1 2006 annual meeting, san antonio, tx, u.s.a, march 12–16, 2006 iron removal from titanium ore by...
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Iron Removal from Titanium Oreby Electrochemical Method
Isao Obana1 and Toru H. Okabe2
1Graduate School of Engineering, The University of Tokyo
2International Research Center for Sustainable Materials, Institute of Industrial Science, The University of Tokyo
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AircraftSpacecraftChemical plantsImplantsArtificial bones, etc.
Applications
Lightweight and high strengthCorrosion resistantBiocompatibleSome titanium alloys : shape memory effect superelasticity
Introduction
Ti ore + C + 2 Cl2 → TiCl4 (+ FeClx) + CO2
Chlorination
TiCl4 + 2 MgReduction
MgCl2
Electrolysis
The Kroll process: Currently employed Ti production processMg & TiCl4 Feed port
SpongeTitanium
→ Ti + 2 MgCl2
→ Mg + Cl2
ReactionContainer
MgCl2
Features of titanium
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2. Chlorine circulation in the Kroll process can be improved.
3. This process can also be applied to the new Ti production processes, e.g., the direct electrochemical reduction of TiO2.
Upgrading Ti ore
(CaCl2)
Ti ore (Ilmenite, FeTiOx) Upgraded Ilmenite (UGI)
TiOx
FeOx Others
TiOxFeOx
Others Upgrade Chloridewastes
Discarded
Ti metal
Ti smelting
Low grade Ti ore
Upgraded Ti ore FeClx(+AlCl3)
(FeTiOX)
(TiO2)
MClx
Chlorine recovery
Selective chlorination
Fe TiCl4
Ti scrap
Advantages:1. Material cost can be
reduced by using low-grade ore.
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Previous study
Ref. R. Matsuoka and T. H. Okabe: Symposium on Metallurgical Technology for Waste Minimization at the 2005 TMS Annual Meeting, San Francisco, California (2005.2.13–17).
The selective chlorination of Ti ore by MgCl2 or CaCl2 is found to be feasible.
Pyrometallurgical de-Fe process
FeOx (s, in Ti ore) + MgCl2 (s, l) → FeClx (l, g) + MgO (s)
CaCl2 (s, l) + H2O (g) → HCl (g) + CaO (s)
FeOx (s, in Ti ore) + HCl (g) → FeClx (l, g) + H2O (g)Susceptor
RF coil
Vacuum pump
Quartz Tube
Deposit
Mixture ofTi oreand MClx
N2 or N2+H2O gas
Condenser
(FeClx)
T = 973~1373 K
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Study objectives
1. Thermodynamic analysis of selective chlorination2. Fundamental experiments of selective chlorination by electrochemical methods 3. Reduction experiment for the sample obtained by selective chlorination
Application of electrochemical methodusing molten salt
Low-grade Ti ore
TiO2 + flux
(FeTiOx)
Fe removal byselective chlorination
Ti powder
Direct reduction of TiO2
obtained after Fe removal
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Fig. Chemical potential diagram for Fe-Cl-O and Ti-Cl-O systems at 1100 K
The selective chlorination of Ti ore by controlling chlorine partial pressuremay be possible using an electrochemical technique.
Thermodynamic analysis (Ti ore chlorination)
Ti ore : FeTixOy
For simplicity, it is assumed to be amixture of TiOx and FeOx
TiCl4 (g)
TiCl3 (s)
–40
–10
–30
–20
–50
–60
0
-40 -10-30 -20 0
CaO (s)/CaCl2 (l) eq.aCaO = 0.1
Fe-Cl-O and Ti-Cl-O system, T = 1100 K
Potential regionfor selective chlorinationof iron from titanium ore
Potential region for chlorinationof titanium
Oxy
gen
part
ial p
ress
ure,
lo
g p
O2 (
atm
)
Chlorine partial pressure, log pCl2 (atm)
C/CO eq.CO/CO2 eq.
H2O (g)/HCl (g) eq.
MgO (g)/MgCl2 (l) eq.
TiCl2 (s)
FeO (s)
Fe2O3 (s)
FeCl2 (l)
Fe3O4 (s)
FeCl3 (g)Fe (s)
TiO (s)
TiO2 (s)
Ti (s)
TiO2 → Stable
FeOx → FeClx (g)
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2 Cl– (in CaCl2) → Cl2 + 2 e–
Anode:
Chlorine chemical potential in molten CaCl2 at anode
can be increased electrochemically.
Cathode :
Ca2+ + 2 e– → Ca
Electrolysis
Fen+ + n e– → Fe
FeOx + Cl2 → FeClx↑ + O2–
e–
Molten salt (CaCl2, MgCl2, etc.)
DC power source
Upgraded orlow-grade Ti ore(e.g., FeTiOx)
FeCl3, AlCl3, O2, CO2 gas
Chlorination by increasing Cl2 potential
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Reactions
CaCl2 (l) = Ca (l) + Cl2 (g) 629 3.26
FeO (s) = Fe (s) + 1/2 O2 (g) 201 1.04
FeO (s) + 1/2 C (s) = Fe (s) + 1/2 CO2 (g) 3 0.02
FeTiO3 (s) + CaCl2 (l) + 1/2 C (s)= TiO2 (s) + FeCl2 (l) + Ca (l) + 1/2 CO2 (g)
438 2.34
a: I. Barin: Thermochemical Data of Pure Substances, 3rd ed. (Weinheim, Federal Republic of Germany, VCH Verlagsgesellschaft mbH, 1997)
FeO (s) + CaCl2 (l) + C (s) = FeCl2 (l) + CO (g) + Ca (l) 409 2.23
Theoretical decomposition voltage
Under a certain condition, the selective chlorination of Fe in Ti ore may proceed below the theoretical decomposition voltage of CaCl2.
Go /kJ mol-1a E o /Va
Table Standard Gibbs energy of decomposition and theoretical voltage of that in several chemical species at 1100 K.
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Iron removal by selective chlorination using an electrochemical method
Low-grade Ti ore
TiO2 + flux
(FeTiOx)
Fe removal byselective chlorination
Ti powder
Direct reduction of TiO2
obtained after Fe removal
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Experimental apparatus
(a) Reaction chamber (b) Reaction cell
Ceramic insulator
Thermocouple
Heater
Rubber plug
Ar inlet
Wheel flange
Stainless steel tube (Electrode)
Molten salt (CaCl2)
Potential lead (Nickel wire)
Mild steel crucible (Cathode)
Graphite crucible (Anode)
Sample
V
A
Height 40 mm
(a) (b)
I.D. 17 mm
O.D. 19 mm
Surface of molten salt
Support rod(Stainless steel tube)
Sample(Ti ore, CaCl2, etc.)
Screw (Stainless steel)
Graphite crucible
Air hole
Holes formolten salt diffusion
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Selective chlorination experiments
Mass of sample i, wi/g
Ti oreCaCl2
Carbonpowder
4.00 ー ーA
B
C
0.74
0.74
2.17
2.17
ー0.18
Voltage,E/V
Time,t”/h
1.5
1.5
1.5
12
3
3
Ilmenite UGI
D
E
1.59
1.59
1.27
1.27
ー 1.5
2.0
3
3
ー
ーー
ーー ー
Experimental conditions:Temperature: Atmosphere: Molten salt: Cathode: Anode:
Exp. No.
Sample
MoltenCaCl2
Mild steelcrucible(Cathode)
Graphite cruciblecontaining Ti ore(Anode)
Voltage monitor/controller
e–
Low initial Fe content
1100 KArCaCl2 (800 g)Mild steel crucible (I.D. 96 mm)Graphite crucible (I.D. 17 mm)
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Results of the selective chlorination experiments
XRF analysis
Fe/Ti ratio decreasedfrom 114% to 7.2% (ilmenite)and from 2.00% to 0.18% (UGI).
Table Analytical results of the samples obtained after electrochemical selective chlorination
0.295.9 1.9 0.1 0.1 2.00
94% of Fe in ilmenite and 92% of Fe in UGI were successfully removed.
Exp. D 0.598.0 0.2 0.1 0.3 0.18
Exp. E 0.296.9 0.3 0.2 0.5 0.28
UGI
0.642.6 48.7 0.3 2.2 114
Exp. A 2.745.7 21.7 12.3 1.4 47.4
Exp. B 0.447.2 3.4 47.9 0.0 7.2
Exp. C 0.130.2 7.5 42.7 0.3 24.7
Ilmenite
a: Average values of the samples obtained from the upper and lower parts of the graphite crucible
Concentration of elementi, Ci (mass%)
VTi Fe Ca Si
Fe/Tiratio,
RFe/Ti (%)
Sample
Exp. X 0.145.1 5.8 40.6 0.5 12.9
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10 20 30 40 50 60 70 80 90 100
XRD analysis
A mixture of CaTiO3 and TiO2
was obtained after Fe removal.
Fig. XRD pattern of the start sample and the sample obtained after Fe removal (Exp. B)
:CaTiO3
:TiO2
Angle, 2θ (degree)
FeTiO3 (s) + CaCl2 (l)
→ CaTiO3 (s) + FeClx (l, g)
FeTiO3 (s) + CaCl2 (l) + C (s)
→ TiO2 (s) + FeClx (l, g) + COx (g) + Ca (s)
Discussion
CaTiO3 can be utilized as a feed material of direct TiO2 reduction processes(e.g., FFC, OS, EMR-MSE processes).
Inte
nsity
, I(a
. u.)
Ilmenite FeTiO3
Result of a selective chlorination experiment
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Low-grade Ti ore
TiO2 + flux
(FeTiOx)
Fe removal byselective chlorination
Ti powder
Direct reduction of TiO2
obtained after Fe removal
Direct reductionof TiO2 afterFe removal by electrochemicalmethod
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Reduction experiment apparatus
Fig. Schematic illustration of the experimental apparatus in this study.
C + x O2– → COx + 2x e–
Anode:
Cathode:
TiO2 + 4 e– → Ti + 2 O2–
Electrolysis
CaCl2 molten salt
Ti crucible
Carbon anode
TiO2 feed
Direct reduction by electrochemical method was applied.
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Reduction experiments
Mass of element i, wi / g
Ti ore CaCl2
2.50R-1
R-2
R-3 0.79
2.50
2.50
Voltage,E/V
Time,t”/h
1.5
3.0
3.0
3
3
3
CaTiO3
R-4 2.50 3.0 3
1.50
1.50
ー
0.76
Exp.
Experimental conditions:Temperature: 1100 K
Atmosphere: Ar
Molten salt: CaCl2 (800 g)
Cathode: Ti crucible (I.D. 18 mm)
Anode: Graphite rod (O.D. 3 mm)
ー
ー
ー
Table Analytical results of the sample obtained after electrochemical selective chlorination
0.295.9 1.9 0.1 0.1 2.00
Exp. D 0.598.0 0.2 0.1 0.3 0.18Exp. E 0.296.9 0.3 0.2 0.5 0.28
UGI
Concentration of element i,Ci (mass%)
VTi Ca SiFe
Fe/Tiratio,
RFe / Ti (%)
Sample
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10 20 30 40 50 60 70 80 90 100
Result of the reduction experimentsXRD analysis
Fig. XRD pattern of the sample obtained after the reduction experiment (Exp. R-2)
Angle, 2θ (degree)
:Ti2O:CaTiO3
Inte
nsity
, I(a
. u.)
CaTiO3 was changed into Ti2O during this reduction experiment.
Fig. XRD pattern (Cu-K) of the obtained powder sample after reduction at 1173 K using the EMR process.
Inte
nsi
ty,
I (a
.u.)
9070503010
: Ti JCPDS # 44-1294
Angle, 2 (degree)
Ti reduction by EMR
In a previous study,low oxygentitanium powderwas obtained.
2500 ppm O
40 60 80 10020
A complete reduction was not achieved in this study.
e-
Carbon anode
TiO2 preform (Cathode)
e-
Current monitor
CaCl2 molten salt
Ca-X alloyRef. T. Abiko, I. Park, and T.H. Okabe, Proceedings of 10th World Conference on Titanium, Ti-2003, (Hamburg, Germany, 13–18 July 2003), 253–260.
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Summary
Ti powder
Reduction byelectrochemical method
Low-grade Ti ore
TiO2 + flux
(FeTiOx)
Iron removal byselective chlorination
Development ofan industrial scale process for producing low-cost titanium
・ The selective chlorination of
Ti ore by using an electrochemical
method was investigated,
and 94% of Fe was
successfully removed directly
from low-grade Ti ore.
・ The feasibility of Ti smelting
process for directly producing
metallic Ti from low-grade Ti ore
was demonstrated.
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Questionand
Answer
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History of Titanium
1791 First discovered by William Gregor, a clergyman and amateur geologist in Cornwall, England.
1795 Klaproth, a German chemist, gave the name titanium to an element re-discovered in Rutile ore.
1887 Nilson and Pettersson produced metallic titanium containing large amounts of impurities.
1910 M. A. Hunter produced titanium with 99.9% purity by the sodiothermic reduction of TiCl4 in a steel vessel.
(119 years after the discovery of the element)
1946 W. Kroll developed a commercial process for the production of titanium: Magnesiothermic reduction of TiCl4...
Titanium was not purified until 1910,and was not produced commercially until the early 1950s.
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024681012141618
1960 1970 1980 1990 2000
(a) Production of titanium sponge in the world (2003).
(b) Transition of production volume of titanium mill products in Japan.
Year
Am
ou
nt
of
tita
niu
m m
ill p
rod
uct
s [k
t]
17.4 kt (2004)
Fig. Current status of titanium production,
Total65.5 kt
USA8 kt
Japan18.5 kt (28% share)
Russia26 kt
Kazakhstan9 kt
China4 kt
(a) production of titanium sponge in the world (2003),(b) transition of production volume of titanium mill products in Japan.
Titanium Production
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Melting point (K)Density (g / cc @298 K)
Specific strength((kgf / mm2) / (g / c
c))
Price (Yen / kg)
Titanium
Ti
19434.5
8 ~ 10
3000
~ 0.1
Aluminum
Al
933.32.7
3 ~ 6
600
20
Iron
Fe
18097.9
4 ~ 7
50
800
Symbol
Production volume(106 ton / year・ world)
Table Comparison between common metals and titanium.
Clarke numbera 0.46 (rank 10) 7.56 (rank 3) 4.7 (rank 4)
a: Values in parentheses are the existence rank in the earth’s crust.
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Fig. Flowchart of the titanium production based on the Kroll process.
Ti feed (TiO2)
Chlorine (Cl2)
Sponge Ti
Ti ingot
MgCl2 + Mg
CO2, FeClx,AlCl3 etc.
Other compounds
MgCl2
Chlorination
Distillation
Reduction
Vacuum distillation
Crushing / Melting
Electrolysis
Crude TiCl4
Pure TiCl4
Sponge Ti + MgCl2 + Mg
H2S etc.
Reductant, Mg
Reductant (C)
Flowchart of the titanium production
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(a) Low grade titanium ore (ilmenite) (b) Up-graded titanium ore (UGI)
Fig. (a) Composition of low grade titanium ore (ilmenite), and (b) that of up-graded titanium ore (up-graded ilmenite, UGI).
FeOx
2%
Others3%
TiOx
95%
TiOx
45%FeOx
45%
Others10%
Composition of titanium ore
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Importance
1. A large amount of chloride wastes (e.g., FeClx) are produced in the Kroll process.
2. Chloride waste treatment is costly, and it causes chlorine loss in the Kroll process.
Ti ore (Ilmenite, FeTiOx) Upgraded Ilmenite (UGI)
TiOx
FeOx Others
TiOxFeOx
Others Upgrade Chloridewastes
Discarded
1. Reduction of disposal cost of chloride wastes2. Minimizing chlorine loss in the Kroll process3. Improvement of environmental burden4. Reduction of material cost using low grade ore
Upgrading Ti ore for minimizing chloride wastes
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This study Advantages:1. Utilizing chloride wastes
from the Kroll process
2. Low cost Ti chlorination
3. Minimizing chlorine loss
in the Kroll process
caused by generation
of chloride wastes
Development of a new environmentally sound chloride metallurgy
Effective utilization of chloride wastes
Ti metal or TiO2 production
TiCl4 feed FeClx (+AlCl3)
Carbo-chlorination
COx
Low-grade Ti ore
Upgraded Ti ore FeClx(+AlCl3)
(FeTiOX)
(TiO2)
MClX
Chlorine recoverySelective chlorination(Cl2)
Fe
FeClx
TiCl4
Ti scrap
Refining process using FeClx
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Reduction (in kiln)
Fe2+ / TiFe = 80~95%
145C° (2.5 kg/cm2) *4 hr*2 step
(90% purity)
Ilmenite Reductant (Heavy oil etc.)
Reduced ore HCl vapor
Leached ilmenite Water Spray acid Fuel
(Synthetic rutile)95% TiO2
1% TiFe
TiO2 HCl aq.
Leaching (in digestor)
Filtration Roasting
HClSol.TiO2 Iron oxide
Calcination Absorber
HCl aq.(18~20% HCl)
Fig. Flowsheet of the Benilite process.
The Benilite process
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Gas + particle Particle
Ilmenite
Gas
Reduced ilmenite
TiO2
(Synthetic rutile) TiO2 92~93% TiFe 2.0~3.5%
TiO2
TiO2
Reduction (in kiln)
Leaching
WasteMag. separator
Acid Leaching
Filtering / Drying
Screen
-1 mm+1 mm
Cyclone
Reduced ore
Coal (low ash) Air
NH4Cl
H2SO4 aq.
Air
Iron oxide + Sol.
Iron oxide Sol.
Thickener
Fig. Flowchart of the Beacher process.
(Non. mag.)
The Beacher process (WLS)
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Thermocouple
Ceramic tube
Fused CaCl2 bath
TiO2 powder
Cathode (stainless steel)
Alumina tube
Anode lead wire (W)
Alumina crucible
Graphite crucible (anode)
Electric furnace
TiO2 (CaCl2) + 4 e- → Ti + 2 O2- (CaCl2)
Fig. Electrochemical reduction of TiO2 in CaCl2. (Ref. Mem. Fac. Eng., Nagoya Univ., 19, (1967) 164-166.)
or TiO2 (CaCl2) + 2 Ca → Ti + 2 CaO
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Fig. The principle of electrochemical deoxidization of titanium. (Ref. Met. Trans. B, 24B, June, (1993) 449-455.)
Cl2 COX
CaCl2 molten salt
O2-
[O] in Ti
Ti
C
e-
Ti
Ca[O] O2-
Carbon anode Ti cathode
e-
O2-
Ca2+ Cl-
Ca2+
Ca2+
Cl-
Cl-
Ca2+
O2-
Ca2+
Ca
CaO (in Ti) + 2 e- → O2- (in CaCl2)
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TiO2 + 4 e- → Ti + 2 O2 (in CaCl2)
Fig. Schematic illustration of the procedure of the FFC process. (Ref. Nature, 407, 21, Sep. (2000) 361.)
Titanium ore
Chlorination orsulfate method
Titanium oxide
Mixing withBinder
Cathodeformation
Calcination
Titanium reduction by FFC process
Recovery oftitanium electrode
Crushingand leaching
FFC titanium
AnodeCathode
Molten saltTiO2
(TiO2 electrode)
TiO2 C
COx
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FFC Process (Fray et al., 2000)
C + x O2- → COx + 2x e-
Anode:
Cathode:
TiO2 + 4 e- → Ti + 2 O2-
Electrolysis
(a1)
(a2)
OS Process (Ono & Suzuki, 2002)
C + x O2- → COx + 2x e-
Anode:
TiO2 + 2 Ca → Ti + 2 O2- + Ca2+
Cathode:
Ca2+ + 2 e- → Ca
Electrolysis(b1)
(b2)
(b3)
e-
CaCl2 molten salt
TiO2
preform
Carbon anode e-
TiO2 powder
CaCl2 molten salt
Carbon anode
Ca
Production process under investigation
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EMR / MSE Process (Electronically Mediated Reaction / Molten Salt Electrolysis)
Production process under investigation
TiO2 + C → Ti + CO2
Over all reaction
(d)
Ca → Ca2+ + 2 e-
Anode:
Cathode:
TiO2 + 4 e- → Ti + 2 O2-
C + x O2- → COx + 2x e-
Ca2+ + 2 e- → Ca
Cathode:
Anode:
Electrolysis
(c4)
(c1)
(c2)
(c3)
(a) TiO2 reduction (b) Reductant production
e-
Carbon anode
TiO2
e-
Ca-X alloy (X = Ag, Ni, Cu,・・・)
e-e-
CaCl2 -CaO molten salt
Current monitor / controller
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(a) FFC Process (Fray et al., 2000)
C + x O2- → COx + 2x e-
Anode:
Cathode:
TiO2 + 4 e- → Ti + 2 O2-
Electrolysis
(a1)
(a2)
(b) OS Process (Ono & Suzuki, 2002)
C + x O2- → COx + 2x e-
Anode:
TiO2 + 2 Ca → Ti + 2 O2- + Ca2+
Cathode:
Ca2+ + 2 e- → Ca
Electrolysis
(b1)
(b2)
(b3)
e-
CaCl2 molten salt
TiO2 preform
Carbonanode
e-
TiO2 powder
CaCl2 molten salt
Carbonanode
Ca
e- Carbon anode
CaCl2molten salt
TiO2 feed
e-
Current monitor / controller
Ca-X alloy
e-
EMR MSE
Fig. Schematic illustration of experimental apparatus for titanium smelting in the future.
(C) EMR / MSE Process (Okabe et al., 2002)
TiO2 + C → Ti + CO2
Over all reaction
(d)
Ca → Ca2+ + 2 e-Anode:
Cathode: TiO2 + 4 e- → Ti + 2 O2-
C + x O2- → COx + 2x e-
Ca2+ + 2 e- → Ca Cathode:
Anode:
Electrolysis
(c4)
(c1)
(c2)
(c3)
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Advantages Disadvantages
Kroll Process ◎ High purity titanium available × Complicated process◎ Easy metal / salt separation Slow production speed○ Established chlorine circulation Batch type process ○ Utilizes efficient Mg electrolysis○ Reduction and electrolysis operation
can be carried out independentlyFFC Process ◎ Simple process Difficult metal / salt separation
○ Semi-continuous process Reduction and electrolysis have to becarried out simultaneously
△ Sensitive to carbon and iron contamination △ Low current efficiency
OS Process ◎ Simple process Difficult metal / salt separation○ Semi-continuous process △ Sensitive to carbon and iron contamination
△ Low current efficiency PRP (Preform ◎ Effective control of purityDifficult recovery of reductant
◎ Flexible scalability
Environmental burden by leaching
◎ Resistant to contamination○ Small amount of fluxes necessary
EMR / MSEProcess
◎ Resistant to iron and carbonDifficult metal / salt separation when oxide
○ Semi-continuous process Complicated cell structure○ Reduction and electrolysis operation
△ Complicated process can be carried out independently
××
×
×
×
××
×
×
ReductionProcess)
Features of several titanium production process
and morphology
contaminationsystem
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Fig. Conceptual image of the new titanium reduction process currently under investigation (EMR / MSE process, Oxide system).
e-
Carbon anode
CaCl2-CaO molten salt
e-
Current monitor / controller
Ca-X reductant alloy
e-
A
A
V
e-
Feed preform(TiO2 + CaCl2)
Product Ti pelletsTi (+ CaO + CaCl2)
VnCOx gas
CaCl2-CaO
TiO2 + 4 e- = Ti + 2 O2-
Ca (Ca-X alloy) = Ca2+ + 2 e-
C + x O2- = COx + 2x e-
Ca2+ + 2 e- = Ca (Ca-X alloy)
O2- , Ca2+
Ca (Ca-X alloy)
Ca
Nighttime electrolysisDaytime reduction
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Stainless steel cover
Stainless steel plate
R reductant
Stainless steel reaction vessel
Ti sponge getter
Feed preform (MO x + flux)
TIG weld
Fig. Schematic illustration of the experimental apparatus for producing titanium powder by means of the preform reduction process (PRP).
MOx + R → M + RO
1. Amount of flux (molten salt) is small.
2. Easy to prevent contamination
from reaction vessel and reductant.
3. Highly scalable.
M = Nb, Ta, TiR = Mg, Ca…
Preform Reduction Process (PRP)
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Reductant vapor
Feed powder
Reductant (R = Ca, Mg)
(a) Conventional Metallothermic Reduction (b) Preform Reduction Process (PRP)
Reductant vapor
Feed preform
Reductant (R = Ca, Mg)
Fig. Metal powder production process: (a) conventional metallothermic reduction, (b) preform reduction process (PRP).
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FeOx (s) + MgCl2 (l) = FeClx (l) + MgO (s)
T = 1100 K, t’ = 1 h,Atmosphere : N2,Ti ore (UGI) : 4 g, MgCl2 : 2 g
Experimental condition
Fig. Experimental apparatus for selective-chlorination of titanium ore using MgCl2 as a chlorine source.
Carbon crucible
Stainless steel susceptor
Glass beads
Stainless steel net
RF coil
Ceramic tube
Glass flange
Vacuum pump
Quartz flange
Deposit
Mixture ofTi oreand MgCl2
ChloridesCondenser
ChlorinationReactor
(FeClx ... )
(Fe-free Ti ore)
N2 or N2+H2O gas
Selective chlorination using MgCl2
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FeOx (s) + MgCl2 (l) = FeClx (l, g) + MgO (s)
Inte
nsity
, I (
a. u
.)
10 30 40 50 60 70 8020
Fig. XRD pattern of the deposit at chlorides condenser. The sample powder was sealed in Kapton film before analysis.
XRD analysis
Deposit obtained after selective-chlorination. → FeCl2 was generated.
90 100
: FeCl2
XRF analysis
Residue after selective-chlorination.→ Fe was selective chlorinated.
Angle, 2θ (deg.)
Table Analytical results of titanium ore, the residue after selective chlorination, and the sample after reduction. These values are determined by XRF analysis.
Concentration of element i, Ci (mass %)
Ti ore (UGI from Ind.)
After heating sample
V
0.75
1.50
Ti
95.10
96.45
Fe
2.29
0.43
Si
0.41
0.44
Al
0.12
0.37
98.30 0.05 0.38 0.12 0.52After reduction sample
Results of previous study
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Fig. Experimental apparatus for chlorination of titanium using FeCl2 as a chlorine source.
Heater
Quartz tube
Sample deposits(on Si rubber, NaOH gas trap and quartz tube)
Carbon crucible
Sample mixture:(e.g., FeCl2+Ti powder)
Ti (s) + 2 FeCl2 (s) = TiCl4 (g) + 2 Fe (s)
XRF analysis Table Analytical results of the samples before and after heating and the sample deposited on quartz tube and Si rubber. These values are determined by XRF analysis.
Concentration of element i, Ci (mass %)
Residue before heating
Residue after heating
Ti
18.4
9.8
Fe
45.3
80.1
Cl
36.2
9.0
Dep. on quartz tube after heating
Dep. on Si rubber after heating
3.5 50.4 46.1
64.9 0.9 34.1
Chlorination of Ti using FeCl2
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Fig. Flowchart of new titanium smelting process from titanium ore discussed in this study.
(CaCl2)
Ti metal
Ti smeltingby electrochemical method
This study
Low-grade Ti ore
Upgraded Ti ore FeClx(+ AlCl3)
(FeTiOx)
(TiO2)
MClx
Selective chlorinationby electrochemical method
Chlorine recovery
Fe
FeClx
TiCl4
Ti scrap
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Iron removal process by electrochemical method
Direct reduction process from Ti ore to Ti metal can be achieved.
Establishment of a new up-grading processof Ti ore by electrochemical method.
Ae-
TiO2 Ti
e-
e- O2-
Ca-X alloy
Molten CaCl2-CaO
Carbon electrode
Ti crucible(Cathode)
Ti reduction Production of reductant
Ti ore(TiO2 + FeOx)
Molten CaCl2
V
Mild steel crucible(Cathode)
Carbon crucible(Anode)
A
TiFeOX
Reference electrode
e-
2. TiO2 reduction process
TiO2 + 4 e- → Ti + O2-
Ca(or Ca-X)Cathode:Anode :
(e.g. EMR-MSE process)
→ Ca2+ + 2 e-
Selective chlorination・Iron removal process
Fen+ + n e- → Fe
2 Cl- → Cl2 + 2 e-
FeOx + Cl2
Cathode:
Anode :Ca2+ + 2 e- → Ca
→ FeClx(l, g) + O
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Fig. Schematic illustrations of the processes investigated in this study.
(a) Iron removal process
2 Cl- → Cl2 + 2 e-
FeOx + Cl2 + C → FeClx + COx
Anode:
Cathode: Ca2+ + 2 e- → Ca
Electrolysis
(a1)
(a2)
(a3)
e-
Carbon crucible containingTi ore + CaCl2 mixture (Anode)
SampleMolten CaCl2 Mild steel crucible (Cathode)
(b) FFC process (Fray et al., 2000)
C + x O2- → COx + 2x e-Anode:
Cathode: TiO2 + 4 e- → Ti + 2 O2-
Electrolysis
(b1)
(b2)
e-
CaCl2 molten salt
TiO2 preform
Carbon anode
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@1100 K
2CaCl2 + O2 → 2CaO + 2Cl2
2MgCl2 + O2 → 2MgO + 2Cl2
4HCl + O2 → 2H2O + 2Cl2
2CO + O2 → 2CO2
FeO + MgCl2 → FeCl2 + MgO
2C + O2 → 2CO
log pCl22 / pO2
= -
8.29
log pO2 = -17.74
log pO2 = -19.85
e.g.
ΔG = -0.28 kJ < 0
log pCl22 / pO2
= 1.49
log pCl22 / pO2
=
0.48
Potential of several reaction
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Ref.a
900 K 1100 K 1300 KFe (s ) + Cl2 (g ) = FeCl2 (s ) -228.93 [1]Fe (s ) + Cl2 (g ) = FeCl2 (l ) -212.65 [1]Fe (s ) + 1.5 Cl2 (g ) = FeCl2 (g ) -183.14 -190.89 -194.39 [1]Fe (s ) + 1.5 Cl2 (g ) = FeCl3 (g ) -236.41 -231.45 -225.62 [1]Fe (s ) + 0.5 O2 (g ) = FeO (s ) -213.15 -200.71 -188.00 [1]2 Fe (s ) + 1.5 O2 (g ) = Fe2O3 (s ) -585.32 -535.98 -486.33 [1]3 Fe (s ) + 2 O2 (g ) = Fe3O4 (s ) -821.79 -762.36 -702.25 [1]Ti (s ) + Cl2 (g ) = TiCl2 (s ) -370.38 -340.24 -310.26 [1]Ti (s ) + Cl2 (g ) = TiCl2 (g ) -258.15 262.11 -265.30 [1]Ti (s ) + 1.5 Cl2 (g ) = TiCl3 (s ) -526.31 -485.79 [1]Ti (s ) + 1.5 Cl2 (g ) = TiCl3 (g ) -495.25 -485.30 -474.73 [1]Ti (s ) + 2 Cl2 (g ) = TiCl4 (g ) -654.50 -630.68 -606.36 [1]Ti (s ) + 0.5 O2 (g ) = TiO (s ) -455.54 -437.16 -418.80 [1]Ti (s ) + 0.5 O2 (g ) = TiO (g ) -32.67 -50.63 -67.66 [1]Ti (s ) + O2 (g ) = TiO2 (s ) -780.23 -744.91 -709.30 [1]2 Ti (s ) + 1.5 O2 (g ) = Ti2O3 (s ) -1267.35 -1215.50 -1163.77 [1]3 Ti (s ) + 2.5 O2 (g ) = Ti3O5 (s ) -2052.96 -1969.32 -1885.27 [1]4 Ti (s ) + 3.5 O2 (g ) = Ti4O7 (s ) -2838.53 -2718.92 -2599.03 [1]
[1] I. Barin, Thermochemical Data of Pure Substances, 3rd ed., (Weinheim, Federal Republic of Germany, VCH Verlagsgesellschaft mbH, 1997).
Reactions Gibbs energy change, ΔG
f (kJ/mol)
a: References
Table Gibbs energy change of formation in the Fe-Ti-O system.
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0.5 1.0 1.5 2.0 2.5
0
-2
-4
-6
-8
-10
-12
Reciprocal temperature, 1000 T-1 / K-1
Vap
or p
ress
ure
, lo
g p i
(at
m)
Temperature, T / K
Ti (s,l)
Fe (s,l)
TiC
l2 (s)
TiCl3 (s)
TiCl4 (l)
FeC
l2 (s,l)
FeCl3 (s,l)
1000 500 4002000
MgC
l2 (s, l)
CaC
l2 (s, l)
Region suitablefor vaporizationof chlorides
Fig. Vapor pressure of iron, calcium, magnesium and titanium chlorides as a function of reciprocal temperature.
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e.g.-40
-10
-30
-20
-50
-60
0
-40 -10-30 -20 0
Fe-Cl-O system, T = 1100 K
CaO (s) / CaCl2 (l) aCaO = 0.1
C / CO eq.CO / CO2 eq.
Oxy
gen
part
ial p
ress
ure,
lo
g p
O2 (
atm
)
Chlorine partial pressure, log pCl2 (atm)
FeO (s)
Fe2O3 (s)
FeCl2 (l)
Fe3O4 (s)
FeCl3 (g)
Fig. Chemical potential diagram for Fe-Cl-O system at 1100 K.
FeOx can be chlorinatedby controlling oxygenand chlorine partial pressure.
Ti ore :mixture of TiOx and FeOx.H2O (g) / HCl (g)
MgO (g) / MgCl2 (l) eq.
Fe (s)
FeOX (s) + MgCl2 (l)
→ FeClX (l, g)↑ + MgO (s, l)
Thermodynamic analysis (FeOx chlorination)
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Fig. Chemical potential diagram for Ti-Cl-O system at 1100 K.
-40
-10
-30
-20
-50
-60
0
-40 -10-30 -20 0
TiO (s)
TiO2 (s)
TiCl4 (g)
Ti2O3 (s)
TiCl3 (s)
Ti3O5 (s)
Oxy
gen
part
ial p
ress
ure,
lo
g p
O2 (
atm
)Ti-Cl-O system, T = 1100 K
Chlorine partial pressure, log pCl2 (atm)
CaO (s) / CaCl2 (l) aCaO = 0.1
C / CO eq.CO / CO2 eq.
Fe / FeCl2 eq.
Since TiCl4 ishighly volatile species,chlorine partial pressuremust be keptin the oxide stable region.
TiCl2 (s)
H2O (g) / HCl (g)
MgO (g) / MgCl2 (l) eq.
Ti4O7 (s)
Ti (s)
Thermodynamic analysis (TiOx chlorination)
Ti ore :mixture of TiOx and FeOx.
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(CaCl2)
Ti metal
Ti smeltingby electrochemical method
This chapter
Low-grade Ti ore
Upgraded Ti ore FeClx(+ AlCl3)
(FeTiOx)
(TiO2)
MClx
Selective chlorinationby electrochemical method
Chlorine recovery
Fe
FeClx
TiCl4
Ti scrap
Fig. Flowchart of the new titanium smelting process discussed in this study.
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Sintered feed preform
Feed preform
Mixing
Slurry
Preform fabrication
Ti ore Flux Binder
Calcination / Iron removal
Flux : CaCl2, MgCl2
Binder: Collodion
FeClx
Fig. Flowchart of the procedure of preform fablication supplied for Fe removal experiment.
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Table Composition of titanium ore (ilmenite) and up-graded ilmenite (UGI) used this study.
Sample name
TiO2 Fe2O3 FeO MnO Al2O3 SiO2 MgO Nb2O5 P2O5 Moisture
ilmenaiteb 52.55 20.91 15.27 1.91c - - - 0.21 0.11 0.61
UGId 95.20 0.99 0.77 0.63 0.61 0.27 < 0.01 0.10
UGIe 96.46 1.60 - 0.03 0.28 0.52 0.03 - - 0.15a: Nominal value.b: Natural ilmenite ore produced in Australia.c: This is value as Mn. d: Up-graded ilmenite by the Beacher process (see Fig. 1-7). The ore was produced in Australia. e: Up-graded ilmenite by the Benilite process (see Fig. 1-6). The ore was produced in India.
Composition (mass%)a
Total Fe
1.22
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Table Starting materials used in this study.
Form
Liquid
Supplier
5.0
Chip 98.0up
Powder 95.0up
Collodiona
Ti
CH3COOH
CaCl2
Ca
Purity orconc. (%)
Wako Pure Chemical., Inc.
Osaka Tokusyu GoukinCo., Ltd.
Kanto Chemicals, Inc.
Sponge 98.0up Toho Titanium Co., Ltd.
Liquid 99.7 Kanto Chemicals, Inc.
Materials
a: 5 mass% nitro cellulose, 23.75 mass% ethanol, 71.25 mass% diethylether.
HCl
2-Propanol
Liquid 35 Kanto Chemicals, Inc.
Liquid 99.5up Kanto Chemicals, Inc.
Aceton
Graphite
99.0up
99.98
Liquid
Crucible
Kanto Chemicals, Inc.
Kanto Chemicals, Inc.
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Experimental apparatus
Electrochemical interface
Electrochemicalcontrol unit
10 Apowersource
Sample
MoltenCaCl2
Mild steel crucible(Cathode)
Graphite cruciblecontaining Ti ore(Anode)
Voltage monitor / controller
e-
Holes oncrucible
Furnace
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Ceramic insulator
Thermocouple
Heater
Rubber plug
Ar inlet
Wheel flange
Reaction chamber
Preform containing Ti ore
Stainless steel tube
Molten salt (CaCl2)
Potential lead (Nickel wire)
Graphite crucible
Mild steel crucible
V1V2
A1A2
Fig. Schematic illustration of the experimental apparatus in a voltage measurement.
Ti ore, sample
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Surface of molten salt
Support rod(Stainless steel tube)
Sample(Ti ore, CaCl2 etc.)
Inlet of molten salt
Screw (Stainless steel)
Graphite crucible
Air hole
Fig. Schematic illustration of the graphite crucible used in this experiment, (a) appearance, (b) inner content.
I.D. 17 mmO.D. 19 mm
40 mm
(a) (b)
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Fig. Variation of the external current from the dipped preform to the graphite crucible.
-4
-2
0
2
4
6
8
0 500 1000 1500 2000 2500Immersion time, t / s
Imm
ersi
on c
urre
nt,
i / m
A Carbon cruciblecontaining Ti ore (Anode)
CaCl2molten salt
TiO2 preform (Cathode)
e-AAi
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Fig. Electromotive force between the dipped preform and the graphite crucible.
-40
-20
0
20
40
60
80
100
120
0 500 1000 1500 2000 2500
Immersion time, t / s
Imm
ersi
on v
olta
ge,
V /
mV
Carbon cruciblecontaining Ti ore (Anode)
CaCl2molten salt
TiO2 preform (Cathode)
VV
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Table Analytical results of various samplesa.
Concentration of element i, Ci (mass%)b
Fe
42.4
33.7
Ti
50.4
50.6
Ca
0.2
7.1
41.441.9 9.6
RFe / Ti (%)
84.1
66.6
98.8
AlSiCl Cr
0.90.0
0.0
3.7
5.3
2.4
2.7
0.0 4.3 2.5
0.6
0.3
40.7 36.1 10.8 88.78.7 2.0 1.3 0.3
50.1 42.2 0.1 84.30.0 4.0 3.3 0.3
Fe / Ti ratioc,
Sample #
a: Ilmenite (FeTiOx) produced in China. b: Determined by X-ray fluorescence analysis. This value excludes carbon and gaseous elements. c: Indicator of iron removal from titanium ore.
A
B
D
C
E
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Fig. Phase diagram for the CaCl2-FeCl2 system [2].
Liquid
674℃
592℃
782℃800
700
600Tem
per
atur
e, T
/ ℃
0 100CaCl2 FeCl2FeCl2 content, xFeCl2
(mol%)20 40 60 80
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Ceramic insulator
Thermocouple
Heater
Rubber plug
Ar inlet
Wheel flange
Reaction chamber
Stainless steel tube
Molten salt (CaCl2)
Potential lead (Nickel wire)
Nickel quasi-reference electrode
Mild steel crucible (working)
Graphite crucible (counter)
Ti ore
A
Fig. Schematic illustration of the experimental apparatus for cyclic voltammetry in molten CaCl2.
V1 V2
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-2
Potential (vs Ni quasi-ref.), E / V
-1 0 1
Cu
rre
nt,
i /
A
2
1
0
-1
2
1
0
-1
2
3.2 V
2 Cl- = Cl2 + 2 e- (on C)
Ca2+ + 2 e- = Ca (on Fe)
(a)
(b)
Fig. Cyclic voltammograms for molten CaCl2 at 1100 K (a) before pre-electrolysis, (b) after pre-electrolysis, cathode sweep; working: Fe rod; counter: C rod, anode sweep; working: C rod; counter: Fe rod, scan rate: 100 mV / s, immersion length: 4 cm.
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Table Standard Gibbs energy of formation and theoretical voltage for reactions in this study.
Reactions
Gibbsenergychange,
ΔG
f / kJ
Theoreticalvoltagefor reactions,
ΔE of / V
Temperature,T / K Ref.a
Fe (s ) + Cl2 (g ) = FeCl2 (l ) -212.65 1.10 1100 [1]Fe (s ) + 1.5 Cl2 (g ) = FeCl2 (g ) -190.89 0.99 1100 [1]Fe (s ) + 1.5 Cl2 (g ) = FeCl3 (g ) -231.45 1.20 1100 [1]Fe (s ) + 0.5 O2 (g ) = FeO (s ) -200.71 1.04 1100 [1]2 Fe (s ) + 1.5 O2 (g ) = Fe2O3 (s ) -535.98 0.93 1100 [1]3 Fe (s ) + 2 O2 (g ) = Fe3O4 (s ) -762.36 0.99 1100 [1]Ti (s ) + 0.5 O2 (g ) = TiO (s ) -437.16 2.27 1100 [1]Ti (s ) + 0.5 O2 (g ) = TiO (g ) -50.63 0.26 1100 [1]Ti (s ) + O2 (g ) = TiO2 (s ) -744.91 1.93 1100 [1]2 Ti (s ) + 1.5 O2 (g ) = Ti2O3 (s ) -1215.50 2.10 1100 [1]3 Ti (s ) + 2.5 O2 (g ) = Ti3O5 (s ) -1969.32 2.04 1100 [1]4 Ti (s ) + 3.5 O2 (g ) = Ti4O7 (s ) -2718.92 2.01 1100 [1]Ca (s ) + Cl2 (g ) = CaCl2 (l ) -629.11 3.26 1100 [1]Ca (s ) + 0.5 O2 (g ) = CaO (s ) -520.78 2.70 1100 [1]CaO (s ) + C (s ) = Ca (s ) + CO (g ) -312.00 1.62 1100 [1]CaO (s ) + 0.5 C (s ) = Ca (s ) + 0.5 CO2 -323.00 1.67 1100 [1]C (s ) + 0.5 O2 (g ) = CO (g ) -209.06 1.08 1100 [1]C (s ) + O2 (g ) = CO2 (g ) -395.92 1.03 1100 [1]Fe (s ) + Ti (s ) + 1.5 O2 (g ) = FeTiO3 -956.61 1.65 1100 [1]2 Fe (s ) + Ti (s ) + 2 O2 (g ) = Fe2TiO4 -1164.70 1.51 1100 [1]
[1] I. Barin, Thermochemical Data of Pure Substances, 3rd ed., (Weinheim, Federal Republic of Germany, VCH Verlagsgesellschaft mbH, 1997).
a: Referencesb: E o = -G o / nF, where n is electron transfer number, and F is Faraday constant.
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-1 0 1 2-2 3
Cu
rre
nt,
i /
A
-1
-1
2
1
0
2
1
0
-1
2
1
0
3.0 V
2 Cl- = Cl2 + 2 e- (on C)
Ca2+ + 2 e- = Ca (on Fe)
1.7 V
C + x O2- = COx + 2x e- (on C)
Ca2+ + 2 e- = Ca (on Fe)
1.7 V
C + x O2- = COx + 2x e- (on C)
Ca2+ + 2 e- = Ca (on Fe)
(a)
(b)
(c)
Potential (vs Ca / Ca2+ ref.), E / V
Fig. Cyclic voltammograms for molten CaCl2 at 1100 K after Ca deposition using various carbon electrode, (a) C rod, scan rate: 100 mV / s, (b) C crucible, scan rate: 100 mV / s, (c) Ti ore holding C crucible, scan rate: 20 mV / s, cathode sweep; working: Fe rod; counter: Carbon, anode sweep; working: Carbon; counter: Fe rod, immersion length: 2 cm.
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Fig. Phase diagram for the CaCl2–Ca system [3].
Te
mp
era
ture
, T
’ / ˚
C
1200
1100
900
800
1000
700
CaCl2 Ca content, xCa (mol%) Ca20 40 600 80 100
Liq. Two liquids
825˚ 828˚
767˚
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Sample
Molten CaCl2
Mild steel crucible(Cathode)
Carbon crucible containingTi ore + CaCl2 mixture(Anode)
e-
Fig. Schematic illustration of experimental apparatus for iron removal by electrochemical method.
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Fig. Schematic illustration of the experimental apparatus for iron removal by electrochemical method.
V
A
Ceramic insulator
Thermocouple
Heating element
Rubber plug
Ar inlet
Wheel flange
Stainless steel reaction chamber
Stainless steel tube
Molten salt (CaCl2)
Potential lead (Nickel wire)
Mild steel crucible (Cathode)
Graphite crucible (Anode)
Ti ore
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S L
Ti ore ( + Fe2O3 etc)
Electrochemical iron removal
Leaching
TiO2 powder
CaCl2
Waste solution
CaCl2
TiO2 + CaCl2
TiO2
Vacuum drying
Separation
CH3COOH aq.,HCl aq.,Distilled water,Isopropanol,Acetone
Fig. Flowchart of the procedure for iron removal experiment by electrochemical method.
Distilled water
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Experiment 1
Experimental condition:Temperature: 1100 KAtmosphere: ArMolten salt: CaCl2 (800 g)Cathode: Mild steel crucible (I.D 96 mm)Anode: Graphite crucible (I.D 17 mm)
Sample
MoltenCaCl2
Mild steelcrucible(Cathode)
Graphite cruciblecontaining Ti ore(Anode)
Voltage monitor / controller
Mass of Ti ore(Ilmenite), w / g
A 4.00B 4.00
4.00C
Voltage,E / V
Time,t’ / h
2.52.01.5
63
12
Exp. No.
e-
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Result 1
XRF analysis
After the electrochemical treatment, Fe in the Ti ore was selectivelychlorinated and removed.
Table Analytical results of the sample obtained after the electrochemical selective chlorination.Concentration of element i,
Ci (mass %)
VTi Fe Ca Si
Ti ore 0.642.6 48.7 2.2 2.2
Exp. A 0.964.2 29.6 0.5 1.8
Fe / Tiratio,
114
49.5
Disscussion
Ti ore (Ilmenite, FeTiOx)
Molten CaCl2
Graphite crucible(Anode)
Unreacted part
Unreacted part wasremained at the bottomof the graphite crucible.
Exp. B 1.255.4 25.3 13.8 1.1 45.6
Exp. C 2.745.7 21.7 12.3 1.4 47.4a: Average of the samples obtained from the upper part and lower part of the graphite crucible.
RFe / Ti (%)
e-Sample
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Mass of feed materials i, wi / g
Table Experimental condition for iron removal from Ti ore by electrochemical methodc.
UGIa
A
a: Upgrade ilmenite by the Benilite process (see Fig.1-6 ). The ore was produced in India (see Table 3-1).b: Ilmenite (FeTiOx) produced in China. c: Temperature: 1100 K, Ar atmosphere.
Exp.
B
Ilmeniteb
C
D
E
F
G
2.76
2.82
2.91
2.88
2.81
2.75
2.92
2.0
1.2
0.5
2.0
1.0
0.5
1.0
1.0
1.0
1.0
3.0
6.0
0.5
1.0
Voltage, V / volts
Reaction time,t / hr
H
I
J
K
L
M
N
4.00
4.03
3.99
4.00
3.93
4.01
4.01
2.5
1.5
1.0
0.5
ー
1.5
1.5
3.0
3.0
6.0
6.0
6.0
9.0
6.0
O
4.00 2.0 13.01.42 1.2 1.0 P
Mass of feed materials i, wi / g
UGIa
Exp.
Ilmeniteb
Voltage, V / volts
Reaction time,t / hr
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Fig. Schematic illustration of electrochemical interface in this experiment.
10 APowerSource
20 cm
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Fig. Current generated by imposed each voltage.
Time, t / second
Cur
rent
, I /
A
0 10000 20000- 0.5
0
0.5
1.0
1.5
2.0
Exp. K
Exp. L
Exp. M
Exp. N
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Exp. Noteb
# Al Si S Cl Ca Sc Ti V Mn Fe NiUGIc
0.0 0.1 nd 0.0 0.1 nd 96.3 0.2 1.0 1.9 0.0 2.00 051227-UGIAUSUGIc 0.4 1.1 0.5 nd 0.1 0.4 92.8 1.2 1.3 2.3 0.0 2.45 050125_UGI
A 0.2 0.4 0.0 nd 38.8 0.2 55.4 1.1 0.4 2.6 0.8 4.65 050125_UGI_P04_1B nd nd nd nd nd nd nd nd nd nd nd nd 050119_UGI_P02C 0.3 1.1 0.1 nd 15.3 0.1 80.2 1.4 0.3 1.3 0.0 1.63 050125_UGI_P05_2D 0.2 0.9 0.0 nd 5.3 0.3 90.1 1.0 0.9 1.3 0.0 1.40 050125_UGI_P06_1E 0.2 0.4 0.0 0.0 45.7 0.2 49.8 1.5 0.6 1.6 0.1 3.27 050125_UGI_P07_2F 0.2 0.8 0.0 nd 30.4 0.1 66.4 1.1 0.4 0.6 nd 0.98 050127_UGI_P10_1G nd 0.1 0.1 nd 11.3 0.1 86.5 1.5 0.2 0.2 nd 0.24 050119_UGI_P01_1H 0.1 0.2 0.0 nd 21.4 0.1 76.4 1.1 0.2 0.4 0.0 0.56 050119_UGI_P03_1b
Ilmenited 1.8 1.8 0.0 nd 0.2 0.2 44.8 0.7 3.3 47.2 0.0 105.3 050420_ilmenite
Ilmenited 2.6 2.6 0.0 nd 0.5 0.2 40.4 0.6 2.9 50.2 0.1 124.4 050420_ilmenite
Ilmenited 0.8 2.0 0.0 nd 0.2 0.3 45.7 0.5 3.2 47.2 0.0 103.2 050615_ilmenite
Ilmenited 1.0 1.4 nd nd 0.2 0.4 45.0 0.5 3.0 48.5 0.1 107.9 050607_ilmeniteI 1.1 0.5 0.0 0.1 9.0 0.3 53.8 0.9 0.9 33.3 0.1 61.9 050425_ilmenite_P33_2J 0.9 1.5 0.1 nd 6.4 0.2 56.0 0.7 0.7 33.5 0.1 59.9 050428_ilmenite_P38_1K 1.0 6.2 0.1 nd 8.1 0.1 58.1 1.1 0.9 24.0 0.5 41.3 050217_ilmenite_P15_1L 1.3 4.5 0.1 nd 21.5 0.1 56.7 1.2 0.8 12.8 0.9 22.6 050217_ilmenite_P14_1M 1.2 2.8 0.1 0.4 20.2 nd 46.7 0.8 1.6 26.1 0.1 55.8 050216_ilmenite_P13_3N 1.2 1.9 0.0 1.7 35.4 0.1 37.7 0.7 0.6 20.5 0.0 54.6 050216_ilmenite_P12_2O 0.1 0.2 0.0 0.2 35.3 0.3 49.1 1.0 1.0 12.8 nd 26.0 050517_ilmenite_P46_2P 0.1 0.5 0.0 0.1 28.5 0.2 41.4 0.8 1.5 26.7 nd 64.6 050516_ilmenite_P45_1Q 0.6 0.6 0.0 0.2 33.4 0.2 52.2 1.2 0.7 10.8 nd 20.7 050502_ilmenite_B_1
a: Determined by XRF analysis. b: Experimental date.c: Upgraded ilmenite produced in Australia.d: Ilmenite (FeTiOx) produced in China.nd: not detected. Below detection limit of XRF (< 0.01%)
Fe / Ti/ %
Composition i , C ia / mass %
Table Analytical results of the samples obtained after iron removal by electrochemical method.
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Ceramic insulator
Thermocouple
Heater
Rubber plug
Ar inlet
Wheel flange
Stainless steel tube (Electrode)
Molten salt (CaCl2)
Potential lead (Ni wire)
Mild steel crucible (Cathode)
V1V2
A1A2
Graphite crucible (Anode)
Ti ore + CaCl2 mixture
100 mm
Fig. Schematic illustration of experimental apparatus in this experiment.
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Fig. Current value passed by imposed certain voltage, and voltage in this experiment, Exp. F.
0
2
4
6
8
10
12
0 3000 6000 9000 12000Time / s
Curr
ent / A
0
0.5
1
1.5
2
2.5
3
Volta
ge / V
Current
Voltage
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Fig. XRD pattern of the obtained sample after selective chlorination experiment.
Inte
nsity
, I (
a. u
.) : CaTiO3
(JCPDS #42-0423)
Angle, 2θ (degree)
: TiO2
(JCPDS #21-1276)
100908070605040302010
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Table Experimental condition and analytical results of the chlorination experiment using ilmenite.
Exp. Ilmemite Carbon CaCl2 Noteb
- Ilmenitec- - - - - - - 105.5 - 050420_ilmenite
A 1.25 - 1.80 2.0 1.5 3 2.52 54.8 0.85 050610_P48B 1.87 - 1.33 1.0 1.8 6 1.72 74.8 1.26 050613_P49C 1.47 - 1.60 1.5 1.8 8 2.83 19.3 0.52 050614_P50
2 D 0.75 - 2.19 4.0 2.0 3 1.59 96.2 0.63 050624_P53E 0.79 - 2.00 3.7 2.0 6 5.09 - - 050725_P55F 0.87 - 2.35 3.7 c c 5.91 7.2 0.97 050803_P56G 3.99 - - - 2.0 3 3.60 54.9 2.60 050811_P57H 0.77 - 2.18 4.0 1.5 3 5.87 57.4 0.48 050811_P58I 0.77 0.18 2.14 4.0 1.5 3 3.09 24.7 0.03 050814_P59J 0.74 - 2.12 4.0 1.5 3 4.49 48.8 0.76 050816_P60K 0.74 - 2.17 4.0 1.5 3 5.00 3500 0.02 050816_P61L 0.72 - 2.19 4.0 - 6 - 34.2 0.55 051014_P62M 0.73 - 2.20 4.0 0.0 6 -0.004 48.7 0.55 051014_P63N 0.62 - 2.26 5.0 1.5 3 0.68 46.2 0.37 051017_P64O 0.61 - 2.25 5.0 1.5 6 0.42 37.7 0.41 051018_P66P 0.74 - - - 1.5 3 0.47 72.7 0.56 051019_P67Q 0.73 0.16 2.00 3.7 2.5 6 1.95 - - 051020_P69R 0.74 - 2.17 4.0 2.5 6 1.81 12.4 0.42 051021_P70S 0.60 - 2.26 5.0 1.5 3 1.27 107.0 0.31 051025_P72T 0.60 - 2.21 5.0 2.0 6 0.79 126.8 0.59 051025_P73U 0.60 - 2.21 5.0 d d 4.10 354.4 0.02 051026_P74V 0.67 - 2.37 5.0 e e - 12.9 0.38 051114_P75
a: Indicator of iron removal from titanium ore. b: Experiment numberc: Ilmenite (FeTiOx) produced in China.d: 2.0 volts 20 minutes, and 1.5 volts 3hourse: 1.8 volts 6 hours, and 3.0 volts 3 hoursf: 2.0 volts, 1.5 volts, 1.8 volts, and 2.0 volts, 1 hour respectively
Obtainedsample,w / g
Mass of feed material i , w i / g
1
Usebath #
CaCl2 / FeOx
ratio,M Ca / Ti / -
Imposedvoltage,
V / volts.
Reactiontime,t / hr
Averagecurrent,
I / A
Fe / Ti
ratioa,R Fe / Ti / %
3(Old)
4
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Table Experimental conditions and analytical results of the chlorination experiment using UGI.
Exp. UGIa CaCl2 Notec
- - - - - - - 2.00d - - 051227_UGIAUSA 1.55 1.27 20 2.0 3 - - - 051219_P77A 1.59 1.26 20 2.0 3 0.28 0.09 0.13 051222_P89B 2.08 0.84 10 2.0 3 - - - 051219_P79B 2.07 0.83 10 2.0 3 4.70 0.15 0.20 051221_P87C 2.46 0.49 5 2.0 3 - - - 051220_P82C 2.46 0.49 5 2.0 3 7.41 0.42 0.25 051221_P86D 1.59 1.27 20 1.5 3 0.18 0.49 0.35 051220_P81E 2.11 0.85 10 1.5 3 0.59 0.55 0.14 051219_P78F 2.45 0.48 5 1.5 3 - - - 051220_P84F 2.45 0.48 5 1.5 3 0.83 1.11 0.29 051221_P85G 2.12 0.58 7 1.5 9.5 0.33 0.76 0.16 051220_P80H 2.08e 0.83 10 1.5 10 - - - 051222_P88
4 I 1.57 1.28 20 f f 2.20 0.02 0.42 051115_P76J 1.59 1.24 20 0.0 3 2.63 1.95 0.05 051220_P83K 1.59g 1.27 20 2.0 6 0.43 0.31 0.15 051222_P90
a: Up-graded ilmenite by the Beacher process (see Fig. 1-6). The ore was produced in Australia. b: Indicator of iron removal from titanium ore.c: Experiment date and numberd: Referencee: Mixture 2.08 g of Ti ore and 0.08 g of carbon powderf: 2 volts 2 hours, and 2 volts 2hoursg: Up-graded ilmenite by the Benilite process (see Fig. 1-5). The ore was produced in India.
5
5
Mass of feed material i , w i / gUsebath
#
Obtainedsample,w 1 / g
Mass decrease ofcarbon crucible,
w2 / g
CaCl2 / FeOx
ratio,M Ca / Ti / -
Imposedvoltage,V / volts
Reactiontime,
t / hour
Fe / Ti
ratiob,R Fe / Ti / %
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(CaCl2)
Ti metal
Ti smeltingby electrochemical method
This chapter
Low-grade Ti ore
Upgraded Ti ore FeClx(+ AlCl3)
(FeTiOx)
(TiO2)
MClx
Selective chlorinationby electrochemical method
Chlorine recovery
Fe
FeClx
TiCl4
Ti scrap
Fig. Flowchart of new titanium smelting process from titanium ore discussed in this chapter.
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Ceramic insulator
Thermocouple
Heater
Rubber plug
Ar inlet
Wheel flange
Reaction chamber
Stainless steel tube
Molten salt (CaCl2)
Potential lead (Nickel wire)
Mild steel crucible
Ti crucible (Cathode)
Mixture of Ti oreafter Fe removal and CaCl2
A
Fig. Schematic illustration of the experimental apparatus for electrochemical reduction of Ti ore after Fe removal.
V
Graphite rod (Anode)
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S L
Ti ore (+Fe2O3 etc)
CaCl2 Mixing
Electrochemical reduction
Leaching
Ti powder
Waste solution
Mixture
CaCl2
Ti + CaCl2
Vacuum drying
CH3COOH aq.,HCl aq.,Distilled water,Isopropanol,Acetone
Fig. Flowchart of the experimental procedure for electrochemical reduction of Ti ore after Fe removal.
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Table Experimental conditions for electrochemical reduction of Ti ore after Fe removal.
Mass of feed material i, Ci / g
Ti ore CaCl2
2.50R1
R2
R3 0.79a
2.50
2.50
Voltage,E / V
Time,t” / h
1.5
3.0
3.0
3
3
3
CaTiO3
R4 2.50 3.0 3
1.50
1.50
ー
0.76b
Exp. No.
ー
ー
ー
a: The sample obtained by selective chlorination exp. A.
b: The sample obtained by selective chlorination exp. D.
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Fig. Phase diagram for the CaCl2–CaO system.
1150 K
1000
950
900
850
800
750
700
CaCl2
10 20
CaO content, xCaO (mol%)30
CaO 0
Te
mp
era
ture
, T
’ / ˚
C