Guangjun Mei

A refractory phosphate ore obtained from Guizhou, China, contains high amounts of detrimental metal impurities (e.g., Fe, Al, and Mg) which affect the deep wet processing of phosphorus products before use. In this study, mineralogy parameters of the ore such as mineral composition, disseminated particle size, mineral liberation degree, and intergrowth relationship were investigated using X-ray fluorescence spectrometer (XRF), X-ray powder diffractometer (XRD), and advanced mineral identification and characterization system (AMICS). The mechanism for flotation separation was also discussed. The results showed that the ore was a fine-grained calcareous-siliceous collophanite with high P₂O₅ grade. The gangue minerals such as quartz, sericite (muscovite), pyrite, and dolomite were finely disseminated and encapsulated by fluoroapatite particles in a rather complex relationship. A double reverse flotation process was carried out based on the separation principle of less flotation and more inhibition. A phosphorous concentrate with a P₂O₅ grade of 35.53%, SiO₂ content of 5.88%, MgO content of 0.91%, sesquioxide (Fe₂O₃ + Al₂O₃) content of 1.98%, MER value of 8.13%, and phosphorus recovery of 75.04% was obtained. Based on the flotation test results and the analysis of process mineralogy parameters, we concluded that the main causes of difficulty in separation of collophanite are fine disseminated particle size, poor mineral liberation degree, and serious argillization. The selection of foam-controlled collectors, efficient dispersing inhibitors and classified desliming process will be necessary for improving flotation index. These results provide a technical reference for subsequent development and utilization of collophanite resources.

Y₂O₃:Eu were prepared through precursors synthesized by leaching tests, removing impurities, enrichment of Y and Eu from residual purified liquors, annealing treatment, and high temperature solid-state reaction method, which is the most suitable for large-scale production. The analysis of product shows that the purity is 99.42%. The resultant powders were characterized by X-ray diffraction (XRD), differential thermal analysis (TG-DTA), scanning electron microscope (SEM), and photoluminescence (PL). Compared with the commercial phosphors, the XRD spectrum of the product samples revealed the synthesized particles to have a pure cubic Y₂O₃:Eu structure without any impurities in the crystalline phase. On the morphology, the Y₂O₃:Eu particles synthesized by a combustion and high temperature solid state process with sintering aids, were large and uniform. For luminescence property, the emission intensity of Y₂O₃:Eu phosphors synthesized by combustion process and high temperature solid state process with sintering aids were higher than those without sintering aids, at 1400 °C.