Mohd Ali Hashim
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Mohd Ali Hashim has a total of 233 co-authors. Here are the top co-authors by number of shared publications:
- Inas Muen AlNashef
Department of Chemical & Petroleum Engineering, Khalifa University of Science and Technology, Abu Dhabi, UAE
47 shared publications - Farouq Sabri Mjalli
Petroleum and Chemical Engineering Department, Sultan Qaboos University, Muscat 123, Oman
41 shared publications - Bhaskar Sen Gupta
Heriot-Watt University Institute of Sustainable Built Environment, School of Energy, Geoscience, Infrastructure and Society Edinburgh
26 shared publications - Maan Hayyan
Energy and Sustainability Research Center (ESRC), A'Sharqiyah University, P.O. Box 42, Ibra 400, Oman; Energy and Sustainable Engineering Department, College of Engineering, A'Sharqiyah University, P.O. Box 42, Ibra 400, Oman
25 shared publications - Adeeb Hayyan
Higher Institution Centre of Excellence (HICoE), UM Power Energy Dedicated Advanced Centre (UMPEDAC), Universiti Malaya, Kuala Lumpur, Malaysia
18 shared publications - Kaveh Shahbaz
College of Science and Engineering James Cook University Townsville Australia
11 shared publications
Latest Publications
- Open Access
- 7 September 2026
- Published by Elsevier in Industrial Crops and Products
- Vol. 252
How effective are deep eutectic solvents in the purification of crude palm oil?
- 7 September 2026
- Published by Elsevier in Industrial Crops and Products
- Vol. 252
Open AccessHow effective are deep eutectic solvents in the purification of crude palm oil?
- Open Access
- 31 August 2026
- Published by MDPI AG in Separations
- Vol. 13 (9) , 246
Multifactor Optimization of Solvolytic Recycling of Polyethylene Terephthalate in Designer Deep Eutectic Solvents
A circular economy for polyethylene terephthalate (PET) aims to achieve complete material recirculation and reduce dependence on fossil-based feedstocks. Among recycling strategies, depolymerization offers the greatest potential for true circularity. This work investigates deep eutectic solvent (DES)-assisted PET depolymerization using a tetrabutylammonium bromide/sulfolane (TBABr/Sulf) system. A four-factor, three-level Box–Behnken design was employed, where reaction time, NaOH concentration, PET/solvent ratio, and water content were selected as independent variables, with PET weight loss as the response. The optimized conditions of 35 min reaction time, 5.9 wt% NaOH, a PET/solvent ratio (g/g) of 0.061, and a 1:1 water-to-DES ratio achieved 97% PET depolymerization and 93.8% TPA recovery. The process achieved a relatively low PET/DES (g/g) utilization ratio of 0.12 and required at least 40% less NaOH than other DES-based alkaline hydrolysis reported in the literature. The identity and quality of the recovered TPA were confirmed by FTIR, NMR, DSC, and elemental analysis. Under microwave-assisted conditions, TBABr/Sulf was successfully reused over three consecutive cycles while maintaining 100% depolymerization efficiency with consistent TPA quality. Collectively, these results demonstrate the technical potential of the proposed DES-assisted PET depolymerization process, particularly in terms of reduced solvent and alkaline requirements, shortened reaction time, and demonstrated solvent recyclability.
- 31 August 2026
- Published by MDPI AG in Separations
- Vol. 13 (9) , 246
Open AccessMultifactor Optimization of Solvolytic Recycling of Polyethylene Terephthalate in Designer Deep Eutectic Solvents
A circular economy for polyethylene terephthalate (PET) aims to achieve complete material recirculation and reduce dependence on fossil-based feedstocks. Among recycling strategies, depolymerization offers the greatest potential for true circularity. This work investigates deep eutectic solvent (DES)-assisted PET depolymerization using a tetrabutylammonium bromide/sulfolane (TBABr/Sulf) system. A four-factor, three-level Box–Behnken design was employed, where reaction time, NaOH concentration, PET/solvent ratio, and water content were selected as independent variables, with PET weight loss as the response. The optimized conditions of 35 min reaction time, 5.9 wt% NaOH, a PET/solvent ratio (g/g) of 0.061, and a 1:1 water-to-DES ratio achieved 97% PET depolymerization and 93.8% TPA recovery. The process achieved a relatively low PET/DES (g/g) utilization ratio of 0.12 and required at least 40% less NaOH than other DES-based alkaline hydrolysis reported in the literature. The identity and quality of the recovered TPA were confirmed by FTIR, NMR, DSC, and elemental analysis. Under microwave-assisted conditions, TBABr/Sulf was successfully reused over three consecutive cycles while maintaining 100% depolymerization efficiency with consistent TPA quality. Collectively, these results demonstrate the technical potential of the proposed DES-assisted PET depolymerization process, particularly in terms of reduced solvent and alkaline requirements, shortened reaction time, and demonstrated solvent recyclability.
- Open Access
- 1 December 2025
- Published by KEAI Publishing in Environmental Pollution and Management
- Vol. 2, 142-149
Removal of antibiotic contaminants from water via adsorption: Analysis of equilibrium isotherms
- 1 December 2025
- Published by KEAI Publishing in Environmental Pollution and Management
- Vol. 2, 142-149
Open AccessRemoval of antibiotic contaminants from water via adsorption: Analysis of equilibrium isotherms
- 19 August 2025
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 27 (35) , 18789-18792
Comment on “Unravelling the kinetics, isotherms, thermodynamics, and mass transfer behaviours of Zeolite Socony Mobil – 5 in removing hydrogen sulphide resulting from a dark fermentative biohydrogen production process” by M. K. A. Asman et al., Phys. Chem. Chem. Phys., 2024, 26, 20409
This critique identifies methodological flaws in the analysis of hydrogen sulfide adsorption on a zeolite adsorbent, as reported by Asman et al. [Phys. Chem. Chem. Phys., 2024, 26, 20409–20426]. Key concerns include fundamental errors in the formulation of both the Temkin adsorption isotherm and the Weber–Morris intraparticle diffusion model, along with inconsistencies in thermodynamic calculations. These flaws undermine the reliability of the study's findings and diminish its contribution to hydrogen sulfide adsorption research.
- 19 August 2025
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 27 (35) , 18789-18792
Comment on “Unravelling the kinetics, isotherms, thermodynamics, and mass transfer behaviours of Zeolite Socony Mobil – 5 in removing hydrogen sulphide resulting from a dark fermentative biohydrogen production process” by M. K. A. Asman et al., Phys. Chem. Chem. Phys., 2024, 26, 20409
This critique identifies methodological flaws in the analysis of hydrogen sulfide adsorption on a zeolite adsorbent, as reported by Asman et al. [Phys. Chem. Chem. Phys., 2024, 26, 20409–20426]. Key concerns include fundamental errors in the formulation of both the Temkin adsorption isotherm and the Weber–Morris intraparticle diffusion model, along with inconsistencies in thermodynamic calculations. These flaws undermine the reliability of the study's findings and diminish its contribution to hydrogen sulfide adsorption research.
- 27 March 2025
- Published by Elsevier in Electrochimica Acta
- Vol. 525
Relaxation dynamics of hydrogen bonds in hydrophobic deep eutectic electrolytes
- 27 March 2025
- Published by Elsevier in Electrochimica Acta
- Vol. 525
Relaxation dynamics of hydrogen bonds in hydrophobic deep eutectic electrolytes
- 25 July 2024
- Published by Elsevier in Science of The Total Environment
- Vol. 948, 174758
Evaluation of biodegradability, toxicity and ecotoxicity of organic acid-based deep eutectic solvents
- 25 July 2024
- Published by Elsevier in Science of The Total Environment
- Vol. 948, 174758
Evaluation of biodegradability, toxicity and ecotoxicity of organic acid-based deep eutectic solvents