Use of biochar prepared from the açaí seed as adsorbent for the uptake of catechol from synthetic effluents

This work proposes a facile methodology for producing porous biochar material (ABC) from açaí kernel residue, produced by chemical impregnation with ZnCl2 (1:1) and pyrolysis at 650.0 °C. The characterization was achieved using several techniques, and the biochar material was employed as an adsorbent to remove catechol. The results show that ABC carbon has hydrophilic properties. The specific surface area and total pore volume are 1315 m2·g−1 and 0.7038 cm3·g−1, respectively. FTIR revealed the presence of oxygenated groups, which can influence catechol adsorption. The TGA/DTG indicated that the sample is thermally stable even at 580 °C. Adsorption studies showed that equilibrium was achieved i

Total Oxidation of Isopropanol in the Liquid Phase, under Atmospheric Pressure and Low Temperature, on Transition Metal Oxides Catalysts Cr2O3 and Fe2O3

Isopropanol oxidation in the liquid phase under atmospheric pressure and low temperature has been studied in the presence of transition metal oxides (Cr2O3 and Fe2O3) prepared by the precipitation method. These solids characterized by structural analyses (FTIR and XRD) and textural analysis (BET) have led to results in line with those reported in the literature. Chromium oxide has a much more developed texture, with a specific surface area and pore volume 5 times larger than iron oxide. Both of the solids show a good specific activity and led to acetone and carbon dioxide to be formed as the only oxidation products of isopropanol. However, chromium oxide is more active. The initial catalytic activity for the latter is varying between 4.87 ∗ 10−6 and 5.79 ∗ 10−6 mol·g−1·s−1 with temperature range from 40 to 80°C. Kinetic study shows that the reaction follows a successive scheme: isopropanol ⟶ acetone ⟶ CO2 involving a redox mechanism. The low value of the activation apparent energy (Ea.(Cr2O3) = 2.87 kJ·mol−1 < Ea. (Fe2O3) = 5.37 kJ·mol−1) justifies the relatively higher activity observed for chromium oxide

Total Oxidation of Isopropanol in Its Liquid Phase, at a Low Temperature in the Presence of Prepared and Characterized Zinc Oxide

The complete oxidation of isopropanol in its liquid phase at a low temperature was studied in the presence of zinc oxide (ZnO). This solid was prepared with the precipitation method. Structural analysis (infrared in Fourier transform and diffraction of X-rays) and textured (adsorption/desorption of N2) were conducted for the wurtzite structure results, an IV type isotherm with a type H3 hysteresis. This solid presents a good catalytic activity against the complete oxidation of isopropanol, a constant of selectivity equal to 1; however, the studied temperatures were 40, 60, and 80°C. In addition, a kinetic study of the oxidation was performed and showed that the reaction follows a successive mechanism isopropanol-acetone-carbon dioxide. The low value of the apparent energy of the activation of this solid confirms the high value of the initial rate of the catalytic oxidation reaction of isopropanol in the temperature range studied

Comparison of phenol adsorption property and mechanism onto different moroccan clays

This study focuses on the removal of phenol from aqueous media using Agouraï clay (Fes-Meknes-Morocco region) and Geulmima clay (Draa Tafilalet region). The characterization of the clay by Fourier Transform Infrared (FTIR) Spectroscopy, X-ray diffraction (XRD), N2 adsorption (BET), Scanning Electron Microscopy (SEM), and Thermogravimetric and differential thermal analysis (DTA/GTA) indicates that it is mainly composed of quartz, kaolinite, and illite. The results showed that raw Clay Agourai (RCA) and raw Clay Geulmima (RCG) adsorbed phenol very quickly and reached equilibrium after 30 min. Thermodynamic parameters reveal the physical nature of the adsorption, the spontaneity, and the sequence of the process. However, the structure and structural characterization of the solid before and after phenol adsorption indicated that the mechanism of the reaction was electrostatic and that hydrogen bonding played an important role in RCG, while kinetic modeling showed the pseudo-second-order model dynamics. The physics-statistics modeling was employed for describing the isotherm adsorption for both systems. It was found that the monolayer model with two different energy sites best describes adsorption irrespective of the system. The model indicates that the receptor density of each clay direct influences the adsorption capacity, demonstrating that the composition of the clay is the main source of the difference. Thermodynamic simulations have shown that the adsorption of phenol is spontaneous and endothermic, irrespective of the system. In addition, thermodynamic simulations show that the RCG could be adsorbed even further since the equilibrium was not achieved for any thermodynamic variable. The strength of this study lies in the determination of the adsorption mechanism of phenol on clay materials and the optimum values of temperature and pH

Valorization of Lignocellulosic Wastes Material for Efficient Adsorption of a Cationic Azo Dye and Sludge Recycling as a Reinforcement of Thermoplastic Composite

This work explored the adsorption of Malachite Green (MG) dye by Acorn Pericarp (AP) in the context of biomass valorization. The Acorn Pericarp was analyzed by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction. The adsorption capacity under optimal experimental conditions was studied at different adsorbent doses, the initial concentration times of the dye and pH. The results presented in this work on the adsorption kinetics of MG showed that the pseudo-first-order model (R2 = 0.9971) better described the adsorption kinetics at 10−5 M. The experimental isotherms showed that Acorn Pericarp adsorption followed the Langmuir isotherm model (R2 = 0.9889). The thermodynamic study showed that MG adsorption is endothermic (ΔH° > 0) and spontaneous (ΔG° < 0). For a sustainable industry, the sludge was converted into reinforcement of polystyrene using in-situ polymerization with 10% by weight of filler. A morphological and structural analysis was performed using SEM and FTIR, the results of characterization showed that the AP sludge was incorporated well into the PS matrix

Green Synthesis of Nickel and Copper Nanoparticles Doped with Silver from <i>Hammada scoparia</i> Leaf Extract and Evaluation of Their Potential to Inhibit Microorganisms and to Remove Dyes from Aqueous Solutions

Hammada scoparia (Pomel) is a powerful plant with important biological properties. In this study, we report on the green synthesis of silver-doped nickel and copper nanoparticles (NPs) in the presence of H. scoparia leaf extract using a self-propagating sol–gel autocombustion process. The synthesized NiO, CuO, Ag-NiO, and Ag-CuO NPs were characterized with Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). Afterward, they were tested for their antimicrobial activity as well as their potential to remove dyes from aqueous solutions using adsorption processes for malachite green (MG) and photocatalytic degradation for methylene blue (MB). Our results showed that the mass of the adsorbent had a significant effect on the adsorption rate, which increased to reach a maximum value of 98%. The Ag-CuO NP showed the best final conversion of MB (97.95%) compared to NiO, CuO, and Ag-NiO. In addition, we noted that the NPs doped with silver had the best performance in the removal of dyes. These results indicated that the photocatalytic performance was significantly improved after the addition of silver. Moreover, the antimicrobial activity showed that the studied NPs had moderate activity against the tested bacteria and a weak activity or were ineffective against Candida albicans. Therefore, the green synthesis of NPs from H. scoparia leaf extract is considered a sustainable alternative to removing dyes from aqueous solutions. However, further investigation should be performed on the other dyes to understand the overall effectiveness of these NPs

Towards an in-depth experimental and theoretical understanding of the cadmium uptake mechanism on a synthesized chitin biopolymer

This work analyzes the adsorption of cadmium, a potentially toxic pollutant, on biopolymers synthesized from shrimp shells, as a promising new adsorbent. Spectroscopic analysis, such as FTIR, ATD/ATG, XRD, and SEM/EDX techniques, were used to characterize chitin before it was exposed to cadmium ions. Experimental data indicate that Cd(II) adsorption proceeds with pseudo-second-order model kinetics and is influenced by increasing temperature. In the equilibrium, the maximum adsorption capacity obtained was 58.82 mg g−1 at a temperature of 308 K. Experiments to obtain adsorption data were performed at T = 298–318 K. The saturated adsorption capacities of Cd(II) range from 57.40 to 59.90 mg g−1. The application of the physics-statistics model indicates that the Cd(II) atoms are adsorbed on the surface of the chitosan forming a monolayer. In addition to that, the results also show that the adsorption affinity increases with the system temperature, resulting in higher affinity and an increase of 30% in the adsorption capacity. The adsorption energy was found to be around 2.5 kJ mol−1, indicating that the adsorption is physical and endothermic. The entropy was found to quickly increases (reaching a maximum value of 6 × 10−22 kJ mol−1 K−1) at low concentrations followed by the equilibrium after the 40 mg L−1, indicating that the equilibrium is quickly reached. The Gibbs free energy indicates that the process is spontaneous (ranging from −1.364 to −1.451 kJ mol−1) and that the energy tends to remain constant after 15 mg L−1. Last, the results indicate that the Cd(II) is adsorbed due to dipole–dipole interactions and possible coordination bounds. The results of tests on the adsorption of cadmium by chitin showed that this biopolymer could replace other more expensive adsorbents