Mesoporous silica materials (MSM) with ordered and controllable porous structure, high surface area, pore volume and thermal stability are very suitable catalyst supports, because they provide high dispersion of metal nanoparticles and facilitate the access of the substrates to the active sites. Since the conventional wet-impregnation and deposition-precipitation methods are not appropriate for the incorporation of gold nanoparticles (AuNPs) into MSM, considerable efforts have been made to develop suitable methods to synthesize Au/MSM catalysts, because the incorporation of AuNPs into the channel system can prevent their agglomeration and leaching. In this review, we summarize the main methods to synthesize active gold catalysts supported on MSM. Examples and details of the preparative methods, as well as selected applications are provided. We expect this article to be interesting to researchers due to the wide variety of chemical reactions that can be catalyzed by gold supported catalysts.

In this study, the proposed adsorbent composed of graphene oxide (GO) functionalized by magnetic nanoparticles of iron oxide (α-γ-Fe₂O₃) was obtained by a simple ultrasonication process. This new material was used for the removal of glyphosate in water. The nanoparticulated iron oxide used was synthesized by means of a modified sol–gel method, which does not use organic solvents. The adsorbent material (GO-α-γ-Fe₂O₃) obtained was characterized by magnetic measurements, and it can be proved that it has superparamagnetic properties, allowing fast and efficient magnetic separation. The equilibrium time for the adsorption of glyphosate when using GO-α-γ-Fe₂O₃ was 2 hours and the maximum removal was 92% at 15°C, with a maximum adsorption capacity of 46.8 mg g⁻¹. Langmuir model and pseudo-second-order kinetic model correlated satisfactorily to the experimental data. The thermodynamic parameters showed that the adsorption of glyphosate on GO-α-γ-Fe₂O₃ was spontaneous, exothermic and thermodynamically favorable at temperature of 15–45°C. Thus the adsorbent material GO-α-γ-Fe₂O₃ proposed in this study is considered a good candidate to be used in the removal of glyphosate from aqueous solutions, presenting high adsorption capacity, low cost and magnetic properties that facilitate the separation of the adsorbent material.

In this work, a valorization of the starch stemming from downgraded potatoes was approached through the preparation of starch nanoparticles using different physical methods, namely liquid and supercritical carbon dioxide, high energy ball milling (HEBM), and ultrasonication on the one hand and enzymatic hydrolysis on the other hand. Starch nanoparticles are beneficial as a reinforcement in food packaging technology as they enhance the mechanical and water vapor resistance of polymers. Also, starch nanoparticles are appropriate for medical applications as carriers for the delivery of bioactive or therapeutic agents. The obtained materials were characterized using X-ray diffraction as well as scanning and transmission electron microscopies (SEM and TEM), whereas the hydrolysates were analyzed using size exclusion chromatography coupled with pulsed amperometric detection (SEC-PAD). The acquired results revealed that the physical modification methods led to moderate alterations of the potato starch granules’ size and crystallinity. However, enzymatic hydrolysis conducted using Pullulanase enzyme followed by nanoprecipitation of the hydrolysates allowed us to obtain very tiny starch nanoparticles sized between 20 and 50 nm, much smaller than the native starch granules, which have an average size of 10 μm. The effects of enzyme concentration, temperature, and reaction medium pH on the extent of hydrolysis in terms of the polymer carbohydrates’ fractions were investigated. The most promising results were obtained with a Pullulanase enzyme concentration of 160 npun/g of starch, at a temperature of 60 °C in a pH 4 phosphate buffer solution resulting in the production of hydrolysates containing starch polymers with low molecular weights corresponding mainly to P-10, P-5, and fractions with molecular weights lower than P-5 Pullulan standards.

The present study proposes development of an adsorbent based on combination of graphene oxide (GO) and iron oxide (α-γ-Fe₂O₃) nanoparticles for atrazine removal from water. The synthesized adsorbent (GO@ α-γ-Fe₂O₃) was characterized using different techniques. Magnetic measurements proved that the adsorbent has superparamagnetic characteristics, thus facilitating its magnetic separation from the working suspensions. The maximum adsorption capacity was 42.5 mg g⁻¹. The Langmuir isotherm and the pseudo-second order kinetic models correlated adequately with the experimental data. The thermodynamic data showed that atrazine adsorption was spontaneous, endothermic and thermodynamically favorable.

Atrazine is a systemic herbicide widely used in weed control. In recent years, it has been largely detected in surface and groundwater in several locations all over the world. Photocatalysis is a green and sustainable technology with huge application prospects in pollution control and the degradation of organic water pollutants. In this work, photodegradation of aqueous atrazine was investigated over pristine graphitic carbon nitride (g-C₃N₄) synthesized via urea pyrolysis and graphene/g-C₃N₄ composite synthesized via the in situ growth method involving direct deposition of g-C₃N₄ nanosheets on the graphene surface. The obtained photocatalysts were characterized using transmission and scanning electron microscopy, Fourier-transformed infrared spectroscopy, UV-visible spectroscopy, photoluminescence spectroscopy, X-ray diffraction, and surface area measurements. It was demonstrated that the composite material exhibited remarkable photocatalytic properties for the efficient degradation of aqueous atrazine under visible light at ambient temperature. After 5 h of reaction, atrazine conversion reached 100% in the presence of graphene/g-C₃N₄ composite, while the pristine g-C₃N₄ allowed 40% conversion under the same conditions, thus demonstrating the positive effect of graphene on the photocatalytic activity of g-C₃N₄. Moreover, graphene/g-C₃N₄ was shown to keep its activity even when it was recycled five times, thus proving its stability and its potential to be used at the industrial scale.