4.7 Article

Fabrication of a reusable polymer-based cerium hydroxide nanocomposite with high stability for preferable phosphate removal

期刊

CHEMICAL ENGINEERING JOURNAL
卷 405, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.126649

关键词

Nanocomposite; Cerium hydroxide; Phosphate; Selective removal; High stability

资金

  1. Open Research Fund of Jiangsu Provincial Key Laboratory of Environmental Engineering [ZX2017010, KF2018-004]
  2. State Key Laboratory of Pollution Control and Resource Reuse Foundation [PCRRF18032]
  3. China Postdoctoral Science Foundation [2020M671624]
  4. Natural Science Foundation of China [51508221]
  5. Graduate Research and Innovation Projects of Jiangsu Province [XSJCX19_091]

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A reusable nanocomposite adsorbent HCO@201 with high stability and specific affinity towards phosphate was developed for efficient phosphate removal from wastewater. The adsorbent showed excellent stability over a wide pH range and high affinity for phosphate, making it a promising option for practical applications in wastewater treatment.
Efficient phosphorus removal from municipal or industrial effluents is a valid channel to combat eutrophication. Adsorption has been regarded as an effective approach for enhanced elimination and potential reclamation of phosphorus from wastewater. However, traditional phosphorus adsorbents often suffer from lack of stability and selectivity under complicated solution chemistry. In the current study, a reusable nanocomposite adsorbent HCO@201 of high stability and specific affinity towards phosphate was newly developed and well characterized, where Ce hydroxide (HCO) nanoparticles were encapsulated inside an aminated macroporous polystyrene host D201. The resultant HCO@201 was extremely stable over a wide pH range. Phosphate adsorption by HCO@201 was a pH-dependent process with highest adsorption capacity of 36.4 mg P/g at pH 7.0 +/- 0.1. Thanks to the inner-sphere complexation between phosphate and the embedded HCO nanoparticles, HCO@201 could preferentially capture phosphate even coexist with high levels of other competing anions (HCO3- , NO3-,Cl- and SO42-) or dissolved organic matters (humic acid). Fixed-bed adsorption tests demonstrated that HCO@201 could efficiently treat similar to 1800 bed volumes (BV) of an actual bio-treated sewage (from influent of 1.83 mg P/L to effluent of 0.5 mg P/L), while only similar to 250 BV for its host D201. The saturated HCO@201 could achieve an efficient in-situ regeneration by a simply desorption method. In conclusion, HCO@201 exhibited an excellent application prospect in efficient phosphate removal from wastewater.

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