posted on 2023-09-18, 13:06authored byEdward J. O’Loughlin, Maxim I. Boyanov, Kenneth M. Kemner
Compared to more abundant metalloids (e.g., As, Se, and
Sb), little
is known regarding the biogeochemistry of tellurium (Te), a critical
metal whose use in CdTe photovoltaic solar cells is driving increasing
global demand for this element. To understand the redox behavior of
Te under ferrugenic/sulfidogenic conditions, we examined the potential
for reduction of Te(VI) and Te(IV) in aqueous suspensions containing
Fe(II) as siderite, vivianite, green rust, magnetite, or mackinawite;
Fe(II)-bearing minerals which are often formed during microbial reduction
of Fe(III) oxides. In the mackinawite systems, complete reduction
of Te(VI) or Te(IV) to Te(0) was observed within 12 h, and near complete
reduction (>90% Te(0)) was observed within 2.5 days in the green
rust
systems. In the presence of siderite, complete reduction of Te(VI)
or Te(IV) to Te(0) occurred within 60 days. We observed >60% reduction
of Te(VI) to Te(IV) within 2.5 days in the magnetite system, but Te(0)
did not form until 120 days; however, complete reduction to Te(0)
was observed within 120 days when starting with Te(IV). With vivianite
there was >80% reduction of Te(VI) to Te(IV) within 12 h, without
further reduction to Te(0) over the duration of the experiment (120
days); in the Te(IV)-vivianite system, there was no evidence of Te(IV)
reduction within 120 days. The reduction of Te(VI) and Te(IV) in soils
and sediments has been largely attributed to direct reduction by microbes;
however, the reduction of Te(VI) and Te(IV) by Fe(II)-bearing minerals
suggests that abiotic or coupled biotic–abiotic processes may
also play a critical role in Te redox chemistry in natural and engineered
environments.