Fekri Abdulraqeb Ahmed Ali

Removal of heavy metal ions using a carboxylated graphene oxide-incorporated polyphenylsulfone nanofiltration membrane

We investigate the removal of heavy metal ions from synthetic contaminated water on a laboratory scale using a carboxylated-graphene oxide (GO)-incorporated polyphenylsulfone (PPSU) nanofiltration membrane (the so called PPSU/carboxylated-GO nanocomposite membrane). The prepared membranes were characterized with respect to the rheology of the doping solutions and based on the morphology, topography, and charge density of the membranes. Spectroscopic analysis of the membranes was also performed. The nanofiltration performance was demonstrated by the removal of five heavy metal ions (arsenic, chromium, cadmium, lead, and zinc). The effects of carboxylated-GO on the membrane molecular weight cut-off, hydraulic permeability, and heavy metal ion removal performance were investigated with respect to different factors, including feed concentration from single ions, transmembrane pressure (TMP) with mixed ions, and permeate flux. The addition of carboxylated-GO produced a membrane with enhanced properties that exhibited superior performance. Increasing the feed concentration and TMP did not affect the removal of anions; however, the removal of cations slightly decreased with the resulting membrane. The maximum removal rates of heavy metal ions were >98% and ∼80% for the anions and cations, respectively, and an enhanced volumetric flux of 27 ± 3 L m−2 h−1 was observed. This result is based on the Donnan exclusion principle, which is attributable to the surface charge of −70 mV and the order of the hydrated metal radii. The prepared PPSU/carboxylated-GO nanocomposite membrane provided impressive heavy metal ion removal and showed an acceptable volumetric flux under the applied parameters; this work demonstrates very economically advantageous conditions for heavy metal ion removal.

Template-free synthesis of nitrogen doped carbon materials from an organic ionic dye (murexide) for supercapacitor application

The present study describes a template-free single step carbonization route to prepare hierarchically structured nitrogen-doped carbon materials (NCMs) by using an organic ionic dye (OID), ammonium purpurate (murexide). These NCMs exhibited moderate specific surface area (307 m2 g−1 for NCM(MDE)-900) and hierarchical macro/meso/microporous structures with abundant nitrogenous functionalities that contributed towards the high specific capacitance displayed by pseudocapacitive contribution. In particular, the NCM(MDE)-800 displayed superior specific capacitance (222 F g−1 at 3 A g−1) and excellent cyclic stability of ∼10 000 cycles at 10 A g−1 in 1 M 1.0 M H2SO4(aq). The material prepared at higher temperature, viz. NCM(MDE)-900, exhibited high rate capability at 50 A g−1, which is 92% of their specific capacitances at 10 A g−1. Further systematic investigations of NCM(MDE)-800 in three different electrolytes, viz. 1.0 M H2SO4(aq), 6 M KOH(aq) and 0.5 M Na2SO4(aq), revealed that 1.0 M H2SO4(aq) is a promising electrolyte for achieving good specific capacitance, high capacitive retention and long term cyclic stability, which might have its origins in the formation of ionic interactions between the active protons in 1.0 M H2SO4(aq) and the alpha carbon atoms with Lewis basic character next to the nitrogen in these NCMs.

Antimicrobial and antifouling properties of versatile PPSU/carboxylated GO nanocomposite membrane against Gram-positive and Gram-negative bacteria and protein

Biofouling is a serious issue in membrane-based water and wastewater treatment as it critically compromises the efficacy of the water treatment processes. This investigation demonstrates the antimicrobial and antifouling properties of a nanocomposite membrane system composed of carboxyl-functionalized graphene oxide (COOH-GO) and polyphenylsulfone (PPSU). The PPSU/COOH-GO nanocomposite membrane exhibited excellent antimicrobial properties, achieving maximum bacteriostasis rates of 74.2% and 81.1% against the representative Gram-negative bacteria (Escherichia coli and Pseudomonas aeruginosa, respectively) and 41.9% against the representative Gram-positive bacterium (Staphylococcus aureus). The PPSU/COOH-GO nanocomposite membrane inhibited the attachment, colonization, and the biofilm formation of three species. Antifouling was assessed through filtration experiments using a model foulant bovine serum albumin (BSA). The fouling mechanisms were investigated by Hermia’s models (complete blocking, intermediate blocking, standard blocking, and cake formation), and the analysis involved fitting the volumetric flux decline experimental data to models. The fouling study revealed a less irreversible fouling and increased flux recovery ratio for the PPSU/COOH-GO nanocomposite membrane. Complete blocking of pores and cake formation were the major fouling mechanisms for the membrane.

Novel route for amine grafting to chitosan electrospun nanofibers membrane for the removal of copper and lead ions from aqueous medium

A novel step wise synthetic route was developed to prepare amine grafted nanofibers (AGNFs) affinity membrane. The chemical structure of the nanofibers (NFs) after grafting was studied by acquiring Fourier Transform Infrared (FT-IR) spectra and Carbon, Hydrogen and Nitrogen (CHN) data. The morphology of the NFs before and after grafting was studied by Field Emission Scanning Electron Microscope (FE-SEM). FT-IR and CHN data confirmed the introduction of new functional groups into the primary structure of chitosan (CH). FE-SEM showed denser membrane with no deterioration of the NFs morphology after grafting. The aqueous stability of the membranes was studied in distilled water. The AGNFs membranes showed good aqueous stabilities (with only ∼ 6% loss in weight until 24 h and remained stable thereafter) which was less than the weight loss by glutaraldehyde treated nanofibers (GNFs) (∼44% loss in weight until 24 h) and pristine NFs (100% loss in weight as soon as the NFs were immersed in distilled water). The maximum adsorption (qm) capacity of AGNFs for Cu (II) and Pb (II) was observed to be 166.67 mg.g-1 and 94.34 mg.g-1. The adsorption capacity of the present systems was much higher for Cu (II) when compared to the already existing conventional and chitosan adsorbents. This increased might be related not just to the size, but more potentially to the increase in the number of nitrogen binding sites (chelating sites). Nitrogen donates lone-pair of electrons for chelation. The combination of processing into nano size and amine grafting (AG) has significantly increased the adsorption capacity of CH NFs membrane.