Great Water Research Articles

Evaluation of baffle-plate bioreactor coupling with adsorption column for the remediation of aquaculture wastewater

In this study, a baffle-plate bioreactor was designed and coupled with an adsorption column for the remediation of aquaculture wastewater. Specifically, baffle-plate was installed in the bioreactor to improve the removal of carbon (C) and nitrogen (N), while the ceramsite prepared from steel slag and river sediment was filled into the column for the adsorptive removal of phosphorus (P). To evaluate the performance of the bioreactor, the operation conditions (e.g., hydraulic retention time (HRT) and C/N ratio) were tentatively optimized. Under the optimal operation conditions, the effects of sulfamethoxazole (SMX) on the performance of the bioreactor and the microbial community were comprehensively investigated. Satisfactorily, the removal rates of NH4+-N, NO3−-N and permanganate index (IMn) were all above 88 % before adding SMX. Moreover, neither IMn nor NH4+-N was influenced by the SMX shock, whereas the NO3−-N removal was significantly deteriorated owing to the inhibitory effect of SMX on denitrifying bacteria. As revealed by the analysis of microbial communities, the microbial abundance obviously increased in the aerobic (e.g., Azohydromonas and Chitinophagaceae) and anaerobic (e.g., Alkaliflexus) zone as compared to the initially inoculated sludge. Nevertheless, the abundance of most denitrifying genera decreased after adding SMX, leading to the inefficient denitrification. In addition, the ceramsite prepared under the optimum conditions had great void fraction (55.2 %) and water absorbency (29.5 %). The average removal rate of phosphorus by the adsorption column was 71.6 %. Overall, these findings may shed new lights into the coupling of bioreactor and adsorption column for the remediation of aquaculture wastewater.

Modeling and Analysis of Lake Water Levels Using System Dynamics and Principal Component Analysis

Understanding the intricate dynamics of the Great Lakes water levels, shaped by environmental factors like rainfall and evaporation, is crucial for devising sustainable water management strategies. This study develops a model to manage the Great Lakes' water levels by analyzing the interconnectedness of the lake network. Utilizing principal component analysis, key variables like rainfall and evaporation were evaluated for their impact on water levels. System dynamics models integrated with flow conservation laws allowed for a detailed hydrodynamic assessment. The study introduces a "narrow seam method" for dry river scenarios, enhancing model accuracy. Annual water level trends from 2000 are depicted, offering insights into future water management practices in response to environmental changes.

Supported Co3O4 catalyst on modified UiO-66 by Ce4+ for completely catalytic oxidation of toluene

Creating a new low-temperature catalyst in decreasing the emission of volatile organic compounds (VOCs) has great significance under different industrial production situations. In particular, the Zr-UiO-66 is optimized by different amounts of cerium, which not only enhances the physicochemical stability but also increases the number of active sites of CexZryUiO-66. Furthermore, the catalysts with Co3O4 nanoparticles supported on CexZryUiO-66 were successfully prepared via impregnation method. In the process of toluene degradation, the Co/Ce1Zr2-UiO-66 attains a 90% conversion rate at 210 °C with a space velocity of 60000 mL/(g·h) and toluene concentration at 1000×10–6. Meanwhile, the carbon dioxide selectivity reaches 100% at 218 °C. The Co/Ce1Zr2-UiO-66 shows great water resistance (3 vol% H2O). Multiple characterization methods were used to figure out the physicochemical properties of the catalysts. It is found that the addition of an appropriate amount of cerium can enhance stability of UiO-66 and surface lattice oxygen proportion. Additionally, the stronger electron transfer between Ce4+ and Co2+ enables the Co/Ce1Zr2-UiO-66 to possess more active surface oxygen species and Co3+ cationic species in all samples.

Enhanced healing of burn wounds by multifunctional alginate-chitosan hydrogel enclosing silymarin and zinc ‎oxide ‎nanoparticles

Multifunctional wound dressings have been applied for burn injuries to avoid complications and promote tissue regeneration. In the present study, we fabricated a natural alginate-chitosan hydrogel comprising silymarin and green-synthesized zinc ‎oxide ‎nanoparticles (ZnO NPs). Then, the physicochemical attributes of ZnO NPs and loaded hydrogels were analyzed. Afterward, wound healing efficacy was evaluated in a rat model of full-thickness dermal burn wounds. The findings indicated that ZnO NPs were synthesized via reduction with phytochemicals from Elettaria cardamomum seeds extract. The microscopic images exhibited fairly spherical ZnO NPs (35-45nm), and elemental analysis verified the relevant composition. The hydrogel, containing silymarin and biosynthesized ZnO NPs, displayed a uniform appearance, smooth surfaces, and a porous structure. Moreover, infrared spectroscopy ‎identified functional groups, confirming the successful loading without adverse interactions. The obtained hydrogel exhibited great water absorption, high porosity, sustainable degradation for several days, and enhanced antioxidant capability of the combined loaded component. In vivo studies revealed faster and superior wound healing, achieving nearly complete closure by day 21. Histopathology confirmed improved cell growth, tissue regeneration, collagen deposition, and neovascularization. It is believed that this multifunctional hydrogel-based wound dressing can be applied for effective burn wound treatment.

Antimicrobial potential and protein binding affinity of a hybrid ternary nanocomposite matrix: Zinc oxide functionalization with poly(vinyl alcohol)-sulphonated graphene oxide-poly pyrrole

The present study focuses on the application of a ternary PVA/sGO/ZnO-NP/PP nanocomposite as an antibacterial and antifungal agent. The process involved utilizing a solution casting technique to fabricate the inorganic–organic blend material, where 4-sulfophthalic acid (SPTA) was used in the sulfonation of graphitic oxide (GO) sheets. The amalgamation of polyvinyl alcohol polymer (PVA) and sulphonated GO (sGO) was achieved through a chemical oxidation polymerization process carried out in a water-based environment. This process developed a PVA/sGO film, in which zinc oxide nanoparticles (ZnO-NP) and pyrrole monomers were introduced. The PVA/sGO film served as the initial stage for the in-situ deposition and formation of polypyrrole (PP), leading to the fabrication of PVA/sGO/ZnO-NP/PP membrane. The structure was stabilized by hydrogen bonding and electrostatic interactions between the components, while SPTA acted as a cross-linker and a sulphonating agent. The Fourier transform infrared (FTIR) spectra of the quad-component composite unraveled the presence of distinctive functional groups, including PVA, sGO, PP, and Zn-O bands. The UV–visible spectra of PVA/sGO/ZnO-NP/PP nanocomposite membrane revealed a peak in the UV-B region, while in-depth X-ray diffraction (XRD) analyses provided strong evidence of its amorphous nature. The scanning electron microscopy (SEM) image showed that the top surface of the organic film was adorned with PP polymeric chains. The membrane exhibited great water retention capabilities due to its high ion exchange capacity (IEC) value.Additionally, the minimal water loss observed underscores its extended shelf life. Due to their inherent hydrophilic properties, the ternary nanocomposite membranes exhibited enhanced hydrophilicity, porosity, zeta potential, and water uptake. The BET and BJH analyses revealed that PVA/sGO/ZnO-NP/PP nanocomposites had a substantial surface area. Remarkably, the nanocomposite membrane exhibited significantly improved antimicrobial efficacy against bacteria and fungi. The type of interactions between Human serum lysozyme (HSL) and nanocomposite at the molecular level was studied through fluorescence spectroscopy. Stern-Volmer plot revealed the occurrence of both static and dynamic quenching. However, the precise mechanisms underlying the antimicrobial and protein binding (HSL) studies of PVA/sGO/ZnO-NP/PP-based nanocomposites require further investigation.

MoS2 supported hydrophilic porous membrane for solar water evaporation

Solar powered interfacial water evaporation has become one of the most direct and sustainable technologies for seawater desalination. However, developing an efficient, stable evaporator with good salt resistance is a critical and challenging. In this work, MoS2-CNT@C membranes synthesized by loading 1T/2H MoS2 flower spheres on the CNT@C hierarchically porous membrane by hydrothermal method are used as solar water evaporators. MoS2-CNT@C membranes, as photothermal conversion materials, have broadband solar absorption capacity and good hydrophilicity. The porous structure of CNT@C membrane can provide great water transport channels, and the decoration of flower spheres MoS2 enhances the internal reflection which can increase the sunlight absorption capacity, resulting in a jump in water evaporation properties. The membrane has a high evaporation rate of 2.53 kg m−2h−1 under one sun illumination. In addition, the evaporation rate of the sample in seawater reaches 2.51 kg m−2h−1, similar to that in the pure water, and remains stable after several evaporation cycles, ensuring that high quality fresh water can be produced during the desalination.

Using Radiometric and Categorical Change to Create High-Accuracy Maps of Historical Land Cover Change in Watersheds of the Great Lakes Basin

Great Lakes Basin landscapes are undergoing rapid land cover and land use (LCLU) change. The goal for this study was to identify changes in land cover occurring in the Great Lakes Basin over three time periods to provide insights into historical land cover changes occurring on a bi-national watershed scale. To quantify potential impacts of anthropogenic changes on important yet vulnerable Great Lakes Wetland ecosystems, the historical changes in land cover over time are assessed via remote sensing. The goal is to better understand legacy effects on current conditions, including wetland gain and loss and the impacts of upland ecosystems on wetland health and water quality. Three key time periods with respect to Great Lakes water level changes and coastal wetland plant invasions were mapped using Landsat-derived land cover maps: 1985, 1995, and 2010. To address change between the three time periods of interest, we incorporate both radiometric and categorical change analysis and open-source tools available for assessing time series data including LandTrendr and TimeSync. Results include maps of annual land cover transition from 1985 to 1995 and 1995 to 2010 basin-wide and by ecoregion and an assessment of the magnitude and direction of change by land cover type. Basin-wide validated change results show approximately 776,854 ha of land changed from c.1980–1995 and approximately 998,400 ha of land changed from c.1995–2010. Both time periods displayed large net decreases in both deciduous forest and agricultural land and net increases in suburban cover. Change by ecoregion is reviewed in this study with many of the change types in central plains showing change in and out of agriculture and suburban land covers, the mixed wood plain ecoregion consisted of a mixture of agricultural, suburban, and forestry changes, and all top five change types in the mixed wood shield consisted of various stages of the forestry cycle for both time periods. In comparison with previous LCLU change studies, overall change products showed similar trends. The discussion reviews why, while most changes had accuracies better than 84%, accuracies found for change from urban to other classes and from other classes to agriculture were lower due to unique aspects of change in these classes which are not relevant for most change analyses applications. The study found a consistent loss in the deciduous forest area for much of the time studied, which is shown to influence the aquatic nitrogen implicated in the expansion of the invasive plant Phragmites australis in the Great Lakes Basin. This underscores the importance of LCLU maps, which allow for the quantification of historical land change in the watersheds of the Great Lakes where invasive species are expanding.

Evaluation of eDNA qPCR monitoring as an early detection tool for a non-native mysid in Great Lakes Waters

Early detection of aquatic invasive species (AIS) is vital to cost-effective prevention of their spread in the Great Lakes. Unfortunately, AIS surveillance has been generally too slow and geographically limited to support this purpose. Environmental DNA (eDNA) detection using quantitative polymerase chain reaction (qPCR) offers more rapid and affordable detection of likely AIS presence, but it does not directly discern live/dead status. Vital status verification using conventional surveys following positive eDNA qPCR detections could resolve this barrier, but only if the latter are adequately reliable and sensitive. Here we explore the reliability and sensitivity of eDNA qPCR monitoring for the bloody red shrimp (Hemimysis anomala), an AIS established in the southern Great Lakes but not yet widely distributed in Lake Superior, against conventional microscopy-based methods. We conducted this comparison using 1) harbor water from Muskegon Lake, MI where H. anomala is established, and 2) raw ballast water from ships transporting ballast from lower Lake Michigan to western Lake Superior. Our studies showed positive eDNA qPCR detections of H. anomala in all harbor and ballast samples for which conventional detection results were positive, and in some samples for which conventional results were negative. These results suggest that qPCR assays with adequate specificity could be an important tool in support of more effective and affordable early detection of target species in Great Lakes water, especially when combined with confirmatory conventional monitoring.

Alignment measurement of immersed tunnels based on laser differential imaging

The precision of underwater alignment for tunnel elements directly impacts the closure state of immersed tunnels. The current global navigation satellite system measurement tower method provides centimeter-level precision; however, this is insufficient due to the tower deformation at great water depths, which fails to meet alignment requirements. In this study, a novel immersed tunnel alignment measurement method using laser differential imaging is developed. A unique sensor layout is designed to measure the axial angle and distance between tunnel elements. The system design is implemented, and its laser data processing scheme is optimized to improve performance base on this sensor layout. The experimental results demonstrate that the accuracy of underwater laser spot extraction is better than 1.16 pixels, and the precision of axial angle and axial distance alignment measurements is better than 25″ and 1.6 mm, with repeatability precision exceeding 10.55″ and 0.53 mm. The laser-based alignment measurement method is not affected by the depth of water, satisfying the required precision of immersed tunnel alignment. These results can be applied to future immersed tunnel installations without measuring towers, providing a novel method for achieving automated and unmanned intelligent construction of immersed tunnels.

Response of deep soil water deficit to afforestation, soil depth, and precipitation gradient

In semi-arid and semi-humid regions, deep soil water resources are crucial for vegetation restoration to mediate the ecosystem sustainability. Yet it is still limited on understanding soil water deficit (SWD) caused by vegetation restoration and its response to soil depth and precipitation. To obtain a more accurate measurement of regional SWD, we conducted a two-year soil water monitoring to a depth of 1800 cm under typical vegetation restoration with a precipitation gradient ranging from 300 mm/y to more than 600 mm/y across the Loess Plateau of China. With increasing precipitation gradient, soil water storages in 0–1800 cm depth under both arable cropland and artificial vegetation significantly increased (p < 0.05). Compared to arable cropland, artificial vegetations (forest and shrub) had a significantly greater SWD regardless of either precipitation gradient or soil depth. In particular, the deep-rooted vegetations (R. pseudoacacia and C. korshinskii) on the Loess Plateau demonstrated the greatest SWD in the 0–1800 cm layer due to their great water consumption. Indeed, a positive relationship between the accumulated SWD and the accumulated root biomass was detected, suggesting that the increased root biomass in soil depth may promote soil water consumption. In addition, the relative SWD in artificial vegetation at a depth of 1800 cm decreased significantly (p < 0.05). These findings reveal that there is a mechanism of precipitation self-regulation on the deep SWD, of which is more sensitive in the sub-shallow soil layers. We conclude that the SWD depends on vegetation restoration, soil depth, and precipitation self-regulation, offering a reference for how afforestation affects deep soil water in the Loess Plateau region. This finding also benefits to mediate water balance processes and develop sustainable land management in water-limited regions around the world.

Physicochemical properties and biological efficacy of 30 DYRK2 Inhibitors for the treatment of prostate cancer

AbstractProstate cancer is the most common cancer among men which has major diagnosis in the United States in 2017. Among DYRK class II members, dual specificity tyrosine phosphorylation‐regulated kinase 2 (DYRK2) is the functional target for prostate cancer treatment. Studies show that subfamilies of DYRKs are also capable to phosphorylate (tyrosine, serine, and threonine) residues, yet little research has been carried out for its inhibitors. In this article, conceptual density theory is used to estimate the physicochemical properties of 30 experimentally synthesized inhibitors targeting DYRK2. The HOMO–LUMO gap showed low reactivity and high chemical activity for the inhibitors. The biological efficacy of these 30 inhibitors is predicted by bioavailability, mutagenicity, and cardiotoxicity measures. The inhibitors showed low toxicity and no blood brain barrier permeability. Results indicated that the physiological actions of these inhibitors involve multiple target interactions. Since the experimental results of the DYRK2 protein showed great water solubility, favorable safety properties, and potential anti‐prostate cancer activities for ligand 24, docking and molecular dynamics simulations from the Galaxy webserver using Gromacs open‐source tools are also performed for (DYRK2‐24) complex (PDB: 7EJV). (DYRK2‐24) showed strong binding affinity and noncovalent interactions.

Investigating the physicochemical, rheological, and sensory properties of low-fat mayonnaise prepared with amaranth protein as an egg yolk replacer.

This study investigated the possibility of using amaranth protein isolate (API) as a plant-based substitute for egg yolk (EY) in the preparation of low-fat mayonnaise (LFM). The alkali extraction/acidic precipitation method was used to isolate amaranth protein; its functional properties were then studied. The results showed that besides its great water and oil absorption capacities, API had better emulsifying capacity and significantly higher (p < .05) emulsion stability at pH 2.0 than alkali pH values. Five mayonnaise samples with different API/EY combination ratios (%) (i.e., 0/0.75, 0.25/0.5, 0.375/0.375, 0.5/0.25, and 0.75/0) were prepared. The color, emulsion stability (ES), freeze-thaw stability (FTS), droplet size, structure, rheology, and sensory properties of samples were examined. API replacement showed no adverse effects on the L* value, ES, and sensory attributes (p > .05). Low API concentrations (0.25% and 0.375%) significantly (p < .05) increased the droplet size and decreased the FTS of LFM emulsion. High API concentrations (0.5% and 0.75%) had no significant effect (p > .05) on droplet size and formed emulsions with more tightly packed oil droplets. The Cross model was chosen best to describe the flow behavior of LFM samples (R 2 = 0.99). The sample with 0.75% API had significantly (p < .05) the highest values of η o (zero-shear viscosity) and λ (relaxation time), indicating greater interaction between the emulsion particles. All samples showed a weak gel structure (G' > G"). In conclusion, API can be considered an appropriate substitute for EY in LFM production, which can benefit human health and offer a new strategy for preparing vegan products.

Synthesis and Characterization of Enhanced Proton-Conducting Nafion&lt;sup&gt;® &lt;/sup&gt;117- Silica Composite Membranes for Fuel Cell Applications

Nafion®/silica nanocomposite membranes were prepared by impregnation method from Nafion® 117 and sol-gel pre-synthesized n-octadecyl-trimethoxy silane (C18TMS) coated silica nanoparticles. The scanning electron microscope (SEM) of pristine silica particles displayed monodispersed nanospheres with diameters ranging from 150-350 nm; while Brunauer-Emmett-Teller (BET) analysis presented 760 m2/g BET surface area, a micropore-mesopore bimodal distribution of micropore systems with respective pore volume at 14.6 Å and 17.0 Å (2.01 x 10-3 cm3/g.Å), as well as the prolific mesopores centered at 29.5 Å (5.64 x 10-2 cm3/g.Å). Characterization of Nafion® 117 based membranes on SEM, Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and x-ray diffraction (XRD), and tensile stress exhibited varying surface morphology with silica loadings, structural interaction between membrane support and the ion exchanger, thermal stabilities (up to 330 °C), crystalline nature, and reasonable mechanical stability of nanocomposite membranes. The maximum water uptake (44.8 %) and proton conductivity of (1.14 x10-2 S/cm) were obtained on low Nafion®/SiO2 (5%) loaded membrane. While both composite membranes displayed the improved reduction in methanol permeability, 2.43x10-07 cm2/s at 80 °C was obtained with high Nafion®/SiO2 (10%) loading. Improved water uptake and proton conductivity substantiate the high ion exchange capacity (IEC) of 1.81 meq.g-1 when compared to IEC of 0.93 meq.g-1 [pristine Nafion®] and 1.46 meq.g-1 [Nafion®/SiO2 (10%)]. The increase in IEC value may be due to the high acid functionalization of additional sulfonic acid groups surrounded by hydrophilic segments of nanosilica, which improves the properties of the membrane. The high proton conductivity coupled with great water retention capabilities indicated that the Nafion®/SiO2 nanocomposite membranes could be utilized as proton exchange membranes for medium temperature methanol fuel cells. Keywords: Fuel cells; nanocomposite membrane; SiO2 nanofillers; methanol permeability; ion exchange capacity

Highly visible-light-active sulfur and carbon co-doped TiO2 (SC-TiO2) heterogeneous photocatalysts prepared by underwater discharge plasma

To promptly and simply create highly crystalline S/C co-doped TiO2 (SC-TiO2) photocatalysts at room temperature and atmospheric pressure, we suggest a novel plasma-assisted sol-gel synthesis method. This method is a simultaneous synthetic process, in which an underwater plasma undergoes continuous reactions to generate high-energy atomic and molecular species that enable TiO2 to achieve crystallinity, a large surface area, and a heterogeneous structure within a few minutes. In particular, it was demonstrated that the heterogeneously structured TiO2 was formed by doping that sulfur and carbon replace O or Ti atoms in the TiO2 lattice depending on the composition of the synthesis solution during underwater plasma treatment. The resultant SC-TiO2 photocatalysts had narrowed bandgap energies and extended optical absorption scope into the visible range by inducing the intermediate states within bandgap due to generation of oxygen vacancies on the surface of TiO2 through synthesis, crystallization, and doping. Correspondingly, SC-TiO2 showed a significant degradation efficiency ([k] = 6.91 h−1) of tetracycline (TC, antibiotics) under solar light irradiation, up to approximately 4 times higher compared to commercial TiO2 ([k] = 1.68 h−1), resulting in great water purification. Therefore, we anticipate that this underwater discharge plasma system will prove to be an advantageous technique for producing heterostructural TiO2 photocatalysts with superior photocatalytic efficiency for environmental applications.

Fluorination modification enhanced the water resistance of Universitetet i Oslo-67 for multiple volatile organic compounds adsorption under high humidity conditions: Mechanism study

The construction of metal–organic frameworks (MOFs) with highly efficient capture for volatile organic compounds (VOCs) adsorption under humid conditions is a significant yet formidable task. Herein, series of fluorinated UiO-67 modified with trifluoroacetic acid (TFA) and 4-fluorobenzoic acid were successfully synthesized for VOCs adsorption under high humidity conditions. Experiments results showed that UiO-67 modified with 4-fluorobenzoic acid (67-F) presented excellent adsorption capacity of 345 mg/g for toluene adsorption and exhibited great water resistance (10.0 vol% H2O, 374 mg/g toluene adsorption capacity). Characterization results indicated that the introduction of 4-fluorobenzoic acid induced the competitive coordination between 4-fluorobenzoic acid and 4,4-biphenyl dicarboxylic acid (BPDC) with Zr4+, causing the formation of abundant defects to provide extra adsorption sites. Meanwhile, the benzene ring in 4-fluorobenzoic acid enhanced the π-π conjugation, causing the further promotion of VOCs adsorption capacity. More importantly, the water resistance mechanism was investigated and elucidated that the introduction of F decreased the surface energy of 67-F and its affinity with water. Meanwhile, the metal complex induced by the fluorinated modification produced an electron-dense pore environment, which greatly improved its chemical and water stability. This work provided a strategy for preparing an adsorbent with high water resistance for real-world VOCs adsorption at high humidity conditions.

Chiral Viologen-Derived Water-Stable Small Band Gap Lead Halides: Synthesis, Characterization, and Optical Properties.

Chiral organic-inorganic metal halides (OIMHs) are attractive for their potential applications in chiral optoelectronics and spintronics, such as circular polarized light emitters, detectors, and chiral-induced spin selectivity. Here, we report three pairs of chiral OIMHs with great water stability constructed from chiral viologens. These OIMHs contain either 1D or 0D structures, however, with small band gaps around 2 eV. Circular dichroism (CD) spectroscopy on transparent thin films of two OIMH pairs showed a wide CD response covering most of the visible light range. Although the chiral center is not directly attached to the pyridinium in these chiral viologens, the chirality is still successfully transferred into both the band gap and the exciton absorption ranges. Liquid and solid CD studies of the chiral viologens further indicate that the chiral induction inside these OIMHs is possibly through chiral crystallization. This work demonstrated the design strategy of water-stable, small band gap chiral OIMHs through chiral viologens. These low-dimensional chiral materials may provide an interesting system to investigate chiral induction, and their broad CD response may enable their potential application as circular photodetectors with a wide detection range.

Photocatalytic Hydrogen Production from Pure Water Using a IEF-11/g-C3N4 S-Scheme Heterojunction.

Construction of S-scheme heterojunction offers a promising way to enhance the photocatalytic performance of photocatalysts for converting solar energy into chemical energy. However, the photocatalytic H2 production in pure water without sacrificial agents is still a challenge. Herein, the IEF-11 with the best photocatalytic H2 production performance in MOFs and suitable band structure was selected and firstly constructed with g-C3N4 to obtain a S-scheme heterojunction for photocatalytic H2 production from pure water. As a result, the novel IEF-11/g-C3N4 heterojunction photocatalysts exhibited significantly improved photocatalytic H2 production performance in pure water without any sacrificial agent, with a rate of 576 μmol/g/h, which is about 8 times than that of g-C3N4 and 23 times of IEF-11. The novel IEF-11/g-C3N4 photocatalysts also had a photocatalytic H2 production rate of up to 92 μmol/g/h under visible light and a good photocatalytic stability. The improved performance can be attributed to the efficient separation of photogenerated charge carriers, faster charge transfer efficiency and longer photogenerated carrier lifetimes, which comes from the forming of S-scheme heterojunction in the IEF-11/g-C3N4 photocatalyst. This work is a promising guideline for obtaining MOF-based or g-C3N4-based photocatalysts with great photocatalytic water splitting performance.

Overview Metode Fitoremediasi Dalam Pengelolaan air Tercemar Timbal (Pb)

Wastewater originating from industry varies greatly depending on the type of industry. Industrial wastewater usually contains many toxic and dangerous chemical compounds (B3) and contains heavy metals. Heavy metals are pollutants that have dangerous effects because they cannot be broken down biologically and stable. Heavy metal elements can be distributed on the earth's surface in water, soil and air. Heavy metal waste pollution containing lead (Pb) is a problem for current environmental conditions. Heavy metals are found in almost all types of industrial waste. The increasing number of industries will cause increased pollution of water sources originating from industrial waste. . Therefore, effective and efficient methods are needed to manage lead-contaminated water. Methods that are easy to apply, low cost and environmentally friendly are highly desirable for managing lead-contaminated water so that the concept of good mining practice can be applied to sustainable development. The most efficient and effective method applied for mining waste management is the phytoremediation method. The results of the research state that several plants have a significant and efficient effect in helping the absorption of the metal lead (Pb) contained in water. Great Duckweed (Spirodela Polyrhiza) and Water Hyacinth (Eichhornia crassipes) are plants that are suitable for implementing phytoremediation methods in managing water contaminated with lead (Pb).

Toward the development of an ecosystem model ensemble to support adaptive management in Lake Ontario

Notwithstanding the continuing advancement of our understanding of the broader ecosystem functioning in Lake Ontario, emerging evidence suggests that there are fundamental knowledge gaps to accurately describe the relationship between exogenous phosphorus (P) loading and in-lake total phosphorus (TP) concentrations. The whole-lake load appears to frequently exceed the Great Lakes Water Quality Agreement (GLWQA) interim target of 7000 metric tonnes·year−1, although the offshore-water P concentrations are consistently below the GLWQA interim substance concentration objective of 10 µg TP·L–1. Contrasting ecological conditions prevail in different locations of Lake Ontario, owing to the significant urban footprint along the shoreline but also the capacity of dreissenid mussels to sequester P in the littoral zone. Specifically, low ambient P levels threaten fisheries productivity in offshore waters, while nuisance benthic algae (predominantly Cladophora) and toxin-producing cyanobacteria blooms affect the water quality in the nearshore zone. The present study offers a technical analysis of the recent and ongoing modelling work that has been conducted in Lake Ontario and can be potentially used to address the multitude of ecosystem management challenges. Our aim is to provide an overview of all the major models developed by identifying their fundamental assumptions, structural attributes, and general consistency against empirical knowledge derived from the system. The existing modelling work has opted for parsimonious representations of the lower food web coupled with granular grid configurations to effectively link hydrodynamic processes and mass transport between nearshore and offshore waters. The establishment of comprehensive ecophysiological modules that will recreate the mechanisms underlying the interplay among bioavailable phosphorus, planktonic dynamics, dreissenid mussels, and Cladophora is a critical undertaking to reproduce the water quality conditions in the nearshore zone of Lake Ontario. Striving to integrate the lower food web with fisheries and ecosystem-service modelling, we also offer a technical analysis of knowledge gaps and monitoring-assessment objectives that should be addressed to ensure that ecosystem processes of management interest are adequately measured and the local modelling enterprise is focused on suitable performance indicators.

Optimal Water Level Study Based on Great Lakes Water Issues

Optimal Water Level Study Based on Great Lakes Water Issues