Acid-base equilibria in organic solvents : Part 2. Cyclic voltammetry in the study of hydrogen-bond formation

The cyclic voltammetric technique is used to study hydrogen-bond formation in some polar organic solvents (S) of electroanalytical interest (1,2-dimethoxy, tetrahydrofuran, dimethylformamide, dimethyl sulphoxide and pyridine). The cathodic shift of the proton reduction caused by stepwise addition of the solvent investigated to a solution of anhydrous perchloric acid in acetonitrile is utilized. The theoretical treatment applied produced evidence that HS⁺ and HS⁺₂ are the only acidic species involved, so that the relevant formation constants can be evaluated. The data obtained mostly compare well with those available in the literature. The features that condition the tendency to hydrogen-bonding and the effect of hydrogen bonding on solvent basicity are discussed.     

Simultaneous determination of concentration,diffusion coefficient and number of electrons for electroactive species by combining suitable electroanalytical measurements

The electroanalytical method described for the simultaneous determination of concentration, the number of electrons involved in the redox process and diffusion coefficient is based on evaluation of the ratios between the currents recorded for the analyte and for an easily standardized reference species dissolved in the same medium. Three different electroanalytical techniques are used in which the currents exhibit, for two techniques at least, different dependences on both the diffusion coefficient and electron number. The approach is applicable to diffusion-controlled processes, regardless of the degree of reversibility involved. Reliability tests with electroactive organic compounds dissolved in dimethyl sulphoxide show that both accuracy and precision are within 10% depending on the chosen combination of techniques.     

Determination of heavy metals in real samples by anodic stripping voltammetry with mercury microelectrodes : Part 1. Application to Wine

Differential-pulse anodic stripping voltammetry with a mercury microelectrode is used for the determination of zinc, cadmium, lead and copper in wine at its natural pH without pretreatment. The effects of the matrix on the stripping peaks are studied in detail by varying the concentration of the metals. Intermetallic (CuZn) interferences and the effects of oxygen are described. The results obtained for the labile metal contents varied from 2 μg l^?1 for cadmium to 148 μg l^?1 for zinc; standard addition plots were linear over about two orders of magnitude above these levels, demonstrating the negligible effect of organic matter. Acidification of the sample with hydrochloric acid to pH 1 allowed the total metal contents to be determined. The reliability of the method was tested by comparison with the results obtained with atomic absorption spectrometry; the differences were within 10–20%.     

Analysis of Roman wall paintings found in Verona

The present paper deals with the analysis of roman wall paintings fragments recovered from twelve buildings of Verona, Italy. The analytical techniques used were Optical Microscopy, Scanning Electron Microscopy (SEM) equipped with an EDS microanalysis detector, Xray powder diffraction (XRD) Fourier Transform infrared spectroscopy (FTIR) and Raman Spectroscopy. The wall preparation generally consisted of three layer: the pictorial layer, an intonachino layer of hydrated lime and a plaster one made of slaked lime and sand. The pigments found in the studied domus are different reflecting the taste and culture of Xa Regio of Italy but also the economical possibilities of the dominus and the building period.     

Analysis of mural paintings in Istria

Fragments of wall paintings from Istria, coming from the Basilica of Guran near Vodnjan, from the cemeterial Church of Saint Simeon in Guran and from the Benedictine monastery of Santa Maria Alta near Bale were studied. The analytical instrumental techniques used were Optical Microscopy, Scanning Electron Microscopy equipped with an EDS microanalysis detector, X Ray diffraction, FTIR infrared Spectroscopy and Raman Spectroscopy. Red and yellow pigments used in Guran and Bale have bean derived from red and yellow istrian bauxites, as already demonstrated for works from 11th to 15th century. The blue pigment found in the paintings of the Bale Chapel is a lapislazzuli blue; this fact confirms the literature data referring to the period from 11th to the 16th century. The materials and pigments used at Bale and Guran fit with the Istrian tradition and history of painting going back to the first Carolingian period.     

An EPR study on ancient and newly synthesised Egyptian blue

Two sets of ancient roman Egyptian blue (EB) samples and one set of EB samples synthesised in our lab, were analysed by EPR spectroscopy, a technique not commonly used in this field. The spectroscopic parameters obtained were used to attempt the discrimination of the provenance and of the manufacturing techniques of the investigated samples.The results obtained show that EPR technique could be very useful for this purpose.Furthermore, the similarity of the obtained parameters between the ancient and new samples testify the successful attempt to reproduce the EB according to the chemical knowledge.     

Acid-base equilibria in organic solvents : Part 3. An Absolute pH Scale from Proton Basicity Evaluated by Cyclic Voltammetry

The relative basicity of some organic solvents of electroanalytical interest (propylene carbonate, sulfolane, 2-methyltetrahydrofuran, methyl formate and morpholine) is evaluated by cyclic voltammetry. Anhydrous perchloric acid is electrogenerated in these solvents and the half-wave potentials of the redox couple H⁺/H₂ are recorded by referring them to a reference system, here bis(biphenyl)chromium (I)/bis(biphenyl)chromium(0), which is independent of the nature of the solvent. The data obtained, together with those found previously for other solvents by following the same procedure, are used to draw an absolute pH scale covering a wide range of basicities from nitromethane to morpholine. The same approach is also utilized to evaluate and compare, on the basis of this absolute pH scale, the strength in the solvents studied of some nitrogen bases which are suitable as titrants in nonaqueous media. The proposed proton basicity scale is compared with other basicity series defined in the literature.     

Electrochemical measurement of mercury concentration profiles in the pore-waters of sediments of the Venice Lagoon by ion-exchange voltammetry at polymer modified electrodes

Glassy carbon electrodes modified with coatings of poly-[1-methyl-3-(pyrrol-1-ylmethyl)pyridinium], poly-MPP, were employed for preconcentrating and detecting the anionic complex HgCl4(2-), which is the prevailing inorganic Hg(II) species in salt waters such as the pore-waters of sediments here examined. The application of ion-exchange voltammetry at poly-MPP coated electrodes in combination with an in situ pore-water sampler allowed the measurement of concentration vs. depth profiles for mercury dissolved in the pore-waters of a salt-marsh and of a mud-flat located in a polluted area of the Venice Lagoon. The trends of the mercury profiles are discussed in comparison with the trends measured from the same location for other trace metals (Zn, Cd, Cu and Pb) and reduced species such as S(-II) and Fe(II).