Search

In this study, zinc oxide nanoparticles (ZnO‐NPs) are synthesized and combined with chitosan (Cs) to create Cs/ZnO‐NPs nanomicelles, aiming to investigate their potential as a novel cancer treatment. The ZnO‐NPs are produced through a sintering process at temperatures ranging from 300 to 700 °C. The most effective nanoparticles are obtained at 600 °C, as determined by X‐ray diffraction (XRD) and Fourier‐transform infrared spectroscopy (FTIR) analyses, which confirmed their crystallinity and purity. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) are employed to characterize the size and shape of the nanoparticles, revealing predominantly spherical and hexagonal structures with stable dimensions. The cytotoxic effects of the Cs/ZnO‐NPs are evaluated against various cancer cell types. The results show that at a concentration of 125 µg mL−1, the Cs/ZnO‐NPs demonstrate significantly higher cancer cell toxicity compared to ZnO‐NPs alone, while remaining non‐toxic to normal cells. This indicates that Cs/ZnO‐NPs have a superior ability to selectively target cancer cells. These findings suggest that Cs/ZnO‐NPs nanomicelles hold promise as an effective and safe nanotherapeutic approach in the realm of cancer treatment, meriting further exploration for clinical applications. [ABSTRACT FROM AUTHOR]

Copper nanoparticles (Cu‐NPs) have garnered substantial interest in the field of nanotechnology due to their exceptional physical and chemical properties and cost‐effectiveness. However, challenges such as particle aggregation and rapid copper oxidation affect nanoscale production. This study systematically investigates the synthesis of colloidal Cu‐NPs using chitosan (Cts) as a stabilizer and reducing agent in the arc discharge system, comparing it to distilled water as a medium. Confirmation of the purity, size, and morphology of the Cu‐NPs is achieved through various physicochemical characterization methods. X‐ray diffraction patterns confirm the synthesis of highly pure face‐centered cubic (fcc) crystal Cu‐NPs. UV–vis analysis reveals absorption peaks at 572–585 nm, indicating pure copper. Fourier‐transform infrared spectroscopy shows peaks at 638 and 597 cm−1, corresponding to Cu─Cts bonds. Transmission electron microscopy images depict spherical nanoparticles ranging from 15 to 45 nm, with smaller sizes at higher Cts concentrations. The catalytic activity of Cu‐NPs in the degradation of 4‐nitrophenol to 4‐aminophenol is assessed, with Cu‐NPs synthesized in distilled water demonstrating superior catalytic properties compared to 0.10 wt.% Cts. This study highlights the efficacy of the arc discharge method in producing pure, uniformly sized Cu‐NPs with potential applications in catalysis. [ABSTRACT FROM AUTHOR]

This study presents a green synthesis approach for the fabrication of zinc oxide-silver nanoparticles (ZnO-Ag-NPs) using Punica granatum fruit peels extract as a natural reducing and stabilizing agent. This eco-friendly method offers a sustainable alternative to conventional methods that often employ toxic or hazardous chemicals. Antibacterial and anti-cancer activities of the green synthesized nanoparticles were then assessed in vitro. X-ray diffraction confirmed the production of ZnO-Ag-NPs with increasing crystallinity in higher pH values. The ZnO-Ag-NPs were found to be agglomerated with spherical AgNPs. Fourier Transform Infrared (FTIR) spectra revealed a broad band in ZnOAg-NPs ranging from 400-1 to 530 cm-1 with reduced intensity as compared to ZnO-NPs, indicating the formation of Ag-NPs on the surface of ZnO-NPs. The synthesized ZnO-Ag-NPs exhibited potent antibacterial activity against a broad spectrum of bacterial strains, particularly Gram-positive bacteria, with superior inhibition activity compared to ZnO-NPs. Moreover, ZnO-Ag-NPs showed a dosedependent anti-proliferative effect on colorectal-, lung-, and cervical cancer cells. ZnO-Ag-NPs showed significantly greater efficacy in inhibiting cancer cell growth at a lower concentration of 31.25 μg/mL, compared to ZnO-NPs which required over 500 μg/mL, possibly due to the presence of silver nanoparticles (Ag-NPs). The results obtained from this study demonstrate the potential of green synthesis approaches in the fabrication of therapeutic nanomaterials for cancer treatment, as well as other biomedical applications. [ABSTRACT FROM AUTHOR]

The main objective of the present work is to investigate the thermal degradation behaviour of the non-catalytic and catalytic co-pyrolysis of empty fruit bunch (EFB) and high-density polyethylene (HDPE) over commercial hydrogen exchanged zeolite socony mobil five (HZSM-5) and rice husk ash (RHA) catalysts via thermogravimetric analyser (TGA). RHA catalysts were produced using the solvent-free method by converting RHA into HZSM-5. XRD characterization was conducted for the synthesized catalysts and RHA catalyst showed less amount of peaks compared to commercial HZSM-5. Non-catalytic and catalytic co-pyrolysis of EFB and HDPE over commercial HZSM-5 and RHA catalysts were conducted using TGA. A fixed EFB-toHDPE mass ratio of 1:1 and a fixed catalyst-to-feedstock mass ratio of 1:1 were used for the TGA experiments. The sample was heated up under pyrolysis conditions at a heating rate of 20 °C/min until 700 °C. The thermal degradation behaviour of EFB and HDPE did not change significantly when RHA catalysts were used, based on the TG curves. Volatilization of matter was maximum between temperatures 240 °C and 500 °C (Phase II) for all cases of the pyrolysis process, where the highest volatilized matter of 93.2 wt% was produced from the catalytic process over commercial HZSM-5, followed by the catalytic process over RHA catalysts with 92.3 wt% of volatilized matter and non-catalytic process with 83.0 wt% of volatilized matter. When using catalysts, 0.44 wt% of solid residual was left when commercial HZSM-5 was used while 0.38 wt% of solid residual was left when RHA catalyst was used. [ABSTRACT FROM AUTHOR]

The main objective of the current work is to investigate the influence of waste chicken eggshell (WCE) as an alternative source of calcium oxide (CaO) on Hydrogen exchanged Zeolite Socony Mobil-5 catalyst (HZSM-5). WCE as promoter was loaded at 1wt.% on HZSM-5 catalyst which act as support via incipient wetness impregnation method. The HZSM-5, commercial CaO, and WCE were individually prepared for comparison with WCE/HZSM-5. Synthesized catalysts were characterized via X-Ray Diffraction to analyse the phase purity, Field Emission Scanning Electron Microscopy to analyse the surface morphology, and Brunauer-Emmett-Teller to analyse the surface area and pore size. The addition of WCE on HZSM-5 has significantly affected the framework structure of HZSM-5 where the crystallinity percentage and average crystal size of HZSM-5 drastically dropped to 44.97 % and 45.00 nm. The original cubic-like structure in HZSM-5 has significantly altered into a netlike structure after the impregnation of WCE. A similar effect of alteration was observed on BET surface area dropped from 365.81 m2 /g (HZSM-5) to 292.14 m2 /g (WCE/HZSM-5). Interestingly, the pore diameter of WCE/HZSM-5, WCE, and HZSM-5 catalysts was similar at 3.88 nm, 3.87 nm, and 3.87 nm respectively. WCE and commercial CaO almost share similar textural properties. Hence, the addition of WCE as an alternative source of calcium oxide into HZSM-5 can provide a high catalytic reaction and stable surface in catalytic cracking of heavy hydrocarbons into small hydrocarbons with longer catalyst lifetimes. [ABSTRACT FROM AUTHOR]

The present study details a more environmentally friendly method for synthesizing iron oxide nanoparticles (Fe3O4‐NPs) utilizing Hibiscus sabdariffa (H. sabdariffa) leaf extract. The produced H. sabdariffa/Fe3O4‐NPs underwent characterization through VSM, XRD, FESEM‐EDX, TEM and FTIR analyses. The FESEM and TEM images revealed that the H. sabdariffa/Fe3O4‐NPs had a narrow distribution and an average particle size of 5±2 nm. Catalytic degradation studies of the synthesized Fe3O4‐NPs exhibited efficient reduction of methyl orange (MO) dye. The degradation of MO catalysed by H. sabdariffa/Fe3O4‐NPs follow the pseudo‐first order kinetics, with a rate constant of 0.0328 s−1 (R2=0.9866). Moreover, in electrochemical sensing studies, the anodic peak current of nitrite (NO2−) for H. sabdariffa/Fe3O4‐NPs/GCE showed a linear relationship with its concentration within the range of 0.5–7.5 mM, achieving a detection limit of 0.29 μM. These findings demonstrate that the modified electrode with Fe3O4‐NPs synthesized using H. sabdariffa leaf extract serve as a novel electrochemical sensor for determining NO2− with high sensitivity and reproducibility. [ABSTRACT FROM AUTHOR]