Molecular speciation of phosphorus in phosphogypsum waste by solid-state nuclear magnetic resonance spectroscopy

Abstract

Phosphogypsum (PG), a waste by-product of the phosphate fertilizer industry as well as a point-source P contaminant, has caused serious environmental problems particularly in estuarine and coastal regions. However, in-depth understanding of P speciation in PG, which is critical for its restoration and management, remains largely unknown. Using solid-state 31P NMR spectroscopy, density functional theory calculations of the NMR parameters and NanoSIMS, we for the first time reported that P in PG ubiquitously exists as phosphate incorporated into gypsum and minor fluorapatite. The occasional presences of mineral phosphate phases mainly associated with Ca and Al were also detected. The molecular environment of the incorporated phosphate is HPO42− substituting for SO42− in the gypsum lattice with the H atom away from the H2O molecules and almost parallel to the a–c plane. A high spatial heterogeneity was observed for the distribution of this phosphate species in PG at the submicron scale. Upon heating, at least 64% of the incorporated phosphate could be converted to the easy-to-recover fluorapatite or amorphous calcium phosphate by thermal treatments at above 750 °C for 2–4 h. This information of P speciation transformation may pave a solid basement for the sustainable recovery of P from PG.