Management of ibuprofen in wastewater using electrospun nanofibers developed from PET and PS wastes.

Electrospinning is a promising technique for the beneficial use and recycling of plastic waste polymers using simple methodologies. In this study, plastic bottles and Styrofoam wastes have been used to develop polyethylene terephthalate (PET) and polystyrene (PS) nanofibers using electrospinning technique separately without any further purification. The effect of the concentration onto the nanofiber's morphology was studied. The fabricated nanofibers were characterized using Field Emission Scanning Electron Microscope (FE-SEM), Fourier Transformed Infrared Spectroscopy (ATR-FTIR), N2 adsorption/desorption analysis, and water contact angle (WCA). Furthermore, the prepared nanofibers were applied for the adsorption of ibuprofen (IBU) from wastewater. Some parameters that can influence the adsorption efficiency of nanofibers such as solution pH, wt.% of prepared nanofibers, drug initial concentration, and contact time were studied and optimized. The results show that the equilibrium adsorption capacity was achieved after only 10 min for 12 wt% PET nanofibers which is equivalent to 364.83 mg/g. For 12 wt% PS nanofibers, an equilibrium adsorption capacity of 328.42 mg/g was achieved in 30 min. The experimental data was fitted to five isotherm and four kinetics models to understand the complicated interaction between the nanofibers and the drug. Langmuir-Freundlich isotherm model showed the best fit for experimental data for both PET and PS nanofibers. The adsorption process was characterized by predominantly physical reaction rather than chemical adsorption for both materials. The reusability study revealed that the synthesized nanofibers maintain their ability to adsorb/desorb IBU for up to five cycles. The results obtained demonstrated that fabricated nanofibers from plastic wastes could perform promising adsorbents for the management of IBU in wastewater. However, further research is needed for the scaling-up the fabrication which is required for real-world applications.

Valorification of Egyptian volcanic tuff as eco-sustainable blended cementitious materials.

Rhyolite rocks extend from southern Egypt to northern Egypt in the Eastern Desert, and no effective economic exploitation of them has been discovered so far. The pozzolanic activities of different volcanic tuffs (VT) supplied from the Eastern Desert located in Egypt have been investigated as natural volcanic pozzolan materials to develop new green cementitious materials for achieving sustainability goals in the construction field. Experimentally in this paper, the pozzolanic activities of seven diverse specimens of Egyptian tuffs taken with standardized proportions of 75:25% (Cement: volcanic tuffs) were investigated. Pozzolanic features of such tuffs are examined comparatively via strength activity index (SAI), TGA, DTA, and the Frattini's test. Chemical composition, petrographic, and XRD analysis were also performed for tuffs samples. The pozzolanic reaction degrees were determined according to the compressive strengths at 7, 28, 60 and 90 days with different replacement ratios (20, 25, 30 and 40%) of tuffs samples. Additionally, the micro-filler effects in mortar and concrete were determined by measuring the heat of hydration in mortar samples and the compressive strength of concrete with different additive ratios for tuffs samples besides, the concrete slump test. The results show that TF6 gives a lower cement heat of hydration value which is less than 270 J/g at 7 days. Also, its performance in concrete is better than silica fume at late strength (28 days) since the concrete index value is 106.2% by compared to the concrete index of silica fume 103.9 and therefore it can be used as an alternative to high price and quality variable silica fume (SF) for producing high-performance green concrete. Due to the good pozzolanic behavior proved by nearly most volcanic tuffs, along with their low cost, this study will be profitable for very auspicious the use of Egyptian volcanic tuffs for developing sustainable and eco­friendly blended cement.

Cost-effective and green additives of pozzolanic material derived from the waste of alum sludge for successful replacement of portland cement.

The major objective of this study was to examine the viability of using 5, 10, or 15 mass% of Activated Alum Sludge waste (AAS) instead of Ordinary Portland Cement (OPC) as a pozzolanic ingredient in concrete. This fundamental inquiry framed the investigation and OPC-AAS-hardened composites were studied to see whether they may benefit from inexpensive nanocomposites in terms of improved physical properties, mechanical strength, and resistance to heat and flame. The investigation set out to see how inexpensive nanocomposite might be put to use and the nanoparticles of CuFe2O4 spinel with an average size of less than 50 nm were successfully manufactured. Many different OPC-AAS-hardened composites benefit from the addition of CuFe2O4 spinel, which increases the composites' resistance to fire and enhances their physicomechanical properties at roughly average curing ages. Synthesized CuFe2O4 spinel was shown to have desirable characteristics by TGA/DTG and XRD. By using these methods, we were able to identify a broad variety of hydration yields, including C-S-Hs, C-A-S-Hs, C-F-S-Hs, and Cu-S-Hs, that enhance the physicomechanical properties and thermal resistivity of OPC-AAS-hardened composites as a whole. The composite material comprising 90% OPC, 10% AAS waste, and 2% CuFe2O4 has several positive economic and environmental outcomes.

Economic and facile approach for synthesis of graphene-titanate nanocomposite for water reclamation.

Graphene and its composites with semiconductor materials have been received highly attention in many research areas because of their unique properties. Efficient application of graphene is hindered by the lack of cost-effective synthesis methods. In this work, an economic and facile route for mass production of graphene-titanate nanocomposite has been discussed. Graphene was prepared by exfoliation of graphite powder in 40% ethanol aqueous solution. Titanate nanotubes were grown on graphene sheets by hydrothermal method, where the dispersed graphene sheets were mixed with titanate solution and then placed in autoclave and placed in oven for 16 h at 160 °C. The prepared composite was characterized by transmission electron microscope (TEM), scanning electron microscope (SEM), Fourier transforms infrared spectroscopy (FTIR), thermogravimetric analysis (TGA). All the obtained results confirmed the synthesis of graphene and its composite with titanate in highly uniform and pure form. The adsorption efficiency of the prepared composite was tested using methylene blue (MB) as a model dye. The adsorption isotherm was investigated using Freundlich and Langmuir models. The adsorption capacity of MB was 270.27 mg/g. The obtained correlation coefficients (R2) by Freundlich and Langmuir model were 0.996 and 0.973, respectively. The adsorption kinetics was investigated and discussed using different models. The thermal stability of the developed composite is improved after MB adsorption.

Preparation and characterization of novel MWCNTs/Fe-Co doped TNTs nanocomposite for potentiometric determination of sulpiride in real water samples.

Novel multiwalled carbon nanotubes/ Fe-Co doped titanate nanotubes nanocomposite (MWCNTs/Fe-Co doped TNTs) facilitated the charge transfer and enhanced sensitivity and selectivity. Herein, three novel modified carbon paste sensors (CPSs) based on MWCNTs (sensor I), Fe-Co doped TNTs (sensor II) and MWCNTs/Fe-Co doped TNTs composite (sensor III) were fabricated for a simple, low cost and high accuracy electrochemical method for the potentiometric determination of sulpiride (SLP). The sensors exhibited excellent Nernstian slopes 57.1 ± 0.4, 56 ± 0.5 and 58.8 ± 0.2 mV decade-1 with detection limits (DL) 7.6 × 10-7, 1.58 × 10-6 and 8.7 × 10-8 mol L-1, quantification limits (QL) 2.5 × 10-6, 5.2 × 10-6 and 2.9 × 10-7 mol L-1 for a long lifetime 20, 18, and 25 weeks for sensors (I), (II), and (III), respectively. The modified sensor (III) was applicable by measuring the concentration of spiked SLP in pure solutions, pharmaceutical products, human urine, and real water samples. The proposed method can be used as an important analytical tool in the quality control of the pharmaceutical industry.

Prostate Cancer Cellular Uptake of Ternary Titanate Nanotubes/CuFe2O4/Zn-Fe Mixed Metal Oxides Nanocomposite.

BACKGROUND: Certainly, there is a demand for stronger recognition of how nanoparticles can move through the cell membrane. Prostate cancer is one of the forcing sources of cancer-relevant deaths among men. AIM OF THE WORK: The current research studied the power of prostate cancer cells to uptake a ternary nanocomposite TNT/CuFe2O4/Zn-Fe mixed metal oxides (MMO). METHODOLOGY: The nanocomposite was synthesized by a chemical method and characterized by a High-resolution transmission electron microscope, Field emission scanning electron microscope, X-ray diffraction, Fourier transmission infra-red, X-ray photoelectron spectroscopy, dynamic light scattering. Besides, it was implemented as an inorganic anticancer agent versus Prostate cancer PC-3 cells. RESULTS: The results revealed cellular uptake validity, cell viability reduction, ultra-structures alterations, morphological changes and membrane damage of PC-3 cells. CONCLUSION: The prepared ternary nanocomposite was highly uptake by PC-3 cells and possessed cytotoxicity that was dose and time-dependent. To conclude, the study offered the potential of the investigated ternary nanocomposite as a promising prostate anticancer agent.

Outstanding features of Cu-doped ZnS nanoclusters.

ZnS and their Cu-doped nanoclusters (NCs) were synthesized successfully using the wet chemical route with different Cu content. The crystalline structure was investigated using x-ray powder diffraction which assured the single-phase formation in cubic symmetry. High-resolution transmission electron microscope indicated the microstructure of NCs with a size ranging from 2-4 nm. A butterfly hysteresis (M-H) loop was observed at room temperature with large values of coercivity for the Cu content of x = 0.05. Photoluminescence emission spectra were recorded from 500-615 nm for pure and Cu-doped ZnS NCs at a 350 nm excitation wavelength. The sample exhibited green fluorescence bands peaking at 535, 544, 552.5, 558.2, and 560.6 nm, which confirmed the characteristic feature of Zn2+ as luminescent centers in the lattice. The additional yellow and orange emissions are due to defect levels or/and impurity centers. The dielectric constant as well as the conductivity values increased with increasing Cu content.

Synthesis and multifunctionality of (CeO2-NiO) nanocomposites synthesized via sonochemical technique.

CeO2, NiO and their nanocomposite were synthesized using facile sonochemical technique. XRD assure single phase CeO2 and NiO while the nanocomposite consists of the two phases only. CeO2 nanoparticles possess cubic shape, NiO was formed in nanorods, and CeO2 decorated the NiO nanorods in the nanocomposite. The magnetic behavior of the nanocomposite lies between those of the two parents with a ferromagnetic tendency. Metal oxide nanoparticles acted as catalyst in the formation of carbon nanofibers (CNFs), while the nanocomposite leads to the production of carbon nanotubes. The photocatalyst (CeO2-NiO) achieved complete dye degradation (100%) in light for the tested dye at 50 min. The decay products were analyzed using GC mass confirming mineralization of Bb red dye.

Microwave synthesis of pure and doped cerium (IV) oxide (CeO2) nanoparticles for methylene blue degradation.

Cerium (IV) oxide (CeO2), samarium (Sm) and gadolinium (Gd) doped CeO2 nanoparticles were prepared using microwave technique. The effect of microwave irradiation time, microwave power and pH of the starting solution on the structure and crystallite size were investigated. The prepared nanoparticles were characterized using X-ray diffraction, FT-Raman spectroscopy, and transmission electron microscope. The photocatalytic activity of the as-prepared CeO2, Sm and Gd doped CeO2 toward degradation of methylene blue (MB) dye was investigated under UV light irradiation. The effect of pH, the amount of catalyst and the dye concentration on the degradation extent were studied. The photocatalytic activity of CeO2 was kinetically enhanced by trivalent cation (Gd and Sm) doping. The results revealed that Gd doped CeO2 nanoparticles exhibit the best catalytic degradation activity on MB under UV irradiation. For clarifying the environmental safety of the by products produced from the degradation process, the pathways of MB degradation were followed using liquid chromatography/mass spectroscopy (LC/MS). The total organic carbon content measurements confirmed the results obtained by LC/MS. Compared to the same nanoparticles prepared by another method, it was found that Gd doped CeO2 prepared by hydrothermal process was able to mineralize MB dye completely under UV light irradiation.

Preparation, characterization and antimicrobial applications of Zn-Fe LDH against MRSA.

Facile and simple processes to get Zn-Fe layered double hydroxide (LDH) with nitrate as the interlayer anion are reported. The method of co-precipitation produced high crystallinity LDH that is marked by XRD, SEM, TEM and FT-IR. Results showed that 99.8% of Cd(+2) removals were at pH11 and 4h. To get the adsorption isotherms, the concentration of metal ions extending from 6 to 18mg/L was utilized. Results supported the Langmuir adsorption model. In contrary, the adsorption process followed the pseudo-second-order reaction kinetics. Interestingly, the prepared LDH shows durable antimicrobial activities against Gram-negative (Proteous vulgaris, Klebsiella pneumoniae, Escherichia coli and Pseudomonas aeruginosa) and Gram-positive (Staphylococcus epidermidis, Staphylococcus aureus, Streptococcus pyogenes and MRSA) and fungi (Candida albicans, Aspergillus fumigatus, Geotricumcandidum, and Trichophyton mentagrophytes). The minimum inhibitory concentration (MIC) of Zn-Fe LDH varied from 0.49 to 15.60µg/mL according to the types of microorganisms. The prepared LDH achieved 90% at pH8.50 which is the pH of wastewater and at the same time exhibited durable antimicrobial activities against MRSA, Gram-negative, Gram-positive and fungi. Results have significant implications in the field of bioremediation of water with little cost, simple operation, high productivity and easiness of the equipment.

Adenosine triphosphate blocks opiate withdrawal symptoms in rats and mice.

The effect of adenosine triphosphate (ATP) on the expression of opiate withdrawal was examined using a chronic model of morphine-dependence. ATP was studied for its ability to modify or block jumping in morphine-abstinent mice. In mice administered 2 mg/kg ATP intravenously, the naloxone ED50 for withdrawal jumping increased by 11-fold in comparison to saline-treated mice. Nalaxone-precipitated morphine-withdrawal in the rats, has been shown to induce a specific pattern of intestinal hypermyoelectric activity and to increase the arterial blood pressure. Administration of ATP at dose of 1 and 2 mg/kg intravenously inhibited the induction of hypermyoelectric activity pattern in 80 and 100% of animals tested respectively. ATP also blocked the increase in mean arterial blood pressure seen during withdrawal in a dose-dependent fashion. Investigations were carried out to determine if blocking of the alpha 2-adrenoreceptors with yohimbine would result in an alteration in antiwithdrawal action of ATP. Yohimbine reversed the effect of ATP in blocking naloxone-precipitated withdrawal on the myoelectric activity of jejunum and colon, however, it failed to antagonize the effect of ATP on withdrawal jumping and to block the effect of ATP on the pressor response produced by naloxone in morphine-dependent animals.