General Chemistry PTC101

Semester: 
Fall

Chemical Kinetics Chem317

Semester: 
Fall
Abdelrahim, A. M., M. A. G. El-Moghny, H. H. Abdelhady, H. S. Wali, M. M. Gamil, S. R. Fahmy, T. M. Abdel-Hamid, G. K. Mohammed, Y. A. Ahmed, and M. S. El-Deab, Tailoring a facile electronic and ionic pathway to boost the storage performance of Fe3O4 nanowires as negative electrode for supercapacitor application, , vol. 14, issue 1, pp. 16807, 2024. AbstractWebsite

Today, high-energy applications are devoted to boosting the storage performance of asymmetric supercapacitors. Importantly, boosting the storage performance of the negative electrodes is a crucial topic. Fe3O4-based active materials display a promising theoretical storage performance as a negative electrode. Thus, to get a high storage performance of Fe3O4, it must be tailored to have a higher ionic and electronic conductivity and outstanding stability. Functionalized graphite felt (GF) is an excellent candidate for tailoring Fe3O4 with a facile ionic and electronic pathway. However, the steps of the functionalization of GF are complex and time-consuming as well as the energy loss during this step. Thus, the in-situ functionalization of the GF surface throughout the synthesis of Fe3O4 active materials is proposed herein. Fe3O4 is electrodeposited at the in-situ functionalized GF surface with the crystalline nanowires-like structure as revealed from the various analyses; SEM, TEM, Mapping EDX, XPS, XRD, wettability test, and Raman analysis. Advantageously, the synthetic approach introduces full homogeneous and uniform coverage of the large surface area of the GF. Thus, Fe3O4 nanowires with high ionic and electronic conductivity are characterized by a higher storage performance. Interestingly, Fe3O4/GF possesses a high specific capacity of 1418 mC cm−2 at a potential scan rate of 10 mV s−1 and this value retained to 54% at a potential scan rate of 50 mV s−1 at an extended potential window of 1.45 V. Remarkably, the diffusion-controlled reaction is the main contributor of the storage of Fe3O4/GF electrode as revealed by the mechanistic studies.

Ahmed, A. M., A. M. Abdelrahim, M. G. Abd El-Moghny, H. H. Abdelhady, N. M. Abd Elhakiem, M. S. Shehate, N. W. Mohamed, S. R. Abdelrahman, and M. S. El-Deab, Tuning heterostructured interface of binary hydroxide/metallic CoNi over Fe3O4 at modified graphite felt for enhanced oxygen evolution reaction, , vol. 72, pp. 107423, 2025. AbstractWebsite

The sluggish kinetics of the oxygen evolution reaction (OER) represents a challenge to the efficient production of hydrogen via alkaline water electrolysis (AWE). The tunable electronic properties of heterostructured materials lead to increased susceptible active sites and synergetic interactions over their constituents. Such materials offer a promising approach for enhanced OER performance. Herein, this work demonstrates a simple and controlled electrodeposition approach to fabricate a highly active and cost-effective heterostructured binary hydroxide/metallic CoNi interface over Fe3O4 electrodeposited at in-situ functionalized graphite felt (denoted as ((CoNi/Fe)Ox@GF) electrocatalyst for the OER. This approach utilizes a simple two-step electrodeposition method with electrochemical activation after each step, involving the in-situ functionalization of graphite felt (GF). The unmodified and modified GF are subjected to various characterization techniques, including XRD, Raman spectroscopy, contact angle, XPS, SEM, EDX mapping, and TEM. The fabricated (CoNi/Fe)Ox@GF electrode with optimized composition exhibits a superb electrocatalytic performance for OER in an alkaline medium (1 M KOH), which requires a marked ultra-low overpotential of 234 mV to afford a current density at 10 mA cm–2, coupled with a low Tafel slope of 34 mV dec–1. It also maintains outstanding stability at 100 mA cm–2, exceeding 24 h in 1 M KOH of continuous operation.

Abu-Ghazala, A. H., H. H. Abdelhady, M. G. Abd El-Moghny, B. B. Saied, A. H. Sayed, S. T. Kenawy, O. H. Khalifa, M. A. Rwash, and M. S. El-Deab, "Boosting biodiesel production from WCO utilizing marble waste powder as precursor for CaO/K2CO3 nanocatalyst at low temperature via RSM optimization", RSC Advances, vol. 15, issue 37: The Royal Society of Chemistry, pp. 30829 - 30848, 2025. AbstractWebsite

This study aims to valorize hazardous industrial marble machining and shaping waste powder as a precursor to prepare a heterogeneous nano-catalyst (CaO/K2CO3) employing the wet-impregnation method for producing biodiesel via the transesterification of waste cooking oil (WCO). Surface and morphological characterization of the thus-prepared nano-catalyst has been performed employing various analytical tools, e.g., XRD, BET, CO2-TPD, FT-IR, HR-TEM, and FE-SEM & mapping EDX. The impact of calcination treatment on the catalytic performance is investigated together with the weight percentage (wt%) of CaO compared to K2CO3. Response surface methodology (RSM) is used to optimize the parametric independent variables, e.g., catalyst loading level, reaction temperature, and time, as well as methanol to WCO molar ratio (M : WCO) via the central composite design (CCD). The experimentally attained optimal reaction parameters for effective biodiesel production (92%) are: 3.2 wt% catalyst loading, operating at 40 °C for 84 min, along with a 5.8 : 1 M : WCO. The proposed nano-catalyst has been recovered and reused effectively for 5 consecutive cycles, with a slight loss in catalytic activity beginning from the 3rd cycle. Additionally, the quality of the obtained biodiesel perfectly fits the American (ASTM D-6751) and the European (EN-14214) standard limits.

Hamed, S. M., A. F. Zedan, H. H. Abdelhady, N. M. Mohamed, and A. M. Fekry, Graphitic carbon nitride/titania nanotube arrays for photoelectrochemical oxidation of methanol under visible light, , vol. 90, pp. 918 - 930, 2024. AbstractWebsite

In this study, the fabrication of ordered and vertically oriented titanium dioxide nanotubes (TiO2 NT) array sensitized with graphitic carbon nitride (g-C3N4) nanosheets (g-C3N4 NS/TiO2 NT) was demonstrated as an attractive class of photocatalysts for the visible-light-driven photoelectrochemical oxidation of methanol. The phase and composition of the fabricated g-C3N4 NS/TiO2 NT structures and their precursors were investigated using X-ray powder diffraction (XRD). The morphological and topological characteristics of the prepared materials were studied using scanning electron microscopy (SEM). Raman spectroscopy was employed to study the electronic properties of composite material. Upon the fabrication, characterization, and use of the prepared structures for photoelectrochemical oxidation of methanol under visible-light illumination (50 W halogen lamp, 0.1 M KOH), the g-C3N4 NS/TiO2 NT array showed a significant increase in the photocurrent (96.2 μA cm−2) compared to the TiO2 NT electrode (79 μA cm−2) with 1.2 times enhancement factor. Moreover, decorating the TiO2 NT array resulted in enhanced dark light density that is 8.7 times more than that of the TiO2 NT electrode. The improved photo- and electrochemical properties of the prepared g-C3N4 NS/TiO2 NT could arise from the synergistic effects of g-C3N4 NS decoration and the unique structural properties of the fabricated vertically aligned TiO2 nanotube arrays. The TiO2 NT/g-C3N4 NS composite modified photo-electrode offers 22.55 times the ambient condition “light off” of the TiO2 NT electrode and 2.3 times the irradiated ones. The present study suggests a simple, stable, reusable, and cost-effective approach for the preparation of g-C3N4 NS/TiO2 NT photocatalyst for designing a DMFC.

Mawlid, O. A., H. H. Abdelhady, and M. S. El-Deab, "Recent Advances in Magnetic Nanoparticle-Based Heterogeneous Catalysts for Efficient Biodiesel Production: A Review", Energy & FuelsEnergy & Fuels, vol. 38, issue 21: American Chemical Society, pp. 20169 - 20195, 2024. AbstractWebsite

Owing to the worldwide concentration on energy security, a recent trend of the energy mix is adopted by gradually replacing fossil fuels with other renewable energy sources. Biodiesel has emerged as a promising candidate. It is renewable, nontoxic, and biodegradable and can be a suitable choice for undertaking this energy issue. Biodiesel can be produced via various procedures, e.g., dilution, microemulsion, pyrolysis, and transesterification. The latter is the most utilized procedure given its effectiveness in which vegetable oils or animal fats and short-chain alcohols are allowed to react in the presence of a catalyst. Different oil feedstocks are identified including edible, nonedible, and algae-based biomass resources. Conventionally, homogeneous catalysts are generalized for biodiesel production because of their high catalytic activity and low cost, albeit, due to high wastewater generation during the purification process of the product, separation problems, and soap production, heterogeneous catalysts have emerged to overcome problems facing the homogeneous catalytic system. Of these, magnetic nanomaterials including magnetite and spinel ferrites are introduced. A literature survey is comprehended in this review concerning magnetic nanocatalysts, preparation methods, and applications. The economic lookout is portrayed by using magnetic catalysts as a future catalytic vision. Besides, the biodiesel’s physicochemical properties including kinematic viscosity, density, cetane number, flash, pour, and cloud points are reviewed for its commercial utilization.Owing to the worldwide concentration on energy security, a recent trend of the energy mix is adopted by gradually replacing fossil fuels with other renewable energy sources. Biodiesel has emerged as a promising candidate. It is renewable, nontoxic, and biodegradable and can be a suitable choice for undertaking this energy issue. Biodiesel can be produced via various procedures, e.g., dilution, microemulsion, pyrolysis, and transesterification. The latter is the most utilized procedure given its effectiveness in which vegetable oils or animal fats and short-chain alcohols are allowed to react in the presence of a catalyst. Different oil feedstocks are identified including edible, nonedible, and algae-based biomass resources. Conventionally, homogeneous catalysts are generalized for biodiesel production because of their high catalytic activity and low cost, albeit, due to high wastewater generation during the purification process of the product, separation problems, and soap production, heterogeneous catalysts have emerged to overcome problems facing the homogeneous catalytic system. Of these, magnetic nanomaterials including magnetite and spinel ferrites are introduced. A literature survey is comprehended in this review concerning magnetic nanocatalysts, preparation methods, and applications. The economic lookout is portrayed by using magnetic catalysts as a future catalytic vision. Besides, the biodiesel’s physicochemical properties including kinematic viscosity, density, cetane number, flash, pour, and cloud points are reviewed for its commercial utilization.

Mawlid, O. A., H. H. Abdelhady, M. G. Abd El-Moghny, A. Hamada, Fatma abdelnaby, M. Kased, S. Al-Bajouri, R. A. Elbohy, and M. S. El-Deab, Clean approach for catalytic biodiesel production from waste frying oil utilizing K2CO3/Orange peel derived hydrochar via RSM Optimization., , vol. 442, pp. 140947, 2024. AbstractWebsite

Energy worldwide crisis devotes the concern of the scientific forums to find better solutions for an efficient and economical energy source instead of the conventional Petro-fuels. Herein, this study addresses the utilization of plant waste-derived heterogeneous catalysts for efficient biodiesel (BD) production from waste frying oil (WFO). Hydrochar is fabricated from orange peels to valorize the waste-to-fuel approach through utilizing plant residue and WFO to make the whole process more economical and environmentally benign. Hydrothermal carbonization of orange peels is used for the fabrication of hydrochar. Then, a novel potassium carbonate/orange peel-derived activated hydrochar (KC/OAH) heterogeneous catalyst is employed for a competent methanolysis of WFO. Various characterization techniques are employed to elucidate the physicochemical properties of the proposed materials. The evaluated optimal mass ratio of the catalyst composition is 2:1 K2CO3: OAH (2-KC/1-OAH). Next, a central composite design (CCD) via response surface methodology (RSM) is utilized to disclose the optimum operational parameters at which the reaction is implemented. Optimum conditions of 4.4 wt %, 6.6:1 methanol to oil molar ratio, and 108 min reaction time at a fixed reaction temperature of 50 °C result in biodiesel conversion of c.a. 89.2 %. A low minimum selling price (MSP) of biodiesel of 1.12 $/kg is developed, which confirms the low cost of the overall process to produce the biodiesel. The significant leaching of K+ (2-KC/1-OAH) necessitates chemical regeneration via re-soaking of the spent catalyst in K2CO3, which restores the activity and provides the same high biodiesel conversion as the genuine catalyst. Ultimately, the physico-chemical properties of the produced biodiesel are found to be compatible with international limits, which elevates the safe usage of this fuel in automobile engines.

Eldine, R. A., H. H. Abdelhady, S. Abd Elhafez, and M. S. El-Deab, Synthesis & Characterization of Novel CaO-based Heterogeneous Catalysts for Efficient Biodiesel Production from Waste Cooking Oil, , vol. 67, issue 8, pp. 13 - 28, 2024. AbstractWebsite

In this study, a series of novel basic heterogeneous catalysts (Ca-based mixed Ce and Cu oxides) with various mass ratios were designed by co-precipitation method to be utilized in biodiesel, Fatty acid methyl ester (FAME) production via the transesterification process of waste oil under the following process conditions (i.e., methanol to waste cooking oil mass ratio of [13:1] at reaction temperature 75 oC for 5 h). The various binary mixed oxides were characterized by several techniques (e.g., Thermo-gravimetric analysis (TGA-DTG), powder X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area measurements, Fourier transform- Infrared (FT-IR) spectroscopy, and surface basicity by back titration). Biodiesel yield is estimated by gas chromatography (GC). The biodiesel optimum yield, of 95 and 94 % yield is achieved by 3CaO-1CeO2@800 oC and 3CaO-1CuO@800 oC catalysts under the reaction condition of 2% wt. catalyst loading level, methanol to waste oil molar ratio of [13:1], reaction temperature of 75 oC, and reaction time of 2 h for the former catalyst, while, catalyst loading of 2% for 1 h at 75 oC and [13:1] M:O molar ratio for the later one, respectively. The high catalytic activity may be attributed to the higher BET surface area and strong basic characteristics, which indicate more accessible active sites for the transesterification process on the catalyst surface. Furthermore, the catalytic materials were reactivated and reused for two to three reaction cycles. The physical characteristics of the produced FAME are found to fulfill the American standard for testing materials (ASTM D-6751) international standards.

Abu-Ghazala, A. H., H. H. Abdelhady, A. A. Mazhar, and M. S. El-Deab, Exceptional room temperature catalytic transesterification of waste cooking oil to biodiesel using environmentally-benign K2CO3/γ-Al2O3 nano-catalyst, , vol. 474, pp. 145784, 2023. AbstractWebsite

This study addresses the exceptional catalytic efficacy of K2CO3/γ-Al2O3 as a heterogeneous nano-catalyst for room-temperature biodiesel production from waste cooking oil (WCO). That is industrial aluminum waste powder (IAWB) is used as a precursor for the synthesis of environmentally benign nano-supporting alumina (γ-Al2O3) which is subsequently loaded with K2CO3. Diverse analytical techniques are applied to study the physicochemical characterization of the prepared nano-catalyst, e.g., XRD, XPS, FT-IR, BET isotherm, CO2−TPD, SEM−EDX, HR−TEM, and AFM. The Box-Behnken Design (BBD) approach is implemented to optimize the parametric conditions for the transesterification reaction via applying Response Surface Methodology (RSM), i.e., catalyst loading, reaction time, and methanol:oil (M:O) molar ratio. The optimum transesterification reaction conditions for biodiesel conversion (98.7%) are 5.8 wt% catalyst loading at 25 °C for 120 min with a 9:1 M:O molar ratio, which is superior to similar repeating catalysts. Kinetic and thermodynamic parameters are estimated, with activation energy (Ea), activation enthalpy (ΔH#), and activation entropy (ΔS#) values of 18.87 kJ mol−1, +16.34 kJ mol−1, and −217.22 J mol−1, respectively. The catalyst maintains its catalytic activity for six successive cycles. Moreover, the physicochemical characterization of the generated biodiesel fuel is congruent with the ASTM D − 6751 and EN − 14,214 international standards. Thus, the proposed catalyst herein is a potential heterogeneous catalyst with robust activity for industrial biodiesel manufacture.