Publications by authors named "Samir Kamel"

Article Synopsis
  • Two types of carbon quantum dots (CQDs) were created using citric acid and dimethyl formamide from cellulose and carboxymethyl cellulose: tree-shaped/fingerprinted (TF-CQDs) and fullerene-like (F).
  • Fluorescence microscopy showed TF-CQDs emitting blue light and F emitting green, indicating that their structures affect their light properties.
  • In tests on removing chromium (Cr(vi)) from water, TF-CQDs were faster at adsorption, reaching equilibrium in 120 minutes, while F took 240 minutes; TF-CQDs followed a first-order model, while F demonstrated both chemical and physical adsorption mechanisms.
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In this study, novel Cu-complexes of heterocyclic cellulose which were synthesized via the reaction of carboxymethyl cellulose (CMC) from bagasse pulp with NHNH to give hydrazide cellulose which easily reacted with CS to form salt and then cyclized in the presence of HCl to afford cellulose oxadiazole, or with hydrazine hydrate to give cellulose triazole. Furthermore, the cellulose oxadiazole and triazole moieties acting as chelating agents with metal ion Cu (II), and all synthesized compounds were examined for their spectral analysis to show the adsorption of Cu (II) on the surface of cellulose through intramolecular hydrogen bonding. Results illustrated that cellulose oxadiazole and Cu- cellulose oxadiazole exhibited antimicrobial activities more than triazole and Cu- cellulose triazole.

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Article Synopsis
  • The study explores ionothermal carbonization (ITC) as a method to create nanostructured carbon materials, known as ionochars, using lignocellulosic biomass in specific ionic liquids (ILs).
  • Previous research focused on how the imidazolium cation affects the properties of these ionochars, but the role of the chloroferrate anion needed further investigation.
  • This research revealed that different anionic components significantly influence the ionochars' texture and morphology, utilizing various analytical techniques to characterize their properties.
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This work aims to enhance the performance of the polyvinyl alcohol (PVA) composite by using cellulose nanocrystal (CNC) as reinforcement and copper nanoparticles (CuNPs)/reduced graphene oxide (rGO) as conducting and antimicrobial reagents. Firstly, rGO was loaded onto CuNPs using an eco-friendly microwave method. Different techniques characterized the components and prepared composites, which indicated the incorporation of cellulose nanocrystals and rGO@CuNPs within the polyvinyl alcohol matrix.

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Exceptionally fast temperature-responsive, mechanically strong, tough and extensible monolithic non-porous hydrogels were synthesized. They are based on divinyl-crosslinked poly(N-isopropyl-acrylamide) (PNIPAm) intercalated by hydroxypropyl methylcellulose (HPMC). HPMC was largely extracted after polymerization, thus yielding a 'template-modified' PNIPAm network intercalated with a modest residue of HPMC.

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Graphene oxide (GO), TiO-NPs, HPMC, and shellac are environmentally green polymers and nanocomposites. This work aimed to create biodegradable composite films made of HPMC/shellac, HPMC/shellac-GO, and HPMC/shellac-GO/TiO-NPs by film casting. TiO-HPMC/shellac-GO matrix's dispersibility and mixing ability were characterized and observed using FTIR and XRD.

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A combination of different eco-friendly materials prepared promising fluorescent quantum dots (QDs) through the one-step process using the microwave heating of urea with cellulose, chitosan, and biochar. Characterizations of the prepared QDs, including the investigation of their structure by infrared spectroscopy, Raman analysis, X-ray diffraction, thermal gravimetric analysis, morphology, and optical properties, were performed. The results showed that QDs possess a small size, high UV absorption, and excitation wavelength-dependent fluorescence.

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A novel adsorbent was prepared using a backbone comprising chemically hybridized dialdehyde cellulose (DAC) with chitosan via Schiff base reaction, followed by graft copolymerization of acrylic acid. Fourier transform infrared spectroscopy (FTIR) confirmed the hybridization while scanning electron microscopy (SEM) revealed intensive covering of chitosan onto the surface of DAC. At the same time, energy dispersive X-ray (EDX) proved the emergence of nitrogen derived from chitosan.

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This study aimed to prepare antifouling and highly mechanical strengthening membranes for brackish and underground water desalination. It was designed from cellulose acetate (CA) loaded anatase. Anatase was prepared from tetra-iso-propylorthotitanate and carboxymethyl cellulose.

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Nowadays, the combined knowledge and experience in biomedical research and material sciences results in the innovation of smart materials that could efficiently overcome the problems of microbial contaminations. Herein, a new drug delivery platform prepared by grafting sodium alginate with β-carboxyethyl acrylate and acrylamide was described and characterized. 9-Aminoacridine (9-AA), and kanamycin sulfate (KS) were separately loaded into the hydrogel in situ during graft polymerization.

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The chromium adsorption behavior from aqueous solution by the amphoteric Janus nitrogen-doped carbon quantum dots (AJ-N-CQDs) was investigated. The pseudo-first-order and the second-order adsorption kinetics models were employed to analyze the experimental data; the second-order adsorption kinetics model presented a better correlation to the experimental data, suggesting a chemisorptions process. The values obtained in the pseudo-first-order are still suitable for describing the Kinetics of Cr(VI) sorption.

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The continuous supply of hydrogen sulfide (HS) gas at high concentrations to tumors is considered a promising and safe strategy for tumor therapy. However, the absence of a durable and cost-effective HS-producing donor hampers its extensive application. Sulfate-reducing bacteria (SRB) can serve as an excellent HS factory due to their ability to metabolize sulfate into HS.

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In this study, novel crosslinked hydrogels based on chitosan (CS) and carrageenan (CRG) loaded with silver and/or copper nanoparticles (Ag/CuNPs) were prepared through a freeze-drying (thawing) process to be applied in biological applications comprising wound dressing. These hydrogels showed porous interconnected structures. The influence of the used nanoparticles (NPs) on the antibacterial properties of the CS/CRG hydrogels was explored.

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Biopolymers have significant pharmaceutical applications, and their blending has favorable characteristics for their pharmaceutical properties compared to the sole components. In this work, sodium alginate (SA) as a marine biopolymer was blended with poly(vinyl) alcohol (PVA) to form SA/PVA scaffolds through the freeze-thawing technique. Additionally, polyphenolic compounds in leaves were extracted by different solvents, and it was found that extracts with 80% methanol had the highest antioxidant activity.

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In this work, we prepared highly swelling, stimuli-responsive hydrogels capable of the highly efficient adsorption of inorganic pollutants. The hydrogels were based on hydroxypropyl methyl cellulose (HPMC) grafted with acrylamide (AM) and 3-sulfopropyl acrylate (SPA) and were synthesized via the growth (radical polymerization) of the grafted copolymer chains on HPMC, which was activated by radical oxidation. These grafted structures were crosslinked to an infinite network by a small amount of di-vinyl comonomer.

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The diagnosis and treatment of many neurological and psychiatric problems depend on establishing simple, inexpensive, and comfortable electrochemical sensors for dopamine (DA) detection. Herein, 2,2,6,6 tetramethylpiperidine-1-oxyl (TEMPO)-oxidized cellulose nanofibers (TOC) were successfully loaded with silver nanoparticles (AgNPs) and/or graphite (Gr) and crosslinked by tannic acid, producing composites. This study describes a suitable casting procedure for the composite synthesis of TOC/AgNPs and/or Gr for the electrochemical detection of dopamine.

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Graphene oxide (GO) and its reduced form (rGO) have recently attracted a fascinating interest due to their physico-chemical properties, which have opened up new and interesting opportunities in a wide range of biomedical applications, such as wound healing. It is worth noting that GO and rGO may offer a convenient access to its ready dispersion within various polymeric matrices (such as cellulose and its derivative forms), owing to their large surface area, based on a carbon skeleton with many functional groups (i.e.

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Wastewater rich in heavy metals and organic compounds represents one of the essential environmental pollutants. Therefore, a practical approach is to fabricate eco-friendly polymer-based systems with a high ability to absorb pollutants. Herein, bionanocomposites consisting of chitosan (Cs) grafted by various monomers, such as acrylamide (Am), acrylic acid (AA), and 4-styrene sulfonic acid (SSA), and hybrid nanoparticles of graphene oxide/titanium dioxide nanoparticles (GO@TiO-NPs) were fabricated.

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In this study, the dielectric behavior of polyanionic electrically conductive superabsorbent hydrogel based on sodium alginate-g-poly(AM-co-ECA-co-AMPS) was investigated by broadband dielectric spectroscopy (BDS). The dielectric spectra obtained from -70 to 70 °C showed a superposition of three distinctive processes, electrode polarization, charge carrier's transport, and a molecular relaxation process. These dynamic processes were further analyzed along with the effect of both temperature and reduced graphene oxide (rGO) content.

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Fluorescent carbon quantum dots (CQDs) were prepared by an economical, green, and single-step procedure with the assistance of microwave heating of urea with bagasse (SCB), cellulose (C), or carboxymethyl cellulose (CMC). The prepared CQDs were characterized using a series of spectroscopic techniques, and they had petite size, intense absorption in the UV, and excitation wavelength-dependent fluorescence. The prepared CQDs were used for Pb(II) adsorption from an aqueous solution.

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Electrochemical conductive hydrogels are being extensively explored in the fabrication of portable batteries and high-performance supercapacitors. Herein, the rational design of a new polyanionic electrically conductive hydrogels based on sodium alginate-g-poly(AM-co-ECA-co-AMPS) are described. rGO was incorporated into the hydrogel during the polymerization process generating rGO@ sodium alginate-g-poly(AM-co-ECA-co-AMPS) composite hydrogels to study the impact of rGO on the performance of the hydrogels.

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We study the microstructure, optical, thermal, dielectric, and mechanical properties of flexible oxidized cellulose (OC) films loaded with different mass fractions of cubic structure BiNaKTiO by blending solution technique and casting method. The films were characterized using infrared, X-ray diffraction, scanning electron microscopy, and UV-visible spectroscopy. The optical results confirmed the formation of crystalline bismuth sodium titanate/OC semiconductor films with a direct energy bandgap (3.

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The current rationale is exploring new eco-friendly UV- shielding films based on cellulose and thiazolidine. Cellulose was oxidized to dialdehyde cellulose (DAC) and tricarboxy cellulose (TCC) by periodate and TEMPO/periodate/hypochlorite, respectively. While E-3-amino-5-(phenyldiazenyl)-2-thioxothiazolidin-4-one (TH) was synthesized by coupling diazonium salt with the 5-methylene of 2-thioxo-4-thiazolidinone.

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The conjugation between drug and biopolymers through an easily hydrolysable bond such as ester linkage, disulfide linkage, or imine-bond have been extensively employed to control the drug release pattern and improve its bioavailability. This work described the conjugation of 9-aminoacridine (9-AA) to Gum Arabic (GA) via Schiff's base, as a pH-responsive bond. First, GA was oxidized to Arabic Gum dialdehyde (AGDA), then a different amount of 9-AA (10, 25, and 50 mg 9-AA) was coupled to defined amount of AGDA, the coupling was confirmed by elemental analysis and different spectroscopic tools.

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