Journal
CHEMOSPHERE
Volume 302, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.134833
Keywords
Nanoscale zero-valent iron; UIO-66 (Zr -O); Vanadium; Mechanism; Recyclability
Categories
Funding
- Youth Scientific Research Talent Support Program of Tianjin Normal University [135302RC1706]
- Young and Middle-aged Backbone Innovative Talents Training Project Foundation of Tianjin [135305JF76]
- Second Level Candidates for the 131 Talent Plan in Tianjin [135305QR06]
- National Natural Science Foundation of China [21307090]
- Tianjin Municipal Natural Science Foundation of China [18JCYBJC96600, 14JCZDJC41000]
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An effective complex of nanoscale zero-valent iron (NZVI) supported on zirconium 1,4-dicarboxybenzene metals-organic frameworks (UIO-66) was synthesized for efficient removal of V5+ from wastewater. The composite demonstrated strong oxidation resistance and a uniform dispersion of NZVI on UIO-66. V5+ could be quickly and completely removed in a wider pH range by the composite, except at pH = 1. The adsorption of V5+ on the composite followed a multi-layer heterogeneous adsorption mechanism, with an adsorbed amount of 397.23 mg V/g NZVI. The presence of nitrate inhibited the removal of V5+ by the composite. The mechanisms of vanadium elimination included physical adsorption, reduction, and co-precipitation, with reduction being the dominant mechanism. The composite showed good reusability after acid leaching.
An effective complex of nanoscale zero-valent iron (NZVI) supported on zirconium 1,4-dicarboxybenzene metals-organic frameworks (UIO-66) with strong oxidation resistance was synthesized (NZVI@UIO-66) for V5+ removal from wastewater. The results demonstrated that NZVI was successfully loaded on UIO-66 with a uniform dispersion, and then the composite was aged in the air which was named A-NZVI@UIO-66. V5+ could be removed quickly and completely using A-NZVI@UIO-66 in a wider pH range except for the pH = 1 condition. The reaction between A-NZVI@UIO-66 and V5+ was an endothermic process. Freundlich model with a better-fitted value showed the adsorption of V5+ on A-NZVI@UIO-66 was multi-layer heterogeneous adsorption and the adsorbed amount of V5+ was 397.23 mg V/g NZVI. Nitrate had a competitive inhibition on V5+ removal by A-NZVI@UIO-66. Mechanisms of vanadium elimination from the aqueous phase by A-NZVI@UIO-66 included physical adsorption, reduction, and complex co-precipitation, particularly the reduction dominated. The subsistent Zr-O bond in A-NZVI@UIO-66 provided a possible double reaction path by playing an electron donor, storage, or conductor role. After acid leaching, A-NZVI@UIO-66 represented good reusability in the removal of V5+ from the practical mine sewage.
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