TY - JOUR
T1 - Dehydroxylation and dissolution of nickeliferous goethite in New Caledonian lateritic Ni ore
AU - Landers, M.
AU - Gilkes, Robert
PY - 2007
Y1 - 2007
N2 - Goethite is a major constituent in ferruginous soils in a lateritic nickel deposit on the Koniambo massif in New Caledonia, and dehydroxylation of nickeliferous goethite may occur naturally due to fire and during the processing of lateritic Ni ore. Goethite started to alter to hematite in 2 h of heating at 230-250 degrees C and had completely altered to hematite at 340 degrees C and higher temperatures. For most heated samples the rate of dissolution of Fe in 1 M HCl followed the cube root equation with a single straight line describing the data, however for samples where both goethite and hematite were present the data did not conform to this equation. There was an approximately 7 fold increase in the rate of dissolution for samples heated to 340 degrees C which can be accounted for by the increase in surface area (2-fold) due to the development of micropores and the increase of structural defects in poorly ordered hematite structures (protohematite and hydrohematite) (3.5-fold) formed by partial dehydroxylation of goethite. For heated samples Ni, Cr, Al, Co and Mn showed congruent dissolution with iron indicating uniform incorporation of these metals in the structures of the iron oxides and complete retention of these metals in crystals during the goethite to hematite transition. V and Cu showed only partial dissolution (i.e. noncongruent dissolution) indicating that some V and Cu may be associated with another less soluble mineral (e.g. ilmenite). (C) 2006 Published by Elsevier B.V.
AB - Goethite is a major constituent in ferruginous soils in a lateritic nickel deposit on the Koniambo massif in New Caledonia, and dehydroxylation of nickeliferous goethite may occur naturally due to fire and during the processing of lateritic Ni ore. Goethite started to alter to hematite in 2 h of heating at 230-250 degrees C and had completely altered to hematite at 340 degrees C and higher temperatures. For most heated samples the rate of dissolution of Fe in 1 M HCl followed the cube root equation with a single straight line describing the data, however for samples where both goethite and hematite were present the data did not conform to this equation. There was an approximately 7 fold increase in the rate of dissolution for samples heated to 340 degrees C which can be accounted for by the increase in surface area (2-fold) due to the development of micropores and the increase of structural defects in poorly ordered hematite structures (protohematite and hydrohematite) (3.5-fold) formed by partial dehydroxylation of goethite. For heated samples Ni, Cr, Al, Co and Mn showed congruent dissolution with iron indicating uniform incorporation of these metals in the structures of the iron oxides and complete retention of these metals in crystals during the goethite to hematite transition. V and Cu showed only partial dissolution (i.e. noncongruent dissolution) indicating that some V and Cu may be associated with another less soluble mineral (e.g. ilmenite). (C) 2006 Published by Elsevier B.V.
U2 - 10.1016/j.clay.2006.08.012
DO - 10.1016/j.clay.2006.08.012
M3 - Article
VL - 35
SP - 162
EP - 172
JO - Applied Clay Science
JF - Applied Clay Science
SN - 0169-1317
IS - 3-4
ER -