Effect of Oxidation on Vivianite Dissolution Rates and Mechanism

Abstract

The interest in the mineral vivianite (Fe$_3$(PO$_4$)$_2$·8H$_2$O) as a more sustainable P resource has grown significantly in recent years owing to its efficient recovery from wastewater and its potential use as a P fertilizer. Vivianite is metastable in oxic environments and readily oxidizes. As dissolution and oxidation occur concurrently, the impact of oxidation on the dissolution rate and mechanism is not fully understood. In this study, we disentangled the oxidation and dissolution of vivianite to develop a quantitative and mechanistic understanding of dissolution rates and mechanisms under oxic conditions. Controlled batch and flowthrough experiments with pristine and preoxidized vivianite were onducted to systematically investigate the effect of oxidation on vivianite dissolution at various pH-values and temperatures. Using X-ray absorption spectroscopy and scanning transmission X-ray microscopy techniques, we demonstrated that oxidation of vivianite generated a core−shell structure with a passivating oxidized amorphous Fe(III)−PO$_4$ surface layer and a pristine vivianite core, leading to diffusion-controlled oxidation kinetics. Initial (<1 h) dissolution rates and concomitant P and Fe release (∼48 h) decreased strongly with increasing degree of oxidation (0−≤ 100%). Both increasing temperature (5−75 °C) and pH (5−9) accelerated oxidation, and, consequently, slowed down dissolution kinetic