Graphene oxide (GO) was modified by a carbodiimide-induced covalent cross-linking with bovine serum albumin (BSA), enriched with numerous amino and carboxyl functional groups, for radioactive uranium (U VI ) removal. The adsorbent was confirmed through scanning electron microscopy, transmission electron microscopy, Fourier transform infrared, X-ray diffraction, atomic force microscopy, and X-ray photoelectron spectroscopy (XPS). We investigated the effect of factors such as the pH, contact time, and initial concentration on the adsorption of U VI . In this work, the adsorption process closely fitted the Langmuir isotherm model, and pseudo-second-order indicates that chemical adsorption dominates the adsorption process of U VI onto GO–BSA composites. These results show that the optimal adsorption amount of U VI of GO–BSA composites was 389 mg g –1 at 298.15 K, pH = 6, C 0 = 200 mg L –1, and t = 80 min. According to kinetics and the thermodynamic model as well as XPS analysis of pre- and postadsorption of U VI, we propose that the adsorption behavior of U VI onto GO–BSA adsorbent is divided into two stages: (1) chelation of the organic functional groups onto the surface of GO–BSA with U VI; (2) movement of U VI into the interior of the material after adsorption onto the surface. Moreover, the composites exhibit good adsorption efficiency in simulated seawater, indicating the potential of GO–BSA composites for U VI removal from seawater.
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Yang et al. (2017) studied this question.
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