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Download pdf 10Th International Symposium On High Temperature Metallurgical Processing Tao Jiang ebook full chapter
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High-Temperature Metallurgical
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10th International
Symposium on
High-Temperature
High-Temperature
Metallurgical
Processing
EDITED BY
Tao Jiang
Jiann-Yang Hwang
Dean
De an Gregurek
Zhiwei Peng
Peng
Jerome P. Downey
Baojun Zhao
Onuralp Yücel
Ender Keskink
Keskinkilic
ilic
Rafael Padilla
The Minerals, Metals & Materials Series
Tao Jiang Jiann-Yang Hwang
• •
Rafael Padilla
Editors
10th International
Symposium
on High-Temperature
Metallurgical Processing
123
Editors
Tao Jiang Jiann-Yang Hwang
Central South University Michigan Technological University
Changsha, China Houghton, MI, USA
Rafael Padilla
University of Concepción
Concepción, Chile
This Springer imprint is published by the registered company Springer Nature Switzerland AG
The registered company address is: Gewerbestrasse 11, 6330 Cham, Switzerland
Preface
This book presents selected papers submitted for the 10th International Symposium
on High-Temperature Metallurgical Processing organized in conjunction with the
TMS 2019 Annual Meeting and Exhibition in San Antonio, Texas, USA. More than
120 abstracts were received. Among them, 90 were selected for oral presentation
and 34 were provided with a poster presentation opportunity. After reviewing the
submitted manuscripts, 75 were accepted for publication in this book.
As the title of symposium suggests, the interest of the symposium is on thermal
processing of minerals, metals and materials that intends to promote physical and
chemical transformations of materials to enable the extraction and production of
valuable materials such as metals, alloys, ceramics and compounds. The sympo-
sium was open to participants from both industry and academia and focused on
innovative high-temperature technologies including those based on non-traditional
heating methods as well as their environmental aspects such as handling and
treatment of emission gases and by-products. Because high-temperature processes
require high energy input to sustain the temperature at which the processes take
place, the symposium addressed the needs for sustainable technologies with
reduced energy consumption and reduced emission of pollutants. The symposium
also welcomed contributions on thermodynamics and kinetics of chemical reac-
tions, phase transformations that take place at elevated temperatures, as well as
simulation of high-temperature metallurgical processes. We hope the book will
serve as a reference for both new and experienced metallurgists, particularly those
who are actively engaged in exploring innovative technologies and routes that lead
to more energy-efficient and environmentally sustainable solutions.
v
vi Preface
Tao Jiang
Jiann-Yang Hwang
Dean Gregurek
Zhiwei Peng
Jerome P. Downey
Baojun Zhao
Onuralp Yücel
Ender Keskinkilic
Rafael Padilla
Contents
vii
viii Contents
xv
xvi About the Editors
Shun Yao, Sheng-li Wu, Bo Song, Ming-yin Kou and Heng Zhou
Abstract A carbon loss mathematical model was established based on the Fe–O–C
balance and traditional engineering method. The coke carbon loss and carbon loss
of coupled direct reduction are calculated based on this model and actual production
data of B# blast furnace in Bayisteel. And then, the model is applied to research the
effect of coal ratio, burden metallization rate, blast temperature, oxygen enrichment
rate and blast humidity on carbon loss of direct reduction and carbon loss of
coupled direct reduction. The results show that burden metallization rate and
oxygen enrichment rate have significant influences on carbon loss of direct
reduction. The burden metallization rate, oxygen enrichment rate and coal ratio
have significant influences on carbon loss of coupled direct reduction. In addition,
comparing with 4# blast furnace in Baosteel, the high-quality coke can observably
reduce carbon loss of coupled direct reduction.
Introduction
Metallurgical coke is the most important and inevitable raw material in the blast
furnace. Metallurgical coke is a fuel, a reductant, a carburetant, a permeable grid in
the blast furnace. And coke is indispensable material in the blast furnace, because it
sustains the passages of liquid metal and slag towards the lower part and of
high-temperature reducing gas towards the upper part, and it is the only material
that remains a solid phase in the high-temperature zones adjacent to the blast
furnace raceways. Coke quality affects the gas permeability, liquid permeability of
the burden and state of hearth [1].
steam gasified coke than CO2 gasified coke. After reacting with CO2 and steam, the
high-temperature compressive strength of coke will decrease with the increasing of
solution loss or temperature. Guo et al. [11] researched the solution loss kinetics
behaviour on coke strength after reaction. The results showed that the temperature
of gradient reaction brings the most serious degradation to three cokes are different
due to different reactivity, and the temperature of the high reactive coke is about
1100 °C which is lower than another two cokes. Liu et al. [12] investigated kinetics
of coke gasification with CO2 by non-isothermal thermogravimetry. The results
showed that when the gasification temperature is higher than 1200 K, both of the
gasification reaction rate and carbon conversion rate increase significantly. When
the gasification temperature reaches about 1500 K, the gasification reaction rate
reaches the maximum. NOMURA et al. [13] investigated the strength of
catalyst-added highly reactive coke after solution loss reaction. This result showed
that the adding method and the types of catalyst have a great influence on the
post-reaction strength of coke.
These researches have important guiding significance to ironmaking process, but
there is few information about the quantization of coke solution loss in the blast
furnace. In this study, a carbon loss calculation model is established based on
traditional engineering method and Fe–O–C balance. The coke carbon loss of direct
reduction and carbon loss of coupled direct reduction in B# blast furnace of
Bayisteel are calculated based on actual production data. Discussions were made on
the influences of different operating factors to coke carbon loss.
Modelling
There are some shortcomings in traditional engineering method, such as using the
assumed direct reduction degree, unchangeable empirical specific heat capacity and
ignoring the effects of blast humidity and pulverized coal. Therefore, the short-
comings of traditional engineering method have been corrected in this work. Firstly,
carbon loss of direct reduction is calculated by this model based on conservation of
carbon. Then the amount of carbon loss of coupled direct reduction can be cal-
culated by the result of carbon loss of direct reduction. This model assumes the
following conditions: all pulverized coal is burned with oxygen; all combustion of
carbon and oxygen is incomplete combustion; it is 0.999:0.001 that the distribution
ratio of iron to hot metal and slag.
RFeðDRÞ
rd ¼ ð1Þ
RFeðpigÞ
where rd represents the direct reduction degree; RFe(DR) represents the amount of Fe
that is generated by direct reduction, kg/t; RFe(pig) represents the amount of Fe in hot
metal, kg/t.
According to Fe–O–C balance, the amount of Fe element produced by direct
reduction could be calculated by carbon loss of direct reduction. The calculating
formula is shown as follows:
56
RFeðDRÞ ¼ RCðDRÞ ð2Þ
12
where RC(total) is the total amount of carbon in coke, kg/t; RC([C]) is the amount of
carbon consumed by hot metal carburization, kg/t; RC(Vad) is the amount of carbon
in volatiles of coke, kg/t; RC(XO) is the amount of carbon consumed by non-ferrous
oxide direct reduction, kg/t; RC(combustion) is the amount of carbon consumed by
combustion of coke in raceway, kg/t; RCðH2 OÞ is the amount of carbon consumed by
oxygen of blast moisture, kg/t; RC(dust) is the amount of carbon in dust, kg/t.
In blast furnace, carbon loss of direct reduction reaction can be divided into coupled
direct reduction carbon loss reaction and molten direct reduction carbon loss
reaction according to different reaction modes. The direct reduction reaction is
coupled by solution loss reaction and indirect reduction reaction, and this direct
reduction reaction is regarded as coupled direct reduction reaction. Therefore, the
amount of carbon consumed by solution loss reaction is same to coupled direct
reduction carbon loss reaction. Besides, molten direct reduction carbon loss reaction
is caused by direct reduction of coke and molten slag.
In this model, the reduction zone of iron oxide in blast furnace is divided into 3
parts as follows:
(1) Indirect reduction zone. In this zone, the direct reduction reaction does not
occur. The indirect reduction reaction equations as follows:
A Mathematical Model for Carbon Loss of Blast Furnace … 7
(2) Coupled direct reduction zone. In this zone, indirect reduction reaction and
solution loss reaction can be coupled into direct reduction reaction. The solu-
tion loss reaction equations are shown as:
Eqn (4) + Eq. (6) and Eq. (5) + Eq. (7) can obtain direct reduction reaction
equation as follows:
(3) Molten direct reduction zone. In this zone, the indirect reduction reaction does
not occur. And coke is the only material that remains a solid phase, the direct
reduction reaction occurs between coke and molten slag. The molten direct
reduction reaction equation is shown as:
The coke consumption in BF is shown in the following ways: iron oxide direct
reduction; hot metal carburization; volatile matter of coke volatile; non-ferrous
oxide direct reduction; combustion in raceway; coke fines are discharged with
gas into dust. The iron oxide direct reduction includes coupled direct reduction
and molten direct reduction, and the coke carbon loss includes carbon loss of
coupled direct reduction and carbon loss of molten direct reduction.
The following assumptions are made for the calculation of coupled direct
reduction carbon loss: the coke carbon loss rate is 30% before coke falling into
the raceway [9, 14]; before coke falling into raceway, the coke carbon loss is
caused by coupled direct reduction, hot metal carburization, coke volatiles and
coke fines that are discharged into dust; the carbon loss of molten direct
reduction is ignored before coke drops into raceway; the hot metal carburization
can be completed 80% before hot metal droplets drop into raceway [15].
The formula for carbon loss of coupled direct reduction is as follows:
where RC(CDR) represents the amount of carbon loss of coupled direct reduction,
kg/t; kLC represents the coke carbon loss ratio, it is 0.3 in assumptions; kCC
represents the completed ratio of hot metal carburization, it is 0.8 in
assumptions.
8 S. Yao et al.
where RC(MR) represents the amount of carbon loss of molten direct reduction,
kg/t.
Based on the carbon loss model, it is investigated that the influence of burden
metallization rate, oxygen enrichment rate and blast humidity on coke carbon loss
and carbon loss of coupled direct reduction. The calculation results are shown in
Fig. 1 and Fig. 2, respectively.
The meanings of these symbols in Fig. 1 are as follows. A represents the effect
of coal ratio on carbon loss of direct reduction. It shows that with the increasing
10 kg/t of the coal ratio, the carbon loss of direct reduction is 0.45 kg/t. The effect
of blast temperature on carbon loss of direct reduction is shown in B. The carbon
loss of direct reduction increases 0.14 kg/t when the blast temperature increasing
50 °C.
The effects of burden metallization rate on carbon loss of direct reduction are
shown in C and D. C represents the carbon loss of direct reduction decreases
1.69 kg/t with the increasing 2% of the burden metallization rate by adding scrap
iron. It can be seen from D that using the pre-reduced burden to increase burden
metallization rate by 2% will reduce the carbon loss of direct reduction by about
7.16 kg/t. The effects of oxygen enrichment rate on carbon loss of direct reduction
are shown in E and F. E represents that an increment in oxygen enrichment rate of
1% under the condition that blast volume is constant will reduce the carbon loss of
direct reduction by about 3.13 kg/t. F represents that an increment in oxygen en-
richment rate of 1% under the condition that bosh gas volume is constant will
reduce the carbon loss of direct reduction by about 1.81 kg/t. The effects of blast
humidity on carbon loss of direct reduction are shown in G and H. G represents that
in order to ensure sufficient heat in the hearth, the blast temperature is increased
during the process of increasing the blast humidity. It can be seen from G that as the
blast humidity increases 5 g/m3, the carbon loss of direct reduction is decreased by
1.15 kg/t. H represents that in order to ensure sufficient heat in the hearth, the
amount of pulverized coal injection is reduced during the process of increasing the
blast humidity. It can be seen from H that with the blast humidity increasing 5 g/m3,
the carbon loss of direct reduction is reduced by 1.15 kg/t.
The meanings of these symbols in Fig. 2 are as follows. A represents the effect
of coal ratio on carbon loss of coupled direct reduction. It shows that with the
increasing 10 kg/t of the coal ratio, the carbon loss of coupled direct reduction is
2.08 kg/t. The effect of blast temperature on carbon loss of coupled direct reduction
is shown in B. The carbon loss of coupled direct reduction decreases 1.6 kg/t when
the blast temperature increasing 50 °C. The effects of burden metallization rate on
carbon loss of coupled direct reduction are shown in C and D. C represents the
carbon loss of coupled direct reduction decreases 1.83 kg/t with the increasing 2%
of the burden metallization rate by adding scrap iron. It can be seen from D that
using the pre-reduced burden to increase burden metallization rate by 2% will
reduce the carbon loss of coupled direct reduction by about 5.26 kg/t. The effects of
oxygen enrichment rate on carbon loss of coupled direct reduction are shown in E
and F. E represents that an increment in oxygen enrichment rate of 1% under the
condition that blast volume is constant will reduce the carbon loss of coupled direct
reduction by about 3.00 kg/t. F represents that an increment in oxygen enrichment
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