The establishment of technology for rapid and complete removal and mineralization of harmful phenolic compounds from water is of great importance for environmental conservation. Visible-light irradiation (λ > 430 nm, light intensity integrated from 420 to 485 nm = 6.0 mW cm) of Au nanoparticle (NP)-loaded TiO (Au/TiO) in dilute aqueous solutions of bisphenol A (BPA) and p-cresol (PC) causes degradation of the phenols. The addition of trimethylstearylammonium chloride (CTAC) enhances the adsorption of BPA on Au/TiO to greatly increase the rate of reaction. Consequently, 10 μM phenols are completely removed from the solutions within 2.5 h irradiation, and prolonging irradiation time to 24 h quantitatively oxidizes BPA to CO. Dynamic light scattering ζ-potential measurements indicate that a CTAC bilayer or admicelle is formed on the Au/TiO particle surface at CTAC concentration >50 μM. The action spectrum for reaction shows that this reaction is driven by the Au NP localized surface plasmon resonance excitation-induced interfacial electron transfer from Au to TiO. We propose a possible reaction scheme on the basis of the experimental results including intermediate analysis.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.langmuir.7b02396 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!