Green Synthesis Process Research Articles

Photocatalytic Degradation of Four Organic Dyes Present in Water Using ZnO Nanoparticles Synthesized with Green Synthesis Using Ambrosia ambrosioides Leaf and Root Extract

Currently, several organic dyes found in wastewater cause severe contamination problems for flora, fauna, and people in direct contact with them. This research proposes an alternative for the degradation of polluting dyes using ZnO nanoparticles (NPs) synthesized by an ecological route using leaf and root extracts of Ambrosia ambrosioides as a reducing agent (with a weight/volume ratio = 4%). Scanning Electron Microscopy (SEM) was used to determine the morphology, showing an agglomeration of cluster-shaped NPs. Using Transmission Electron Microscopy (TEM), different sizes of NPs ranging from 5 to 56 nm were observed for both synthesized NPs. The composition and structure of the nanomaterial were analyzed by infrared spectroscopy (FT-IR) and X-ray diffraction (XRD), showing as a result that the NPs have a wurtzite-like crystalline structure with crystallite sizes around 32–37 nm for both samples. Additionally, the bandgap of the NPs was calculated using Ultraviolet Visible Spectroscopy (UV–Vis), determining values of 2.82 and 2.70 eV for the NPs synthesized with leaf and root, respectively. Finally, thermogravimetric analysis demonstrated that the nanoparticles contained an organic part after the green synthesis process, with high thermal stability for both samples. Photocatalytic analysis showed that these nanomaterials can degrade four dyes under UV irradiation, reaching 90% degradation for methylene blue (MB), methyl orange (MO) and Congo red (CR) at 60, 100 and 60 min, respectively, while for methyl red (MR) almost 90% degradation was achieved at 140 min of UV irradiation. These results demonstrate that it is effective to use Ambrosia ambrosioides root and leaf extracts as a reducing agent for the formation of ZnO NPs, also evidencing their favorable application in the photocatalytic degradation of these four organic dyes.

Sustainable synthesis of pyrochlore gadolinium zirconate through the molten salt method: A green approach

Gadolinium zirconate (GZO) with pyrochlore phase exhibits exceptional promise for thermal barrier coatings due to its notable low thermal conductivity. Current synthesis methods for GZO, however, are frequently complex, energy-intensive, and environmentally hazardous. A more sustainable and eco-friendly synthesis route for GZO is thus imperative. This research introduces a green synthesis process for pyrochlore GZO utilizing the molten salt method.Experimental synthesis at varying temperatures revealed changes in the phase composition of GZO via the molten salt method. Fluorite GZO formed at 1200 °C, while pyrochlore GZO appeared at 1400 °C. XRD refinement, TEM, and Raman spectroscopy confirmed these results. Density Functional Theory (DFT) calculations established the minimum theoretical synthesis temperature for pyrochlore GZO at 1370 °C. Limiting factors for reactions at different temperatures during the molten salt synthesis process were identified. DFT calculations and experiments verified that the fluorite structure GZO transitions to pyrochlore GZO at temperatures exceeding 1370 °C. Property tests on pyrochlore GZO samples synthesized through two pathways showed minimal differences. This study thus lays a theoretical foundation for the eco-friendly synthesis of pyrochlore GZO material using the molten salt method and offers insights for future process development.

Dynamic Simulation and Optimization for Load Regulation Strategies of the Green Ammonia Synthesis Process

Dynamic Simulation and Optimization for Load Regulation Strategies of the Green Ammonia Synthesis Process

Exploring sustainable synthesis paths: a comprehensive review of environmentally friendly methods for fabricating nanomaterials through green chemistry approaches.

This comprehensive review delves into the burgeoning field of nanotechnology, where the synthesis of nanoparticles (NPs) is strategically tailored to specific applications. Embracing the principles of green chemistry, nanotechnology increasingly utilizes environmentally friendly materials, such as plant extracts or microorganisms, as capping or reducing agents and solvents in the synthesis process. Notably, plant-based synthesis demonstrates enhanced stability and faster rates compared to microorganisms. The synthesized materials exhibit unique properties ranging from antimicrobial and catalytic effects to antioxidant activities and they are finding applications across diverse fields. Green synthesis processes, characterized by mild conditions in terms of temperature and reagents, stand in stark contrast to traditional chemical synthesis methods. This review focuses on the synthesis of various metal and metal oxide NPs, including Ag, Au, Zn, Fe, Mg, Ti, Sn, Cu, Cd, Ni, Co, and Ag NPs and their oxides, using plant extracts and microorganisms. We provide a comprehensive analysis of the advantages, disadvantages, and applications associated with each synthesis method. Additionally, we explore the future prospects of green synthesis and its limitations and challenges, offering insights into its evolving role in nanotechnology.

Sustainable synthesis of silver nanoparticles from Azadirachta indica: antimicrobial, antioxidant and in silico analysis for periodontal treatment.

This study explores potential application of silver nanoparticles (AgNPs) to treat periodontal infection using Azadirachta indica leaf extract. The eco-friendly green synthesis process uses Azadirachta indica as a natural stabilizer and reducer, allowing AgNPs to be formed. Experimental AgNPs were characterized through transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), Zeta potential, ultraviolet-visible spectroscopy (UV-Vis) etc. The antimicrobial, antioxidant potential of AgNPs was tested to identify its efficacy against periodontal infections. AgNPs were found spherical, nanosized (86nm), with negative surface charge (-26.9mV). TEM study depicted clear formation of discrete nanosize particles with smooth surface texture. Results showed strong antibacterial and anti-oxidant action of experimental AgNPs, preventing biofilm growth and bacterial viability. A higher binding affinity was observed between Quercetin and the selected protein, which is implicated in bacterial growth and biofilm formation on teeth. The study suggests that Azadirachta indica derived AgNPs could be a safe, efficacious, and eco-friendly alternative in place of conventional therapies to treat periodontal infection. Future in vivo studies are however warranted.

Use of Dialysis Membranes for the Purification of Fe/Ni and Fe/Cu Nanoparticles Synthesized from Green Tea Extract

AbstractTo ensure the quality and effectiveness of nanoparticle material for specific applications, it is essential to eliminate contaminants or unreacted substances produced during the green synthesis process using leaf extract. In this study, dialysis membranes with a molecular weight cut‐off (MWCO) of approximately 12,000–14,000 Dalton (Da) were employed to remove metal ions, chlorides, and polyphenols from the zerovalent bimetallic nanoparticles (BNPs) suspension, instead of using centrifugation or filtration, which causes solvent loss to the environment. Our research results showed that the efficiency of removing impurities and residual components achieved by the dialysis membrane was relatively high. Furthermore, alterations in specific characteristics of BNPs following dialysis were also observed and discussed.

Experimental evaluation of green nanofluids in heat exchanger made oF PDMS

Conventional methods for synthesizing metallic nanoparticles face challenges such as instability and environmental concerns. Therefore, new, simpler, and more eco-friendly methods are being explored. In this context, the study reports a green synthesis process to produce magnetic iron oxide nanoparticles using an aqueous extract of the alga Chlorella vulgaris. This process leverages natural resources to create a sustainable nanofluid known as green nanofluid. To evaluate the characteristics of this nanofluid, experimental measurements of wettability, viscosity, thermal conductivity, and qualitative stability analysis were conducted. An experimental setup consisting of a heat exchanger made of polydimethylsiloxane (PDMS) was used to assess the thermal performance and the results were compared to theoretical equations and numerical simulation. Additionally, thermographic imaging of temperature gradients as the fluids passed over the heated surface of the serpentine channel were made. The main findings confirmed that the nanofluid was more stable than that obtained by traditional methods and had a more uniform temperature distribution over the heat exchanger. The higher concentration exhibited superior thermal performance compared to DI-Water. Moreover, the green nanofluid was used at a weight concentration of 0.1 wt%, provided thermal performance results of nearly 4.5% superior to those estimated by the numerical model and 6.4% higher than those experimentally obtained with the base fluid, respectively. Finally, the results obtained for the nanofluid also showed an average increase of around 5% in the viscosity of the base fluid, with a more significant sedimentation at a concentration of 0.1 wt%.

Antibacterial Activity of Zinc Oxide Nanoparticles Synthesized by Green Eichhornia Crassipes Extract Method

Purpose: Zinc Oxide Nanoparticle (ZnO NPs) production has become more common because of the benefits of the green strategy, which include its ease of use, environmental friendliness, and cheap operating costs. In order to accomplish the goal of green chemistry, the green synthesis process also uses safe solvents like water and ethanol. ZnO NPs are among the metal oxide-NPs used in antibacterial and bioremediation applications. Materials and Methods: Energy Dispersive X-ray spectroscopy (EDX), Fourier Transform Infrared spectroscopy (FT-IR), X-Ray Diffractometer (XRD), and Field Emission Scanning Electron Microscopy (FESEM) were used to analyze the green-produced ZnO NPs. Results: ZnO nanoparticles have an average size of 22.89 nm, which is corroborated by FESEM pictures, indicating that the particles are tiny. The excellent purity of ZnO NPs has been confirmed by EDX data. The antibacterial activity of ZnO NPs was assessed against a few dangerous pathogens. Zinc oxide nanoparticles were shown to have an interesting antibacterial action against both gram-positive and gram-negative bacteria at micromolar concentrations because they exhibit the maximum diameter of inhibition zone at concentrations 100 mg/ml of S. aureus, E. coli, K. pneumonia, Acintobacret spp, S. fecalis reaching (27,19,18,17, and 14) mm, respectively while S. pneumonia were resistant.The ZnO NPs recorded at a concentration of 12.5 mg/ml lowest areas of the inhibition zone against the same isolates reaching (16, 11, 11, 12, and 10) mm while S. pneumonia were resistant, respectively, as well. Conclusion: ZnO NPs, since they have excellent antibacterial properties, and are biocompatible, they will open up a new line of inquiry for antibacterial agent research because they are stable, nontoxic, and harmless.

CsPbBr3@PbSO4 nanocomposites with near-unity photoluminescence and ultrastability via in-water in situ embedding synthesis strategy

Perovskite quantum dots (PQDs) are emerging as promising nanomaterials for optoelectronic applications. However, developing a cost-effective green synthesis process that simultaneously possesses satisfactory photoluminescence quantum yield (PLQY) and stability remains a severe challenge. Here, CsPbBr3@PbSO4 nanocomposites with a near-unity PLQY of 99.8 % and robust ambient stability are synthesized in situ in water via 4-Bromobenzenesulfonic acid and ditetradecylamine ligands. Notably, these nanocomposites show no decline in PLQY even after being immersed in water for over 250 days, and also exhibit superior stability against heating, ultrasonication, UV irradiation, anion exchange, and erosion by polar solvents. First-principles calculations reveal that CsPbBr3@PbSO4 nanocomposites can form a natural quantum well structure, which effectively promotes the radiative recombination of carriers in CsPbBr3 QDs. Meanwhile, the remarkable stability is attributed to the ultrahigh decomposition enthalpy of PbSO4 that serves as a strong barrier preventing the invasion of anions and polar media into the embedded CsPbBr3 QDs. Finally, besides the convenient application of green fluorescent paper, a fingerprint recognition is demonstrated by fabricating a bright-green LED integrated with the CsPbBr3@PbSO4 nanocomposites powder and a commercial UV chip. This work provides a new strategy for green synthesis and practical application of high-efficient and ultrastable PQDs.

Cross-domain fault diagnosis for multimode green ammonia synthesis process based on DA-CycleGAN

Green ammonia is a crucial strategy for reducing carbon emissions and promoting sustainable development. However, in industrial applications, the production load of the ammonia synthesis section must be adjusted to accommodate fluctuations in renewable energy generation and hydrogen production. Consequently, the green ammonia synthesis process operates under multiple conditions with varying production loads. The operations of this multimode process introduce new challenges for process safety. Traditional fault diagnosis methods experience significant performance degradation when production conditions change. In new conditions, only a small number of normal samples can be obtained, and no fault samples are available. To address this issue, a novel transfer learning method named DA-CycleGAN is proposed for the multimode green ammonia synthesis process. This method combines a two-dimensional generation model based on CycleGAN (Cycle-Consistent Generative Adversarial Networks) with domain adaptation to enhance model performance in cross-domain tasks. The feasibility of the proposed method was initially validated using the benchmark Tennessee-Eastman process for fault diagnosis. Subsequently, a case study of the green ammonia synthesis process demonstrated that it significantly enhances performance in multimode processes, ensuring process safety and reducing losses for industrial applications.

Exploration of green catalytic Hantzsch process for synthesis of polyhydroquinoline derivatives and their in silico & in vitro evaluation as anti-tubercular agents

Polyhydroquinolines (PHQ) were long known for various pharmacological activities and numerous methods were reported for their synthesis by using different reaction conditions and catalysts. An attempt has been made to synthesize PHQs by following the environmental friendly green chemical approaches by using reusable and recyclable catalyst and solvent materials. Twelve compounds (2A-2L) were synthesized with varied substitutions on the aromatic ring by following the Hantzsch one-pot approach with bleaching earth clay and polyethylene glycol. Use of novel reaction conditions has improved the yield and drastically reduced the time required for the completion of the reaction. The DFT analysis revealed the structural features and the stability of the compound, and later the compounds were subjected to molecular docking against two key proteins of the M. tuberculosis H37 Ra InhA and DprE1. It was found that few of the compounds showed excellent binding interactions compared to the co-crystalized ligand. Later, all the synthesized compounds were subjected to the in vitro antimycobacterial activity using the Kirby-Bauer disk diffusion method, MICs were calculated by REMA assay and the hemolytic assay was performed to check cytotoxicity. Compounds 2K and 2E were found to show better inhibitory activity than the standard rifampin. The antimycobacterial activity of the PHQ compounds might be due to the interaction of the InhA and DprE1, which can be correlated positively and supported by the structural features and the in silico interaction data. Parallelly, molecular dynamic simulation studies were carried out with ligand 2K for the time frame of 100 ns against both targets InhA and DprE1 revealing the formation of stable complexes which further validate the ligand 2K as a potential lead molecule for further studies. The compounds can be further subjected to lead optimization for improved activity.

A promising sustainable green nanosilver formula for p-nitrophenol and methylene blue remediation from wastewater

In an attempt to create wastewater treatment “green” techniques that are both economically feasible and sustainable without using any dangerous chemicals, barley grain (Hordeum vulgare L.) water extract was used to phyto-synthesize silver nanoparticles (Ag°). Barley grains served as a natural reductant and stabilizer at the same time. The role of different synthesis conditions and their effect on the efficiency of the green synthesis process were studied and confirmed with characterization using several techniques (UV–vis, SEM, EDX, sizing distribution, and FTIR). The Ag°9 formula catalytic reduction was inspected against p-nitrophenol (PNP) and methylene blue (MB) as a model of nitroaromatic components and dyes, respectively. The removal studies were conducted using the target pollutants in a single or mixed liquid state. Remarkably, the Ag°9 particle size was around 20 nm, and its final concentration in the current formula was 2.2 × 10−7 mol L−1. The adsorption mechanism of the PNP and MB was pseudo-second order. The good fit with the pseudo-second-order kinetic model suggests that chemisorption occurs in the sorption process. The formula catalytic activity to remove PNP and MB was 99 and 66% at levels 60 and 500 µL from the Ag°9 formula, respectively, within less than 5 min.

Development and characterization of an aluminum-enhanced graphene oxide nanocomposite: An Eco-friendly and sustainable catalyst for electrochemical Friedel-crafts reactions

This study focuses on the development and characterization of an eco-friendly and sustainable aluminum-modified graphene oxide nanocomposite (AlNPs/GO-Gu) as a catalyst for electrochemical Friedel-Crafts reactions. The catalyst exhibits remarkable efficiency in the synthesis of benzophenone derivatives 4(a-l) through the reaction of benzoyl chloride 1(a-h) and benzene 2(a-f). The nanocomposite was thoroughly characterized using various analytical techniques, including Brunauer-Emmett-Teller (BET), Fourier Transform Infrared Spectroscopy (FT-IR), Thermogravimetric analysis (TGA) and transmission electron microscopy (TEM) spectroscopy, scanning electron microscopy (SEM), energy dispersive X-ray (EDS). The results confirmed the successful integration of Al with graphene oxide, leading to modified catalytic activity. The electrochemical Friedel-Crafts reaction, mediated by this nanocomposite catalyst, demonstrates high selectivity and yields of benzophenone derivatives 4(a-l) in good to excellent yields (89–94 %). Moreover, this environmentally friendly approach avoids the use of hazardous reagents and promotes sustainable synthesis methodologies. The Al-modified graphene oxide nanocomposite exhibits excellent reusability, making it a promising candidate for green and sustainable organic synthesis processes. This research offers insights into the development of catalysts with improved catalytic performance while prioritizing environmental sustainability, creating fresh opportunities for the field of organic synthesis and catalysis.

An investigation of silver nanoparticles made from plectranthus amboinicus leaves and their antibacterial and photocatalytic activities

In the present research, silver nanoparticles (AgNPs) were prepared utilizing Plectranthus amboinicus using a simple green synthesis process. UV, FT-IR, XRD, TEM, SEM, EDX and DLS were used to characterize the prepared AgNPs. The SPR band appears at 448 nm in the UV–visible spectrum. The FTIR spectrum of the synthesized materials confirmed the presence of potential functional groups in the P.amboinicus leaf extract, as well as silver nanoparticles. The peaks in the PXRD is indexed with the database entry (110) reveals the crystalline nature and the FCC structures of silver nanoparticles. The SEM image reveals the existence of spherical shaped AgNPs, while the EDX image reveals the presence of silver element. TEM pictures indicate the spherical shape of AgNPs with sizes ranging from 20 to 30 nm. Additionally, these biosynthesized NPs photocatalytic activity was investigated against methylene blue under sun irradiation, and after 60 min of exposure, they demonstrated an efficiency of 94 %.Furthermore, the most effective antibacterial agent is Pseudomonas aeruginosa, as evidenced by a 14 mm AgNPs inhibition zone. As a result, we conclude that the synthesized Plectranthus amboinicus AgNPs have more medicinal and industrial potential.

Recovery of lithium from the desorption solutions of salt lakes using β-diketone synergistic extraction system

Lithium has become increasingly important because of its irreplaceable role in lithium-ion batteries. Addressing the complex process and high energy consumption of the current adsorption-membrane integrated process for lithium extraction from high Mg/Li ratio salt lake brine, this study put forward an integrated process of adsorption-solvent extraction. Taking the desorption solution of adsorption method as raw material, the process parameters and extraction mechanism of lithium by the novel extraction system were investigated. A novel process of lithium recovery from the desorption solutions of salt lakes by solvent extraction was proposed for the first time. The composition of the extraction system was studied and determined to be HTTA-P113-kerosene. Compared with the previously reported neutral ligands (TOPO, Cyanex923), P113 not only exhibited excellent synergistic extraction ability but also had good miscibility and a green synthesis process. The effects of saponification degree, extraction time, temperature and phase ratio on lithium extraction and βLi/Na were systematically investigated. Through the four-stage countercurrent extraction, more than 99.2 % of lithium could be extracted by the organic phase consisting of 0.4 mol L−1 HTTA, 0.4 mol L−1 P113, saponification degree of 80 % at O/A ratio of 1:1 and equilibrium pH of 6.78. Furthermore, after the scrubbing and stripping process, the lithium-rich solution containing 21.64 g L−1 Li+ and 0.037 g L−1 Na+ was obtained. The Li2CO3 products with a purity of 99.5 % were successfully prepared from the lithium-rich solution by precipitation method. Finally, the extraction mechanism was studied via the slope analysis method and FT-IR spectra. It was indicated that the extracted lithium species were Li(TTA)(P113).

Green Sonochemical Synthesis of rGO Nanosheets‐Decorated by SnO2 Nanoparticles for Nitrogen Gas‐Sensing Applications

In recent years, the development of efficient and environmentally friendly synthesis methods for nanomaterials has gained significant attention in various research fields, particularly in gas‐sensing applications. Among these methods, ultrasonic synthesis stands out for its simplicity, cost‐effectiveness, and ecofriendly nature. Herein, a simple and green ultrasonic synthesis process is used to synthesize the SnO2 nanoparticles‐decorated rGO nanosheets. The obtained X‐ray diffraction reveals the tetragonal rutile‐type crystal structure. The transmission electron microscopy images reveal the decoration of SnO2 nanoparticles on the surfaces of the rGO sheets. SnO2 nanoparticles of size 4–8 nm are identified on the surfaces of the rGO sheets. Furthermore, the optical absorbance and photoluminescence spectra of the nanocomposites validate charge migrations occurring at the interface of SnO2 and the rGO sheets. Compared to the pristine SnO2 nanoparticles, the green ultrasonically synthesized SnO2 nanoparticles‐decorated SnO2/rGO nanocomposite exhibits better sensing performance against NO2 gas and shows selectivity for NO2 gas at 200 °C. The SnO2/rGO nanocomposite demonstrates high NO2 sensing with appealing sensing properties such as excellent responsiveness (67% at 400 °C), rapid reaction time (18 s), and short recovery time (25 s).

Tungsten-Doped ZnO as an Electron Transport Layer for Perovskite Solar Cells: Enhancing Efficiency and Stability.

This study delves into enhancing the efficiency and stability of perovskite solar cells (PSCs) by optimizing the surface morphologies and optoelectronic properties of the electron transport layer (ETL) using tungsten (W) doping in zinc oxide (ZnO). Through a unique green synthesis process and spin-coating technique, W-doped ZnO films were prepared, exhibiting improved electrical conductivity and reduced interface defects between the ETL and perovskite layers, thus facilitating efficient electron transfer at the interface. High-quality PSCs with superior ETL demonstrated a substantial 30% increase in power conversion efficiency (PCE) compared to those employing pristine ZnO ETL. These solar cells retained over 70% of their initial PCE after 4000 h of moisture exposure, surpassing reference PSCs by 50% PCE over this period. Advanced numerical multiphysics solvers, employing finite-difference time-domain (FDTD) and finite element method (FEM) techniques, were utilized to elucidate the underlying optoelectrical characteristics of the PSCs, with simulated results corroborating experimental findings. The study concludes with a thorough discussion on charge transport and recombination mechanisms, providing insights into the enhanced performance and stability achieved through W-doped ZnO ETL optimization.

Sulfur-modified polyurethane adhesives: Green synthesis process and disassembly-responsive characteristics

Polyurethane adhesives have been widely used in industrial production and daily life for their excellent properties. With the urgent need for social progress, the intelligent responsiveness of polyurethane adhesives has become more and more important. Here, we demonstrate a stimulus-responsive polyurethane adhesive. Starting from the structural design, sulfur (S8) is added into the polyurethane adhesive for the first time using the inverse vulcanized mechanism, and the controllable disassembly response of the polyurethane adhesive under the condition of thermal stimulation is realized. In addition, the stimulus response of the adhesive can also be activated through the permeation process of methoxide anion (CH3O−), and the rapid disassembly response property is displayed in the methanol solution of CH3ONa, to realize the recovery of the bonding substrate. Simultaneously, the implementation of the inverse vulcanized mechanism imparts the adhesive with a diminished water absorption swelling rate and heightened cross-link density. On the surface of the metal substrate, it shows excellent bonding properties, with a lap shear adhesion strength reaching 2.8 MPa. It is worth noting that the adhesive also exhibits excellent underwater durability. After 36 h of underwater soaking treatment, its adhesion can still be maintained at 2.4 MPa. This work reveals the mechanism of rapid disassembly of polyurethane adhesives at the molecular level. By density functional theory (DFT) calculation, it is found that the minimum bond energy of the S-S bond in a polyurethane adhesive system is 134 KJ·mol−1, and the disassembly response can be triggered by heating to 53.79℃. At the same time, the mechanism of the disassembly response induced by CH3O− is further analyzed using an electrostatic potential (ESP) diagram. This work utilizes sulfur (S8) and castor oil (CO) as raw materials, which can be sourced from industrial or agricultural by-products. It breaks away from traditional polyurethane adhesive preparation methods and offers a "green" strategy that can be synthesized through a solvent-free one-pot process, thus providing a new way of thinking about obtaining sustainable polymers from industrial and agricultural by-products.

Nanotechnology and malaria: Evaluation of efficacy and toxicity of green nanoparticles and future perspectives.

Malaria is a global health problem that causes 1.5-2.7 million deaths worldwide each year. Resistance to antimalarial drugs in malaria parasites and to insecticides in vectors is one of the most serious issues in the fight against this disease. Moreover, the lack of an effective vaccine against malaria is still a major problem. Recent developments in nanotechnology have resulted in new prospects for the fight against malaria, especially by obtaining metal nanoparticles (NPs) that are less toxic, highly biocompatible, environmentally friendly, and less expensive. Numerous studies have been conducted on the synthesis of green NPs using plants and microorganisms (bacteria, fungi, algae, actinomycetes, and viruses). To our knowledge, there is no literature review that compares toxicities and antimalarial effects of some of the existing metallic nanoparticles, revealing their advantages and disadvantages. Hence, the purpose of this work is to assess metal NPs obtained through various green synthesis processes, to display the worth of future malaria research and determine future strategies. Results revealed that there are very few studies on green NPs covering all stages of malaria parasites. Additionally, green metal nanoparticles have yet to be studied for their possible toxic effects on infected as well as healthy erythrocytes. Morever, the toxicities of green metal NPs obtained from various sources differed according to concentration, size, shape, synthesis method, and surface charge, indicating the necessity of optimizing the methods to be used in future studies. It was concluded that studies on the toxic properties of green nanoparticles would be very important for the future.

Green synthesis and characterisation of ZnO from citrus hystrix extracts for photocatalytic application

The purpose of this ongoing research project is to enhance the quality of zinc oxide (ZnO) powder synthesised through a green synthesis process using extracts from C. hystrix. The objective is to explore the potential of C. hystrix as a sustainable source for the production of ZnO nanoparticles with improved properties. Through a series of experimental procedures, including characterisation techniques such as x-ray diffraction (XRD), scanning electron microscopy (SEM), and UV–vis spectroscopy, the synthesised ZnO powder’s structural, morphological, and optical properties are evaluated. Additionally, the photocatalytic activity of the biosynthesised ZnO powder is assessed for its effectiveness in degrading organic pollutants under UV illumination. By systematically optimising the synthesis parameters and understanding the underlying mechanisms, this research endeavours to contribute to the advancement of green synthesis approaches for producing high-quality ZnO nanoparticles that demonstrate enhanced performance, thereby fostering sustainable and eco-friendly nanomaterial synthesis processes. Following the successful production of eco-friendly ZnO through green synthesis, the optimum sample will undergo several experiments using a doping method with various chemical substances.