Cellulosic polysaccharides have increasingly been recognized as a viable substitute for the depleting petro-based feedstock due to numerous modification options for obtaining a plethora of bio-based materials. In this study, cellulose triacetate was synthesized from pure cellulose obtained from the waste lignocellulosic part of date palm (Phoenix dactylifera L.). To achieve a degree of substitution (DS) of the hydroxyl group of 2.9, a heterogeneous acetylation reaction was carried out with acetic anhydride as an acetyl donor. The obtained cellulose ester was compared with a commercially available derivative and characterized using various analytical methods. This cellulose triacetate contains approximately 43.9% acetyl and has a molecular weight of 205,102 g·mol⁻¹. The maximum thermal decomposition temperature of acetate was found to be 380 °C, similar to that of a reference sample. Thus, the synthesized ester derivate can be suitable for fabricating biodegradable and “all cellulose” biocomposite systems.

In the present work, a nitrogen-rich activated carbon (PAnAC) was prepared using polyaniline (PAn) as a precursor to represent one possible conversion of nitrogen-containing polymeric waste into a valuable adsorbent. PAnAC was fabricated under the chemical activation of KOH and a PAn precursor (in a 4:1 ratio) at 650 °C and was characterized using FTIR, SEM, BET, TGA, and CHN elemental composition. The structural characteristics support its applicability as an adsorbent material. The adsorption performance was assessed in terms of adsorption kinetics for contact time (0–180 min), methyl orange (MO) concentration (C₀ = 50, 100, and 200 ppm), and adsorbent dosages (20, 40, and 80 mg per 250 mL batch). The kinetic results revealed a better fit to a pseudo-second-order, specifically nonlinear equation compared to pseudo-first-order and Elovich equations, which suggests multilayer coverage and a chemical sorption process. The adsorption capacity (q_e) was optimal (405.6 mg/g) at MO C₀ with PAnAC dosages of 200 ppm and 40 mg and increased as MO C₀ increased but decreased as the adsorbent dosage increased. The adsorption mechanism assumes that chemisorption and the rate-controlling step are governed by mass transfer and intraparticle diffusion processes.

This study aimed to assess the role of polymeric sources (polypyrrole, polyaniline, and their copolymer) of nitrogen (N)-doped activated carbons (indexed as PAnAC, PPyAC, and PnyAC, respectively) on their adsorption efficiency to remove methyl orange (MO) as a model cationic dye. The adsorbents were characterized using FTIR, SEM, TGA, elemental analysis, and surface area. The kinetic experiments were performed in batches at different MO concentrations (C₀) and adsorbent dosages. The adsorption kinetic profiles of pseudo-first-order, pseudo-second-order (PSO), Elovich, intraparticle diffusion, and liquid film diffusion models were compared. The results showed a better fit to the PSO model, suggesting a chemisorption process. The adsorption capacity (q_e, mg/g) was found to have increased as MO C₀ increased, yet decreased as the adsorbent quantity increased. At the adsorption operating condition, including MO C₀ (200 ppm) and adsorbent dose (40 mg), the calculated q_e values were in the order of PAnAC (405 mg/g) > PPyAC (204 mg/g) > PnyAC (182 mg/g). This trend proved the carbon precursor’s importance in the final properties of the intended carbons; elemental analysis confirmed that the more nitrogen atoms are in the activated carbon, the greater the number of active sites in the adsorbent for accommodating adsorbates. The diffusion mechanism also assumed a rate-limiting step controlled by the film and intraparticle diffusion. Therefore, such an efficient performance may support the target route’s usefulness in converting nitrogenous-species waste into valuable materials.

This study aimed to synthesize new bisphenol A-glycidyl methacrylate (BisGMA) derivatives, targeting a reduction in its viscosity by substituting one of its OH groups, the leading cause of its high viscosity, with a chlorine atom. Hence, this monochloro-BisGMA (mCl-BisGMA) monomer was synthesized by Appel reaction procedure, and its structure was confirmed using Fourier transform infrared spectroscopy, ¹H and ¹³C-nuclear magnetic resonance spectroscopy, and mass spectroscopy. The viscosity of mCl-BisGMA (8.3 Pa·s) was measured under rheometry conditions, and it was found to be more than 65-fold lower than that of BisGMA (566.1 Pa·s) at 25 °C. For the assessment of the viscosity changes of model resins in the presence of mCl-BisGMA, a series of resin matrices, in which, besides BisGMA, 50 wt % was triethylene glycol dimethacrylate, were prepared and evaluated at 20, 25, and 35 °C. Thus, BisGMA was incrementally replaced by 25% mCl-BisGMA to obtain TBC0, TBC25, TBC50, TBC75, and TBC100 blends. The viscosity decreased with temperature, and the mCl-BisGMA content in the resin mixture increased. The substantial reduction in the viscosity value of mCl-BisGMA compared with that of BisGMA may imply its potential use as a dental resin matrix, either alone or in combination with traditional monomers. However, the various properties of mCl-BisGMA-containing matrices should be evaluated.

The growth of plants highly depends on the soil’s water availability and properties. Hydrogels (HGs) have been used for decades to enhance soil water retention, whereas developing eco-friendly and sustainable HGs for agricultural applications is still necessary to ensure water and food security. In this study, renewable and cost-effective HGs were prepared from all-lignocellulose fibers of date palm biomass after carboxymethylation followed by citric acid (CA) crosslinking. HGs showed high equilibrium swelling capacity (EWC%), even in salty media, whereas purified HGs showed about 700–400 EWC% in deionized water. Further, HGs’ effect on germination was studied on Chico III tomato, mint, Basilico red, and chia seeds. The results revealed that HGs enhanced the soil properties, with taller and healthier plants observed in HG-amended soil. FTIR, thermal analysis, and microscope imaging were utilized to evaluate HGs’ and raw materials’ characteristics. The findings in this study support the idea that all-lignocellulose could be used for HG production without separation.

Mevacor/Poly(vinyl acetate-co-2-hydroxyethyl methacrylate) drug carrier systems (MVR/VAC-HEMA) containing different Mevacor (MVR) contents were prepared in one pot by free radical copolymerization of vinyl acetate with 2-hydroxyethyl methacrylate using an LED lamp light in the presence of camphorquinone as a photoinitiator and Mevacor as a drug filler. The prepared material was characterized by FTIR, ¹H NMR, DSC, SEM and XRD methods. Different parameters influencing the efficiency in the Mecvacor-water solubility and the drug delivery of this system, such as the swelling capacity of the carrier, the amount of Mevacor loaded and the pH medium have been widely investigated. The results obtained revealed that the Mevacor particles were uniformly dispersed in their molecular state in the copolymer matrix forming a solid solution; the cell toxicity of the virgin poly(vinyl acetate-co-2-hydroxy ethyl methacrylate) (VAC-HEMA) and MVR/VAC-HEMA drug carrier system exhibited no significant effect on their viability when between 0.25 and 2.00 wt% was loaded in these materials; the average swelling capacity of VAC-HEMA material in water was found to be 45.16 wt%, which was practically unaffected by the pH medium and the solubility of MVR deduced from the release process reached more than 22 and 37 times that of the powder dissolved directly in pH 1 and 7 media, respectively. The in vitro MVR release kinetic study revealed that the MVR/VAC-HEMA system containing 0.5 wt% MVR exhibited the best performance in the short gastrointestinal transit (GITT), while that containing 2.0 wt% is for the long transit as they were able to considerably reduce the minimum release of this drug in the stomach (pH1).