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Complex Formation during Dissolution of Metal Oxides in Molten Alkali Carbonates
Author(s) -
Qingfeng Li,
Flemming Borup,
Irina Petrushina,
Niels J. Bjerrum
Publication year - 1999
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/1.1391954
Subject(s) - dissolution , solubility , non blocking i/o , electromotive force , inorganic chemistry , oxide , alkali metal , chemistry , carbonate , metal , molten salt , electrochemistry , mole fraction , nickel , lithium (medication) , electrode , organic chemistry , catalysis , medicine , physics , quantum mechanics , endocrinology
Dissolution of metal oxides in molten carbonates relates directly to the stability of materials for electrodes and construction of molten carbonate fuel cells. In the present work the solubilities of PbO, NiO, Fe{sub 2}O{sub 3}, and Bi{sub 2}O{sub 3} in molten Li/K carbonates have been measured at 650 C under carbon dioxide atmosphere. It is found that the solubilities of NiO and PbO decrease while those of Fe{sub 2}O{sub 3} and Bi{sub 2}O{sub 3} remain approximately constant as the lithium mole fraction increases from 0.43 to 0.62 in the melt. At a fixed composition of the melt, NiO and PbO display both acidic and basic dissolution as the partial pressure of carbon dioxide varies. By combination of solubility and electromotive force measurements, a model is constructed assuming the dissolution involves complex formation. The possible species for lead are proposed to be [Pb(CO{sub 3}){sub 2}]{sup {minus}2} and/or [Pb(CO{sub 3}){sub 3}]{sup {minus}4}. A similar complex chemistry for nickel oxide dissolution might be expected.

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