Thermal and mineral properties of Al-, Cr-, Mn-, Ni- and Ti-substituted goethite
Thermal and mineral properties of Al-, Cr-, Mn-, Ni- and Ti-substituted goethite
Clays and Clay Minerals (April 2006) 54 (2): 176-194
- aluminum
- cation exchange capacity
- cell dimensions
- chemical properties
- chromium
- clay mineralogy
- crystal chemistry
- crystallinity
- dehydroxylation
- endothermic reactions
- experimental studies
- ferrihydrite
- geochemistry
- goethite
- hematite
- manganese
- metals
- nickel
- oxides
- recrystallization
- substitution
- thermal properties
- titanium
- unit cell
Mineralogical and thermal characteristics of synthetic Al-, Cr-, Mn-, Ni- and Ti-bearing goethites, synthesized via alkaline hydrolysis of metal-ferrihydrite gels, were investigated by powder X-ray diffraction and differential thermal analysis. Shifts in unit-cell dimensions were consistent with size of substituent metal ions and confirmed the incorporation of Al (super 3+) , Cr (super 3+) , Mn (super 3+) , Ni (super 2+) and Ti (super 4+) in the goethite structure. A weight loss of 6.2 wt.% for goethite containing 12.2 mol.% Ti, being significantly less than for stoichiometric goethite, is consistent with the replacement of Fe by Ti in the goethite structure coupled with the substitution of O (super 2-) ions for OH (super -) (i.e. proton loss). These data provide the first confirmation of the direct replacement of Fe by Ti within goethite. Formation of multiple dehydroxylation endotherms for goethite containing 4.5 mol.% Al, 15.3 mol.% Mn and 12.2 mol.% Ti was not attributed to the decomposition of surface OH groups or related simply to the crystallinity of precursor goethite ("high-a" vs. "low-a") as defined by the magnitude of a. Instead, endotherm doublet formation was associated with weight loss due to the dehydroxylation of goethite remaining after initial phase transformation to protohematite and to the evolution of OH (super -) associated with the rapid increase in crystallite size of protohematite directed primarily along the a direction. Development of the first endotherm is due to initial dehydroxylation and transformation to protohematite. With continued heating of well ordered goethite or goethite containing moderate to high levels of substituent cations, domain growth along the a direction is delayed or inhibited to a critical point that provides enough thermal energy to enable goethite transformation to proceed to completion and for proto-hematite domain growth to occur. This results in the formation of a second endotherm. For less well ordered goethite and/or goethite containing only low levels of foreign metal cations, protohematite domain growth is not inhibited and proceeds continuously with heating to give only a single endotherm.