Published October 2021 | Version v1
Journal article

Highly efficient uranium (VI) capture from aqueous solution by means of a hydroxyapatite-biochar nanocomposite: Adsorption behavior and mechanism

  • 1. School of Civil Engineering, Guangzhou University, Guangzhou, 510006 (China)
  • 2. Guangdong Provincial Key Laboratory for Radionuclides Pollution Control and Resources, School of Environmental Science and Engineering, Guangzhou University, Guangzhou, 510006 (China)
  • 3. Department of Soil Science and Agricultural Chemistry, Engineering Polytechnic School, Universidade de Santiago de Compostela, 27002, Lugo (Spain)
  • 4. College of Ecology and Environment, Hainan University, Haikou City, 570100 (China)
  • 5. National Engineering Laboratory for Improving Quality of Arable Land, Institute of Agricultural Resources and Regional Planning, Chinese Academy of Agricultural Sciences, Beijing, 100081 (China)
  • 6. Key Laboratory of Industrial Ecology and Environmental Engineering, School of Environmental Science and Technology, Dalian University of Technology, Dalian, 116024 (China)
  • 7. Department of Environment and Soil Sciences, University of Lleida, 25198, Lleida (Spain)

Description

The exploration and rational design of easily separable and highly efficient sorbents with the sufficient capability of retaining radioactive and toxic uranium U(VI) is paramount. In this study, a hydroxyapatite (HAP) biochar nanocomposite (BR/HAP) was successfully fabricated from rice straw biochar (BR), to be used as a new and efficient adsorbent for removing U(VI) from aqueous solution. Both BR and the BR/HAP composite were characterized via Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and X-ray photo electron spectroscopy (XPS) techniques. Batch test results showed that BR/HAP exhibited remarkably higher adsorption capacity than the raw BR. A pseudo-second order kinetic model thoroughly explained the adsorption kinetics, providing the maximum U(VI) adsorption capacities (qe) of 110.56 mg g−1 (R2 = 0.98) and 428.25 mg g−1 (R2 = 0.99), for BR and BR/HAP, respectively, which was indicative of the rate-limited sorption via diffusion or surface complexation after rapid initial adsorption steps. The Langmuir isotherm model fitted the experimental data to accurately simulate the adsorption of U(VI) onto BR and BR/HAP (R2 = 0.97 and R2 = 0.99). The thermodynamic results showed negative values for ΔG°, clearly indicating that the reaction was spontaneous, as well as positive values for ΔH° (11.04 kJ mol−1 and 28.86 kJ mol−1, respectively) and ΔS° (88.97 kJ mol−1 K−1, and 183.42 kJ mol−1 K−1), making clear the endothermic nature of U(VI) adsorption onto both sorbents, with an increase in randomness at a molecular level. FTIR spectroscopy and XPS spectrum further confirmed that the primary mechanisms were ion exchange with UO22+ and surface complexion by –OH and –COOH. In addition, BR/HAP showed an excellent reusability, making it a promising candidate as a new sorbent for U(VI) removal from wastewater. In view of that, it would be interesting to perform future research to explore practical implications of this sorbent material regarding protection from environmental and public health issues related to that pollutant.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.envres.2021.111518

Additional details

Identifiers

DOI
10.1016/j.envres.2021.111518;
PII
S0013935121008124;

Publishing Information

Journal Title
Environmental Research
Journal Volume
201
Journal Page Range
vp.
ISSN
0013-9351
CODEN
ENVRAL

Optional Information

Copyright
Copyright (c) 2021 Elsevier Inc. All rights reserved.