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.

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 m 2 /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.

No abstract

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 data presented in this article are generated as part of the research article entitled “from a naturally occurring material (clay mineral) to the production of porous ceramic membranes” (Elgamouz and Tijani, 2018) [1]. This article describe how clays as very abundant versatile materials that have many properties not available in pure materials namely, silica, alumina and zirconia can be used for the preparation of ceramic membranes (Karaborni et al., 1996; Oun et al., 2017; Hollanders et al., 2016; de Oliveira Henriques et al., 2017) [2], [3], [4], [5]. This paper presents data obtained at different stages of the fabrication of a clay-zeolite composite ceramic membrane made from a largely available clay from the central region of Morocco (Meknes). The data include the characterization of the clay powder using XRD, FTIR, thermogravimetric (TGA and TDA) analysis of the clay powder. The data of porosity, mesoporosity, specific surface area, volumes of the pores, volumes of mesopores, diameters of the pores using mercury intrusion porosimetry and adsorption desorption of nitrogen data that was computed from BET and BJH theories of the clay supports at different firing temperatures (700, 750, 800, 850 and 900 °C). Data obtained from measurement of nitrogen permeation of support alone and that of the silicalite membranes are also represented.