Open Access
Steering the synthesis of Fe3O4 nanoparticles under sonication by using a fractional factorial design
(Elsevier, 2021) Echeverría Morrás, Jesús; Moriones Jiménez, Paula; Garrido Segovia, Julián José; Ugarte Martínez, María Dolores; Cervera Gabalda, Laura María; Garayo Urabayen, Eneko; Gómez Polo, Cristina; Pérez de Landazábal Berganzo, José Ignacio; Ciencias; Zientziak; Estadística, Informática y Matemáticas; Estatistika, Informatika eta Matematika; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa; Gobierno de Navarra / Nafarroako Gobernua
Superparamagnetic iron oxide nanoparticles (MNPs) have the potential to act as heat sources in magnetic hyperthermia. The key parameter for this application is the specific absorption rate (SAR), which must be as large as possible in order to optimize the hyperthermia treatment. We applied a Plackett-Burman fractional factorial design to investigate the effect of total iron concentration, ammonia concentration, reaction temperature, sonication time and percentage of ethanol in the aqueous media on the properties of iron oxide MNPs. Characterization techniques included total iron content, Fourier Transform Infrared Spectroscopy, X-Ray Diffraction, High Resolution Transmission Electron Microscopy, and Dynamic Magnetization. The reaction pathway in the coprecipitation reaction depended on the initial Fe concentration. Samples synthesized from 0.220 mol L−1 Fe yielded magnetite and metastable precipitates of iron oxyhydroxides. An initial solution made up of 0.110 mol L−1 total Fe and either 0.90 or 1.20 mol L−1 NH3(aq) led to the formation of magnetite nanoparticles. Sonication of the reaction media promoted a phase transformation of metastable oxyhydroxides to crystalline magnetite, the development of crystallinity, and the increase of specific absorption rate under dynamic magnetization.
Open Access
Kinetics of the acid-catalyzed hydrolysis of tetraethoxysilane (TEOS) by 29Si NMR spectroscopy and mathematical modeling
(Springer, 2018) Echeverría Morrás, Jesús; Moriones Jiménez, Paula; Arzamendi Manterola, Gurutze; Garrido Segovia, Julián José; Gil Idoate, María José; Cornejo Ibergallartu, Alfonso; Martínez Merino, Víctor; Química Aplicada; Kimika Aplikatua; Institute for Advanced Materials and Mathematics - INAMAT2
Tetraethoxysilane (TEOS) is widely used to synthesize siliceous material by the sol–gel process. However, there is still some disagreement about the nature of the limiting step in the hydrolysis and condensation reactions. The goal of this research was to measure the variation in the concentration of intermediates formed in the acid-catalyzed hydrolysis by 29Si NMR spectroscopy, to model the reactions, and to obtain the rate constants and the activation energy for the hydrolysis and early condensation steps. We studied the kinetics of TEOS between pH 3.8 and 4.4, and four temperature values in the range of 277.2–313.2 K, with a TEOS:ethanol:water molar ratio of 1:30:20. Both hydrolysis and the condensation rate speeded up with the temperature and the concentration of oxonium ions. The kinetic constants for hydrolysis reactions increased in each step kh1 < kh2 < kh3 < kh4, but the condensation rate was lower for dimer formation than for the formation of the fully hydrolyzed Si(OH)4. The system was described according to 13 parameters: six of them for the kinetic constants estimated at 298.2 K, six to the activation energies, and one to the equilibrium constant for the fourth hydrolysis. The mathematical model shows a steady increase in the activation energy from 34.5 kJ mol−1 for the first hydrolysis to 39.2 kJ mol−1 in the last step. The activation energy for the condensation reaction from Si(OH)4 was ca. 10 kJ mol−1 higher than the largest activation energy in the hydrolytic reactions. The decrease in the net positive charge on the Si atom contributes to the protonation of the ethoxy group and makes it a better leaving group.
Open Access
Comprehensive kinetics of hydrolysis of organotriethoxysilanes by 29Si NMR
(American Chemical Society, 2019) Moriones Jiménez, Paula; Arzamendi Manterola, Gurutze; Cornejo Ibergallartu, Alfonso; Garrido Segovia, Julián José; Echeverría Morrás, Jesús; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2
The kinetics of several representative hybrid precursors were studied via 29Si NMR: three alkyl precursors, methyltriethoxysilane, ethyltriethoxysilane, and propyltriethoxysilane; as well as two unsaturated radicals, vinyltriethoxysilane and phenyltriethoxysilane. The reaction rate is related to the chemical shift of 29Si in the NMR spectra, which gives information about the electronic density of the Si atoms and the inductive effects of substituents. The concentration of the precursors decreased exponentially with time, and the intermediate products of hydrolysis and the beginning of the condensation reactions showed curves characteristic of sequential reactions, with a similar distribution of the species as a function of the fractional conversion. For all of the precursors, condensation started when the most hydrolyzed species reached a maximum concentration of 0.30 M, when the precursor had run out. A prediction following the developed mathematical model fits the experimental results in line with a common pathway described by eight parameters.
Open Access
Tunability of hybrid silica xerogels: surface chemistry and porous texture based on the aromatic precursor
(MDPI, 2023) Rosales Reina, María Beatriz; Cruz Quesada, Guillermo; Padilla-Postigo, Nataly; Irigoyen-Razquin, Marian; Alonso-Martínez, Ester; López Ramón, María Victoria; Espinal Viguri, Maialen; Garrido Segovia, Julián José; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
The interest in new materials with specific properties has increased because they are essential for the environmental and technological needs of our society. Among them, silica hybrid xerogels have emerged as promising candidates due to their simple preparation and tunability: when they are synthesised, depending on the organic precursor and its concentration, their properties can be modulated, and thus, it is possible to prepare materials with à la carte porosity and surface chemistry. This research aims to design two new series of silica hybrid xerogels by co-condensation of tetraethoxysilane (TEOS) with triethoxy(p-tolyl)silane (MPhTEOS) or 1,4-bis(triethoxysilyl)benzene (Ph(TEOS)2 and to determine their chemical and textural properties based on a variety of characterisation techniques (FT-IR, 29Si NMR, X-ray diffraction and N2 , CO2 and water vapour adsorption, among others). The information gathered from these techniques reveals that depending on the organic precursor and its molar percentage, materials with different porosity, hydrophilicity and local order are obtained, evidencing the easy modulation of their properties. The ultimate goal of this study is to prepare materials suitable for a variety of applications, such as adsorbents for pollutants, catalysts, films for solar cells or coatings for optic fibre sensors.
Open Access
Fiber optic sensors based on hybrid phenyl-silica xerogel films to detect n-hexane: determination of the isosteric enthalpy of adsorption
(Beilstein-Institut, 2017) Echeverría Morrás, Jesús; Calleja, Ignacio; Moriones Jiménez, Paula; Garrido Segovia, Julián José; Kimika Aplikatua; Institute for Advanced Materials and Mathematics - INAMAT2; Química Aplicada; Gobierno de Navarra / Nafarroako Gobernua, 269/01/08
We investigated the response of three fiber optic sensing elements prepared at pH 10 from phenyltriethoxysilane (PhTEOS) and tetraethylsilane (TEOS) mixtures with 30, 40, and 50% PhTEOS in the silicon precursor mixture. The sensing elements are referred to as Ph30, Ph40 and Ph50, respectively. The films were synthesized by the sol–gel method and affixed to the end of optical fibers by the dip-coating technique. Fourier transform infrared spectroscopy, N2 adsorption–desorption at 77 K and X-ray diffraction analysis were used to characterize the xerogels. At a given pressure of n-hexane, the response of each sensing element decreased with temperature, indicating an exothermic process that confirmed the role of adsorption in the overall performance of the sensing elements. The isosteric adsorption enthalpies were obtained from the calibration curves at different temperatures. The magnitude of the isosteric enthalpy of n-hexane increased with the relative response and reached a plateau that stabilized at approximately −31 kJ mol−1 for Ph40 and Ph50 and at approximately −37 kJ mol−1 for Ph30. This indicates that the adsorbate–adsorbent interaction was dominant at lower relative pressure and condensation of the adsorbate on the mesopores was dominant at higher relative pressure.
Open Access
Hybrid xerogels: study of the sol-gel process and local structure by vibrational spectroscopy
(MDPI, 2021) Cruz Quesada, Guillermo; Espinal Viguri, Maialen; López Ramón, María Victoria; Garrido Segovia, Julián José; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
The properties of hybrid silica xerogels obtained by the sol-gel method are highly dependent on the precursor and the synthesis conditions. This study examines the influence of organic substituents of the precursor on the sol-gel process and determines the structure of the final materials in xerogels containing tetraethyl orthosilicate (TEOS) and alkyltriethoxysilane or chloroalkyltri-ethoxysilane at different molar percentages (RTEOS and ClRTEOS, R = methyl [M], ethyl [E], or propyl [P]). The intermolecular forces exerted by the organic moiety and the chlorine atom of the precursors were elucidated by comparing the sol-gel process between alkyl and chloroalkyl series. The microstructure of the resulting xerogels was explored in a structural theoretical study using Fourier transformed infrared spectroscopy and deconvolution methods, revealing the distribution of (SiO)4 and (SiO)6 rings in the silicon matrix of the hybrid xerogels. The results demonstrate that the alkyl chain and the chlorine atom of the precursor in these materials determines their inductive and steric effects on the sol-gel process and, therefore, their gelation times. Furthermore, the distribution of (SiO)4 and (SiO)6 rings was found to be consistent with the data from the X-ray diffraction spectra, which confirm that the local periodicity associated with four-fold rings increases with higher percentage of precursor. Both the sol-gel process and the ordered domains formed determine the final structure of these hybrid materials and, therefore, their properties and potential applications.
Open Access
Photocatalytic enhancement of anatase supported on mesoporous modified silica for the removal of carbamazepine
(MDPI, 2025-10-08) Cruz Quesada, Guillermo; Rosales Reina, María Beatriz; Velo-Gala, Inmaculada; Fernández-Poyatos, María del Pilar; Álvarez-Merino, Miguel Ángel; García-Ruiz, Cristian; López Ramón, María Victoria; Garrido Segovia, Julián José; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2
TiO2 is the most used material for the photocatalytic removal of organic pollutants in aqueous media. TiO2, specifically its anatase phase, is well-known for its great performance under UV irradiation, high chemical stability, low cost and non-toxicity. Nevertheless, TiO2 presents two main drawbacks: its limited absorption of the visible spectrum; and its relatively low specific surface area and pore volume. Regarding the latter, several works in the literature have addressed the issue by developing new synthesis approaches in which anatase is dispersed and supported on the surface of porous materials. In the present work, two series of materials have been prepared where anatase has been supported on mesoporous silica (MSTiR%) in situ through a hydrothermal synthesis approach, where, in addition to using tetraethoxysilane (TEOS) as a silicon precursor, three organotriethoxysilanes [RTEOS, where R = methyl (M), propyl (P) or phenyl (Ph)] were used at a RTEOS:TEOS molar percentage of 10 and 30%. The materials were thoroughly characterized by several techniques to determine their morphological, textural, chemical, and UV-vis light absorption properties and then the most promising materials were used as photocatalysts in the photodegradation of the emerging contaminant and antiepileptic carbamazepine (CBZ) under UV irradiation. The materials synthesized using 10% molar percentage of RTEOS (MSTiR10) were able to almost completely degrade (~95%), 1 mg L−1 of CBZ after 1 h of irradiation using a 275 nm LED and 0.5 g L−1 of catalyst dose. Therefore, this new synthesis approach has proven useful to develop photoactive TiO2 composites with enhanced textural properties.
Open Access
Volatile compounds other than CO2 emitted by different microorganisms promote distinct posttranscriptionally regulated responses in plants
(Wiley, 2019) García Gómez, Pablo; Almagro Zabalza, Goizeder; Sánchez López, Ángela María; Bahaji, Abdellatif; Ameztoy del Amo, Kinia; Ricarte Bermejo, Adriana; Baslam, Marouane; López Gómez, Pedro; Morán Juez, José Fernando; Garrido Segovia, Julián José; Muñoz Pérez, Francisco José; Baroja Fernández, Edurne; Pozueta Romero, Javier; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias; Gobierno de Navarra / Nafarroako Gobernua
A 'box-in-box' cocultivation system was used to investigate plant responses to microbial volatile compounds (VCs) and to evaluate the contributions of organic and inorganic VCs (VOCs and VICs, respectively) to these responses. Arabidopsis plants were exposed to VCs emitted by adjacent Alternaria alternata and Penicillium aurantiogriseum cultures, with and without charcoal filtration. No VOCs were detected in the headspace of growth chambers containing fungal cultures with charcoal filters. However, these growth chambers exhibited elevated CO2 and bioactive CO and NO headspace concentrations. Independently of charcoal filtration, VCs from both fungal phytopathogens promoted growth and distinct developmental changes. Plants cultured at CO2 levels observed in growth boxes containing fungal cultures were identical to those cultured at ambient CO2. Plants exposed to charcoal-filtered fungal VCs, nonfiltered VCs, or superelevated CO2 levels exhibited transcriptional changes resembling those induced by increased irradiance. Thus, in the 'box-in-box'' system, (a) fungal VICs other than CO2 and/or VOCs not detected by our analytical systems strongly influence the plants' responses to fungal VCs, (b) different microorganisms release VCs with distinct action potentials, (c) transcriptional changes in VC-exposed plants are mainly due to enhanced photosynthesis signaling, and (d) regulation of some plant responses to fungal VCs is primarily posttranscriptional.
Open Access
The narrative of a line of research from a feminist perspective: fiber optic sensors and actor-network theory (ANT)
(MDPI, 2022) Aliende Urtasun, Ana; Garrido Segovia, Julián José; Soziologia eta Gizarte Lana; Institute for Advanced Materials and Mathematics - INAMAT2; Sociología y Trabajo Social
The narrative of a line of research from a feminist perspective involves describing the situated practices that contribute to understanding inequality in the construction of the social relationships that build links between human and nonhuman materialities. This paper aims to link feminist epistemology and actor–network theory to the expert network that produces, sustains and manages the design of the chemical zone of a fiber optic sensor (FOS) and of new smart materials, tracing the path of a university research group with important scientific publications that has also developed a line of work in the field of science, technology and society (STS). We are interested in the generalized division of labor and the role of science and technology in the creation of symbols in our culture, particularly in the field of expert knowledge, where research carried out by men and women constructs trajectories of academic success that are predominantly male. The transversal incorporation of gender analysis into the production of FOSs helps reveal the processes that have, up to this point, excluded women from prominent positions in publications. © 2022 by the authors.
Open Access
Mobility of heavy metals in soils amended with sewage sludge
(Agricultural Institute of Canada, 2001) Morera Luzán, María Teresa; Echeverría Morrás, Jesús; Garrido Segovia, Julián José; Química Aplicada; Kimika Aplikatua
Sewage sludges added to arable land can improve soil fertility and physical properties. However, the concentrations of heavy metals commonly found in sludges limits their application to soil. The purpose of this paper is to evaluate the mobility of heavy metals (Cd, Cu, Ni, Pb and Zn) in four soils amended with different rates (0, 80, 60 and 320 t ha-1) of anaerobically stabilized urban sewage sludge. Total metal content in the sewage sludge was Zn much greater than Cu > Pb > Ni much greater than Cd. Sludge, soils and sludge-soil mixtures were fractionated by the Tessier sequential extraction procedure. The fractions extracted by H2O2/HNO3 and NH2OH.HCl were the most abundant pools for metals under study. The apparent mobility of metals in the sludge was Zn approximate to Cd approximate to Ni > Pb > Cu. The addition of sewage sludge in soils increased the percentages of metal extracted in non-residual fractions. ANOVA showed that the most significant increases were those of Zn, followed by Cu and Pb; there were no statistical differences (P < 0.05) for Ni and Cd. Exchangeable Zn from sludge was immobilized in basic soils. The other trace metals showed no fraction redistribution. The soils and sludge-treated soil samples were also extracted with EDTA and DTPA. Extraction with EDTA was more sensitive to soil type, whereas extraction with DTPA showed wider variation with metals. Both chelates seemed to be more effective to assess the mobility of metals added with the sludges at low concentrations than the Tessier's chemical partitioning.