Publications by authors named "Giuliana Aquilanti"

The significance of thermochromic materials in a wide range of applications makes their research and development highly desirable. Herein, three new thermochromic isomorphous supramolecular materials based on the 5,5'-indigodisulfonate ion of the indigo carmine dye, with formulas [Cu(HO)](CHNOS)·2HO (), [Ni(HO)](CHNOS)·2HO (), and [Co(HO)](CHNOS)·2HO (), are reported. These materials exhibit thermochromic properties, with a color change from red-bronze to grayish-red after the first step of their dehydration process completed around 80 °C (conversion of to [Cu(HO)(CHNOS) ()]), and then, this grayish-red color becomes lighter after the second step, which is completed around 230 °C (conversion of to [Cu(CHNOS)] ()).

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Among different Prussian Blue Analogues (PBAs), manganese hexacyanoferrate (MnHCF), with open framework and two abundant electroactive metal sites, exhibits high potential for the grid-scale aqueous rechargeable zinc-ion batteries (ARZIBs) application. Until now, the intercalation mechanism of Zn into MnHCF has not been clearly illustrated. In this work, combining different synchrotron X-ray techniques, the structural and microscopic evolution of MnHCF in 3 m ZnSO electrolyte is comprehensively studied, and a thorough understanding of the intercalation/release dynamic, in terms of local and long-range domain, is provided.

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Article Synopsis
  • Terbium-161 is a promising alternative for medical treatments due to its beta decay energy and half-life similar to lutetium-177.
  • The separation of terbium-161 from gadolinium-160 and its decay product dysprosium-161 is complicated by their similar chemical properties.
  • A new method combines electrochemical oxidation of terbium (3+) to terbium (4+) with anion exchange chromatography to improve purification efficiency for therapeutic applications.
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In this contribution, a comprehensive study of nanostructured BiTe (BT) thermoelectric material was performed using a combination of synchrotron radiation-based techniques such as XAFS, and XRF, along with some other laboratory techniques such as XRD, XPS, FESEM, and HRTEM. This study aims to track the change in morphological, compositional, average and local/electronic structures of BiTe of two different phases; nanostructure (thin film) and nanopowders (NPs). BiTe nanomaterial was fabricated as pellets using zone melting process in a one step process, while BiTe thin film was deposited on sodalime glass substrate using a vacuum thermal evaporation technique.

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  • Bimetallic metal-organic frameworks (MOFs) have potential for reactivity with biomolecules but face challenges like stability and synthesis control.
  • A new synthesis method for Zr/Ce-MOFs in a water/acetic acid mixture creates stable materials with effective nanozymatic reactivity, even for typically unstable high-cerium MOFs.
  • Advanced characterization techniques confirm that modifications in synthesis and Ce incorporation lead to superior nanozymes, suggesting similar approaches could enhance the development of other bimetallic MOF nanozymes for biotechnology.
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Glioblastoma multiforme (GBM) is the most common and devastating primary brain tumor among adults. It is highly lethal disease, as only 25% of patients survive longer than 1 year and only 5% more than 5 years from the diagnosis. To search for the new, more effective methods of treatment, the understanding of mechanisms underlying the process of tumorigenesis is needed.

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High-entropy oxides (HEOs) have emerged as promising anode materials for next-generation lithium-ion batteries (LIBs). Among them, spinel HEOs with vacant lattice sites allowing for lithium insertion and diffusion seem particularly attractive. In this work, electrospun oxygen-deficient (Mn,Fe,Co,Ni,Zn) HEO nanofibers are produced under environmentally friendly calcination conditions and evaluated as anode active material in LIBs.

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We aimed to evaluate the magnesium content in human cirrhotic liver and its correlation with serum AST levels, expression of hepatocellular injury, and MELDNa prognostic score. In liver biopsies obtained at liver transplantation, we measured the magnesium content in liver tissue in 27 cirrhotic patients (CIRs) and 16 deceased donors with healthy liver (CTRLs) by atomic absorption spectrometry and within hepatocytes of 15 CIRs using synchrotron-based X-ray fluorescence microscopy. In 31 CIRs and 10 CTRLs, we evaluated the immunohistochemical expression in hepatocytes of the transient receptor potential melastatin 7 (TRPM7), a magnesium influx chanzyme also involved in inflammation.

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A γ-alumina support functionalized with transition metals is one of the most widely used industrial catalysts for the total oxidation of volatile organic compounds (VOCs) as air pollutants at higher temperatures (280-450 °C). By rational design of a bimetal CuFe-γ-alumina catalyst, synthesized from a dawsonite alumina precursor, the activity in total oxidation of toluene as a model VOC at a lower temperature (200-380 °C) is achieved. A fundamental understanding of the catalyst and the reaction mechanism is elucidated by advanced microscopic and spectroscopic characterizations as well as by temperature-programmed surface techniques.

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Manganese hexacyanoferrates (MnHCF) are promising positive electrode materials for non-aqueous batteries, including Na-ion batteries, due to their large specific capacity (>130 mAh g ), high discharge potential and sustainability. Typically, the electrochemical reaction of MnHCF associates with phase and structural changes, due to the Jahn-Teller (JT) distortion of Mn sites upon the charge process. To understand the effect of the MnHCF structure on its electrochemical performance, two MnHCF materials with different vacancies content are investigated herein.

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Juncus acutus has been proposed as a suitable species for the design of phytoremediation plans. This research aimed to investigate the role played by rhizosphere minerals and water composition on Zn transformations and dynamics in the rhizosphere-plant system of J. acutus exposed to different Zn sources.

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Metabolism of metals in microalgae and adaptation to metal excess are of significant environmental importance. We report a three-step mechanism that the green microalga Chlorella sorokiniana activates during the acquisition of and adaptation to manganese (Mn), which is both an essential trace metal and a pollutant of waters. In the early stage, Mn2+ was mainly bound to membrane phospholipids and phosphates in released mucilage.

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Copper sulfide has attracted increasing attention as conversion-type cathode material for, especially, solid-state lithium-based batteries. However, the reaction mechanism behind its extraordinary electroactivity is not well understood, and the various explanations given by the scientific community are diverging. Herein, the CuS reaction dynamics are highlighted by examining the occurring redox processes via a cutting-edge methodology combining X-ray absorption fine structure spectroscopy, and chemometrics to overcome X-ray diffraction limitations posed by the poor material's crystallinity.

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Biotransformation of toxic selenium ions to non-toxic species has been mainly focused on biofortification of microorganisms and production of selenium nanoparticles (SeNPs), while far less attention is paid to the mechanisms of transformation. In this study, we applied a combination of analytical techniques with the aim of characterizing the SeNPs themselves as well as monitoring the course of selenium transformation in the mycelium of the fungus Phycomyces blakesleeanus. Red coloration and pungent odor that appeared after only a few hours of incubation with 10 mM Se indicate the formation of SeNPs and volatile methylated selenium compounds.

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Synchrotron radiation-based techniques [X-ray absorption near-edge structure (XANES) and X-ray fluorescence (XRF)] combined with inductively coupled plasma-mass spectrometry (ICP-MS) were used for the assessment of heavy metals concentrations as well as lead (Pb) and nickel (Ni) speciation in airborne particulate matter (PM) over two residential sites in Greater Cairo. Nineteen 24 h high-volume samples collected at Giza (G) Square and Helwan (H) University (Egypt) were selected for this study. Mean concentrations of heavy metals in PM at both sites were found to have the same descending order of Pb > Cu > Ni > Cd > Co > As, of which concentrations of Pb, Cu, Ni and Cd in H samples were higher than those in G samples.

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X-ray absorption fine-structure (XAFS) spectroscopy can assess the chemical speciation of the elements providing their coordination and oxidation state, information generally hidden to other techniques. In the case of trace elements, achieving a good quality XAFS signal poses several challenges, as it requires high photon flux, counting statistics and detector linearity. Here, a new multi-element X-ray fluorescence detector is presented, specifically designed to probe the chemical speciation of trace 3d elements down to the p.

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A thorough understanding of the implications of chronic low-dose exposure to engineered nanomaterials through the food chain is lacking. The present study aimed to characterize such a response in L. (zucchini) upon exposure to a potential nanoscale fertilizer: copper oxide (CuO) nanoparticles.

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Solid friable residues (i.e. Ash) from combusted oil shale are a major environmental issue because they are highly enriched with toxic elements following combustion.

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Article Synopsis
  • * Hand-Held XRF showed that the inkwell and its lid are made of a bronze alloy and that the lid contains higher levels of lead, suggesting environmental contamination and degradation of the artifact.
  • * Further techniques like XRPD, XAS, and FTIR indicated the ink contains silicates and clay minerals, with the primary composition of the ink being amorphous carbon from burned organic material mixed with Arabic gum as a binding agent.
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Ru/Al O is a highly stable, but less active catalyst for methanation reactions. Herein we report an effective approach to significantly improve its performance in the methanation of CO /H mixtures. Highly active and stable Ru/γ-Al O catalysts were prepared by high-temperature treatment in the reductive reaction gas.

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The role and distribution of iron (Fe) species in physical soil fractions have received remarkably little attention in field-scale systems. Here, we identify and quantify the Fe phases into two fractions (fine sand, FSa, and fine silt and clay, FSi + Cl), isolated from an agricultural soil unamended and amended with different organic materials, by Fe K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy. The linear combination fitting and wavelet transform of EXAFS data revealed noticeable differences between unamended FSa and FSi + Cl fractions.

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  • Manganese hexacyanoferrate (MnHCF) is a cost-effective and environmentally safe material that has superior electrochemical performance compared to other similar compounds.
  • The presence of water significantly impacts its electrochemical behavior, as both interstitial and adsorbed water influence reaction dynamics.
  • This study employs advanced techniques to explore how variations in ion content affect the structural and electronic properties of MnHCF during sodium release and lithium insertion, revealing notable reversible changes in the material's electronic state.
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Zinc incorporation into marine bivalve shells belonging to different genera (Donax, Glycymeris, Lentidium, and Chamelea) grown in mine-polluted seabed sediments (Zn up to 1% w/w) was investigated using x-ray diffraction (XRD), chemical analysis, soft x-ray microscopy combined with low-energy x-ray fluorescence (XRF) mapping, x-ray absorption spectroscopy (XAS), and transmission electron microscopy (TEM). These bivalves grew their shells, producing aragonite as the main biomineral and they were able to incorporate up to 2.0-80 mg/kg of Zn, 5.

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The chemistry of copper(I) with water-soluble phosphines is an emergent area of study which has the objective of finding ligands that stabilize copper in its lower oxidation state. Cu(I) has been found relevant in the mechanism of copper transports into cells, and the accessibility of this oxidation state has implications in oxidative stress processes. For these reasons the possibility to deal with stable, water soluble copper(I) is an attractive approach for devising new biologically relevant metal-based drugs and chelating agents.

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Following the Q2XAFS Workshop and Satellite to IUCr Congress 2017 on `Data Acquisition, Treatment, Storage - quality assurance in XAFS spectroscopy', a summary is given of the discussion on different aspects of a XAFS experiment that affect data quality. Some pertinent problems ranging from sources and minimization of noise to harmonic contamination and uncompensated monochromator glitches were addressed. Also, an overview is given of the major limitations and pitfalls of a selection of related methods, such as photon-out spectroscopies and energy-dispersive XAFS, and of increasingly common applications, namely studies at high pressure, and time-resolved investigations of catalysts in operando.

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