Transformation and destabilization of graphene oxide in reducing aqueous solutions containing sulfide. (23rd September 2014)

• Record Type: Journal Article
• Authors: Fu, Heyun; Qu, Xiaolei; Chen, Wei; Zhu, Dongqiang
• Is Part Of: Environmental toxicology and chemistry. Volume 33:Number 12(2014:Dec.)
• Page Start: 2647
• Page End: 2653
• Publication Date: 2014-09-23
• Subjects: Graphene oxide -- Sulfide -- Colloidal stability -- Reductive transformation -- Surface hydrophobicity; Pollution -- Environmental aspects -- Periodicals; Environmental chemistry -- Periodicals; 615.902
• DOI: 10.1002/etc.2730
• Languages: English
• ISSNs: 0730-7268

Abstract

Abstract: The colloidal stability of carbon nanomaterials is a key factor controlling their fate and bioavailability in natural aquatic systems. The authors report that graphene oxide nanoparticles could be destabilized in reducing aqueous solutions containing a low concentration (0.5 mM) of sulfide, a naturally occurring reductant. Spectroscopic characterization using combined X‐ray photoelectron, Fourier‐transform infrared, X‐ray diffraction, and Raman analyses revealed that the surface oxygen‐containing groups (mainly epoxy groups) of graphene oxide were significantly reduced after reacting with sodium sulfide. The destabilization of graphene oxide was likely caused by the enhanced surface hydrophobicity of the reduced graphene oxide, whereas electrostatic repulsion played a minimal role. Solution pH was found to affect both the deoxygenation process and the aggregation behavior of graphene oxide. Coexisting humic acid reduced the reaction efficiency and stabilized graphene oxide through steric hindrance. These findings suggest for the first time that the colloidal behavior of carbon nanomaterials might change drastically when they enter natural reducing environments containing sulfide such as anaerobic aquifers and sediments. Environ Toxicol Chem 2014;33:2647–2653 . © 2014 SETAC