Ahmad M. Mohammad Alakraa

In the current study, a cleaned glassy carbon (abbreviated as C) electrode was modified by the sequential electrodeposition of gold (AuNPs) and palladium (PdNPs) nanoparticles (denoted as Pd-Au/C) for the catalytic electro-oxidation of methanol (EOM). Interestingly, the catalyst showed a higher (~ 5 times increase) oxidation peak current, Ip, and a lower (~ 9 times decrease) charge transfer resistance (Rct) than the Au-unmodified Pd/C catalyst. This finding recommended the significant lowering of the catalyst’s surface poisoning together with enhanced charge transfer kinetics as the enhancement origin of EOM. Besides, the effects of NaOH concentration in the electrolyte and scan rate during oxidation were optimized to achieve an optimized EOM electrocatalysis. © The Author(s), under exclusive license to Springer Nature Switzerland AG 2024.

To quickly move the formic acid (FA) fuel cells closer to a real commercialization, an inexpensive, efficient, and durable electrocatalyst for the direct FA electro-oxidation (FAEO) was developed. This involved a sequential modification of a glassy carbon (GC) substrate with palladium nanocubes (ca. 70 nm, nano-Pd) and iron oxide nanowires (nano-FeOx, ca. 40 nm and 150 nm in average diameter and length, respectively). The deposition sequence and loading level of nano-FeOx in the catalyst were optimized to minimize the catalyst's poisoning with CO that might probably release from a parallel dehydration of FA or from CO2 reduction. Surprisingly, the FeOx/Pd/GC catalyst exhibited a high (21.6 mA cm−2) specific activity for FAEO, which denoted ca. 7 times that of the “pristine” Pd/GC catalyst. This was synchronized with a better (up to fivefold increase in turnover frequency) “long-termed” stability that extended for 90 min of continuous electrolysis at room temperature. A successful effort was dedicated to improving more the catalyst's stability by activating the catalyst electrochemically at –0.5 V vs Ag/AgCl/KCl (sat.) in 0.2 mol L−1 NaOH. The CO stripping agreed perfectly with the impedance analysis in appending the observed enhancement in the catalytic efficiency of FAEO to a favorable electronic modulation at the Pd surface that boosted the oxidative desorption of poisoning CO species at a lower potential. © 2022 The Authors

The modification of Pt nanoparticles (nano-Pt, assembled electrochemically onto a glassy carbon (GC) substrate) with hybrid multivalent nickel (nano-NiOx) and iron (nano-FeOx) oxide nanostructures was intended to steer the mechanism of the formic acid electro-oxidation (FAO) in the desirable dehydrogenation pathway. This binary modification with inexpensive oxides succeeded in mediating the reaction mechanism of FAO by boosting reaction kinetics “electron transfer” and amending the surface geometry of the catalyst against poisoning. The sequence of deposition was optimized where the a-FeOx/NiOx/Pt/GC catalyst (where “a” denotes a post-activation step for the catalyst at −0.5 V in 0.5 mol L−1 NaOH) reserved the best hierarchy. Morphologically, while nano-Pt appeared to be spherical (ca. 100 nm in average diameter), nano-NiOx appeared as flowered nanoaggregates (ca. 56 nm in average diameter) and nano-FeOx (after activation) retained a plate-like nanostructure (ca. 38 nm in average diameter and 167 nm in average length). This a-FeOx/NiOx/Pt/GC catalyst demonstrated a remarkable catalytic efficiency (125 mA mgPt−1) for FAO that was ca. 12.5 times that of the pristine Pt/GC catalyst with up to five times improvement in the catalytic tolerance against poisoning and up to −214 mV shift in the FAO's onset potential. Evidences for equipping the a-FeOx/NiOx/Pt/GC catalyst with the least charge transfer resistance and the highest stability among the whole investigated catalysts are provided and discussed. © 2023 The Royal Society of Chemistry.

This study aims at investigating the catalytic performance of Pd, Pd/Pt, and Pd/Au nanocatalysts toward the 2-propanol electro-oxidation reaction (2POR) in an alkaline medium. The catalyst components (Pd, Pt, and Au) were sequentially electrodeposited onto the glassy carbon (GC) electrode surface and further characterized using electrochemical (cyclic voltammetry (CV)) and materials (field-emission scanning electron microscopy (FE-SEM) coupled with energy-dispersive X-ray (EDX)) characterization methods. The Pd/Au/GC catalyst showed the highest catalytic activity in terms of the highest oxidation current (0.386 mA) and the highest stability in terms of the highest obtained current after 1800 s of continuous electrolysis. This behaviour was attributed to the enhancement in the charge transfer kinetics where the Pd/Au/GC catalysts acquired the lowest charge transfer resistance (Rct, 1.85 kΩ) during the 2POR. © 2023 Kareem Ayman et al.

Phytoremediation is a promising, cost-effective, and eco-friendly process for wastewater treatment. Herein, the dry biomasses of Vossia cuspidata (Roxb.) Griff. leaves (PL) and rhizomes including aerial stems (PR) were used to effectively remediate methylene blue (MB) dyes. Interestingly, the adsorption uptake and removal efficiency of MB by PR were higher than those of PL; exceeding 97 and 91% in 35 and 25 min for 0.1 and 0.4 g/L MB, respectively. The MB diffusion within the PL and PR was insignificant and the adsorption kinetics was principally controlled by the surface MB–adsorbent interaction, as consistently approved by the pseudo-second order kinetic model. In addition, the adsorption increased rapidly with the plant dosage with high dependence on the initial MB concentration. Moreover, the impact of shaking speed on the adsorption was minor but temperature played a critical role where the highest efficiencies were recorded at 30 and 40 °C on PL (91.9%) and PR (93.3%), respectively. The best removal efficiencies were attained with PR at pH 6, but with PL at pH 8. The Temkin isotherm could perfectly simulate the experimental data (R2 > 0.97); suggesting a linear decrease of the adsorption heat of MB with the plant coverage. © 2023, The Author(s).

In this study, the formic acid electro-oxidation reaction (FAEOR) was catalyzed on a Pd-Au co-electrodeposited binary catalyst. The kinetics of FAEOR were intensively impacted by changing the Pd2+:Au3+ molar ratio in the deposition medium. The Pd1-Au1 catalyst (for which the Pd2+:Au3+ molar ratio was 1:1) acquired the highest activity with a peak current density for the direct FAEOR (Ip) of 4.14 mA cm−2 (ca. 13- times higher than that (ca. 0.33 mA cm−2) of the pristine Pd1-Au0 catalyst). It also retained the highest stability that was denoted in fulfilling ca. 0.292 mA cm−2 (ca. 19-times higher than 0.015 mA cm−2 of the pristine Pd1-Au0 catalyst) after 3600 s of continuous electrolysis at 0.05 V. The CO stripping and impedance measurements confirmed, respectively, the geometrical and electronic enhancements in the proposed catalyst. © 2022 The Author(s)

With the growing warning for accrediting the traditional combustion of fossil fuels for energy production, not only for their limited supply but also for their environmental risks (air pollution, climate change, …. etc), it became necessary to realize alternative greener and abundant sources for energy. Instead, the interest to sustain biodiesel for the energy production has recently been renewed as a replacement for petroleum diesel in conventional diesel engines. This was due to its renewable nature, low toxicity, high degradability and unique physical properties (high flash points & lubrication). Castor oil, in particular, appeared promising for biodiesel production with extremely low cloud and pour points; making it suitable for tropical climates. Blending petroleum diesel with castor oil biodiesel has been proven efficient for enhancing both the environmental effect and the kinematic flow properties of the mineral fuel. Nonetheless, because of the current market price of conventional diesel, the blended product appeared cost-ineffective; steering research to tune the use of castor oil biodiesel alone. In this study, a simple method is recommended to produce biodiesel from castor oil by a transesterification process. The effect of mixing time of oil and alcohol is optimized with a thorough analysis to optimize the best condition for the biodiesel production © 2006-2022 Asian Research Publishing Network (ARPN). All rights reserved

The aim of this study is to highlights the importance to shift from the use of traditional fossil fuels to biodiesel as a clean energy source. A simulation study has been conducted using ASPEN HYSIS software for the biodiesel production form castor oil. The simulation was run and the properties of the produced biodiesel were highlighted. The optimum conditions resulted in 88 % conversion. © 2006-2022 Asian Research Publishing Network (ARPN). All rights reserved.

This study aims to mitigate the CO poisoning of platinum (Pt) surfaces during formic acid electro-oxidation (FAEO), the essential anodic reaction in the direct formic acid fuel cells (DFAFCs). For this purpose, a glassy carbon (GC) electrode was amended sequentially with Pt (n-Pt), gold (n-Au), and cobalt oxide (n-CoOx) nanostructures. Fascinatingly, the ternary modified n-CoOx/n-Au/n-Pt/GC catalyst (for which n-Pt, n-Au, and n-CoOx were sequentially and respectively assembled onto the GC surface) exhibited a remarkable electrocatalytic enhancement toward FAEO, which surpassed ca. 53 times that of the Pt/GC catalyst. Additionally, it exhibited a much (ca. 18 times) higher stability after 3000 s of continuous electrolysis. The observed enhancement was proven to originate from driving the reaction mechanism principally to the desirable direct dehydrogenation pathway on the expense of the poisoning dehydration path. The impedance and CO stripping measurements confirmed the prevailing of both the electronic and third body effects in the catalytic enhancement. © 2022 The Authors

This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeOx) and nickel (nano-NiOx) nanowire oxides assembled sequentially onto a bare platinum (bare-Pt) substrate was recommended for the formic acid electro-oxidation reaction (FAOR). While nano-NiOx appeared as fibrillar nanowire bundles (ca. 82 nm and 4.2 μm average diameter and length, respectively), nano-FeOx was deposited as intersecting nanowires (ca. 74 nm and 400 nm average diameter and length, respectively). The electrocatalytic activity of the catalyst toward the FAOR depended on its composition and loading sequence. The FeOx/NiOx/Pt catalyst exhibited ca. 4.8 and 1.6 times increases in the catalytic activity and tolerance against CO poisoning, respectively, during the FAOR, relative to the bare-Pt catalyst. Interestingly, with a simple activation of the FeOx/NiOx/Pt catalyst at −0.5 V vs. Ag/AgCl/KCl (sat.) in 0.2 mol L−1 NaOH, a favorable Fe2+/Fe3+ transformation succeeded in mitigating the permanent CO poisoning of the Pt-based catalysts. Interestingly, this activated a-FeOx/NiOx/Pt catalyst had an activity 7 times higher than that of bare-Pt with an ca. −122 mV shift in the onset potential of the FAOR. The presence of nano-FeOx and nano-NiOx enriched the catalyst surface with extra oxygen moieties that counteracted the CO poisoning of the Pt substrate and electronically facilitated the kinetics of the FAOR, as revealed from CO stripping and impedance spectra. © 2022 The Royal Society of Chemistry.

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