Effect of mechanochemical activation of natural phosphorite structure as well as phosphorus solubility

• Published in: PloS one 2019-11, Vol.14 (11), p.e0224423-e0224423
• Main Authors: Fang, Nana, Shi, Yuanliang, Chen, Zhenhua, Sun, Xun, Zhang, Lei, Yi, Yanli
• Format: Article
• Language: English
• Subjects: Acids; Activated carbon; Activation; Agricultural chemicals; Apatite; Apatites; Apatites - chemistry; Biology and Life Sciences; Carbonates; Carbonates - chemistry; Citric acid; Citric Acid - chemistry; Crystal defects; Dietary minerals; Durapatite - chemistry; Earth Sciences; Ecological effects; Ecology; Electron microscopy; Fertilizers; Fluorapatite; Halides; Hydroxyapatite; Hydroxyapatites; Infrared spectroscopy; Minerals - chemistry; Organic acids; Particle size; Phase transitions; Phosphate minerals; Phosphates; Phosphates - chemistry; Phosphorite; Phosphorus; Phosphorus - chemistry; Phosphorus content; Physical Sciences; Research and Analysis Methods; Scanning electron microscopy; Solubility; Spectroscopy; Spectrum analysis; X-Ray Diffraction
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0224423

Mechanochemical treatment of phosphate rock is considered as an effective and ecologically clean way of treating the medium- and low-grade phosphorite which could be used as fertilizer instead of the high-grade phosphorite. In order to investigate the effects of different milling times on the mechanochemically activated phosphorite (lower total phosphorus content) by more efficient milling equipment with enhanced milling speed, phosphorus solubility in citric acid and structural characteristics of natural and mechanochemically activated phosphorite from Yichang, China were studied using scanning electron microscope, infrared spectroscopy and X-ray diffraction. Phosphorus solubility in citric acid increased proportionately with the milling time until 30 min (57.51%), but then gradually reached an equilibrium with the maximum (59.03%) in 50 min. These changes were mainly manifested in considerably reduced particle size, decreased crystallinity and increased structural defects of phosphorite due to substitution of PO43- with CO32- and the incorporation of OH-. With the incorporation of CO32- and OH-, the non-activated carbonate-fluorapatite (type B) was transformed into a mixture of carbonate-fluorapatite, hydroxyapatite, fluorocarbon hydroxyapatite and/or carbonate apatite, respectively during the process of mechanochemical activation. As a result of the structural and phase transformations after mechanochemical activation, phosphorus solubility remarkably increased.