Nanoscale zerovalent iron (nZVI) supported by natural and acid-activated sepiolites: the effect of the nZVI/support ratio on the composite properties and Cd2+ adsorption
2017
Habish, Amal Juma | Lazarević, Slavica | Janković-Častvan, Ivona | Jokić, Bojan | Kovač, Janez | Rogan, Jelena | Janaćković, Đorđe | Petrović, Rada
Natural (SEP) and partially acid-activated (AAS) sepiolites were used to prepare composites with nanoscale zerovalent iron (nZVI) at different (SEP or AAS)/nZVI ratios in order to achieve the best nZVI dispersibility and the highest adsorption capacity for Cd²⁺. Despite the higher surface area and pore volume of AAS, better nZVI dispersibility was achieved by using SEP as the support. On the other hand, a lower oxidation degree was achieved during the synthesis using AAS. X-ray photoelectron spectroscopy (XPS) analysis of the composite with the best nZVI dispersibility, before and after Cd²⁺ adsorption, confirmed that the surface of the nZVI was composed of oxidized iron species. Metallic iron was not present on the surface, but it was detected in the subsurface region after sputtering. The content of zerovalent iron decreased after Cd²⁺ adsorption as a result of iron oxidation during Cd²⁺ adsorption. The XPS depth profile showed that cadmium was present not only at the surface of the composite but also in the subsurface region. The adsorption isotherms for Cd²⁺ confirmed that the presence of SEP and AAS decreased the agglomeration of the nZVI particles in comparison to the pure nZVI, which provided a higher adsorption capacity. The results showed that the prevention of both aggregation and oxidation during the synthesis was necessary for obtaining an SEP/AAS–nZVI composite with a high adsorption capacity, but oxidation during adsorption was beneficial for Cd²⁺ removal. The formation of strong bonds between Cd²⁺ and the adsorbents sites of different energy until monolayer formation was proposed according to modeling of the adsorption isotherms.
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