Search Results (28)

This study evaluates the feasibility of nitrogen recovery from wastewater via electrochemical methods as an alternative nutrient source for agricultural applications. Ammonium nitrogen (NH₄⁺-N) and phosphate (PO₄³⁻-P) contamination poses significant environmental risks and challenges water resource management globally. The electrochemical precipitation of struvite (MgNH₄PO₄·6H₂O) offers a promising solution for nutrient recovery, with potential applications as a slow-release fertilizer. Experimental results demonstrate that increased current density (from 2.5 to 7.5 mA/cm²) and reduced electrode distance (1 cm) significantly enhance NH₄⁺ and PO₄³⁻ consumption and struvite precipitation. Increasing the amperage from 2.5 to 7.5 mA·cm⁻² at a 1 cm electrode distance raised the ammoniacal nitrogen incorporation from 1.59 to 5.34 g/100 g, signifying greater struvite production. The Mg and P concentrations were 15.44 and 12.60 g/100 g, respectively, for this higher amperage, although lower than the concentrations seen with 2.5 mA·cm⁻² (22.16 and 14.52 g/100 g). The majority of Mg (60%) and P (93.6%) were, however, incorporated within struvite. Additionally, this study reveals that Mg is primarily incorporated as struvite when using higher current densities, while lower current densities yield greater Mg incorporation in non-struvite forms, such as magnesium carbonate. Findings suggest that optimizing current density and electrode distance can improve nitrogen and phosphorus recovery efficiencies, making electrochemical struvite production a viable, sustainable approach for nutrient recycling. This method not only reduces dependence on synthetic fertilizers but also supports sustainable agricultural practices by transforming wastewater contaminants into valuable resources. Full article

Water quality is a crucial determinant in decision-making processes aimed at optimizing resource allocation across various industries. Pollutant impurities that hinder the sufficient supply of water have a deleterious impact on the quality and are damaging to living species, especially aquatic life. Various chemical and biological treatments are used to reduce water pollution levels. A technology involving a mixture of anaerobic and aerobic beneficial microbes is becoming popular for its eco-friendly characteristics. Effective Microorganism (EM) technology utilizes naturally existing microorganisms that can purify and restore the environment. The study investigated the application of Effective Microorganism-Activated Solution (EMAS), TeMo Decomposer (TeMo), and Lactic Acid Bacteria (LAB) to enhance water quality. Additionally, microbial testing will be carried out to identify bacteria present in each EM. EM-based rehabilitation of polluted and degraded water bodies significantly contributes to the restoration of aquatic habitats and ecosystems. This study aimed to assess the water quality at Tasik Alumni, Kampus Pauh, Perlis, Malaysia. Four sampling points in Tasik Alumni were chosen to reflect the water quality status of the lake. The sampling was conducted once at four points locations in Tasik Alumni. Seven water quality measures, including pH, dissolved oxygen (DO), biochemical oxygen demand (BOD), chemical oxygen demand (COD), ammoniacal nitrogen (NH₃-N), total suspended solid (TSS), and turbidity, were analysed ex-situ and categorised according to Water Quality Index (WQI) and National Water Quality Standard (NWQS) classifications. The Tasik Alumni was categorised as mildly contaminated. The results clearly showed the efficiency of this technique in restoring and conserving water quality in a degraded or polluted lake. Full article

Urbanization growth has intensified the challenge of managing and treating increasing amounts of municipal solid waste (MSW). Landfills are commonly utilized for MSW disposal because of their low construction and operation costs. However, this practice produces huge volumes of landfill leachate, a highly polluting liquid rich in ammoniacal nitrogen (NH₃-N), organic compounds, and various heavy metals, making it difficult to treat in conventional municipal wastewater treatment plants (WWTPs). In recent years, research has shown that microbial biofilms, developed on carriers of different materials and called “moving bed biofilm reactors” (MBBRs), may offer promising solutions for bioremediation. This study explored the biofilm development and the nitrification process of moving bed biofilms (MBBs) obtained from high ammonia-selected microbial communities. Using crystal violet staining and confocal laser-scanning microscopy, we followed the biofilm formation stages correlating nitrogen removal to metagenomic analyses. Our results indicate that MBBs unveiled a 10-fold more enhanced nitrification rate than the dispersed microbial community present in the native sludge of the Porto Sant’Elpidio (Italy) WWTP. Four bacterial families, Chitinophagaceae, Comamonadaceae, Sphingomonadaceae, and Nitrosomonadaceae, accumulate in structured biofilms and significantly contribute to the high ammonium removal rate of 80% in 24 h as estimated in leachate-containing wastewaters. Full article

The excessive mineralization of organic molecules during anaerobic fermentation increases the availability of nitrogen and carbon. For this reason, the development of downstream processing technologies is required to better manage ammonia and carbon dioxide emissions during the storage and land application of the resulting soil organic amendment. The present work investigated classical distillation as a technology for valorizing ammoniacal nitrogen (NH₄⁺-N) in anaerobic digestate. The results implied that the direct isolation of ammonium bicarbonate (NH₄HCO₃) was possible when applying the reactive distillation to the food waste digestate (FWD) with a high content of NH₄⁺-N, while the addition of antifoam to the agrowaste digestate (AWD) was necessary to be able to produce an aqueous solution of NH₄HCO₃ as the distillate. The reason was that the extraction of NH₄HCO₃ from the AWD required a higher temperature (>95 °C) and duration (i.e., steady state in batch operation) than the recovery of the inorganic fertilizer from the FWD. The titration method, when applied to the depleted digestate, offered the quickest way of monitoring the reactive distillation because the buffer capacity of the distillate was much higher. The isolation of NH₄HCO₃ from the FWD was attained in a transient mode at a temperature below 90 °C (i.e., while heating up to reach the desired distillation temperature or cooling down once the batch distillation was finished). For the operating conditions to be regarded as techno-economically feasible, they should be attained in the anaerobic digestion plant by integrating the heat harvested from the engines, which convert the biogas into electricity. Full article

Herein, the development of a niobium-based metal–organic framework (Nb-MOF) designed to serve as a catalytic support for the production of hydrogen (H₂) from sodium borohydride (NaBH₄) is reported. The Nb-MOF was synthesized via a solvothermal method using niobium ammoniacal oxalate (AmOxaNb) as the metal source and 1,4-benzenedicarboxylic acid (BDC) as the ligand. The resulting MOF was characterized by Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). The characterization study confirmed the successful synthesis of Nb-MOF. The catalytic activity was optimized by examining five key factors: (i) platinum (Pt) and cobalt (Co) bimetallic compositions (ranging from 1:0 to 0:1 mmol), (ii) NaBH₄ concentration (0.2, 0.3, 0.4, and 0.5 mol L⁻¹), (iii) the Nb-MOF/Pt–Co catalyst dose (0.05, 0.10, 0.20, and 0.40 mmol), (iv) sodium hydroxide (NaOH) concentration (0.01, 0.05, 0.1, and 0.2 mol L⁻¹), and (v) system temperature (293.15, 298.15, 303.15, 313.15, and 323.15 K). The optimal catalyst was identified as Nb-MOF supporting a Pt-Co bimetallic composition in a 0.4:0.6 mmol ratio, achieving a hydrogen generation rate (HGR) of 1473 mL min⁻¹ g_cat⁻¹ and an activation energy of 19.2 kJ mol⁻¹. Furthermore, this catalyst maintained its efficiency over 20 cycles, demonstrating significant potential as a sustainable solution for H₂ evolution from NaBH₄. Full article

Total ammoniacal nitrogen (TAN) occurs in various wastewaters and its recovery is vital for environmental reasons. Forward osmosis (FO), an energy-efficient technology, extracts water from a feed solution (FS) and into a draw solution (DS). Asymmetric FO membranes consist of an active layer and a support layer, leading to internal concentration polarization (ICP). In this study, we assessed TAN recovery using a polymeric thin-film composite FO membrane by determining the permeability coefficients of NH₄⁺ and NH₃. Calculations employed the solution–diffusion model, Nernst–Planck equation, and film theory, applying the acid–base equilibrium for bulk concentration corrections. Initially, model parameters were estimated using sodium salt solutions as the DS and deionized water as the FS. The NH₄⁺ permeability coefficient was 0.45 µm/s for NH₄Cl and 0.013 µm/s for (NH₄)₂SO₄ at pH < 7. Meanwhile, the NH₃ permeability coefficient was 6.18 µm/s at pH > 9 for both ammonium salts. Polymeric FO membranes can simultaneously recover ammonia and water, achieving 15% and 35% recovery at pH 11.5, respectively. Full article

The emergence of 2D materials has significantly expanded the wide range of nanomaterials with diverse applications. Notably, their high conductivity, catalytic efficiency, and hydrophobicity have fueled heightened research interests for water treatment applications. This research aimed to investigate the synthesis and characterization of MXene and reduced graphene oxide (rGO) nanocomposites with silver nanoparticles (Ag) for enhanced catalytic activity in the decomposition of Direct Blue-24 dye. In this study, we employed well-established methods, previously documented in the literature, to prepare two distinct nanocomposites. Novel nanocomposites, namely reduced graphene oxide–silver nanoparticles (rGO–Ag) and MXene–silver nanoparticles (MXene–Ag), were synthesized using the hydrothermal and direct reduction method with an ammoniacal solution (aqueous solution). Comprehensive characterization using advanced tools revealed that the introduced Ag particles integrated seamlessly onto the parent nanofilms of the Carbon derivatives, forming a secondary phase with enhanced catalytic functionality. These nanocomposites demonstrated significant improvements in the catalytic decomposition reactions in simulated wastewater. Verification involved the reduction reaction of Direct Blue-24 dye at known nanocomposite concentrations. The results indicated that MXene–Ag exhibited a superior catalytic activity of 98% in 10 min compared to the rGO–Ag nanocomposite films, which achieved 96% in 35 min. The results indicated that MXene–Ag nanocomposites exhibited a 20–25% increase in catalytic efficiency compared to the rGO–Ag nanocomposites. The outcomes of this research hold promise for practical applications in textile wastewater management and various industrial sectors dealing with mutagenic and carcinogenic chemicals containing azo and/or phthalocyanine products. Full article

Iron oxides (hematite, Fe₂O₃, and magnetite, Fe₃O₄), previously used as electron mediators in the galvanic system with zero-valent aluminum (ZVAl), have been shown to recover Au upon cementation in Au–Cu ammoniacal thiosulfate media selectively, and this warrants further investigation. This research is focused on investigating the role of the semiconductive properties of metal oxides by performing a cementation experiment by mixing 0.15 g of electron mediators (Fe₃O₄, Fe₂O₃, TiO₂ (anatase and rutile)) and 0.15 g of zero-valent aluminum powder as an electron donor in various electrochemical experiments. The results revealed that upon the cementation experiment, synthetic Fe₂O₃ and Fe₃O₄ were consistently able to selectively recover Au at around 90% and Cu at around 20%. Compared to activated carbon (AC), TiO₂, in anatase and rutile forms, obtained selective recovery of gold, but the recovery was utterly insignificant compared to that of iron oxides, obtaining an average of 93% Au and 63% Cu recovery. The electrochemical and surface analysis supports the results obtained upon the cementation process, where TiO₂, upon cyclic voltammetry (CV), obtained two reduction peaks centered at −1.0 V and −0.5 V assigned to reducing Au and Cu ions, respectively. Furthermore, various electrochemical impedance spectroscopic analyses revealed that the flat band potential obtained in the Mott–Schottky plot is around −1.0 V and −0.2 V for iron oxides and titanium oxides, respectively, suggesting that the electrons travel from semiconductor interface to electrolyte interface, and electrons are accessible only to Au ions in the electrolyte interface (reduction band edge around −1.0 V). The determination of this selective cementation mechanism is one of a kind. It has been proposed that the semiconductive properties of Fe₂O₃, Fe₃O₄, and, by configuring their relative energy band diagram, the travel of electrons from the iron oxide–electrolyte interface facilitate the selective cementation towards Au(S₂O₃)₂³⁺ ions in gold–copper ammoniacal thiosulfate solutions. Full article

Membrane contactors are among the available technologies that allow a reduction in the amount of ammoniacal nitrogen released into the environment through a process called transmembrane chemical absorption (TMCA). This process can be operated with different substances acting as trapping solutions; however, strong inorganic acids have been studied the most. The purpose of this study was to demonstrate, at laboratory scale, the performance of citric acid as a capturing solution in TMCA processes for recovering ammonia as an organic fertilizer from anaerobic digestor reject water using membrane contactors in a liquid–liquid configuration and to compare it with the most studied solution, sulfuric acid. The experiments were carried out at 22 °C and 40 °C and with a feed water pH of 10 and 10.5. When the system was operated at pH 10, the rates of recovered ammonia from the feed solution obtained with citric acid were 10.7–16.5 percentage points (pp) lower compared to sulfuric acid, and at pH 10.5, the difference decreased to 5–10 pp. Under all tested conditions, the water vapor transport in the system was lower when using citric acid as the trapping solution, and at pH 10 and 40 °C, it was 5.7 times lower. When estimating the operational costs for scaling up the system, citric acid appears to be a better option than sulfuric acid as a trapping solution, but in both cases, the process was not profitable under the studied conditions. Full article

Zinc oxide dust (ZOD) is an industrial solid waste produced in the production process of wet smelting Zn, with large output and great pollution to the environment. The recycling of metallurgical solid waste such as zinc oxide dust is very important to achieve the sustainable development of the circular economy. An experimental study of zinc (Zn) leaching from zinc oxide dust using an ultrasound-enhanced ammonia–ammonium chloride system was performed. The effects of ultrasonic power, leaching time, total ammonia concentration, and other factors on the leaching rate of zinc from zinc oxide dust were investigated. The results revealed that the leaching rate of Zn reached up to 80.70% under the condition of ultrasound power of 1000 W, reaction time of 15 min, total ammonia concentration of 6 mol/L, [NH₃]:[NH₄⁺] of 1:1, L/S of 5:1, temperature of 45 °C, and stirring speed of 100 r/min. The conventional leaching was conducted under similar conditions, except that the time was controlled to 40 min and the zinc leaching rate was 71.15%. The leaching rate of Zn in the ultrasound condition was improved by 9.55% compared with that in the conventional leaching process. XRD, laser particle size, and SEM-EDS analyses were conducted to study the leaching residues of ZOD. The analysis results showed that in the ultrasound condition, the largest leaching rate of soluble ZnO phases was achieved after 15 min of leaching. Under the ammoniacal system, it was difficult to leach ZnFe₂O₄, Zn₂SiO₄, and ZnS phases, which partly accounted for the low zinc leaching rate. Additionally, through ultrasound-enhanced treatment, the ZnO particles encapsulated in ZOD particles were broken into smaller sizes and exposed to the leaching solution. Thus, the leaching rate of Zn was improved. The experimental results show that ultrasound can tremendously improve the effect of Zn extraction from ZOD, shorten reaction time, and help reduce energy consumption and environmental pollution, making it a promising application in the treatment of secondary Zn resources. Full article

Background and Objectives: The aim of this quantitative research was to investigate the effect of gravitational forces on the marginal integrity of different bulk-fill composites by micro-CT imaging. Materials and Methods: Fifty caries-free human third molars extracted for prophylactic purposes were used in this study. Each tooth was prepared with two proximal box cavities, with dimensions of 3 mm × 3 mm × 5 mm. Five distinct groups, each comprising 20 cavities, thus totaling 100 cavities for this study: (1, Group CON): Clearfil Majesty Flow + Clearfil Majesty Esthetic (as the control); (2, Group FBR): Filtek Bulk-fill Flowable Restorative + Clearfil Majesty Esthetic; (3, Group XTB): Voco Extrabase + Clearfil Majesty Esthetic; (4, Group SDR): SDR + Clearfil Majesty Esthetic; and (5, Group SNC): Sonicfill. When restoring the mesial cavities, the occlusal surfaces of the teeth in the mold were positioned upwards, counteracting the force of gravity. In contrast, for the restoration of the distal cavities, the occlusal surfaces were aligned downwards, to be parallel with the gravitational pull. After restorative procedures, each tooth was treated with 5000 thermal cycles. A solution of ammoniacal silver nitrate (AgNO₃) was employed as a tracing agent. The micro-CT scans were conducted and the total volume of silver nitrate and the total volume of restorations within the relevant region of interest were calculated in “mm³” with software. Two-way ANOVA and Tukey tests were performed at a significance level of p = 0.05 with Graphpad Prism v 8.2.1 software. Results: Both gravity effect and interaction showed no statistical differences (p > 0.05). Statistically significant differences were observed in the restorative materials (p < 0.05). Conclusions: Gravitational forces do not emerge as a major factor affecting the marginal integrity of flowable bulk-fill composites in class II restorations. The chemical composition of the composites plays a more crucial role, with the XTB composite showing higher microleakage ratios compared to the others. Full article

The leaching of Cu in ammoniacal solutions has proven an efficient method to recover Cu from waste printed circuit boards (WPCBs) that has used by many researchers over the last two decades. This study investigates the feasibility of a counter-current leaching circuit that would be coupled with an electrowinning (EW) cell. To accomplish this objective, the paper is divided into three parts. In Part 1, a leaching kinetic framework is developed from a set of experiments that were designed and conducted using end-of-life waste RAM chips as feed sources and Cu(II)-ammoniacal solution as the lixiviant. Various processing parameters, such as particle size, stirring rates, initial Cu(II) concentrations, and temperatures, were evaluated for their effects on the Cu recovery and the leaching rate. It was found that the particle size and initial Cu(II) concentration were the two most important factors in Cu leaching. Using a 1.2 mm particle size diameter and 40 g/L of initial Cu(II) concentration, a maximum Cu recovery of 96% was achieved. The Zhuravlev changing-concentration model was selected to develop the empirically fitted kinetic coefficients. In Part 2, kinetic data were adapted into a leaching function suitable for continuously stirred tank reactors. This was achieved via using the coefficients from the Zhuravlev model and adapting them to the Jander constant concentration model for use in the counter-current circuit model. Part 3 details the development of a counter-current circuit model based on the relevant kinetic model, and the circuit performance was modeled to provide a tool that would allow the exploration of maximum copper recovery whilst minimizing the Cu(II) reporting to electrowinning. A 4-stage counter-current circuit was modeled incorporating a feed of 35 g/L of Cu(II), achieving a 4.12 g/L Cu(II) output with 93% copper recovery. Full article

Ammonium thiosulfate leaching is a promising alternative to the conventional cyanide method for extracting gold from ores. However, strategies for recovering gold from the leachate are less commercially used due to its low affinity to gold. The present study investigated the recovery of gold from the leachate using iron oxides (hematite, Fe₂O₃ or magnetite, Fe₃O₄). Cementation experiments were conducted by mixing 0.15 g of aluminum powder as an electron donor and 0.15 g of an electron mediator (activated carbon, hematite, or magnetite) in 10 mL of ammonium thiosulfate leachate containing 100 mg/L gold ions and 10 mM cupric ions for 24 h at 25 °C. The results of the solution analysis showed that when activated carbon (AC) was used, the gold was recovered together with copper (recoveries were 99.99% for gold and copper). However, selective gold recovery was observed when iron oxides were used, where the gold and copper recoveries were 89.7% and 21% for hematite and 85.9% and 15.4% for magnetite, respectively. An electrochemical experiment was also conducted to determine the galvanic interaction between the electron donor and electron mediator in a conventional electrochemical setup (hematite/magnetite–Al as the working electrode, Pt as the counter electrode, Ag/AgCl as the reference electrode) in a gold–thiosulfate medium. Cyclic voltammetry showed a gold reduction “shoulder-like” peak at −1.0 V using hematite/Al and magnetite/Al electrodes. Chronoamperometry was conducted and operated at a constant voltage (−1.0 V) determined during cyclic voltammetry and further analyzed using SEM-EDX. The results of the SEM-EDX analysis for the cementation products and electrochemical experiments confirmed that the gold was selectively deposited on the iron oxide surface as an electron mediator. Full article

Leachate generation is among the main challenging issues that landfill operators must handle. Leachate is created when decomposed materials and rainwater pass through the waste. Leachate carries many harmful pollutants, with high concentrations of BOD, COD, colour, heavy metals, ammoniacal nitrogen (NH₃-N), and other organic and inorganic pollutants. Among them, COD, colour, and NH₃-N are difficult to be completely eliminated, especially with a single treatment. They should be handled by appropriate treatment facilities before being safely released into the environment. Leachate remediation varies based on its properties, the costs of operation and capital expenditures, as well as the rules and regulations. Up until now, much scientific and engineering attention was given to the development of comprehensive solutions to leachate-related issues. The solutions normally demand a multi-stage treatment, commonly in the form of biological, chemical, and physical sequences. This review paper discussed the use of contemporary techniques to remediate landfill leachate with an emphasis on concentrated COD, colour, and NH₃-N levels with low biodegradability that is normally present in old landfill or dumping grounds in developing countries. A semi-aerobic type of landfill design was also discussed, as this concept is potentially sustainable compared to others. Some of the challenges and future prospects were also recommended, especially for the case of Malaysia. This may represent landfills or dumpsites in other developing countries with the same characteristics. Full article

The worldwide increment of food waste requires innovative management solutions, aligned with sustainability, energy, and food security. Anaerobic digestion (AD), followed by nutrient recovery, may be considered an interesting approach. This study proposed a co-digestion of apple pomace (AP) with swine manure (SM) to study the effect of different proportions of AP (0, 7.5, 15, and 30%, on a volatile solids (VS) basis) on the methane production and the stability of the process. Subsequently, the gas-permeable membrane (GPM) technology was applied to recover nitrogen (N) as ammonium sulfate (bio-based fertilizer) from the digestates produced after the AD of 7.5% of AP and SM, and SM alone. The results showed that the co-digestion of 7.5% and 15% of AP with SM presented a methane production similar to the AD of SM alone (with 412.3 ± 62.6, 381.8 ± 134.1, and 421.7 ± 153.6 mL g VS⁻¹ day⁻¹, respectively). The later application of the GPM technology on the resulting digestates, with SM alone and with 7.5% of AP with SM, showed total ammoniacal N recovery rates of 33 and 25.8 g N m⁻² d⁻¹, respectively. Therefore, the AP valorization through the AD process, followed by N recovery from the digestate, could be a good management strategy. Full article