Sequence closed-loop recovery of fluoride, phosphate, and sulfate anions from phosphogypsum leachate via precipitation-electrodialysis-crystallization approaches
            
                编号:56
                访问权限:仅限参会人
                更新:2024-05-16 19:33:12
                                浏览:1672次
                口头报告
            
            
            
                摘要
                Phosphogypsum (PG) is a large-scale industrial by-product generated during the production of phosphoric acid, typically being deposited in landfills worldwide. The leaching of fluoride (F–), phosphate (PO43–), and sulfate (SO42–) anions from PG into water bodies through rainfall results in significant environmental pollution. Herein, we proposed a stepwise precipitation combined with electrodialysis and crystallization strategy for efficient recovery and valorization of multiple anions from PG leachate. Our method demonstrates effectiveness both theoretically and practically. Consequently, fluoride anions were precipitated as CaF2 and Ca5(PO4)3F at pH 4.7, with a recovery rate of 98.80%; phosphate anions as MgNH4PO4·H2O at pH 8.5, with a recovery rate of 99.91%; and sulfate anions through electrodialysis and crystallization with a recovery rate of 99.89%, ensuring effluent met discharge standards. In addition, the concentrated sulfate-rich solution was employed for electrochemical production of persulfate, yielding ammonium persulfate salts after cooling crystallization. Our integrated approach for multiple anions recovery from PG leachate offers significant environmental and economic benefits, providing valuable insights and references for future research and practical productions.
 
             
            
                关键词
                phosphogypsum,leachate,Recovery,fluoride,phosphate,sulfate
             
            
            
                    稿件作者
                    
                        
                                    
                                        
                                                                            
                                    Xiang-Yang Lou
                                    Shenzhen Institute & Information Technology
                                
                                             
                          
    
发表评论