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The aim of this project is to fabricate a highly stable Fe3O4-OA-MWCNT composite and its colloidal suspension in polyalphaolefin (PAO) base fluid for heat transfer applications. The nanocomposite was produced in three mass ratios (0.5 : 1, 1 : 1, and 1.5 : 1) to explore the concentration effects on the stability of the nanocomposite. XRD analysis and FTIR spectroscopy were conducted to inspect the phase and composition of the synthesized nanocomposite. The crystallite sizes (3.75 nm, 7.74 nm, and 7.52 nm) and dislocation densities of each composite were calculated, and it was revealed that the samples with high concentration of iron oxide nanoparticles showed small defects in their lattices. Dispersion stability of ferrofluids was also examined by natural deposition method for 365 days. The ferrofluids displayed high stability for more than one year with no sign of sedimentation. Thermal conductivity of the nanofluid was also measured via. A transient plane source method and a linear trend with slight deviation were observed. [ABSTRACT FROM AUTHOR]

Nanotechnology has emerged as a promising multidisciplinary field. It has shown several applications including diagnostics, imaging and structural design. Nanoparticles can be synthesized via chemical and physical approaches, carrying many threats to the ecosystem. To overcome these threats, sustainable routes for the synthesis of nanoparticles were implemented. Green synthesis is the most fascinating and attractive alternative to chemical synthesis as it offers more advantages. Nontoxic and eco-friendly secondary metabolites from plants are used as reducing and capping agents. This process is comparatively simple and cost-effective. A gold salt is simply reduced by biomolecules (phenols, alkaloids, proteins, etc.) present in the extracts of these plants. In this review, we have emphasized the synthesis and antimicrobial potential of gold nanoparticles using various plant extracts and their proposed mechanisms. Abbreviation: Au: aurum; gold; DLS: dynamic light scattering; EDAX: energydispersive X-ray analysis; EDS: energy-dispersive spectroscopy; FTIR: Fourier transform infrared spectroscopy; HRTEM: highresolution transmission electron microscopy; NPs: nanoparticles; UV–VIS: ultra violet-visible spectroscopy; SEM: scanning electron microscopy; XRD: X-ray Diffraction [ABSTRACT FROM PUBLISHER]

In the present work, pristine anatase titanium oxide (TiO2), vanadium oxide (V2O5), and yttrium oxide (Y2O3) nanopowders (NPs), and tri-phase TiO2–Y2O3–V2O5 nanocomposite (NC) were prepared via a simple co-precipitation method. The grown products were characterized by employing a range of techniques, including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–vis), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX) analysis. The XRD diffraction pattern confirmed the formation of NC having TiO2 tetragonal, Y2O3 cubic, and V2O5 orthorhombic phases. FTIR spectra evident the presence of metal–oxygen bond in NPs and NC. The energy bandgap (2.55 eV) of NC is found in the range of visible region specified its use as an efficient photocatalyst under sunlight illumination. EDX analysis confirmed the existence of Ti, Y, and V in the nanocomposite. The antibacterial studies against Staphylococcus aureus, Klebsiella pneumonia, and Proteus vulgaris bacteria by varying concentrations (10, 20, 30, and 40 mg ml−1) showed that the NC has higher antibacterial activity than individual oxides. The photocatalytic activity exhibited that NC has the highest degradation efficiency 99.29%, 90.69%, and 99.83% against methylene blue (MB), safranin-O (SO), and methyl orange (MO) dyes as compared to pristine TiO2, V2O5, and Y2O3 NPs under 80 min direct sunlight irradiation. Furthermore, the grown NC is a good candidate for treating organic pollutants and bacteria inactivation. [ABSTRACT FROM AUTHOR]

Essential oils are complex volatile compounds, extracted from specific plant species, with promising therapeutic potentials. However, their volatile nature presents a major hindrance in using them as therapeutic agents. In the current study, we successfully encapsulated oregano essential oil (OEO) into Poly (l-lactic acid-co-e-caprolactone) /Silk Fibroin (PLCL/SF) polymers through electrospinning. The nanofibrous membrane (NF) was fabricated and characterized for various physico-chemical and biological attributions. Homogenous and bead free morphology was confirmed by scanning electron microscopy (SEM). Attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) confirmed the successful loading of OEO and its physical interaction with the blend of PLCL/SF. Moreover, thermogravimetric analysis (TGA) also confirmed the successful loading and thermostability of the OEO. Although a significant change was noted in tensile strength due to the loading of OEO, the mechanical behaviour still falls into the acceptable ranges required for skin tissue engineering. Similarly, fabricated material was evaluated for its biological significance. Liquid chromatography-mass spectrometry (LC-MS) was employed to determine the release behaviour of OEO from electrospun membranes. LC-MS data, noted for 48 h, confirmed the biphasic release of OEO. Furthermore, NF membranes have shown strong antioxidant and anti-tumor activities. This material is promising and can be implanted to avoid the recurrence of the tumor after its surgical removal. [ABSTRACT FROM AUTHOR]

Objective: The green synthesis method for nanoparticles is getting more attention globally, due to its lesser cost, non-hazardous, and eco-friendly nature. The novelty of the present work is to investigate the anti-bacterial and degradation activity of the green synthesized Iron Oxide NPs. Methods: In this study, the Iron Oxide NPs were synthesized through a green synthesis route from leaves of Ficus Palmata. UV-Vis confirmed Iron Oxide NP’s peaks between (230–290 nm), while Fourier transforms infrared spectroscopy analysis showed that several groups were involved in reduction and stabilization. Results: Results indicated that the highest photo thermal activity was shown in light and it was almost 4 folds greater than the control. Similarly, Iron Oxide NPs showed excellent antimicrobial potential against bacterial species “Salmonella typhi” “Xanthomonas Oryzae” and “Lactobacillus” at low concentrations (150 µg/mL). Hemolytic assay results showed that the toxicity was lesser than 5% at both dark and light conditions. Moreover, we also evaluated the photo-catalytic potential of Iron Oxide NPs against methylene orange. Results indicated that almost complete degradation was noted after 90 min in the presence of continuous light. All tests were performed in triplicates. All the data was subjected to P-test (P < 0.5) using Excel and graph pad (V.5.0). Conclusion: Iron Oxide NPs holds a promising future and could be used in treating diseases, and microbial pathogenesis and also could be used as a vector in drug delivery. Moreover, they can also eradicate persistent dyes and could be used as an alternative to remediate pollutants from the environment. [ABSTRACT FROM AUTHOR]

Trigonella foenum-graecum and Zingiber officinale are used as traditional medicinal plants for the treatment of infectious and inflammatory diseases. However, a comparative analysis and bioactivities of T. foenum-graecum and Z. officinale lack some necessary information for therapeutic purposes. This study was designed to evaluate the biochemical characterizations and biological efficacy of T. foenum-graecum and Z. officinale as antioxidant, antidiabetic, antiamnesic, and cytotoxic agents. Antioxidant activity was determined by DPPH free radical scavenging assay. Antidiabetic potentials were evaluated by glycation, alpha-amylase, and acetylcholinesterase inhibition assays. We performed biochemical characterization through analyses of high-performance liquid chromatography (HPLC) and FTIR (Fourier transform infrared spectroscopy). Results revealed that total phenolic contents (TPCs) (g GAE/100 g) of T. foenum-graecum and Z. officinale were 5.74 ± 0.81 g and 6.15 ± 0.06 g, respectively, and total flavonoid contents (TFCs) varied from 1.51 ± 0.58 g CE/100 g to 17.54 ± 0.58. DPPH scavenging potentials of T. foenum-graecum and Z. officinale extract were 50.27% and 88.82%, respectively. Antiglycation potentials of T. foenum-graecum and Z. officinale showed a maximum activity at 16–29% and 96%. Alpha-amylase and alpha-glucosidase inhibition ranged from 9.43–24.95 and 10.52–27.89 and 54.97%, respectively. All the test samples of T. foenum-graecum and Z. officinale showed acetylcholinesterase inhibition potential at 0.37–46.88%. HPLC analysis of T. foenum-graecum revealed the presence of quercetin, gallic acid, caffeic acid, vanillic acid, syringic acid, and cumeric acid, while Z. officinale revealed the quercetin, gallic acid, vanillic acid, benzoic acid, chlorogenic acid, p.Coumaric acid, ferulic acid, and cinnamic acid. FTIR analysis revealed the presence of aldehydes, ketones, aromatic compounds, amines, and carbonyl groups in T. foenum-graecum, while alcohol, alkane, alkene, ketone, amine, and ether are bioactives present in the methanolic extract of Z. officinale. It was concluded that a comparative analysis of T. foenum-graecum and Z. officinale showed that Z. officinale showed higher therapeutic effects. [ABSTRACT FROM AUTHOR]

Natural soil (NS)-based geopolymers (GPs) have shown promise as environmentally friendly construction materials. The production of ordinary Portland cement is known to release significant amounts of greenhouse gas (CO2) into the atmosphere. The main objective of this work is to synthesize a geopolymer (GP) from an uncommon aluminosilicate-based NS and a sodium silicate (SS) activating solution that would not only minimize the emission of harmful gases, but also offer improved mechanical strength. Samples of different compositions were produced by varying the wt.% of NS from 50% to 80% and adding a balancing amount of SS solution. The drying and curing of the samples were carried out in an electric oven at specific temperatures. The degree of geopolymerization in the samples was measured by Fourier transform infrared spectroscopy, and microstructural analysis was performed using a scanning electron microscope. Mechanical tests were conducted to evaluate the range of compressive strength values of the prepared GP samples. A minimum compressive strength of 10.93 MPa at a maximum porosity of 37.56% was observed in a sample with an NS to SS ratio of 1:1; while a ratio of 3:1 led to the maximum compressive strength of 26.39 MPa and the minimum porosity of 24.60%. The maximum strength (26.39 MPa) was found to be more than the reported strength values for similar systems. Moreover, an improvement in strength by a factor of three has been observed relative to previously developed NS-based GPs. It may be inferred from the findings that for the given NS, with almost 90% aluminosilicate content, the extent of geopolymerization increases significantly with its increasing proportions, yielding better mechanical strength. [ABSTRACT FROM AUTHOR]

The current study was designed to analyze the presence or absence of common adulterants in milk and milk products from six different regions of Faisalabad, Pakistan. Purposely, 54 samples from six different regions of Faisalabad were collected. Results revealed that milk of Faisalabad's regions was adulterated with water, starch, urea, glucose, cane sugar, soap, synthetic milk and neutralizers. The results for starch, formalin, vegetable fat, artificial color, nitrates, sodium chloride, coal tar dyes, hydrogen peroxide, annatto, detergent, sulphate adulteration was found to be non-significant. The results for soap, synthetic milk, urea, sugar cane, neutralizers and glucose were significant. It was noted that R2 milk samples had more bacterial load (3.92x108 CFU/mL) followed by R1 (3.38x108 CFU/mL). Among milk products, cream samples collected from R6 had the maximum bacterial count (1.74x108 CFU/mL). The milk samples were also analyzed for the presence of added urea by Fourier Transform Infrared Spectroscopy (FTIR). [ABSTRACT FROM AUTHOR]