TY - JOUR
T1 - Reduction of CaTiO3 in molten CaCl2 - As basic understanding of electrolysis
AU - Suzuki, Ryosuke O.
AU - Noguchi, Hiromi
AU - Hada, Hiromasa
AU - Natsui, Shungo
AU - Kikuchi, Tatsuya
N1 - Publisher Copyright:
© 2017 The Japan Institute of Metals and Materials.
PY - 2017
Y1 - 2017
N2 - Electrochemical decomposition of CaTiO3 at the cathode was examined in a scheme of titanium metal production from natural deposit, Ilmenite (TiFeO3). Based on the possible precipitation of CaTiO3 from TiFeO3, the electrochemical decomposition of CaTiO3 is here examined using combination of the calciothermic reduction and the electrolysis of CaO in the same molten salt. Inhomogeneous reduction in the cathodic basket is related with buoyancy of Ca and insufficient dehydration. By optimizing the cooling conditions, CaO content in the molten salt, and dehydration method, an industrial level of 0.42 mass%O could be achieved as powder form.
AB - Electrochemical decomposition of CaTiO3 at the cathode was examined in a scheme of titanium metal production from natural deposit, Ilmenite (TiFeO3). Based on the possible precipitation of CaTiO3 from TiFeO3, the electrochemical decomposition of CaTiO3 is here examined using combination of the calciothermic reduction and the electrolysis of CaO in the same molten salt. Inhomogeneous reduction in the cathodic basket is related with buoyancy of Ca and insufficient dehydration. By optimizing the cooling conditions, CaO content in the molten salt, and dehydration method, an industrial level of 0.42 mass%O could be achieved as powder form.
KW - Calciothermic reduction
KW - Calcium chloride
KW - Molten salt electrolysis
KW - Titanium production
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U2 - 10.2320/matertrans.MK201625
DO - 10.2320/matertrans.MK201625
M3 - Article
AN - SCOPUS:85016042531
SN - 1345-9678
VL - 58
SP - 341
EP - 349
JO - Materials Transactions
JF - Materials Transactions
IS - 3
ER -