Publications by authors named "Leonarda Francesca Liotta"

Herein, we present a paper that attempts to bridge the gap between CO oxidation catalytic tests performed in a model stream and a more realistic exhaust gas stream by incorporating characterization methods that allow for active probing of the catalyst surface. The results have shown that it is not just the abundance of a given type of species on the surface that impacts the activity of a system but also the ease of extraction of ions from their surface (time-of-flight secondary ion mass spectrometry) and the response of the support to change in the feed composition (dynamic in situ X-ray diffraction (XRD) with variable atmosphere). The study utilizes the method of doping a catalyst (RuO/CZ) with a small amount of alkali-metal (K or Na) carbonates in order to slightly modify its surface to gain insight into parameters that may cause discrepancies between model stream activity and complex stream activity.

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The grafting of trialkoxysilanes is the most common method for the surface functionalization of silica gel, and it is usually carried out in the presence of toluene or other solvents such as acetonitrile or acetone. Here, we replaced these solvents with alcohols to afford silica materials containing alkoxy groups linked to the silicon atom. The grafting of -dimethyl-3-amino- or 3-amino-propyltrimethoxysilane was carried out in the presence of several alcohols containing an unsubstituted alkyl chain (C7 and C14), a PEG functionalized chain, or an amino-substituted chain (-dimethylamino, pyridyl).

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In this study, vermiculite was explored as a support material for nickel catalysts in two key processes in syngas production: dry reforming of methane with CO and steam reforming of ethanol. The vermiculite underwent acid or base treatment, followed by the preparation of Ni catalysts through incipient wetness impregnation. Characterization was conducted using various techniques, including X-ray diffraction (XRD), SEM-EDS, FTIR, and temperature-programmed reduction (H-TPR).

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Catalytic total oxidation is an effective technique for the treatment of industrial VOCs principally resulting from industrial processes using solvents and usually containing mono-aromatics (BTEX) and oxygenated compounds (acetone, ethanol, butanone). The aim of this work is to deposit gold nanoparticles on CoAl mixed oxide issued from layered double hydroxide (LDH) precursor by using the deposition precipitation (DP) method, which is applied with two modifications, labeled method (A) and method (B), in order to enhance the interaction of the HAuCl precursor with the support. Method (A) involves the hydrolysis of the HAuCl precursor after addition of the support, while in method (B), the gold precursor is hydrolyzed before adding the support.

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Dry reforming of methane with ratio CH/CO = 1 is studied using supported Ni catalysts on SBA-15 modified by CeMnO mixed oxides with different Ce/Mn ratios (0.25, 1 and 9). The obtained samples are characterized by wide-angle XRD, SAXS, N sorption, TPR-H, TEM, UV-vis and Raman spectroscopies.

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Cu (10 wt%) materials on silica nanotubes were prepared via two different synthetic approaches, co-synthesis and wetness impregnation on preformed SiO nanotubes, both as dried or calcined materials, with Cu(NO)2.5HO as a material precursor. The obtained silica and the Cu samples, after calcination at 550 °C for 5 h, were characterized by several techniques, such as TEM, N physisorption, XRD, Raman, H-TPR and XPS, and tested for toluene oxidation in the 20-450 °C temperature range.

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For this study, the synthesis of TiO nanomaterials was performed via a novel sol-gel method employing titanium butoxide as a metal precursor, Pluronic F127 as a templating agent, toluene as a swelling agent, and acidic water or ethanol as the reaction solvents. The method was designed by tailoring certain reaction parameters, such as the sequence of toluene addition, magnetic stirring, the type of reaction solvent, and the calcination conditions. Analysis of the specific surface area and porosity was carried out via N physisorption, whereas the morphological features of the solids were investigated via transmission electron microscopy.

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In this work, formulations of "environmentally compatible" silicone-based antifouling, synthesized in the laboratory and based on copper and silver on silica/titania oxides, have been characterized. These formulations are capable of replacing the non-ecological antifouling paints currently available on the market. The texture properties and the morphological analysis of these powders with an antifouling action indicate that their activity is linked to the nanometric size of the particles and to the homogeneous dispersion of the metal on the substrate.

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The reaction of octakis(3-chloropropyl)octasilsesquioxane with four equivalents of 1-hexylimidazole or 1-decylimidazole gave two products labelled as HQ-POSS (hexyl-imidazolium quaternized POSS) and DQ-POSS (decyl-imidazolium quaternized POSS) as regioisomer mixtures. An investigation of the biological activity of these two compounds revealed the higher antimicrobial performances of HQ-POSS against Gram-positive and Gram-negative microorganisms, proving its broad-spectrum activity. Due to its very viscous nature, HQ-POSS was adsorbed in variable amounts on the surface of biologically active oxides to gain advantages regarding the expendability of such formulations from an applicative perspective.

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In the present study CeO, MnO and CeMnO mixed oxide (with molar ratio Ce/Mn = 1) were prepared by sol-gel method using citric acid as a chelating agent and calcined at 500 °C. The silver catalysts (1 wt.% Ag) over the obtained supports were synthesized by the incipient wetness impregnation method with [Ag(NH)]NO aqueous solution.

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Microbial fuel cells (MFCs) provide new opportunities for the sustainable production of energy, converting organic matter into electricity through microorganisms. Moreover, MFCs play an important role in remediation of environmental pollutants from wastewater with power generation. This work focuses on the evaluation of ferroelectric perovskite materials as a new class of non-precious photocatalysts for MFC cathode construction.

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The electrochemical reduction of molecular oxygen is a fundamental process in Solid Oxide Fuel Cells and requires high efficiency cathode materials. Two LaBaSrCoFeO-based perovskite compounds were prepared by solution combustion synthesis, and characterized for their structural, microstructural, surface, redox and electrochemical properties as potential cathodes in comparison with BaSrCoFeO and LaSrCoFeO perovskites. Results highlighted that calcination at 900 °C led to a "bi-perovskite heterostructure", where two different perovskite structures coexist, whereas at higher calcination temperatures a single-phase perovskite was formed.

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In the last years, the use of clay minerals for pharmaceutical purposes has increased due to their interesting properties. Hectorite (Ht) is a clay belonging to the smectite group which has attracted attention for applications in biology, tissue engineering and as drug carrier and delivery system. However, the mechanisms involved in Ht cellular uptake and transport into cells, are still unclear.

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The present work is the first investigation of the electrocatalytic performances of ZrPO as a cathode in a single-chamber Microbial Fuel Cell (MFC) for the conversion of chemical energy from wastewater to bioelectricity. This catalyst was prepared by a coprecipitation method, then characterized by X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), ultraviolet-visible-near-infrared spectrophotometry (UV-Vis-NIR), and cyclic voltammetry analyses. The acid-basic characteristics of the surface were probed by using 2-butanol decomposition.

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Two sets of four different supported catalyst materials were prepared. One set was obtained by polymerization of a bis-vinylimidazolium salt, which formed a poly(ionic liquid) coating on SiO2, TiO2, boron nitride BN, and carbon nitride C3N4. The other set was, instead, obtained by immobilizing Keggin heteropolyacid H3PW12O40 onto poly-imidazolium functionalized materials.

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Silica, titania, and mixed silica-titania powders have been used as supports for loading 5 wt% Cu, 5 wt% Ag, and 2.5 wt% Cu-2.5 wt% Ag with the aim of providing a series of nanomaterials with antifouling properties.

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Three different carbon nanoforms (CNFs), single-walled and multi-walled carbon nanotubes (SWCNTs, MWCNTs) and carbon nanohorns (CNHs), have been used as supports for the direct polymerization of variable amounts of a bis-vinylimidazolium salt. Transmission electron microscopy confirmed that all CNFs act as templates on the growth of the polymeric network, which perfectly covers the nanocarbons forming a cylindrical (SWCNTs, MWCNTs) or spherical (CNHs) coating. The stability of these hybrid materials was investigated in the conversion of CO into cyclic carbonate under high temperature and CO pressure.

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The catalytic dehydration of fructose to 5-hydroxymethylfurfural (HMF) in water was performed in the presence of pristine NbO and composites containing Nb and Ti, Ce or Zr oxides. In all experiments, fructose was converted to HMF using water as the solvent. The catalysts were characterized by powder X-ray diffraction, scanning electron microscopy, N physical adsorption, infrared and Raman spectroscopy and temperature-programmed desorption of NH.

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Paper-TiO-AgO floating photocatalysts were produced under mild condition and their photocatalytic activity for the degradation of aromatic amine under sunlight stimulant was investigated. Characterizations by Raman, XRD, XPS, DRS and PL confirmed the presence of TiO and AgO, and the morphology of the appended TiO/AgO layer was probed by FE-SEM. The photocatalytic activity of the prepared samples was investigated by the degradation of aniline (AN) in water under simulated sun-light illumination and constrained conditions, i.

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Controlling Vacancies and heterointerfaces of nano/microstuctures is very challenging, importantly, which tailors the electromagnetic (EM) parameters to develop the high-performance electromagnetic wave (EMW) absorbers. Herein, we report a strategy using various sulfur-source modifying FeO nanosphere by one-step hydrothermal method to prepare a series of FeS-based composites. Diverse sulfur sources determine their morphologies, crystal structures and compositions, and further affect EMW absorption abilities.

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Carbon fiber (CF) is a significant multifunction material, which is extensively used in aircraft because of its superb performance. However, its microwave absorption properties (MAPs) are seriously restricted as a result of the impedance mismatch issue. To address this issue, an efficient strategy is conducted by a series of CF@MoS and CF@MoS@FeO composites that are fabricated by in-situ grown MoS nanosheets (MoS-NS) and FeO nanoparticles (FeO-NPs) on the surface of CF.

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Multiwalled carbon nanotubes (MWCNTs) were easily and efficiently functionalised with highly cross-linked polyamines. The radical polymerisation of two bis-vinylimidazolium salts in the presence of pristine MWCNTs and azobisisobutyronitrile (AIBN) as a radical initiator led to the formation of materials with a high functionalisation degree. The subsequent treatment with sodium borohydride gave rise to the reduction of imidazolium moieties with the concomitant formation of secondary and tertiary amino groups.

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The aim of this study was to develop smart materials with stimuli-responsive properties for the long-term protection of steel. The idea was to obtain a tailored and controlled release of protective agents in response to the environment stimuli. First, the protective efficacy of three inhibitors containing a carboxylic moiety, such as -aminobenzoic (pAB), succinic (SA), and caffeic (CA) acids, was investigated in alkaline chloride solutions.

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A facile method to produce paper-TiO decorated with AgBr nanoparticles by a mild hydrothermal process at 140 °C was reported. The synthesis method was based on the immersion of the paper in a ready-made suspension of TiO/AgBr, comprising TiO sol solution prepared in acidic conditions and AgBr solution (10 M). A paper-TiO sample was prepared and used as reference.

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Polyhedral oligomeric silsesquioxanes (POSS) have been employed as molecular building blocks for the synthesis of imidazolium cross-linked networks, to be used as heterogeneous catalysts for the conversion of carbon dioxide into cyclic carbonates. Two hybrid materials with different nucleophilic species (bromide and iodide) have been prepared and characterized by means of elemental analysis, C and Si solid-state NMR spectroscopy, thermogravimetric analysis and IR spectroscopy. The solids were tested as the sole catalyst under metal- and solvent-free reaction conditions showing full selectivity toward the formation of cyclic carbonates.

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