Application In Wastewater Treatment Research Articles

Polydopamine assisted synthesis of N-doped Al2O3/PDA/MnO2 for enhanced catalytic ozonation of MB in waste water

In this study, a novel N-doped Al2O3/PDA/MnO2 ozonation catalyst were fabricated by sequential coating of polydopamine (PDA) via self-polymerization and MnO2 loading via calcination processes. The ozonation catalyst was characterized by XRD and XPS, confirming the successful preparation of N-doped Al2O3/PDA/MnO2. The decoration of PDA polymer can enhance the loading and dispersion properties of MnO2 on Al2O3 spheres. In contrast, the apparent rate constant of N-doped Al2O3/PDA/MnO2 ozonation catalyst for methylene blue (MB) degradation was 2.67 times than that of undoped Al2O3/MnO2. This work provides a general strategy for exploring novel polymer-assisted functional Al2O3 based ozonation catalyst for waste water treatment applications.

Sulfonated Covalent Organic Frameworks Anchoring Cobalt as High-Efficient and Stable Catalysts for Peroxymonosulfate Activation.

Heterogeneous cobalt-based catalysts are highly effective in activing peroxymonosulfate (PMS) and produce free radicals to deal with recalcitrant organic pollutants in water. However, unfeasible recyclability and gradual performance degradation remain challenging due to the easy agglomeration and leaching of active cobalt species. Herein, a strategy is proposed to construct stably anchored and highly dispersed Co2+ sites on dual functional sulfonated covalent organic frameworks (COF-Co). The sulfonic acid groups are able to realize the targeted binding with cobalt ions through a two-step cation-exchange method, leading to strong combination with active Co2+ sites and utmost utilization efficiencies. Moreover, the super-hydrophility of sulfonic acid groups favors the rapid accessibility of organic molecules to the catalyst and accelerates the degradation. Remarkably, COF-Co exhibits high activity in PMS activation, effective oxidation for tetracycline degradation (92% within 30min at 30mg L-1) and other coloring contaminants, and excellent recycle stability. This work can guide the rational design of efficient and environmentally friendly PMS-activated catalyst with great potential for application in wastewater treatment.

Electrospinning of Sodium Alginate/Copper Oxide Nanofibrous Composite Membrane and Its Application of Cationic Dye Adsorption

AbstractDye wastewater is becoming one of the most significant sources of water pollution, and its impact on human survival is immeasurable. In this study, we successfully synthesized a nanofiber membrane with environmentally friendly and efficient properties using electrospinning of a mixture of sodium alginate (SA) and copper oxide (CuO) nanoparticles, aimed at effective dye removal. The adsorption performance of the SA/CuO nanofiber membrane was evaluated using the cationic dye methylene blue (MB). The maximum adsorption capacity of the nanofiber membrane was increased significantly with the addition of CuO nanoparticles, reaching a maximum value of 1633.4 mg g−1, almost twice as much as that of pure SA membrane. The adsorption kinetics follows the pseudo‐second‐order model, where chemisorption acts as the rate‐limiting step. The adsorption isotherm data indicate that the adsorption is monolayer. The nanofibrous membranes showed better dye removal under an alkaline environment. After four cycles of adsorption/desorption, the MB removal efficiency remained at 70.1% of the original adsorption capacity. The addition of CuO nanoparticles facilitated the adsorption of MB dyes, while the form of the nanofibrous membrane is easily recoverable and reusable. Therefore, the as‐prepared SA/CuO nanofibrous composite membrane is a potentially favorable adsorbent material for wastewater treatment applications.

The Fabrication of Lithium Niobate Nanostructures by Solvothermal Method for Photocatalysis Applications: A Comparative Study of the Effects of Solvents on Nanoparticle Properties

In this work, we report, for the first time, a comparative study on the effects of different solvents on the properties of LiNbO3 (LN) nanostructures. The solvothermal synthesis method was successfully used with three different solvents: 1—water, 2—methanol, and 3—benzyl. The structural and optical properties of the as-prepared nanoparticles were studied using transmission electron microscopy (TEM), X-ray diffraction (XRD), UV-Vis absorbance, Raman spectroscopy, and photoluminescence (PL). Nanoparticles of a very small size, with an average size between 3 and 10 nm, were obtained for the first time. The photocatalytic activities of the three synthesized LiNbO3 nanoparticles were studied in relation to the photodegradation of a complex and heavy reactive black 5 dye for a wastewater treatment application. The LiNbO3 synthesized with deionized water showed a higher photocatalytic activity than those synthesized using other solvents, such as methanol or benzyl.

Co-culture systems of microalgae and heterotrophic microorganisms: applications in bioproduction and wastewater treatment and elucidation of mutualistic interactions.

In recent years, reducing the concentration of carbon dioxide in the atmosphere has become an important issue. Microalgae have a higher photosynthetic efficiency and growth rate than higher plants; thus, biological carbon dioxide fixation using microalgae is attracting particular attention as an efficient carbon dioxide fixation method. However, under dilute atmospheric conditions, microalgae exhibit lower growth rates and reduced carbon dioxide fixation efficiency. In recent years, technology that can efficiently fix carbon dioxide, even in the atmosphere, using a microalgae co-culture system that co-cultivates microalgae and heterotrophic microorganisms has attracted attention. In such a co-culture system, it is believed that a mutualistic relationship is established between microorganisms through the exchange of various compounds. This review focuses on the application of a co-culture system of microalgae and heterotrophic microorganisms for bioproduction and wastewater treatment. In addition, research to elucidate the mutualistic relationships in microalgal co-culture systems using analytical methods that have been widely used in recent years, such as next-generation sequencing technology, is also discussed. In the future, it is expected that the use of microalgae co-culture systems will expand on an industrial scale through the development of key technologies, such as efficient genetic modification techniques for microalgae and their heterotrophic microorganism partners, large-scale cultivation facilities that can efficiently cultivate microalgae, and stable control techniques for co-culture systems using advanced technology.

Physical and enhanced photocatalytic MO dye degradation behaviour of Zn doped β-Ga2O3 microrods

This work explored the effects of Zn doping on the structural, micrographic, optical and photocatalytic behaviour of gallium oxide (β-Ga2O3) microrods. The X-ray diffractogram (XRD) and Raman spectral analyses confirmed the monoclinic structure of β-Ga2O3, with a shift to lower angles in the XRD pattern indicating Zn incorporation into the Ga2O3 lattice. The Scanning electron microscopy (SEM) images revealed a rod-like shape, with the diameter decreasing from 604 nm to 573 nm with Zn doping. Further analysis using TEM, HR-TEM, SAED, EDX, and elemental mapping confirmed the shape, crystallinity, crystal structure, and elemental distribution. The interplanar spacings were measured as 0.4 and 0.2 nm, corresponding to the (002) and (−311) planes of β-Ga2O3. UV–Vis diffuse reflectance spectroscopy (UV–Vis DRS) showed a slight shift in the absorption edge, while photoluminescence (PL) analysis demonstrated strong UV and weak visible light emission. Photocatalytic results revealed a high efficiency of dye degradation,(i.e) 98 % (20 ppm) and 89 % (30 ppm) against methyl orange (MO) dye aqueous solution over 150 min, with a rate constant of 0.02/min and 0.01/min, respectively for 1.5 wt% Zn doping. This suggests that the Zn-doped material holds promise as a photocatalyst for wastewater treatment applications.

Catalytic Degradation of Bisphenol A in Water by Non-Thermal Plasma Coupled with Persulfate

Bisphenol A (BPA) has become prevalent in the environment due to its extensive use in industrial materials, thus raising significant concerns regarding its potential toxicity and health effects. In this study, an efficient and eco-friendly non-thermal plasma (NTP) was used to catalyze persulfate (PS) for BPA decomposition, and the results showed that the integrated system could effectively degrade BPA. The best performance was attained at a PS to BPA mass ratio of 5:1, with a degradation rate of 91.3% following a 30 min treatment. The degradation rate of BPA increased with increasing input voltage and frequency; conversely, it decreased with an increase in BPA’s initial concentration. Higher BPA degradation rates could be achieved in alkaline environments. Radical quenching experiments revealed that SO4−•, OH•, O2−• and 1O2 were important active substances involved in BPA degradation. Nine intermediate products were identified by liquid chromatography–mass spectrometry (LC-MS), and four degradation pathways were deduced. Additionally, a toxicity analysis of intermediate products was performed. The significant decrease in chemical oxygen demand (COD) during the actual wastewater treatment suggested that the NTP/PS system has good applicability in actual wastewater treatment.

Novel Venturi injector reactor design and application in ammonia nitrogen wastewater treatment

The Venturi injector reactor has a robust and durable design and is highly efficient and reliable. The flow field control in the Venturi reactor is an effective way to enhance gas−liquid mass transfer. In this study, a novel Venturi injector reactor with an expandable self-priming air inlet and a second water inlet in the diffusion section was designed by combining particle image velocimetry (PIV) experiments with a computational fluid dynamics simulation. This novel design increased the gas holdup, generated smaller and more uniform bubbles, and enhanced mass transfer. Furthermore, we applied the novel Venturi device to the biological degradation of ammonia nitrogen wastewater. The total gas holdup in the novel Venturi was higher than in the conventional Venturi injector reactor by 0.0056 on average. The minimum bubble diameter was approximately 0.71 mm. Moreover, the ammonia nitrogen removal efficiency of the novel Venturi equipment with the second inlet was 2 and 1.1 times higher than that of conventional aeration and conventional Venturi device, respectively. This study provides a theoretical basis and practical significance for improving the performance and efficient degradation of the ammonia nitrogen concentration in Venturi injector reactors.

Implementation of an Upflow Fixed Bed Bioreactor for Denitrification Coupled to Methane Oxidation: Performance and Biomass Development Under Anoxic Conditions

Denitrification coupled to methane oxidation (DOM) has been shown to be an appropriate process for wastewater treatment applications, since it can reduce greenhouse gas emissions and nitrogen discharges, making wastewater treatment plants more environmentally sustainable. Study of DOM has focused on laboratory-scale application using membrane biological reactors (MBR) or sequency batch reactors (SBR), which have been shown to be able to retain DOM biomass and therefore appropriate for use with this process. However, it is necessary to expand knowledge of the behavior of this process using other configurations, with a view to scaling up. Therefore, in this study, an upflow fixed bed bioreactor (UFBR) was implemented using plastic carriers such as bioballs and Biochips® to carry out the DOM process under anoxic conditions. The reactor reached stable nitrogen removal conditions after approximately 400 days of continuous operation, forming a biomass composed of denitrifying methane-oxidizing microorganisms where the genus Anaerolinea and Methylocystis predominated. Once the biomass was formed and the DOM process was stabilized, maximum nitrite and nitrate removal rates of 17.6 mgN-NO2−/L-d and 8.9 mgN-NO3−/L-d, respectively, and a removal efficiency of methane up to 77% were obtained. This demonstrates the feasibility of the application of the DOM process under anoxic conditions using fixed bed bioreactors, which is promising for further nitrogen removal from wastewater using a varied reactor configuration easily to scaled-up.

Conversion of Lignin to Nitrogenous Chemicals and Functional Materials.

Lignin has long been regarded as waste, readily separated and discarded from the pulp and paper industry. However, as the most abundant aromatic renewable biopolymer in nature, lignin can replace petroleum resources to prepare chemicals containing benzene rings. Therefore, the high-value transformation of lignin has attracted the interest of both academia and industry. Nitrogen-containing compounds and functionalized materials are a class of compounds that have wide applications in chemistry, materials science, energy storage, and other fields. Converting lignin into nitrogenous chemicals and materials is a high-value utilization pathway. Currently, there is a large amount of literature exploring the conversion of lignin. However, a comprehensive review of the transformation of lignin to nitrogenous compounds is lacking. The research progress of lignin conversion to nitrogenous chemicals and functional materials is reviewed in this article. This article provides an overview of the chemical structure and types of industrial lignin, methods of lignin modification, as well as nitrogen-containing chemicals and functional materials prepared from various types of lignin, including their applications in wastewater treatment, slow-release fertilizer, adhesive, coating, and biomedical fields. In addition, the challenges and limitations of nitrogenous lignin-based materials encountered during the development of applications are also discussed. It is believed that this review will act as a key reference and inspiration for researchers in the biomass and material field.

Low-Cost Biosorbents Derived from Corn Husks for the Exclusion of Fe(II) and Cr(VI) Ions Undertaken Aqueous Media: Application for Wastewater Treatment

Low-Cost Biosorbents Derived from Corn Husks for the Exclusion of Fe(II) and Cr(VI) Ions Undertaken Aqueous Media: Application for Wastewater Treatment

Synthesis of magnetic zirconium oxide-iron oxide nanoparticles composite using chemical precipitation process for Pb (II) adsorption

The exploration and utilization of natural raw zircon minerals in Indonesia, particularly in Central Kalimantan, remain largely untapped in their potential as high-tech and commercially valuable substances with eco-friendly properties, particularly in water and industrial wastewater treatment. The primary objective of this research is to enhance the development and synthesis of natural raw zircon minerals by converting them into zirconium oxide and integrating them with magnetic nanoparticles. The magnetic nanoparticle composite material for zirconium oxide (MNP@ZrO2) was synthesized using the chemical co-precipitation method. Zirconium and its oxides have gained significant application in water and wastewater treatment in recent years. Through chemical co-precipitation processes (MNP@ZrO2), the natural raw zircon minerals were transformed into zirconium oxides and combined with magnetic nanoparticles due to their exceptional potential as effective adsorbents for anions and cations in water and industrial treatment processes. In the utilization of Scanning Electron Microscopy (SEM), magnetic nanoparticles with a diameter of less than 50 nm emerged on the surface of the zirconium crystals within the magnetic nanoparticle composites. X-ray diffraction (X-RD) analysis indicated that the treatment of zirconium minerals resulted in 11.19% decrease in the Crystallinity Index and a significant reduction of 98% in silica content. By maintaining a pH level of approximately 7 ± 0.2 over 360 min with a stirring rate of 150 rpm, and at ambient temperature, the optimal conditions for Pb (II) adsorption were achieved with the adsorption capacity of 68.98 mg/g using MNP@ZrO2 as adsorbent. The successful synthesis of magnetic zirconium oxide-iron oxide nanoparticles at various pH levels using the chemical co-precipitation process has facilitated a comprehensive assessment of their performance in Pb (II) adsorption.

A Novel Approach for Nanosponge: Wool Waste as a Building Block for the Synthesis of Keratin-Based Nanosponge and Perspective Application in Wastewater Treatment.

Wool waste is a huge environmental problem that needs to be addressed in order to avoid the continuous accumulation of biohazardous waste in landfills. In recent years, wool has proven to be an excellent source of keratin that can be used for various purposes. But never before has keratin from wool waste been used as a building block to synthesize a well-known class of biopolymers called nanosponges. Typically, nanosponges are produced by the reaction of cyclodextrins with an appropriate cross-linker to obtain an insoluble hyper-cross-linked polymer, which has applications in various fields. For this reason, a novel, affordable approach for the synthesis of a novel class of nanosponge using wool keratin as the building block has been presented. The keratin nanosponge was synthesized by reacting keratin with pyromellitic dianhydride as a cross-linking agent. The formation of a cross-linked polymer was successfully confirmed by CHNS-elemental analysis, TGA, DSC, FTIR-ATR, SEM, and water absorption capacity measurements. Surprisingly, the keratin-based nanosponge showed ∼50% uptake of heavy metals after only 24 h of contact time. The adsorption kinetics was also evaluated, indicating a pseudo-second-order model fit and the mechanism is predominantly the intraparticle diffusion process. The novel synthesized nanosponge proved to be a possible alternative for wastewater treatment.

Electrolysis for ammonia removal and hydrogen generation in urban wastewater: Innovative approaches to the water crisis

The global water crisis poses significant challenges, with millions lacking access to clean drinking water and increasing water scarcity affecting urban areas worldwide. This study explores the electrolysis of urban wastewater as a two-fold solution for ammonia (un-ionized NH3, and ionized NH4+) removal and hydrogen gas (H2) production. Traditional treatment methods often fail to remove ammonia efficiently, underscoring the need for innovative approaches. Electrolysis, known for its versatility, energy efficiency, and environmental friendliness, emerges as a promising solution in wastewater treatment applications. This research utilized a dimensionally stable electrode (DSA) comprising a Ru-Ir anode and a stainless-steel cathode to electrochemically oxidize ammonia and produce H2. The study investigates the effects of current density, J (83.33–416.6 A/m2) on the treatability of urban wastewater. Maximum H2 production was achieved at J of 416.6 A/cm2 after 300 min reaction time. Under optimal conditions (333.3 A/m2, 0.5 mm inter-electrode distance, and 300 min of operation), the process achieved removal efficiencies of 98.94 % for ammonia, 78.18 % for total suspended solids (TSS), 50.73 % for chemical oxygen demand (COD), and complete removal (∼100 %) of total coliforms. Gas chromatography (GC) assessed the composition of gases of interest generated during electrolysis. This approach addresses environmental pollution and freshwater scarcity and generates an energy resource, presenting a scalable solution for cities worldwide facing similar challenges.

The high adsorption performance of banana (Musa ABB Cv. Kluai ‘Namwa’) beaded materials modified with zinc and magnesium oxides for cadmium removal

Wastewater contaminated with cadmium is a concern because of its toxicity, persistence, and bioaccumulation to the environment, ecosystem, and human health, so it is required to remove cadmium(II) ions before releasing them to receiving water. Banana powder beads (BPB), banana powder doped ZnO beads (BPZB), banana powder doped MgO beads (BPMB), and banana powder doped ZnO + MgO beads (BPZMB) were synthesized as the novel cadmium adsorbents, and their characterizations, cadmium adsorption performances, cadmium adsorption patterns and mechanisms, thermodynamic study, and reusability were investigated. BPMB had the highest specific surface area of 16.60 m2/g and the smallest pore size of 1.69 nm than other materials. BPB was an amorphous structure, whereas BPZB, BPMB, and BPZMB were crystalline structures presenting their specific metal oxide peaks of ZnO or MgO. They were coarse surfaces and had a spherical shape consisting of C, O, Ca, Cl, and Na. Their main functional groups were O–H, C–H, C=O, C–O, and N–H. The points of zero charge of BPB, BPZB, BPMB, and BPZMB were 5.37, 6.75, 9.87, and 9.43. The cadmium removal efficiencies of BPB, BPZB, BPMB, and BPZMB were 89.18%, 96.62%, 99.59%, and 97.85%, and their qm values were 90.09, 232.56, 454.55, and 303.03 mg/g, respectively. Thus, the metal oxide helped to improve material efficiency, especially MgO. The Freundlich and pseudo-second-order kinetic models were good fit models for describing their adsorption patterns and mechanisms. The increasing temperature affected to decrease their cadmium adsorptions. They could be reused in more than 3 cycles of more than 73% of cadmium adsorption. The electrostatic interaction played an important role in describing their cadmium adsorptions. Therefore, BPBM was a good cadmium adsorbent for application in industrial wastewater treatment since it had a higher performance of cadmium adsorption than other materials.

Luffa cylindrica as a biosorbent in wastewater treatment applications: a comprehensive review

Luffa cylindrica as a biosorbent in wastewater treatment applications: a comprehensive review

Evaluation of a mixture of livestock wastewater and food waste as a substrate in a continuous-flow microbial electrolysis cell

While the efficiency of microbial electrolysis cell (MEC) systems has improved remarkably, their application in continuous reactors and wastewater treatment remains poorly understood. This study evaluated the performance of a continuous-flow MEC using livestock wastewater and food waste as substrates. The MEC system achieved a hydrogen production rate of 5.2 L/L/day using acetate as a substrate, and a rate of 2.9–4.6 L/L/day when real wastewater mixtures were used. In terms of chemical oxygen demand (COD) removal, the system demonstrated high efficiency, with values ranging from 42.3 % to 62.2 % depending on the wastewater composition. Volatile fatty acid (VFA) removal reached up to 72.8 %. The current density averaged 9.9 A/m2 with acetate and decreased to 7.0 and 6.1 A/m2 in phases using wastewater, reflecting the adaptation of the microbial community to the more complex substrates. The microbial community was dominated by Firmicutes, Bacteroidetes, Proteobacteria, and Synergistetes, with Proteobacteria showing a particularly high abundance near the anion exchange membrane (AEM) on the anode. The MEC process demonstrates substantial promise as a sustainable technology for both biohydrogen production and wastewater treatment. With further optimization and scaling, MECs could play a crucial role in the circular economy by converting waste into clean energy while simultaneously treating wastewater, offering a pathway toward more sustainable industrial and environmental practices.

Effect of Hydrodynamic Shear Stress on Algal Cell Fate in 3D Extrusion Bioprinting

The 3D bioprinting of aquatic photosynthetic organisms holds potential for applications in biosensing, wastewater treatment, and biofuel production. While algae cells can be immobilized in bioprinted cell‐friendly matrices, there is a knowledge gap regarding the thresholds of hydrodynamic shear stress that affect the cells’ functionality and viability during bioprinting. This study examines the effect of hydrodynamic shear stress on the fate of Chlamydomonas reinhardtii cells. Computational fluid dynamics models based on the Navier–Stokes equations are developed to numerically predict the shear stresses experienced by the cells during extrusion. Parallelly, cell culture experiments are conducted to evaluate the functionality, growth rates, and viability of algae cells within bioprinted constructs. By correlating cell culture and simulation results, the causal link between shear stress in the nozzle and cell viability and function has been characterized. The findings highlight that cell viability and function are significantly impacted by process factors. Notably, algae cell function is more sensitive to shear stress than cell viability. Functional impairments occur at maximum shear stresses around 5 kPa, while viability remains unaffected. Beyond 14 kPa, both functionality and viability decline significantly and irreversibly. The results emphasize the importance of assessing viability and function after bioprinting, rather than just viability.

Synthesis, optical absorption, luminescence, chromaticity, and catalytic properties of undoped CuO and Gd-doped CuO nanostructures for LED devices and waste water treatment applications

The first objective of this present investigation is the co-precipitation synthesized of undoped and various concentrations of Gd-doping in the CuO material as a photocatalyst and methylene blue dye under passing solar light radiation, followed by obtaining their photocatalytic degradation efficiency of 88–96%. Using photoluminescence (PL) data of synthesized undoped and 1%, 3%, and 5 wt% Gd-doped CuO to make a chromaticity diagram for identifying the colour coordinates to scrutinize the applications of light-emitting devices. To trace the diffraction peaks, related crystal system, and vibrational bond of undoped and Gd-doped CuO materials by XRD and FT-IR studies. The morphological structure has been varied in each Gd-dopant concentration when compared to undoped CuO nanostructures through SEM studies. The aforementioned material has a narrow band gap and strong visible emission, as identified by UV–visible and PL spectra.

Enhanced photodegradation of organic dyes using copper and zinc aluminate nanophotocatalysts

This study aims to enhance the photocatalytic efficiency of CuxZn1-xAl2O4 (x = 0.0, 0.2, 0.4, 0.6, and 0.8) nanophotocatalysts synthesized via a sol-gel self-combustion method. Rietveld analysis confirmed the formation of single-phase spinels with a face-centered cubic structure and Fd-3m space group symmetry, while electron density distribution analysis supported the ionic character of bonding within the material. Subsequent UV–visible spectroscopy revealed that the addition of Cu(II) reduced the band gap from 4.66 eV to 2.54 eV, facilitating enhanced light absorption. Consequently, the catalyst with x = 0.8 deteriorated 95 % of methyl orange (MO) and 93 % of rhodamine-B (RhB) in 120 min of visible light irradiation, following a pseudo-first-order kinetic model. The Cu0.8Zn0.2Al2O4 sample demonstrated significant reusability and stability, with degradation rates of 93–79 % for RhB and 95–81 % for MO after four cycles. Scavenging studies indicated that photoexcited holes (h), hydroxyl radicals (OH•), and superoxide radicals (O₂•⁻) were key factors in the degradation process. This study presents an improved approach for enhancing the photodegradation performance of the Cu0.8Zn0.2Al2O4 catalyst for pharmaceutical and wastewater treatment applications.