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Background Trace amounts of nitrogen and phosphorus can easily trigger eutrophication damage in surface water, while cost-effective adsorption treatment is in prospect for clearing these pollutants simultaneously and efficiently. In this study, engineered adsorbents decorated with ZnFe-LDH by alkaline coprecipitation (3-6 mm, with modified ceramsite as CZF and modified volcanic rock as VZF) were prepared for NH 4 + and H 2 PO 4 - co-adsorption from aqueous solutions.Results Coexisting ions showed great effects on phosphate adsorption, especially Ca 2+ and CO 3 2- , and humic acid exhibited only a limited shielding impact on co-adsorption properties. Though comprehensive tests presented that the maximum captured amount of ammonium and phosphate occurred at pH 7, the isotherm and kinetic results suggest that two adsorbents preferentially adsorbed each pollutant. Specifically, the maximum uptake quantity of NH 4 + (15.55 mg-N g -1 ) and H 2 PO 4 - (11.21 mg-P g -1 ) were achieved by VZF and CZF, respectively, and controlled by physisorption and chemisorption distinctively, revealing that contaminants were cleared in disparate ways. Performances of seven consecutive adsorption/desorption cycles using 5% NaOH regenerant suggested that CZF retained 71.9% of PO 4 - removal efficiency, and VZF retained 47.9% of the NH 4 + adsorption rate, implying the strong reusability of ZnFe-LDH-modified adsorbents. A dynamic study has assessed that with 1 kg of combined modified adsorbents, approximately 527 L of polluted runoff flow could be continuously treated to below the National limits within one adsorption cycle.Conclusion Comparing with other parallel adsorbents, ZnFe-LDH-modified adsorbent is promising in eliminating eutrophication due to their superior capacity, stability, renewability, and non-toxicity.

Ammonium is strongly related to eutrophication and a key control of eutrophication in aquatic systems, especially in agricultural runoff. In this study, a novel Fe-Mn binary oxide-modified lava (FMML) granular adsorbent was synthesized for ammonium removal from aqueous solutions by co-precipitation method. The kinetic data were described by pseudo-second-order kinetic model well and intraparticle diffusion had effects on ammonium adsorption. For pH between 4.0 and 10.0, the adsorption efficiency was >80%, and its optimum was recorded at pH 7.0. FMML exhibited strong ammonium adsorption selectivity under the single presence of cations like Na + , K + , Ca 2+ , and Mg 2+ . The optimum adsorbent dose and particle size were 4 g/L and 3-5 mm, respectively, for an aqueous solution containing 10 mg/L of ammonium under normal conditions (298 K and pH 7.0). Furthermore, the adsorption process was endothermic, following both the Langmuir (R 2 > 0.98) and Freundlich (R 2 > 0.96) models. Compared with other adsorbents, the FMML can be prepared following a simpler protocol. After 30 times of adsorption-regeneration cycle, the FMML also had a relatively high ammonium adsorption capacity; hence, we see it as a prospective adsorbent for ammonium adsorption from aqueous solutions. © 2019 Water Environment Federation • Practitioner points• Fe-Mn binary oxide-modified lava with Fe/Mn ratio 3:1 was prepared using co-precipitation method. • Adsorption maximum of modified lava was 20.8 mg/g (298 K and pH 7.0). • Adsorption was sensitive to changes in adsorbent dose, particle size, and pH. • Inorganic cations decreased ammonium adsorption in order of Na + > K + > Ca 2+ > Mg 2+ . • Mechanisms for ammonium removal by FMML include diffusion, electrostatic attraction, oxidation, and complexation reaction.