# Integrating VNIR–SWIR Spectroscopy and Handheld XRF for Enhanced Mineralogical Characterization of Phosphate Mine Waste Rocks in Benguerir, Morocco: Implications for Sustainable Mine Reclamation

## TL;DR

This study combines two analytical techniques to better understand phosphate mine waste in Morocco, helping to guide sustainable reuse and reclamation efforts.

## Contribution

The novel integration of VNIR–SWIR spectroscopy and HHXRF provides a rapid and low-impact method for mineralogical characterization of mine waste.

## Key findings

- The combined workflow successfully identified carbonate–clay–phosphate mineral assemblages in mine waste samples.
- Elemental ratios and spectral data align to reveal localized phosphate enrichment and mineral variability.
- The method offers reproducible and actionable insights for sustainable mine reclamation planning.

## Abstract

Phosphate is a crucial non-renewable mineral resource, mainly utilized in producing fertilizers that support global agriculture. As phosphorus is an indispensable nutrient for plant growth, phosphate holds a key position in ensuring food security. While deposits are distributed worldwide, the largest reserves are concentrated in Morocco. The Benguerir phosphate mining in Morocco generates heterogeneous waste (i.e., including overburden, tailings, and phosphogypsum) that complicates management and valorization, which is the beneficial reuse or value recovery from waste materials (e.g., use in cover systems, buffering, or other engineered applications). Therefore, it is essential to characterize their mineralogical properties to evaluate their environmental impact and possibilities for reuse or site revegetation. To do so, we integrate VNIR–SWIR reflectance spectroscopy with HandHeld X-ray fluorescence (HHXRF) to characterize phosphate waste rock and assess its reuse potential. For this purpose, field samples (n = 104) were collected, and their spectral reflectance was measured using an ASD FieldSpec 4 spectroradiometer (350–2500 nm) under standardized laboratory conditions. Spectra were processed (Savitzky–Golay smoothing, convex-hull continuum removal) and matched to ECOSTRESS library references; across the dataset, library matching achieved mean RMSE = 0.15 ± 0.053 (median 0.145; 0.085–0.350), median SAM = 0.134 rad, median SID = 0.029, and mean R2 = 0.748 ± 0.170, with 84% of spectra yielding R2 > 0.70. In parallel, HHXRF major and trace elements were measured on all samples to corroborate spectral interpretations. Together, these analyses resolve carbonate–clay–phosphate assemblages (dolomite commonly dominant, with illite/smectite–kaolinite, quartz, and residual carbonate-fluorapatite varying across samples). Elemental ratios (e.g., Mg/Ca distinguishing dolomite from calcite; K/Al indicating illite) reinforce spectral trends, and phosphate indicators delineate localized enrichment (P2O5 up to 23.86 wt % in apatite-rich samples). Overall, the combined workflow is rapid, low-impact, and reproducible, yielding coherent mineralogical patterns that align across spectroscopic and geochemical lines of evidence and providing actionable inputs for selective screening, targeted material reuse, and more sustainable mine reclamation planning.