Advanced Water Purification Research Articles

Elucidating the dynamics of carbamazepine uptake using date pit-derived activated carbon: A comprehensive kinetic and thermodynamic analysis

Water contamination with pharmaceuticals such as Carbamazepine (CBZ) presents a significant environmental challenge. This study investigates the use of activated carbon derived from waste date pits (DPAC) for the removal of CBZ from water. The impact of several parameters such as pH, temperature, CBZ concentration, and flow rate on the adsorption were assessed. The generated DPAC demonstrated a specific surface area of 309 m2/g, a pore volume of 0.264 cm³/g, and the pores are mainly distributed at 1.86, 2.73, and 3.43 nm. The Langmuir, Freundlich, Sips, and Toth isotherms were used to fit the experimental data, and the results indicate the occurrence of monolayer adsorption and heterogeneous surface conditions. The Linear Driving Force model was used for kinetic analysis, showing improved fit at higher concentrations. Thermodynamic analyses revealed the process to be endothermic, spontaneous, and entropically driven. The DPAC achieved an adsorption capacity of 14.89 mg/g and maintained 94 % effectiveness after the first regeneration cycle and 70 % after four cycles. This study highlights the potential of DPAC as a sustainable adsorbent for advanced water purification.

Fundamental Insights into the Direct Electron Transfer Mechanism on Ag Atomic Cluster.

The nonradical oxidation pathway for pollutant degradation in Fenton-like catalysis is favorable for water treatment due to the high reaction rate and superior environmental robustness. However, precise regulation of such reactions is still restricted by our poor knowledge of underlying mechanisms, especially the correlation between metal site conformation of metal atom clusters and pollutant degradation behaviors. Herein, we investigated the electron transfer and pollutant oxidation mechanisms of atomic-level exposed Ag atom clusters (AgAC) loaded on specifically crafted nitrogen-doped porous carbon (NPC). The AgAC triggered a direct electron transfer (DET) between the terminal oxygen (Oα) of surface-activated peroxodisulfate and the electron-donating substituents-containing contaminants (EDTO-DET), rendering it 11-38 times higher degradation rate than the reported carbon-supported metal catalysts system with various single-atom active centers. Heterocyclic substituents and electron-donating groups were more conducive to degradation via the EDTO-DET system, while contaminants with high electron-absorbing capacity preferred the radical pathway. Notably, the system achieved 79.5% chemical oxygen demand (COD) removal for the treatment of actual pharmaceutical wastewater containing 1053 mg/L COD within 30 min. Our study provides valuable new insights into the Fenton-like reactions of metal atom cluster catalysts and lays an important basis for revolutionizing advanced oxidation water purification technologies.

Sustainable H2O2 production in a floating dual-cathode electro-Fenton system for efficient decontamination of organic pollutants

Electrochemical advanced oxidation processes (EAOPs) based on natural air diffusion electrode (NADE) promise efficient and affordable advanced oxidation water purification, but the sustainable operation of such reaction systems remains challenging due to severe cathode electrowetting. Herein, a novel floating cathode (FC) composed of a stable hydrophobic three-phase interface was established by designing a flexible catalytic layer of FC. This innovative electrode configuration could effectively prolong the service life of the cathode by mitigating the interference of H2 bubbles from the hydrogen evolution reaction (HER), and the H2O2 production rate reached 37.59 mg h−1·cm−2 and realize a long-term stable operation for 10 h. Additionally, an FC/carbon felt (CF) dual-cathode electro-Fenton system was constructed for in situ sulfamethoxazole (SMX) degradation. Efficient H2O2 production on FC and Fe(III) reduction on CF were synchronously achieved, attaining excellent degradation efficiency for both SMX (ca. 100%) with 2.5 mg L−1 of Fe(Ⅱ) injection. For real wastewater, the COD removal of the FC/CF dual-cathode electro-Fenton system was stabilized at exceeding 75%. The practical application potential of the FC/CF dual-cathode electro-Fenton system was also demonstrated for the treatment of actual landfill leachate in continuous flow mode. This work provides a valuable path for constructing a sustainable dual-cathode electro-Fenton system for actual wastewater treatment.

Optimization of Dissolved Silica Removal from Reverse Osmosis Concentrate by Gedaniella flavovirens for Enhanced Water Recovery

Photobiological treatment of reverse osmosis concentrate (ROC) using brackish diatoms is a green and sustainable technology that can enhance water recovery by removing dissolved silica from ROC while producing beneficial biomass. This study aimed to determine the optimum conditions for the photobiological treatment of ROC obtained from a full-scale advanced water purification facility using Gedaniella flavovirens Psetr3. While light color presented minor impacts on the silica uptake rate, the impact of color intensity was significant. The uptake rate improved from 28 ± 1 to 48 ± 7 mg/L/day by increasing photosynthetically active radiation (PAR) from 50 to 310 µmol m−2 s−1. Increasing the PAR further did not improve the performance. The optimum temperature was around 23–30 °C. While the silica uptake was slower at 10 °C, G. flavovirens Psetr3 was unable to survive at 40 °C. Experiments using sunlight as a light source verified the impact of temperature on the silica uptake and the detrimental effect of ultraviolet radiation on this diatom. The sunlight-based treatment effectively removed N-nitrosodimethylamine. The results of this study are being used in subsequent pilot-scale investigations and full-scale technoeconomic analysis and will contribute to the further development of this sustainable water technology.

Harmonizing nature’s blueprint: enhanced synthesis of CuO nanoparticles using Trigonella foenum-graecum for advanced water purification

Harmonizing nature’s blueprint: enhanced synthesis of CuO nanoparticles using Trigonella foenum-graecum for advanced water purification

Investigation of the adsorption behaviour of toxic heavy metals and bacteria on two allotropes of low dimensional boron nitride: Implications for detection and elimination

In this research, the focus was on two 2D allotropes of boron nitride (BN), specifically Haeck-BN and Twin-BN. They exhibit unique structural and electronic characteristics, making them suitable for sensing applications. High surface area materials offer numerous affinity sites for heavy metal ions and toxic molecules. Using density functional theory (DFT), the adsorption mechanisms of various contaminants in gas (solvent) phase on both pristine and doped Haeck-BN and Twin-BN were investigated. Pronounced adsorption of arsenic (As) and lead (Pb) was observed on pristine Twin-BN sheets, with adsorption energies of −2.83 eV (−2.86 eV) and −2.03 eV (−2.39 eV), respectively. Haeck-BN showed weaker interactions, with adsorption energies of −1.48 eV (−1.55 eV) for As and −0.64 eV (−0.92 eV) for Pb. Significant adsorption of specific amino acids, integral components of bacterial cell walls, was noted on both pristine and silver-modified sheets. The electronic properties showed significant shifts upon molecular adsorption, confirming their sensitivity towards foreign contaminants. The high adsorption energies of amino acids suggest potential applications in efficient bacterial inactivation for water purification. While real-world scenarios pose challenges, the calculations provide valuable insights for potential use of these nanosheets in advanced water purification membrane technology.

Spin‐Regulated Fenton‐Like Catalysis for Nonradical Oxidation over Metal Oxide@Carbon Composites

AbstractThe spin state of the transition metal species (TMs) has been recognized as a critical descriptor in Fenton‐like catalysis. The raised spin state of dispersed TMs in carbon will enhance the redox processes with adsorbed peroxides and improve the oxidation performance. Nevertheless, establishing the spin‐activity correlations for the encapsulated TM nanoparticles remains challenging because of the difficulties in fine‐tuning the spin state of TM species and the insufficient understanding of orbital hybridization states upon interaction with peroxides. Here, the advantage of the fast‐temperature heating/quenching of microwave thermal shock is taken to engineer the structure and spin state of encapsulated TMs within the N‐doped graphitic carbons. The reduced TMs particle size and enhanced TMs‐carbon coupling increase surface entropy and regulate eg electron filling of the high‐spin TM‐N coordination, endowing electrons with high mobility and facilitating peroxymonosulfate (PMS) adsorption. The strong interactions further uplift the PMS O 2p band position toward the Fermi level and thus elevate the oxidation potential of surface‐activated PMS (PMS*) as the dominant nonradical species for pollutant degradation. The deciphered orbital hybridizations of engineered high‐spin TM and PMS enlighten the smart design of spin‐regulated nanocomposites for advanced water purification.

Humic substances mediated superior photochemical pollutant conversion on defective TiO2 in environmentally relevant matrices: The key roles of oxygen vacancy in surface interactions, oxidant activation and radical generation

Ubiquitous humic substances usually exhibit strong interfering effects on target pollutant removal in advanced water purification. This work aims to develop a photochemical conversion system on the nonstoichiometric TiO2 for pollutant removal in environmentally relevant matrices. In this synergistic reaction system, the redox-reactive humic substances and defective oxygen vacancies can serve as the organic electron transfer mediator and the key surface reactive sites, respectively. This system achieves a superior pollutant degradation in real surface water at low oxidant concentrations. Reactive oxygen vacancies on the TiO2 surface and sub-surface are of considerable interest for this photochemical reaction system. By engineering defective oxygen vacancies on high-energy {001} polar facet, the surface and electronic interactions between tailored TiO2 and humic substances are greatly strengthened for the promoted electron transfer and oxidant activation. Rendered by the strong surface affinity and molecular activation, defective oxygen vacancies thermodynamically and dynamically promote reactive chain reactions for free radical formation, including the selective O2 reduction to ·O2− and the H2O2 activation to ·OH. Our findings take new insights into environmental geochemistry, and provide an effective strategy to in-situ boost the humic substances-mediated water purification without secondary pollution. Environmental implicationHumic substances are widely distributed in aquatic environment, thus playing important roles in environmental geochemistry. For example, humic substances can achieve good surface adsorption through electrostatic adsorption, ligand exchange and electronic interactions with typical TiO2 to form reactive ligand-metal charge transfer complexes for pollutant degradation. Inspired by the unique properties of surface and sub-surface oxygen vacancies, the defective TiO2 was designed to refine the humic substances-mediated photochemical reactions. A superior reactivity was measured for pollutant degradation. Our findings provide an effective strategy to boost naturally photochemical decontamination in environmentally relevant matrices.

Per- and poly-fluoroalkyl substances removal in multi-barrier advanced water purification system for indirect potable reuse.

The study evaluated the removal efficacy of per- and poly-fluoroalkyl substances (PFAS) across various advanced water treatment (AWT) processes in a field-scale AWT train using secondary effluent samples from a full-scale water reclamation facility (WRF). Samples collected from April to October 2020 revealed PFCAs as the dominant PFAS compounds in the WRF secondary effluent, with PFPeA having the highest average concentration and PFSAs in notably lower amounts. Temporal fluctuations in total PFAS concentrations peaked in September 2020, which may reflect the seasonality in PFAS discharges related to applications like AFFFs and pesticides. In assessing AWT processes, coagulation-flocculation-clarification-filtration system showed no notable PFAS reduction, while ozonation resulted in elevated PFBS and PFBA concentrations. Biological activated carbon (BAC) filtration effectively removed long-chain PFAS like PFOS and PFHxS but saw increased concentrations of short-chain PFAS post-treatment. Granular activated carbon (GAC) filtration was the most effective treatment, reducing all PFSAs below the detection limits and significantly decreasing most PFCAs, though short-chain PFCAs persisted. UV treatment did not remove short-chain PFCAs such as PFBA, PFPeA, and PFHxA. The findings highlight the efficacy of AWT processes like GAC in PFAS reduction for potable reuse, but also underscore the challenge presented by short-chain PFAS, emphasizing the need for tailored treatment strategies. PRACTITIONER POINTS: Secondary effluents showed higher concentrations of PFCAs compared to PFSAs. Advanced water treatment effectively removes long-chain PFAS but not short-chain. Ozonation may contribute to formation of short-chain PFAS. BAC is less effective on short-chain PFAS, requiring further GAC treatment.

Mesoporous Magnetic/Polymer Hybrid Nanoabsorbent for Rapid and Efficient Removal of Heavy Metal Ions from Wastewater.

As an advanced water purification technology, magnetic nanoabsorbents are highly attractive for their sustainability, robustness, and energy efficiency. However, magnetic responsiveness and high adsorptive capacity are irreconcilable during the design and synthesis of a high-performance magnetic nanoabsorbent. Here, we address this issue by designing a kind of mesoporous magnetic polymer hybrid microspheres, where functional polymers such as polyrhodanine and polypyrrole were attached to the pore walls in the interior of mesoporous Fe3O4 microspheres through in situ polymerization. Due to the integrated large saturation magnetic moment, porous structure, and dense polymer layer, the mesoporous magnetic polymer hybrid microspheres demonstrated fast magnetic responsiveness, excellent recycling performance, and high adsorption capacities toward Pb(II) ions (189 mg g-1) for polyrhodanine and Cr(VI) ions (199 mg g-1) for polypyrrole. Furthermore, their potential application in wastewater treatment was verified by a self-made magnetic separation column, where the designed magnetic nanoabsorbent exhibits significant advantages including rapid separation of heavy metal ions and high outflow. This study provided a promising magnetic polymer hybrid nanoabsorbent for realizing efficient removal of heavy metal ions from wastewater.

Microbially mediated synthesis of vivianite by Desulfosporosinus on the way to phosphorus recovery

Desulfosporosinus metallidurans can be utilized in advanced water purification methods and for recovering phosphorus from industrial waste sludge.

Engineered diatomic catalyst empowered electro-Fenton processes for advanced water purification

This work introduces the selection and preparation of DACs for the 2 + 1e− ORR EF process and concludes with a discussion on challenges and future directions for the intelligent design of electrodes and reactors in EF purification technologies.

Capabilities of Novel Carbon Nano Adsorbents in Evaluating the Extraction of 2-Nitrophenol and Heavy Metal from Aqueous Solutions

This study primarily focused on evaluating the efficacy of Metal Oxide-infused Carbon Nano Adsorbents (CNAs), which included both Carbon Nanotubes and Carbon Nanofibers, in removing Cd+2, Cr+3, and 2-NP from water solutions. We synthesized and analyzed four distinct types of CNAs, each impregnated with either Al2O3, TiO2, Fe2O3, or Cu2O3. The metal content in these CNAs was determined by comparing their dry and calcined weights. To investigate their properties, we utilized various techniques such as Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, Energy-Dispersive X-ray Spectroscopy (EDX), and Thermal Gravimetric Analysis (TGA). These methods helped us understand their morphological traits, surface areas, pore structures, metal oxide distributions, and thermal stabilities, thereby confirming their adsorption effectiveness for pollutants. The findings indicated that CNAs altered with metal oxides showed higher surface areas and adsorption abilities than their unmodified counterparts. Specifically, CNAs/TiO2 exhibited the most significant increase in surface area (140 m2/g) and pore volume (0.460 cm3/g), which resulted in an enhanced adsorption capacity for Cd+3 at 11.4 (mg/g), surpassing the 9.5 (mg/g) capacity of pure CNAs with surface area (90 m2/g) and Pore volume (0.331 cm3/g). Similarly, CNAs/Al2O3 demonstrated an increased surface area of 100 (m2/g), surpassing that of pure CNAs. This enhancement led to a significant improvement in adsorption capacities, elevating the uptake for Cr+3 from 32.2 to 52 (mg/g) and for 2-NP from 24.8 to 49.6 (mg/g). This enhancement in adsorption efficiency is attributed to the increased surface area and improved surface chemistry due to the incorporation of Titania and Alumina, which proved more effective than modifications with copper oxide and Ferric oxide. These insights emphasize the significance of selecting appropriate metal oxides for modifying CNAs, as this can greatly impact their ability to target various contaminants, thus contributing to the development of more advanced water purification methods using CNAs/MO.

Transforming Horticulture: The Influence of Nanotechnology on Crop Enhancement

Nanotechnology, a field of science and engineering focused on manipulating matter at the nanoscale, has garnered significant attention for its transformative potential across various industries. At the nanometer level, materials exhibit unique properties and behaviors, making it possible to engineer novel solutions with precision and efficiency. Nanotechnology finds applications in diverse areas, from medicine and electronics to energy and environmental remediation. Its ability to create nanoscale structures, devices, and materials has led to groundbreaking innovations, such as drug delivery systems for targeted therapies, ultra-efficient solar cells, and advanced water purification technologies. However, the rapid development of nanotechnology also raises important ethical, safety, and regulatory considerations that require careful attention. As nanotechnology continues to advance, it promises to reshape industries, enhance scientific understanding, and address some of the world's most pressing challenges.

Constructing an orderly electron transport channel on boron regulated biomass carbon fiber for selective ROS generation and water decontamination

Antibiotic pollution has raised widely attention due to the difficult biodegradation and lasting toxicity to public health, metal-free material based heterogeneous catalysis is a highly-promise and eco-friendly technology for organics elimination. Herein, boron doped biomass carbon fiber (B-CF) was synthesized to construct orderly electron transport channels for enhancing catalytic performance and deeply purifying organics polluted water. Integrating systematical quenching experiments and EPR detection, O2·- and 1O2 are found to be dominating reactive oxygen species (ROS) for norfloxacin (NOR) degradation rather than ∙OH or SO4∙-. Adsorption, catalytic degradation in pristine CF/peroxodisulfate (PDS) and B-CF/PDS systems, electrochemical tests, and theory calculations were compared and the results suggested B-CF surface can trigger intense electron transfer via simultaneous activating NOR and PDS, and electrons transferred from NOR to B-CF-PDS compound, resulting in selective and remarkably enhanced ROS generation. Moreover, it was found that B-CF exhibited surprising adsorption capacity for NOR (834.4 mg g−1), and it can also remove SO42- from the solution through electrostatic attraction. This B-CF/PDS system is efficient within a wide operation pH from 3 to 11 and exhibits long lasting activity (> 274 h maintaining over 80% efficiency). This study unveils the highly selective formation of O2-· and 1O2 and solves the short lifetime of catalysts in persulfate-based catalysis, which provides feasible technology for advanced water purification.

Heteroatom-modulated NiCo2O4 apparent energy activation of PMS for tetracycline removal: Mechanism and toxicity analysis

Heteroatom doping to reconfigure the electronic structure of heterogeneous catalysts is expected to lead to the development of advanced oxidation water purification materials with superior performance and greater stability. Herein, a series of catalysts with different elemental doping was developed by a simple and environmentally friendly one-step self-propagating combustion method to remove Tetracycline (TC). After S-doping, the normalized kinetic constant of TC was significantly increased from 30.49 to 159.41 min−1M−1 within 30 min, which is even higher than most recent heterogeneous catalysts. The prepared S-doped NiCo2O4 (NCO–S) exhibits an extremely promising catalytic performance for oxidation (92.8 %) and mineralization (65.9 %) of TC in a wide pH range (3–11). The resistance to interference is excellent for inorganic ions and even in real water samples. Quenching experiments, electron paramagnetic resonance (EPR), and electrochemical analyses demonstrated that the non-radical oxidation pathway, including electron transfer and 1O2, dominated the degradation process after S doping. It is speculated that possible intermediates and toxicological studies are discussed, finding that the overall degradation process is moving towards low toxicity to reveal prospects for large-scale applications. This work not only provides a way to remove TC, but may also inspire the design of more efficient and stable materials for water treatment and other applications.

Catalytic transformation of microplastics to functional carbon for catalytic peroxymonosulfate activation: Conversion mechanism and defect of scavenging

Plastic wastes were catalytically transformed into different structured carbons as effective catalysts for peroxymonosulfate activation to degrade organic pollutants in water and the catalytic conversion mechanism was comprehensively investigated. A salt template-based carbonization approach was successfully developed to catalytically converting high-density polyethylene (HDPE) into diverse carbon materials, such as core-shell carbon composites, nanosheets, and their hybrids. The morphology and proportions of structure defective carbon were found to be controlled by a NiCl2 to HDPE ratio. Carbon nanosheets performed excellent catalytic efficiency in peroxymonosulfate activation toward phenol oxidation, due to a high content of reactive defects via a nonradical electron-transfer mechanism. More importantly, deliberate experiment design and kinetic analyses were employed to illustrate the artifact of radical scavengers (e.g., ethanol) in mechanistic investigation for nonradical/radical reaction. This work provides an upcycle approach for waste plastics into carbocatalysts and new insight to the conversion process and advanced water purification.

Enteric virus removal by municipal wastewater treatment to achieve requirements for potable reuse

Primary and secondary treatment of municipal wastewater contributes to virus removal upstream of advanced purification to produce water for potable reuse. In this study, virus occurrence by cultivable and molecular methods was measured over a 24-month period in raw wastewater influents and secondary effluents from two municipal wastewater treatment plants that together provide the recycled water source for an advanced water purification facility. Using a rank-paired, covariance-based statistical approach, virus log removal values were determined for four wastewater treatment processes that operate in parallel at the two facilities (two activated sludge processes, trickling filter process, and trickling filter/solids contactor process). The trickling filter process exhibited the lowest observed removal of cultivable enteric virus with a median removal of 1.0 log10 (or 90% removal) and a 5th percentile log removal of 0.73 (or 82%), compared to the greatest removal observed for one of the activated sludge processes (median log removal of 2.4 or 99.6% and 5th percentile of 2.1 or 99.2%). Median log removal observed for male-specific (MS) and somatic (SOM) coliphage was 1.8 (98.6% removal) and 0.5 (70%), respectively, for trickling filter and 2.9 (99.9%) and 2.0 (99%) for activated sludge. Thus, coliphage removal was fairly similar to removal observed for cultivable enteric virus. The cultivable enteric virus 5th percentile removal (0.7) from the trickling filter treatment process was proposed to the state regulator for credit towards state requirements for virus removal related to groundwater augmentation with purified recycled water. Receiving pathogen removal credits for secondary wastewater treatment would allow for an improved margin (safety factor) of credits beyond the minimum required; and in this case may also increase the number of viable future groundwater recharge sites closer to drinking water production wells by reducing the underground travel time otherwise required to obtain sufficient credits.

Permeate quality, advanced oxidation process treatability, and cost for two concentrate treatment technologies to enhance recovery for potable reuse

Abstract Closed circuit reverse osmosis (CCRO) and forward osmosis-RO (FO-RO) were evaluated at a pilot scale to generate additional permeate from RO concentrate – achieving a recovery of 61% for CCRO and 35% for FO-RO – at a full-scale advanced water purification facility. This study assessed permeate water quality, suitability of the permeate for treatment by an ultraviolet-advanced oxidation process (UV-AOP), and cost/footprint for a conceptual 10- or 20-mgd system. Both technologies demonstrated inorganic, organic, and microbiological constituent removal suitable for blending with primary RO permeate. Virus challenge testing with MS coliphage demonstrated ≥3.7-log removal by both technologies. Pilot-scale UV/hydrogen peroxide AOP treatment of CCRO or FO-RO permeate yielded similar performance (∼1.4-log N-nitrosodimethylamine removal and ∼0.5-log 1,4-dioxane removal) as the full-scale UV-AOP that treats the RO permeate from the purification facility. The estimated full-scale total unit cost (capital plus operation and maintenance costs) of product water produced by the two technologies was estimated to range from $0.91 to $1.12 per cubic meter, depending on the design flow rate of RO concentrate treated, and is estimated to be similar between the two technologies given the +50%/–30% expected accuracy of the Class 5 cost estimate.

Multidisciplinary collaborations for advanced water purification devices

Multidisciplinary collaborations for advanced water purification devices