4.6 Article

Enhanced phosphate removal by zero valent iron activated through oxidants from water: batch and breakthrough experiments

Journal

RSC ADVANCES
Volume 11, Issue 63, Pages 39879-39887

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ra05664f

Keywords

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Funding

  1. National Key R&D Program of China [2019YFC1805900]
  2. National Natural Science Foundation of China [41571302, 41807338]
  3. Science and Technology Project of Guangzhou [201803030036]
  4. Water Resource Science and Technology Innovation Program of Guangdong Province [2016-26]

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Oxidants such as hydrogen peroxide, hypochlorite, and persulfate were used to promote zero-valent iron corrosion and enhance phosphate removal efficiency. The addition of oxidants increased the surface corrosion of iron, creating more reaction-adsorption sites for phosphate removal. Different oxidants had varying effects on the corrosion of ZVI and phosphate removal, and adjusting the dosing of oxidants could optimize the removal of phosphate from water.
In this study, oxidants including hydrogen peroxide (H2O2), hypochlorite (ClO-) and persulfate (S2O82-) were employed to promote zero-valent iron (ZVI) corrosion and enhance phosphate (P) removal from water through batch and breakthrough experiments. Characterization results indicated that the addition of oxidant can cause large-scale corrosion of the iron surface. This subsequently generates more iron ions and active minerals, resulting in a large number of reaction-adsorption sites for P removal. Therefore, compared with the ZVI alone system (29.4%), the removal efficiency of P by oxidant/ZVI system (H2O2 : ClO- : S2O82- = 33.2% : 54% : 67.1%) was improved. For the oxidant/ZVI system, H2O2 can promote the corrosion of ZVI to a certain extent. However, the solution pH could be increased during the corrosion process. This leads to inhibition of P removal performance by the H2O2/ZVI system, which only increased by 12.9% to 33.2%. The reaction between NaClO and ZVI consumes less H+, and the reaction product Cl- can pierce the passivation layer on the surface of the ZVI through the pitting effect. As such, the NaClO/ZVI system attained a 54% P removal rate. Compared with H2O2 and NaClO, a better P removal effect of about 67.1% can be achieved by using Na2S2O8, since the oxidation corrosion process of Na2S2O8 does not consume H+, and it also has the strongest oxidizing properties. Furthermore, an appropriate increase in oxidant dosing (0.1-2 mM) could improve the efficiency at which of P is removed. Five batch cycle experiments showed that the oxidant/ZVI system has a higher removal capacity and longer life-span. In the long-term column running, the P removal capacity and operation life of the NaClO/ZVI column are 9.6 times and 3.2 times higher than that of the ZVI column, respectively. This work demonstrates that an oxidant/ZVI system can be an efficient method for P removal in water, which also provides a new idea for solving the problem of ZVI corrosion passivation.

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