Abstract

Nanoscale zero-valent iron particles have large specific surface area and high reaction activity, and have been increasingly used for the degradation of environmental contaminants. However, rapid aggregation and deactivation hinder their wide applications. In this work, nanoscale zero-valent iron (NZVI) particles were prepared in vesicles, which were formed by self-assembly of amphiphilic block copolymer poly(1-vinylpyrrolidone-co-vinylacetate) (PVV) in aqueous tetrahydrofuran medium, and characterized with the aid of XRD, FTIR, SEM-EDX, TEM, XPS and DLS techniques. It was found that the NZVI particles were well encapsulated in the vesicles, and they could be stored directly in the air as solids, but the dried NZVI particles could be easily released from the vesicles once they were put in water. These NZVI particles showed some unique features, such as uniform nanometer size distribution (from 70 to 100nm), vesicle-like morphology, and good dispersion. Activity and stability of the NZVI in vesicles were examined by using Cr(VI) and nitrobenzene as the model pollutants, and compared with the bare NZVI particles synthesized with the same procedures but without PVV. A dramatic difference in activity and stability was observed for the two different NZVI particles. The NZVI in vesicles showed a good chemical stability in the air, and still maintained its high reactivity in water. Such excellent performance might be attributed to the encapsulation of the NZVI by vesicles, which could impede well the strong agglomeration of metal particles in water and prevent metal particles from being oxidized in the air.

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