Abstract

Arsenic-contaminated groundwater is widely used in agriculture. To meet the increasing demand for safe water in agriculture, an efficient and cost-effective method for As removal from groundwater is urgently needed. We hypothesized that Fe (oxyhydr)oxide (FeOOH) minerals precipitated in situ from indigenous Fe in groundwater may immobilize As, providing a solution for safely using As-contaminated groundwater in irrigation. To confirm this hypothesis and identify the controlling mechanisms, we comprehensively evaluated the transport, speciation changes, and immobilization of As and Fe in agricultural canals irrigated using As-contaminated groundwater. The efficiently removed As and Fe in the canals accumulated in shallow sediment rather than subsurface sediment. Linear combination fitting (LCF) analysis of X–ray absorption near edge spectroscopy (XANES) indicated that As(V) was the dominant As species, followed by As(III), and there was no FeAsO4 precipitate. Sequential extraction revealed higher contents of amorphous FeOOH and associated As in shallower sediment than in the subsurface layer. Stoichiometric molar ratio calculations, SEM‒EDS, FTIR, and fluorescence spectroscopy collectively demonstrated that the microbial reductive dissolution of amorphous FeOOH proceeded via reactive dissolved organic matter (DOM) consumption in subsurface anoxic porewater environment facilitating high labile As, whereas in surface sediment, the in situ-generated amorphous FeOOH was stable and strongly inhibited As release via adsorption. In summary, groundwater Fe2+ can efficiently precipitate in benthic surface sediment as abundant amorphous FeOOH, which immobilizes most of the dissolved As, protecting agricultural soil from contamination. This field research supports the critical roles of the phase and reactivity of in situ-generated FeOOH in As immobilization and provides new insight into the sustainable use of contaminated water.

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