Green Synthesis Route Research Articles

Mechanistic insights into the stepwise lithium-mediated electrochemical nitrogen reduction for enhanced ammonia synthesis

The lithium-mediated electrochemical nitrogen reduction reaction (Li-NRR) is a sustainable route for green NH3 synthesis. It accelerates the N2 reduction by reacting the inert N ≡ N with active Li metal. However, the study on the mechanism of the Li-NRR process remains limited. Herein, a novel stepwise Li-NRR system is established to separately optimize the major steps of Li-NRR: lithium-ion reduction, lithium nitridation, and Li3N protonation. It is revealed that during the Solid Electrolyte Interface (SEI) decomposition, the carbon chains in organic species become shorter, and LixBFy is converted to LiF, which is similar to the continuous Li-NRR. Contrary to the continuous Li-NRR, the O/C ratio decreases as the SEI decomposes due to the absence of ethanol. Commercial Cu, Ni, and Zn are employed as cathodes in the experiments at various currents. The highest Faraday efficiency of 33.2 % and ammonia yield rate of 1404.5 μg h−1 cm−2 are achieved on Zn electrode owing to its superior electron transfer and enhanced Li+ diffusion than those of Cu and Ni. The current has also been found to affect Faraday efficiency through the portion of active lithium in coulomb efficiency experiments. Moreover, the LiCl generated in protonation process is found to facilitate lithium cycling.

Engineering 2D Photocatalysts for Solar Hydrogen Peroxide Production

AbstractSolar energy can be utilized in photocatalysis technology to realize light‐driven hydrogen peroxide (H2O2) production, a green chemical synthesis route. Designing high‐performance photocatalysts is critical to achieving practical solar H2O2 production. During the past decade, significant research progress is made in photocatalytic materials for H2O2 production. Particularly 2D materials‐based photocatalysts stand out due to their unique physical and chemical properties. This review highlights the intricate relationship between 2D material innovation and photochemical H2O2 production. It starts with the fundamental principles of photochemical H2O2 generation, focusing on crucial steps such as photon absorption, carrier dynamics, surface reactions, and the challenges that 2D materials can solve at each step. Then, various 2D materials‐based photocatalysts for solar H2O2 production are introduced in detail. Engineering strategies to optimize the photocatalytic performance are discussed afterward. Finally, the challenges and future opportunities for designing 2D materials‐based photocatalysts for solar H2O2 production are outlined. This review is expected to inspire the engineering of 2D materials‐based photocatalysts for the green synthesis of H2O2 and the conversion of solar energy to other chemicals.

Novel deep eutectic solvent catalysed Single-Pot open flask synthesis of Tetrasubstituted-1H-Pyrroles

Pyrrole and its analogs have garnered immense attention due to their multifaceted biological significance and versatile applications, ranging from medicinal agents to fundamental biological pigments. Despite their prominence, pyrrole synthesis with multiple substituents is complex and calls for innovative approaches to green chemistry. This study delves into synthesizing novel 3,5-dimethyl-1H-pyrroles via multicomponent reactions (MCRs) employing deep eutectic solvents (DES). Due to their eco-friendly nature, these DESs provide a safer substitute for traditional solvents. Specifically, a novel three-component DES (3CDES) was formulated, showcasing promising catalytic activity for multiple cycles with excellent product generation. The synergy between MCR and DES elucidates their combined potential in fostering a sustainable and efficient green synthesis route with the E-factor of 0.1699.

A Green Route for Sustainable Nanoporous Solid Acid Catalyst Synthesis Using Bio Template and Analysis of Its Progressive Transformation of CO2

Green chemistry approach is a most important area in the modern chemical world. The nano (meso) porous materials have the specific application in separation, adsorption and catalysis. A green template (Egg white) is used as a bio template for the synthesis of nanoporous material to replace the hazardous templates. It is a bio-degradable template; it does not create any environmental issues. The synthesized material is characterized by various spectroscopic techniques to confirm its structural formation. Based on pore size, the catalyst named as AlSiO4-14. The synthesized catalyst (AlSiO4-14) is active at 175oC. This low temperature activity will not produce coke formation at the same time it does not require any regeneration and the catalyst is continuously active for catalytic reactions. The catalytic activity of carbon dioxide decomposition is achieved at lower temperature. The complete carbon dioxide decomposition of AlSiO4-14 is 43 % is a great impact of the material.

Adsorptive removal of heavy metal ions from aqueous solution by using green synthesized copper oxide nanoparticles

Metal nanoparticles can be synthesized by “green synthesis” methods, an efficient and environmentally friendly process that involves combination of metal salt solution with plant extract. Due to low cost, ideal surface area, plenty of active sites, and high adsorption capabilities, copper oxide nanoparticles (CuO-NPs) have drawn a lot of attention as effective adsorbents. Our present study is primarily concerned about green synthesis route of producing copper oxide nanoparticles (CuO-NPs) from flower extract of Nyctanthesarbor-tristis. The prepared CuO-NPs was used in the adsorption of toxic metal ions including U(VI), Pb(II), Cr(VI), and Cd(II) from water samples was studied. Different analytical techniques like UV-visible spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy and field emission scanning electron microscopy has been used for analyzing the properties of prepared copper oxide nanoparticles. A batch experiment has also been conducted to determine the efficacy of the synthesized copper oxide nanoparticles toward the adsorption of toxic metal ions including U(VI), Pb(II), Cr(VI), and Cd(II) from water samples at various parameters, such as the impact of pH, contact time and adsorbent dosage. According to the results, the adsorption capacity (qmax) of CuO-NPs for U(VI), Pb(II), Cr(VI), and Cd(II) metal ions are 200, 155.27, 131.57 and 90.90 respectively. The kinetic studies showed that the pseudo-second order kinetics model has best fits to the data (R2= 0.85, 0.91, 0.89, 0.92 for U(VI), Pb(II), Cr(VI), and Cd(II) respectively. The study also included pseudo-first order, Elovich models and intra particle diffusion. In light of these findings, copper oxide nanoparticles were found to be a promising nano-adsorbent for the treatment of water.

Green-route synthesis of ZnO nanoparticles via Solanum surattense leaf extract: Characterization, biomedical applications and their ecotoxicity assessment of zebrafish embryo model

Biogenic synthesis (green synthesis) of metal or metal oxide nanoparticles has recently become important to researchers due to its improved antibacterial properties and associated applications. The present investigation has been carried out to produce zinc oxide nanoparticles (ZnO NPs) using a leaf aqueous extract of Solanum surattense as a reducing and stabilizing agent. The synthesized NPs have been studied using UV–visible, FT-IR, XRD, SEM-TEM, and EDX analysis. The highest UV peak produced by the synthesized ZnO NPs was 294 nm. The resulting ZnO NPs were crystalline, confirmed by XRD measurements. FT-IR demonstrates the presence of OH stretching and CC bending, functional groups of the plant extract stabilizing activity on the NP's outer layer. SEM & TEM investigation confirmed that the NPs were spherical, and their diameters were 25.14 ± 7.4 nm. At a 100 μg/mL concentration, the NPs showed significant antibiofilm activity against Streptococcus mutans and Enterococcus faecalis. Furthermore, the ZnO NPs had remarkable antibacterial activity against two targeted bacteria. In ABTS and DPPH scavenging tests, ZnO NP's antioxidant functions significantly surpassed the ascorbic acid standard. The ZnO NPs significantly inhibited the MDA-MB-231 human breast cancer cell line in vitro, and their IC50 value was 40 μg/mL. The pkCSM server and ADMETlab2 online services analyzed the pharmacokinetics characteristics. Tetratriacontane and streptomycin binding energies have been identified to be -8.7 and -7.6 kcal/mol, respectively. Lastly, the appearance of shorter bodies was observed only at doses above 5 mg/mL in the toxicity test done on zebrafish eggs. The work shows that phyto-synthesized ZnO NPs employing S. surattense extract may be an alternative biological agent in the future.

Green Synthesis of Bimetallic Nanoparticles and its Catalytic Activity of Multicomponent Reactions and Antibacterial Activity

AbstractThis present research work focuses on synthesizing Ag−Cu bimetallic nanoparticles utilizing an aqueous extract leaf of Excoecaria agallocha, employing a green synthesis route. The incorporation of silver (Ag) with copper (Cu) induces synergistic effects that enhance reaction kinetics and reduce the multicomponent reaction time. The catalysts synthesized through this environmentally friendly approach were thoroughly characterized using various analytical techniques, including HR‐TEM, XRD, SEM‐EDX, UV‐Vis Spectrophotometry, and FT‐IR. The UV‐visible spectrum displayed a peak at 257 nm, while the FT‐IR spectrum exhibited peaks at 574 cm−1, indicative of bimetallic peak reductions attributed to the influence of plant metabolites. HR‐TEM and XRD revealed the crystalline with (111), (200), (111), (200), and (220) plane values and shapes of BMNPs. Furthermore, the Ag−Cu bimetallic nanoparticles demonstrated outstanding catalytic performance with high product yield, along with notable reusability and recyclability and excellent antimicrobial activity when compared with commercial antibacterial chloramphenicol.

Environmentally-friendly preparation of Sn(II)-BDC supported heteropolyacid as a stable and highly efficient catalyst for esterification reaction

Facilitating energy resource deficiency and environmental contamination, this work focuses on sustainable biodiesel production through the esterification reactions of oleic acid (OA) with methanol. To address the reaction, a novel heterogeneous acid catalyst, 12-tungstophosphoric acid (TPA) immobilized on Sn-based MOFs (Sn(II)-BDC) was synthesized via a simple, green solvent, and easy-to-implement synthesis strategy for the first time, and applied effectively for esterification process of OA to produce biodiesel. The structure and composition of as-obtained catalyst have been verified using XRD, FTIR, N2 physisorption, SEM, EDX, TG, Py-FTIR, TPD-NH3, and XPS techniques. The obtained TPA/Sn(II)-BDC catalyst was found to be the best with 60 wt% of TPA loading, which resulted in an OA conversion of 91.7 % at optimized conditions of 0.15 g catalyst loading and methanol to OA molar ratio of 20:1 at temperature of 120 °C in 4 h, and the excellent performance arises from available pores structure, large amounts of acidic sites, good stability and the synergistic catalytic effect of TPA and Sn(II)-BDC. Furthermore, the composite catalyst reusability has been studied for five cycles, and it exhibits an acceptable conversion. This research provides a green and large-scale synthesis route for the sustainable production of biofuels by constructing heteropolyacids/Sn-based MOFs synergistic catalysts.

Synthesis, characterization and antimicrobial activity of Cassia fistula mediated Cobalt doped Copper oxide nanoparticle against Salmonella typhi a step toward antibacterial nanomedicine

The green synthesis route is becoming an emerging field of study in nanotechnology due to its biodegradability, eco-friendly nature, and non-hazardous nature. Among a variety of industrial metal nanoparticles (NPs), copper oxide nanoparticles (CuONPs) are the most attractive topic for researchers because of their effective surface area to volume ratio, chemical properties, and antimicrobial activity. The current study consists of the synthesis of Copper oxide nanoparticles (CuONPs) using Cassia fistula extract as a reducing and capping agent and studies its antibacterial activity. The formation of Cassia Fistula mediated CuONPs was identified by color change and was confirmed by FTIR and UV-visible spectrophotometry, revealing an absorbance peak at 235 nm. A shift of 45 nm was observed when the NPs were coated with PEG. Astonishingly, CuONPs showed a virtuous result on 485 ug/ml, showing only 3% of hemolysis; meanwhile, many different concentrations of NPs were used to check whether it would exceed the standard value. However, none of the diluted concentrations were above the standard value, making them biocompatible. The MIC test was performed, showing 250 ml and 350 ml of diluted CuONPs were prominent concentrations for the elimination of bacteria. ROS quantification and identification showed that the ROS produced followed the Type II mechanism in which the singlet oxygen transfers energy to triplet oxygen. We settled that CuONPs possess the ability to delimit the bacteria, specifically Salmonella typhi.

Energy recovery and clean water remediation using antibiofouling polysaccharide coated PAN hollow fiber membrane obtained via green route synthesis

Biofouling is an important biological constrain in the water treatment process, and the control or management strategies using green principles have gained recent attention. Antibiofouling agents based on the biological source are now extensively studied due to their high efficacy and are environmentally friendly. In this present study, Poly Acrylo Nitrile (PAN)/Ulvan hollow fibre membranes of four different modules were fabricated for water treatment studies by testing against B. subtilis and E. coli along with separation efficiency studies on proteins such as albumin, pepsin, and clay. Ulvan (Ulv), green seaweed sulfated polysaccharide extracted from Ulva fasciata, was coated on PAN hollow fibres, fabricated using a wet-spinning process. Ulvan was dip-coated on membrane surface followed by cross-linking and resultant changes in terms of performance and morphology. PAN/Ulv hollow fibre membranes were examined for the pure water flux and protein separation analysis to analyse the membrane efficiency. SEM was used to analyse the membrane structure and ATR- FTIR for the determination of functional groups. Ulvan coated (310 C) hollow fibre membrane showed better performance than the other three membranes with a flux of 398.1 L m−2 h−1. Higher sample concentration of suspended solids paved simpler route for enhanced COD sequestration efficacy. Pepsin, albumin, and clay particles were rejected by the 310C Ulvan adorned membranes at rates greater than 80%. By incrementing suspended particles beyond 3200 mg/L, the greatest power recovery was reduced that portrays an adverse influence of bio-fouling process on membrane operation. Experimental results demonstrated that synthesised 310 C membrane possessed better separation performance and antifouling characteristics for aquatic water systems.

Aqueous Electrocatalytic Reduction as a Low‐Carbon and Green Route for Chemical Synthesis and Environmental Remediation

AbstractThe green electricity‐driven electrocatalytic reduction of organic compounds in aqueous solution has merged as a sustainable and green platform for organic electrosynthesis, upcycling of chemical waste, and environmental remediation. Compared with the thermocatalytic hydrogenation process, the electrocatalytic reduction of organic compounds uses water as a proton source, which enables its operation at ambient conditions with simplified reaction schemes and significantly reduces operation cost and energy consumption. Most studies have demonstrated the development of electrocatalysts to boost the current efficiency, conversion, and product selectivity of the electrocatalytic reduction processes. Still, little attention has been paid to the mechanism (e. g., electron/proton transfer route) and related energetics behind the electrocatalytic reduction process. This Concept overviews the recent development of the electrocatalytic reduction systems for environmental remediation, pollutant upcycling, and valorization of biomass‐derived chemicals. This Concept highlights the underlying mechanisms and aims to provide instructive guidance on designing efficient and selective electrocatalytic systems.

Green-route synthesis and ab-initio studies of a highly efficient nano photocatalyst:Ce/zinc-oxide nanopetals

In the present work, Zinc-oxide nanostructures and Ce/Zinc-oxide nanopetals were synthesized by a new environmentally friendly green synthesis method using the Withania coagulans plant. Cerium nitrate Ce(NO3)3 and zinc nitrate Zn(NO3)2 were used as precursors. The prepared nanostructures were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and ultraviolet spectroscopy (UV–vis). Crystal planes (100), (002), (101), (102), (110), (103), (200), (112) and (201) at 2θ 31.75°, 34.35°, 36.2°, 47.55°, 56.6°, 62.75°, 66.3°, 67.9°, and 69.09° respectively confirmed the hexagonal wurtzite crystal structure of Zinc-oxide. Angular shifts for Ce1% doped Zinc-oxide and Ce3% doped Zinc-oxide nanopetal nanostructures were observed in the (100) and (101) planes of the crystal. More specifically, using Scherrer's equation, the crystallite sizes of Zinc-oxide, Ce1% doped Zinc-oxide nanopetals, Ce3% doped Zinc-oxide nanopetals, and Ce5% doped Zinc-oxide nanopetals were 16.48 ± 02 nm, 17.8 ± 2 nm, 18.8 ± 2 nm, and 18.87 ± 2 nm, respectively. The pure Zinc-oxide grain had the appearance of a nanoflower. On the other hand, the nanopetal structure of Ce5% doped Zinc-oxide nanopetals had oval-shaped nanopetal morphology. The absorption peaks were observed at 373, 376.4, 377, and 378 nm for Zinc-oxide, Ce1% doped Zinc-oxide nanopetals, Ce3% doped Zinc-oxide nanopetals, and Ce5% doped Zinc-oxide nanopetals, respectively, which results in a progressive redshift. The gap energies of Zinc-oxide, Ce1% doped Zinc-oxide nanopetals, Ce3% doped Zinc-oxide nanopetals, and Ce5% doped Zinc-oxide nanopetals were 2.796, 2.645, 2.534, and 2.448 eV, respectively. Photodegradation under visible light (>400 nm) indicates the high efficiency of the photocatalyst based on Ce5% doped Zinc-oxide nanopetals. DFT calculations, structural changes, charge analysis, and electronic band structures were carried out to confirm the experiment.

A green synthesis route of cyclohexanol via transesterification reaction intensified by reactive distillation technology

With the increasing demand of cyclohexanol in nylon industry, it is significant to develop a safe, green and economical process to produce cyclohexanol. For this purpose, a novel reactive distillation process through cyclohexyl acetate transesterification with methanol was proposed in this work. The NKC-9 catalyst was preferred to establish the reaction kinetic model based on pseudo-homogeneous model. Seven reactive distillation experiments with pilot-scale for cyclohexanol synthesis were explored to prove feasibility of reactive distillation processes and accuracy of model by comparing simulated results, which ensured the establishment of the process simulation. Furthermore, three reactive distillation processes of cyclohexanol production were designed and optimized by the sequential iterative algorithm based on minimum total annual cost. After optimization of pressure and recycled stream flow, a novel double column of reactive and pressure-swing hybrid distillation process showed the minimized total annual cost per ton product, which was 170.90 $/kg. Finally, total annual cost of transesterification, hydrolysis and hydrogenation processes were compared, and transesterification process demonstrated economic advantage. This work would provide a guidance for cyclohexanol green production by reactive distillation through cyclohexyl acetate transesterification, while a whole, economical and atomic economical reactive distillation process of cyclohexanol production could be established in the future.

Co-precipitation vs. Green Synthesis: A Comparative Analysis of Structure, Morphology, Optical Properties, and Antibacterial Activity of Ag/ZnO Nanocomposite

Ag/ZnO nanocomposites were successfully prepared through co-precipitation (CS) and a green synthesis (GS) route mediated by Moringa Oleifera. The confirmation of their formation was evident from the simultaneous presence of Ag and ZnO reflections in powder X-ray diffraction. Field emission scanning electron microscopy (FESEM) analysis disclosed an average particle size of approximately 22 nm and 146 nm for CS and GS samples, respectively. The CS sample exhibited a disstinctive flower-like morphology, indicating a unique self-assembly and growth pattern, while the GS sample displayed an almost rectangular shape. Structural composition and functional groups in the nanocomposites were analyzed using FT-IR spectroscopy. The direct band gaps were determined as 3.12 eV for CS and 3.10 eV for GS samples using a Tauc plot derived from UV-Vis NIR spectrometry. Notably, the antibacterial evaluation of the green-synthesized Ag/ZnO exhibited a pronounced zone of inhibition against both gram-positive (S. aureus) and gram-negative (E. coli) bacteria, demonstrating superior efficacy compared to chemically prepared Ag/ZnO. Overall, the study highlights the successful synthesis, structural characterization, and enhanced antibacterial properties of Ag/ZnO nanocomposites via a green route mediated by Moringa Oleifera. GRAPHICAL ABSTRACT

Omnipotent plant sources assisted green synthesis of Silver Nanoparticle - A promising Chemical Sensing tool

This article aims to analyze the various sensor applications of silver nanoparticles synthesized from green materials, particularly plant-based sources. The current shape in the field of nanotechnology is the synthesis of metal nanoparticles via environmentally friendly and more reliable green materials. The green route synthesis is found to be a promising method because of its congenial properties. It is economical, affable, and reproducible. Heavy metals have been dispersed widely in the environment, and they are well known for their virulent effects. Numerous methods are available to sense and detect those metals. The headway in the domain of nanotechnology is to synthesize AgNPs from green plants and to steer clear of the hazardous effects of metals. Efficacious synthetic routes via plant-mediated synthesized AgNPs open up easy and efficient sensing of hazardous metals in the environment. AgNPs have attracted many researchers because they have good biocompatibility and other outstanding properties. Remarkable electronic, catalytic, and optical properties have enabled AgNPs to be used as sensors in medical, biological, and chemical fields. This review highlights the application of PAGS-AgNPs as a chemical sensor for detecting heavy metals and organic compounds in the environment.

Comparative study of the efficiency of conventional and green-prepared iron nanoparticles for catalytic ozonation

This study aimed at the preparation of green and conventionally prepared iron nanoparticles (Fe-C-NPs), their characterization and application as catalysts of ozonation to remove emerging contaminants and disinfection. It is the first time that a study has compared the chemical and morphological characteristics of Fe-C-NPs and related them to their efficiency as catalysts in ozonation. Green Fe-C-NPs were prepared with eucalyptus and mulberry leaves extract and the conventional Fe-C-NPs prepared using ammonia as reducing agent. The green synthesis routes are low cost and environmental friendly, thereby reducing the risk of harmful effects of toxic chemicals and derivative compounds. The Fe-C-NPs were characterized by FTIR, SEM, XRD, XPS and VSM, and were applied in the degradation of malachite green, methylene blue, sulfamethoxazole, atrazine, and acetaminophen in ultrapure water and secondary effluent as well as in the inactivation of disinfection indicators. As expected, the implementation of Fe-C-NPs in catalytic ozonation resulted in enhanced efficacy compared to ozonation alone. However, the green Fe-C-NPs showed equivalent or better efficiency compared to the conventionally Fe-C-NPs, showing better efficiencies in cleaner water matrices. When applied to remove micropollutants and promote disinfection in secondary effluents, the green Fe-C-NPs showed equivalent efficiencies in comparison with conventional Fe-C-NPs. It highlights that nanomaterials produced by green routes can be an alternative to traditional nanomaterials that use of toxic reagents on its production.

Facile green synthesis route for new ecofriendly photo catalyst for degradation acid red 8 dye and nitrogen recovery

This study novelty is that new photo catalyst prepared from sustainability low cost precursors. Dark red color hydrogel composites have been easily prepared from gelatin biopolymer using a simple sol–gel method. Gelatin doped by cobalt chloride, and silver nanoparticles (SNPs) in the presence of traces amount of sodium dodecyl sulfate surfactant and calcium chloride. Water-insoluble Gelatin composites are thermally stable photocatalysts for the degradation of toxic anionic acid red 8 dye. Promising photodynamic activity confirmed by fluorescence emission at λmax 650 nm. Optical absorption in Vis. light enhanced photo catalytic activity. Silver nanoparticles enhanced crystallinity, and improved optical properties and porosity. Dopants by CoCl2 and silver nanoparticles increased band gap of gelatin composites from (1.82 to 1.95) indicating interfacial charge separation. Low band gaps improved photo catalytic activity. Optical band gaps (Eg) lower than 2.0 eV indicates high catalytic activity in the photo degradation acid red 8 dye using Vis. light, wavelength 650 nm. Percent removal efficiency (%Re) of the dye at 500 ppm initial concentration, pH 1, contact time 30 min., and 0.20 g L−1 dose photo catalyst reached 95%. pH not affects removal efficiency. So, gelatin composites removed AR8 dye by photodegradation mechanism rather than adsorption due to photodynamic activity. Kinetics of photodegradation followed pseudo first order kinetic with rate constant k1 5.13 × 10−2 min.−1 Good electrical conductivity and magnetic properties (effective magnetic moment (µeff 4.11 B.M) improved dye degradation into simple inorganic species. Nutrients NH4+, and NO3− degradation products recovered by using alumina silicate clay via a cation exchange mechanism.

Synthesis and Characterization of Parthenium hysterophorus-Mediated ZnO Nanoparticles for Methylene Blue Dye Degradation

Herein, zinc oxide nanoparticles (ZnO NPs) were synthesized using Parthenium hysterophorus whole plant aqueous extract as reducing and capping agents. The synthesized ZnO NPs were characterized via UV-Vis spectroscopy, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and dynamic light scattering (DLS). An intrinsic optical absorbance of ZnO NPs occurred at 337 nm in the UV-Vis spectrum. The FTIR analysis revealed the presence of secondary metabolites responsible for reducing and stabilizing the nanoparticles. Furthermore, SEM and TEM images revealed that ZnO NPs were spherical with an average particle size of 38 nm. The XRD analysis revealed that ZnO NPs had a hexagonal wurtzite crystal structure with a crystallite size of 42.6 nm. The synthesized nanoparticles were investigated for degradation ability against methylene blue dye at varying conditions of ZnO NPs’ dosage, methylene blue concentrations, pH, temperature, and interaction time. Degradation efficiency of 55.69% was obtained at optimal conditions using 50 mg of ZnO NPs, 5 mg/L of MB dye concentration, and pH 12 and at 65°C within 32 minutes. Due to their novel green synthesis route, Parthenium hysterophorus-mediated ZnO NPs are promising candidates for removing persistent organic dyes from aquatic environments.

Reducing the environmental footprint of solid-electrolytes - a green synthesis route for LATP

We present a simplified, CO2-free and energy efficient synthesis to produce high-purity LATP with competitive electrochemical properties.

Sunlight assisted degradation of methylene blue dye by zinc oxide nanoparticles green synthesized using Vitex negundo plant leaf extract

Zinc oxide nanoparticles (ZnO NPs) were formed through a simple green synthesis route using Vitex negundo (V. negundo) leaf extract as reducing and capping source. Morphological, structural, chemical and optical features of the prepared ZnO NPs were examined by field emission SEM, XRD, EDAX, PL, FTIR and UV–vis DRS, respectively. FESEM images precisely visualized morphology of the ZnO NPs as spherical with particles size ranges between 5 and 35 nm having a mean diameter of ∼ 19 nm. XRD pattern revealed formation of hexagonal wurtzite structured ZnO NPs with high crystallinity. Further, the observed asymmetric stretching vibration of Zn-O bond confirmed the formation of hexagonal wurtzite structured ZnO NPs. Photocatalytic activity of the ZnO NPs was assessed against methylene blue (MB) dye degradation under natural sunlight illumination. Results of the photocatalytic experiment disclosed an impressive MB dye degradation efficiency of 98.50 % at 60 min. Moreover, green synthesized ZnO NPs exhibited a maximum mineralization (TOC removal) efficiency of 92.34 % at 5 h of sunlight illumination.