliding interface for the liquid phase, and the liquid
1940 Zhang, Meng, L. Guo, and Z. Guo

Because of the strong couplings among the gas,


Table III. The operating parameters for the liquid, and solid phases and because each equation
simulated traditional blast furnace simultaneously requires an iterative solution, a
parallel computer cluster is used to solve the model
Operating and reduce the convergence time. When the three-
Phases parameters Values
phase continuity equation residuals are less than
Gas Blast rate, blast 1700 m3 min1, 1423 K, 0.001, the calculation is complete.
temperature, 1.7%, 1.66%, 1.2 9 105 Pa,
humidity, oxygen and 2.2 9 105 Pa NUMERICAL SOLUTION AND OPERATION
enrichment rate, PARAMETERS
top pressure, and
blast pressure Solution Procedure
Solid Daily output of iron, 2100 t day1, 76.66%,
Well-established sequential solution procedures
Fe2O3 content, coke 370 kg t1, 82.28%, 298 K,
rate, fixed carbon and 170 kg t1 are employed to calculate the comprehensive
content of coke, momentum, mass and energy transfers through the
charge tempera- steps shown in Fig. 2. The parameters are calcu-
ture, and coal injec- lated through iterations with given operational
tion ratio conditions.
Liquid [C], [Si], [S], [P], 4.6, 0.5, 0.025, 0.084,
and [Mn] content in and 0.15% Blast Furnace Structure and Computational
hot metal Grid
In this model, the study object is a blast furnace
with a hearth diameter of 6.8 m, a height of
19.95 m, and an effective volume of 750 m3. A body-
fitted coordinates (BFC) grid was generated in this
Table IV. The operating parameters of the oxygen area. The geometrical parameters and mesh distri-
blast furnace for the basic case in the GF–FOBF butions of the blast furnace are shown in Fig. 3. No
process shaft tuyeres of a traditional blast furnace were
available.
Operating
Phases Parameters Values Operating Parameters for the Blast Furnace
3 1
Gas Blast rate, blast 536.7 m min , 29 8 K, The operational results of a traditional blast fur-
temperature, oxy- 90.0%, 1.2 9 105 Pa nace were calculated using the model, and the
gen concentration, simulation results were compared with actual pro-
and top pressure duction data to verify the validity of the model. The
Solid Daily output of iron, 3150 t day1, 76.66%,
Fe2O3 content, coke 205 kg t1, 82.28%, 298 K,
main operating parameters of the actual production
rate, fixed carbon 200 kg t1 blast furnace are shown in Table III. On the basis of
content of coke, the model validation, the boundary conditions and
charge tempera- internal parameters of the model were modified to
ture, and coal injec- obtain the oxygen blast furnace mathematical
tion ratio model. In the simulations of the oxygen blast fur-
Liquid [C], [Si], [S], [P], 4.6%, 0.5%, 0.025%, 0.084%, nace, one set of parameters was set as the base case.
and [Mn] content in 0.15% The operating parameters are shown in Table IV.
hot metal Two rows of tuyeres are present in the oxygen
blast furnace. The recycling gas volumes, composi-
phase can pass freely through the slag interface in tions, and temperatures of these tuyeres are shown
the lower portion of the blast furnace. in Table V. To ensure the reasonable setting of the
  inlet boundary conditions, all conditions were cal-
Tg;wall þ Ts;wall culated by a comprehensive mathematical model
Qg;wall ; Qs;wall ¼ 0:5Awall hwall  Twall
2 established on balancing the chemical reactions and
(18) maintaining the conservation of material and en-
ergy under the corresponding operating conditions.
where Qg,wall and Qs,wall are the gas and solid heat
loss of the furnace wall, respectively, W; Awall is the RESULTS AND DISCUSSION
furnace wall area, m2; and Tg,wall and Ts,wall are the
temperatures of the gas phase and solid phase near Model Validation
the furnace wall, respectively, K. The convective To verify the validity and accuracy of the model,
heat-transfer coefficient hwall and the furnace wall the model was used to calculate the parameters of a
temperature Twall are set to 20 W m2 K1 and traditional blast furnace. Figure 4 shows the tem-
298 K, respectively. perature distribution of the three phases, and the
Numerical Study of the Gas Distribution in an Oxygen Blast Furnace Part 1: Model Building 1941
and Basic Characteristics

Table V. Recycling gas parameters for the oxygen blast furnace

Recycling Gas composition (vol.%)

Region CO CO2 H2 H 2O O2 N2 Gas volume (m3 t21) Temperature (K)


Recycling gas into shaft 80.5 – 8.4 – – 11.1 358.0 1173
Recycling gas into hearth 80.5 – 8.4 – – 11.1 400.0 1173

Table VI. Comparisons of the calculated top gas compositions and the measured values for a traditional
blast furnace

Top gas compositions CO CO2 H2 H2O O2 N2


Calculated values (vol.%) 22.5 20.3 1.5 3.1 0.1 52.5
Measured values (vol.%) 21.9 20.2 1.9 2.3 0.3 53.4

Fig. 4. (a) Gas, (b) solid, and (c) liquid temperature field in a traditional blast furnace (K).

dashed line represents the cohesive zone. From this surements. The cohesive zone displays an inverted
figure, the calculated temperature fields match well V-shape.
with the temperature distribution trends obtained The calculated top gas components were com-
by anatomical blast furnace or other actual mea- pared with the values noted during actual produc-
1942 Zhang, Meng, L. Guo, and Z. Guo

tion (Table VI). Minimal differences were noted be- Basic Characteristics of the Gas Distribution
tween these two sets of values, reflecting the high in an Oxygen Blast Furnace
credibility of the calculated results of the model.
To determine the basic characteristics of the gas
distribution in an oxygen blast furnace, the base
case for an oxygen blast furnace was calculated with
the multifluid model. CO and CO2 replaced N2 as
the main components of the gaseous phase in the
oxygen blast furnace, and their distributions are
essential to the smooth operation of the blast fur-
nace. Therefore, CO and CO2 can be used to char-
acterize the distribution of the gas phase in oxygen
blast furnaces.
Figure 5 shows the calculated concentration dis-
tributions of CO and CO2 in the oxygen blast fur-
nace. Below the shaft tuyere in the furnace, the
contours of CO and CO2 are parallel to the hori-
zontal plane and their volume fractions decrease or
increase as the height increases, whereas their
contours becomes parallel to the vertical direction
above the shaft tuyere. In the upper and top part of
the furnace, the CO volume fraction distribution
also presents a gradually decreasing trend from the
edge to the center of the furnace, whereas the CO2
volume fraction shows an opposite trend. This phe-
nomenon mainly results from the collisions of the
recycling gas injected into the blast furnace through
the shaft tuyere with the charge temperature and
the gas ascending from the hearth. These collisions
hamper the horizontal movement of the recycling
gas and promote an upward movement, causing an
uneven distribution of the recycling gas.
Figure 6a and b shows the radius distributions of
CO and CO2 at different heights above the shaft
tuyere in the oxygen blast furnace used in the GF–
FOBF process, respectively. From this figure, the
CO concentration decreases from the edge to the
center at the identical height above the shaft tuyere.
In addition, as the height increases, the CO con-
Fig. 5. Volume fraction distributions of (a) CO and (b) CO2 in the centration decreases, whereas the CO2 concentra-
oxygen blast furnace. tion shows an opposite trend. At the top of oxygen

Fig. 6. Radial distributions of (a) CO and (b) CO2 at different heights in the oxygen blast furnace.
Numerical Study of the Gas Distribution in an Oxygen Blast Furnace Part 1: Model Building 1943
and Basic Characteristics

Fig. 7. The experimental results from the literature: (a) volume fraction distribution of shaft recycling in the upper furnace and (b) radial
distribution of the shaft recycling gas at different heights of the furnace shaft.

blast furnace, the concentration differences of the model considers the chemical reactions and high
CO and CO2 between center and edge reach a temperatures that are ignored in this previous
maximum (7.8% and 11.7%, respectively). These experiment. The similarity between the simulation
values can be used to represent the uneven distri- results and the experimental results shows that the
bution degree of the reducing gas. However, both model is appropriate for studying the gas distribu-
remain stable in the central portion (the inner one tion in an oxygen blast furnace. Furthermore, the
third of the blast furnace). This phenomenon indi- model is more accurate and comprehensive to con-
cates that the recycling gas from the shaft tuyere sider completely the actual conditions.
can only penetrate to two thirds of the radial
direction. Natsui et al.19,20 called the infiltration of CONCLUSION
the recycling gas toward the center the radial eddy
diffusion effect; this effect results from the irregular The gas distribution in an oxygen blast furnace
distribution of the gas in the radial direction caused was studied with a recently established multifluid
by turbulent diffusion. Because the even distribu- model. The main findings of this study are sum-
tion of recycling gas is essential to reducing the marized as follows:
burden, distributing the temperature, and utilizing 1. Because of the introduction of the shaft tuyere,
the reducing gas, the magnitude of the radial eddy the uneven distribution of the recycling gas
diffusion effect plays a significant role in the uti- becomes a severe problem. Below the shaft
lization of the recycling gas in an oxygen blast fur- tuyere, the reducing gas is evenly distributed.
nace. However, the recycling gas is unevenly dis-
To further validate the application of the oxygen tributed above the shaft tuyere. The distribu-
blast furnace multifluid model in the study of the tions of CO and CO2 can be used to demonstrate
gas distribution, the simulation results of the gas this problem.
distribution in the blast furnace was compared with 2. The gas distribution in an oxygen blast furnace
the experimental results of the gas distribution in displays concentration differences of CO and
an oxygen blast furnace obtained by Liu et al.21 CO2 between the center and edge at the top of
Figure 7a and b show the typical gas distribution in the furnace, reaching 7.8% and 11.7%, respec-
the upper furnace and the radial distributions of the tively. The recycling gas from the shaft tuyere
recycling gas injected through the shaft tuyere in only penetrates two thirds of the radius; i.e., the
the experimental study, respectively. The volume recycling gas is concentrated at the edge of the
fraction distribution trend is similar to the distri- blast furnace. Therefore, the recycling gas uti-
bution in Fig. 5a. The recycling gas injected through lization is seriously affected.
the shaft tuyere is concentrated at the edge of the
blast furnace. The upper part of the furnace is di-
ACKNOWLEDGEMENT
vided into two parts: the hearth gas-affected zone
and the shaft recycling gas-affected zone. For the This research was supported by the National
radial distribution of recycling gas, the experimen- Natural Science Foundation of China (Grant No.
tal data measured at different heights of the furnace 51134008) and National Program on Key Basic Re-
is similar to the radial distribution of CO shown in search Project of China (973 Program) (Grant No.
Fig. 6a. Small differences are noted because the 2012CB720401).
1944 Zhang, Meng, L. Guo, and Z. Guo

REFERENCES 11. H. Nogami, M.S. Chu, and J. Yagi, Rev. Metall. 102, 189
(2005).
1. M.S. Qin and Y.T. Zhang, Ironmak. Steelmak. 15, 287 12. M.S. Chu, H. Nogami, and J. Yagi, ISIJ Int. 44, 2159 (2004).
(1988). 13. S. Ergun, Chem. Eng. Prog. 48, 89 (1952).
2. R. Murai, M. Sato, and T. Ariyama, ISIJ Int. 44, 2168 (2004). 14. J.F. Richardson and R.A. Meikle, Trans. Inst. Chem. Eng.
3. J.L. Meng, H.Q. Tang, and Z.C. Guo, Appl. Mech. Mater. 39, 348 (1961).
268, 356 (2013). 15. P.C. Carman, Chem. Eng. Res. Des. 75, S32 (1997).
4. T. Inada, A. Kasai, K. Nakano, S. Komatsu, and A. Ogawa, 16. W.E. Ranz and W.R. Marshall, Chem. Eng. Prog. 48, 141
ISIJ Int. 49, 470 (2009). (1952).
5. T. Iwamura, H. Sakimura, Y. Maki, T. Kawai, and Y. Asano, 17. P.J. Mackey and N.A. Warner, Metall. Trans. 3, 1807 (1972).
Trans. Iron Steel Inst. Jpn. 22, 764 (1982). 18. E.R.G. Eckert and R.M. Drake, Heat Mass Transfer, 2nd ed.
6. J. Yagi, ISIJ Int. 33, 619 (1993). (New York: McGraw-Hill Book Co., 1976), p. 173.
7. M.S. Chu, H. Nogami, and J. Yagi, ISIJ Int. 44, 801 (2004). 19. S. Natsui, S. Ueda, H. Nogami, J. Kano, R. Inoue, and T.
8. K. Meijer, M. Denys, J. Lasar, J.P. Birat, G. Still, and B. Ariyama, ISIJ Int. 51, 1410 (2011).
Overmaat, Ironmak. Steelmak. 36, 249 (2009). 20. S. Natsui, S. Ueda, H. Nogami, J. Kano, R. Inoue, and T.
9. M.S. Chu and J. Yagi, Steel Res. Int. 81, 1043 (2010). Ariyama, ISIJ Int. 51, 51 (2011).
10. M.S. Chu, X.F. Yang, F.M. Shen, J. Yagi, and H. Nogami, J. 21. J.Z. Liu, Q.G. Xue, X.F. She, and J.S. Wang, Beijing Keji
Iron. Steel Res. Int. 13, 8 (2006). Daxue Xuebao 36, 817 (2014).

You might also like