Activated carbon has been widely used to remove hazardous Cr(VI); however, the impact of CrO precipitate on gradually declining removal ability as pH increases has received little attention. Herein, to investigate the effect of CrO, SEM-EDX (scanning electron microscope-energy dispersive X-ray analysis) coupling elements mapping of chromium-loaded powdered activated carbon (PAC) revealed that a chromium layer was formed on the PAC exterior after being treated with Cr(VI) at pH 7. XPS (X-ray photoelectron spectroscopy) study confirmed that 69.93% and 39.91% CrO precipitated on the PAC surface at pH 7 and pH 3, respectively, corresponding to 17.77 mg/g and 20 mg/g removal capacity. Exhausted PAC had a removal efficiency of 92.43% after CrO being washed by HSO solution, which was much higher than the removal efficiency of 51.27 % after NaOH washing. This further verified that the intrinsically developed CrO precipitate on PAC under neutral conditions limited the durability of PAC as an adsorbent. Consecutive elution assessments confirmed that adsorption and reduction ability both declined as pH increased. Raman spectroscopy and C 1s spectra of materials demonstrated two distinct Cr(VI) removal mechanisms under pH 3 and pH 7. In conclusion, the exhausted AC after Cr(VI) adsorption can be rejuvenated after the surface coated CrO is washed by the acid solution, which can expand the longevity of AC and recover Cr(III).
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