A green and cost-effective technique for the preparation of silver nanoparticles (Algae-AgNPs) as a colorimetric sensor for hydrogen peroxide (H₂O₂) is described. Silver nanoparticles were capped using the green algae (Noctiluca scintillans) extract at an optimum time of 3 h at 80 °C. The pH of the plant extract (pH = 7.0) yields nanoparticles with a mean size of 4.13 nm and a zeta potential of 0.200 ± 0.02 mV and negative polarity, using dynamic light scattering (DLS). High-resolution transmission electron microscopy (HRTEM) analysis showed regular spherical particles with the average size of 4.5 nm. Selected area electron diffraction (SAED) results revealed the polycrystalline nature of the silver nanoparticles. The obtained patterns were indexed as (111), (200), (220), and (311) reflections of the fcc (face centered cubic) silver crystal based on their d-spacing of 2.47, 2.13, 1.49, and 1.27 Å, respectively. The apparent color change from brown to colorless was observed when nanoparticles reacted with H₂O₂. Linear responses were obtained in three different ranges (nM, µM, and mM). Limits of detection (LOD) of 1.33 ± 0.02 and 1.77 ± 0.02 nM and quantitation limits (LOQ) of 7.31 ± 0.03 and 9.67 ± 0.03 nM were obtained for Abs and ΔAbs calibration curves, respectively. 10% v/v Algae-AgNPs solution inhibited Staphylococcus aureus over Escherichia coli, while a 50% reduction of tumor cell growth of MDA-MB-231 human breast adenocarcinoma was obtained.

The commercial value of any clay depends on its physical and chemical properties, these could help in tuning the characteristics of ceramic membrane supports required at extreme filtration conditions. The characteristics of two clay minerals named SA and CH were studied at various firing temperatures. The composition in oxides of both raw materials consisted of quartz (44.40 ± 0.60 to 46.98 ± 0.57 m%), alumina (13.16 ± 0.56 to 19.64 ± 0.48 m%), iron oxide (4.85 ± 0.46 to 6.37 ± 0.70 m %), and relatively smaller amounts of alkaline-earth oxides (3.34 ± 0.43 to 5.98 ± 0.33 m% calcium oxide and 1.98 ± 0.18 to 5.87 ± 0.34 m% for magnesium oxide). XRD of the investigated samples indicated the presence of kaolinite and illite as pure clay fractions in the clay mineral. SEM showed that the clay minerals were constituted from fine poorly crystalline particles with particles' size more than 5 μm. The specific surface areas of the clay minerals were found to vary between 94.5 ± 6.3 to 138.6 ± 4.2 m2/g using methylene blue stain test, indicating that, the clay minerals fall within chlorite, illite, and kaolinite categories. The porosity of the clay supports made from both clays were found to be maximal with values of 23.45% ± 0.66 and 21.61% ± 0.60 for SA and CH clay materials respectively at 700°C. These values were a direct result of capillary movements of water in the specimen pores that were opened to the outside leading to the highest number macropores and mesopores in the specimen.

Developing heterogeneous catalyst using chitosan (CS) and magnetic Fe₃O₄ as support has been remarkably attractive due to their availability, low cost and non-toxicity. In this work, a heterogeneous catalyst (denoted as Fe₃O₄@CS@MS@Ag) was fabricated by the deposition of silver nanoparticles on magnetic chitosan via an easy and facile modification of its surface with methyl salicylate (MS). The catalyst was characterized using Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), X-ray diffractometer (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). To the best of our knowledge, for the first time, CS decorated Fe₃O₄ (Fe₃O₄@CS) has shown the catalytic activity for the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) in presence of NaBH₄. Surface modified magnetic chitosan (Fe₃O₄@CS@MS) also acts as active catalyst towards the reduction of 4-NP. However, catalytic efficiency has increased fourfold when silver-nanoparticles-deposited magnetic chitosan (Fe₃O₄@CS@MS@Ag) used as our target catalyst. The catalyst was separated with external magnet after each cycle of catalytic reaction and reused effectively five times with almost 90% efficiency.