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Filippo Mangani

Publications and source records attributed to Filippo Mangani.

9 recordsLinked to original sources
PubMed2003

Variable-gradient generator for micro- and nano-HPLC.

A new, simple device generates accurate nano- and microflow rate gradients from any conventional HPLC system. The core of the new device is represented by an electric-actuated, computer-controlled, multiposition HPLC valve. The valve hosts six reservoirs for as many different mobile-phase compositions of increasing strength. A low flow rate stream pushes the weakest solvent through the column as long as required and at the desired flow rate, until the chromatographic run is started. From this time on, the electric actuation allows one to select which reservoir will be on-line with the column and for how long, thus generating a specific solvent gradient, through a sequence of controlled segments of precise mobile-phase composition. This permits one not only to exactly reproduce the programmed slope but also to achieve different gradient shapes (i.e., linear, convex, concave) for different separation needs. The new device has proven to be reliable and reproducible even at the lowest flow rate tested (250 nL x min(-1)) and in different chromatographic conditions.

Journal Article↗
PubMed2003

The weathering of natural and artificial stones in the baroque church of S. Pietro in Valle (Fano-Italy).

The church of San Pietro in Valle in Fano is with good reason considered one of the outstanding examples of baroque art in Central Italy. Currently the church is in a serious degradation status. For this reason, and in order to devise a correct conservative restoration project, a scientific study has been carried out, aimed at characterizing mortars used for the application of marble decorations and the different degradation products occurring in the church (i.e. pulverizations, encrustations, salt efflorescences, and condensation water). In the following, results obtained analyzing the different sample typologies by optical microscopy, X-ray diffraction, electron scanning microscopy with energy-dispersion micro-analytical system, ion chromatography, and head-space solid phase microextraction-gas chromatography-mass spectrometry will be reported.

Architecture↗
PubMed2002

Trace level determination of organophosphorus pesticides in water with the new direct-electron ionization LC/MS interface.

A new LC/MS method for the determination of organophosphorus pesticides in water, based on the use of direct-electron ionization (EI) interface, is presented. Direct-EI is a new device that, in a very simple fashion, couples a nano-HPLC system with a mass spectrometer equipped with electron ionization capability. The nanoscale liquid flow allows for a direct introduction of eluate into the ion source and, after nebulization, for its ionization under typical EI conditions. Library-matchable EI spectra are generated for a choice of full scan or SIM detection of the analytes. In our case, a selection of organophosphorus pesticides, commonly distributed in local sugar beet cultivation, were considered. The new interface permits a very sensitive detection of the analytes in a wide range of linear response (0.09-9 ng). When applied to a real sample, the method allowed detecting four different pesticides at a concentration level of approximately 3 ng x L(-1).

Chromatography, High Pressure Liquid↗
PubMed2002

A simple approach for coupling liquid chromatography and electron ionization mass spectrometry.

A miniaturized, aerosol based interface for directly coupling a liquid chromatograph with a mass spectrometer is presented. The interface is entirely within the electron ionization (EI) source of the mass spectrometer and no additional, external devices are needed. This simple and effective approach exploits micro-flow nebulization technology providing a new interface suitable for a variety of applications of environmental and biological interest. The new interface provides necessary linearity, ruggedness, sensitivity, and reproducibility of response for trace level analysis, and readily interpretable mass spectra for unambiguous identification of unknown compounds of small to medium molecular weight.

Journal Article↗
PubMed2002

Characterization of the surface interacting ability of carbon black by means of electron paramagnetic resonance analysis of adsorbed Cu2+, supported by surface analysis and atomic absorption.

Electron paramagnetic resonance (EPR) has been used to investigate the adsorption capability and the surface interacting ability towards Cu(II) solutions (CuCl2, Cu(NO3)2, CuSO4 in water or ethanol) of various carbon blacks, both graphitized and ungraphitized, selected on the basis of the surface area, namely, Carbograph1 (area = 100 m2/g), Carbograph4 (area = 210 m2/g), and Carbograph5 (area = 560 m2/g), which were indicated as C1g, C4g, C5g (g = graphitized), and C1ng, C4ng, C5ng (ng = ungraphitized). The EPR analysis was supported by surface analysis, for evaluating the surface area, the pore volume and the porosity, and by atomic absorption to obtain the adsorbed Cu(II) amounts. Graphitization provokes a decrease in surface area, but C1g, at low surface area, showed a unexpected increase of the adsorption ability ascribed to the formation of new surface porosity closed by graphite layers. The carbon samples showed a broad unresolved EPR signal due to mobile unpaired electrons in the carbon matrix. Graphitized samples presented a narrower signal than ungraphitized samples, which increases in width with the increase in surface area (with the exception of C5ng due to the high exposition of the wide surface to oxydizing external agents) and upon prolonged thermal treatment. The signal intensity of the carbon paramagnetic centers decreases upon Cu(II) adsorption. Computer aided analysis of the EPR spectra of the solids after Cu(II) adsorption allowed to extract structural information on the Cu-surface site complexes. The Cu2+ ions coordinated with surface polar sites, mainly oxygenated. Adsorption depends on the different Cu(II) salts, caused by the salt solubility and the interacting ability of the counter-ion. In several cases the solutions concentrated in the carbon porosity leading to precipitation of the salt. Ethanol solutions are more adsorbed at the carbon surface than water solutions; Cu(II) partially retains its solvation shell and partially presents electron transfer to the carbon surface. Adsorption is favored to ungraphitized carbons with respect to the graphitized ones due to both the higher surface area, and the higher hydrophilicity of the surface. In summary, these carbon powders, widely used for chromatographic applications, show an adsorption capability towards Cu(II) solutions higher than expected due to both a definite porosity, and the presence of polar groups which are not eliminated with chemical surface treatments.

Carbon↗
PubMed2002

Measurements of chlorofluorocarbons and their replacement compounds at Monte Cimone: results obtained after eighteen months of observations.

Chlorofluorocarbons and their substitutes are anthropogenic compounds strongly involved in global change phenomena. Therefore, their atmospheric mixing-ratios are monitored on a worldwide scale. In order to evaluate source strength of these compounds in Southern Europe, in 1999 a research activity, monitoring these compounds in the atmosphere of the Monte Cimone (MO, Italy) was started. Air samples, collected on a weekly base, were analyzed using a GC-MS methodology recently devised by our group. The reported results, obtained after eighteen months of observation, are relative to four fully halogenated halocarbons and four hydrogenated halocarbons.

Air Pollutants↗
PubMedDate not supplied

New liquid chromatography/electron ionization mass spectrometry methods in water analysis.

A method to extract and analyze organic compounds from water is presented. A solid phase micro-trap (micro-SPE) directly connected to the micro-analytical column is used. Sensibility and specificity needed for trace analysis are guaranteed by mass spectrometric electron ionization (EI) detection. A new micro-HPLC/EI-MS interface called Capillary-EI (Cap-EI) is described. The ultimate evolution of this interface is also presented: in this extremely simplified interface the analytes are nebulized, vaporized and ionized in the small volume of the ion source. This interface, called Direct-EI, exploits nano- and micro-HPLC columns with a mobile phase flow rates ranging from 0.3 to 1.5 microL/min. Contemporary use of micro SPE, Cap-EI or Direct-EI gives us a powerful technique to identify and quantify organic pollutants at part per billion level (ppb).

Chromatography, High Pressure Liquid↗