Degradation Experiments Research Articles

Investigation of Degradation and Biocompatibility of Indirect 3D-Printed Bile Duct Stents.

This study proposes a bile duct stent based on indirect 3D printing technology. Four ratio materials were synthesized from lactic acid (LA) and glycolide (GA) monomers by melt polymerization: PLA, PLGA (70:30), PLGA (50:50), and PLGA (30:70). The four kinds of material powders were preliminarily degraded, and the appearance was observed with an optical microscope (OM) and a camera. The weight and appearance of the four materials changed significantly after four weeks of degradation, which met the conditions for materials to be degraded within 4-6 weeks. Among them, PLGA (50:50) lost the most-the weight dropped to 13.4%. A stent with an outer diameter of 10 mm and an inner diameter of 8 mm was successfully manufactured by indirect 3D printing technology, demonstrating the potential of our research. Then, the degradation experiment was carried out on a cylindrical stent with a diameter of 6 mm and a height of 3 mm. The weight loss of the sample was less than that of the powder degradation, and the weight loss of PLGA (50:50) was the largest-the weight dropped to 79.6%. The nano-indenter system measured the mechanical properties of materials. Finally, human liver cancer cells Hep-3B were used to conduct in vitro cytotoxicity tests on the scaffolds to test the biocompatibility of the materials. A bile duct stent meeting commercial size requirements has been developed, instilling confidence in the potential of our research for future medical applications.

Unveiling Impurities: A Comprehensive RP-HPLC Method for Accurate Atorvastatin Impurity Analysis in Pharmaceuticals Using Accuracy Profile Approach.

Accurate determination of active pharmaceutical ingredients and impurities is essential for ensuring the safety and effectiveness of medications. This study focuses on the validation of a high-performance liquid chromatography (HPLC) method for quantifying Atorvastatin and its impurities, addressing a critical aspect of pharmaceutical analysis. The primary objective is to conduct a comprehensive validation study for the HPLC method, covering specificity assessment, response function establishment, and a detailed analysis of precision, trueness, and tolerance intervals. The emphasis is on demonstrating the method's precision, accuracy, and stability-indicating capabilities across various concentrations and compounds. The HPLC method is validated through rigorous assessments, including specificity, response function establishment, and analyses of precision, trueness, and tolerance intervals. Induced degradation experiments are conducted to explore Atorvastatin's behavior under extreme conditions. Insights into the compound's synthesis and degradation pathways are provided through a proposed mechanism for intramolecular esterification. The results affirm the precision, accuracy, and stability-indicating capabilities of the validated HPLC method. The method effectively differentiates between Atorvastatin and its impurities, showcasing its suitability for pharmaceutical quality control. The validated HPLC method emerges as a robust and reliable tool for Atorvastatin analysis, contributing significantly to pharmaceutical research and quality control. Its application ensures the safety and efficacy of medications, reinforcing its role in pharmaceutical analysis. This study not only validates a crucial HPLC method for Atorvastatin analysis but also provides insights into the compound's behavior under extreme conditions and its synthesis and degradation pathways. The validated method serves as a cornerstone in pharmaceutical research and quality control, ensuring medication safety and efficacy.

Application of novel dual-ligand co metal-organic framework/graphene oxide for electrocatalytic oxidative degradation of bisphenol A in marine wastewater

The adjustment of the electron distribution of 2D metal-organic frameworks (2D-MOFs), as a hot anode candidate for electrocatalytic oxidation, is crucial for its application. In this work, a new electron distribution was achieved with dual-ligand connection and graphene oxide (GO) loading and the complex of dual-ligand 2D-MOF/GO (Co-IH/GO) exhibit faster electron transfer efficiency (Rct = 62.5) and more active sites (ID/IG = 1.01). Co-IH/GO demonstrated excellent electrocatalytic performance and achieved 100 % electrocatalytic degradation of bisphenol A (BPA) within 10 min. In addition, superior properties of stability, temperature tolerance, and pH tolerance were achieved, after 5 cycles of degradation, the catalyst was able to maintain 100 % degradation efficiency, Capable of maintaining good degradation performance over a temperature range of 25 °C–45 °C and a wide pH range of pH = 5–11. Both experimental and electron paramagnetic resonance analysis results indicated that 1O2 acted as the dominant active substrate. With the involvement of Cl− in marine wastewater, activated chlorine was also generated during the reaction, which contributed to fast BPA degradation. Furthermore, the established dual-ligand 2D-MOF/GO electrocatalytic system exhibited superior activity for the degradation of dyes and complex microflora, while the solar-driven degradation experiment shed light on the independence of fossil and stationary sources of energy.

Hygrothermal Degradation of Epoxy Electrical Insulating Material-Testing and Mathematical Modeling.

The degradation of electrical insulating materials has been a subject of interest for decades as they are commonly applied in many fields of electrical engineering. Suitably modeling such a process is important since the known and well-described degradation process reveals the effect of ambient conditions, and this allows us to possibly estimate a material's remaining useful life. However, not many studies are dealing with the effect of the hygrothermal degradation of impregnating mono-component epoxy resins in the context of electrical engineering. Therefore, this study deals with this issue and discusses both the dielectric response (based on the measurement of relative permittivity, dissipation factor, and dielectric strength) and the mechanical response (based on measurements of tensile strength and Shore D hardness) to a hygrothermal degradation experiment. In addition, the results of thermal analyses are presented for the evaluation of the pristine specimen manufacturing process and possible post-curing processes. Furthermore, this study presents several methodologies for modeling the degradation process, including a novel methodology in this area based on Bayesian experimental design. As an outcome, mechanical parameters are proven to be specific in terms of the actual condition of the material and the Bayesian enhanced degradation model seems to be superior to the conventional evaluation methods in this particular study.

Study of photocatalytic degradation of dyeing wastewater with CdS nanoparticles anchored on cotton short staple-based carbon aerogels

The photocatalytic technology is widely recognized as an effective solution for both the energy crisis and environmental issues. Developing cost-effective alternatives to noble metal-based photocatalytic catalysts is crucial for the degradation of organic pollutants in dye wastewater; however, it remains a challenging task. In this study, a novel approach was presented, wherein a cotton-based carbon aerogel was synthesized using short staple cotton cellulose as the raw material. CdS nanoparticles were then anchored onto the three-dimensional porous structure of the carbon aerogel. The resulting materials were thoroughly characterized and analyzed using various techniques, including XRD, SEM, Mapping, XPS, BET, and UV-Vis spectroscopy, and their performance was extensively assessed. Experimental results indicated that the degradation efficiency of 20 ml (15 mg/L) methylene blue solution reached 95.7 % within 90 min, achieving near-complete degradation within 120 min using 10 mg catalyst material. Furthermore, photocatalytic degradation experiments were conducted on commonly used reactive red dye (K-type) and reactive yellow dye (M-type) that are typically employed in textile dyeing and finishing processes. For 20 ml of waste liquid, after 90 min, the degradation rates of the reactive red and yellow dyes reached 91.4 % and 94.4 %, respectively, with complete degradation achieved within 120 min. Free radical quenching experiments demonstrated that hydroxyl radicals (•OH) and superoxide radicals (•O2-) played a central role in mediating the photocatalytic degradation of organic pollutants using the CdS/carbon aerogel (CdS/CA) composite material. Overall, the research findings suggest that the CdS/CA composite material exhibited highly desirable attributes, effectively adsorbing and photodegrading methylene blue as well as organic dyes in dye wastewater. These results provide valuable insights for the development of cost-effective photocatalytic materials and the efficient degradation of dyes.

Efficient degradation of halogenated disinfection by products in a three-dimensional electrode reactor with MnO2/NiMn-LDH/C as particle electrodes: Performance prediction and mechanism exploration

In this work, an in situ novel MnO2/NiMn-LDH/C composite material was designed and used as a particle electrode in a three-dimensional electrochemical continuous flow system, which degraded dichloroacetamide (DCAcAm) because a suitable nickel-manganese metal ratio leads to the construction of MnO2 and NiMn-LDH, and the addition of carbon contributes to the formation of a hierarchical structure. The effects of different conditions were explored by single factor experiments and response surface design experiments. A high removal rate of 89 % was obtained under optimal conditions (current density of 12 mA/cm2, flow rate of 0.5 mL/min, electrolyte concentration of 0.175 mol/L, and a pollutant concentration of 10.5 g/L). According to density functional theory (DFT) calculations, electron paramagnetic resonance (EPR) measurements and free radical quenching experiments, the corresponding electrocatalytic mechanism and reaction pathways were clarified. The application of response surfaces was utilized to predict degradation performance. The results of the recycling experiments show the good stability of this electrode. Finally, the actual chlorin wastewater degradation experiment results showed that the COD and TOC of this wastewater decreased by 76.03 % and 72.41 %, respectively, after 90 min of electrocatalytic degradation. This study offers a novel theoretical framework and technical support for the control of HAcAms.

Ranitidine degradation in layered double hydroxide activated peroxymonosulfate system: impact of transition metal composition and reaction mechanisms.

Ranitidine, a competitive inhibitor of histamine H2 receptors, has been identified as an emerging micropollutant in water and wastewater, raising concerns about its potential impact on the environment and human health. This study aims to address this issue by developing an effective removal strategy using two types of layered double hydroxide (LDH) catalysts (i.e., CoFeLDH and CoCuLDH). Characterization results show that CoFeLDH catalyst has superior catalytic properties due to its stronger chemical bond compared to CoCuLDH. The degradation experiment shows that 100% degradation of ranitidine could be achieved within 20min using 25mg/L of CoFeLDH and 20mg/L of peroxymonosulfate (PMS). On the other hand, CoCuLDH was less effective, achieving only 70% degradation after 60min at a similar dosage. The degradation rate constant of CoFeLDH was 10 times higher than the rate constant of CoCuLDH at different pH range. Positive zeta potential of CoFeLDH made it superior over CoCuLDH regarding catalytic oxidation of PMS. The catalytic degradation mechanism shows that sulfate radicals played a more dominant role than hydroxyl radicals in the case of LDH catalysts. Also, CoFeLDH demonstrated a stronger radical pathway than CoCuLDH. XPS analysis of CoFeLDH revealed the cation percentages at different phases and proved the claim of being reusable even after 8 cycles. Overall, the findings suggest that CoFeLDH/PMS system proves to be a suitable choice for attaining high degradation efficiency and good stability in the remediation of ranitidine in wastewater.

A putative endonuclease reduces the efficiency of oral RNA interference in Nilaparvata lugens.

The RNA interference (RNAi) efficiency of double-stranded RNA (dsRNA) delivery to insects by various methods is different and the reduced efficacy of feeding dsRNA is partly due to the presence of DNA/RNA non-specific endonuclease in the insect gut. However, the mechanism leading to the low RNAi efficiency of Nilaparvata lugens by feeding remains elusive. In this study, we identified a putatively DNA/RNA non-specific endonuclease gene in the N. lugens genome database that was highly expressed in the first nymphal instar and the midgut. Different expression levels of NldsRNase after feeding and injection suggested that NldsRNase might interfere with oral RNAi in N. lugens. A co-delivery RNAi strategy further revealed that the presence of NldsRNase reduces RNAi efficiency. In vitro dsRNA degradation experiments also showed that the stability of dsRNA was higher in a gut mixture from nymphs injected with dsNldsRNase. These results support the idea that the low oral RNAi response observed in N. lugens is likely due to the presence of NldsRNase. Our study provides insight into the differences in RNAi response between the injection and feeding of dsRNA in N. lugens and sheds light on the mechanisms underlying the reduced efficacy of RNAi via feeding. These findings may help to inform the development of more-effective RNAi-based strategies controlling N. lugens and other insect pests. © 2024 Society of Chemical Industry.

Sustainable green synthesis and characterization of nanocomposites for synergistic photocatalytic degradation of Reactive Orange 16 in textile wastewater using CuO@A-TiO2/Ro-TiO2

This paper explores the photocatalytic degradation of Reactive Orange 16 (RO16) dye in textile wastewater employing a novel CuO@A-TiO2/Ro-TiO2 nanocomposite. The nanocomposite was synthesized via a hydrothermal technique, resulting in a monoclinic phase of leaf-shaped CuO loaded on a hexagonal wurtzite structure of rod-shaped ZnO, as confirmed by FE-SEM and XRD analyses. Optical experiments revealed band gap energies of 1.99 eV for CuO, 2.19 eV for ZnO, and 3.34 eV for the CuO@A-TiO2/Ro-TiO2 nanocomposite. Photocatalytic degradation experiments showcased complete elimination of a 100 mg/L RO16 solution (150 mL) after 120 min of UV light illumination and 100 min of sunlight illumination, emphasizing the nanocomposite's efficiency under both light sources. The study further delves into the application of the CuO@A-TiO2/Ro-TiO2 nanocomposite for the degradation of actual textile wastewater samples under sunlight irradiation. The results underscore the nanocomposite's remarkable efficacy in treating RO16 in textile wastewater, positioning it as a promising candidate for sustainable and efficient wastewater treatment applications. This research contributes valuable insights into the development of advanced photocatalytic materials for textile dye degradation in wastewater treatment.

Combined metabolomics and proteomics to reveal the mechanism of S. oneidensis MR-1 degradation malathion enhanced by FeO/C

Iron oxide @ biochar (FeO/C) promotes bacterial growth and facilitates electron transfer, thereby effectively promoting malathion degradation by Shewanella oneidensis MR-1 (S. oneidensis MR-1). This study elucidated the underlying mechanism of FeO/C-enhanced malathion degradation by S. oneidensis MR-1 through a combination of metabolomics and proteomics analysis. The kinetic fitting results from the degradation experiment indicated that 0.1 g/L FeO/C exerted the most significant enhancement effect on malathion degradation by S. oneidensis MR-1. Observations from Scanning Electron Microscopy and Laser Scanning Confocal Microscopy, along with physiological and biochemical analysis, showed that FeO/C enhanced the growth and oxidative response of S. oneidensis MR-1 under malathion stress. In addition, metabolomics and proteomics analysis revealed an increase in certain electron transfer related metabolites, such as coenzymes, and the upregulation of proteins, including coenzyme A, sdhD, and petC. Overall, spectroscopic analysis suggested that Fe2+, which was reduced from Fe3+ by S. oneidensis MR-1 in FeO/C, promoted electron transfer in S. oneidensis MR-1 to enhance the degradation of malathion. This study offers enhanced strategies for efficient removal of malathion contaminants.

Two Paenibacillus spp. strains promote grapevine wood degradation by the fungus Fomitiporia mediterranea: from degradation experiments to genome analyses

Ascomycetes, basidiomycetes and deuteromycetes can degrade wood, but less attention has been paid to basidiomycetes involved in Esca, a major Grapevine Trunk Disease. Using a wood sawdust microcosm system, we compared the wood degradation of three grapevine cultivars inoculated with Fomitiporia mediterranea M. Fisch, a basidiomycete responsible for white-rot development and involved in Esca disease. The grapevine cultivar Ugni blanc was more susceptible to wood degradation caused by F. mediterranea than the cultivars Cabernet Sauvignon and Merlot. Solid-state Nuclear Magnetic Resonance (NMR) spectroscopy showed that F. mediterranea preferentially degrades lignin and hemicellulose over cellulose (preferential, successive or sequential white-rot). In addition, co-inoculation of sawdust with two cellulolytic and xylanolytic bacterial strains of Paenibacillus (Nakamura) Ash (Paenibacillus sp. (S231-2) and P. amylolyticus (S293)), enhanced F. mediterranea ability to degrade Ugni blanc. The NMR data further showed that the increase in Ugni blanc sawdust degradation products was greater when bacteria and fungi were inoculated together. We also demonstrated that these two bacterial strains could degrade the wood components of Ugni blanc sawdust. Genome analysis of these bacterial strains revealed numerous genes predicted to be involved in cellulose, hemicellulose, and lignin degradation, as well as several other genes related to bacteria-fungi interactions and endophytism inside the plant. The occurrence of this type of bacteria-fungus interaction could explain, at least in part, why necrosis develops extensively in certain grapevine varieties such as Ugni blanc.

Improved photocatalytic degradation of malachite green, crystal violet and antibacterial activity of mesoporous Zn1-xCoxO nanoflakes

ABSTRACT The photocatalytic ability of the Zinc Oxide nanoparticles can be significantly enhanced through transition metal doping. In this work, Zn1-xCoxO nanoparticles were synthesised by a chemical coprecipitation method at room temperature. XRD studies indicated non-monotonic decrease in the Scherrer’s crystalline size from 19.79 nm for the pristine ZnO NPs to 14.81 nm for 2.5% Co2+ doped ZnO nanocrystals. The morphology of the nanoparticles was revealed by FESEM to resemble nanoflakes, and the existence of Co, Zn and O elements was verified by EDS findings. Tauc plots demonstrated a shrinkage of the optical band gap from 3.15 eV to 2.98 eV. The mesoporous nature and noteworthy increase in specific surface area (from 22.198 m2/gm to 54.159 m2/gm) were revealed by BET analysis of the N2 adsorption of the nanoflakes. Further, the degradation experiments of cationic dyes Malachite Green (MG) and Crystal Violet (CV) were carried out in the presence of synthesised catalysts under a high-pressure mercury vapour (450W-UV) lamp. Among the doped ZnO nanocatalysts, 2.5% Co2+ doped ZnO nanoflakes showed the most efficient photocatalytic degradation against MG (97.87%) and CV (93.27%) in 20 minutes. Furthermore, antibacterial activity was investigated against pathogenic bacteria Staphylococcus aureus, Bacillus subtilis and Escherichia coli which revealed improved bactericidal effects of 2.5% Co2+ doped ZnO nanoflakes. Hence, the current finding explored 2.5% Co2+ doped ZnO nanoflakes can serve as dual role efficient and potential candidate for eradication of organic as well as microbial contaminants from wastewater.

Redox-Responsive Hydrogels Loaded with an Antibacterial Peptide as Controlled Drug Delivery for Healing Infectious Wounds.

Infectious wounds occur when harmful microorganisms such as bacteria or viruses invade a wound site. Its problems associated include delayed healing, increased pain, swelling, and the potential for systemic infections. Therefore, developing new wound dressing materials with antibacterial effects is crucial for improving the healing process. Here a redox-degradable hydrogel loaded with an antibacterial peptide (vancomycin) in a straightforward gram-scale synthesis, is developed. The hydrogel structure consists of a disulfide bond-containing hyperbranched polyglycerol (SS-hPG) that is cross-linked by 4-arm polyethylene glycol-thiol (4-arm PEG-SH). The polymerization mechanism and full characterization of SS-hPG are described as this synthesis is reported for the first time. Rheology is used to ascertain the hydrogel's mechanical characteristics, such as stiffness, and self-healing, determining these properties for different ratios and concentrations of both gel components. The incorporation of disulfide bonds in the hydrogel is proved by conducting degradation experiments in reductive environments. Fluorescein isothiocyanate-albumin (FITC-BSA) and vancomycin both are loaded into the gel, and the guest release kinetics is assessed for both slow and on-demand releases. Finally, the in vitro and in vivo experiments prove that the vancomycin-loaded hydrogel acts as an antibacterial barrier for wound dressing and accelerates the healing of infectious wounds in a mouse model.

Visible light-induced photocatalytic degradation of tetrabromobisphenol A on platinized tungsten oxide

In this study, we investigated the degradation of the flame retardant tetrabromobisphenol A (TBBPA) using platinized tungsten oxide (Pt/WO3), synthesized via a simple photodeposition method, under visible light. The results of degradation experiments show a significant enhancement in TBBPA degradation upon surface platinization of WO3, with the degradation rate increasing by 13.4 times compared to bare WO3. The presence of Pt on the WO3 surface stores conduction band electrons, which facilitates the two-electron reduction of oxygen and enhances the production of valence band holes (hVB+) and hydroxyl radicals (●OH). Both hVB+ and ●OH are significantly involved in the degradation of TBBPA in the visible light-irradiated Pt/WO3 system. This was verified through fluorescence spectroscopy employing coumarin as a chemical probe and oxidizing species-quenching experiments. The analysis of degradation products and their toxicity assessment demonstrate that the toxicity of TBBPA-contaminated water is significantly reduced after Pt/WO3 photocatalysis. The degradation rate of TBBPA increased with increasing Pt/WO3 dosage, reached an optimum at a Pt content of 0.5 wt%, but decreased with increasing TBBPA concentration. The decrease in degradation efficiency of Pt/WO3 was minor, both in the presence of various anions and after repeated use. This study proposes that Pt/WO3 is a viable photocatalyst for the degradation of TBBPA in water under visible light.

Photocatalytic activity of Ho3+-Yb3+ activated BiVO4 upconverting phosphors

The BiVO4:Ho3+-Yb3+ upconverting phosphors have been synthesized by using the chemical co-precipitation method and optimized with 0.7 % Ho3+ + 6 % Yb3+ combination through frequency upconversion emission study. The synthesized phosphors have been characterized through XRD (X-Ray diffraction), FESEM (Field emission scanning electron microscopy), HR-TEM (High resolution- Transmission electron microscopy), UV–vis diffuse reflectance spectroscopy (DRS), Raman, and FT-IR (Fourier transform infrared spectroscopy). The XPS (X-ray photoelectron spectroscopy) analysis has been performed to study the elemental composition, chemical, and electronic states of the atoms present in the optimized sample. The specific surface area of the pure and optimized phosphors has been determined through BET (Brunauer-Emmett-Teller) analysis. From the XRD analysis, it is clear that on doping, the crystal structure of BiVO4 changes from monoclinic to tetragonal structure. The values of rate constants for the photocatalytic performance of the upconverting codoped and pure BiVO4 phosphors under the illumination with an artificial solar lamp for degradation of MB dye are found to be 0.00498 min−1 and 0.00269 min−1, respectively. To verify these results, the same experiment has also been performed under the visible LED (Light-emitting diode) light illumination. This enhancement of ∼ 85 % in the rate constant of the photocatalytic performance ensured the utilization of the NIR portion of the light by the codoped BiVO4 phosphors through the frequency upconversion process. The material’s recycling photocatalysis experiment for three cycles has been performed to check its reusability. The upconversion emission and XRD analysis of the materials after photocatalysis have been performed. From this study, it is confirmed that the stability of the sample is better even after three cycles of photocatalytic dye degradation experiment.

Preparation of chitosan/Tenebrio molitor larvae protein/curcumin active packaging film and its application in blueberry preservation

With growing concerns about postharvest spoilage of fruits, higher requirements have been placed on high-performance and sustainable active packaging materials. In this study, we prepared curcumin-based functional composite films using chitosan (CS) and Tenebrio molitor larvae protein (TMP) as the substrates. The effects of curcumin concentration on the structural and physicochemical properties of the composite films were determined. Curcumin was equally distributed in the polymer film through physical interactions. Furthermore, the curcumin composite film with 0.3 % addition exhibited a 27.39 % increase in elongation at break (EBA), a 37.04 % increase in the water vapor barrier, and strong UV-blocking properties and antioxidant activity compared with the control film (CS/TMP). The degradation experiment of the composite film on natural soil revealed that the composite film exhibited good biodegradability and environmental protection. Furthermore, the applicability of functional composite films for preserving blueberries was investigated. Compared with the control film and polyethylene (PE) films, the prepared composite films packaging treatment reduced the decay rate and weight loss rate of blueberries during storage, delayed softening and aging, and maintained the quality of blueberries. Using sustainable protein resources (TMP) and natural polysaccharides as packaging materials provides an economically, feasible and sustainable way to achieve the functional preservation of biomass materials.

Novel FeOOH-decorated La-doped Bi4O5I2 microspheres for boosting photocatalysis-Fenton synergy degradation of emerging contaminants

Photocatalytic-Fenton synergistic degradation of pollutants in wastewater is considered a promising technology for environmental treatment. Herein, FeOOH quantum dots decorated La-doped Bi4O5I2 hybrids were prepared using an in-situ deposition strategy and applied for the removal of 2,4-dinitrophenylhydrazine. The FeOOH-1/La10-Bi4O5I2 sample exhibits the highest catalytic activity in degradation experiments, eliminating 93.8 % of 2,4-dinitrophenylhydrazine within 30 min at a reaction rate constant of 0.117 min−1. In addition, the impacts of several operational parameters on the catalytic activity were comprehensively examined, including H2O2 concentration, catalyst dosage, reaction solution pH and co-existing ions. In degradation process of 2,4-dinitrophenylhydrazine, the major reactive oxygen species are ·OH and ·O2–, with ·OH generated by Fenton reaction. Optical property characterization, cyclic voltammetry tests, and photoelectrochemical measurements confirmed that the FeOOH-1/La10-Bi4O5I2 composite has excellent light absorption capacity, abundant active centers, and excellent carrier separation efficiency. Finally, the degradation mechanism of FeOOH-1/La10-Bi4O5I2 composites for 2,4-dinitrophenylhydrazine is rationally discussed based on experimental and theoretical calculations. This study presents a fresh design idea for developing bismuth oxyhalide-based composites with high activity.

Functionalized sea urchin-like MnO2 with chitosan to load CaCo layered double hydroxides for advanced catalytic oxidation of antibiotics through activation of peroxymonosulfate

Novel composite catalysts based on the functionalization of sea urchin-like MnO2 with chitosan (CS) to load CaCo layered double hydroxides were prepared by a simple hydrothermal method, and the physicochemical properties of the resulting MnO2@CS-CaCo LDHs were analyzed by various characterization methods. Then advanced oxidation processes (AOPs) were constructed based on MnO2@CS-CaCo LDHs through activation of peroxymonosulfate (PMS) to degrade ciprofloxacin (CIP), norfloxacin (NOR) and sulfamethoxazole (SMX) in water. Sea urchin-like MnO2 modified by CS created a unique interface and a variety of active functional groups for the loading of CaCo LDHs where MnO2 particles were uniformly attached to the surface of CaCo LDHs. The results showed that the MnO2@CS-CaCo LDHs composites had excellent catalytic performances compared with monomeric MnO2, MnO2@CS and CaCo LDHs, and the enhanced catalytic performances were mainly due to the synergistic effects between LDHs, CS and MnO2. Under optimal experimental conditions, the removal efficiencies of CIP and NOR reached up to 96.45 % and 96.58 % within 20 min, respectively, and the removal of SMX was 93.12 % within 30 min. Quenching experiments demonstrated that 1O2 was the main active oxygen species for catalytic degradation through a non-radical pathway. In addition, the degradation efficiency of NOR was still as high as 93.78 % after the 10th cycle of degradation experiments, indicating that the composite catalysts had excellent reproducibility and stability. Finally, the activation mechanisms of MnO2@CS-CaCo LDHs/PMS and degradation pathways of SMX were proposed. The catalytic performances of MnO2@CS-CaCo LDHs/PMS for removal of three drugs in actual water bodies were further evaluated their practical application ability.

Oxygen vacancy-rich β-Bi2O3/Bi2O2SiO3 Z-Scheme heterojunction: A strategy to enhance visible light-driven photocatalytic removal of ARB and ARGs

Oxygen vacancy-rich β-Bi2O3/Bi2O2SiO3 (BO/BOS) Z-Scheme heterojunction was prepared by hydrothermal method-assisted calcination. Under visible light, β-Bi2O3/Bi2O2SiO3 photocatalyst demonstrated superior photocatalytic efficacy in degrading antibiotics and antibiotic-resistant Escherichia coli (AR E. coli) compared to individual β-Bi2O3 and Bi2O2SiO3. The experimental results showed that BO/BOS-450 sample possessed the best photocatalytic activity against tetracycline (2 h, 80.8%), amoxicillin (4 h, 57.9%) and AR E. coli (3 h, 107.43 CFU·mL−1). BO/BOS-450 sample showed 91.8% electrostatic capture of AR E. coli in the bacterial capture experiment. In the antibiotic-resistant genes (ARGs) degradation experiment, BO/BOS-450 sample was able to bring the log10 (Ct/C0) value of tetA to -3.49 after 2 h. Oxygen vacancies (OVs) were verified through HR-TEM, XPS and EPR analyses. ESR experiments aligned with the quenching experiment results, confirming that the crucial active species were ‧O2- and h+ during photocatalytic sterilization. A small-scale sewage treatment equipment was designed for the effective removal of ARB from real water samples.

Efficacy and mechanism of activation peroxymonosulfate for tetracycline degradation by AC-MIL-101(Fe)-derived magnetic CuO/Fe2O3/CuFe2O4

In this work, magnetic CuO/Fe2O3/CuFe2O4 (CFC-0.50) composites were prepared by using a complex of the metal–organic skeleton AC-MIL-101(Fe) and Cu as a precursor. The compositional structure of the catalysts was observed via XRD, FTIR, SEM, and TEM, and the physicochemical properties of the catalyst materials were analyzed via characterization methods such as BET and VSM. Degradation experiments using TC as the target antibiotic were performed to screen the optimal catalyst, CFC-0.50, by modulating different doping ratios of Cu/AC-MIL-101(Fe) to study the effects of changes in key parameters of the catalyst environment on the degradation efficiency of TC and to investigate the stability and applicability of CFC-0.50. The reaction mechanism of the CFC-0.50/PMS/TC system was proposed by using XPS to study the chemical shape of the catalyst before and after the reaction and supplemented by quenching experiments, EPR, and EIS and LSV. The intermediate products of the reaction system were analyzed via LCMS, and possible degradation pathways were proposed.