4.7 Article

Lanthanum ion modification of aminated cyclomatrix polyphosphazene-coated porous carbon nanosheets for rapid, efficient and selective removal of phosphate

期刊

APPLIED SURFACE SCIENCE
卷 593, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.apsusc.2022.153359

关键词

Polyphosphazene; Phosphate removal; Modification; Adsorption selectivity; Adsorption mechanism

资金

  1. National Natural Science Foundation of China [21101141]
  2. Outstanding Young Talent Research Fund of Zhengz-hou University [1521320002]
  3. Key Scientific Research Project of Col-leges and Universities in Henan Province [21A430036]
  4. Foundation of Henan General Science and Technology Project [212102210206]

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In this study, a fast, efficient, and selective adsorbent, PCNs@PCP-La, was developed for phosphate removal from water. PCNs@PCP-La exhibited high uptake capacity, wide pH range applicability, rapid adsorption kinetics, excellent selectivity, and good reusability.
Phosphate removal has been the top priority in eutrophic wastewater treatment. Herein we reported a fast, efficient and selective adsorbent, PCNs@PCP-La, for phosphate removal from an aqueous medium. The adsorbent was fabricated via two steps: (1) synthesis of PCNs@PCP composite through in situ polymerization of hexachlorocyclotriphosphazene and polyethyleneimine on the porous carbon nanosheets; and (2) lanthanum ion (La3+) modification of PCNs@PCP via an impregnation process to create PCNs@PCP-La hybrid. Multiple characterizations showed that the atomically dispersed La3+ ions could be facilely chelated with nitrogen-rich cyclomatrix polyphosphazene framework, significantly improving the application efficiency of La3+ ions as active adsorption sites. Comparative tests confirmed that PCNs@PCP-La had a high phosphate uptake capacity of up to 121.2 mg P g(-1) (pH = 4.0) at 298 K and performed well even in a wide pH range (3.0-9.0). Also, PCNs@PCP-La showed a particularly short saturated adsorption time (5 min), indicating a fast adsorption kinetic process. Meanwhile, PCNs@PCP-La presented a superior adsorption selectivity for phosphate under interference with coexisting anions/cation and humic acid, and owned an attractive reusability (after 5th cycles, 85% capacity retention). The plausible adsorption mechanism can be ascribed to electrostatic attraction, inner-sphere complexation, and the formation of LaPO4 center dot 0.5H(2)O precipitates between adsorbent and adsorbate.

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