Hematite-goethite ratios at pH 2–13 and 25–170 °C: A time-resolved synchrotron X-ray diffraction study

Si Athena Chen, Peter J. Heaney, Jeffrey E. Post, Peter J. Eng, Joanne E. Stubbs

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15 Scopus citations

Abstract

Iron (oxyhydr)oxides are sensitive indicators of pH, Eh, temperature, microbial activity, and climate conditions in the Critical Zone. The most ubiquitous and environmentally significant iron oxides in most soils are two-line ferrihydrite, goethite, and hematite. Here we present a comprehensive study of the transformation of two-line ferrihydrite to hematite and goethite over a wide range of temperature (25–170 °C) and initial pH (2−13) conditions through ex situ batch and in situ synchrotron X-ray diffraction (XRD) experiments. Within the high time resolution of our experiments, goethite and hematite nucleated nearly simultaneously from ferrihydrite in nearly equal concentrations by mass. Hematite increased in abundance relative to goethite until a steady-state ratio was achieved, and both phases ceased growth on the depletion of ferrihydrite. Higher temperatures and lower water activities favored hematite formation at all pH values studied. In both our batch and our time-resolved, angle-dispersive synchrotron X-ray diffraction experiments, hematite was favored relative to goethite at an initial pH of 3 to 5. In contrast, goethite preferentially formed in neutral (initial pH 7–8) and highly alkaline conditions (initial pH ≥ 11). Surprisingly, mildly alkaline conditions (initial pH 9–11) induced the precipitation of a highly Fe-deficient (Feocc = ~0.80–0.90) variety of hematite known as “hydrohematite” in greater concentrations than goethite. Our results are useful for the application of hematite-goethite ratios as paleoclimate proxies for soil and sediment systems with low pH buffering capacities.

Original languageEnglish
Article number120995
JournalChemical Geology
Volume606
DOIs
StatePublished - Sep 20 2022
Externally publishedYes

Funding

Funding for this research was provided by the National Science Foundation Grant EAR-1552211 and EAR-1925903, the Pennsylvania State University Biogeochemistry dual-title Ph.D. program, and the Hiroshi and Koya Ohmoto Graduate Fellowship from the Pennsylvania State University Geosciences Department. Synchrotron XRD was performed at the GSECARS (University of Chicago) Beamline 13-BM-C at the APS. GSECARS is supported by NSF EAR-1634415 and DOE GeoSciences DE-FG02-94ER14466. APS is operated under DOE Contract No. DE-AC02-06CH11357. We acknowledge Devon Chenot for his help with pH measurements. We thank four anonymous reviewers for their helpful suggestions and comments. Funding for this research was provided by the National Science Foundation Grant EAR-1552211 and EAR-1925903 , the Pennsylvania State University Biogeochemistry dual-title Ph.D. program, and the Hiroshi and Koya Ohmoto Graduate Fellowship from the Pennsylvania State University Geosciences Department . Synchrotron XRD was performed at the GSECARS (University of Chicago) Beamline 13-BM-C at the APS. GSECARS is supported by NSF EAR-1634415 and DOE GeoSciences DE-FG02-94ER14466 . APS is operated under DOE Contract No. DE-AC02-06CH11357. We acknowledge Devon Chenot for his help with pH measurements. We thank four anonymous reviewers for their helpful suggestions and comments.

Keywords

  • 2-line Ferrihydrite
  • Goethite
  • Hematite
  • Iron Oxides
  • Time-resolved X-ray diffraction

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