R. M. Ahmed

Prof. R. M. Ahmed

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Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 March 2024 in Scientific Reports
Verified
Journal Article
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MIManar A. Ibrahim
Manar A. Ibrahim
GNG. M. Nasr
G. M. Nasr
RAR. M. Ahmed
R. M. Ahmed
NKNermeen A. Kelany
Nermeen A. Kelany
The ability of wound dressing materials to tackle skin pathogens colonization that is associated with open wound infections is limited. Recently, green-synthesized metal oxide nanoparticles has received a lot of attention to overcome this limitation. However, titanium dioxide nanoparticles (TiO2-NPs) exhibit exceptional antibacterial properties. In this work, several concentrations (0, 1, 3, and 5 wt.%) of TiO2 NPs prepared using Aloe vera leaf extract were added to a blend of polyvinyl alcohol and sodium alginate (PVA:SA). This nanocomposite was designed to enhance the healing process of wounds. The interaction between the PVA:SA composite and the TiO2 NPs was confirmed by FTIR. The thermal behavior of the nanocomposite films was investigated using DSC and TGA. The experimental results indicate that the glass transition temperatures of the nanocomposites increased by increasing the added amount of TiO2 NPs to be 53.7 °C (1 wt.%), 55.8 °C (3 wt.%), and 60.6 °C (5 wt.%), which were consistently lower than the glass transition temperature of the matrix material (69.6 °C). The Dynamic Mechanical Analysis was examined. The nanocomposite doped with 5 wt.% of TiO2 NPs detected a high storage modulus (21.6 × 108). Based on swelling and degradation studies, the prepared PVA:SA:TiO2 nanocomposite films have an excellent swelling rate, and the inclusion of TiO2 NPs increases the stability of the polymeric matrix. The PVA:SA:TiO2 nanocomposite films exhibited a superior antibacterial efficacy against Gram-positive bacteria such as Bacillus cereus and Staphylococcus aureus, compared to their effectiveness against Gram-negative bacteria like Escherichia coli. Moreover, the nanocomposite films were biocompatible with Human Skin Fibroblast. Therefore, the developed PVA:SA:TiO2 nanocomposite films suit wound dressing applications.

30 March 2023 in Coatings
Verified
Journal Article
Open access
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RAR. M. Ahmed
R. M. Ahmed
NKNermeen A. Kelany
Nermeen A. Kelany
MIManar A. Ibrahim
Manar A. Ibrahim
GAGhadah M. Al-Senani
Ghadah M. Al-Senani
Ayman Mohamed MostafaAyman Mohamed Mostafa
Ayman Mohamed Mostafa
In this study, a polyvinyl alcohol–sodium alginate blend, PVA:SA 3:1 (w:w), was doped with different contents of TiO2 nanoparticles (NPs) prepared by aloe vera leaf extract to form the investigated nanocomposites. The nonlinear parameters of third-order susceptibility (χ(3)) and refractive index (n2) were detected by using UV-Vis spectroscopy and Z-scan techniques. Some different optical parameters were also determined, including the refractive index (n), optical dielectric parameters, volume and surface energy loss functions, and some others. The best solar skin protection factor (SSPF) was investigated by 5 wt.% of TiO2 NPs doped in PVA:SA 3:1, which was about 84.6% compared to the corresponding value of the host blend (41%). The studied nanocomposites were examined for their utility in the optical limiting of CUT-OFF laser filters utilizing a continuous He-Ne laser working at 632.2 nm. As a result, our finding demonstrated that TiO2 NPs doped in the host blend of PVA:SA positively influences a laser light blocking for the investigated laser source. Using the estimated gap energies values, different models were used to deduce theoretical values of the linear refractive index (n). The presence of Ti peaks in the EDX spectrum confirmed the doping of TiO2 NPs in the nanocomposites. SEM showed that the TiO2 NPs are homogeneously dispersed through the host blend with some agglomerates. XRD spectra showed that the values of the lattice strain εstr. detected at 2ϴ = 19.78° are 0.058, 0.055, and 0.060, corresponding to 1, 3, and 5 wt.% of TiO2 NPs doped in the PVA:SA blend.

12 August 2021 in Journal of Materials Science: Materials in Electronics
Verified
Journal Article
Closed access
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RAR. M. Ahmed
R. M. Ahmed
MAM. M. Atta
M. M. Atta
ETE. O. Taha
E. O. Taha

16 November 2020 in International Journal of Polymer Analysis and Characterization
Verified
Journal Article
Closed access
RAR. M. Ahmed
R. M. Ahmed
AIA. A. Ibrahiem
A. A. Ibrahiem
AEA. S. El-Bayoumi
A. S. El-Bayoumi
MAM M. Atta
M M. Atta
Composites of polyvinylchloride (PVC) embedded with different ratios of graphene nano-platelets (GnP) were prepared by the casting method. Some techniques as X-ray diffraction technique (XRD), Fourier transform infrared (FT-IR), optical microscopy, and scanning electron microscopy (SEM) were investigated. The crystalline structure of GnP dominated by increasing its ratio to 2.5 wt.% in the hosting matrix compared to the amorphous structure of the pristine PVC. Microstructural analysis showed uniform distribution of GnP in PVC with some aggregates. Also, the article represents a study of the impact of GnP loading on PVC dielectric parameters such as dielectric loss, electric modulus, ac conductivity, and their dependencies on frequency and temperature. The permittivity ε' displayed an increase in its values with increasing GnP content due to the creation of a strengthened interfacial polarization phenomenon. The values of the activation energy of the polymer were decreased with increasing the content of GnP due to the growing number of conductive networks in the composites. Therefore, GnP enhanced considerably the conductivity of the polymer composites. The mechanical strength of PVC improved with increasing GnP content in which the tensile strength increased up to ∼100%. However, Young’s modulus of PVC enhanced remarkably to be about 109%. In contrast, the elongation at break of PVC decreased by GnP reinforcement from 139.5 to 28.4% by incorporate 0.25% GnP.


1 March 2020 in Acta Physica Polonica A
Verified
Journal Article
Open access
RAR. Ahmed
R. Ahmed
AIAli IBRAHIM
Ali IBRAHIM
EEE. El-Said
E. El-Said