The abatement of nutrient compounds from aqueous waste and wastewater is currently a priority issue. Indeed, the uncontrolled discharge of high levels of nutrients into water bodies causes serious deteriorations of environmental quality. On the other hand, the increasing request of nutrient compounds for agronomic utilizations makes it strictly necessary to identify technologies able to recover the nutrients from wastewater streams so as to avoid the consumption of natural resources. In this regard, the removal and recovery of nitrogen and phosphorus from aqueous waste and wastewater as struvite (MgNH₄PO₄·6H₂O) represents an attractive approach. Indeed, through the struvite precipitation it is possible to effectively remove the ammonium and phosphate content of many types of wastewater and to produce a solid compound, with only a trace of impurities. This precipitate, due to its chemical characteristics, represents a valuable multi-nutrients slow release fertilizer for vegetables and plants growth. For these reasons, the struvite precipitation technology constantly progresses on several aspects of the process. This manuscript provides a comprehensive review on the recent developments in this technology for the removal and recovery of nutrients from aqueous waste and wastewater. The theoretical background, the parameters, and the operating conditions affecting the process evolution are initially presented. After that, the paper focuses on the reagents exploitable to promote the process performance, with particular regard to unconventional low-cost compounds. In addition, the development of reactors configurations, the main technologies implemented on field scale, as well as the recent works on the use of struvite in agronomic practices are presented.

Nitrate is a widespread water contaminant that can pose environmental and health risks. Various conventional techniques can be applied for the removal of nitrate from water and wastewater, such as biological denitrification, ion exchange, nanofiltration, and reverse osmosis. Compared to traditional methods, the chemical denitrification through zero-valent metals offers various advantages, such as lower costs, simplicity of management, and high efficiencies. The most utilized material for chemical denitrification is zero-valent iron (ZVI). Aluminium (ZVA), magnesium (ZVM), copper (ZVC), and zinc (ZVZ) are alternative zero-valent metals that are studied for the removal of nitrate from water as well as from aqueous solutions. To the best of our knowledge, a comprehensive work on the use of the various zero-valent materials that are employed for the removal of nitrate is still missing. Therefore, in the present review, the most recent papers concerning the use of zero-valent materials for chemical denitrification were analysed. The studies that dealt with zero-valent iron were discussed by considering microscopic (mZVI) and nanoscopic (nZVI) forms. For each Fe⁰ form, the effects of the initial pH, the presence or absence of dissolved oxygen, the initial nitrate concentration, the temperature, and the dissolved ions on the nitrate removal process were separately evaluated. Finally, the different materials that were employed as support for the nanoparticles were examined. For the other zero-valent metals tested, a detailed description of the works present in the literature was carried out. A comparison of the various features that are related to each considered material was also made.

The composting process of organic fraction of municipal solid waste, besides to the residual compost, generates a wastewater that is characterized by a high organic load. The application of anaerobic processes represents an advantageous solution for the treatment and valorization of this type of wastewater. Nevertheless, few works have been focused on the anaerobic digestion of compost leachate. To overcome this dearth, in the present paper an extensive experimental investigation was carried out to develop and analyse the anaerobic treatment of young leachate in completely stirred tank reactors (CSTR). Initially, it was defined a suitable leachate pretreatment to correct its acidic characteristics that is potentially able to inhibit methanogenic biomass activity. The pretreated leachate was fed to the digester over the start-up phase that was completed in about 40 days. During the operational period, the organic load rate (OLR) changed between 4.25 kg_COD/m³d and 38.5 kg_COD/m³d. The chemical oxygen demand (COD) abatement was higher than 90% for OLR values up to 14.5 kg_COD/m³d and around to 80% for applied loads equal to 24.5 kg_COD/m³d. At this OLR, it was reached the maximum daily biogas production of about 9.3 L_biogas/(L_reactord). The CH₄ fraction was between 70%–78% and the methane production yield in the range 0.34–0.38 LCH₄/g_CODremoved. The deterioration of biogas production started for OLR values that were over the threshold of 24.5 kg_COD/m³d when a volatile fatty acids (VFA) accumulation occurred and the pH dropped below 6.5. The maximum ratio between VFA and alkalinity (ALK) tolerable in the CSTR was identified to be 0.5 gCH₃COOH/gCaCO₃. Through an economic analysis, it was proven that the digestion of compost leachate could ensure significant economic profits. Furthermore, the produced digestate had characteristics that were compatible for agricultural applications.

The definition of technologies capable of removing and recovering nutrients from polluting effluents is a key environmental challenge. Through these technologies, it would be possible to protect aquatic systems and prevent the consumption of natural resources for the production of commercial fertilizers. In this regard, the application of the precipitation processes of struvite-type compounds is an attractive approach. Indeed, these processes are potentially able to remove nutrients from many effluents and produce a precipitate reusable as a slow-release fertilizer. The scientific community has largely focused on the precipitation of magnesium ammonium phosphate (MgNH₄PO₄·6H₂O, MAP), while the recovery of the analogous magnesium potassium phosphate (MgKPO₄·6H₂O, MPP) has received extensive attention in the last decade. Research on this topic is continuously progressing to improve the precipitation process in different aspects (working conditions, reaction units, interference elimination, etc.). Until now, there has been no paper that comprehensively reviewed the applicability of MPP precipitation for the removal and recovery of nutrients from aqueous waste. To fill this gap, the present paper aimed to provide an exhaustive analysis of the literature reports on MPP processes to help researchers understand the theoretical and applicative aspects, the main problems, and the need for further research. In this regard, the applications in the treatment of various aqueous wastes were considered. The theoretical concepts, the main process parameters, and the effects of inhibiting substances and impurities are presented. Moreover, the development of reactor configurations and their working conditions are evaluated. Finally, the potential use of MPP as a fertilizer and some economic evaluations are reported. On the basis of the conducted analysis, it emerged that the recovery of MPP was mainly affected by the pH, dose, and nature of reagents, as well as the presence of competitive ions. The optimal pH values were reported to be between 9 and 11. Reagent overdoses with respect to the theoretical values improved the process and the use of pure reagents guaranteed superior performance. The stirred-tank reactors and fluidized bed reactors were the most used units with high process yields. The applicability of MPP in agronomic practices appears to be a suitable option.