AI Article Synopsis

  • Wood fiber is an affordable, renewable material with the ability to adsorb dyes, and when enhanced with nanoscale zero-valent iron (EWF-nZVI), it gains magnetism and stronger dye degradation capabilities.
  • Characterization methods revealed EWF-nZVI exhibits a strong magnetism of 96.51 emu/g and efficiently removes dyes according to pseudo-second-order kinetics and Langmuir isotherm models, achieving high removal capacities, particularly for Congo red.
  • After multiple cycles, EWF-nZVI demonstrated reasonable regeneration efficiencies and operates through mechanisms including redox degradation and electrostatic adsorption, highlighting its potential for large-scale water treatment applications.

Article Abstract

Wood fiber as a natural and renewable material has low cost and plenty of functional groups, which owns the ability to adsorb dyes. In order to improve the application performance of wood fiber in dye-pollution wastewater, Eucalyptus wood fiber loaded nanoscale zero-valent iron (EWF-nZVI) was developed to give EWF magnetism and the ability to degrade dyes. EWF-nZVI was characterized via FTIR, XRD, zeta potential, VSM, SEM-EDS and XPS. Results showed that EWF-nZVI owned a strong magnetism of 96.51 emu/g. The dye removal process of EWF-nZVI was more in line with the pseudo-second-order kinetics model. In addition, the Langmuir isotherm model fitting results showed that the maximum removal capacities of Congo red and Rhodamine B by EWF-nZVI were 714.29 mg/g and 68.49 mg/g at 328 K, respectively. After five adsorption-desorption cycles, the regeneration efficiencies of Congo red and Rhodamine B were 74 % and 42 % in turn. The dye removal mechanisms of EWF-nZVI included redox degradation (Congo red and Rhodamine B) and electrostatic adsorption (Congo red). In summary, EWF-nZVI is a promising biomass-based material with high dye removal capacities. This work is beneficial to promote the large-scale application of wood fiber in water treatment.

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http://dx.doi.org/10.1016/j.ijbiomac.2024.131141DOI Listing

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