Adsorption of selenium( vi ) onto nano transition alumina

• Published in: Environmental science. Nano Vol. 5; no. 7; pp. 1661 - 1669
• Main Authors: Jordan, Norbert, Franzen, Carola, Lützenkirchen, Johannes, Foerstendorf, Harald, Hering, David, Weiss, Stephan, Heim, Karsten, Brendler, Vinzenz
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 2018
• Subjects: Adsorption; Aluminum oxide; Analytical methods; Charge distribution; Environment models; Environmental impact; Fourier transforms; Infrared reflection; Infrared spectroscopy; Ionic strength; Modelling; Molecular chains; pH effects; Selenium; Sodium chloride; Spectroscopy; Spectrum analysis; Surface charge; Surface chemistry; Surface properties; Transitional aluminas; Trustworthiness; Uptake
• ISSN: 2051-8153; 2051-8161
• DOI: 10.1039/C8EN00293B

The adsorption of selenium( vi ) onto nano transition alumina (γ/δ-Al 2 O 3 ) was investigated at both macroscopic and molecular levels. The uptake of selenium( vi ) was found to decrease upon increasing pH (5–10) and ionic strength (0.01–0.1 mol L −1 NaCl). At the molecular level, in situ attenuated total reflection Fourier-transform infrared (ATR FT-IR) spectroscopy established the predominant formation of a bidentate outer-sphere surface complex throughout the investigated pH range. The acid–base surface properties of transition alumina (surface charge) together with the Se( vi ) adsorption edges were successfully described using a 1-p K charge distribution surface complexation model involving one outer-sphere selenium( vi ) surface species, namely {(AlOH 2 0.5+ ) 2 SeO 4 2− } as suggested by the IR studies. Blind predictions of literature data yielded good agreement in particular in NaCl systems. These new spectroscopy based results can be implemented in reactive transport models to enable more consistent and trustworthy prognostic modeling of the environmental fate of selenium( vi ).