AAArwa O. Al-Ahmadi

Arwa O. Al-Ahmadi

*This is an algorithmically generated author record based on publicly available information.

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Arwa O. Al-Ahmadi has a total of 7 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Isothermal Crystallization Kinetics of Poly (3-hydroxybutyrate/ Poly(ethylene-co-vinyl acetate) Blends Enhanced by NH4Cl as a Nucleating Agent

    by Safaa H. El-Taweel, Arwa O. Al-Ahmadi

    The isothermal crystallization kinetics of poly (3-hydroxybutyrate) (PHB)/NH4Cl composites, PHB/poly(ethylene-co-vinyl acetate), with vinyl acetate contents of 80% (EVA80) blends and PHB/EVA80/1 wt% NH4Cl composites were investigated by using differential scanning calorimetry (DSC). The Avrami approach was applied to estimate the kinetic parameters of the PHB samples under isothermal crystallization conditions. It was found that the values of The Avrami rate constant, k, of PHB were increased with the incorporation of NH4Cl, declining EVA80 content in the PHB blends, and decreasing crystallization temperature. Moreover, the Avrami exponent, n, remained unchanged in spite of the change in the crystallization temperature, EVA80 content, and presence of NH4Cl. The activation energy, EA, calculated using the Arrhenius equation, for PHB/NH4Cl was much lower than that of pure PHB and PHB/EVA80, suggesting that the NH4Cl induced heterogeneous nucleation. The EA values for PHB/EVA80/1 wt% NH4Cl increased as the EVA80 content was increased, indicating a retardation effect of EVA80. Furthermore, a modified Lauritzen–Hoffmann treatment (LH) was used to evaluate the nucleation constant, Kg, of the PHB samples based on the assumption that U* was 13.8 kJ/mol and the equilibrium melting temperatures were 470 K, intercepts of HL equation,  ln⁡1/t0.5, were 25.9 for all PHB samples. The Kg values indicated that the crystallization of PHB in its composites and blends, described here, occurred in regime III. The maximum degradation rate temperatures of the PHB/NH4Cl composites were higher than that of PHB, by 9 oC. No significant change in thermal stability was detected by the addition of EVA80.


  • Open Access

    Cationic Cyclopentadienyliron Complex as a Novel and Successful Nucleating Agent on the Crystallization Behavior of the Biodegradable PHB Polymer

    by Safaa H. El-Taweel, Arwa O. Al-Ahmadi, Omaima Alhaddad, Rawda M. Okasha

    Cationic cyclopentadienyliron (CpFe+) is one of the most fruitful organometallic moieties that has been utilized to mediate the facile synthesis of a massive number of macromolecules. However, the ability of this compound to function as a nucleating agent to improve other macromolecule properties has not been explored. This report scrutinizes the influence of the cationic complex as a novel nucleating agent on the spherulitic morphology, crystal structure, and isothermal and non-isothermal crystallization behavior of the Poly(3-hydroxybutyrate) (PHB) bacterial origin. The incorporation of the CpFe+ into the PHB materials caused a significant increase in its spherulitic numbers with a remarkable reduction in the spherulitic sizes. Unlike other nucleating agents, the SEM imageries exhibited a good dispersion without forming agglomerates of the CpFe+ moieties in the PHB matrix. Moreover, according to the FTIR analysis, the cationic organoiron complex has a strong interaction with the PHB polymeric chains via the coordination with its ester carbonyl. Yet, the XRD results revealed that this incorporation had no significant effect on the PHB crystalline structure. Though the CpFe+ had no effect on the polymer’s crystal structure, it accelerated outstandingly the melt crystallization of the PHB. Meanwhile, the crystallization half-times (t0.5) of the PHB decreased dramatically with the addition of the CpFe+. The isothermal and non-isothermal crystallization processes were successfully described using the Avrami model and a modified Avrami model, as well as a combination of the Avrami and Ozawa methods. Finally, the effective activation energy of the PHB/CpFe+ nanocomposites was much lower than those of their pure counterparts, which supported the heterogeneous nucleation mechanism with the organometallic moieties, indicating that the CpFe+ is a superior nucleating agent for this class of polymer.


  • Open Access

    Corrosion and corrosion inhibition of cast Iron in hydrochloric acid (HCl) solution by cantaloupe (Cucumis melo) as green inhibitor

    by M Emran Khadijah, O Al Ahmadi Arwa, A Torjoman Bayan, M Ahmed Najla, N Sheekh Sara

    The effect of cantaloupe juice and seed extracts on corrosion of cast iron in 1.0 M hydrochloric acid (HCl) solution using hydrogen evolution measurements (HEM) and mass loss measurements (MLM) were investigated. Cantaloupe extracts inhibited the corrosion of cast iron in 1.0 M HCl solution. The inhibition efficiency increased with concentration of the extracts. The adsorption of the inhibitor molecules on cast iron surface was in accordance to Langmuir adsorption isotherms. In absence of inhibitors, the corrosion rate of cast iron increases with HCl concentration. The fractional reaction order observed in HCl solution indicates the formation of intermediates through the dissolution process or multiple steps mechanism of cast iron dissolution in HCl solution. Key words: Cantaloupe (Cucumis melo), corrosion, cast iron, HCl concentrations, adsorption isotherm.