Catalytic fuel cell used as an analytical tool for methanol and ethanol determination. Application to ethanol determination in alcoholic beverages

A small direct catalytic methanol 'fuel cell' was used for analytical purposes. Three different formats were investigated for methanol and ethanol determination: two different Open Circuit Voltage (OCV) formats and a potentiostatic (i.e. amperometric) format; the latter was used if the current supplied by the cell was recorded. The measurement times using one or other of these three formats were much different. The time required by the potentiostatic format was more short for a suitable analytical measurement. The cell was used to check ethanol content in several commercial wine and beer samples and the possibility of using the fuel cell for the analytical measures in real samples, discussed. Lastly the results were compared with those obtained using two conventional amperometric enzyme sensors and statistical tests carried out. (C) 2016 Elsevier Ltd. All rights reserved

Amperometric enzyme sensor to check the total antioxidant capacity of several mixed berries. comparison with two other spectrophotometric and fluorimetric methods

The aim of this research was to test the correctness of response of a superoxide dismutase amperometric biosensor used for the purpose of measuring and ranking the total antioxidant capacity of several systematically analysed mixed berries. Several methods are described in the literature for determining antioxidant capacity, each culminating in the construction of an antioxidant capacity scale and each using its own unit of measurement. It was therefore endeavoured to correlate and compare the results obtained using the present amperometric biosensor method with those resulting from two other different methods for determining the total antioxidant capacity selected from among those more frequently cited in the literature. The purpose was to establish a methodological approach consisting in the simultaneous application of different methods that it would be possible to use to obtain an accurate estimation of the total antioxidant capacity of different mixed berries and the food product

Suitable classification of mortars from ancient roman and renaissance frescoes using thermal analysis and chemometrics

Background Literature on mortars has mainly focused on the identification and characterization of their components in order to assign them to a specific historical period, after accurate classification. For this purpose, different analytical techniques have been proposed. Aim of the present study was to verify whether the combination of thermal analysis and chemometric methods could be used to obtain a fast but correct classification of ancient mortar samples of different ages (Roman era and Renaissance). Results Ancient Roman frescoes from Museo Nazionale Romano (Terme di Diocleziano, Rome, Italy) and Renaissance frescoes from Sistine Chapel and Old Vatican Rooms (Vatican City) were analyzed by thermogravimetry (TG) and differential thermal analysis (DTA). Principal Component analysis (PCA) on the main thermal data evidenced the presence of two clusters, ascribable to the two different ages. Inspection of the loadings allowed to interpret the observed differences in terms of the experimental variables. Conclusions PCA allowed differentiating the two kinds of mortars (Roman and Renaissance frescoes), and evidenced how the ancient Roman samples are richer in binder (calcium carbonate) and contain less filler (aggregate) than the Renaissance ones. It was also demonstrated how the coupling of thermoanalytical techniques and chemometric processing proves to be particularly advantageous when a rapid and correct differentiation and classification of cultural heritage samples of various kinds or ages has to be carried out

Bioethanol in biofuels checked by an amperometric organic phase enzyme electrode (OPEE) working in “substrate antagonism” format

The bioethanol content of two samples of biofuels was determined directly, after simple dilution in decane, by means of an amperometric catalase enzyme biosensor working in the organic phase, based on substrate antagonisms format. The results were good from the point of view of accuracy, and satisfactory for what concerns the recovery test by the standard addition method. Limit of detection (LOD) was on the order of 2.5 × 10−5 M. © 2016 by the authors; licensee MDPI, Basel, Switzerland

Comparison between a direct-flow SPR immunosensor for ampicillin and a competitive conventional amperometric device: analytical features and possible applications to real samples

In this research, we developed a direct-flow surface plasmon resonance (SPR) immunosensor for ampicillin to perform direct, simple, and fast measurements of this important antibiotic. In order to better evaluate the performance, it was compared with a conventional amperometric immunosensor, working with a competitive format with the aim of finding out experimental real advantages and disadvantages of two respective methods. Results showed that certain analytical features of the new SPR immunodevice, such as the lower limit of detection (LOD) value and the width of the linear range, are poorer than those of a conventional amperometric immunosensor, which adversely affects the application to samples such as natural waters. On the other hand, the SPR immunosensor was more selective to ampicillin, and measurements were more easily and quickly attained compared to those performed with the conventional competitive immunosensor

Characterization of Rome’s rainwater in the early of 2018 aiming to find correlations between chemical-physical parameters and sources of pollution: a statistical study

Analysis of rainwater in historical cities plays a key role to save ancient monuments from atmospheric agents. In this study we sampled the Rome’s rainwater from February to July of 2018 and we analysed them to determine their chemical and physical parameters: pH, redox potential, conductivity, temperature, and the concentration of the main inorganic ions (Na+, K+, Ca++, Mg++, F−, Cl−, NO3−, SO4−−). The volume of the daily fallen rainwater, the speed and direction of the wind in the sampling site were also collected. In order to find a correlation between all the above data we used the Principal Component Analysis (PCA). Results evidenced that there aren’t authentic “acid rains” as the minimum pH value that we found is 5.2. In some cases high concentrations of nitrates and sulphates were found with maximum values of 12.4 ppm and 18.7 ppm respectively. We also found no correlation between the rainwater’s composition and the seasonal period; on the contrary, the speed and direction of the wind, especially when coming from the sea or industrial country near Rome, play a noticeable role on the rainwater composition. [Figure not available: see fulltext.] © 2020, The Author(s)

A flow SPR immunosensor based on a sandwich direct method

In this study, we report the development of an SPR (Surface Plasmon Resonance) immunosensor for the detection of ampicillin, operating under flow conditions. SPR sensors based on both direct (with the immobilization of the antibody) and competitive (with the immobilization of the antigen) methods did not allow the detection of ampicillin. Therefore, a sandwich-based sensor was developed which showed a good linear response towards ampicillin between 10-3 and 10-1 M, a measurement time of ≤20 min and a high selectivity both towardsβ-lactam antibiotics and antibiotics of different classes. © 2016 by the author

Applications of biopolymers to processes of environmental control

Two new methods of insolubilizing in cellulose triacetate membranes, natural or synthetic polyelectrolytes, able to bind heavy metal ions, were experimented and discussed. The efficiency of the obtained membranes was tested by monitoring the cupric ion adsorption with a copper ion selective electrode (ISE

Cascade Superfluorescence in Er:YLF

We report the analysis of paired photon pulses arising from two cascading transitions in continuously pumped Erbium-doped YLiF$_4$ 1% and 0.01% crystals at 1.6 K. The dependence of the pulse peak intensity on the squared number of involved Erbium ions, between 10$^{11}$ and 10$^{13}$, definitely identifies the cooperative nature of the two pulsed emissions, that are generated by the subsequent, spontaneous formation of coherent states. The observed fluctuations of the time interval between the paired pulses and, most importantly, its correlation with the second pulse duration, demonstrate that the Erbium ions coherence is indeed seeded by vacuum fluctuations