Arwa O. Al-Ahmadi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Arwa O. Al-Ahmadi has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Safaa H. El-Taweel
Chemistry Department, Faculty of Science, Cairo University, Orman-Giza, 12613, Egypt
4 shared publications A Torjoman Bayan
Chemistry Department (Applied Chemistry) Faculty of Science Taibah University Saudi Arabia
1 shared publication- Khadijah Mohammed Emran Abdalsamad
Chemistry Department, College of Science, Taibah University, Al-Madinah Al-Monawarah, Saudi Arabia
1 shared publication M Ahmed Najla
Chemistry Department (Applied Chemistry) Faculty of Science Taibah University Saudi Arabia
1 shared publicationN Sheekh Sara
Chemistry Department (Applied Chemistry) Faculty of Science Taibah University Saudi Arabia
1 shared publication- Omaima A. Alhaddad
College of Sciences, Chemistry Department, Madina Monawara, Taibah University, Al-Madina 30002, Saudi Arabia
1 shared publication
Latest Publications
- 21 February 2020
- Published by Springer Nature in Polymer Bulletin
- Vol. 78 (2) , 729-751
Thermal behavior and soil biodegradation for blends of poly(hydroxybutyrate)/ethylene vinyl acetate copolymer (EVA 60) with 1 mass% NH4Cl
- 21 February 2020
- Published by Springer Nature in Polymer Bulletin
- Vol. 78 (2) , 729-751
Thermal behavior and soil biodegradation for blends of poly(hydroxybutyrate)/ethylene vinyl acetate copolymer (EVA 60) with 1 mass% NH4Cl
- 26 March 2019
- Published by Taylor & Francis in Journal of Macromolecular Science, Part B
- Vol. 58 (4) , 518-534
Isothermal Crystallization Kinetics of Poly (3-hydroxybutyrate/ Poly(ethylene-co-vinyl acetate) Blends Enhanced by NH4Cl as a Nucleating Agent
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, 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, 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 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, 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, were 25.9 for all PHB samples. The 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.- 26 March 2019
- Published by Taylor & Francis in Journal of Macromolecular Science, Part B
- Vol. 58 (4) , 518-534
Isothermal Crystallization Kinetics of Poly (3-hydroxybutyrate/ Poly(ethylene-co-vinyl acetate) Blends Enhanced by NH4Cl as a Nucleating Agent
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, 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, 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 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, 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, were 25.9 for all PHB samples. The 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.- 22 February 2019
- Published by Springer Nature in Journal of Thermal Analysis and Calorimetry
- Vol. 137 (5) , 1657-1672
Non-isothermal crystallization kinetics of poly(3-hydroxybutyrate)/EVA 80 blends enhanced by NH4Cl as a nucleating agent
- 22 February 2019
- Published by Springer Nature in Journal of Thermal Analysis and Calorimetry
- Vol. 137 (5) , 1657-1672
Non-isothermal crystallization kinetics of poly(3-hydroxybutyrate)/EVA 80 blends enhanced by NH4Cl as a nucleating agent
- Open Access
Cationic Cyclopentadienyliron Complex as a Novel and Successful Nucleating Agent on the Crystallization Behavior of the Biodegradable PHB Polymer
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 AccessCationic Cyclopentadienyliron Complex as a Novel and Successful Nucleating Agent on the Crystallization Behavior of the Biodegradable PHB Polymer
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
- 31 March 2015
- Published by Academic Journals in African Journal of Pure and Applied Chemistry
- Vol. 9 (3) , 39-49
Corrosion and corrosion inhibition of cast Iron in hydrochloric acid (HCl) solution by cantaloupe (Cucumis melo) as green inhibitor
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.
- 31 March 2015
- Published by Academic Journals in African Journal of Pure and Applied Chemistry
- Vol. 9 (3) , 39-49
Open AccessCorrosion and corrosion inhibition of cast Iron in hydrochloric acid (HCl) solution by cantaloupe (Cucumis melo) as green inhibitor
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.