Magnetite nanoparticles were synthesized by a simple and ecofriendly method using onion peel (MNp-OP) and corn silk extract (MNp-CS), in order to develop new low-cost adsorbents for arsenic removal from groundwater. As a point of comparison, magnetite nanoparticles were also synthesized with a conventional chemical process (MNp-CO). The antioxidant potential of onion peel and corn silk extracts was determined using ferric reducing antioxidant power (FRAP) and free radical (DPPH) scavenging assays, including the total phenolics, flavonoids and tannins contents. The synthesized magnetite nanoparticles were characterised using different techniques (Scanning electron microscope/Energy dispersive spectroscopy (SEM/EDS), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR) and Brunauer-Emmett-Teller (BET) surface area analyzer). The adsorption capacity of MNp-OP and MNp-CS and the arsenic removal mechanism of these novel adsorbents was investigated through kinetic and equilibrium experiments and their corresponding mathematical models. Characterisation of MNp-OP and MNp-CS shows high BET specific surface areas of 243 m2/g and 261 m2/g, respectively. XRD and FTIR analysis confirmed the formation and presence of magnetite nanoparticles. The arsenic adsorption mechanism on MNp-OP, MNp-CS and MNp-CO involves chemisorption, intraparticle and external diffusion. Maximal adsorption capacities of MNp-OP, MNp-CS and MNp-CO were 1.86, 2.79, and 1.30 mg/g respectively. The green synthesis applied using onion peel and corn silk extracts was cost effective and environmentally friendly, and results in adsorbents with a high capacity for arsenic and magnetic properties, making them a very promising alternative approach in the treatment of arsenic contaminated groundwater.

Functionalized multiwalled carbon nanotubes (MWCNTs) have drawn wide attention in recent years as novel materials for the removal of heavy metals from the aquatic media. This paper investigates the effect that the functionalization (oxidation) process duration time (3 h or 6 h) has on the ability of MWCNTs to treat water contaminated with low levels of Cu(II), Ni(II) and Cr(VI) (initial concentrations 0.5–5 mg L−1) and elucidates the adsorption mechanisms involved. Adsorbent characterization showed that the molar ratio of C and O in these materials was slightly lower for the oxMWCNT6h, due to the higher degree of oxidation, but the specific surface areas and mesopore volumes of these materials were very similar, suggesting that prolonging the functionalization duration had an insignificant effect on the physical characteristics of oxidized multiwalled carbon nanotubes (oxMWCNTs). Increasing the Ph of the solutions from Ph 2 to Ph 8 had a large positive impact on the removal of Cu(II) and Ni(II) by oxMWCNT, but reduced the adsorption of Cr(VI). However, the ionic strength of the solutions had far less pronounced effects. Coupled with the results of fitting the kinetics data to the Elowich and Weber–Morris models, we conclude that adsorption of Cu(II) and Ni(II) is largely driven by electrostatic interactions and surface complexation at the interface of the adsorbate/adsorbent system, whereas the slower adsorption of Cr(VI) on the oxMWCNTs investigated is controlled by an additional chemisorption step where Cr(VI) is reduced to Cr(III). Both oxMWCNT3h and oxMWCNT6h have high adsorption affinities for the heavy metals investigated, with adsorption capacities (expressed by the Freundlich coefficient KF) ranging from 1.24 to 13.2 (mg g−1)/(mg l−1)n, highlighting the great potential such adsorbents have in the removal of heavy metals from aqueous solutions.

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