Attia, N. F., M. A. Nour, and S. E. A. Elashery, "Innovative engineering of scalable, renewable and spherical organic nanoparticles for high fire safety, UV protection and antibacterial properties of polyvinyl alcohol nanocomposites films", Scientific Reports, vol. 14, issue 1, pp. 28841, 2024. AbstractWebsite

A novel and environmentally friendly route was developed for production of sustainable flame retardant, antibacterial and UV protective nanoparticles for polymeric films nanocomposites. For the first time, dried molokhia leaves were engineered into spherical nanoparticles with an average size of 8.5 nm via an eco-friendly, one-pot solid-state ball-milling method. The engineered nanoparticles were proved using spectroscopic and microscopic techniques. The sustainable nanoparticles were employed as an efficient and green flame retardant, antibacterial and UV protective materials for polyvinyl alcohol (PVA) nanocomposite films. The distinct compatibility between PVA chains and spherical nanoparticles afford excellent homogeneous dispersion of each nanoparticle in the polymer matrix. Compared to blank PVA film which burned at a rate of 125 mm/min, the novel nanoparticles achieved significant flame retardancy for polymer nanocomposites films recording zero rate of burning. Their outstanding charring ability and naturally doped elemental composition were attributed to their higher flame retardancy achieved. Moreover, the newly developed multifunctional nanoparticles integrated outstanding UV protection feature to developed polymer nanocomposite films recording UV protection factor superiority of more than 900% compared to nanoparticle free film. Noteworthy to note that, the nanoparticles afford excellent inhibition to bacterial growth against Escherichia coli and Staphylococcus aureus over the surface of developed polymer nanocomposite films achieving clear inhibition zone of 9 and 7.6 mm compared to zero mm for pristine polymer film, respectively. In addition, a proposed and clarified flame retardancy mechanism was presented. Additionally, an assessment was conducted regarding the economic feasibility of producing sustainable multifunctional nanoparticles on an industrial scale.

Elashery, S. E. A., M. M. El-Bouraie, E. A. Abdelgawad, N. F. Attia, and G. G. Mohamed, "Adsorptive performance of bentonite-chitosan nanocomposite as a dual antibacterial and reusable adsorbent for Reactive Red 195 and crystal violet removal: kinetic and thermodynamic studies", Biomass Conversion and Biorefinery, vol. 15, pp. 2511-2524, 2025.
Attia, N. F., A. Policicchio, G. Conte, R. G. Agostino, A. Alkahlawy, and S. E. A. Elashery, "Green fabrication of cost-effective and sustainable nanoporous carbons for efficient hydrogen storage and CO2/H2 separation", International Journal of Hydrogen Energy, vol. 92, pp. 1160-1171, 2024. AbstractWebsite

In this study, sustainable nanoporous carbon materials that are efficient, renewable, cost-effective and adaptable were developed. These microporous feature carbon adsorbents were synthesized utilizing a straightforward and efficient method. Plum stones are residual fruit materials that offer a financially feasible and sustainable carbon source with exceptional porosity and desirable elemental composition. The plum stones underwent carbonization and were subsequently chemically modified with polyaniline nanofibers and then subjected to chemical activation using different activating agents. This yielded sustainable nanoporous carbon with a high degree of porosity, in conjunction with doping with precious high electron density elements such as O, N and S. The sustainable nanoporous carbons that have been developed exhibits exceptional microporosity, with BET-SSA of 1705 m2 g−1 and a pore volume of 0.726 cm3 g−1, besides, the dominance of ultramicropores of 0.6 nm size. This in addition to convenient doping of oxygen, nitrogen and sulfur elements which are crucial for H2 uptake. The developed nanoporous carbon demonstrated highly promising capabilities for storing H2 molecules at cryogenic and ambient temperatures. The sustainable adsorbent achieved hydrogen storage capacities of 4.63 and 0.45 wt% at 77, 296 K, and a pressure of 40 and 80 bar, respectively. This H2 storage capacity at RT is often regarded as one of the highest reported in the literature for nanoporous adsorbents. Moreover, study investigated the separation selectivity of developed adsorbents for CO2/H2 based on uptake ratio at 30 bar and RT. The results demonstrated a significant separation selectivity reaching a value of 382.5 for the CO2/H2, which is regarded as one of the most elevated values documented in the existing literature for nanoporous carbon materials. Thus, the presented sustainable nanoporous materials have shown great promise for hydrogen storage, pre-combustion CO2 capture and H2 purification applications at ambient temperature.

Attia, N. F., A. Policicchio, A. M. Zakria, C. P. Bonaventura, S. Bartucci, A. Alkahlawy, M. A. Nour, N. A. A. El-Ghany, A. M. Rabie, and S. E. A. Elashery, "Rational fabrication of ultramicroporous flexible porous carbon fabrics for efficient capture of CO2 andCO2/N2 and CO2/H2 separation", Surfaces and Interfaces, vol. 56, pp. 105584, 2025. AbstractWebsite

An innovative flexible nanoporous carbon fabrics were developed for selective capture of CO2 and its separation over N2 and H2 gases. The as developed flexible porous fabrics was fabricated using viscose rayon fabrics coated with various nanocoatings includes phosphorylated cellulose nanocrystals (P-CNC), polyaniline nanofibers (PANI-NFs) and graphene sheets derived from mandarin shell in conjunction with polyvinyl alcohol (PVA). Afterwards, they were carbonized and subsequently chemically activated with green potassium dihydrogen orthophosphate as an activating agent. The developed flexible porous carbon fabrics achieved superior microporosity with specific surface area and total pore volume of 753 m2 g-1 and 0.309 cm3 g-1, respectively. This is in addition to existence of ultramicropores of size 0.61 nm and rich doping with oxygen, nitrogen and phosphorus species, in conjunction with precious metals residues. Besides, their flexibility, easier processability and safe handling properties, they achieved high CO2 uptake of 5.72 and 38.7 wt.% at 1 and 30 bar and room temperature, respectively. This superior CO2 uptake at pre-and post-combustion conditions was ascribed to ultramicropores and high electron density adsorption sites which affords easier adsorption and interaction of CO2 molecules with pore walls. Moreover, the flexible porous fabric records superior removal of CO2 over N2 from flue gas recording separation selectivity of CO2/N2 of 36.5 at 30 bar and room temperature based on uptake ratio. Additionally, they achieved outstanding separation selectivity of CO2 over H2 gas achieving CO2/H2 of 280.

Jung, M., J. Park, J. Zhou, T. Park, Y. - C. Nah, S. E. A. Elashery, S. G. Kang, N. F. Attia, R. Muhammad, and H. Oh, "Thermally regulated gating phenomenon in bio-derived ultra-narrow nanoporous carbon for enhancing hydrogen isotope separation", Fuel, vol. 382, pp. 133754, 2025. AbstractWebsite

The temperature-triggered gating in flexible nanoporous frameworks exhibits dynamic nanopore regulation under external stimuli, leading to optimum pore sizes and enhanced selectivity for isotopologue separation. In this work, we report one of the very rare observations of temperature-responsive gating in efficient bio-derived ‘nanoporous carbon’ material. The distinctive characteristics of this material, such as its suitable pore sizes for Kinetic Quantum Sieving (KQS) that lead to strong diffusion limitation, as well as its capacity to operate at higher temperatures, overcome the limitations of existing crystalline porous materials. It is remarkable that this activated carbon derived from biological sources, even without any strong binding sites, can release hydrogen isotopologues at a higher temperature of 180 K in comparison to MOF-74(Ni), which possesses many open metal sites but releases mostly at 90–100 K. The separation performance is also demonstrated to reach up to 120 K, and only six separation cycles are needed to enrich from a low concentration of 4 % to –92 % D2 in a mixture of deuterium (D2/H2). This finding suggests that inexpensive porous carbon’s thermal pore size modulation can significantly increase the operating temperature for precise separation of hydrogen isotopologues.

Park, J., M. Jung, S. E. A. Elashery, H. Oh, and N. F. Attia, "Molecular Imprinting as a Tool for Exceptionally Selective Gas Separation in Nanoporous Polymers", Chemistry – An Asian Journal, vol. 20, no. 2, pp. e202401205, 2025. AbstractWebsite

Abstract The alarming rise in atmospheric CO2 levels, primarily driven by fossil fuel combustion and industrial processes, has become a major contributor to global climate change. Effective CO2 capture technologies are urgently needed, particularly for the selective removal of CO2 from industrial gas streams, such as flue gas and biogas, which often contain impurities like N2 and CH4. In this study, we report the design and synthesis of novel molecularly imprinted polymers (MIPs) using 4-vinylpyridine (4VP) and methacrylic acid (MAA) as functional monomers, and thiophene (Th) and formaldehyde (HC) as molecular templates. The MIPs were specifically engineered to create selective molecular cavities within a nanoporous polymer matrix for the efficient capture of CO2. By adjusting the molar ratios of the template to functional monomers, we optimized the molecular imprinting process to enhance CO2 selectivity over N2 and CH4. The resulting MIPs exhibited outstanding performance, with a maximum CO2/N2 selectivity of 153 at 25 bar and CO2/CH4 selectivity of 25.3 at 1 bar, significantly surpassing previously reported porous polymers and metal-organic frameworks (MOFs) under similar conditions. Furthermore, we conducted heat of adsorption studies, which revealed the strong and selective interaction of CO2 with the imprinted cavities, confirming the superior adsorption properties of the synthesized MIPs. The study demonstrates that molecular imprinting can effectively enhance both CO2 capture capacity and selectivity, providing a cost-efficient and scalable solution for industrial CO2 separation and purification processes.

Attia, N. F., R. Shoaib, I. ul Islam, S. E. A. Elashery, and H. Ameen, "2D Metal Chalcogenides Gas Chemical Sensors", Advanced Two-Dimensional Nanomaterials for Environmental and Sensing Applications: CRC Press, 2024.
Attia, N. F., S. E. A. Elashery, M. A. Nour, A. Policicchio, R. G. Agostino, M. Abd-Ellah, S. Jiang, and H. Oh, "Recent advances in sustainable and efficient hydrogen storage nanomaterials", Journal of Energy Storage, vol. 100, pp. 113519, 2024.
Attia, N. F., S. E. A. Elashery, F. El-Sayed, M. Mohamed, R. Osama, E. Elmahdy, M. Abd-Ellah, H. R. El-Seedi, H. B. Hawash, and H. Ameen, "Recent advances in nanobased flame-retardant coatings for textile fabrics", Nano-Structures & Nano-Objects, vol. 38, pp. 101180, 2024.
Frag, E. Y., S. E. A. Elashery, G. G. Mohamed, and A. A. E. Sleim, "Elucidating the Performance of Thick Film Screen Printed Electrodes in Detection of a Local Anesthetic", Journal of Analytical Chemistry , vol. 78, pp. 1426–1436, 2023.
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