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Speciation analysis and formation mechanism of iron-phosphorus compounds during chemical phosphorus removal process.
Ping, Qian; Zhang, Bingqian; Zhang, Zhipeng; Lu, Kexin; Li, Yongmei.
Affiliation
  • Ping Q; State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, PR China; Shanghai Institute of Pollution Control and Ecological Security, Shanghai, 200092, PR China. Electronic address: pingqian@tongji.edu.cn.
  • Zhang B; State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, PR China.
  • Zhang Z; State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, PR China.
  • Lu K; State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, PR China.
  • Li Y; State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, PR China; Shanghai Institute of Pollution Control and Ecological Security, Shanghai, 200092, PR China. Electronic address: liyongmei@tongji.edu.cn.
Chemosphere ; 310: 136852, 2023 Jan.
Article in En | MEDLINE | ID: mdl-36241115
ABSTRACT
Iron (Fe) salt was applied extensively to remove phosphorus (P) in wastewater treatment plants (WWTPs). Exploring the formation mechanism of iron-phosphorus compounds (FePs) during the chemical P removal (CPR) process is beneficial to P recovery. In this study, the performance of P removal, FePs speciation analysis and the kinetics of P removal under different conditions (pH, Fe/P molar ratio (Fe/Pmol), type of Fe salt, dissolved organic matters) were comprehensively investigated. More than 95% of P was removed under the optimal conditions with pH = 4.7, Fe/Pmol = 2, FeCl3 or polymeric ferric sulfate (PFS) as the coagulant. The FePs formation mechanism was considerably influenced by reaction conditions. Iron-phosphate compounds were the dominant FePs species (>76%) at pH < 6.2, while more iron oxides were formed at pH ≥ 6.2 with decreased P removal efficiency. When the initial Fe/Pmol was 2, iron-phosphate compound was the only product that was formed by the reaction between PO43- and Fe(III) or Fe(II) ions directly. More iron oxides were generated when the initial Fe/Pmol was 1 or 3. At Fe/Pmol = 1, the Fe(III) was hydrolyzed to form iron oxides and trapped PO43-, while at Fe/Pmol = 3, iron-phosphate compounds were produced firstly and the remaining Fe(III) was hydrolyzed to form iron oxides. The pseudo-second-order kinetic model simulated the chemical P removal process well. The reaction rate of P with Fe(II) was slower than that with Fe(III), but complete removal was still achieved when the reaction time was more than 30 min. Poly-Fe salt exhibited a fast P removal rate, while the removal efficiency depended on its iron content. Organic matters in wastewater with large molecular weight and multiple functional groups (such as humic acids) inhibited P removal rate but hardly affect the removal amount. This study provides an insight into CPR by Fe salts and is beneficial for P recovery in WWTPs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ferric Compounds / Iron Compounds Language: En Journal: Chemosphere Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ferric Compounds / Iron Compounds Language: En Journal: Chemosphere Year: 2023 Document type: Article
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