4.7 Article

Preparation of biochar-interpenetrated iron-alginate hydrogel as a pH-independent sorbent for removal of Cr(VI) and Pb(II)

期刊

ENVIRONMENTAL POLLUTION
卷 287, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2021.117303

关键词

Alginate hydrogel; Biochar; Reduction; Adsorption; pH-independent

资金

  1. National Natural Science Foundation of China [41977117, 41771349, 41977085]
  2. High-levelForeign Expert Recruitment Program of Jiangsu Province [BX2020050]
  3. Qing-Lan Project of Yangzhou University
  4. High-level Talent Support Plan of Yangzhou University
  5. Key Research and Development Program of Zhejiang Province [2019C02053]

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A pH-independent interpenetrating polymeric network was fabricated for removal of Cr(VI) and Pb(II) from aqueous solution. The Fe-SA-C exhibited excellent pH buffering capacity and high adsorption performance due to the crosslinking of graphitic biochar and iron-alginate hydrogel. The functionalized, conductive, and positively-charged Fe-SA-C extended its applicability for removal of heavy metals over a wide pH range.
Herein, a pH-independent interpenetrating polymeric networks (Fe-SA-C) were fabricated from graphitic biochar (BC) and iron-alginate hydrogel (Fe-SA) for removal of Cr(VI) and Pb(II) in aqueous solution. Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and scanning electron microscope (SEM) results demonstrated that graphitic BC interpenetration increased surface porosity and distorted surfaces of Fe-SA, which boosted availability of hydroxyl (-OH) group. Fe3+ as a cross-linking agent of the alginate endowed Fe-SA-C with positive surfaces (positive zeta potential) and excellent pH buffering capacity, while excessive Fe3+ was soldered on Fe-SA-C matrix as FeO(OH) and Fe2O3.Cr(VI) removal at pH of 3 by Fe-SA-C (20.3 mg g(-1)) were 30.3% and 410.6% greater than that by Fe-SA and BC, respectively. Fe-SA-C exhibited minor pH dependence over pH range of 2-7 towards Cr(VI) retention. Greater zeta potential of Fe-SA-C over Fe-SA conferred a better electrostatic attraction with Cr(VI). FTIR and XPS of spent sorbents confirmed the reduction accounted for 98.5% for Cr(VI) removal mainly due to participation of -OH. Cr(VI) reduction was further favored by conductive carbon matrix in Fe-SA-C, as evidenced by more negative Tafel corrosion potential. Reductively formed Cr(III) was subsequently complexed with carboxylic groups originating from oxidation of -OH. Thus, Cr(VI) removal invoked electrostatic attraction, reduction, and surface complexation mechanisms. Pb(II) removal with excellent pH independence was mainly ascribed to surface complexation and possible precipitation. Thus, the functionalized, conductive, and positively-charged Fe-SA-C extended its applicability for Cr(VI) and Pb(II) removal from aqueous solutions in a wide pH range. This research could expand the application of hydrogel materials for removal of both cationic and anionic heavy metals in solutions over an extended pH range.

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