High Surface Area Research Articles

Antimony removal using zero-valent iron-manganese bimetallic nanomaterial: Adsorption behavior and mechanism

Although the effectiveness of zero-valent iron (ZVI) and zero-valent manganese (ZVMn) in heavy metal removal is well-established, their combined synergistic potential for antimony (Sb) remediation from wastewater has remained largely unexplored. Addressing this gap, this study introduced a magnetic zero-valent iron-manganese bimetallic material (ZVIM), synthesized via the borohydride reduction method, to investigate its capabilities and underlying mechanisms for Sb reduction and adsorption. The ZVIM, characterized by a high specific surface area of 220 m²/g, exhibited a high adsorption capacity (614.6 mg/g for Sb(III) and 241.7 mg/g for Sb(V)), facilitating over 96.7 % removal for both Sb(III) and Sb(V). The adsorption conformed to the pseudo-second-order kinetic model, and the isotherm data aligned with the Freundlich model, indicative of a heterogeneous adsorption process. The removal of Sb(III) predominantly occurred via surface complexation and electrostatic adsorption to the positively charged ZVIM surface, accompanied by a partial oxidation of Sb(III) to Sb(V). In contrast, the elimination of Sb(V) was primarily facilitated through surface complexation mechanism, encompassing both reduction and electrostatic adsorption. The outcomes of this study shed light on the intricate interactions between Sb species and the ZVIM, revealing the material as a promising candidate for the efficacious removal of Sb from wastewater.

Preparation of porous (Mo2/3Y1/3)2AlC and its hydrogen evolution reaction performance

Porous (Mo2/3Y1/3)2AlC MAX phase ceramic was prepared by reaction sintering method using Mo, Y, Al, and graphite powder as raw materials. The influence of changes in Al content on the purity of the obtained samples was investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), Archimedes method, and bubble point method. The conditions for obtaining a pure phase were identified, and the transformation path of the phase during sintering and the mechanism of pore formation were provided. The linear sweep voltammetry (LSV) cure and cyclic voltammetry (CV) cure of MAX were tested using an electrochemical workstation. It can be calculated that MAX exhibits good hydrogen evolution reaction (HER) performance under alkaline conditions due to its high electrochemical active surface area (ECSA) of 373.2 and small Tafel slope of 41.7 ​mV·dec−1.

Impact of Ag2O on the gas sensing properties of the star-shaped BaTiO3/ZnO heterostructures

In this work, star-shaped heterostructures of Ag2O/BaTiO3/ZnO were proposed as resistive-type gas sensors. Through combined analyzes of XRD, SEM, and EDS, the structure, surface morphology, and the elemental composition of the synthesized materials were confirmed. The star-shaped morphology of BaTiO3/ZnO was found to be intact even after loading with different quantities of Ag2O, as revealed by the SEM analysis. The impact of loading different amounts of Ag2O (ranging from 1 % to 3 %) on the sensors' ability to detect volatile organic compounds (VOCs) and carbon dioxide (CO2) was concretely gauged by their response, response/recovery times, selectivity, and long-term stability. For the detection of ethanol/acetone, CO2, and methanol, a 1:2 M ratio of BaTiO3/ZnO with 1 % and 2 % Ag2O, and a 1:3 M ratio of BaTiO3/ZnO with 1 % Ag2O were determined as the optimum content, respectively. From the gas sensing analysis, Ag2O/BaTiO3/ZnO sensors with different amounts of Ag2O additive gave different optimal temperatures for different target gases. Lower operating temperatures, i.e. 180 °C, and 260 °C for CO2 and VOCs, respectively, rapid responsivity with a response time of <1 s for VOCs, and fast recovery times (as low as 10, 13, and 6 s for ethanol, acetone, and methanol vapors, respectively) were observed. More importantly, the sensor exhibited good selectivity for several possible interferences. The underlying reasons for the acceleration of the gas molecules adsorption, hence the fast sensor response, are the high specific surface area established by the star-shaped morphology, and compatible energy band alignment at the p/n interface coupled with the catalytic effect induced by Ag2O.

Turning waste into wonder: Arsenic removal using rice husk based activated carbon

In this study, rice husk activated carbon (RHAC) was synthesized by physicochemical activation, which consists of heat treatment with CO2 gasification and KOH chemical treatment to eliminate arsenic (As) from the polluted water. Initial arsenic concentrations, solution pH, solution temperature and contact time are the parameters that have been tested in this study. The characterization study showed that RHAC has a high BET surface area (815.52 m2/g) and its pore structure was found to be mesoporous with an average pore diameter of 2.96 nm. Characterization studies, including X-ray diffraction analysis (XRD), Raman spectroscopy and scanning electron microscopy (SEM) were employed to determine the RHAC’s performance. The adsorption of As towards RHAC followed the Freundlich isotherm model and pseudo-first order with adsorption process was favorable at higher arsenic concentrations. The mechanism study also signified that the adsorption of As-RHAC was limited by film-diffusion. Thermodynamic studies indicated that the As-RHAC adsorption system was endothermic, random, spontaneous, feasible in nature and governed by the chemisorption process. Desorption and regeneration studies of RHAC showed that it can be utilized up to 5 cycles and is stable for the water treatment facilities.

Anchoring effect of transition metal dihaloalkanes in lithium-sulfur batteries: A first-principles study

Suppressing the shuttle effect by enhancing the sulfur electrode structure is an effective method to achieve long-term cycle stability of lithium-sulfur batteries. In which, two-dimensional materials are widely used to improve the performance of lithium-sulfur batteries because of their high specific surface area and high electrical conductivity. In this paper, the anchoring effect of NbX2 (X= S,Se,Te) on polysulfides, and the conductivity, stability and diffusion behavior of the adsorption system are studied by using density functional theory calculation. The results show that NbX2 (X= S,Se,Te) has good electrical conductivity and stability, where NbS2 has moderate adsorption strength (0.84–3.28 eV) for lithium polysulfides, and the interaction of S atoms on the surface of Li2S and Nb atoms on the substrate surface is the main source of adsorption energy. In addition, the diffusion potential barrier is low (0.12 eV). The calculated results show that NbS2 may be a potential choice as an anchoring material for Li-sulfur batteries.

Harnessing the power of ternary nanocomposites: Iron oxide, multiwalled carbon nanotubes, and bentonite for superior ciprofloxacin adsorption

Water contamination from antibiotics can have detrimental effects on one’s health. Consequently, treating the polluted water is required to fix this issue. Fe3O4-multiwalled Carbon Nanotubes (MWCNTs)-Bentonite nanocomposite has been successfully prepared using a customized co-precipitation process. The synthesized nanocomposite was used as an adsorbent to extract the ciprofloxacin from aqueous solutions. The synthesized nanocomposite was examined using several characterization methods. Scanning electron microscopy demonstrates that the Fe3O4 nanoparticles and bentonite are well-decorated on MWCNTs. The nanocomposite exhibits a high BET surface area of 221.577 m2/g and a pore volume of 0.411 cm3/g. According to the analysis, the average pore diameter was found to be 3.717 nm. Additionally, the adsorption model agreed with the Jovanovic model, which had a 137.35 mg/g adsorption capacity, with a χ2 of 2.161, and a good nonlinear R2 value of 0.999. Moreover, adsorbent was found to be highly stable even after 4 cycles. The ΔS and ΔH values were found to be positive, which suggested an endothermic process. The synthesized nanocomposite proved to be a viable option for water treatment applications, and there is no literature available on CIP antibiotic adsorption using Fe3O4-MWCNT-Bentonite nanocomposite.

Facile manufacturing of carbon nanotube/ZIF-67-derived cobalt composite aerogel with high-efficiency electromagnetic wave absorption

Developing high-efficiency electromagnetic wave (EMW) absorbers by designing dielectric/magnetic components and microstructure in a straightforward, scalable method is highly desirable yet challenging. Here, we introduce a novel hierarchical composite aerogel-based EMW absorber composed of conductive carbon nanotubes (CNTs) and magnetic metal-organic framework (MOF) derivatives, integrated with sustainable cellulose nanofibers (CNF) derived carbon. This composite was prepared using a scalable freeze-casting followed by carbonization approach. Freeze casting enabled the creation of porous monoliths with high specific surface areas and customizable pore sizes and porosities, crucial for enhancing EMW reflection and scattering. Carbonization enhanced composite conductivity and stabilized the cobalt (Co)/carbon nanoparticles derived from ZIF-67 within the carbon matrix. CNF-derived carbon facilitated the efficient integration of ZIF-derived Co nanoparticles and CNTs, resulting in a robust 3D aerogel structure. The synergistic effects of CNT conductive paths and Co nanoparticles' magnetic losses provided an efficient route to enhance EMW absorption. Moreover, the creation of numerous heterogeneous interfaces augmented polarization losses, significantly enhancing EMW loss capability. Remarkably, the composite achieved outstanding EMW absorption, with a minimum reflection loss of -71.03 dB at a filling ratio of merely 10 wt.% and an effective absorption bandwidth of 4.64 GHz, comparable to leading EMW absorbers reported to date.

Preparation of CeO2QDs-g-C3N4/C composites and electrochemical determination of aflatoxin B1

The presence of Aflatoxin B1 (AFB1) in food represents a significant threat to human health, leading to the development of cancer. The key factor for effective trace detection technology lies in the utilization of sensor materials that exhibit excellent selectivity and high sensitivity properties. In this study, a successfully synthesis of g-C3N4/C with a high specific surface area uses melamine and houttuynia cordata stem as starting materials. A CeO2QDs-g-C3N4/C composite was prepared by hydrothermally anchoring cerium oxide quantum dots (CeO2QDs) onto the surface of g-C3N4/C, the high redox efficiency of CeO2QDs and the small size limitation effect significantly improve the sensing performance. The composite was characterized by XRD, XPS, SEM, TEM, and N2 adsorption-desorption. The results revealed that, the CeO2QDs-g-C3N4/C composite sensor material exhibited significant advantages with a large specific surface area, a well-defined micropore structure, and abundant reactive sites. In addition, electrochemical activity tests are conducted using EIS, CV, and DPV for the purpose of electrochemical investigations. The CeO2QDs-g-C3N4/C/GCE exhibits exceptional electrocatalytic activity against AFB1, with a wide linear response range of 100-1300 pg ml-1, an impressively low detection limit (LOD) of 6.61 fg ml-1 (S/N=3), and a sensitivity of 0.985 pg μM ml-1μA-1. Furthermore, the stability, repeatability, and interference experimental response errors all remain below 5%. It is also noteworthy that, the sensor material demonstrates excellent practicality in AFB1 assays conducted on real samples, which serves to illustrate its immense potential for applications in food safety evaluation.

Synthesis and Characterization of Carbon Nano Sphere-doped Gd: Alpha Sb2O4 Nanostructure for High-Performance Energy Storage Applications

Background: To enhance the super capacitive properties of nanocomposites, the effective method is to combine carbon nanospheres with mesoporous structures with Gd3+:α-Sb2O4 inorganic nanocomposites (NC) to form hybrid electrodes. An as-prepared hybrid electrode material possesses increased energy density, high rate of reversibility and cyclic stability when incorporated in electrochemical cyclic voltammetric studies. Methods: In the present investigation, various wt % of C-nanospheres (Cx) (5 %, 10% and 20%) were decorated over Gd3+: α-Sb2O4 nanocomposites and were synthesized by coprecipitation method. XRD, SEM, EDX, UV-visible, and XPS are only a few of the analytical techniques used to describe the as-prepared hybrid nanocomposites. Electrochemical cyclic voltammetry was carried out in a 6 M KOH solution, three-electrode system. Results: The crystal structure and morphology of Cx: Gd3+@ α-Sb2O4 NC showed a mixed hexagonal phase and agglomerated tiny irregularly shaped morphology that appeared as the Cx concentration increased. Redshift in optical absorption peak appeared (near UV-edge), and the optical band gap (Eg) value increased from 3.53 eV to 3.65 eV. The electrochemical supercapacitor showed the highest specific capacitance of 989 F/g at the current density of 1 A/g for C20%:Gd3+@α-Sb2O4 NC compared with Cx:Gd3+@α-Sb2O4 (x = 5% and 10%) and undoped Gd3+:α-Sb2O4 NC. The change in phase angle and Rs value of 1.98 was attributed to the ideal supercapacitor properties. The cyclic stability after 5000 cycles with 79.71% capacitive retention was exhibited by C20%:Gd3+@α-Sb2O4 NC. Conclusion: The present research introduces ease of synthesis of hybrid electrode materials possessing high active surface area, increased energy density, high cyclic stability, and reversibility in an aqueous solution.

Optimized strategies for efficient CO2 trapping using hydrate technology by pressure adjustment

The hydrate-based method enhances oceanic CO2 storage capacity and is deemed beneficial for controlling greenhouse gas emissions. However, the non-uniform CO2 hydrate crystal interface in the sub-seabed storage layer acts as a barrier, slowing down mass transfer kinetics. This work employed in-situ nuclear magnetic resonance (NMR) technology to compare three different pressure adjustment strategies and observe CO2 bubble dispersion after hydrate dissociation, secondary nucleation, and crystal growth mechanism, along with pore water changes. The presence of micro/nano CO2 bubbles with high internal pressure and high specific surface area in the dissociation liquid significantly accelerated secondary micro-structural phase transition rates. The optimal hydrate-based CO2 storage efficiency reached up to 81.7 %. Moreover, the secondary formation of CO2 hydrates distributed more uniformly within the large, medium, and small pores and led to a significantly increased residual water conversion rate (reaching up to 88 %) in medium pores. The post-secondary formation of high-density hydrates resulted in low fluid mobility (T1/T2 mostly distributed in the range of 0 ∼ 10) and exhibited a mixed wettability state between pore fluids. Utilizing the “memory effects” of CO2 hydrate effectively overcame late-stage mass transfer barriers of solid hydrates films. Our findings extend the understanding of CO2 hydrate formation kinetics under pressure adjustment strategies.

Synergic effect between La-MOF and MXene: Revolutionizing TPU with improved mechanical strength and fire safety

Two-dimensional MXene nanosheets with lamellar structure and high specific surface area are considered promising flame retardants for polymers. However, MXene easily accumulates in polymer materials, resulting in the impairment of their mechanical properties. Metal-organic frameworks (MOFs) not only address this issue effectively but also improve compatibility with polymer materials due to their organic components. In this work, lanthanide rare-earth MOF (La-MOF) were successfully grown in-situ on the MXene surface to prepare hybrid flame retardants (La-MOF@MXene), then added to thermoplastic polyurethane (TPU). The La-MOF suppressed the accumulation of MXene in TPU, and the synergistic effect between them improved the fire safety and mechanical strength of TPU composites. The peak heat release rate of the TPU composites with the addition of 3 wt% La-MOF@MXene was 473.3 kW/m2, which represented a 49.4 % decrease compared to that of pure TPU. Besides, due to the synergic properties of MXene and La-MOF, La-MOF@MXene further reduced total smoke, CO2, and CO of TPU composites in fires. Moreover, with the addition of 3.0 wt% La-MOF@MXene, the tensile strength and elongation at break of TPU composites dramatically improved to 42.4 MPa and 686 %, respectively. Therefore, this study provides a novel paradigm for preparing hybrid flame retardants that can improve the fire safety and mechanical properties of TPU composites, exhibiting broad application prospects.

Multiphase lattice engineering of bimetallic phosphide-embedded tungsten-based phosphide/oxide nanorods on carbon cloth: A synergistic and stable electrocatalyst for overall water splitting

The hierarchical design of the three-dimensional (3D) nanoarchitecture, comprising multiple phases within an interconnected network on a conductive substrate, offers a high specific surface area, abundant exposed active sites, and rapid electron transport. In our study, we synthesized a hybrid catalyst by integrating (Fe,CO)-P nanoparticles into uniformly grown W-(O,P) nanorods on carbon cloth (CC) using a straightforward method, demonstrating notable electrocatalytic performance. The as-synthesized (Fe,CO)-P/W-(O,P)@CC exhibited remarkable performance in both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) for overall water splitting. It achieves overpotentials of 210 and 61.3 mV for the OER and HER, respectively, at a current density of 10 mA cm−2 in a 1 M KOH solution. As a bifunctional electrocatalyst in overall water splitting, (Fe,CO)-P/W-(O,P)@CC needs only 1.50 V to attain a current density of 10 mA cm−2, surpassing traditional Pt/C@CC and IrO2@CC counterparts (1.53 V @ 10 mA cm−2). The synergistic effects between (Fe,Co)-P and the W-(O,P)@CC nanohybrid heterostructure enhance the charge transfer, further promoting the activity of this hybrid electrocatalyst. This study reveals a promising avenue for advanced water electrolysis applications.

Effect of CeO2 on the preparation of functional ceramsite and the adsorption effect of ammonia-nitrogen wastewater treatment

This study investigates the effect of rare earth oxide CeO2 on the physical properties of ceramsite and its efficiency in treating ammonia-nitrogen wastewater. Ceramsite was prepared from solid waste with 10% coal gangue added as a pore-forming agent. Ceramsite sample I with CeO2 and sample II without CeO2 were prepared using pure reagents. The process parameters for both samples were optimized using an orthogonal test. Additionally, the effects of CeO2 on ceramsite performance and the treatment of ammonia-nitrogen wastewater were studied, and the adsorption mechanism of CeO2 on ammonia-nitrogen wastewater was clarified. The process parameters for preparing ceramsite sample Ⅰ were: preheating for 30 min at 600 °C, followed by roasting for 20 min at 1090 °C. The parameters for preparing ceramsite sample Ⅱ were: preheating for 30 min at 600 °C, followed by roasting time for 15 min at 1090 °C. The presence of CeO2 increased the porosity of the ceramsite by 0.89% and the specific surface area by 0.66 m2/g. Under neutral environmental conditions of water samples, CeO2 increased the removal rate of ammonia nitrogen by 1.85%. Ceramsite has a high porosity and specific surface area, indicating that it has abundant internal pores, a large contact area with ammonia-nitrogen, a strong ability to remove ammonia nitrogen, and resistance to erosion and water flow shear, which are conducive to the treatment of ammonia-nitrogen wastewater.

Study on porous carbon materials derived from Chitosan

Abstract The materials with high specific surface area, uniform pore size distribution, and high nitrogen content were prepared by using chitosan as raw material and a low co-soluble mixture (lithium nitrate, potassium nitrate, and potassium sulfate) as a pore-forming agent and salt template agent. The CO2 adsorption capacity of the material was tested at 25°C (2.15 mmol/g) and 0°C (2.88 mmol/g). It was found that more pores and higher nitrogen content were conducive to the adsorption of CO2 by the material.

Thin film microextraction of apixaban from plasma based on the covalent organic framework coated on a mesh prior to liquid chromatography-tandem mass spectrometry

In this research, a new covalent organic framework was synthesized and utilized as a coating in thin film microextraction for the extraction of apixaban from plasma samples. This coating was applied to the mesh modified through immersion in a HF solution. The resulting sorbent was characterized using various techniques. The extracted drug was then analyzed using liquid chromatography-tandem mass spectrometry. By combining the high specific surface area and selectivity of the covalent organic framework, along with integrating the innovative thin film microextraction method and a sensitive analysis system, an efficient analytical approach was achieved. The target analyte was preconcentrated and extracted by immersing of the covalent organic framework-coated mesh as an absorbent into the biological sample. Subsequently, a sonication process was conducted for a specific duration. Following this, the adsorbed analyte was desorbed using acetonitrile as the elution solvent. The effective parameters of the proposed technique were optimized by using “one-parameter-at-a-time” strategy and the optimal conditions were selected. By integrating the developed method notable achievements were made in the terms of low limits of detection and quantification (0.17 and 0.56 µg/L, respectively), a wide linear range (0.05–250 µg/L), intra- and inter day precisions (with relative standard deviations of ≤14 %), as well as satisfactory extraction recoveries (53 % and 54 % in plasma and deionized water, respectively). Hence, it can be concluded that the introduced technique exhibits high efficiency and reliability when applied to biological samples.

Shape-controllable synthesis of lignin-derived boron-doped nanoporous carbons for dye adsorption and electrochemical H2O2 production

Lignin-derived nanocarbon materials (LNCMs) have attracted intense attention due to their excellent properties and promising applications in renewable energy technologies. However, lignins tend to melt and agglomerate during pyrolysis, make it difficult to control the morphology and pore structure of the resulting carbon. In this study, boron-doped porous nanocarbon (BFC) in various shapes (sphere, band, and sheet) were synthesized using ammonium borate as a crosslinking agent to prevent lignin melting, assisted by liquid nitrogen freeze-drying and potassium phosphate (KP) templating. The effects of BFC structure on methylene blue adsorption and electrochemical generation of H2O2 were investigated. The results show that KP-1/1-8BFC exhibits a high specific surface area (912.89 m2/g) and a hierarchical micro-mesoporous structure, achieving a remarkable adsorption capacity of 473.9 mg/g for methylene blue and rapid kinetics. The selectivity of KP-1/20-8BFC for electrochemical production of H2O2 reaches 85%. This study offers theoretical guidance for the controllable synthesis of LNCMs, contributing to the advancement of sustainable energy solutions.

Valorization of coffee cherry waste ash as a sustainable construction material

This study explores the potential of treated coffee cherry waste (T-CCW) as a partial replacement of cement in mortar. T-CCW was characterized and incorporated into pastes and mortars at 5% to 25% cement replacement. The main objectives were to examine the fresh and hardened properties, hydration, and environmental assessment. Results showed that the high specific surface area and porous structure of T-CCW particles increased water demand and accelerated setting times. T-CCW incorporation of up to 15% enhanced compressive strength at all curing ages due to improved hydration and limited pozzolanic reactions. Ultrasonic pulse velocity indicated good homogeneity and compactness in T-CCW blended mortars. Microstructural analysis revealed that T-CCW enhanced cement hydration, leading to a denser matrix. Environmental analysis showed a reduced embodied carbon and cement intensity index compared to the control mix. Overall, the optimal performance was observed at 15% T-CCW replacement, significantly improving engineering properties and environmental impact. Further, the fishbone diagram addresses various factors to optimize the use of T-CCW as a cementitious composite. These findings demonstrate the potential of T-CCW as a sustainable construction material, offering a promising pathway towards environmentally friendly and resource-efficient building practices while addressing waste management in the coffee industry.

Electrocatalytic oxygen reduction at non-metalated and pyrolysis free hypercrosslinked polymers

Oxygen reduction is one of the core steps of non-emissive zero carbon energy conversion. Therefore, enhancement of its sluggish kinetics is extremely important. Very recently researchers focused on oxygen electrocatalysis at porous polymers. Here we applied the non-metalated and pyrolysis free hypercrosslinked polymers with high specific surface area and abundant active sites. Electrode modified with the copolymer prepared from the twisted triphenylbenzene and N containing triphenyl amine exhibits electrocatalytic ORR in alkaline medium. Tafel slope value (0.067 V dec−1) indicates the efficient electrocatalytic activity and fast reaction kinetics. The lack of H2O2 product detected by scanning electrochemical microscopy suggests 4-electron path. The electrocatalytic activity of electrodes modified with hypercrosslinked polymers prepared from single monomers is also seen.

BN fiber aerogels with high solar reflectivity and thermal insulation for green buildings

There exists more than one-third of the stock of buildings that do not meet energy-saving building standards, so there is an urgent need for breakthroughs in the field of green buildings. Herein, we successfully prepared boron nitride (BN) fiber aerogels by sol-gel, freeze-drying and high-temperature pyrolysis. When the molar ratio of C3N6H6 to H3BO3 was 1:2 and the roasting temperature was 1000 °C, the BN fiber aerogel was produced with high specific surface area (257.690 m2/g) and high porosity (99 %). BN fiber aerogels, with their low thermal conductivity (0.043 W/(m·K)) and stable mechanical properties (no change after 45 cycles at 30 % strain), offered possibilities for thermal insulation in green buildings. Its hydrophobic properties protect the wall from the natural environment. In particular, it had a solar reflectivity of 98.6 %, which exceeds most reflective coating materials, enabling the cooling of green construction on hot summer days. The high-temperature resistance of BN fiber aerogels could be applied in special environments such as blast furnace plants and thermoelectric power plants.

Kinetic and optimization study of ultrasound-assisted biodiesel production from waste coconut scum oil using porous CoFe2O4@sulfonated graphene oxide magnetic nanocatalysts: CI engine approach

In this study, CoFe2O4@sulfonated graphene oxide (SGO) heterogeneous nanocatalyst was synthesized and utilized to produce biodiesel from waste coconut scum oil (WCSO). The structural features of CoFe2O4@SGO nanocatalyst were evaluated by SEM, TEM, EDX, FTIR, XRD, CO2/TPD, VSM, and BET analyses. According to these analyses, CoFe2O4@SGO nanocatalyst has high specific surface area, suitable functional groups, and good reactivity. The highest biodiesel yield using CoFe2O4@SGO nanocatalyst in optimal conditions (MeOH/WCSO ratio=12.41, temperature= 64.73 oC, catalyst concentration= 2.24%, and ultrasonic time= 33.08 min) was 96.87%. The yield of biodiesel decreased from 96.91% to 90.17% after six reuse cycles, which demonstrates the significant stability of CoFe2O4@SGO nanocatalyst in the transesterification process. After 7 reuse steps, XRD and CO2/TPD analyzes revealed that the catalytic activity and crystallinity of the nanocatalyst were almost retained. The kinetic behavior of biodiesel generation showed that the transesterification reaction is endothermic. Enhancing the concentration of biodiesel in the fuel mix had a positive impact on the reduction of CO and UHC emissions, as well as diesel engine parameters such as cylinder pressure, BP, EGT, BSFC, and BTE. Owing to the high biodiesel yield, significant reusability, and positive impacts on the diesel engine, CoFe2O4@SGO nanocatalyst is recommended for industrial applications.