Degradation Percentage Research Articles

Insights into Novel Doping Effect of Fe-Doped ZnS Nanostructures Derived from Oxystelma Esculentum: Kinetics-Based Photocatalysis, Nitrogen Fixation, and Antifungal Efficacy

Implementing greener approaches is a sustainable and eco-friendly methodology for nanocomposite synthesis. This work reports the sustainable fabrication of Fe-doped ZnS (Fe0.3Zn0.7S) nanocomposite and its broad-spectrum applications. The systematic characterization was carried out using several advanced analytical techniques. DLS, Zeta potential, SEM, XPS, and TEM performed morphological and size assessments of the engineered nanocomposite. Eventually, XRD provided valuable insights into the crystalline behavior of nanocomposite. The nanocomposites were then treated against the organic dye Safranin O, which displayed 93% degradation within an hour with the rate constant value of 0.0326 min−1. Parameters influencing the percentage degradation, such as temperature, pH, etc., were also discussed. Moreover, an LCMS test was also conducted to evaluate the presence of reactive intermediates. Safranin O’s degradation was confirmed by identifying intermediate products, such as compounds with m/z values of 335.84, 321.81, 306.79, 292.77, and 257.32, which were indicative of progressive dye breakdown. Finally, the photocatalytic enactment examination verified that the prepared nanocomposite’s nitrogen fixation rate (38.96 µmolg−1) was way greater (~4 times) than the pristine compound. In addition, prepared nanoparticles demonstrated a befitting ability to eliminate a wide range of threatening pathogenic fungi. The doping of Fe into ZnS further enhanced the inhibition against Fusarium oxysporum.

Remediation of antibiotics-contaminated wastewater through photocatalytic techniques: implications for SDGs that support a more sustainable future and a healthy planet

ABSTRACT This paper aims to provide information on the remediation of various antibiotics from contaminated wastewater by photocatalytic treatment techniques. The review includes the mechanism of action of pharmaceuticals, pharmaceuticals as environmental pollutants, antibiotics and their metabolites, toxicity and health implication of antibiotics-contaminated wastewater, measures to manage antibiotics in the environment, the different wastewater treatment technologies, the degradation and mechanism of antibiotics via photocatalysis, and the Sustainable Development Goals (SDGs) relating to the treatment of antibiotics-contaminated wastewater. Photocatalysis has more advantages than other treatment techniques due to its simplicity, cost-effectiveness, and higher percentage degradation of antibiotics in wastewater. The use of photocatalytic methods to purify antibiotic-contaminated wastewater has substantial ramifications for several SDGs, hence promoting a healthier world and a more sustainable future. This paper is presumed to offer some insight on the treatment technique that is more efficient and suitable for antibiotics-contaminated wastewater that can be explored on an industrial scale.

Biosynthesis, characterization of Ag2O nanoparticles for enhancement of antioxidant and photo degradation activities

Silver oxide (Ag2O) nanoparticles were synthesized via Biosynthesis methods using Croton macrotachyus leaf extract silver sulphate (Ag2SO4) was used as precursors and the extract was used in the reactions as reducing, stabilizing and capping agents which is a very easy and inexpensive synthesis method. Metal oxide nanoparticles characterized using UV–visible, TGA, Fourier transform infrared(FTIR),powder X-ray diffraction(XRD), X-ray photoelectron(XPS), and Scanning Electron Microscopy(SEM) with Energy Dispersive X-Ray(EDX) and Transmission Electron Microscopy(TEM), High Resolution Transmission Electron Microscope(HRTEM), and Selected Area Electron (SAED) which is used for determination of crystalline size, morphology,particle size and oxidation state with composition of elements in the sample. Metal oxide nanoparticles have a significant photo catalytic performance under visible light source confirmed that study supported Ag2O spherical structure, which exhibits enhanced photo catalytic activity and anti-oxidant activities as well as the size of the Ag2O nanoparticles was between 16 nm and 21 nm from the XRD(Scherrer equation),SEM & TEM) imaje software and Photo catalytic activity of Ag2O NPs were assessed against methylene blue (MB) dye degradation under natural sunlight illumination for 60 min. This sustainably photo degraded in direct solar irradiance with remarkable degradation percentage which is greater than 96.35 % and Scavenging activities Ag2O nanoparticles enhanced DDPH scavenging activities was 88 %

Enhanced cathodic electrodes from V2O5 nanorods: Pioneering organic dye degradation and optimized catalysis for sustainable supercapattery devices

Encapsulating the essence of multifunctionality, the synthesized Vanadium Pentoxide (V2O5) nanorods (NRs) are adaptable innovators of visible-light photocatalytic degradation and sustainable supercapattery device fabrication. Meanwhile, the physicochemical properties are investigated by precise instruments. The V2O5 NRs demonstrate improved photocatalytic performance over a 100-min duration, effectively catalyzing the methylene blue (MB) degradation with a remarkable degradation percentage of 98.37 % (25 mg catalysis) and shows a lower wavelength shift due to MB molecular braking. In a groundbreaking twist, this work utilises tainted V2O5 NRs, ingeniously repurposing them to energy storage tenacities. In addition, the electrochemical assessment of tainted V2O5 NRs demonstrated subtle changes after MB degradation, increasing the specific capacity (Cs) value from 794 to 933C.g−1 due to developing reduced particle agglomeration. Moreover, the better Cs value of tainted V2O5 NRs reached 95.02 % after 500 cycles (5 A.g−1). The fabricated asymmetric supercapattery (ASC) device demonstrates superior ion diffusion processes, as evidenced by Dunn's method calculations, particularly at a scan rate of 5 mV.s−1. Additionally, the assembled device underscored their unique positioning between battery and capacitor materials, distinctly supported by a “b” value of 0.8 and superior capacity retentivity. They reached a superior power (P = 191.75 W.kg−1) with energy (E = 50 Wh.kg−1) and better cyclic stability, maintaining their performance over 4000 cycles at 5 A. g−1 (91.3 %). Furthermore, under exposure to the light of a yellow light emitting diode (LED) for 30 s, the real-time consequences of after cyclic stability material of tainted V2O5 NRs are investigated, providing meaningful insights into their performance dynamics.

Toxic Dye Degradation Employing Phoenix dactylifera Seed Extract for the Green Synthesis of Silver Nanoparticles: Characterization and Application.

This research highlights the facile green synthesis of silver nanoparticles (AgNPs) using Phoenix dactylifera seed extracts and its photocatalytic application for the degradation of toxic dyes. The AgNPs synthesis was confirmed by the appearance of its representative absorption peak at 416 nm in UV-visible absorption spectroscopy. Moreover, the reduction of silver ions to Ag was justified through Fourier transform infrared (FTIR) spectroscopy. X-ray diffraction pattern revealed crystalline AgNPs structure with particle size ranging from 5 to 15 nm calculated using the Debye-Scherrer equation. The rectangular-like structural morphology of synthesized AgNPs was observed in scanning electron micrographs. The as-synthesized AgNPs demonstrated higher photocatalytic activity for the degradation of malachite green (MG) and congo red (CR) followed by methylene blue (MB), and crystal violet (CV) under UV irradiation. In addition, rate constant (k) and percentage degradation were also calculated. The present study presents a facile green synthesis pathway and its potentially successful manipulation in the reduction of toxic dyes under the illumination of UV-light.

Degradation of salicylic acid coordinated to Fe3O4 nanoparticles by H2O2

Salicylic acid (SA) has strong tendency to form complexes with iron (III). Depending upon the concentrations of SA, the complexes formed are FeR+, FeR2+, FeR32+where R represents salicylate ion (-OC₆H₄COO-). Fe3O4 nanoparticles binds with the salicylate ions through the sites having Fe3+ and at the site containing Fe2+ reacts with H2O2 to produces OH* radicals. The OH* radicals oxidise the salicylic acid attached to Fe3O4 nanoparticles. Thus, the degradation occurs through the formation of SA-Fe3O4 nanoparticles complexes and then followed by the reaction with H2O2 at the nanoparticle site. FT-IR, TGA were used to confirm the synthesis of Fe3O4 nanoparticles as well as to investigate SA-Fe3O4 nanoparticles complex formation and the degradation of the complex by H2O2. Spectrophotometric studies were employed for the monitoring of the degradation of SA at the surface. Here, the nanoparticles act as platform to which both the reactants SA and H2O2 get activated and the degradation reaction occurs. The concentrations of SA, H2O2, nanoparticle dosage, surfactants and polymers were changed and the % degradation were noted. It has been observed that the degradation percentage decreased with the increase in nanoparticle dosage, [surfactant] and [polymers]. The [H2O2] and [HClO4] gave peaked-like curve for the degradation of SA for the plot of % degradation versus concentrations of H2O2 and HClO4. Degradation of SA was observed maximum at [H2O2](= 8.0 × 10−4 mol dm−3) and at [HClO4] (= 1.0 × 10−2 mol dm−3).

Silk fibroin/gelatin electrospun nanofibrous dressing loaded with roxadustat accelerates wound healing in diabetic rats via HIF-1α stabilization

Diabetes presents significant health risks, including diabetic foot ulcers, which can lead to amputation or death if left untreated. It has been acknowledged that hypoxia-inducible factor-1 alpha (HIF-1α) dysfunction in diabetic wounds delays healing and tissue repair. This study explores the therapeutic potential of roxadustat (ROX), a novel HIF-1α stabilizer, within an optimized electrospun gelatin/silk fibroin nanofibrous dressing (ROX-NF). The dressing's properties were optimized using a 22 full factorial design, with varied gelatin (GN) and silk fibroin (SF) amounts as factors and responses including degradation, porosity, swelling, drug release, and drug content percentages. In vitro characterization of the optimized ROX-NF showed a degradation rate of 90.24 ± 1.29 %, porosity of 84.41 ± 3.04 %, cumulative drug release of 93.13 ± 3.05 % over 48 h, and a high drug content of 99.12 ± 0.02 %, with structural analyses confirming successful ROX integration within the nanofibrous matrix. Additionally, in vivo evaluation of the optimized ROX-NF in diabetic rat models demonstrated accelerated wound closure, achieving 5.17 ± 1.2 % wound area by day 14 compared to 19.3 ± 2.8 % with ROX dispersion. Histological analysis revealed enhanced collagen deposition, neovascularization, and organized epidermal and dermal layers. Furthermore, PCR, ELISA, and Western blot assays demonstrated a marked upregulation of key wound healing markers, including HIF-1α, TGF-β, VEGF, and collagen I, in the ROX-NF group relative to ROX dispersion. These findings underscore the efficacy of combining ROX with nanofiber characteristics, offering a promising approach for diabetic wound management through accelerated wound closure and enhanced tissue regeneration.

Waste upcycling of Sapota peels as a green route for the synthesis of silver nanoparticles and their application as catalytic and colorimetric detection of Co2+ and Hg2+

Biochemical synthesis of nanoparticles (NPs) using plant part extracts as capping and reducing agents has drawn considerable attention in research with a growing focus on green chemistry. The present study utilized Sapota (Manilkara zapota L.) peel extract to synthesize silver nanoparticles (SP-AgNPs) using ultrasonic vibration. Different characterization techniques such as UV-vis spectroscopy, dynamic light scattering, Fourier Transform Infrared Spectroscopy, Field emission scanning electron microscope, High resolution transmission electron microscopy, and X-ray diffraction were employed to check the production of SP-AgNPs. The AgNPs were crystalline in nature and had an average particle size of 27.906 nm. The research primarily focused on two aspects: the catalytic activity of SP-AgNPs in degrading environmental pollutants and their ability to act as colorimetric sensors for toxic metal ions. SP-AgNPs exhibited significant catalytic activity in the decomposition of various pollutants such as Methyl Orange (0.035 ± 0.090 min−1, 92.89 ± 1.79%), Crystal Violet (0.1097 ± 0.1016 min−1, 85.56 ± 2.21%) and Cosmic Brilliant Blue G-250 (0.0697 ± 0.0275 min−1, 79.56 ± 1.80%). The high degradation percentages and reaction rate constants indicate the efficiency of SP-AgNPs in pollutant degradation. Additionally, the study demonstrated the effectiveness of SP-AgNPs as sensors for detecting toxic metal ions, particularly Co2+ and Hg2+ with limits of detection 54.40 ± 1.43 µM and 10.70 ± 0.16 µM. With impressive sensitivity and low detection limits, SP-AgNPs showed promise in detecting these ions, which are often found in environmental contaminants. Moreover, their plant-based synthesis, low toxicity, and cost-effectiveness make them attractive options for environmental remediation efforts.Graphical abstract

Electrochemical Treatment of Doxycycline-Containing Wastewater from Pharmaceutical Industry in Batch and Once-Through Continuous Mode

Abstract Doxycycline (DOXY), a widely used antibiotic during COVID-19, was overused, leading to concerns about contamination of aquatic environments and environmental problems. The present study used the Ti/TiO2-RuO2-IrO2 electrode for DOXY's electrochemical oxidation (EO) in batch and once-through continuous mode operations. Process parameters were optimized using a response surface methodology (RSM)-Box-Behnken Design (BBD) model. The impact of key input parameters, including time (t), current density (j) (mA/cm2), and pH, on the percentage of DOXY degradation and energy consumption was systematically investigated. Under optimal conditions pH = 3, t = 73 min, and j = 11.63 mA/cm2, DOXY degradation achieved 91% with an energy consumption of 5.283 kWh/m³. In the once-through continuous mode EO process, optimal conditions reached 91% DOXY degradation with an energy consumption of 13.98 kWh/m³, achieved at a residence time (Rt) of 139 min, elapsed (Et) time of 100 min and at j = 20.40 mA/cm2. The EO process utilizing Ti/TiO2-RuO2-IrO2 electrodes demonstrates significant potential for the degradation of DOXY, primarily due to its enhanced degradation efficiency. This method's superior performance highlights its viability as a highly effective approach for the treatment of DOXY-contaminated wastewater.

Broad photoluminescence and photocatalysis from functional carbonaceous material-metallized porphyrin composites for UV-Vis light harvesting

Abstract Carbon in its many form has attracted huge attraction over the years owing to its biocompatibility, processability, stability and optical properties for its utilization in UV-Vis light harvesting in pure as well as modified schemes such as composite. This study reports green precursor synthesis as well as optical, structural, luminescence and catalysis study of functional carbonaceous material (FCM) in pure and composite form. This high-order self-assembly of FCM possess extraordinary photophysical and chemical properties with its functional groups rich surface making it suitable for π-π* transitions. Further its composite formation with a high absorption coefficient (more than 20,000 cm-1 in broad visible range 400-700 nm) and non-radiative (near IR) fluorescence quenching exhibiting metallized porphyrin is shown to be suitable for photocatalysis applications. These conclusions have been established using XRD, FESEM, EDX, FTIR, UV-Vis, FL and Raman spectroscopy measurements. Broad range photoluminescence for pure FCM (300-550 nm) as well as its porphyrin-based composite (400-550 nm) and further the application of composite in the photocatalytic ability for the degradation of standard methylene blue dye for degradation percentage of 62% in 120 mins in visible light while 30% in 180 mins in dark shows the correlation for sustainable synthesis and application of FCM-porphyrin composite.

Investigation of photocatalytic and corrosion resistance properties of Zr-Ag doped SnO2 Nanoparticles: The impact of calcination temperature

Herein, the synthesis of Zr-Ag doped SnO2 nanoparticles at different calcinating temperatures via simple chemical methods for photocatalytic and corrosion resistance application has been discussed. The XRD analyses describe that increasing the temperature revealed a polycrystalline nature with an increased crystallite size. The SEM and EDX analyses have confirmed the agglomerated surface morphology and the occurrence of elements in the samples. The Optical properties were evaluated using UV–vis absorption spectroscopy. Redshifts were detected, and samples’ band gap energies decreased from 3.54–3.14 eV. The photocatalytic performance of the nanoparticles in degrading safranin dye under sunlight was evaluated at various calcination temperatures. A degradation percentage of 96.5 % was observed at 500 °C. However, the calcination temperature does not appear to significantly impact the photocatalytic activity, as evidenced by the comparable results of 400 °C (95.7 %) and 600 °C (93.8 %). The electrochemical behavior of the synthesized nanoparticles coated in an MS plate was investigated through electrochemical impedance spectroscopy (EIS) and linear sweep voltammetry studies under an acidic environment. Further, the dense coatings and the annealing temperature provide well-refined grains, leading to dual protection for the MS alloy and enhancing corrosion resistance.

ZnO/CuO heterojunction prepared by sol-gel: characterization and photocatalytic evaluation

ZnO, CuO and the ZnO/CuO heterojunction were prepared using zin acetate and copper acetate by sol-gel method. The materials were characterized by: TGA, XRD, XPS, SEM, TEM, EDS and UV-Vis. The heterostructure showed a synergistic effect compared to pure materials. The XPS results confirm the existence of a heterostructure. The morphology is a combination of characteristic morphologies of ZnO and CuO. The bandgap of ZnO decreases with the incorporation of CuO. The photocatalytic efficiency of the heterostructure increases; the degradation percentages were better for the heterostructures in both radiations: Ultraviolet and Visible.

Effect of rGO on photocatalytic performance of Fe2O3-ZnO/rGO nanocomposite

The methods of removing various pollutants from water, due to the limitation of drinking water resources and also the increase in the production of pollutants from various industries, have been widely considered. A green technique that has emerged as a promising process in the degradation of numerous organic pollutants from water is the photocatalytic process. Here, Fe2O3-ZnO/rGO nanocomposites with 0.5, 1, 2 mass percentages of rGO nanosheets were successfully fabricated. These nanocomposites have been characterized by XRD analysis, FESEM, Raman spectroscopy and UV-vis spectrophotometer. Next, the photocatalytic activity of Fe2O3-ZnO/rGO nanocomposites in removing RhB dye was studied. Fe2O3-ZnO/1% rGO nanocomposite showed the best photocatalytic performance with a degradation percentage of 100% in 180 min with a rate constant of 0.020 min−1 and a half-life of 34.7 min. Finally, this optimal photocatalytic activity was attributed to the smaller optical gap of this nanocomposite.

Biosynthesis of gold and silver nanoparticle using water hyacinth (Eichhornia crassipes) extract for photocatalytic degradation of organophosphate and organochlorine pesticide

The study aimed to assess the efficiency of synthesized gold (Au) and silver (Ag) nanoparticles in the degradation of organochlorine and organophosphate pesticides through photocatalysis. The synthesis of gold and silver nanoparticles was achieved using Eichhornia crassipes (water hyacinth extract). Photocatalytic degradation tests were conducted on organochlorine and organophosphate pesticides using gold and silver nanoparticles, with the absorbance of the samples measured by a UV spectrophotometer. The photocatalytic degradation rates of organochlorine and organophosphate were determined, with varied concentrations of the synthesized nanoparticles. The results showed high degradation rates at lower concentrations (10–20 ppm), with degradations of 51.789%, 47.954%, 47.983%, 44.088%, 41.565%, and 36.749% for 25/75, 50/50, and 75/25 Au nanoparticle ratios, respectively. The results also revealed that higher degradation rates were observed at longer reaction times (70–80 minutes), with percentage degradations of 44.344% and 49.987%, 41.754% and 45.937%, 36.773% and 40.458% for 25/75, 50/50, and 75/25 Au nanoparticle ratios, respectively. Lower degradation efficiencies were observed at shorter reaction times (10–20 minutes), with percentage degradations of 15.356% and 19.982%, 13.746% and 17.082%, and 10.976% and 15.167% for 25/75, 50/50, and 75/25 ratios, respectively. Additionally, the results showed high degradation rates at lower concentrations (10–20 ppm) for Ag nanoparticles, with percentage degradations ranging from 40.814% to 44.822% across AgNP ratios (25/75, 50/50, 75/25), indicating efficient degradation at lower concentrations. Conversely, at higher concentrations (60–80 ppm), the degradation efficiency was notably lower, with percentage degradations ranging from 7.004% to 13.539% across different AgNP ratios. In conclusion, Au nanoparticles exhibited higher photocatalytic efficiency than Ag nanoparticles, particularly in degrading organophosphate (Sniper) pesticides. It is recommended that these synthesized nanoparticles be considered as environmentally friendly and cost-effective options for pesticide degradation.

Optimization and reusability of photocatalytic g-C3N4/W-TiO2/PVDF membranes for degradation of sulfamethazine.

Pharmaceuticals and personal care products (PPCPs) are prevalent emerging pollutants in the aquatic environment. The photocatalysis process has proven high efficiency in degrading PPCPs; however, the fate and repercussions of photocatalyst residuals are a major concern. To avoid that, we developed a composite from graphitic carbon nitride/tungsten doped with titanium dioxide (g-C3N4/W-TiO2) and loaded it on polyvinylidene fluoride (PVDF) membranes by the phase-inversion method. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and other different analyses implied the successful synthesis of g-C3N4/W-TiO2 composite and coating on PVDF membranes. A Box-Behnken design (BBD) was used to optimize the operational parameters, including pH, g-C3N4 ratio in the composite, and initial SMZ concentration by the response surface methodology (RSM). The highest SMZ degradation percentage was 98.60% after 240min of irradiation. Liquid chromatography with tandem mass spectrometry (LC-MS/MS) along with suspect screening was used to identify the intermediate transformation products and propose the SMZ degradation pathway. The loss in membrane activity after five cycles of photocatalytic degradation was about 18%. According to the current study, the photocatalytic membrane g-C3N4/W-TiO2/PVDF is promising for removing sulfonamide antibiotics from wastewater.

Synergistic degradation of refractory organic pollutant by underwater bubbling plasma combined with heterogeneous Fenton process

Excessive discharge of the refractory organic pollutants endangers the development of the society and economy, thus seeking an efficient wastewater abatement method is an urgent need. Herein, Iron (Ⅱ) sulfide (FeS) was employed as the heterogeneous catalyst and coupled with underwater bubbling plasma (UBP) for the elimination of the refractory organic pollutant, malachite green (MG). FeS catalyst was synthesized using the solvothermal method and subsequently characterized comprehensively, focusing on its microstructure, specific surface area, chemical bonds and elements valence states. The UBP system combined with FeS (UBP/FeS) exhibited the robust synergism with a maximum synergistic factor of 1.89. The MG degradation percentage and rate constant were up to 94.7% and 0.237 min−1 within 12 min. The parameter experiments revealed that FeS dosage, pulse frequency, initial MG concentration and solution conductivity of 150 mg/L, 56 Hz, 5 mg/L and 21.8 μS/cm, respective, were more conducive for MG elimination. The MG removal efficiency reached 86.2% after five consecutive applications of FeS. Reactive substances including ·OH, ·O2−, eaq, O3 and H2O2 were confirmed to contribute to MG elimination. Additionally, the conversion circle between ≡ Fe(Ⅱ) and ≡ Fe(Ⅲ) promoted the catalytic conversion of H2O2 and O3 into ∙OH. The comparison of UV–vis spectra and total organic carbon of MG solution before and after reaction revealed the superior degradation of MG in the UBP/FeS system. Hypotheses regarding to the decomposition pathways of MG were formulated based on the identified intermediates. The toxicity level of MG solution was lightened after reaction. The above results indicate that UBP/FeS has the advantages of quick degradation and high efficiency, representing a promising approach for refractory pollutants treatment.

Preparation and evaluation of injectable sustained-release Alendronate-loaded lipid liquid crystal on ovariectomy-induced osteoporosis in rats

Alendronate, a bisphosphonate compound, is used to treat osteoporosis by inhibiting bone resorption. However, oral consumption of Alendronate can cause severe gastrointestinal side effects, such as heartburn, difficulty swallowing, constipation or diarrhea, flatulence, and esophageal irritation or pain. To overcome this problem, an injectable sustained-release formulation of alendronate based on lipid liquid crystal (LLC) using phosphatidylcholine (PC), sorbitan monooleate (SMO), glycerol di-oleate (GDO), and N-methyl-2-pyrrolidone (NMP) or ethanol solvents was recommended. This compound was added as a base to one side of a coupling syringe, while alendronate powder was added to the other. After combining the two syringes, the resulting formulations were transferred into tubes containing PBS for in-vitro evaluation. In formulations containing ethanol, the cumulative percentage of drug release, water content, and degradation were higher than in those with NMP. Furthermore, LLC gel formulations with ethanol solvent had lower viscosity and a cubic structure, whereas LLC containing NMP had a hexagonal structure, indicating slower and longer release of alendronate in LLC-NMP formulations. In-vivo evaluations of subcutaneous injections of alendronate based on LLC formulation in rats with ovariectomy-induced osteoporosis showed significant advancements in osteogenesis markers, including RUNX2, OPG, VEGF, and Type 1 Collagen, according to Western blot analysis. These finding highlight alendronate's potential not only as a bone resorption inhibitor but also as a bone formation stimulator. Additionally, histopathology results revealed no osteoclast activity or osteoarthritis reactions in the LLC formulation group. Hence, an injectable LLC formulation containing PC, SMO and NMP could be a suitable option for developing a sustained-release LLC formulation of alendronate for osteoporosis treatment.

Fruit Extract Mediated Formation of Luminescent Titanium Dioxide Nanometer-Sized Particles: An Innovative Strategy in Domain of Photodecomposition and Germicidal Properties.

Discoveries in nanotechnologies are placing a great deal of attention on greener strategies that use harmless substances and moderated reactions to promote healthy development. This work used a straightforward, innovative, and cost-effective sustainable approach to produce bio-augmented TiO2 nanometer-sized particles (NMSP) by applying a water-based extract of the star fruit as a stabilization and reduction agent. A variety of techniques, comprising UV-Vis, XRD, FT-IR, FE-SEM with EDAX, and TEM, have been employed to investigate the formed TiO2 NMSP. The germicidal properties of formed TiO2 NMSP towards germs have been investigated by implementing an agar-based pore plate technique. Congo red and methylene blue dyes have been applied to assess photodecomposition activity. The TiO2 NMSP exhibited significant germicidal efficacy versus many pathogenic microbes. The maximum degradation percentages of Congo red and methylene blue were 89.2% and 83.7%, achieved after 60 and 70 min, respectively. Consequently, it is determined that the selected NMSP composition enhanced germicidal and photodecomposition capabilities. The combined effort may serve as an effective method for eliminating color degradation concerning effluent and could potentially be employed in the field of medicine to address antibiotic resistance.

Development of flexible and mesoporous CdS/ZnS/PVDF nanocomposites with remarkable organic dye degradation performance under natural sunlight

The engineering of polymer-based nanocomposites is a highly promising strategy for improving both the efficiency and stability of catalysts used in wastewater treatment. In this work, we explore the efficacy of flexible CdS/ZnS/PVDF nanocomposite films towards degradation of Malachite Green dye under low energy visible light and ambient sunlight. Films with varying weight percentage of CdS/ZnS nanofillers (0 %, 5 %, 10 %, 15 %, 20 %) were successfully prepared by solution casting method and the physiochemical properties were characterized using various techniques such as XRD, SEM, AFM, EDX, BET, UV–Vis DRS and FTIR. Pore diameter of 5.5 nm was observed, indicating that CdS/ZnS is mesoporous in nature. Under the optimum photocatalytic condition of 15 ppm dye concentration and pH 9, 15 wt% CdS/ZnS/PVDF showed the maximum photodegradation efficiency of 93.5 % in 30 min. The sample exhibited excellent reusability for five consecutive runs of the experiments which show a degradation percentage of 92.1 % in the fifth run and the scavenging study established that superoxide radicals play the major role in the photodegradation process. The experiments under natural sunlight on three separate days showed a remarkable photodegradation performance of 89 %, 93.4 % and 93.6 % highlighting the potential of CdS/ZnS/PVDF nanocomposites for sustainable wastewater treatment under natural sunlight.

Catalytic degradation of aromatic dyes using triazolidine-thione stabilized Nickel nanoparticles

Nanoparticles have been extensively studied for many years due to their important roles in catalysis, metallurgy and high temperature superconductors. But, Nanoparticles are extremely unstable and easily react with other substances. So, to control the size and the shape of nanoparticles they must be stabilized. Organic Ligands have gain more attention for stabilizing Nanoparticles. In the present work, Nickel Nanoparticles have been synthesized by reduction method and then stabilized by synthesized 5-phenyl triazolidine-thione based organic ligand to achieve larger surface area and good catalytic activity. Stabilized Nickel NPs of different ratios were synthesized for analyzing their catalytic performance against dyes that has become one of the most serious environmental problem causing drastic water pollution. The prepared thione stabilized Nickel nanoparticles were confirmed by UV-Visible and Infrared Spectroscopy. UV/Vis analysis displayed the peak at 236 nm which confirms the metallic Ni NPs formation while, in FTIR peak around 720-750cm-1 is due to the nickel and sulphur bond stretching vibrations. The size, surface morphology and the quality of the stabilized Ni Nanoparticles were analyzed by Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD) analysis. SEM images showed uneven morphology with variously sized and shaped particles. Large surface area is visible which is advantageous for catalytic degradation of pollutants. The degradation process was studied by using UV-visible Spectroscopy. The catalytic behavior of stabilized nanoparticles was evaluated by using various parameters i.e. time, concentration and size of NPs. These parameters were optimized during degradation process to get maximum degradation in short period of time. Maximum percentage degradation of Methylene blue, Methyl Orange and Rhodamine B dyes were achieved up to 90%, 88% and 81% respectively, in short duration of time. All the three ratios of thione stabilized Ni Nanoparticles showed good degrading performance for all dyes, but 1:2 thione stabilized Ni NPs had shown maximum catalytic performance.