Higher Degradation Rate Research Articles

Construction of polarized 2D/2D g-C3N4/BiOCl nanosheet dual piezoelectric Z-scheme heterojunction and its efficient charge separation mechanism

A multi-electric field synergistic strategy based on heterojunction construction and polarization engineering enhances carrier separation and migration, achieving excellent piezoelectric photocatalytic performance of g-C3N4 based materials. Here, through the in-situ growth of BiOCl nanosheets (BOCs) on g-C3N4 nanosheets (GCNs), a 2D/2D Z-scheme GCNs/BOCs heterojunction was successfully fabricated, and its outstanding piezo-photocatalytic property was demonstrated. Compared to individual BOCs and GCNs, the high degradation rate (97.64 %) of rhodamine B (RhB) can be achieved over the optimal composite (GCNs/BOCs-50) after 50 min irradiation. Inspiringly, the polarized GCNs/BOCs-50 composite degraded RhB almost completely within 30 min under the simultaneous light irradiation and ultrasound, which reduced the photocatalytic time by 40 %, and its k reached 0.1410 min−1 (12.59 and 2.48 times that of BOCs and GCNs). This work is of great significance for designing a novel heterojunction photocatalysts using polarized ferroelectric materials.

Study on methane degradation by microbial agents based on chelating wetting agent carriers

Due to the low permeability characteristics of the deep gas-containing coal seam, the conventional prevention and control measures that cannot solve the problems of gas outbursts are unsatisfactory for the prevention and control of the coal and gas outbursts disaster. Therefore, in this study, a strain of methane-oxidizing bacteria M07 with high-pressure resistance, strong resistance, and high methane degradation rate was selected from coal mines. The growth and degradation abilities of M07 in chelating wetting agent solutions to assess its adaptability and find the optimal agent-to-M07 ratio. It provides a new method for integrating the reduction of impact tendency and gas pressure in deep coal mines. The experimental results show that M07 is a Gram-positive bacterium of the genus Bacillus, which has strong resistance and adaptability to high-pressure water injection. By degrading 70 mol of methane, M07 produces 1 mol of carbon dioxide, which can reduce gas pressure and reduce the risk of gas outbursts in coal mines. As the experiment proves, the best effect was achieved when the M07 concentration of the chelating wetting agent was 0.05%. The methane-oxidizing bacteria based on the chelating wetting agent as carriers prove a new prevention and control method for the integrated prevention and control of coal and gas outbursts in coal mines and also provide a new idea for microbial application in coal mine disaster control.

Biomass guided the formation of spherical catalysts for efficient photodegradation of tetracycline hydrochloride

Developing and evaluating advanced antibiotic degradation photocatalysts remains challenging owing to the lack of rational structural designs and molecular oxygen activation. In this study, a nanofluoral-biochar-modified bismuth vanadate (m-BiVO4) material with a specific structure was prepared via surface-assisted polymerization. The results show that the yeast-derived carbon material significantly broadened the capture range of n–p* visible light and improved the electron delocalization and carrier separation rates. Under visible light irradiation, m-BiVO4 exhibited a high photocatalytic degradation rate, and the degradation rate of 10 mg/L tetracycline (TC) reached 89.9 % within 180 min, almost three times that of the control group. An EPR test and free radical capture experiment showed that ·OH and ·O2– were the main active substances in the TC degradation process. Cyclic experiments also showed that the material had great stability and potential for reuse. The intermediate in the degradation pathway was identified using liquid chromatography-tandem mass spectrometry, the degradation pathway of TC in the composite system was predicted, and a corresponding degradation pathway was proposed. In this study, the synergistic effect of morphology adjustment and component cutting was realized using biomass templates, providing a new method for designing photocatalysts with specific structures.

Unveiling a Novel Antidote for Deoxynivalenol Contamination: Isolation, Identification, Whole Genome Analysis and In Vivo Safety Evaluation of Lactobacillus rhamnosus MY-1.

Deoxynivalenol (DON) is a global contaminant found in crop residues, grains, feed, and animal and human food. Biodegradation is currently the best solution for addressing DON pollution. However, efficient detoxification bacteria or enzymes that can be applied in complex matrices are lacking. The aim of this study was to isolate a DON-detoxifying probiotic strain with a high degradation rate, a good safety profile, and a clear genetic background. One hundred and eight bacterial strains were isolated from 300 samples collected from a school farm and surrounding livestock farms. A new DON-degrading strain, Lactobacillus rhamnosus MY-1 (L. rhamnosus MY-1), with a degradation rate of 93.34% after 48 h and a comprehensive degradation method, was identified. Then, MY-1 at a concentration of 1 × 108 CFU/mL was administered to mice in a chronic intoxication experiment for 28 days. The experimental group showed significantly higher weight gain and exhibited good production performance compared to the control group. The length of the ileal villi in the experimental group was significantly longer than that in the control group. The expression of pro-inflammatory cytokines decreased, while the expression of anti-inflammatory factors increased in the experimental group. Whole-genome analysis revealed that most of the MY-1 genes were involved in carbohydrate metabolism and membrane transport, with a cluster of secondary metabolite genes encoding antimicrobial properties. In summary, this study successfully identified a Lactobacillus strain with good safety performance, high DON degradation efficiency, and a clear genetic background, providing a new approach for the treatment of DON contamination.

Direct electron transfer mediated electrochemical activation of persulfates by reticulated vitreous carbon (RVC) cathode

The electrochemical activation of peroxymonosulfate (PMS) and peroxydisulfate (PDS) for pollutant degradation has gained increasing attention. In this work, reticulated vitreous carbon (RVC) electrodes were prepared at a low cost and investigated for the cathodic activation of PMS/PDS for Acid Orange 7 degradation. The RVC was characterized by SEM, TGA, XRD, Raman spectroscopy, XPS, EIS, and compression test. The superior activity outperformed previous reports in terms of low current density operation (1–10 mA/cm2), high degradation rates (0.13–0.49 min−1), low energy consumption (0.03–0.23 kWh/m3/order) without involvement of catalysts. The process was optimized for current density, PMS dosage, pollutant concentration, pH, water matrix, and supporting electrolyte. Under the optimal current density (3 mA/cm2), the addition of 0.5 mM of PMS boosted the degradation rate by 9.6 times to 0.4470 min−1 and reduced the electrical energy consumption by 90.1 % to 0.0243 kWh/m3/order in 50 mM of Na2SO4. Moreover, up to 117 mg/L of H2O2 was produced in 1 hour by the reduction of oxygen, with current efficiencies between 78–24 %. The process showed little deterioration in 10 cycles, worked for a variety of pollutants, and was not affected by the water matrix. The H-cell experiments confirmed that 90 % degradation took place on the cathode. Scavenging experiments and electrochemical tests suggested that the transitional state of PMS* and O2•− mediated the direct electron transfer mechanism for AO7 degradation. Eighteen degradation products were identified by HPLC-MS and categorized into 4 degradation pathways. Finally, their toxicity was assessed by the ECOSAR programme.

Ag nanoparticle-mediated LSPR effect and electron transfer for enhanced oxidative degradation process of g-C3N5 nanoflowers

The design of photocatalytic system with broad-spectrum response to sunlight and rapid electron transfer is critical for efficient destruction of diverse contaminants in various environmental situations. Herein, self-assembled supramolecular strategy was employed to anchor Ag nanoparticles on the nanoflower-like g-C3N5 surface to construct Schottky-type catalyst (ACN-1) for efficient degradation of organic contaminants. The localized surface plasmon resonance (LSPR) effect significantly improves photocatalytic activity of materials by boosting rapid transfer of interlayer energy and photogenerated electrons and extending the absorption edge of catalysts into near-infrared light region. In actual water samples, ACN-1 entirely eliminated tetracycline (k = 1.0787 min−1) within 40 min and maintained high degradation rate (more than 80 %) under various water quality parameters. Furthermore, ACN-1 demonstrated remarkable suitability to microcystin-LR (98.9 %, k = 0.08098 min−1), sulfamethoxazole (81.2 %, k = 0.02984 min−1), and methylene blue (91.4 %, k = 0.04072 min−1). Quenching experiments and ESR tests showed that main active species in system were 1O2, •O2−, and h+. Finally, five photodegradation pathways and 26 intermediates of TC were elucidated by combining ESR signals, LC-MS and Fukui index. After photodegradation treatment, the toxicity of solution was drastically reduced and the mineralization reached 62.48 %. This study provides new insights into the design and interaction mechanisms of novel g-C3N5-based catalysts and effectively contributes to remediation strategies for emerging pollutants in water.

Effect of physical and chemical co-application of biochar and sulfidated nano scale zero valent iron on the NB degradation in soil: Key roles of biochar

Sulfidated nano zero-valent iron (S-nZVI) can efficiently degrade nitrobenzene (NB) in water. However, its practical application in soil remediation is constrained by limited contact with soil-sorbed NB, leading to sparse research. Herein, Biochar (BC), with its notable adsorption capacity, was coupled with S-nZVI to assess the role of physical (S-nZVI + BC) and chemical (S-nZVI@BC) co-application of BC and S-nZVI, respectively, on enhancing NB degradation in soil. Regardless of the physical or chemical co-application, there was a remarkable advantage after addition of BC relative to S-nZVI alone. In physical co-application, the NB degradation rate of S-nZVI + BC increased as the increasing BC concentration from 0 to 3.5 g·L−1, attributed to enhanced NB desorption via the solubilization effect of BC, facilitating interaction with S-nZVI. Beyond this concentration, no significant improvement was observed, possibly due to BC obstructing reactive sites on S-nZVI surface. In chemical co-application, the S-nZVI@BC (S-nZVI/BC mass ratio of 1:1) exhibited a high NB degradation rate constant (1.097 h−1) during reaction. Apart from solubilization effect, BC in S-nZVI@BC endowed S-nZVI with a higher anti-oxidation property, hydrophobicity, electron transfer capacity, and dispersion effect, accounting for the higher reactivity of S-nZVI@BC over S-nZVI + BC. Besides, the water/soil ratio and initial soil pH significantly affected NB degradation rate, with the optimum water/soil ratio and initial soil pH being 3 and 5, respectively. Our finding broadens the applicability of BC and may offer a highly effective way in soil remediation.

Iron-based metal organic framework (Fe-MOF)-doped sesame stalk biochar enhances antibiotic degradation: Important role of free radicals and comparison of multiple degradation processes

A novel iron-based metal organic framework-doped sesame stalk biochar (Fe-MOF@SBC) composite was successfully synthesized using sonication and used for the degradation of sulfamethoxazole (SMX), norfloxacin (NOR), erythromycin (ERY) and tetracycline (TC) in aqueous solution. The characterization results indicated that Fe oxide was successfully loaded on the biochar. The Fe-MOF@SBC composite presented a porous structure enriched in micropores and mesopores. Adsorption mechanisms, including pore filling, π–π electron donor–acceptor (EDA) interactions, hydrophobic interactions, hydrogen bonding and electrostatic interactions, and the catalytic effect of the Fe-MOF@SBC composite facilitated antibiotic degradation. Specifically, single-layer and multilayer adsorption occurred, and abundant oxygen-containing functional groups were involved in the degradation of NOR, which might be one reason for the high degradation rate of NOR by the Fe-MOF@SBC composite. Scavenging experiments combined with electron paramagnetic resonance (EPR) analysis indicated that free radicals such as •OH, O2−• and 1O2 played vital roles in the degradation of SMX, NOR, ERY and TC. Furthermore, the proposed degradation pathways and possible intermediates of SMX, NOR, ERY and TC were identified, which indicated that the adsorption properties and free radical (•OH, O2−• and 1O2) activity of the Fe-MOF@SBC composite strongly promoted the removal of SMX, NOR, ERY and TC.

MgCa-Based Alloys Modified with Zn- and Ga-Doped CaP Coatings Lead to Controlled Degradation and Enhanced Bone Formation in a Sheep Cranium Defect Model.

Mg-based biodegradable metallic implants are gaining increased attraction for applications in orthopedics and dentistry. However, their current applications are hampered by their high rate of corrosion, degradation, and rapid release of ions and gas bubbles into the physiological medium. The aim of the present study is to investigate the osteogenic and angiogenic potential of coated Mg-based implants in a sheep cranial defect model. Although their osteogenic potential was studied to some extent, their potential to regenerate vascularized bone formation was not studied in detail. We have studied the potential of magnesium-calcium (MgCa)-based alloys modified with zinc (Zn)- or gallium (Ga)-doped calcium phosphate (CaP) coatings as a strategy to control their degradation rate while enhancing bone regeneration capacity. MgCa and its implants with CaP coatings (MgCa/CaP) as undoped or as doped with Zn or Ga (MgCa/CaP + Zn and MgCa/CaP + Ga, respectively) were implanted in bone defects created in the sheep cranium. MgCa implants degraded faster than the others at 4 weeks postop and the weight loss was ca. 50%, while it was ca. 15% for MgCa/CaP and <10% in the presence of Zn and Ga with CaP coating. Scanning electron microscopy (SEM) analysis of the implant surfaces also revealed that the MgCa implants had the largest degree of structural breakdown of all the groups. Radiological evaluation revealed that surface modification with CaP to the MgCa implants induced better bone regeneration within the defects as well as the enhancement of bone-implant surface integration. Bone volume (%) within the defect was ca. 25% in the case of MgCa/CaP + Ga, while it was around 15% for undoped MgCa group upon micro-CT evaluation. This >1.5-fold increase in bone regeneration for MgCa/CaP + Ga implant was also observed in the histopathological examination of the H&E- and Masson's trichrome-stained sections. Immunohistochemical analysis of the bone regeneration (antiosteopontin) and neovascularization (anti-CD31) at the defect sites revealed >2-fold increase in the expression of the markers in both Ga- and Zn-doped, CaP-coated implants. Zn-doped implants further presented low inflammatory reaction, notable bone regeneration, and neovascularization among all the implant groups. These findings indicated that Ga- and Zn-doped CaP coating is an important strategy to control the degradation rate as well as to achieve enhanced bone regeneration capacity of the implants made of Mg-based alloys.

Smart Doped Polyaniline Coating for Wireless Anodic Protection of AISI 304 Stainless Steel in a Corrosive Medium Containing Sulfate and Chloride Ions: Electrochemical and DFT Evaluations.

Polyaniline (PANI) coatings have the capability of in situ anodic protection of stainless steels (SSs). However, these coatings have a high degradation rate in sulfuric acid. Also, the protection of SSs in a medium contaminated with chloride ions is an unsolved challenge. Therefore, the present work aims to modify the electrodeposited PANI coating with different dopants to find the optimal coating for the anodic protection of 304 SS in chloride-contaminated sulfuric acid. Thus, CH3COO-, HSO4-, NO3-, H2PO4-, and NaSO4- were doped electrochemically in PANI to determine the most effective corrosion depressor. Density functional theory (DF)T calculations determined that the lowest Gibbs free energy (more spontaneous doping) is for HSO4- doping by 24 kcal/mol. The band gap energy is <0.5 eV for the PANI/H2SO4 coating, indicating the very high conductivity of this coating. Monte Carlo simulation revealed that the highest deformation energy is related to PANI/H2SO4 at 1877 kcal/mol (stronger adsorption). Mott-Schottky and energy-dispersive spectroscopy (EDS) results showed that PANI doped with sulfuric acid creates a p-type semiconductor (Ni-rich), while the rest of the dopants lead to the formation of an n-type semiconductor passive film (Fe/Cr-rich). Despite the relatively low corrosion resistance of PANI/H2SO4 in the early days, its resistance improved over time by more than 1 order of magnitude. Therefore, this seems to be a more favorable option for long-term anodic protection. Thus, in this work, the corrosion behavior of the passive film formed at the interface of PANI and SS was comprehensively evaluated.

New Insight into the Degradation of Sunscreen Agents in Water Treatment Using UV-Driven Advanced Oxidation Processes

This study evaluates, for the first time, the effects of UV/PMS and UV/H2O2/PMS processes on the degradation of sunscreen agents in synthetic and natural water matrices and compares their effectiveness with the more conventional UV/H2O2. Investigations were conducted using a mixture of organic UV filters containing 4-methylbenzylidene camphor (4-MBC) and 2-ethylhexyl-4-methoxycinnamate. Among the investigated UV-driven AOPs, UV/PMS/H2O2 was the most effective in synthetic water, while in natural water, the highest degradation rate was observed during the degradation of EHMC by UV/PMS. The degradation of UV filters in the UV/PMS system was promoted by sulfate radical (68% of the degradation), with hydroxyl radical contributing approximately 32%, while both radical species contributed approximately equally to the degradation in the UV/H2O2/PMS system. The Vibrio fischeri assay showed an increase in inhibition (up to 70%) at specific stages of UV/H2O2 treatment when applied to natural water, which further decreased to 30%, along with an increase in UV fluence and progressive degradation. The Pseudomonas putida test recorded minor toxicity (&lt;15%) after treatments. Magnetic biochar utilized in conjunction with UV-driven AOPs exhibited superior performance in eliminating residual contaminants, providing an efficient and sustainable approach to mitigate sunscreen agents in water treatment.

Economic Consequences Based on Reversible and Irreversible Degradation of PV Park in the Harsh Climate Conditions of Iraq

Photovoltaic (PV) system reliability and durability investigations are essential for industrial maturity and economic success. Recently, PV systems received much interest in Iraq due to many reasons—for instance, power shortage, global warming and pollution. Despite this interest, the precise economic implications of PV system reliability in harsh climates like Iraq remain uncertain. This work assesses the economic implications of PV system component reliability and soiling in Iraq using field experience and historical data. This study identifies the most common failure modes of PV systems installed in Iraq and similar climatic regions, and also ranks their severity. Simulations explore scenarios of PV module degradation rates, inverter lifetimes, soiling rates, and cleaning intervals, revealing that soiling has the most detrimental effect, with cleaning frequency leading to Levelized Cost of Electricity (LCOE) losses of over 30%, depending on the location. Inverter lifetime contributes to LCOE losses between 4 and 6%, depending on the PV system’s location. This study also evaluates the impact of tilt angle as a mitigation strategy for reducing soiling loss and its economic implications, finding that installing PV modules at higher tilt angles could reduce the economic impact of soiling by approximately 4.4%. Additionally, the optimal cleaning strategy identified is fully automated dry cleaning with robots, outperforming other strategies economically. Overall, the findings highlight that the LCOE in Iraq is relatively high compared to the global weighted average for utility-scale PV systems, primarily due to high soiling and degradation rates. The LCOE varies within the country, influenced by different degradation rates. This study aims to assist PV stakeholders in Iraq and the Middle East and North Africa (MENA) region in accurately estimating solar bankability; moreover, increasing reliability by minimizing the technical and financial risks by considering key parameters specific to these regions.

Rational Bi[sbnd]Mo[sbnd]O nanospheres decorated g-C3N4 for photocatalytic performance of dye degradation

Developing a superior heterostructured composite, optimizing performance through synergies from complementary advantages in diverse materials, remains an ongoing challenge. The rise in organic contaminants in freshwater bodies possesses a major threat to human health. Various dyes such as Rhodamine B, Eosin Y and Methylene Blue are found in excess concentration due to industrial usage and their removal is important for environmental remediation and contaminant-free water. In this study, we report synthesis and fabrication of Bi2MoO6/g-C3N4 (BM/CN) composite photocatalyst and Rhodamine B photodegradation studies. The composite photocatalysts have been characterized using XRD, TGA, FT-IR, UV–Vis, TRPL, SEM, TEM, XPS, electrochemical, and BET studies over g-C3N4, Bi2MoO6, and Bi2MoO6 (10–40 wt%) supported on g-C3N4 photocatalysts. The photocatalytic studies are performed using various composite photocatalysts of BM/CN show 30%-Bi2MoO6 supported on g-C3N4 (30BM/CN) exhibits maximum visible light activation for dye degradation with 3.6 and 2.4-fold higher rate of degradation than bare g-C3N4 and Bi2MoO6, respectively. Higher surface area, broad light absorption, enhanced lifetime, lower charge transfer and higher transient photocurrents of the composite photocatalysts compared to g-C3N4 and Bi2MoO6. Moreover, study is aided with scavenger tests to support the proposed mechanism.The increased photoactivity of 30BM/CN is due to the synergistic interplay of improved charge generation and a reduction in the electron-hole (e−/h+) recombination rate.

Transformed construction from type-II WO3/BaTiO3 heterojunction to Z-scheme WO3/Ba0.5Sr0.5TiO3 and WO3/SrTiO3 photocatalytic systems: Enhanced photocatalytic activity and mechanism insight

In this study, type-II heterojunction WO3/BaTiO3 and Z-scheme WO3/SrTiO3 or WO3/Ba0.5Sr0.5TiO3 nanocomposite photocatalysts were constructed for photodegradation of organic pollutants in wastewater under visible light. The photocatalytic performance of three WO3/titanate systems were estimated. Some influencing factors such as molar ratio of WO3 and titanates, light irradiation time, catalyst dose, and initial concentration of organic pollutants on the photocatalytic activity were investigated. The stability and reusability of three WO3/titanates systems were examined. Moreover, the production of some radicals in the three WO3/titanates photocatalytic systems was demonstrated, and the three WO3/titanates photocatalytic reaction mechanisms were compared. The results reveal that the configurations of WO3/titanates photocatalytic systems are transformed from type-II heterojunction WO3/BaTiO3 with lower activity to Z-scheme WO3/SrTiO3 and WO3/Ba0.5Sr0.5TiO3 with higher activity via the change of titanates. The WO3/titanate nanocomposites show higher photocatalytic activity at 3.0:1.0 M ratio of WO3 and titanates, and WO3/Ba0.5Sr0.5TiO3 nanoparticles have superior photocatalytic activity. The order of photocatalytic activity is as follows: WO3/Ba0.5Sr0.5TiO3 > WO3/SrTiO3 > WO3/BaTiO3. Several organic pollutants, such as rhodamine B, methyl parathion, direct brilliant yellow-4R, and methylene blue, can be efficiently degraded using WO3/Ba0.5Sr0.5TiO3 under visible light, and the RhB has higher degradation rate. After four cycles, WO3/titanate nanocomposites still have relatively high stability and reusability. •OH plays a major role in three WO3/titanates photocatalytic degradation. It is expected that the Z-scheme WO3/Ba0.5Sr0.5TiO3 photocatalytic technology creates a good foreground for disposing of dyes and pesticides in water and wastewater.

Comparative study on physical properties of bio-based PA56 fibers and wearability of their fabrics

Abstract Bio-based polyamide 56 (PA56) has significant advantages in reducing oil dependence and reducing carbon emissions. This study compared the physical properties of bio-based PA56 and conventional polyamide 66 (PA66) fibers and their fabrics. The results showed that due to the odd arrangement structure of carbon atoms in PA56 fiber molecules, its crystallinity and orientation were lower than those of PA66. At the same time, PA56 had a higher degradation rate and coloring rate due to its smaller crystallinity and higher moisture content and gave PA56 fabrics better instantaneous cooling and moisture absorption and drying properties. In addition, the molecular structure characteristics of PA56 also lead to a lower stiffness and soft feel of the fabric, which is beneficial for improving the curling phenomenon of the fabric. Overall, bio-based PA56 fibers can meet the applications in the textile and clothing field and can largely replace PA66, which is worthy of further research and utilization.

Recent Advances in Magnesium-Magnesium Oxide Nanoparticle Composites for Biomedical Applications.

Magnesium (Mg) is considered an attractive option for orthopedic applications due to its density and elastic modulus close to the natural bone of the body, as well as biodegradability and good tensile strength. However, it faces serious challenges, including a high degradation rate and, as a result, a loss of mechanical properties during long periods of exposure to the biological environment. Also, among its other weaknesses, it can be mentioned that it does not deal with bacterial biofilms. It has been found that making composites by synergizing its various components can be an efficient way to improve its properties. Among metal oxide nanoparticles, magnesium oxide nanoparticles (MgO NPs) have distinct physicochemical and biological properties, including biocompatibility, biodegradability, high bioactivity, significant antibacterial properties, and good mechanical properties, which make it a good choice as a reinforcement in composites. However, the lack of comprehensive understanding of the effectiveness of Mg NPs as Mg matrix reinforcements in mechanical, corrosion, and biological fields is considered a challenge in their application. While introducing the role of MgO NPs in medical fields, this article summarizes the most important results of recent research on the mechanical, corrosion, and biological performance of Mg/MgO composites.

Rational design of NiO nanoflakes and porous GCN nanocomposite for synergic effectiveness on photocatalytic degradation of industry effluents and biological activity

Nanotechnology can alter matter at the nanoscale and generate new materials, gadgets, and technologies with unique features and functions, revolutionizing medicine, energy, electronics, and materials science. This study synthesizes nickel oxide nanoflowers utilizing Strychnos potatorum seed extract as reducing and stabilizing agents in an eco-friendly way. The porous GCN and NiO nanocomposite enhances NiO for multifunctional capabilities. UV–Vis, FTIR, EDX, XRD, and FESEM were used to synthesize and characterize NiO nanoflowers. Further synthesized bimetallic nanoparticles were tested for antibacterial, antioxidant, and catalytic properties. It showed increased antioxidant activity, CV and RB dye degradation, and antibacterial activity against S. aureus and E.Coli. Scavenging was enriched with nanoparticles. The highest degradation rate was 98.2 % for CV dye in 90 min. Nanoparticle concertation at 100 µl/mL inhibited E.Coli the most (18 mm). NiO nanoflowers and NiO-GCN nanocomposite synthesized from Strychnos potatorum seed extract may be a novel antioxidant, antibacterial, and catalytic agent for industrial dye-contaminated wastewater.

Photocatalytic application towards the degradation of ciprofloxacin and algae by Z-scheme 2D/3D heterojunction of Bi12O17Cl2/UiO-66-NH2

With the continuous emergence of antibiotics in natural water bodies, the crisis of water environment is becoming increasingly serious. To efficiently remove antibiotics, a novel 2D/3D Z-scheme heterojunction of Bi12O17Cl2/UiO-66-NH2 was constructed by in situ growth technology. The formation of Z-scheme heterojunction between Bi12O17Cl2 and UiO-66-NH2 not only significantly improves the transfer rate and separation efficiency of charge carriers, but also greatly prolongs the lifetime of electrons and improves their light absorption ability. Free radical capture experiments and ESR spectra display that ⋅O2− and ⋅OH radicals dominate the degradation process of ciprofloxacin. The synthesized Z-scheme heterojunction shows a high degradation rate of 83.5 % for antibiotic ciprofloxacin within 60 min, much higher than those of Bi12O17Cl2, UiO-66-NH2 monomers and many other reported photocatalysts. The heterojunction Bi12O17Cl2/UiO-66-NH2 also exhibits excellent degrading performance towards antibiotics in three actual water bodies (tap water, lake water and the effluent of domestic sewage treatment plant). Meanwhile, the as-prepared photocatalyst can effectively degrade Microcystis aeruginosa and algal toxin Microcystin-LR in surface water bodies contaminated by algae and antibiotics. The QSAR analysis indicates that the toxicities of both ciprofloxacin and its intermediates are greatly reduced. The degradation pathways of ciprofloxacin were analyzed via Density Functional Theory calculations and QSAR analysis. This study provides an excellent synthesis method of Z-scheme heterojunction for the purification of surface water bodies contaminated by algae and antibiotics via photocatalytic technology.

A sustainable electrochemical strategy utilizing pulsed alternating current and dual carbon felt electrodes for enhanced degradation of organic pollutants: Oxidation performance and mechanisms

In this work, a novel electrochemical (EC) oxidation system utilizing pulsed alternating current (PAC) and dual carbon felt (CF) electrodes has been established for sustainable degradation of sulfamethoxazole (SMX) with no addition of extra oxidant. The EC/PAC system showed high degradation efficiency and energy efficiency compared to the pulsed direct current (PDC) and direct current (DC) systems. The EC/PAC process was effective across a wide pH range of 3–11 for SMX removal. The results showed that the 1O2 confined to the CF electrode surface was the dominant oxidative specie that was generated from dissolved oxygen in the system. Under PAC conditions, the cathode and anode were rapidly switched on the same CF electrode, increasing the generation of 1O2 for enhanced SMX oxidation. Furthermore, the EC/PAC system demonstrated resistance to interference from various anions of different concentration levels found in natural environment. In contrast to the EC/PDC system, the EC/PAC system emerged as a promising option for more efficient H2O2 production. High-resolution mass spectrometry results revealed the SMX degradation pathways and byproducts, which were then evaluated for toxicity removal. Overall, the EC/PAC system offers a green and sustainable solution to future wastewater treatment, with high degradation rates, energy efficiency, and sustainability.

Floatable Cu2(OH)PO4/rGO Aerogel for Full Spectrum Driven Photocatalytic Degradation of Organic Pollutants.

Photocatalytic technology is an attractive option for environmental remediation because of its green and sustainable nature. However, the inefficient utilization of solar energy and powder morphology currently impede its practical application. Here, we designed a floatable photocatalyst by anchoring 0D Cu2(OH)PO4 (CHP) nanoparticles on 2D graphene to construct 0D/2D CHP/reduced graphene oxide (rGO) aerogels. The CHP/rGO aerogels have interconnected mesopores that provide a large surface area, promoting particle dispersion and increasing the number of active sites. Moreover, the optical response of the CHP/rGO aerogel has been significantly expanded to cover the full spectrum of the solar light. Notably, the 20%CHP/rGO aerogel displayed a high degradation rate (k = 0.178 min-1) taking methylene blue (MB) as a model pollutant under light irradiation (λ > 420 nm). The enhanced photocatalytic activity is ascribed to the rapid electron transfer in the CHP/rGO heterostructures, as supported by the DFT theoretical calculations. Our research highlights the utilization of full spectrum responsive photocatalysts for the elimination of organic pollutants from wastewater under solar light irradiation, as well as the potential for catalyst recovery using floatable aerogels to meet industrial requirements.