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Among the innovative materials used by 20th-century artists, polyurethane (PUR) has been shown to be highly unstable, and therefore artworks made of it are now in need of careful conservation strategies. This study presents a multi-analytical investigation of PUR foam scenic objects originally made between the 1960s and 1970s during the Italian Arte Viva movement. The main components in the foam and additives were characterized through micro attenuated total reflectance infrared spectroscopy (μ-ATR-FTIR) and pyrolysis coupled with gas chromatography and mass spectrometry (Py-GC/MS). Painted samples were further investigated through μ-FTIR and Raman spectroscopy to define binders and pigments. The use of μ-ATR-FTIR in combination with evolved gas analysis-mass spectrometry (EGA-MS) allowed the variable conditions of the artworks to be assessed and attained some insights into the chemical processes responsible for aging. At the same time, morphological changes due to the degradation phenomena were recorded through optical (OM) and scanning electron microscopy (SEM). The detailed characterization of the PUR foam and painting materials was helpful in attaining some insights into harmful environmental parameters for the artworks, thus informing preventive conservation.

Saliva is an easily sampled matrix containing a variety of biochemical information, which can be correlated with the individual health status. The fast, straightforward analysis of saliva by vibrational (ATR-FTIR and Raman) spectroscopy is a good premise for large-scale preclinical studies to aid translation into clinics. In this work, the effects of saliva collection (spitting/swab) and processing (two different deproteinization procedures) were explored by principal component analysis (PCA) of ATR-FTIR and Raman data and by investigating the effects on the main saliva metabolites by reversed-phase chromatography (RPC-HPLC-DAD). Our results show that, depending on the bioanalytical information needed, special care must be taken when saliva is collected with swabs because the polymeric material significantly interacts with some saliva components. Moreover, the analysis of saliva before and after deproteinization by FTIR and Raman spectroscopy allows to obtain complementary biological information.

The rapid identification of beached marine micro-plastics is essential for the determination of the source of pollution and for planning the most effective strategies for remediation. In this paper, we present the results obtained by applying the laser-induced breakdown spectroscopy (LIBS) technique on a large sample of different kinds of plastics that can be found in a marine environment. The use of chemometric analytical tools allowed a rapid classification of the pellets with an accuracy greater than 80%. The LIBS spectrum and statistical tests proved their worth to quickly identify polymers, and in particular, to distinguish C-O from C-C backbone pellets, and PE from PP ones. In addition, the PCA analysis revealed a correlation between appearance (surface pellets roughness) and color (yellowing) , as reported by other recent studies. The preliminary results on the analysis of metals accumulated on the surface of the pellets are also reported. The implication of these results is discussed in view of the possibility of frequent monitoring of the marine plastic pollution on the seacoast.

The introduction of "deep learning" algorithms for feature identification in digital imaging has paved the way for artificial intelligence applications that up to a decade ago were considered technologically impossible to achieve, from the development of driverless vehicles to the fully automated diagnostics of cancer and other diseases from histological images. The success of deep learning applications has, in turn, attracted the attention of several researchers for the possible use of these methods in chemometrics, applied to the analysis of complex phenomena as, for example, the optical emission of laser-induced plasmas. In this paper, we will discuss the advantages and disadvantages of convolutional neural networks, one of the most diffused deep learning techniques, in laser-induced breakdown spectroscopy (LIBS) applications (classification and quantitative analysis), to understand the real potential of "deep LIBS" in practical everyday use. In particular, the comparison with the results obtained using "shallow" artificial neural networks will be presented and discussed, taking as a case study the analysis of six bronze samples of known composition.

Raman spectroscopy is an emerging tool in the research and diagnosis of different diseases, including neurodegenerative disorders. In this work, blood serum samples collected from healthy controls and dementia patients were analysed by Raman spectroscopy to develop a classification model for the diagnosis of dementia of Alzheimer's type (DAT). Raman spectra were processed by means of multivariate tools for multivariate analysis. Lower concentration levels of carotenoids were detected in blood serum from patients, which allowed for a good discrimination with respect to controls, such as 93% of correct predictions on the test set with random forest. We also hypothesize that carotenoid levels might be informative about the severity and progression of the disease, since the intensity of carotenoid signals decreased from the early stage to more severe patients. These encouraging results suggest the possibility to use Raman spectroscopy for the analysis of alternative biofluids (e.g. saliva) and the unobtrusive diagnosis of other neurodegenerative disorders., (© 2022. The Author(s).)

Exfoliated black phosphorus (bP) embedded into a polymer is preserved from oxidation, is stable to air, light, and humidity, and can be further processed into devices without degrading its properties. Most of the examples of exfoliated bP/polymer composites involve a single polymer matrix. Herein, we report the preparation of biphasic polystyrene/poly(methyl methacrylate) (50/50 wt.%) composites containing few-layer black phosphorus (fl-bP) (0.6-1 wt.%) produced by sonicated-assisted liquid-phase exfoliation. Micro-Raman spectroscopy confirmed the integrity of fl-bP, while scanning electron microscopy evidenced the influence of fl-bP into the coalescence of polymeric phases. Furthermore, the topography of thin films analyzed by atomic force microscopy confirmed the effect of fl-bP into the PS dewetting, and the selective PS etching of thin films revealed the presence of fl-bP flakes. Finally, a block copolymer/fl-bP composite (1.2 wt.%) was prepared via in situ reversible addition-fragmentation chain transfer (RAFT) polymerization by sonication-assisted exfoliation of bP into styrene. For this sample, 31 P solid-state NMR and Raman spectroscopy confirmed an excellent preservation of bP structure.

The knowledge of the spectroscopic parameters of the elemental emission lines is important for diagnostics of laser-induced plasmas and the application of calibration-free/fundamental parameters analytical methods. In this paper, we used the recently proposed time-independent extended C-sigma method for determining, for the first time, the transition probabilities and Stark broadening coefficients of several neutral (TIECS) and ionic silver emission lines. The method allows for a compensation of self-absorption in the plasma, thus providing a measure of the spectroscopic parameters which is not affected by the optical thickness of the plasma.

The bio-engineering technologies of medical devices through nano-structuring and coating was recently proposed to improve biocompatibility and to reduce microbial adhesion in the prevention of implantable device-related infections. Our aim was to evaluate the ability of new nano-structured and coated materials to prevent the adhesion and biofilm formation, according to the American Standard Test Method ASTM-E2647-13. The materials composition was determined by X-ray Fluorescence and Laser Induced Breakdown Spectroscopy. Silver release was evaluated by Inductively Coupled Plasma Mass Spectrometry analysis. The gene expression levels of the Quorum Sensing Las and Rhl system were evaluated by the ΔΔCt method. The Log bacterial density (Log CFU/cm 2 ) on TiAl6V4 was 4.41 ± 0.76 and 4.63 ± 1.01 on TiAl6V4-AgNPs compared to 2.57 ± 0.70 on CoCr and 2.73 ± 0.61 on CoCr-AgNPs (P < 0.0001, A.N.O.V.A.- one way test). The silver release was found to be equal to 17.8 ± 0.2 µg/L after the batch phase and 1.3 ± 0.1 µg/L during continuous flow. The rhlR gene resulted in a 2.70-fold increased expression in biofilm growth on the silver nanoparticles (AgNPs) coating. In conclusion, CoCr showed a greater ability to reduce microbial adhesion, independently of the AgNPs coating. The silver release resulted in promoting the up-regulation of the Rhl system. Further investigation should be conducted to optimize the effectiveness of the coating., Competing Interests: The authors declare no conflicts of interest.

In this article, we compare two analytical methods that have been recently proposed: the columnar density Saha-Boltzmann plot method of Cristoforetti and Tognoni (Cristoforetti, G.; Tognoni, E. Spectrochim. Acta, Part B, 2013, 79-80, 63-71) and the C-sigma model of Aragon and Aguilera (Aragon, C.; Aguilera, J. A. J. Quant. Spectrosc. Radiat. Trans. 2014, 149, 90-102). Both methods are based on the exploitation of self-absorbed lines for the characterization of plasmas in laser-induced breakdown spectroscopy experiments. However, although the two methods can be safely applied in many cases, their usefulness is limited in many practical cases of interest because of the intrinsic constraints of the used plasma model or because of the complexity of the numerical treatment. The two methods are presented here and critically discussed. Finally, an extended C-sigma approach is proposed to merge the advantages of the two methods, overcoming their intrinsic limitations and simplifying the numerical treatment.

In exploiting the analytical capabilities of plasma-based spectroscopy method, the evaluation of plasma parameters, particularly the plasma temperature, is a crucial step. In this work, a modified Saha-Boltzmann plot, which uses the columnar densities of atomic and ionic ground levels, is utilized to calculate the plasma temperature in a laser-induced plasma from an aluminum alloy target. The columnar densities are here calculated by quantifying the self-absorption of resonance lines. It is demonstrated that this is a promising method for accurate determination of plasma temperature. To validate the capability of this technique, plasma emission is measured at different gate delay times. For each delay, excitation temperature is calculated both by the conventional Saha-Boltzmann plot (by using the excited states) and by exploiting the new Columnar Density Saha-Boltzmann (CD-SB) plot. The results suggest that at later times of the plasma evolution, the CD-SB plot can be more suitable for the determination of plasma temperature than conventional Saha-Boltzmann plot. These findings provide a new approach for physical characterization of plasmas and give access to a wealth of information about the state of plasma.

In this work, a critical review of the current nondestructive probing and image analysis approaches is presented, to revealing otherwise invisible or hardly discernible details in manuscripts and paintings relevant to cultural heritage and archaeology. Multispectral imaging, X-ray fluorescence, Laser-Induced Breakdown Spectroscopy, Raman spectroscopy and Thermography are considered, as techniques for acquiring images and spectral image sets; statistical methods for the analysis of these images are then discussed, including blind separation and false colour techniques. Several case studies are presented, with particular attention dedicated to the approaches that appear most promising for future applications. Some of the techniques described herein are likely to replace, in the near future, classical digital photography in the study of ancient manuscripts and paintings.

Black phosphorus (bP) has been recently investigated for next generation nanoelectronic multifunctional devices. However, the intrinsic instability of exfoliated bP (the bP nanoflakes) toward both moisture and air has so far overshadowed its practical implementation. In order to contribute to fill this gap, we report here the preparation of new hybrid polymer-based materials where bP nanoflakes (bPn) exhibit a significantly improved stability. The new materials have been prepared by different synthetic paths including: (i) the mixing of conventionally liquid-phase exfoliated bP (in dimethyl sulfoxide, DMSO) with poly(methyl methacrylate) (PMMA) solution; (ii) the direct exfoliation of bP in a polymeric solution; (iii) the in situ radical polymerization after exfoliating bP in the liquid monomer (methyl methacrylate, MMA). This last methodology concerns the preparation of stable suspensions of bPn-MMA by sonication-assisted liquid-phase exfoliation (LPE) of bP in the presence of MMA followed by radical polymerization. The hybrids characteristics have been compared in order to evaluate the bP dispersion and the effectiveness of the bPn interfacial interactions with polymer chains aimed at their long-term environmental stabilization. The passivation of the bPn is particularly effective when the hybrid material is prepared by in situ polymerization. By using this synthetic methodology, the nanoflakes, even if with a gradient of dispersion (size of aggregates), preserve their chemical structure from oxidation (as proved by both Raman and 31 P-solid state NMR studies) and are particularly stable to air and UV light exposure. The feasibility of this approach, capable of efficiently exfoliating bP while protecting the bPn, has been then verified by using different vinyl monomers (styrene and N -vinylpyrrolidone), thus obtaining hybrids where the nanoflakes are embedded in polymer matrices with a variety of intriguing thermal, mechanical, and solubility characteristics., Competing Interests: The authors declare no competing financial interest.

The "Monetiere" of Florence hosts the most important collection of Etruscan coins in the world. In the framework of the longstanding collaboration between the Monetiere and the Applied Laser and Spectroscopy Laboratory in Pisa, the Etruscan gold coin collection of the museum was studied. The measurements were performed at the Monetiere, using a portable energy-dispersive X-ray fluorescence (XRF) instrument. The quantitative determination of the gold alloys used for the realization of the coins was obtained applying the fundamental parameters method to the XRF spectra; as a result, using the self-organizing maps method, we were able to classify the coins in four main groups. The main parameter determining the classification is the quantity of silver in the alloy. The results obtained shed some light about the origin of the coins under study.

The laser-induced breakdown spectroscopy (LIBS) technique was used for analyzing the composition of an ancient Roman mortar (5th century A.D.), exploiting an experimental setup which allows the determination of the compositions of binder and aggregate in few minutes, without the need for sample treatment. Four thousand LIBS spectra were acquired from an area of 10 mm 2 , with a 50 µm lateral resolution. The elements of interest in the mortar sample (H, C, O, Na, Mg, Al, Si, K, Ca, Ti, Mn, Fe) were detected and mapped. The collected data graphically shown as compositional images were interpreted using different statistical approaches for the determination of the chemical composition of the binder and aggregate fraction. The methods of false color imaging, blind separation, and self-organizing maps were applied and their results are discussed in this paper. In particular, the method based on the use of self-organizing maps gives well interpretable results in very short times, without any reduction in the dimensionality of the system.

In the occasion of the celebrations for the 150th anniversary of the founding of Italy (1861-2011), it was decided to analyse the artwork "The Italian Flag" (La Bandiera Italiana) created by the artist Fernando Melani (Pistoia, 1907-1985), one of the precursors of the Poor Art artistic movement in Italy. This project is a follow-up to a previous study which was mainly focused on the pigments and dyes found in his home-studio. The main goal of this paper is to identify a correct diagnostic plan, based on the use of a combination of non-invasive and micro-invasive methodologies, in order to determine the state of preservation and define the best conservation procedures for a contemporary artwork. Visible, infrared and infrared false colour images as well as the Fibre Optic Reflectance Spectroscopy (FORS) technique were applied in situ to analyse The Italian Flag. Laser Induced Breakdown Spectroscopy (LIBS), Fourier Transform Infrared (FT-IR) and micro-Raman spectroscopies, Pyrolysis-Gas Chromatography/Mass Spectroscopy (Py-GC/MS), High Performance Liquid Chromatography with Diode Arrays Detection (HPLC-DAD) and Mass Spectrometric Detection (HPLC-ESI-Q-ToF) were all applied to three small samples detached from the three painted (green-blue, white and red-yellow, respectively) areas of the flag. The combination of the data obtained with all these techniques made possible a comprehensive understanding of both the chemical composition and physical behaviour of the materials used by the artist and supported curators in defining the preventive conservation of this artwork., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Limits of detection have been studied for several elements in aluminium and steel alloys, at atmospheric pressure in air, by use of the single and collinear double-pulse configurations of laser-induced breakdown spectroscopy. For this purpose, calibration plots were constructed for Mg, Al, Si, Ti, Cr, Mn, Fe, Ni, and Cu using a set of certified aluminium alloy samples and a set of certified steel samples. The investigation included optimization of the experimental conditions to furnish the best signal-to-noise ratio. Inter-pulse delay, gate width, and acquisition delay were studied. The detection limits for the elements of interest were calculated under the optimum conditions for the double-pulse configuration and compared with those obtained under the optimum conditions for single-pulse configuration. Significantly improved detection limits were achieved, for all the elements investigated, and in both aluminium and steel, by use of the double-pulse configuration. The experimental findings are discussed in terms of the measured plasma conditions (particle and electron density, and temperature).

The influence of crater depth on plasma properties and laser-induced breakdown spectroscopy (LIBS) emission has been evaluated. Laser-induced plasmas were generated at the surface and at the bottom of different craters in a copper sample. Plasmas produced at the sample surface and at the bottom of the craters were spatially and temporally resolved. LIBS emission, temperature, and electronic number density of the plasmas were evaluated. It is shown that the confinement effect produced by the craters enhances the LIBS signal from the laser-induced plasmas.

The concentration of the main minerals present in human hair is measured on several subjects by Calibration-Free Laser-Induced Breakdown Spectroscopy (CF-LIBS) and compared with the results obtained through a commercial analytical laboratory. The possibility of using CF-LIBS for mineral analysis in hair is discussed, as well as its feasibility for the fast and inexpensive determination of the occurrence of heavy-metal poisoning in hair.