Abstract
Structural Fe in clay minerals is an important, albeit poorly characterized, redox-active phase found in many natural and engineered environments. This work develops an experimental approach to directly assess the redox properties of a natural Fe-bearing smectite (ferruginous smectite, SWa-1, 12.6 wt % Fe) with mediated electrochemical reduction (MER) and oxidation (MEO). By utilizing a suite of one-electron-transfer mediating compounds to facilitate electron transfer between structural Fe in SWa-1 and a working electrode, we show that the Fe2+/Fe3+ couple in SWa-1 is redox-active over a large range of potentials (from EH = -0.63 V to +0.61 V vs SHE). Electrochemical and spectroscopic analyses of SWa-1 samples that were subject to reduction and re-oxidation cycling revealed both reversible and irreversible structural Fe rearrangements that altered the observed apparent standard reduction potential (EHφ) of structural Fe. EHφ-values vary by as much as 0.56 V between SWa-1 samples with different redox histories. The wide range of E H-values over which SWa-1 is redox-active and redox history-dependent EHφ-values underscore the importance of Fe-bearing clay minerals as redox-active phases in a wide range of redox regimes.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 9369-9377 |
| Number of pages | 9 |
| Journal | Environmental Science and Technology |
| Volume | 46 |
| Issue number | 17 |
| DOIs | |
| State | Published - Sep 4 2012 |
All Science Journal Classification (ASJC) codes
- General Chemistry
- Environmental Chemistry
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