Microwave Method Research Articles

Optimization of Sargassum bovianum Extraction Techniques for Germination of Wheat, Canola, and Corn Under Different Salinity Stress

Seaweeds are a cheap, eco-friendly, and rich source of plant growth stimulators that can mitigate the adverse effects of salinity stress. This study examined the impact of Sargassum bovianum extracts obtained through different techniques using pressure, heat, and microwave radiations on the germination and growth of wheat, corn, and canola seeds under varying salinity levels (500, 3500, and 6500 µS cm−1). The findings showed that pressure, microwave, and acidic extraction methods were the most effective in extracting polysaccharides, alginate, and nutrients from S. bovianum. Seaweed extract significantly improved the mean germination time (MGT) and germination index (GI) of wheat under high salinity stress and had a positive effect on wheat plumule length (PL) and germination percentage (GP). However, seaweed extract had no significant impact on canola seeds in salinity stress, except for improved canola PL. The PL and seedling vigor index (SVI) of corn were enhanced in low salinity levels, but most treatments reduced PL and SVI in high salinity. This study suggests that using heat, pressure, and microwave techniques for seaweed extraction results in higher polysaccharides and alginate content, leading to improved germination and plant growth, particularly in wheat and canola. These findings can help growers optimize the germination and growth of these important crops.

Improving phosphorus availability in sewage sludge ash through a novel microwave‐based technology

AbstractThis work is connected with the increasing demand for fertilizers and the associated supply risks and market volatility in the European Union (EU). It highlights the reliance on phosphorus from Moroccan phosphate rocks and the environmental issues stemming from the overuse of phosphate‐based fertilizers. The paper suggests a shift in perspective, viewing waste as a valuable resource. Specifically, it explores the potential of recycling phosphorus from sewage sludge ash, which contains a high phosphorus concentration. The focus is on comparing two methods of phosphorus extraction from sewage sludge ashes: classical wet‐chemical extraction and a new microwave‐based technology. There is an increase in phosphorus bioavailability with the microwave treatment, making it a promising approach for waste management. An initial economic evaluation suggests that the microwave method is highly competitive, especially when compared with wet‐chemical extraction technologies. The resulting material from the microwave treatment is classified as a straight solid inorganic macronutrient fertilizer according to EU regulations.

Physicochemical and therapeutic studies of microwave-synthesized ZnO and Cr-doped ZnO nanoparticles for biomedical applications

Highly stable Zinc Oxide (ZnO) and Chromium (Cr) doped ZnO nanoparticles (NPs) are increasingly studied for biomedical applications due to their low toxicity, biodegradability, and affordability. In this paper, ZnO NPs and Cr doped ZnO NPs have been prepared by a microwave method. The prepared samples were studied with their physicochemical characteristics and successively investigated their impact on the antimicrobial, antioxidant, and biocompatibility properties. Correlations between physicochemical and biomedical properties were assessed. The NPs demonstrated strong, concentration-dependent antibacterial effects against E. coli and X. citri, with maximum inhibition zones of 15.53 mm (PZnO), 13.33 mm (CZnO), 13.56 mm (ZCr2), 14.03 mm (ZCr4), and 15.0 mm (ZCr6) for E. coli, and 13.73, 13.46, 14.50, 14.70, and 15.26 mm, respectively, for X. citri. They also showed significant antifungal activity against A. niger and R. stolonifer. Antioxidant activity, measured via DPPH radical scavenging, revealed inhibition rates of 58.52–92.27 % (PZnO), 56.27–90.65 % (CZnO), 51–85 % (ZCr2), 54–87 % (ZCr4), and 57.75–87.59 % (ZCr6). Hemolysis assays indicated biocompatibility, with hemolysis percentages below 5 % for all NPs at concentrations up to 500 µg/mL. These findings suggest that ZnO and Cr doped ZnO NPs are promising candidates for biomedical applications, offering antimicrobial and antioxidant properties with minimal toxicity to human erythrocytes.

X-ray communication system with high-repetition-rate pulsed X-ray source and LYSO(Ce) and YAP(Ce) scintillators

X-ray communication offers significant advantages over traditional microwave methods due to its shorter wavelength and higher theoretical bandwidth, enabling efficient space communication and penetration through complex electromagnetic environments. However, current systems face limitations in X-ray emission modulation and high-precision timing detection. To meet the high-frequency transmission demands of space missions, we developed a pulsed X-ray emission source capable of high-frequency modulation. Additionally, we identified specific scintillators with distinct advantages for different transmission frequency ranges, allowing for performance optimization. Experimental results demonstrated a successful transmission rate of 10 MHz, validating the feasibility of MHz-frequency X-ray communication.

Structural studies of racemic and diastereomeric 2-amino-3-carbonitrile-based chromene derivatives

In this study, we present a comprehensive exploration of sixteen novel 2-amino-4-aryl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitriles synthesized through a streamlined multicomponent microwave method. These chromene derivatives, obtained in remarkable yields (92-94%), exhibit a fascinating array of stereochemical complexities. The influence of electron-withdrawing groups was subtly evident in chemical shifts, underscoring the nuanced interplay between structure and substituent effects. Infrared spectroscopy confirmed characteristic NH₂ functionalities across the series, with notable deviations in compounds featuring electron-withdrawing groups. Compounds studied by single crystal X-Ray diffraction, were all in the monoclinic crystal system, with interesting molecular disorder in select diastereomers. Intermolecular hydrogen bonding networks formed between the amino functional group and the chromenone O atom or a solvent O atom, lead to motifs similar to the previously reported motifs by our group including an extra N—Hb…O3-interaction involving the amino and the methoxy substituent in compound 3c. Hirshfeld surface analysis further showed the contributions of key intermolecular contacts, while energy calculations highlighted the dominant role of electrostatics in motif stabilization. This work not only enriches the structural landscape of chromene derivatives but also opens avenues for future investigations into their potential applications in material science and beyond.

Rapid Preparation of Platinum Catalyst in Low-Temperature Molten Salt Using Microwave Method for Formic Acid Catalytic Oxidation Reaction.

In this paper, platinum nanoparticles with a size of less than 50 nm were rapidly and successfully synthesized in low-temperature molten salt using a microwave method. The morphology and structure of the product were characterized by SEM, TEM, EDX, XRD, etc. The TEM and SEM results showed that the prepared product was a nanostructure with concave and uniform size. The EDX result indicated that the product was pure Pt, and the XRD pattern showed that the diffraction peaks of the product were consistent with the standard spectrum of platinum. The obtained Pt/C nanoparticles exhibited remarkable electrochemical performance in a formic acid catalytic oxidation reaction (FAOR), with a peak mass current density of 502.00 mA·mg-1Pt and primarily following the direct catalytic oxidation pathway. In addition, in the chronoamperometry test, after 24 h, the mass-specific activity value of the Pt concave NPs/C catalyst (10.91 mA·mg-1Pt) was approximately 4.5 times that of Pt/C (JM) (2.35 mA·mg-1Pt). The Pt/C NPs exhibited much higher formic acid catalytic activity and stability than commercial Pt/C. The microwave method can be extended to the preparation of platinum-based alloys as well as other catalysts.

Comparison of the potential risk from arsenic exposure when eating fish grown in natural and artificial conditions, using the example of rainbow trout

Introduction. Due to the increasing share of fish and fish products in the human diet, hygienic problems are also increasing, especially with the growing of aquaculture sector. The task of determining the level of arsenic toxicity is becoming extremely important. Although the toxicity mechanisms of inorganic arsenic are generally well understood, the impact of speciation of its other (organic) compounds on the likelihood of carcinogenic and non-carcinogenic effects has been largely unexplored. Material and methods. The objects of study were samples of fillet and caviar of salmon fish – rainbow trout (wild and aquaculture). The quantitative determination of arsenic-containing substances was carried out using high-performance liquid chromatography-mass spectrometry with inductively coupled plasma. The samples were prepared using microwave methods. The risk level was calculated based on recommendations R 2.1.10.3968–23. Results. As the result of this work the information about concentration of arsenic (organic and inorganic compounds) in fillets and caviar of fish from the salmon family - rainbow trout was shown. It has been established that the content of inorganic and organic arsenic compounds practically does not differ, depending of the habitat of trout. The levels of carcinogenic and non-carcinogenic risk of inorganic arsenic were calculated. Limitations. Determination of arsenic concentration was carried out in rainbow trout, which had been grown in natural and artificial conditions. Conclusion. It has been established that inorganic arsenic makes the greatest contribution to the health risk. However, the magnitude of the risk does not exceed the acceptable sanitary and hygienic standards, while the conditions for growing fish have practically no effect on these values.

Synthesis and Study Biological Activity of Some New Substituted Thiazolidin-4-one Derivatives

The microwave (MW) method was used to create a series of new thiazolidin-4-one derivatives containing benzothiazole and azo groups. Azoaldehyde derivative A was synthesized via the coupling reaction of 2-aminobenzothiazole diazonium ions and 2-hydroxybenzaldehyde. The resultant azoaldehyde A was then subjected to condensation reactions with the primary aromatic amines using the MW method to give azoimines derivatives S1-S5. Finally, compounds S1-S5 were reacted with α-mercaptoacetic acid by the MW method to generate the thiazolidin-4-one derivatives T1-T5. The novel-produced compounds T1-T5 were identified by FT-IR, 1H NMR, and 13C NMR spectroscopy. The DPPH was used to determine the antioxidant activity of the novel-produced compounds T1-T5. The obtained results for T1 and T5 were excellent as antioxidants in comparison with ascorbic acid, while in the antibacterial study, it was discovered that T2, T3, and T5 were found to be more successful than Gentamycin as a control drug against Staphylococcus aureus in an antibacterial investigation, while T3 was found to be more effective than the reference drug against Escherichia coli.

Comparison of microwave and pulsed electric field methods on extracting antioxidant compounds from Arvaneh plant (Hymenocrater platystegius Rech. F)

Improving the quality of extracts derived from medicinal plants is a critical concern due to their extensive use across various industries. The Arvaneh plant (Hymenocrater platystegius Rech. F), a species native to the Khorasan province in Iran and belonging to the mint family, was the focus of this study. We optimized the extraction of Arvaneh plant using both microwave (MW) and pulsed electric field (PEF) techniques. The MW method was tested at different processing times (90, 180, and 270 s) and power levels (180, 540, and 900 W), while the PEF method was evaluated with varying electric field intensities (0.25, 3.25, and 6.25 kV/cm) and pulse numbers (10, 45, and 80) using a central composite design (CCD). The results revealed that extraction efficiency, total phenolic content, and total flavonoid content were significantly higher with the PEF method compared to the MW method (p < 0.05). Moreover, the PEF technique showed superior performance in preserving the antioxidant properties of the extract, as assessed by DPPH and FRAP methods. GC/MS analysis confirmed the presence of 27 bioactive compounds in the Arvaneh extract obtained through PEF-assisted extraction. In conclusion, the PEF method proved to be highly efficient for extracting bioactive compounds from the Arvaneh plant.

Effects of 910 MHz Solid-State Microwave Cooking on the Quality Properties of Broccoli (Brassica olearacea L. var. Italica Plenck), Carrots (Daucus carota subsp. Sativus), and Red Peppers (Capsicum annuum L. cv. Kapya).

Domestic microwave ovens offer rapid cooking but face challenges such as non-uniform temperature distribution and hot spots. A novel solid-state heating system, which precisely controls microwave frequency and power, provides a promising alternative to traditional microwave ovens utilizing magnetron systems. This study compared the effects of solid-state microwave cooking on the quality of broccoli, red peppers, and carrots with those of traditional microwave and conventional cooking. The traditional microwave cooking used in this study operated at 2450 MHz, while the solid-state system functioned between 902 and 928 MHz. Weight loss was highest for conventional cooking, reaching a maximum of 34%, whereas microwave cooking resulted in a maximum of 11.65% and solid-state microwave cooking in 17.04%. The total phenolic content obtained through conventional cooking ranged between 61.58 and 116.51 mg GAE (gallic acid equivalents)/100 g dry basis, while microwave cooking resulted in a range of 88.04-110.92 mg, and solid-state microwave cooking achieved values between 76.14 and 122.91 mg. Furthermore, reductions in chlorophyll content were observed to be 68.2%, 25.6%, and 35.7% for conventional, microwave, and solid-state microwave cooking, respectively. Lycopene content after conventional cooking decreased to 224.73 mg/100 g dry basis, compared to 289.55 mg after microwave cooking and 242.94 mg after solid-state microwave cooking. β-carotene content showed a decrease of 14.5% in conventional cooking, while both microwave methods showed an increase of 14.7%. These results suggest that solid-state microwave cooking may have promising positive effects on food quality.

Green Engineered CuO/SnO2/HNT Composites: Illuminating the Photocatalytic Path for Organic Pollutant Remediation and Zebrafish Embryo Toxicity Evaluation.

Photocatalysis stands out as a promising technique for treating organic contaminants, yet the quest for visible light active composite materials, crafted through cost-effective, eco-friendly, and uncomplicated processes, poses formidable challenges. Here, we introduce a successful endeavor, the synthesis of a CuO/SnO2 (CS) composite via a microwave method, employing Carissa edulis fruit extract as a reducing as well as capping agent. Various loadings of CS-HNT composites were prepared by ultrasonically incorporating CS onto nanotubular halloysite (HNT) clay. Employing a suite of types of characterization, including XRD, XPS, FT-IR, FE-SEM, HR-TEM, ζ potential, UV-vis-DRS, TGA, BET, and EIS, we meticulously explored the morphology, structure, stability, surface area, electrochemical, and optical properties of the developed CS-HNT composites. HR-TEM observations unveiled the formation of a heterojunction between cubic CuO and spherical SnO2 on the HNT clay surface. Optical and EIS analysis highlighted that the 20CS-HNT composite displayed significant absorption in the visible region, efficient electron-hole pair separation, and enhanced interfacial charge transport relative to other loadings. Photocatalytic evaluations and optimization studies revealed that the 20CS-HNT photocatalyst achieved notable removal efficiencies, eliminating 85% of Congo red (CR) and 80% of tetracycline (TC) within 90 min and 74% of ATZ in 3 h under visible light conditions. Scavenging investigations, the fluorescence probe method, and a NBT transformation study underscored the pivotal roles of hydroxyl and superoxide radicals in pollutant removal. The reusability trials highlighted the exceptional stability and recyclability of the photocatalyst, even after five cycles. In addition, zebrafish embryo toxicity tests revealed improved survival and hatching rates in photocatalyst-treated samples compared to those of controls. Moderate toxicity was observed in treated TC, while the treated CR sample showed non-lethal toxicity. In essence, this study unveils a straightforward and efficacious approach for developing photocatalysts for large-scale wastewater treatment. Furthermore, it proposes the adoption of safe clay-based bimetal oxide photocatalysts in diverse environmental applications.

In-situ synthesis nano PtRuW/WC HER catalyst for acid hydrogen evolution by microwave method

Abstract One of the primary challenges in electrocatalysis for the hydrogen evolution reaction (HER) lies in the development of highly efficient catalysts suitable in acidic environments. Tungsten carbide-based materials have long been proposed as potential substitutes for Pt due to their “Pt-like” electronic properties in the HER process. However, tungsten carbide still falls short of the performance exhibited by commercial precious-metal catalysts. Herein, PtRuW/WC was prepared by a microwave heating method and acted as a HER electrocatalyst. The microwave method not only enhances the diffraction peaks of the substrate tungsten carbide, but also facilitates the growth of metal ions at specific sites. The PtRuW/WC catalyst demonstrates outstanding performance in acidic HER, characterized by a minimal overpotential of 40.7 mV at 10 mA/cm2 (η10). Furthermore, it exhibits exceptional stability in acidic solutions, showing no substantial degradation during 20 h at 1000 mA/cm2. The catalyst-assembled PEM electrolytic water electrode further proves that PtRuW/WC has excellent electrolytic water performance and makes some efforts for the development of commercial PEM electrolytic water.

Sustainable synthesis of MOF for COVID-19 detection using a 23 factorial design

The emergence of the COVID-19 pandemic has underscored the urgent requirement for rapid and accurate diagnostic methods to detect the virus and control its spread. Metal Organic Frameworks (MOFs) have gained significant interest in biosensing applications because of their exceptional properties. This study investigates the microwave synthesis of zeolitic imidazolate framework-8 (ZIF-8) and explores its potential as a fluorescent biosensor for detecting COVID-19 RNA sequences. The microwave method enables a rapid, eco-friendly, and efficient synthesis of ZIF-8. Characterization tests including PXRD, FE-SEM, TGA, and FT-IR confirmed the high crystallinity and thermal stability of ZIF-8. To optimize the biosensor’s performance, a 23 factorial design is pursued. The factorial design allows determining the individual and simultaneous effects of the control parameters such as ZIF-8 concentration, buffer pH, and solution temperature on the quenching efficiency. The results demonstrate that the parameters combination of 25 °C, pH 8.0, and 0.7 mg/mL ZIF-8 concentration results in the highest quenching percentage of 72.41 %. The study of the quenching mechanism confirms that the P-DNA can form electrostatic and π-π stacking interactions with ZIF-8, to produce a P-DNA@ZIF-8 complex. It is also found that photoinduced electron transfer is more dominant than fluorescence resonance energy transfer in the quenching mechanism. The biosensor showed a high sensitivity towards the target COVID-19 RNA with a very low detection limit of 12.02 pM, a fast detection time of 40 minutes, and high selectivity to the target RNA. This study shows the potential of ZIF-8 as a feasible and environmentally friendly material for swiftly and accurately detecting COVID-19 RNA sequences.

Self-Nanoemulsifying Drug Delivery System Combined with a Polymeric Amorphous System of Glibenclamide for Enhanced Drug Dissolution and Stability.

Self-nanoemulsifying drug delivery systems (SNEDDS) have been widely applied to improve the dissolution and bioavailability of hydrophobic medications like glibenclamide (GB). However, the acid liability of GB limits its loading in SNEDDS formulation owing to the expected drug degradation. The present study investigated the ability of a polymeric amorphous system (PAS) to amorphize raw GB and facilitate its integration within dispersed SNEDDS. Liquid-SNEDDS (L-SNEDDS), solid-SNEDDS (S-SNEDDS), and combined systems (SNEDDS + PAS) were prepared for this purpose. The physicochemical properties of the prepared formulations were examined using a zeta-sizer, SEM, DSC, PXRD, and dissolution apparatus. In addition, GB integrity within formulations following incubation in a stability chamber was also investigated. The prepared formulations were able to be dispersed within the nanosize range. SEM, DSC, and PXRD showed that freeze-drying (FD) was superior to the microwave (MW) method in GB amorphization. Even though L-SNEDDS and S-SNEDDS were able to increase the dissolution efficiency (DE) of GB, drug degradation was observed. However, PAS prepared using FD was able to increase the DE of GB from 2.5% to 84.2% and protect the drug from chemical degradation. The present study revealed that a combined system (SNEDDS + PAS) is a promising approach to enhance the stability of acid-labile drugs and facilitate the integration of amorphous drugs within a dispersed SNEDDS formulation.

Exploring microwave activation as a novel method for activating coal gangue: Focus on microwave activation mechanisms and hydration characteristics of cementitious supplementary materials

To support the decarbonization of the cement industry, coal gangue (CG) has potential as a supplementary cementitious material. The calcination process significantly impacts the phase transformation of clay minerals and the pozzolanic activity of CG. This study involved calcination of CG at 600 ℃ and 800 ℃ using both microwave and thermal activation methods. Employ XRD, XPS, FTIR, TG, and SEM to examine the impact of calcination mechanism on the crystal structure, element binding energy, chemical bonds, microstructure, and mineral composition of CG. The results indicate that the transformation of kaolinite in CG to metakaolin is completed around 600 °C. Microwave activation increased the reactive aluminate content in CG, enhancing pozzolanic activity and promoting secondary hydration with cement. This process generated additional C-(A)-S-H gels and AFm phases, which filled matrix pores, increased system density, and improved mechanical properties. The optimal activation method for CG was identified as microwave activation at 600 °C.

Synthesis, photophysical properties, and in-silico nonlinear optics of 3-hydroxy-N-phenyl-2-naphthamide and its acetate, acrylate, and benzoate derivative

In this study, we report the successful growth of single crystals of 3-hydroxynaphthalene-2-carboxanilides (NAS) with a monoclinic structure in the P21/c space group and space group number of 14 for the first time. We have developed a yield and time-effective modified synthetic procedure using a synthetic reactor by replacing the traditional microwave method. Additionally, acylated derivatives of NAS, including novel acryloyl derivative (NAS AC), are synthesized with a modified procedure, replacing pyridine with triethylamine.We investigate the structural, photophysical, and quantum chemical properties of N-(4-acetylphenyl)-2-oxo-2H-chromene-3-carboxamide (NAS) and its acylated derivatives (NAS AC, NAS ACT, NAS BZ). Photophysical studies reveal significant Stokes shifts observed in different solvents, including time-enhanced fluorescence in DMSO, attributed to solvent relaxation processes. Natural bond orbital (NBO) analysis, molecular electrostatic potential (MEP) maps, and frontier molecular orbital (FMO) provide insights into electronic interactions and asymmetric charge distribution. Low-lying LUMO values of these compounds (-2.31 eV to -1.95 eV) support candidature for the electron acceptor applications. Nonlinear optical properties were thoroughly investigated, with NAS displaying the highest static first-order hyperpolarizability (17.89 × 10−30 esu) and NAS BZ exhibiting the highest second-order hyperpolarizability (113.09 × 10−36 esu), indicating significant nonlinear optical responses. Thermal stability (TGA and DTA) highlights the significant range of temperatures for the NLO applications.

Exploration and Design of Carbon Dot-Based Long Afterglow Materials Using Active Machine Learning and Quantum Chemical Simulations.

Long afterglow materials based on carbon dots (CDs) have attracted extensive attention in the field of optics due to their low cost and nontoxic properties. However, the targeted synthesis of specific properties of complex and unknown structures such as CDs remains a daunting challenge. In this study, the powerful nonlinear fitting ability of machine learning was used to explore the afterglow properties of CDs. The XGBoost algorithm demonstrates high prediction accuracy in determining the optimal excitation wavelength, optimal emission wavelength, and afterglow lifetime. Using Bayesian optimization, we screened and synthesized the CDs-based long afterglow materials with the longest lifetime reported so far by a one-step microwave method. By combining quantum chemical calculations with experimental data, we revealed the structure-function relationship between CDs and their precursors through electron-hole analysis. These results show that machine learning can establish nonlinear correlations between precursors and materials with unknown structures, clarify their intrinsic relationships, simplify the material design process, and thus accelerate the development of advanced materials.

POTENTIAL USES OF DRIED APRICOT PULP IN OBTAINING FUNCTIONAL PRODUCTS

In this study, apricot pulp samples dried by hot air, microwave and microwave-hot air combination methods were ground into powder. By analyzing certain parameters of the obtained apricot pulp powder samples (total phenolic content, antioxidant capacity and color values), the apricot pulp powder obtained by the drying method (300 W-60ºC) determined by prioritizing the functional properties in yogurt and bread production, was used in 5 different ratios (10%, 20%, 30%, 40% and 50%).

Modification of Chitosan Isolation Method from Pearl Oyster Shell (Pinctada maxima sp) as A Source of Natural Polymer

Abstract Chitosan is natural polymer with abundant availability and unique characteristics. The purpose of this study was to investigate the effects of various isolation methods on chitosan properties. Chitosan was obtained by isolation method using oyster pearl shell (Pinctada maxima sp.). The parameters of the deacetylation process are the comparison of heating method with microwave method and the comparison of microwave power. Chitosan was characterized for degree of deacetylation (DD) and functional groups by FTIR, and viscosity by Brookfield viscometer. The microwave method was faster than the heating method. Then, the larger mass of shell and %NaOH produced a higher DD of 89.75%. However, the use of 60g mass and 60% NaOH resulted in an already high DD of 81.96%. Furthermore, variation microwave power showed the highest DD at high power. FTIR spectrum analysis showed the appearance of chitosan functional groups, OH and NH2 groups. The viscosity value decreased as the microwave power increased. Based on this study, different isolation methods affect the quality of chitosan. However, it’s necessary to conduct more detailed research related to changes in chemical structure. Therefore, oyster shells can produce chitosan as a source of natural polymers with different characteristics.

Green synthesis of carbon dots nanoparticles from edible swiftlet nest and evaluation of their antioxidant activity

Edible swiftlet nest (ESN) confers various health benefits to humans, including immune system enhancement, anti-inflammatory properties, bone strengthening, and antioxidative effect. ESN is notably rich in protein and minerals, with its proteins serving as non-enzymatic antioxidants capable of binding free radicals. However, the antioxidant capacity of ESN is comparatively lower than that of other free radical scavengers, such as carbon dots nanoparticles (CNPs). CNPs features charged ligands on their surface that act as electron donors for free radical binding. The presence of the carbon chain forming proteins in ESN suggests their potential as the primary source for CNPs formation. The enhancement of hydroxyl groups and delocalized electrons is imperative for enhancing the antioxidant activity of ESN. This study aims to enhance the antioxidant activity of ESN by converting it into CNPs nanoparticles. The results demonstrated the effective synthesis of CNPs from the ESN solution using microwave methods. This was evidenced by XRD patterns indicating CNPs formation, and an average particle size of 4.86 nm as indicated by TEM analysis. The optimal microwave heating duration of 30 min yielded CNPs with a prominent emission spectrum peak at 425 nm and significantly high intensity. Absorbance data revealed the presence of C=C bonds, consistent with aromatic CNPs bonds observed in FTIR studies. CNPs possessed hydroxyl and carboxyl linkages, suggesting their potential as antioxidants. The percent inhibition results indicated that CNPs exhibited a substantial percentage (62.5%) at a concentration of 50 mg ml−1. The free radical scavenging activity of the CNPs significantly elevated compared to ESN.