Removal and recovery of high levels of arsenic (As) in copper smelting wastewater present a great environmental challenge. A novel approach was investigated for the first time using TiO 2 for As adsorptive removal from wastewater and subsequent spent adsorbent regeneration and As recovery using NaOH. EXAFS results demonstrate that As(III), as the only As species present in the raw water, does not form an aqueous complex with other metal ions. An average of 3890 ( 142 mg/L As(III) at pH 1.4 in the wastewater was reduced to 59 ( 79 µg/L in the effluent with final pH at 7 in the 21 successive treatment cycles using regenerated TiO 2 . Coexisting heavy metals including Cd, Cu, and Pb with concentrations at 369 mg/L, 24 mg/ L, and 5 mg/L, respectively, were reduced to less than 0.02 mg/ L. As(III) adsorption followed pseudosecond-order rate kinetics, and the adsorption behavior was described with the charge distribution multisite surface complexation model. Approximately 60% As(III) in the waste solution after the TiO 2 regeneration process was recovered by thermo vaporization and subsequent precipitation of sodium arsenite, as suggested by the EDX and XPS analysis. This "zero" sludge process sheds new light on successful As remediation technology for acidic metallurgical industry wastewater.

Coexisting arsenic (As) and fluoride (F) in groundwater poses severe health risks worldwide. Highly efficient simultaneous removal of As and F is therefore of great urgency and high priority. The purpose of this study was to fabricate a novel composite adsorbent and explore the mechanism for concurrent removal of As(V) and F at the molecular level. This bifunctional adsorbent with titanium and lanthanum oxides impregnated on granular activated carbon (TLAC) exhibits a pronounced As(V) and F adsorption capacity over commercially available iron-and aluminumbased adsorbents for synthetic and real contaminated groundwater samples. Synchrotron-based X-ray microfluorescence analysis demonstrates that La and Ti were homogeneously distributed on TLAC. Extended X-ray absorption fine structure spectroscopic results suggest that As(V) formed bidentate binuclear surface complex as evidenced by an averaged Ti−As bond distance of 3.34 Å in the presence of F. Adsorption tests and Fourier transform infrared spectroscopy analysis indicate that F was selectively adsorbed on lanthanum oxides. The surface configurations constrained with the spectroscopic results were formulated in the charge distribution multisite complexation model to describe the competitive adsorption behaviors of As(V) and F. The results of this study indicate that TLAC could be used as an effective adsorbent for simultaneous removal of As(V) and F.

Surface-enhanced Raman scattering (SERS) analysis of environmental hydrophobic pollutants without chemical functionalization of a bare nanoparticle (NP) substrate presents a challenge. The motivation for our study is to develop a highly reproducible and robust portable SERS sensor for detection and identification of polycyclic aromatic hydrocarbons (PAHs) using bare Au NPs. Our hypothesis is that the coffee ring effect could separate PAHs from the bulk solution and concentrate them on the closely packed Au NP ring, consequently enhancing their Raman scattering. This premise was confirmed with the commonly used citrate-reduced Au NPs in 20 nm, having no structural uniqueness. Because of the coffee ring effect, however, closely packed but not aggregated Au NP arrays were formed and, consequently, facilitated the separation and concentration of hydrophobic PAHs. As a result, a prominent SERS enhancement can be obtained on the ring because of the electromagnetic mechanism. A mixture of six PAHs with different numbers of benzene rings, namely, naphthalene, anthracene, pyrene, benzo[a]pyrene, benzo[g,h,i]perylene, and indeno[1,2,3-cd]pyrene, could be readily identified in river water. This portable SERS sensor based on the coffee ring effect provides a robust and versatile approach in PAH detection without the need for stringent structural requirements for Au NPs.