Adsorption and desorption of chromium with humic acid coated iron oxide nanoparticles

Abstract

Presence of carcinogenic chromium, i.e., Cr(VI), in different industrial effluents necessitates design and development of effective abatement technologies. Nanosorbent consisting of iron oxide nanoparticles functionalized with soil-derived humic acid was employed for removal of Cr(VI). The point of zero charge for both humic acid and nanoparticles as estimated from pH shift experiments was between pH 8 and 9. Adsorption isotherm from batch experiments at neutral pH followed Langmuir model with projected maximum adsorption capacities for humic acid coated nanoparticles (24.13 mg/g) much higher than its uncoated counterpart (2.82 mg/g). Adsorption was process very fast and kinetics could be described with pseudo-second-order model (R2 > 0.98), for both nanoparticles. High E4/E6 ratio of extracted humic acid and Fourier transform infrared spectroscopy of coated nanoparticles (20–100 nm) indicated enrichment of hydroxyl, carboxylic, and aliphatic groups on surface leading for the better adsorption. Humic acid coated and uncoated nanoparticles regenerated with EDTA, NaOH, urea, Na2CO3, and NaCl treatments retained 35.90–59.67 and 26.37–36.28% of their initial adsorption capacities, respectively, in 2nd cycle. Experimental controls (virgin nanoparticles subjected to an identical regenerating environment) revealed irreversible surface modification as the cause for loss of their adsorption capacities.