Dr. Valdes-Morales, Hector

In this study, a hydrophobic synthetic zeolite, namely ZSM-5 is chosen as an adsorbent/ catalyst for toluene removal. Experimental results showed that toluene adsorption onto ZSM-5 was favourable, following a Langmuir adsorption isotherm model. ZSM-5 zeolite was regenerated using gaseous ozone at low temperature. Adsorbed toluene was oxidised, releasing mainly CO2 and H2O. Traces of oxidation by-products such as acetic acid and acetaldehyde were formed and remained adsorbed after the oxidativate regeneration with ozone. After four successive cycles of adsorption/ozonation, the adsorption efficiency was not affected (92%–99%). These results showed that volatile organic compound (VOC) removal by adsorption onto ZSM-5 zeolite followed by ozone regeneration could be used as a promising hybrid process for the control of VOC emissions in terms of efficiency.

This article presents the adsorption of Methylene Blue (MB) onto diatomite, in order to develop a low-cost treatment technology as a process alternative for dye removal. Diatomite used in this work was taken from the Nador area in the northeast of Morocco. Diatomite is characterised by different physical–chemical methods (X-ray diffraction, nitrogen adsorption-desorption isotherm, scanning electron microscopy and Fourier transform infrared). Results showed that the adsorption of MB onto diatomite mineral is affected by various operating parameters like contact time, initial dye concentration, adsorbent dosage, pH and temperature. Adsorption equilibrium is reached after 1.5 h of contact time. Maximum MB removal is obtained at pH = 12. MB removal rate decreases as pH decreases. Adsorption equilibrium data are fitted to Langmuir, Freundlich, Redlich–Peterson and Toth models. Adsorption data are well described by Langmuir isotherm model indicating that a homogeneous adsorption occurs. A maximum adsorption capacity (or monolayer coverage) of 11 mg g–1 is obtained at 45°C. A value of the enthalpy of adsorption of 12.78 kJ mol–1 is found confirming the endothermic nature of adsorption process, while a Gibb’s free energy change (∆G°) falling in the range −30.8 to −35.34 kJ mol–1 confirms the spontaneity of the process. Adsorption kinetics are fitted to a pseudo-second-order kinetic model. Experimental results indicate that the Moroccan diatomite could be used as a potential adsorbent for the removal of cationic dye molecules, at lower cost.

This study aims to evaluate the technical feasibility of applying a low-cost alternative natural bioadsorbent obtained from the cone of the Moroccan cypress Cupressus sempervirens to remove dyes from contaminated waters. Methylene Blue (MB) and Congo Red (CR) dyes are used to represent basic and acid compounds present in wastewater of textile industries. The cone of this medium-sized coniferous evergreen tree was obtained from the Fez area and was characterised by different physical– chemical methods, including nitrogen adsorption–desorption isotherms, Fourier transform infrared spectroscopy, scanning electron microscopy, Boehm titration method and the pH of the point of zero charge (pHpzc). Additionally, the influence of operating conditions such as contact time, initial dye concentration, binary mixture of dye solutions, bioadsorbent dosages and solution pH were evaluated. Experimental results reveal that the adsorption processes take place very rapidly, reaching equilibrium at 30 and 45 min for MB and CR, respectively. Maximum adsorption capacities result to be pH dependents. Hence, MB adsorption is favoured under basic pH conditions, while CR is favoured at acidic pH. A pseudo-second-order kinetic model provides the best fit of the experimental data of MB and CR adsorption onto the biomaterial. Adsorption isotherm data are well represented by Langmuir, Freundlich and Dubinin–Radushkevich models. Langmuir model gives the best fit with a maximum monolayer sorption capacity of 144 and 25.02 mg g–1 for MB and CR, respectively. Experimental results indicate that the cone of Cupressus sempervirens could be used as a potential, low-cost bioadsorbent for the elimination of dyes from contaminated waters.

Ethylene is a plant growth regulator that induces accelerated softening and ripening of fruits during transport and storage. Among the most applied methods for ethylene control, adsorption appears as a cheap and efficient technique. In this work, the effect of the incorporation of transition metals into natural Chilean zeolite on ethylene adsorption is investigated. Natural zeolite mainly composed of clinoptilotite and mordenite is modified using copper and zinc nitrate solutions and calcined under oxygen flow at 623 K, generating different transition metal modified zeolites. Parent and modified zeolites were characterised by X-ray diffraction, X-ray fluorescence spectroscopy and nitrogen adsorption. Zeolite surface modifications were assessed by diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Experimental results reveal the incorporation of Cu2+ and Zn(2+ )as new compensating cations into the zeolite framework. Ethylene adsorption isotherms show an enhancement on the adsorption capacity of Cu-exchanged zeolite. This result is not only associated to the higher micropore surface area of this sample, but also to the higher affinity of ethylene molecules to copper cations incorporated on this zeolite. DRIFTS operando experiments of ethylene adsorption in the absence and in the presence of moisture reveal a competitive mechanism of water and ethylene molecules toward hydroxyl sites. Si-OH-Al and Si-OH sites are rapidly occupied with water, reducing the adsorption of ethylene.