Application of response surface methodology for uranium(VI) adsorption using hydroxyapatite prepared from eggshells waste material: study of influencing factors and mechanism

Abstract Hydroxyapatite (HAp) was synthesized from biowaste hen eggshells by wet precipitation method in which calcium hydroxide and phosphoric acid were used as precursors. The effectiveness of uranium(VI) adsorption onto HAp was investigated by batch adsorption experiments from aqueous solutions. The obtained HAp powder was characterized by X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectrometry, point of zero charge and Scanning electron microscope. The factors and levels used during the experiments were pH (2–5), adsorbent mass (0.01–0.05 g), and initial U(VI) concentration (100–310 mg L−1). A Box–Behnken design combined with analysis of variance was used to interpret the main effect influencing the adsorption. The results showed that pH was the most significant parameter affecting U(VI). The kinetic data correlates well with the pseudo-second-order model. The adsorption isotherms fitted the Langmuir-1 type model with the qmax = 175.22 mg g−1 at 25 °C. The calculated value of the mean free energy indicates the chemisorption process. Under optimal conditions, the uranium effluent derived from the precipitation of ammonium uranyl carbonate removal performance of 98% was achieved. This study proved that HAp prepared from eggshell was an ecofriendly and low-cost adsorbent and was very effective for the adsorption of U(VI) from aqueous solutions.</jats:p

Adsorption of Uranium (VI) onto Natural Algerian Phosphate: Study of Influencing Factors, and Mechanism

The goal of this study was to use natural phosphate (NP) abundant in Algeria, as an adsorbent for the removal of uranium (VI) from aqueous solutions in batch adsorption. A full 23 factorial extended experimental design was investigated. The factors and levels used during the experiments were; pH (X1) (1–5), initial U(VI) concentration (X2) (30–60 mg L−1) and adsorbent dose (X3) (5–30 g L−1). The properties of NP were characterized by XRF, SEM, EDS, XRD and FTIR before and after adsorption. The effects of factors were explored by response surface methodology. The equilibrium data of U(VI) adsorption onto NP fitted to the Langmuir − 1 model at a maximum monolayer capacity of 11.11 mg g−1 with the kinetics being pseudo-second-order. The characterization of the filtered solid after adsorption revealed the formation of a new lamellar crystal phase of autunite Ca(UO2)2(PO4)2(H2O)6. The calculated value of the mean free energy indicates the chemisorp- tion process. Under optimal conditions, the uranium effluent derived from the precipitation of ammonium uranyl carbonate removal performance of 100% was achieved