Fawwaz H. Jumean
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Fawwaz H. Jumean has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Mustafa Khamis
College of Arts and Sciences, American University of Sharjah, University City, Sharjah 26666, United Arab Emirates
5 shared publications N.M. Abdo
Department of Biology, Chemistry and Environmental Sciences, American University of Sharjah, POB 26666, Sharjah, United Arab Emirates
4 shared publications- Taleb Hassan Ibrahim
Department of Chemical Engineering, American University of Sharjah, Sharjah P.O. Box 26666, United Arab Emirates
3 shared publications - Amir Sada Khan
Department of Chemical Engineering, College of Engineering, American University of Sharjah, Sharjah P.O. Box 26666, United Arab Emirates
1 shared publication - Baraa A. Atallah
Department of Biology, Chemistry and Environmental Sciences, American University of Sharjah, Sharjah 26666, UAE
1 shared publication - Mohamed Badrelzaman
Department of Chemical Engineering, American University of Sharjah, Sharjah 26666, UAE
1 shared publication
Latest Publications
- Open Access
Efficient Extraction of Methylene Blue from Aqueous Solution Using Phosphine-Based Deep Eutectic Solvents with Carboxylic Acid
Methylene blue (MB), an organic thiazine dye, has numerous industrial and medical applications. However, MB is a wastewater contaminant that is harmful to humans and aquatic life. Hence, its removal from water bodies is essential. In this work, five novel deep eutectic solvents (DESs) were synthesized using different precursors, screened, and studied for the extraction of methylene blue (MB) from aqueous solution using liquid–liquid extraction. The first, TOP-SA, was synthesized using trioctylphosphine (TOP) as a hydrogen bond acceptor (HBA) and 2-hydroxy benzoic acid as a hydrogen bond donor (HBD). Among these, TOP-SA had the highest MB removal efficiency. The effects of pH, contact time, initial MB concentration, volumetric ratio, temperature, and ionic strength were studied and optimized. A 99.3% removal was achieved in 5 min for a 200 mg dm−3 MB solution mixed in a 1:10 ratio with TOP-SA at 25.0 °C. The structural properties of TOP-SA and its interactions with MB were investigated using FTIR. TOP-SA’s toxicity was investigated using human cells in vitro. TOP-SA was found to be comparatively less toxic and is a more efficient MB remover than other literature reported ionic liquids (ILs).
Open AccessEfficient Extraction of Methylene Blue from Aqueous Solution Using Phosphine-Based Deep Eutectic Solvents with Carboxylic Acid
Methylene blue (MB), an organic thiazine dye, has numerous industrial and medical applications. However, MB is a wastewater contaminant that is harmful to humans and aquatic life. Hence, its removal from water bodies is essential. In this work, five novel deep eutectic solvents (DESs) were synthesized using different precursors, screened, and studied for the extraction of methylene blue (MB) from aqueous solution using liquid–liquid extraction. The first, TOP-SA, was synthesized using trioctylphosphine (TOP) as a hydrogen bond acceptor (HBA) and 2-hydroxy benzoic acid as a hydrogen bond donor (HBD). Among these, TOP-SA had the highest MB removal efficiency. The effects of pH, contact time, initial MB concentration, volumetric ratio, temperature, and ionic strength were studied and optimized. A 99.3% removal was achieved in 5 min for a 200 mg dm−3 MB solution mixed in a 1:10 ratio with TOP-SA at 25.0 °C. The structural properties of TOP-SA and its interactions with MB were investigated using FTIR. TOP-SA’s toxicity was investigated using human cells in vitro. TOP-SA was found to be comparatively less toxic and is a more efficient MB remover than other literature reported ionic liquids (ILs).
- Open Access
Scale-Up of Self-Regenerating Semi-Batch Adsorption Cycles through Concurrent Adsorption and Reduction of Cr(VI) on Sheep Wool
A previous publication by our group reported that adsorption of Cr(VI) on sheep wool reached 99% when allowed a long residence time, with concurrent reduction to Cr(III). In this study, the process was scaled up by optimizing a pilot plant based on semi-batch adsorption cycles. This yielded Cr(III), which is about 300 times less toxic than Cr(VI), and can be precipitated using lime at high pH. Since the reduction step is slower than the adsorption one, an adsorption column was designed to perform semi-batch operation cycles, whereby the extended “off cycle” allows reduction to take place. Since reduction of Cr(VI) frees active sites on wool, the plant acts in lieu of in situ regeneration, accompanied by additional adsorption of Cr(VI). The results show that 97% of the column efficiency can be recovered within 24 h of “off cycle”. Wastewater from a local electroplating industry was treated by this method with high removal of Cr(VI), reaching the limit permitted by environmental standards. This study also reveals that typical concentrations of heavy metals, present in wastewater produced from electroplating, had no substantial antagonistic interference with Cr(VI) adsorption.
Open AccessScale-Up of Self-Regenerating Semi-Batch Adsorption Cycles through Concurrent Adsorption and Reduction of Cr(VI) on Sheep Wool
A previous publication by our group reported that adsorption of Cr(VI) on sheep wool reached 99% when allowed a long residence time, with concurrent reduction to Cr(III). In this study, the process was scaled up by optimizing a pilot plant based on semi-batch adsorption cycles. This yielded Cr(III), which is about 300 times less toxic than Cr(VI), and can be precipitated using lime at high pH. Since the reduction step is slower than the adsorption one, an adsorption column was designed to perform semi-batch operation cycles, whereby the extended “off cycle” allows reduction to take place. Since reduction of Cr(VI) frees active sites on wool, the plant acts in lieu of in situ regeneration, accompanied by additional adsorption of Cr(VI). The results show that 97% of the column efficiency can be recovered within 24 h of “off cycle”. Wastewater from a local electroplating industry was treated by this method with high removal of Cr(VI), reaching the limit permitted by environmental standards. This study also reveals that typical concentrations of heavy metals, present in wastewater produced from electroplating, had no substantial antagonistic interference with Cr(VI) adsorption.
- Open Access
Cyclic Sequential Removal of Alizarin Red S Dye and Cr(VI) Ions Using Wool as a Low-Cost Adsorbent
Alizarin red S (ARS) removal from wastewater using sheep wool as adsorbent was investigated. The influence of contact time, pH, adsorbent dosage, initial ARS concentration and temperature was studied. Optimum values were: pH = 2.0, contact time = 90 min, adsorbent dosage = 8.0 g/L. Removal of ARS under these conditions was 93.2%. Adsorption data at 25.0 °C and 90 min contact time were fitted to the Freundlich and Langmuir isotherms. R2 values were 0.9943 and 0.9662, respectively. Raising the temperature to 50.0 °C had no effect on ARS removal. Free wool and wool loaded with ARS were characterized by Fourier Transform Infrared Spectroscopy (FTIR). ARS loaded wool was used as adsorbent for removal of Cr(VI) from industrial wastewater. ARS adsorbed on wool underwent oxidation, accompanied by a simultaneous reduction of Cr(VI) to Cr(III). The results hold promise for wool as adsorbent of organic pollutants from wastewater, in addition to substantial self-regeneration through reduction of toxic Cr(VI) to Cr(III). Sequential batch reactor studies involving three cycles showed no significant decline in removal efficiencies of both chromium and ARS.
Open AccessCyclic Sequential Removal of Alizarin Red S Dye and Cr(VI) Ions Using Wool as a Low-Cost Adsorbent
Alizarin red S (ARS) removal from wastewater using sheep wool as adsorbent was investigated. The influence of contact time, pH, adsorbent dosage, initial ARS concentration and temperature was studied. Optimum values were: pH = 2.0, contact time = 90 min, adsorbent dosage = 8.0 g/L. Removal of ARS under these conditions was 93.2%. Adsorption data at 25.0 °C and 90 min contact time were fitted to the Freundlich and Langmuir isotherms. R2 values were 0.9943 and 0.9662, respectively. Raising the temperature to 50.0 °C had no effect on ARS removal. Free wool and wool loaded with ARS were characterized by Fourier Transform Infrared Spectroscopy (FTIR). ARS loaded wool was used as adsorbent for removal of Cr(VI) from industrial wastewater. ARS adsorbed on wool underwent oxidation, accompanied by a simultaneous reduction of Cr(VI) to Cr(III). The results hold promise for wool as adsorbent of organic pollutants from wastewater, in addition to substantial self-regeneration through reduction of toxic Cr(VI) to Cr(III). Sequential batch reactor studies involving three cycles showed no significant decline in removal efficiencies of both chromium and ARS.
- 20 September 2011
- Published by Elsevier in Thermochimica Acta
Calorimetric determination of enthalpy changes for the proton ionization of 3-[N-morpholino]propanesulfonic acid (MOPS), 4-[N-morpholino]butanesulfonic acid (MOBS) and 3-[N-morpholino]-2-hydroxypropanesulfonic acid (MOPSO) in water–methanol mixtures
- 20 September 2011
- Published by Elsevier in Thermochimica Acta
Calorimetric determination of enthalpy changes for the proton ionization of 3-[N-morpholino]propanesulfonic acid (MOPS), 4-[N-morpholino]butanesulfonic acid (MOBS) and 3-[N-morpholino]-2-hydroxypropanesulfonic acid (MOPSO) in water–methanol mixtures
- 4 July 2008
- Published by Elsevier in Thermochimica Acta
- Vol. 475 (1-2) , 22-24
Calorimetric determination of enthalpy changes for the proton ionization of N-tris(hydroxymethyl)methyl-4-aminobutanesulfonic acid (TABS), N-tris(hydroxymethyl)methyl-3-aminopropanesulfonic acid (TAPS) and 3-[N-tris(hydroxymethyl)methylamino]-2-hyroxypropane sulfonic acid (TAPSO) in water–methanol mixtures
- 4 July 2008
- Published by Elsevier in Thermochimica Acta
- Vol. 475 (1-2) , 22-24
Calorimetric determination of enthalpy changes for the proton ionization of N-tris(hydroxymethyl)methyl-4-aminobutanesulfonic acid (TABS), N-tris(hydroxymethyl)methyl-3-aminopropanesulfonic acid (TAPS) and 3-[N-tris(hydroxymethyl)methylamino]-2-hyroxypropane sulfonic acid (TAPSO) in water–methanol mixtures
- 1 August 2006
- Published by Elsevier in Thermochimica Acta
- Vol. 447 (1) , 112-114
Calorimetric determination of enthalpy changes for proton ionization of N-[2-hydroxyethyl]piperazine-N′-[2-ethane sulfonic acid] (HEPES) and N-[2-hydroxyethyl]piperazine-N′-[2-hydroxypropane sulfonic acid] (HEPPSO) in water–methanol mixtures
- 1 August 2006
- Published by Elsevier in Thermochimica Acta
- Vol. 447 (1) , 112-114
Calorimetric determination of enthalpy changes for proton ionization of N-[2-hydroxyethyl]piperazine-N′-[2-ethane sulfonic acid] (HEPES) and N-[2-hydroxyethyl]piperazine-N′-[2-hydroxypropane sulfonic acid] (HEPPSO) in water–methanol mixtures