Ferrocene-functionalized graphitic carbon nitride as an enhanced heterogeneous catalyst of Fenton reaction for degradation of Rhodamine B under visible light irradiation. (September 2017)

• Record Type: Journal Article
• Authors: Lin, Kun-Yi Andrew; Lin, Jyun-Ting
• Is Part Of: Chemosphere. Volume 182(2017)
• Page Start: 54
• Page End: 64
• Publication Date: 2017-09
• Subjects: Ferrocene -- Graphitic carbon nitride -- Rhodamine B -- Hydrogen peroxide; Pollution -- Periodicals; Pollution -- Physiological effect -- Periodicals; Environmental sciences -- Periodicals; Atmospheric chemistry -- Periodicals; 551.511
• DOI: 10.1016/j.chemosphere.2017.04.152
• Languages: English
• ISSNs: 0045-6535

Abstract

Abstract: To enhance degradation of Rhodamine B (RhB), a toxic xanthene dye, an iron-doped graphitic carbon nitride (CN) is prepared by establishing a covalent bond (−CN−) bridging ferrocene (Fc) and CN via a Schiff base reaction. The π-conjugation between the aromatic Fc and CN can be much enhanced by the covalent bond, thereby facilitating the bulk-to-surface charge transfer and separation as well as reversible photo-redox reactions during photocatalytic reactions. Thus, the resulting Fc-CN exhibits a much higher catalytic activity than CN to activate hydrogen peroxide (HP) for RhB degradation, because the photocatalytically generated electrons from CN can activate HP and effectively maintain the bivalence state of Fe in Fc, which also induces the activation of HP. The RhB degradation by the Fc-CN activated HP process (Fc-CN-HP) is validated to involve OH by examining the effect of radical probe agent as well as electron paramagnetic resonance (EPR) spectroscopic analysis. Fc-CN is also proven to activate HP for RhB degradation over multiple times without loss of catalytic activity. Through determining the degradation intermediates, RhB is indeed fully decomposed by Fc-CN-HP into much lower-molecular-weight organic compounds. These features indicate that Fc-functionalization can be an advantageous technique to enhance the catalytic activity of CN for activating HP. The results obtained in this study are essential to further design and utilize Fc-functionalized CN for Fenton-like reactions. The findings shown here, especially the degradation mechanism and pathway, are also quite important for treating xanthene dyes in wastewater. Graphical abstract: Highlights: Ferrocene (Fc) is covalently bound to graphitic carbon nitride (CN) to form Fc-CN. Fc-CN exhibits a much higher photocatalytic activity than CN to activate H2 O2 (HP). RhB can be fully decomposed by Fc-CN activated HP (Fc-CN-HP). Fc-CN can be re-used to activate HP over multiple cycles without efficiency loss. Intermediates of RhB degradation are reported and a degradation pathway is proposed.