Open Access
Photocatalytic degradation of trimethoprim on doped Ti-pillared montmorillonite
(Elsevier, 2019) González, Beatriz; Trujillano, Raquel; Vicente, Miguel Ángel; Rives, Vicente; Korili, Sophia A.; Gil Bravo, Antonio; Institute for Advanced Materials and Mathematics - INAMAT2
Montmorillonite pillared with titanium and doped with Cr3+ or Fe3+ has been tested for the photo-degradation of the antibiotic trimethoprim (trimethoxybenzyl-2,4-pyrimidinediamine) under different conditions, namely, in the dark or in UV light, with or without catalyst, finding excellent catalytic performance under photocatalytic conditions. The degradation by-products were preliminary analysed by mass spectrometry. The results suggested that the molecule broke in two halves, corresponding to its two existing rings. The process continued with the breakage of new fragments from the trimethoxybenzene half, these fragments later reacted with the methoxy groups in this part of the molecule, giving species with m/z values higher than that for the starting molecule, and with the breakage of new fragments.
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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
Progress in the synthesis and applications of hexaaluminate-based catalysts
(Taylor & Francis, 2020) 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
The development of materials that can exhibit thermal resistance at very high temperatures, thus allowing them to be applied as catalysts and thermal insulators, amongst other possible uses, is a research subject of great interest. This is the case for hexaaluminates, a class of hexagonal aluminate compounds with a unique structure that are stable at very high temperatures up to 1600°C and exhibit exceptional resistance to sintering and thermal shock, thus making them attractive catalysts for high-temperature applications. In this review, the structure of hexaaluminates is presented first. The most recent advances in synthetic methods (sol-gel, reverse microemulsion, hydrothermal synthesis, carbon-templating, solution combustion synthesis, and freeze-drying methods) are discussed subsequently, with the aim of maximizing textural properties and including in their structure metals known to be active in catalytic applications, such as combustion of CH4, partial oxidation, and dry reforming of CH4 to produce synthetic gas, and the decomposition of N2O. Finally, other applications, such as their function as a thermal barrier, are also addressed.
Open Access
Evidence for the synthesis of La-hexaaluminate from aluminum-containing saline slag wastes: correction of structural defects and phase purification at low temperature
(Elsevier, 2021) Torrez Herrera, Jonathan Josué; Fuentes Ordóñez, Edwin Gustavo; Korili, Sophia A.; Gil Bravo, Antonio; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
The synthesis of a lanthanum hexaaluminate from the aluminum extracted from a saline slag waste is presented for the first time. Briefly, a refluxing 2 M solution of HCl is used to extract the aluminum, giving 8.9 gAl/dm3 along with other metals in lower concentrations. This solution is used to synthesize the hexaaluminate by mixing with a stoichiometric amount of lanthanum nitrate. The results showed the formation of pure phase hexaaluminate at 1473 K, as well as predominance of the hexaaluminate phase at temperatures of 1273 and 1373 K. These results also indicate that the pure hexaaluminate phase can be obtained at a much lower temperature than when commercial aluminum solutions are used improving the applications as catalyst and thermal barrier material. It was also found that the presence of other metals in solution allows the structural problems and purity of the La-hexaaluminate phase to be corrected when working with stoichiometric ratios.
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
Bimetallic (Pt-Ni) La-hexaaluminate catalysts obtained from aluminum saline slags for the dry reforming of methane
(Elsevier, 2021) 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
This work describes the synthesis of platinum-nickel/lanthanum hexaaluminates (PtNi/LHA) and their performance in terms of stability and catalytic activity in the dry reforming of methane (DRM) at 973 K. An Al solution (9.40 g/L) obtained from an Al 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. After calcination at 1473 K for 2 h, the presence of LHA was confirmed. Wet impregnation of the synthesized support was used to obtain an initial Ni/LHA catalyst (10 wt% NiO) and the modified PtNi/LHA catalysts (0.2–1 wt% Pt). The support and catalysts were characterized by X-ray diffraction (XRD), N2 adsorption at 77 K, temperature- programmed reduction (TPR), scanning electron microscopy (SEM) and transmission electron microscopy (HR- TEM). The 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 all cases. The presence of Pt promoted NiO reducibility. The PtNi/LHA catalysts synthesized were found to be active and very stable in the DRM reaction after reaction for 50 h. The catalytic behavior was evaluated from the CO2 and CH4 conversions, as well as the H2/CO selectivity, with values of between 89% and 92% in almost all the time range evaluated. The presence of Pt improved the stability and catalytic performance of Ni/LHA thus improving resistance to coke formation.
Open Access
Adsorption recovery of Ag(I) and Au(III) from an electronics industry wastewater on a clay mineral composite
(University of Science and Technology Beijing, 2019) Rakhila, Youness; Elmchaouri, Abdellah; Mestari, Allal; Korili, Sophia A.; Abouri, Meriem; Gil Bravo, Antonio; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias
The aim of this work is to investigate the ability of an adsorbent of a clay mineral composite to remove and recover gold and silver ions from wastewater. The composite was prepared by mixing phosphogypsum (PG), obtained from an industrial waste, and a natural clay mineral. The materials were characterized before and after use in adsorption by several techniques. Batch adsorption experiments were carried out, and the effects of the contact time and the pH and temperature of solution on the removal processes were investigated. The optimum pH for the adsorption was found to be 4. The adsorption of these metal ions reached equilibrium after 2 h of contact. The pseudo-first- and the pseudo-second-order kinetic models, as well as the Freundlich and the Langmuir isotherm equations, were considered to describe the adsorption results. The maximum adsorbed amount of 85 mg·g−1 Ag(I) and 108.3 mg·g−1 Au(III) was found. The recovery of the adsorbed gold and silver ions from the adsorbent was also analyzed. Strong acids appeared to be the best desorption agents to recover gold and silver ions. The use of aqua regia gave regeneration rates close to 95.3% and 94.3% for Ag(I) and Au(III), respectively. Finally, the removal of gold and silver ions from an industrial wastewater was tested in batch experiments, and percentage recoveries of 76.5% and 79.9% for Ag(I) and Au(III), respectively, were obtained. To carry out the industrial application of the proposed methodology, an economic viability study is required.
Open Access
Effect of high pressure on the reducibility and dispersion of the active phase of Fischer-Tropsch catalysts
(MDPI, 2019) Yunes, Simón; Vicente, Miguel Ángel; Korili, Sophia A.; Gil Bravo, Antonio; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias
The effect of high pressure on the reducibility and dispersion of oxides of Co and Fe supported on -Al2O3, SiO2, and TiO2 has been studied. The catalysts, having a nominal metal content of 10 wt.%, were prepared by incipient wetness impregnation of previously calcined supports. After drying at 60 °C for 6 h and calcination at 500 °C for 4 h, the catalysts were reduced by hydrogen at two pressures, 1 and 25 bar. The metal reduction was studied by temperature-programmed reduction up to 750 °C at the two pressures, and the metal dispersion was measured by CO chemisorption at 25 °C, obtaining values between 1% and 8%. The physicochemical characterization of these materials was completed by means of chemical analysis, X-ray diffraction, N2 adsorption-desorption at -196 °C and scanning electron microscopy. The high pressure lowered the reduction temperature of the metal oxides, improving their reducibility and dispersion. The metal reducibility increased from 42%, in the case of Fe/Al2O3 (1 bar), to 100%, in the case of Fe/TiO2 (25 bar).
Open Access
Titania-triethanolamine-kaolinite nanocomposites as adsorbents and photocatalysts of herbicides
(Elsevier, 2021) Ferreira, Ana Vera de Toledo Piza Figueiredo; Barbosa, Lorrana Vietro; Souza, Suelen Delfino de; Ciuffi, Katia J.; Vicente, Miguel Ángel; Trujillano, Raquel; Korili, Sophia A.; Gil Bravo, Antonio; Faria, Emerson H. de; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias
Kaolinite-titania adsorbents/photocatalysts were prepared by functionalizing a kaolinite with titanium(IV) triethanolaminate isopropoxide by the sol–gel route. These materials were characterized by various techniques and applied in adsorption studies (kinetic and equilibrium) of the herbicides diuron, hexazinone, and tebuthiuron. Photodegradation studies were also conducted with the materials submitted to heat-treatment at 400, 700, or 1000 °C. The basal spacing increased from 0.71 to 1.08 nm when pure kaolinite was functionalized with titanium triethanolaminate units. The materials displayed FTIR bands of –CH, –NH2, and Ti–OH groups, thereby confirming that titanium alkoxide was present in the kaolinite interlayer space. The pseudo second-order model was the best for describing the kinetic adsorption process. In the equilibrium study, the Langmuir model best described the adsorption mechanism. The photodegradation studies showed that the kaolinite-titania nanocomposites heat-treated at 400 and 700 degraded diuron, hexazinone, and tebuthiuron efficiently due to the presence of metakaolin and formation of the anatase phase. © 2021 Elsevier B.V.
Open Access
Synthesis of zeolite a from metakaolin and its application in the adsorption of cationic dyes
(MDPI, 2018) Pereira, Priscila Martins; Ferreira, Breno Freitas; Oliveira, Nathalia Paula; Gil Bravo, Antonio; Korili, Sophia A.; Kimika Aplikatua; Institute for Advanced Materials and Mathematics - INAMAT2; Química Aplicada
The present work reports the synthesis of zeolites from two metakaolins, one derived from the white kaolin and the other derived from the red kaolin, found in a deposit in the city of São Simão (Brazil). The metakaolins were prepared by calcination of the kaolins at 600 ◦C; zeolite A was obtained after alkali treatment of the metakaolins with NaOH. The resulting solids were characterized by powder X-ray diffraction, thermal analysis, scanning electron microscopy, and nitrogen adsorption/desorption at −196 ◦C, which confirmed formation of zeolite A. The zeolites were applied as adsorbents to remove methylene blue, safranine, and malachite green from aqueous solutions. The zeolites displayed high adsorption capacity within short times (between one and five minutes); qt was 0.96 mg/g. The equilibrium study showed that the zeolites had higher adsorption capacity for malachite green (qe = 55.00 mg/g) than for the other two cationic dyes, and that the Langmuir isotherm was the model that best explained the adsorption mechanism.