Synthetic Water Research Articles

Fe3O4 nanoparticles decorated on N-doped graphene oxide nanosheets for elimination of heavy metals from industrial wastewater and desulfurization

Finding an effective and excellent pertinent single catalyst material for multipurpose application for the purification of hydrocarbons in fuels (desulfurization), and for efficient removal of heavy metals from industrial effluent is greatly endowed. In the present work, a hybrid nanocomposite of ultrafine magnetite (Fe3O4) nanoparticle embedded on the surface of in-situ nitrogen doped layered GO (NGO) sheets were fabricated by sol-gel method and treatment with microwave irradiation technique is reported for the first time. The results show a high removal efficiency of 97 % for multiple heavy metals (Pb2+, Cd2+, Cu2+, Cr+2, Mn+2etc.) in industrial effluent and as well as in synthetic water with a very good retention performance of 99 %. The composites were tested against the elimination of sulfur from thiophene is 1.495 mmol g−1 is reported high is due to coupling and coordination of nitrogen with FeO and C. Recycling studies showed that the developed composites had excellent recyclability, with <82 % removal at the 5th cycle; its feasibility was evaluated using industrial effluent water and in synthetic water. Surface phenomena studies presented here revealed that the adsorptive removal processes of heavy metals involved π electron donor-acceptor interactions, ion exchange, and electrostatic interactions, along with surface complexation that showed an excellent synergism. A high stability, and retention performance is better than the pure Fe3O4 and NGO sheets. We hope that this study will motivate and give further scope for scientists working on magnetite-based graphene nanocomposites.

Filtro empacado con residuos de lodos de Al para la eliminación de fósforo como sistema de pulimento en una planta de tratamiento de aguas residuales

Recently, using residual aluminum sludge (Al-sludge) from drinking water treatment plants for phosphorus removal has been assessed and it has shown to be highly efficient. However, most of the studies have been conducted using synthetic water. Only a few works have applied this method to real wastewater (WW), and none of them have been tested in continuous mode, as a polishing step, in a pilot-scale, decentralized wastewater treatment plant (WWTP). This paper aimed to evaluate the performance of an immersed filter packed with a bed of residual Al-sludge as a polishing system for Phosphorous removal, in a pilot-scale, decentralized WWTP. The study determined at laboratory-scale the capacity for phosphorus removal through batch and continuous tests using both synthetic and real wastewater and evaluated the effect of retention time. Based on the results, an Al-sludge immersed filter (Al-sludge Filter) at pilot-scale was constructed, implemented, and evaluated as a polishing step for the effluent of a decentralized-WWTP. The results showed that during continuous testing with real WW, the phosphorus removal capacity was 2.55 mg P-PO43-∙g-1 per gram of Al sludge using a retention time of 120 min. The Al-sludge filter as a polishing system presented an average removal efficiency of 94 ± 8 % and an effluent concentration of under 0.50 mg P-PO43-∙l-1 during the first 20 operational days. For the next 17 days, the system removed 85 ± 9 % on average, showing an effluent concentration of under 1.0 mg P-PO43-∙l-1. From operational day 32 onwards, the removal efficiency was 63.6 ± 10.7 %, with an average effluent concentration of 2.20 ± 0.39 mg P-PO43-∙l-1.

Modeling the health impact of wastewater contamination events in drinking water networks

Pathogen intrusion in drinking water systems can pose severe health risks. To better prepare in planning and responding to such events, computational models that capture the intrusion and health impact dynamics are needed. This study presents a novel benchmark testbed that integrates current knowledge on pathogen transport and fate in chlorinated systems and can assess infection risk from contamination events. The model considers organic matter degradation, chlorine decay mechanisms, pathogen inactivation kinetics, as well as stochastic water demands.We studied modeling of wastewater intrusion events that can occur anywhere within a chlorinated and non-chlorinated network. We applied the Quantitative Microbial Risk Assessment framework focusing on three pathogens: enterovirus, Campylobacter, and Cryptosporidium, and their respective dose-response models. Synthetic household-level water demand time series were used to model the individual water consumption timing and calculate the infection risk (exposure via ingestion).Model outcomes indicate that while chlorination aids mitigation, larger contaminations can still lead to infections due to chlorine resistance (for Cryptosporidium) and chlorine depletion at the contamination point. In our example scenarios, chlorine-susceptible pathogens infected of the downstream population, while chlorine-resistant ones infected the entire downstream population. Enterovirus infection risk is higher, despite the concentrations in the contamination source being lower, due to the lower susceptibility to chlorine than Campylobacter. In non-chlorinated networks, the modeled wastewater contamination events led to infection risk in the total population, depending on the contamination location. Hydraulic uncertainty had a limited influence on infection risk. Furthermore, Campylobacter’s infection risk is more sensitive to the initial concentration in the contamination source whereas enterovirus infection risk to the inactivation rate. The model further indicates that the time window for effective mitigation of the magnitude of a waterborne outbreak is short (within hours).

Use of native macrophyte Echinodorus subalatus for grey water treatment applying alternative bed substrate in constructed wetlands

ABSTRACT Two vertical flow constructed wetland (VFCW 1 and VFCW 2) with native macrophyte Echinodorus subalatus (Mart.) were operated. In VFCW 1, the substrates used were ceramic brick, washed sand, seashells (Anomalocardia brasiliana), and ceramic brick and sand in VFCW 2. The system was operated for 74 days, in batches, with cycles of 168 h, and fed with synthetic grey water. The presence of seashells in VFCW 1 was a differential factor (p < 0) for the removal of anionic surfactant (94.09 ± 7.77%), COD (88.43 ± 5.43%) and total phosphorus (45. 98 ± 9.86%) when compared to VFCW 2. The Langmuir isotherm was used to calculate the substrate adsorption capacity for total phosphorus, anionic surfactant, and COD. The results showed that adsorption on support materials was not the primary mechanism of pollutants removal. From 16S sequencing, it was observed that phylum Firmicutes was the most abundant (96.5%), followed by phylum Proteobacteria (3.5%). The results suggest that using seashells as an alternative substrate improved pollutant removal efficiency.

Innovative eco-friendly methyl orange removal: Mechanism, kinetic, and thermodynamic study using starch cryogel-integrated mesoporous silica nanoparticles

This study introduces a novel, eco−friendly composite, uncalcined mesoporous silica nanoparticles incorporated into a starch cryogel (MSNs-Cry), designed for the effective removal of methyl orange (MO) from water. MSNs−Cry integrates uncalcined mesoporous silica nanoparticles (MSNs) within a starch cryogel network, leveraging the high adsorption capacity of MSNs. The composite achieved a maximum adsorption capacity of 18.98 mg g⁻1 and demonstrated high removal efficiencies of 99.00 % ± 0.21 % in synthetic water (10 mg L−1 MO) and 92.77 % ± 1.76 % in real wastewater containing 0.43 mg L−1 MO. The Langmuir isotherm model provided a superior fit (R2 = 0.9930) compared to the Freundlich model (R2 = 0.9180), and the adsorption kinetics followed a pseudo−second−order model (R2 = 0.9917). The primary adsorption mechanisms included electrostatic attraction, hydrophobic interactions, and hydrogen bonding. The process was endothermic (ΔH° = 31.3 kJ mol−1), spontaneous, and more favorable at higher temperatures (ΔG° = −34.2 to −38.6 kJ mol−1 at 298–318 K). In the presence of sodium silicate at 13.1 times the MO concentration, removal efficiency drops by 35.77 %, and with sodium sulfate and urea at 100 times the MO concentration, it decreases by 8.65 %. Despite these challenges, MSNs−Cry effectively removes MO in the presence of the anionic dye Congo Red and metal ions, demonstrating its selective adsorption capabilities. The tablet form of MSNs−Cry prevents the loss of uncalcined MSNs, mitigating potential environmental and operational impacts. Additionally, the composite's effectiveness at a natural pH of 6.65 eliminates the need for pH adjustment, offering a cost−effective solution for real−world applications. This study establishes MSNs−Cry as a promising material for sustainable water purification.

Modeling Many-Body Interactions in Water with Gaussian Process Regression.

We report a first-principles water dimer potential that captures many-body interactions through Gaussian process regression (GPR). Modeling is upgraded from previous work by using a custom kernel function implemented through the KeOps library, allowing for much larger GPR models to be constructed and interfaced with the next-generation machine learning force field FFLUX. A new synthetic water dimer data set, called WD24, is used for model training. The resulting models can predict 90% of dimer geometries within chemical accuracy for a test set and in a simulation. The curvature of the potential energy surface is captured by the models, and a successful geometry optimization is completed with a total energy error of just 2.6 kJ mol-1, from a starting structure where water molecules are separated by nearly 4.3 Å. Dimeric modeling of a flexible, noncrystalline system with FFLUX is shown for the first time.

Removal of chromium and copper from synthetic water samples using passion fruit peels

In this work, modified passion fruit husk was used as biomass for the removal of chromium and copper present in the waters. PH, contact time, and particle size were considered experimental factors. Stirring speed, dosage, and temperature were considered constants. The results showed a 69% decrease in chromium using a pH 4, 90 min, and 300 μm composition. For copper, 74.4% was removed at pH 4, with 120 min and 300 μm, based on initial concentrations of 30 ppm for both metals. The results showed that passion fruit peel is a potential effective removal agent for chromium and copper in synthetic waters. This supports its possible application in the purification of metal-contaminated water, which could contribute to environmental protection.

Enhancing phosphorus removal: the impact of alkaline environment in eutrophic water systems

Abstract Excessive phosphorus input leads to poor water quality and eutrophication. However, limited research has directly explored the influence of pH on phosphorous in actual aquatic systems. This study investigated the effect of pH on phosphorus removal in synthetic, eutrophic, and black-odorous water. The pH levels ranging from 3.5 to 12.0 were adjusted using H2SO4, NaOH, and cement with a 0.5 ± 0.03 interval, followed by a 25 ± 1 °C static water bath for 24 h. Results showed that NaOH-adjusted pH removed &gt;65% TP from eutrophic water (pH ≥9.50) and black-odorous water (pH ≥11.0). Meanwhile, cement-adjusted pH removed &gt;84%, &gt;90%, and &gt;82% TP from the synthetic solution (pH ≥11.0), eutrophic water (pH ≥9.5), and black-odorous water (pH ≥9.5), respectively. The alkaline environment enhanced the formation of Ca-P in eutrophic water and black-odorous water, and cement strengthened the chemical precipitation of phosphorus by providing additional Ca2+. This study lays the groundwork for pH adjustment strategies in eutrophic water, holding significant implications for water resource management and environmental protection.

Magnetically separable sorbent based on activated carbon derived from a new precursor Rhizoclonium hookeri for facile oil spill clean-up

A huge quantity of synthetic toxic materials ends-up in water bodies causing long-lasting environmental and economic impacts due to catastrophic oil spill. Exploring marine algae as sorbent materials for oil spill remediation is a relatively new area and holds great potential. Herein, macroalgae Rhizoclonium hookeri (RH) derived magnetically recoverable RH-activated carbon (RHAC@Fe3O4) composite has been proposed as an innovative and robust strategy for oil spill clean-up. The application of RHAC@Fe3O4 composite was investigated for oil removal by varying time (10–60 min), dosage (0.2–1 g) and temperature (20, 30, 40 °C) to ascertain its optimal performance using both unused and used motor oil. Characterization studies showed that KOH activation resulted in developing pore structure and surface functionalities in the algal biochar. The percentage of oil uptake from simulated oil spill was over 90 % in 30 min at room temperature using 0.8 g composite. Moreover, Fe3O4 loading onto carbon material allowed magnetic separation as a convenient alternative to filtration for the recovery of oil laden composite. Apart from superior oil removal ability, synthesized composite demonstrated robust performance up to four cycles in synthetic sea water matrices. Comparative study revealed better oil sequestration efficiency of RHAC@Fe3O4 (93 %) as compared to its precursors, i.e. algal biochar (71 %) and AC (88 %). Based on these findings, it is advocated that designed RHAC@Fe3O4 composite being eco-friendly, economical and readily recoverable with enhanced oil uptake ability could potentially be an innovative platform for oil spill clean-up applications.

Nanobubble-enabled foam fractionation to remove algogenic odorous micropollutants

Due to climate change and environmental pollution, natural lakes and reservoir water suffer increasingly serious algal blooms and associated water quality problems due to the presence of algal or algogenic organic matter (AOM) such as algal odour and toxins. Effective removal of these micropollutants, especially in the event of algal blooms, is critical to aesthetic values of water bodies, drinking water security and human health. The study investigated the removal efficiency of two common odorous compounds, trans-1,10-dimethyl-trans-9-decalol (geosmin) and 2-Methylisoborneol (2-MIB), using foam fractionation enabled by air nanobubbles with addition of two common cationic and anionic surfactants, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB), to enhance foaming ability and stability. The results showed that the cationic surfactant (i.e., CTAB), a low pH, and high ionic strength significantly promoted the removal of geosmin and 2-MIB. For example, the removal tests using the synthetic water determined that the conditions of pH = 7, [CTAB] = 20 mg·L−1 and IS = 10 mM as NaCl resulted in both the highest geosmin removal rate of 91.81% and highest 2-MIB removal rate of 85.0%. The removal of two odorous compounds in real lake water was evaluated, which yielded removal rates of 83.2% for geosmin and 48.1% for 2-MIB, highlighting the minor inhibition from water matrixes on the removal performances. Compared to microbubbles, nanobubbles enabled greater surface areas of foam and higher removal efficiencies. The study provided new insights into the use of foam fractionation with air nanobubbles to enhance the removal of odorous compounds from impaired water and mitigate the negative environmental and health impacts of harmful algal blooms (HABs).

Highly efficient radium removal from mine wastewater with fly ash NaP1 zeolite

This study investigates the application of NaP1 zeolite, synthesized hydrothermally from F-class fly ash, for treating radium-contaminated mine water. The objective was to assess the efficiency of NaP1 zeolite in removing radium ions from real mine water samples. Three samples with high concentrations of 226Ra and 228Ra and total dissolved cation contents ranging from 48.9 to 89.0 g/L were treated using sequential batch and fixed bed experiments. The NaP1 zeolite demonstrated high treatment efficiency for radium-sulfate and radium-strontium water, with removal rates of 97 % and 82 % for the 1st liter, and 54 % for the 53th and 9th liters, respectively. However, for radium-barium water, the maximum treatment efficiency was 45 % for the 1st liter, dropping to 0 % after 4th liter. This decline was attributed to the competitive adsorption of barium ions, which reduced the radium removal efficiency more rapidly than in the other water types. An additional experiment with synthetic barium water confirmed that 10 g of NaP1 zeolite adsorbed 1 g of Ba from one liter of distilled water. These results highlight the potential of NaP1 zeolite for radium removal in certain contexts, although its efficiency may be hindered by the presence of competing ions such as barium.

Examining plasma-generated ozone and nitric oxide's role in synthetic textile dye water remediation and ecotoxicological analysis

Synthetic dyes produced by the textile dyeing industry and released into wastewater contribute significantly to water pollution. This study explores the efficacy and versatility of a novel multi-electrode dielectric barrier discharge (MEDBD) plasma system that mainly generates ozone (O3 generator) and nitric oxide (NO generator) selectively to degrade various synthetic textile dyes, namely Methylene Blue (MB), Congo Red (CR), Methyl Orange (MO), Crystal Violet (CV), and Evans Blue (EB). Plasma achieved selective enrichment of O3 and NO by utilizing optimized plasma generation duty cycles of 15% and 100%, respectively. The proposed O3 generator plasma involves plasma-generated aqua electron impact, excited species, and reactive oxygen species notably O3, which degrades synthetic textile dyes into simple forms such as CO2, H2O, and N2. This approach achieved over 95% degradation of the above synthetic textile dyes when employing the O3 enriched plasma with 2.44 ± 0.21 W of power. Ecotoxicological evaluation, including microbial, human cell, and phytotoxicity evaluations of the O3 generator plasma for MB and CR dye-contaminated water, underscored the potential of this plasma system for environmentally friendly dye degradation. Overall, this study promotes MEDBD plasma, particularly the O3 generator, as a sustainable and efficient solution for treating synthetic dye-contaminated water across industries.

Assimilation of ground-based GNSS data using a local ensemble Kalman filter

Tropical cyclones become increasingly nonlinear and dynamically unstable in high-resolution models. The initial conditions are typically sub-optimal, leaving scope to improve the accuracy of forecasts with improved data assimilation. Simultaneously, the lack of real ground-based GNSS observations over the ocean poses significant challenges when evaluating the assimilation results in oceanic regions. In this study, an Observation System Simulation Experiment is carried out based on a tropical cyclone case. Assimilation experiments using the WRF-PDAF framework are conducted. Conventional and GNSS observation operators are implemented. A diverse array of synthetic observations, encompassing temperature (T), wind components (U and V), precipitable water (PW), and zenith total delay (ZTD), are assimilated utilizing the Local Error-Subspace Transform Kalman filter (LESTKF). The findings highlight the improvement in forecast accuracy achieved through the assimilation process over the ocean. Multiple observation types further improve the forecast accuracy. The study underscores the crucial role of GNSS data assimilation techniques. The assimilation of GNSS data presents potential for advancing weather forecasting capabilities. Thus, the construction of ground-based GNSS observation stations over the ocean is promising.

Organic Capillary Barriers for Soil Water Accumulation in Agriculture: Design, Efficiency and Stability

Acute shortage of water resources and high unproductive water losses are the key problems of irrigated agriculture in arid regions. One of the possible solutions is to optimize soil water retention using natural and synthetic polymer water absorbers. Our approach uses the HYDRUS-1D design to optimize the placement of organic water absorbents such as peat and composite hydrogels in the soil profile in the form of water-storing capillary barriers. Field testing of the approach used a water balance greenhouse experiment with the cultivation of butternut squash (butternut squash (Cucurbita moschata (Duchesne, 1786)) under sprinkler irrigation with measurement of the soil moisture profile and unproductive water losses in the form of lysimetric water outflow. In addition, the biodegradation rate of organic water absorbents was studied at the soil surface and at a depth of 20 cm. Organic capillary barriers reduced unproductive water losses by 40–70%, retaining water in the topsoil and increasing evapotranspiration by 70–130% with a corresponding increase in plant biomass and fruit yield. The deepening of organic soil modifiers to the calculated depth not only allowed capillary barriers to form, but also prevented their biodegradation. The best results in soil water retention, plant growth and yield according to the “dose-effect” criterion were obtained for a composite superabsorbent with peat filling of an acrylic polymer matrix. The study showed good compliance between the HYDRUS design and the actual efficiency of capillary barriers as an innovative technology for irrigated agriculture using natural and synthetic water absorbents.

Digital One-Step Competitive Detection of a Small Molecule in Synthetic and Environmental Waters.

Optical methods for single-molecule analysis hold the promise of accurate, sensitive, and rapid detection of target molecules. Here, we demonstrate the efficiency of such an approach for the competitive detection of small molecules in water. Our biosensing method is based on a combination of a single-DNA biochip for the parallelization of tethered particle motion real-time measurements with antibodies and modified targets as molecular competitors. The antibodies are coupled to the particles tethered to the surface by a long DNA bearing in its middle the molecular competitor bound to the antibodies. Competitive target binding leads to a detectable conformational change of the DNA tethers from looped to unlooped in proportions related to the target concentration. We thus managed to detect fluorescein, chosen as a model of a target molecule, in freshwater of various qualities, from solutions prepared with ultrapure water to more complex matrices such as river water and wastewater treatment plant effluent samples. Similar dose-response curves were obtained under these various conditions in a wide range of concentrations from nanomolar to micromolar with a limit of detection around 2 nM.

Enhanced microplastics removal from sewage effluents via CTAB-modified magnetic biochar: Efficacy and environmental impact

Sewage treatment plants (STPs) are identified as a significant pathway of microplastics (MPs) re-entry into the environment through effluent discharge, thereby emphasizing the need for reliable and efficient treatment methods. This study investigated MPs removal from sewage effluents using cetyl trimethyl ammonium bromide (CTAB)-modified magnetic biochar (RH-MBC-CTAB) as an adsorbent. Biochars from different biomass were synthesized, surface modified, characterized, and compared for their MPs removal efficacy from aqueous matrices. Batch adsorption studies were initially conducted on synthetic water with 1 μm sized polystyrene (PS) MPs using different MP concentrations (1–10 mg/L) and varying adsorbent dosages (1–10 mg/50 mL) to assess the effect of different process parameters, viz. pH (2–10), humic acid (6–25 mg/L), and competitive ions (0.01–0.2 M). The maximum MPs removal (98%) was achieved at the favorable conditions: initial MPs concentration: 10 mg/L, RH-MBC-CTAB dose: 7 mg/50 mL, pH 4, mixing speed: 180 rpm, and contact time: 3 min. Electrostatic attraction and hydrogen bonding were likely to remove MPs while the MPs adsorption was best fitted by the pseudo-second-order kinetics model (R2 = 0.91) and Langmuir isotherm model (R2 = 0.94) with the maximum adsorption capacity of 247.52 mg/g. Further, the application of RH-MBC-CTAB on the real-time sewage effluents from sequencing batch reactor (SBR) and moving bed biofilm reactor (MBBR)-based STPs spiked with MPs showed up to 96% MPs removal. The reusability results revealed that developed RH-MBC-CTAB could maintain good stability for up to three reusability cycles, therefore offering extensive potential for the removal of MPs from sewage effluents.

Formulation and evaluation of melatonin as fast dissolving oral strips using combined polymers

Background and objective: Fast-dissolving oral thin film (FDOF) is a novel and most advanced form of solid dosage form that dissolves or disintegrates in 1 minute when put in the mouth without water or chewing. Pre-gastric absorption of FODFs from the mouth, pharynx, and esophagus as saliva flows down into the stomach would improve the therapeutic benefit of the drug as oral films disintegrated in the mouth. The study is designed and purposed to use most water soluble, best type and concentration of polymers to be selected for use in combination to formulate melatonin oral thin films. Different types of synthetic water soluble polymers were utilized the preparation of films (hydroxypropyl methyl cellulose HPMC15M, sodium carboxy methyl cellulose NACMC). Methods: Solvent casting method was performed for preparation of twelve placebo films at the beginning, to obtain and select suitable polymer type and concentration for use in combination to be formulated for drug loading. The films were evaluated for their characteristics like mechanical properties (thickness and folding endurance), surface pH and disintegration time. Percentage of release and assay of melatonin was taken. Comparison studies were performed on melatonin films from this study with melatonin oral disintegrating tablets release profiles. Best batch could be selected. Drug-excipient compatibility carried out as pre formulation study to see whether there is interaction between the drug and excipients used. Results: Results from FT-IR showed no interaction between melatonin and polymers used, the prepared formulations were clear, transparent, non-sticky and easily removed from the plate surface with the thickness ranging from (0.04-0.07) mm depending on the polymer concentration. The times required for the films to disintegrate was ranging from 21-26 seconds, and the majority of melatonin was released within first 2 minutes within the dosage form. Conclusion: Melatonin can be formulated as fast dissolving oral films using combination of water-soluble polymers by solvent casting method to obtain ease of administration without using water during administration, fast onset of action resulted from rapid disintegration.

Valorization of ladle furnace slag and functional enhancement of post-adsorption materials

Carbonating metallurgical slags plays a pivotal role in achieving efficient mineral CO2 sequestration and waste valorization.This research introduces a novel integrated approach that combines the carbonation of Ladle Furnace Slag (LFS) with the simultaneous degradation of Methyl Orange (MO) in synthetic water. The comprehensive characterization of LFS was conducted using X-ray Diffraction (XRD), X-ray Fluorescence (XRF), Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), Brunauer-Emmett-Teller (BET) analysis, and Scanning Electron Microscopy (SEM). The adsorption experiments reveal the high LSF capacity for MO degradation (149.25 mg/g) following pseudo-second-order kinetics (R2 = 0.99) and Langmuir isotherm (R2 = 0.98). The adsorption process was primarily governed by chemical and electrostatic interactions. Analysis of LFS-loaded MO indicated a reduction in Ca(OH)2phases, responsible for CO2mineralization and the formation of calcite (CaCO3). Furthermore, the study explored the reusability of LFS-MO composites through chemical and thermal modifications. Pyrolysis of carbonated LFS with KOH impregnation exhibited potential for regenerating Ca(OH)2phases, while thermal modification induced significant mineral and microstructural changes, creating new active sites at various temperatures. Additionally, the Fenton-like reaction followed by thermal modification resulted in a highly organized and microporous LFS structure with enhanced surface area and porosity. Moreover, modification with ZnSO4followed by thermal activation promoted the formation of ZnO nanoxides on the LFS surface. This research proposes an innovative carbonating approach for metallurgical slags and wastewater treatment, extending their utility and enhancing industrial sustainability. Carbonated LFS-MO composites hold promise for applications in construction, CO2capture, and wastewater treatment, thereby fostering sustainable industrial practices with ongoing research and development efforts.

Proton Conducting Metal-Organic Frameworks (MOFs) via Post Synthetic Transmetallation and Water Induced Structural Transformations.

Post Synthetic Modification (PSM) of Metal-Organic Frameworks (MOFs) is a crucial strategy for developing new MOFs with enhanced functional properties compared to their parent one. PSM can be accomplished through various methods:1) modification of organic linkers; 2) exchange of metal ions or nodes; and 3) inclusion or exchange of solvent/guest molecules. Herein, PSM of bimetallic and monometallic MOFs containing biphenyl dinitro-tetra-carboxylates (NCA) are demonstrated. The tetra carboxylate NCA, produces monometallic Cd-MOF-1 and Cu-MOF-1 and bimetallic CoZn-MOF in solvothermal reactions with the corresponding metal salts. The CoZn-MOF undergoes post-synthetic transmetallation with Cd(NO3)2 and Cu(NO3)2 in aqueous solution to yield Cd-MOF-2 and Cu-MOF-2, respectively. Additionally, green crystals of Cu-MOF-1 found to undergo a single-crystal-to-single-crystal (SCSC) transformation to blue crystals of Cu-MOF-3 upon dipped into water at room temperature. These MOFs demonstrate notable proton conductivities ranging from 10-3 to 10-4 S cm-1 under variable temperatures and humidity levels. Among them, Cu-MOF-3 achieves the highest proton conductivity of 1.36×10-3 S cm-1 at 90 °C and 98 % relative humidity, attributed to its continuous and extensive hydrogen bonding network, which provides effective proton conduction pathways within the MOF. This work highlights a convenient strategy for designing proton-conducting MOFs via post-synthetic modification.

Electrofiltration-Enabled Nitrate Reduction Reactivity of Carbon Nanotube Electrified Membrane for Drinking Water Treatment

Electrocatalytic nitrate reduction could enable nitrate removal in drinking water without generating concentrated waste streams. However, current processes heavily rely upon metal catalysts with high activity to achieve sufficient nitrate removal, which increases treatment costs and can inevitably lead to leaching of metals into treated water. In this study, we elucidate how electrified filtration enables sufficient nitrate conversion to meet drinking water standards in metal-free defective CNTs by tunable matching of mass transport and reaction timescales. The metal-free carbon nanotube (CNT)-based electrified membrane (EM) was employed as a porous flow-through cathode to decrease the diffusion boundary layer. Computational fluid dynamics simulations revealed that the flow-through mode mitigates diffusion limitations to enhance overall reaction activity, as compared to the conventional flow-by mode at the same flow rate. Additionally, the nitrate reduction rate could be tuned by controlling the nitrate advection rate using permeate flux (0 to 60 L h-1 m-2). A maximum removal efficiency of 86.9% was reached when the mass transport rate matched the reaction rate across a range of applied potentials. Furthermore, defects in CNTs were identified as the catalytic active sites. We employed density functional theory and molecular dynamics simulations to gain insight into CNT defect-catalyzed nitrate reduction under electrofiltration. Finally, the long-term stability, tolerance of environmental interferences, and sufficient nitrate removal and N2 selectivity to meet drinking water standards were demonstrated in synthetic surface water, suggesting that the CNT-EM and flow-through reactor may provide a promising solution for decentralized nitrate destruction in drinking water.