Zafar Khan Ghouri

Amorphous SiO2 NP-Incorporated Poly(vinylidene fluoride) Electrospun Nanofiber Membrane for High Flux Forward Osmosis Desalination

Novel amorphous silica nanoparticle-incorporated poly(vinylidine fluoride) electrospun nanofiber mats are introduced as effective membranes for forward osmosis desalination technology. The influence of the inorganic nanoparticle content on water flux and salt rejection was investigated by preparing electrospun membranes with 0, 0.5, 1, 2, and 5 wt % SiO2 nanoparticles. A laboratory-scale forward osmosis cell was utilized to validate the performance of the introduced membranes using fresh water as a feed and different brines as draw solution (0.5, 1, 1.5, and 2 M NaCl). The results indicated that the membrane embedding 0.5 wt % displays constant salt rejection of 99.7% and water flux of 83 L m(-2) h(-1) with 2 M NaCl draw solution. Moreover, this formulation displayed the lowest structural parameter (S = 29.7 μm), which represents approximately 69% reduction compared to the pristine membrane. Moreover, this study emphasizes the capability of the electrospinning process in synthesizing effective membranes as the observed water flux and average salt rejection of the pristine poly(vinylidine fluoride) membrane was 32 L m(-2) h(-1) (at 2 M NaCl draw solution) and 99%, respectively. On the other hand, increasing the inorganic nanoparticles to 5 wt % showed negative influence on the salt rejection as the observed salt flux was 1651 mol m(-2) h(-1). Besides the aforementioned distinct performance, studies of the mechanical properties, porosity, and wettability concluded that the introduced membranes are effective for forward osmosis desalination technology.

Influence of copper content on the electrocatalytic activity toward methanol oxidation of Co(χ)Cu(y) alloy nanoparticles-decorated CNFs.

In this study, CoCu alloy nanoparticles-incorporated carbon nanofibers are introduced as effective non precious electrocatalyst for methanol oxidation in alkaline medium. The introduced electrocatalyst has been synthesized by simple and effective process; electrospinning. Typically, calcination, in nitrogen atmosphere, of electrospun nanofibers composed of cobalt acetate, copper acetate and poly (vinyl alcohol) leads to form carbon nanofibers decorated by CoCu nanoparticles. The nanofibrous morphology and alloy structure have been confirmed by SEM, TEM and XRD analyses. Investigation of the electrocatalytic activity indicates that copper content has strong influence, the alloy nanoparticles having the composition Cu5%Co95% showed distinct high performance; 100 times higher than other formulations. Overall, the introduced study revealed the veil about the distinct role of copper in enhancing the electrocatalytic activity of cobalt-based materials.

ZnO@C (core@shell) microspheres derived from spent coffee grounds as applicable non-precious electrode material for DMFCs

Although numerous reports have introduced non precious electrocatalysts for methanol oxidation, most of those studies did not consider the corresponding high onset potential which restricts utilization in real fuel cells. In this study, an −90 mV [vs. Ag/AgCl] onset potential non-precious electrocatalyst is introduced as an applicable anode material for the direct methanol fuel cells. Moreover, the proposed material was prepared from a cheap and abundantly existing resource; the spent coffee grounds. Typically, the spent coffee grounds were facilely converted to core@shell (ZnO@C) microspheres through a two-step approach, involving chemical activation and a subsequent calcination at temperature of 700 °C. Activation of the carbon derived from the spent coffee grounds was performed with ZnCl2 which acts as pore-forming agent as well as a precursor for the ZnO. The structure and morphology were characterized by (XRD), (SEM), and (TEM) analyses while the electrochemical characterizations was evaluated by cyclic voltammetry (CV) technique. Besides the comparatively very low onset potential, the introduced microspheres exhibited relatively high current density; 17 mA/cm2. Overall, based on the advantages of the green source of carbon and the good electrocatalytic activity, the spent coffee grounds-derived carbon can be considered a promise anode material for the DMFCs.

Photocatalytic degradation and antibacterial investigation of nano synthesized Ag₃VO₄ particles @PAN nanofibers

Well-dispersed Ag₃VO₄ nanoparticles @polyacrylonitrile (PAN) nanofibers were synthesized by an easily controlled, template-free method as a photo-catalyst for the degradation of methylene blue. Their structural, optical, and photocatalytic properties have been studied by X-ray diffraction, transmission electron microscopy, field-emission scanning electron microscopy equipped with rapid energy dispersive analysis of X-ray, photoluminescence, and ultraviolet–visible spectroscopy. The characterization procedures revealed that the obtained material is PAN nanofibers decorated by Ag₃VO₄ nanoparticles. Photocatalytic degradation of methylene blue investigated in an aqueous solution under irradiation showed 99% degradation of the dye within 75 min. Finally, the antibacterial performance of Ag₃VO₄ nanoparticles @PAN composite nanofibers was experimentally verified by the destruction of Escherichia coli. These results suggest that the developed inexpensive and functional nanomaterials can serve as a non-precious catalyst for environmental applications.

Stable N-doped & FeNidecorated graphene non-precious electrocatalyst for Oxygen Reduction Reaction in Acid Medium

NiFe nanoparticles-decorated & N-doped graphene is introduced as an effective and stable non-precious electrocatalyst for ORR in the acid medium. Compared to conventional Pt/C electrodes under the same conditions, the proposed nanocatalyst shows closer onset potential and current density. Typically, the observed onset potentials and current densities for the synthesized and Pt/C electrodes are 825 and 910 mV (vs. NHE) and −3.65 and −4.31 mA.cm−2 (at 5 mV.s−1), respectively. However, the most important advantage of the introduced metallic alloy-decorated graphene is its distinct stability in acid medium; the retention in the electrocatalytic performance after 1,000 successive cycles is approximately 98%. This finding is attributed to the high corrosion resistance of the NiFe alloy. The kinetic study indicates that the number of the transferred electrons is 3.46 and 3.89 for the introduced and Pt/C (20 wt%) electrodes, respectively which concludes a high activity for the proposed nanocomposite. The suggested decorated graphene can be synthesized using a multi-thermal method. Typically, nickel acetate, iron acetate, graphene oxide and urea are subjected to MW heating. Then, sintering with melamine in an Argon atmosphere at 750 °C is required to produce the final electrocatalyst. Overall, the introduced NiFe@ N-doped Gr nanocomposite shows remarkable electrochemical activity in the acid medium with long-term stability.

Surfactant/organic solvent free single-step engineering of hybrid graphene-Pt/TiO2 nanostructure: Efficient photocatalytic system for the treatment of wastewater coming from textile industries

In this study, hybrid graphene-Pt/TiO2 nanostructure were synthesized by single-step, inexpensive and surfactant/organic solvent free route; hydrothermal technique. The physicochemical properties of hybrid graphene-Pt/TiO2 nanostructure were carefully analyzed by multiple techniques, including X-ray diffractometer (XRD), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscope (FESEM) and transmission electron microscope (TEM). The synthesized hybrid nanostructures were utilized as photocatalyst for the degradation of methylene blue (MB) dye under natural environment at average ambient temperature and mean daily global solar radiation, of about 22–25 °C and 374.9 mWh/cm2, respectively. The activity performance indicated considerable degradation of methylene blue (MB) dye and was in the following order Gr (13%), TiO2 (60%) and hybrid graphene-Pt/TiO2 nanostructure (90%) over 21 min under the natural light illumination. The physiochemical characterization suggests that, the tightly attached metalized TiO2 nanoparticles (Pt-TiO2) on the high surface area graphene sheets improved utilization of visible light and increased separation and transfer of photo-excited electron (ē) hole (h+) pairs. Notably, the hybrid graphene-Pt/TiO2 nanostructure exhibited an excellent cyclic stability for methylene blue (MB) dye removal. Finally, the kinetic behavior indicated that the photocatalytic degradation reaction of the dye obeyed the pseudo-first order (Langmuir-Hinshelwood) kinetics model.

Effective NiMn Nanoparticles-Functionalized Carbon Felt as an Effective Anode for Direct Urea Fuel Cells

The internal resistances of fuel cells strongly affect the generated power. Basically, in the fuel cell, the anode can be prepared by deposition of a film from the functional electrocatalyst on a proper gas diffusion layer. Accordingly, an interfacial resistance for the electron transport is created between the two layers. Electrocatalyst-functionalized gas diffusion layer (GDL) can distinctly reduce the interfacial resistance between the catalyst layer and the GDL. In this study, NiMn nanoparticles-decorated carbon felt is introduced as functionalized GDL to be exploited as a ready-made anode in a direct urea fuel cell. The proposed treated GDL was prepared by calcination of nickel acetate/manganese acetate-loaded carbon felt under an argon atmosphere at 850 °C. The physiochemical characterizations confirmed complete reduction for the utilized precursors and deposition of pristine NiMn nanoparticles on the carbon felt fiber. In passive direct urea fuel cells, investigation the performance of the functionalized GDLs indicated that the composition of the metal nanoparticles has to be optimized as the GDL obtained from 40 wt % manganese acetate reveals the maximum generated power density; 36 mW/m2 at room temperature and 0.5 M urea solution. Moreover, the electrochemical measurements proved that low urea solution concentration is preferred as utilizing 0.5 M solution resulted into generating higher power compared to 1.0 and 2.0 M solution. Overall, this study opens a new avenue toward functionalization of the GDL as a novel strategy to overcome the interfacial resistance between the electrocatalyst and the GDL.

Validation of Total Mercury in Marine Sediment and Biological Samples, Using Cold Vapour Atomic Absorption Spectrometry

A method for the measurement of total mercury (T-Hg) in environmental samples using cold vapour atomic absorption spectrometry (CV AAS) has been validated yielding a dynamic range (0.04–10.00 μg/kg) and high certified reference material (CRM) recovery (>90%). The validation was carried out according to International Union of Pure and Applied Chemistry (IUPAC) validation and Eurachem Guides. A freeze-dried and homogenised sample was weighed and then digested using Suprapur acids (HNO3, H2SO4, and HF) with potassium dichromate solution in a hot block digestion system. A calibration curve was constructed (R2 > 0.999). Two CRMs (Marine Sediment Reference Material (PACS-3) and Trace Elements in Muscle Tissue (Trace Elements and Methylmercury in Mussel Tissue (NIST2976)) were utilised for quality assurance and control. The limit of quantification (LOQ) calculated as 0.04 µg/kg, and uncertainty (U) calculated as 2%. The obtained results showed the suitability of this method for direct mercury measurement in environmental samples. Additionally, the proficiency of this method was recognised by accreditation under the standard of International Organization for Standardization (ISO/IEC 17025:2017) for competence of testing and calibration laboratories.

Leaching of Some Essential and Non-Essential Heavy Metals from Modern Glazed Ceramic Crockeries Imported into Qatar from China, India and Spain

In this study, the leaching potential of ceramic crockeries available in Qatar market has been evaluated using inductively coupled plasma mass spectrometry (ICP-MS). Ceramic crockeries decorated with glaze matter containing various essential (Zinc, Iron, and Barium, etc.) and non-essential heavy metals (lead and cadmium) can adulterate the foodstuff and/or can release deadly metals into the food substance. Chines, Indian, and Spanish ceramic crockeries were randomly selected from the products available in the local Qatari market and analyzed to determine the level of leachable essential and non-essential heavy metals. Leaching studies were performed according to the ASTM 738-94 standard test methods for specific metals leaching into 4% acetic acid solutions over 24 hours exposure time. ASTM 738-94 is a precise and standard method and particularly designed for the determination of some heavy metals extracted by acetic acid from the glazed ceramic surface. Results show that all the ceramic crockeries contain both leachable essential and non-essential heavy metals. However, the concentration of these heavy metals is not potentially high to cause any adverse effect on human health.

CoNi Nanoparticles/CNT Composite as Effective Anode for Direct Urea Fuel Cells

This Publication was made possible by NPRP grant # [8-1344-1-246] from the Qatar National Research Fund (a member of Qatar Foundation). The findings achieved herein are solely the responsibility of authors.