4.7 Article

Mechanistic insights of hexavalent chromium remediation by halloysite-supported copper nanoclusters

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 421, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2021.126812

Keywords

Chromium (VI); Copper-nanoclusters; Halloysite-nanotube; CuNCs@HNT; Adsorption; Regeneration-reuse

Funding

  1. Bangabandhu Science and Technology Fellowship Trust
  2. Ministry of Science and Technology, the Government of Bangladesh
  3. Cooperative Research Centre for Contamination Assessment and Remediation of the Environment (CRC CARE), Australia [care 6.47.01]

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In this study, a multi-functional material, copper nanoclusters (CuNCs)-halloysite nanotubes (HNT) composite (CuNCs@HNT), was successfully synthesized and applied for the remediation of Cr(VI) pollution. The material showed a high adsorption capacity, effective adsorption under different pH conditions, and involved chemisorption, multiphase diffusion, and multi-molecular layer distribution during the adsorption process. This biocompatible, low-cost, and stable composite has practical potential for the remediation of similar toxic metals.
Chromium (Cr) pollution is a significant environmental concern with remediation challenge. Hexavalent chromium (Cr(VI)) is more toxic than trivalent chromium (Cr(III)) due to its mutagenicity and oncogenicity. In this investigation, a multi-functional material, copper nanoclusters (CuNCs)-halloysite nanotubes (HNT) composite (CuNCs@HNT), has been synthesised in an eco-friendly manner and utilised for Cr(VI) remediation. Advanced analytical tools confirmed the seeding of ultra-fine CuNCs onto HNT surfaces. The maximum adsorption capacity of CuNCs@HNT is 79.14 +/- 6.99 mg/g at pH 5 +/- 0.1 with an increment at lower pHs. This performance was comparable for real surface stream water as well as other reported materials. The pseudo-second-order kinetic-, intra-particle diffusion- and Freundlich isotherm models well fit the experimental data implying that the chemisorption, multiphase diffusion and multi-molecular layer distribution occurred during adsorption. The Fourier-transform infrared and the x-ray photoelectron spectra also ensured the transformation of Cr(VI) to Cr (III) indicating the material's suitability for concurrent adsorption and reduction of Cr(VI). While coexisting cations and anions did not overwhelm this adsorption, CuNCs@HNT was regenerated and reused five successive times in adsorption-desorption cycles without significant loss of adsorption capacity and material's integrity. Therefore, this multi-functional, biocompatible, low-cost and stable CuNCs@HNT composite may have practical application for similar toxic metals remediation.

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