田畑 陽久

Photo-oxidation of aqueous Fe(II) (Fe2+ and FeOH+) to Fe(III) (Fe3+) was likely involved in the formation of iron oxide deposits on early Mars and Earth. Previous studies have reported the photo-oxidation reaction rate (i.e., quantum yield, phi = the number of oxidized ferrous ions divided by the number of photons absorbed by ferrous ions) under acidic conditions (pH 0.4-3.0). However, the quantum yield has not been systematically investigated using chemical actinometry in the range of weakly acidic to neutral pH, where the photo-oxidation would have occurred on early Mars and Earth. We report quantum yields for the photo-oxidation of aqueous Fe(II) species over a pH range of 0.5-7.6 with Hg and Xe lamps (with and without optical filters) based on measured Fe(II) concentrations and photon fluxes. The quantum yield under continuous UV and visible light (>200 nm, Xe lamp) varies with pH: phi = 0.103 (+/- 0.005) + 2.17 (+/- 0.27) x [H+](0.5) at pH = 3.0-7.0. Our quantum yield is a few times higher than those reported by the previous studies that used a Hg lamp, indicating the wavelength dependence of the quantum yield. At higher pH (7.1-7.6), with a UV cutoff at <= 300 nm (filtered Xe lamp), photo-oxidation of Fe (II) is attributed to oxidation of FeOH+, with a quantum yield of 0.08 +/- 0.01. Based on these quantum yields, we estimated Fe (III) (hydro)oxide precipitation rates in the early Gale lakes on Mars, and in Archean oceans on Earth. Results suggest that photo -oxidation may account for the amounts of Fe(III) (hydro)oxides in Gale sediments, assuming aqueous Fe(II) was supplied to the lakes through upwelling groundwater. Photo-oxidation of Fe(II) in Archean oceans on Earth could have been several times more intense than previously thought. (C) 2021 Elsevier Ltd. All rights reserved.