Open Access
Efficient recovery of aluminum from saline slag wastes
(Elsevier, 2019) Yoldi Sangüesa, María; Fuentes Ordóñez, Edwin Gustavo; Korili, Sophia A.; Gil Bravo, Antonio; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias; Gobierno de Navarra / Nafarroako Gobernua, PI017 CORRAL
This work presents the procedure to improve the aluminum extracted from a hazardous waste from the recycling of aluminum, aluminum that could be used in the production of value-added materials, as well as with the generation of non-hazardous waste. The aluminum waste was treated under reflux and stirring with NaOH aqueous solutions taking into account two concentrations (1 and 2 mol/dm3), various times of extraction (1, 2 and 4 h) and 4th consecutive steps of extraction in order to obtain solutions with Al3+. The activation of the waste by milling is also analyzed. After extraction, the solution is filtered to separate an aqueous solution that contain the extracted Al3+ and a residual waste. A maximum of 7.54 g/dm3 of aluminum was extracted in the first step, for a total accumulated of 9.59 g/dm3 of aluminum. The extracted aluminum can be used to synthesize added-value products applied as adsorbents and catalysts. Finally, the residual waste generated was characterized by N2 adsorption at −196 °C, X-ray diffraction, X-ray fluorescence, energy-dispersive X-ray and scanning electron microscopy in order to apply it as in future works adsorbent or catalyst.
Open Access
Layered double hydroxides for CO2 adsorption at moderate temperatures: synthesis and amelioration strategies
(Elsevier, 2023) Santamaría Arana, Leticia; Korili, Sophia A.; Gil Bravo, Antonio; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
Curving the CO2 atmospheric levels is one of the challenges of this century, given its direct impact on climate change. Of the several strategies of CO2 capture and storage, sorption-enhanced water–gas shift (SEWGS) process, a combination of CO2 adsorption and the water–gas shift reaction, has been appointed as one of the most promising techniques due to is low energy consumption and high efficiency. SEWGS operating settings at both moderate temperature (200–450 ◦C) and high pressure (more than 10 bar) bring the need to find an adsorbent capable of working at these conditions. Calcined layered double hydroxides (LDH) have been proven to give the best results in this range of pressure/temperatures even though its performance can be greatly improved. Herein, a state-of-art of the research accomplished up until now is presented. Several strategies can be followed to improve the adsorbents performance: the synthesis method, LDH composition, modifications employed to promote their adsorption capacity or how the adsorption conditions can affect their efficiency
Open Access
Comparative removal of emerging contaminants from aqueous solution by adsorption on an activated carbon
(Taylor & Francis, 2019) Gil Bravo, Antonio; Taoufik, Nawal; García Mora, Ana María; Korili, Sophia A.; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias
Batch sorption experiments were performed to study the adsorption of six emerging pollutants from aqueous solutions using a commercial granular activated carbon as adsorbent. Caffeine, clofibric acid, diclofenac, gallic acid, ibuprofen and salicylic acid were selected as representative contaminants. The activated carbon was characterized by nitrogen adsorption at 77 K, and through the determination of point of zero charge. The effects of several operational parameters, such as pH, initial concentration of organic molecules, mass of adsorbent and contact time, on the sorption behaviour were evaluated. The contact time to attain equilibrium for maximum adsorption was found to be 40 min. The kinetic data were correlated to several adsorption models, and the adsorption mechanism found to follow pseudo-second-order and intraparticle-diffusion models with external mass transfer predominating in the first 15 min of the experiment. The equilibrium adsorption data were analysed using the Freundlich, Langmuir and Toth isotherm equation models. The similar chemical structure and molecular weight of the organic pollutants studied to make the adsorption capacity of the activated carbon used very similar for all the molecules.
Open Access
Literature review on the recycling postconsumer plastic waste from pyrolysis
(American Chemical Society, 2025-06-12) Aznárez Salvatierra, María Aránzazu; Korili, Sophia A.; Gil Bravo, Antonio; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Gobierno de Navarra / Nafarroako Gobernua; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
Environmental problems associated with postconsumer plastic waste are numerous and are expected to worsen due to the increasing volume of waste generated. Currently, in the European Union, only 35% of plastic waste is recycled, which implies that plastic waste treatment is mostly focused on incineration and landfilling, which are less priority options than recycling according to the waste hierarchy. In order to increase the recycled plastic rate, chemical recycling technologies for plastic waste have been considered as a complement to mechanical recycling, which is currently the most widely used technology. The chemical recycling idea presented in this work is based on the pyrolysis of plastic waste, which is one of the most interesting chemical recycling processes. This paper presents a chemical recycling technology for postconsumer plastic waste (polyolefins and polystyrene with an approximate ratio of 2,6) based on the pyrolysis process and subsequent cascade processes, such as the catalytic reforming of the naphtha obtained through pyrolysis. The objective of the presented technology is to maximize the production of aromatic compounds, benzene, toluene, and xylene, which will close the circle of materials by being precursors of recycled plastics of comparable quality to virgin. This work also considers the Life Cycle Assessment (LCA) of plastic waste pyrolysis and the advantages and challenges of the described technology.
Open Access
Effect of gold nanoparticles on SiO2@g-C3N4 catalyst for the degradation of amoxicillin
(Elsevier, 2024-11-12) Santamaría Arana, Leticia; Korili, Sophia A.; Gil Bravo, Antonio; López de Luzuriaga Fernández, José Manuel; Monge Oroz, Miguel; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
Gold nanoparticles in different proportions (0.5 and 1 %) have been grafted at the surface of a SiO2@g-C3N4 nanotube-based composite (SiO2 nanotubes obtained from halloysite clay) and also g-C3N4 (for comparison purposes) to test their degradation capacity over the antibiotic amoxicillin proving that the introduction of these nanoparticles on the catalyst modifies the degradation mechanism followed by the pollutant. Results obtained show that the introduction of the appropriate percentage of gold NPs in the composite improves amoxicillin degradation efficiency and establish a direct correlation between the presence of gold NPs and the production of ∙O2.
Open Access
Effect of the surface properties of Me2+/Al layered double hydroxides synthesized from aluminum saline slag wastes on the adsorption removal of drugs
(Elsevier, 2020) Santamaría Arana, Leticia; Devred, F.; Gaigneaux, E. M.; Korili, Sophia A.; Gil Bravo, Antonio; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa; Gobierno de Navarra / Nafarroako Gobernua, PI017-PI039 CORRAL
This work presents the synthesis of Me2+ (Co, Mg, Ni and Zn)/Al layered double hydroxides (LDH) with a 3:1 M ratio by the co-precipitation method. Structural characterization and comparison of the series has been achieved using powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), nitrogen physisorption at 77 K, thermogravimetry measurements (TGA), temperature-programmed reduction (TPR), X-ray photoelectron spectroscopy (XPS), ammonia temperature-programmed desorption (NH3-TPD) and point of zero charge (pHpzc). Batch experiments were performed to analyze the adsorption capacity of the different LDH on diclofenac and salicylic acid, as example of emergent pollutants. The pH, mass of adsorbent, contact time and concentration of pollutant were the parameters used to compare the adsorption performance of the synthesized materials. Samples showed different behavior and the equilibrium was reached at different times, Mg6Al2 and Zn6Al2 showed lower equilibrium times but had higher adsorption capacity. Various adsorption and isotherm equation models were employed to study both the kinetic and equilibrium results and, in general, the removal of diclofenac was greater than that of salicylic acid. 1-Butanol conversion was also used as a means of acidity and basicity characterization and the results were compared with the adsorption performance of the samples in order to explain the results found. A relationship between the amount of pollutants adsorbed and the butenes formed in the dehydrogenation reaction of 1-butanol was found.
Open Access
Progress and perspectives in the catalytic hydrotreatment of bio-oils: effect of the nature of the metal catalyst
(American Chemical Society, 2024) Gil Bravo, Antonio; Sancho Sanz, Iris; Korili, Sophia A.; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
In recent years, there has been a surge of interest in transforming biomass into fuel, driven by its potential as the only realistic renewable carbon resource. Several conversion methods have been explored to achieve this, including gasification for producing synthesis gas, fast pyrolysis or hydrothermal liquefaction for obtaining bio-oils, and hydrolysis for generating aqueous sugars. Bio-oils offer environmental benefits due to their lower CO2 emissions, but their direct use as fuels is hindered by limitations such as thermal instability, high viscosity and acidity, and low calorific value. Consequently, advancements in treatment methods are necessary before bio-oils can be used as direct fuels. This review focuses on the catalytic hydrotreatment of bio-oils, which has been shown to be an effective approach for the removal of heteroatoms at moderate temperatures (between 300 and 450 °C) but at high pressures (up to 20 MPa). Oxygenated compounds are transformed into H2O, and N and S are transformed into NH3 and H2S, respectively. The analysis examines how process temperature, residence time, hydrogen pressure, solvent selection, and type of catalyst influence the properties of the improved bio-oil. Mo/W sulfide-supported catalysts have been traditionally used as active phases in hydrotreatment processes, as the presence of S limits catalyst deactivation, while the presence of Ni or Co as promoters enhances hydrogenation reactions. New research trends are exploring alternative catalyst formulations, such as metal phosphides, carbides, nitrides, and mesoporous materials as supports with controlled acid-basic properties.
Embargo
Zeolite synthesis from industrial wastes
(Elsevier, 2019) Yoldi Sangüesa, María; Fuentes Ordóñez, Edwin Gustavo; Korili, Sophia A.; Gil Bravo, Antonio; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias; Gobierno de Navarra / Nafarroako Gobernua, PI017 CORRAL
Conventional synthesis conditions for each type of zeolite are tabulated and reported by the International Zeolite Association Structure Commission (IZA) and most of them are synthesized from commercial reagents, but they can also be synthesized from industrial by-products rich in Si and/or Al. In zeolite synthesis from wastes, concentration of alkali source, temperature, reaction time, liquid/solid ratio and type of waste determine the textural properties, crystal structure, Si/Al ratio and ion exchange characteristics of the fabricated zeolite and its applications. This work summarizes the main methods that have been developed to synthesize zeolites using industrial wastes as Al and/or Si sources, the parameters of synthesis and the advantages and limitations of each synthesis process. The main characteristics and the applications of these synthetic waste zeolites are also reported.
Open Access
A comparative study of the catalytic performance of nickel supported on a hibonite-type La-hexaaluminate synthesized from aluminum saline slags in the dry reforming of methane
(Elsevier, 2022) Torrez Herrera, Jonathan Josué; Korili, Sophia A.; Gil Bravo, Antonio; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
In this work, a hibonite-type Ni/La-hexaaluminate (Ni/LHA) synthesized from an industrial waste is used and compared as catalyst in the dry reforming of methane (DRM) at 973 K. The structure, catalytic behavior, and stability during a run time of at least 50 h of three Nicatalysts obtained from two commercial supports and two preparation methods were used for comparison. An aluminum solution (9.40 g/L) obtained from an aluminum saline slag waste by acid extraction was used to synthesize the hexaaluminate by mixing with a stoichiometric amount of lanthanum nitrate and methanol/Peg400/PegMn400 under hydrothermal conditions at 493 K for 16 h. The Ni/LHA catalyst (10 wt% NiO) was obtained by impregnation of the synthesized support, calcined previously at 1473 K for 2 h. The resulting solids were characterized by several techniques as: X-ray diffraction (XRD), N2 adsorption at 77 K, temperature-programmed reduction (TPR), scanning electron microscopy (SEM) and transmission electron microscopy (HR-TEM). In order to compare the catalytic behavior and properties of the Ni/LHA catalyst, three Ni catalysts obtained from two commercial supports (g-Al2O3 and SiO2) and two preparation methods (wet impregnation (I) and precipitation-deposition (PD)) were synthesized. Analysis of the TPR patterns for the catalysts allowed the type of metal support interaction and NiO species to be determined, with a weak interaction with the support being observed in Ni/LHA and NieI/ SiO2. The NiO species observed, with crystallite sizes between 9.7 and 40.4 nm, confirm the X-ray structural analyses. The Ni/LHA catalyst was found to be active and very stable in the DRM reaction after 50 h. The catalytic behavior was evaluated from the CO2 and CH4 conversions, as well as the H2/CO selectivity, with values of 99% over almost all the time range evaluated. The behavior of this catalyst is comparable to that of NieI/Al2O3 and NiPD/SiO2. The results found indicating that the strong interaction of nickel with the support favors the stability of the catalysts in the DRM reaction.
Open Access
Development of ceramic-MOF filters from aluminum saline slags for capturing CO2
(Elsevier, 2023) Torrez Herrera, Jonathan Josué; Korili, Sophia A.; Gil Bravo, Antonio; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
This study describes the procedures followed to synthesize ceramic-MOF filters using aluminum saline slag wastes. Briefly, the raw aluminum saline slags were washed at 80 ◦C to significantly reduce the saline content and eliminate gases. The pretreated material was mixed with glucose (G/S ratios between 0.2 and 1.6) and acetone by stirring for 4 h. After this time, the resulting solid was dried at 60 ◦C and then at 190 ◦C. During the glucose caramelization step, PegMn400 was also added and the temperature increased to 1200 ◦C. The obtained solid was impregnated with precursor solutions to achieve a supported ZIF-8 MOF. The ceramic-MOF filters were characterized by X-ray diffraction (XRD), N2 adsorption at 77 K, X-ray fluorescence (XRF), scanning electron microscopy (SEM) and transmission electron microscopy (HR-TEM), thereby confirming the presence of a structure that allows dispersion of the synthesized and supported ZIF-8. Finally, the performance of these ceramic-MOF filters as CO2 adsorbents was evaluated in the temperature range 50–300 ◦C, with isosteric heats of 19 kJ/mol being obtained using the Clausius-Clapeyron equation.