Search Results (2)

Phosphorus (P) pollution is a leading cause of water eutrophication, and metal-modified biochar is an effective adsorbent with the ability to alter the migration capacity of phosphorus. This study uses bamboo as the raw material to prepare metal-modified biochar (ZFCO-BC) loaded with Fe and Ca under N₂ conditions at 900 °C, and investigates its adsorption characteristics for phosphate. Batch experimental results show the adsorption capacity of the ZFCO-BC gradually increases (from 4.0 to 69.1 mg/g) as the initial phosphate concentration increases (from 2 to 900 mg/L), mainly through multilayer adsorption. Additionally, as the pH increases from 1 to 7, the adsorption capacity of the ZFCO-BC climbs to reach its maximum value of 48.4 mg/g with an initial phosphate concentration of 150 mg/L. At this pH, phosphate primarily exists as H₂PO₄⁻ and HPO₄²⁻, which both readily react with Fe³⁺ and Ca²⁺ in the biochar. Furthermore, the addition of CO₃²⁻, HCO₃⁻, NO₃⁻, SO₄²⁻, F⁻, and Cl⁻ each affect the removal rate of phosphate by less than 10%, indicating the ZFCO-BC has a highly efficient and selective phosphate adsorption capacity. A multi-column adsorption experiment designed to achieve long-term and efficient phosphorus removal treated 275.5 pore volumes (PVs) of water over 366 h. The cyclic adsorption–desorption experiment results show that 0.5 M NaOH can effectively leach phosphate from the ZFCO-BC. Observations at the molecular level from P K-edge XANES spectra confirm the removal of low-concentration phosphate is primarily dominated by electrostatic attraction, while the main removal mechanism for high-concentration phosphate is chemical precipitation. This study demonstrates that ZFCO-BC has broad application prospects for phosphate removal from wastewater and as a potential slow-release fertilizer in agriculture. Full article

Under hydrothermal conditions emulating natural hydrothermalites, three oxo-salts with sodium and transition metal cations were obtained in the form of single crystals. Their compositions and crystal structures were studied using scanning electron microscopy, microprobe X-ray spectral analysis, and X-ray single-crystal diffraction. The sodium cobalt silicate, i.e., Na₂CoSiO₄, a structural analog of the mineral liberite, is well known as an ionic conductor. Its crystal structure consists of a framework derived from β-tridymite, built using the Co- and Si-centered tetrahedra sharing vertices. The sodium oxocuprate phosphate chloride Na₂Cu₃O(Cu₀.₈Na₀.₂)(PO₄)₂Cl belongs to a group of compounds, including fumarolic minerals, characterized by the presence of oxo-centered pyroxene-like chains in their structures. The crystal structure of mineralogically probable sodium vanadium phosphate hydroxide (Na₃V(OH)(HPO₄)(PO₄)) is based on chains built using octahedra centered by magnetically active V³⁺. Magnetic susceptibility measurements indicate an antiferromagnetic arrangement of V³⁺ ions and no transition to an ordered state up to 2 K. Full article