Search Results (5)

Phosphorus (P) recovery from wastewater is considered to be a positive human intervention towards sustainable P use in the global P cycle. This study investigated the feasibility of synthesizing a superparamagnetic nano-sorbent that was functionalized by lanthanum silicate nanorods (NR_La-Si) using drinking water treatment sludge (DWTS), evaluating both its P adsorption capacity and fertilization effect. The DWTS-based La-modified P nano-sorbent (P-sorbent _D) exhibited complicated but single-layer-dominant adsorption for phosphate, with a maximum adsorption capacity up to 26.8 mg/g, which was superior to that of most of the similar sludge-based P-sorbent. The NR_La-Si-modified P-sorbent _D was identified with several characterization techniques and the leaching metal elements from the nano-sorbent were tested, which were below the limits proposed by the Food and Agriculture Organization of the United Nations. In addition, the growth and vigorousness of Arabidopsis thaliana indicated that the exhausted P-sorbent _D could be used as a potential water-soluble moderate-release P fertilizer, which was also confirmed by the well-fitted P uptake model and the P desorption pattern from the sorbent–fertilizer. The doped lanthanum silicate nanorods could play the dual role of P complexation enhancement and health/growth promotion. In light of this, this study proposed a new way of reclaiming DWTS as a P-sorbent for fertilization, offering new insights into the path toward “closing the P loop”. Full article

Superparamagnetic magnetic nanoparticles (MNPs, Fe₃O₄) were first synthesized based on a chemical co–precipitation method, and the core–shell magnetic silica nanoparticles (MSNPs, Fe₃O₄@SiO₂) were obtained via hydrolysis and the condensation of tetraethyl orthosilicate onto Fe₃O₄ seed using a sol–gel process. Following that, MSNPs were immobilized using a three–step grafting strategy, where 8-hloroacetyl–aminoquinoline (CAAQ) was employed as a metal ion affinity ligand for trapping specific heavy metal ions, and a macromolecular polymer (polyethylenimine (PEI)) was selected as a bridge between the surface hydroxyl group and CAAQ to fabricate a network of organic networks onto the MSNPs’ surface. The as–synthesized MSNPs–CAAQ nanocomposites possessed abundant active functional groups and thus contained excellent removal features for heavy metal ions. Specifically, the maximum adsorption capacities at room temperature and without adjusting pH were 324.7, 306.8, and 293.3 mg/g for Fe³⁺, Cu²⁺, and Cr³⁺ ions, respectively, according to Langmuir linear fitting. The adsorption–desorption experiment results indicated that Na₂EDTA proved to be more suitable as a desorbing agent for Cr³⁺ desorption on the MSNPs–CAAQ surface than HCl and HNO₃. MSNPs–CAAQ exhibited a satisfactory adsorption capacity toward Cr³⁺ ions even after six consecutive adsorption–desorption cycles; the adsorption efficiency for Cr³⁺ ions was still 88.8% with 0.1 mol/L Na₂EDTA as the desorbing agent. Furthermore, the MSNPs–CAAQ nanosorbent displayed a strong magnetic response with a saturated magnetization of 24.0 emu/g, and they could be easily separated from the aqueous medium under the attraction of a magnet, which could facilitate the sustainable removal of Cr³⁺ ions in practical applications. Full article

Phosphorus (P) management in the “water-energy-resource-nexus” in wastewater treatment plants (WWTPs) remains a longstanding challenge. P adsorption from the P-enriched digested sludge liquor (DSL) is a comparatively more practical and economically viable approach for P recovery in WWTPs. However, high concentrations of impurities in DSL might pose a negative and interferential effect on P adsorption, hindering the application of sorbents or precipitation methods. Given such a situation, highly efficient and cost-effective sorbent towards P reclamation from DSL is highly needed. Therefore, this study aims to develop a novel complex agent containing aluminum coagulant and superparamagnetic nano-sorbent (SNS) that can be used in magnetic seeding coagulation for P recovery. The complex agents with different PACl: SNS ratios showed varied turbidity removal rates and P recovery efficiencies and the optimal ratio was 15 mg PACl: 15 g SNS. PAC and SNS showed significant interaction because PAC could enhance P adsorption by shielding the interferential effect of colloidal impurities. In addition, the complex is highly regenerative, with turbidity and P removal rate stably maintained at 70–80% after 10 adsorption/regeneration cycles. The cost–benefit analysis of the dosing complex agent showed a dosing cost of 0.154 EUR/m3, admittedly much higher than the conventional magnetic seeding coagulation, which could probably be covered by the profit if the expensive and rare P product is reclaimed. This work indicated that the complex agent was superior due to its high adsorption capacity, easy separation, and repeated dosing, and therefore had the potential for P recovery from DSL. Full article

We report in the present study the in situ formation of magnetic nanoparticles (Fe₃O₄ or Fe) within porous N-doped carbon (Fe₃O₄/N@C) via simple impregnation, polymerization, and calcination sequentially. The synthesized nanocomposite structural properties were investigated using different techniques showing its good construction. The formed nanocomposite showed a saturation magnetization (M_s) of 23.0 emu g⁻¹ due to the implanted magnetic nanoparticles and high surface area from the porous N-doped carbon. The nanocomposite was formed as graphite-type layers. The well-synthesized nanocomposite showed a high adsorption affinity toward Pb²⁺ toxic ions. The nanosorbent showed a maximum adsorption capacity of 250.0 mg/g toward the Pb²⁺ metallic ions at pH of 5.5, initial Pb²⁺ concentration of 180.0 mg/L, and room temperature. Due to its superparamagnetic characteristics, an external magnet was used for the fast separation of the nanocomposite. This enabled the study of the nanocomposite reusability toward Pb²⁺ ions, showing good chemical stability even after six cycles. Subsequently, Fe₃O₄/N@C nanocomposite was shown to have excellent efficiency for the removal of toxic Pb²⁺ ions from water. Full article

Solid phase extraction using magnetic nanoparticles has represented a leap forward in terms of the improvement of water quality, preventing the contamination of industrial effluents from discharge in a more efficient and affordable way. In the present work, superparamagnetic iron oxide nanoparticles (MNP) with different surface charges are tested as nanosorbents for the removal of chromium(VI) in aqueous solution. Uniform magnetic nanoparticles (~12 nm) were synthesized by a microwave polyol-mediated method, and tetraethyl orthosilicate (TEOS) and (3-aminopropyl) triethoxysilane (APTES) were grafted onto their surface, providing a variation in the surface charge. The adsorptive process of chromium was evaluated as a function of the pH, the initial concentration of chromium and contact time. Kinetic studies were best described by a pseudo-second order model in all cases. TEOS@MNP barely removed the chromium from the media, while non-grafted particles and APTES@TEOS@MNP followed the Langmuir model, with maximum adsorption capacities of 15 and 35 mg_Cr/g, respectively. The chromium adsorption capacities abruptly increased when the surface became positively charged as the species coexisting at the experimental pH are negatively charged. Furthermore, these particles have proven to be highly efficient in water remediation due their 100% reusability after more than six consecutive adsorption/desorption cycles. Full article