Dong Wanqiang, Deng Xiangyi, Chai Liqi, Zhang Yuefei, Chen Haodong, Wu Hanjun, Chi Ru'an
School of Resources and Safety Engineering, Wuhan Institute of Technology, Wuhan 430205, China.
School of Chemistry and Enviromental Engineering, Wuhan Institute of Technology, Wuhan 430205, China.
Molecules. 2024 Dec 24;30(1):5. doi: 10.3390/molecules30010005.
As a large-volume industrial solid waste generated during the production of wet-process phosphoric acid, the primary disposal method for phosphogypsum (PG) currently involves centralized stockpiling, which requires substantial land use. Additionally, PG contains impurities, such as phosphorus, fluorine, and alkali metals, that may pose potential pollution risks to the surrounding environment. However, the mechanisms governing the co-release of phosphorus and fluorine impurities alongside valuable metal cations during leaching remain unclear, posing challenges to efficient disposal and utilization. This study compares the leaching characteristics of cations and anions in PG of different particle sizes through static pH leaching experiments. Using Visual MINTEQ simulation combined with XRD, XPS, and FT-IR characterization methods, we analyzed the leaching mechanisms and key controlling factors for various metal elements and inorganic elements, like phosphorus and fluorine, under different pH conditions. The experimental results show that Ca, Al, Fe, Ti, Ba, Sr, Y, and PO in PG are more easily released under acidic conditions, while Si, Zn, Co, and F are primarily influenced by the content of soluble components. The dynamic "dissolution-crystallization" reaction of CaSO·HO significantly impacts the leaching of fluorine, and the XRD, XPS, and FT-IR characterization results confirm the presence of this reaction during the leaching process. This research provides theoretical guidance for the environmental risk assessment of stockpiled PG and the recovery of phosphorus, fluorine, and valuable metal resources from PG.
作为湿法磷酸生产过程中产生的大宗工业固体废弃物,磷石膏(PG)目前的主要处置方式是集中堆存,这需要大量土地。此外,磷石膏含有磷、氟和碱金属等杂质,可能对周边环境造成潜在污染风险。然而,浸出过程中磷和氟杂质与有价金属阳离子共释放的机制尚不清楚,给高效处置和利用带来了挑战。本研究通过静态pH浸出实验比较了不同粒径磷石膏中阳离子和阴离子的浸出特性。采用Visual MINTEQ模拟结合XRD、XPS和FT-IR表征方法,分析了不同pH条件下各种金属元素以及磷和氟等无机元素的浸出机制和关键控制因素。实验结果表明,磷石膏中的Ca、Al、Fe、Ti、Ba、Sr、Y和PO在酸性条件下更容易释放,而Si、Zn、Co和F主要受可溶性组分含量的影响。CaSO·HO的动态“溶解-结晶”反应对氟的浸出有显著影响,XRD、XPS和FT-IR表征结果证实了浸出过程中存在该反应。本研究为堆存磷石膏的环境风险评估以及从磷石膏中回收磷、氟和有价金属资源提供了理论指导。