Abstract

Fluoride (F) contamination is widely distributed due to natural or anthropogenic causes. A series of mesoporous goethite (α-FeOOH) were synthesized by hydrothermal treatment for rapid F removal from water. The morphology of adsorbents was found to be controlled by varying the hydrothermal and calcination conditions. A highly crystallized FeOOH can be prepared at hydrothermal temperature of 80 °C without further calcination. The sorption isotherm data could be adequately described by Freundlich model and kinetic data followed pseudo-second-order kinetic model. The highest adsorption capacity is as high as 80.1 mg/g. Mesoporous FeOOH exhibited high adsorption capacity in a wide pH range of 3–10 with final pH falling into a stable range (pH 5–6). The presence of Cl- and NO3- seldom impacted the adsorption performance, while addition of high concentrations of CO32- and PO43- (30 mg/L) weakened the adsorption capacity up to 18.2%. For the recycle tests with real F-contaminated groundwater, the removal efficiency dropped slightly from 93.1% (at cycle 1) to 91.8% (at cycle 5), suggesting the adsorbents is powerful for practical use. The FTIR, SEM, and XPS characterization results all confirmed the adsorption of F and revealed that the major adsorption mechanism is the ion-exchange between F ions and hydroxyl groups on the surface of FeOOH.

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