Isotopic analysis of lead present in the cinnabar of Roman wall paintings from the Xth Regio "(Venetia et Histria)" by ICP-MS

The analysis of Roman wall paintings coming from Verona, Vicenza, Padova, Pordenone and Trieste evidentiated the presence of cinnabar. In this work, the isotopic composition (206)Pb, (207)Pb and (208)Pb of trace of lead present in cinnabar is reported, via ICP-MS measurements. The isotopic ratio values are compared with the values obtained from samples coming from Roman wall paintings of Pompeii and from the mines of Almaden (Spain) Monte Amiata (Grosseto Italy) and Idria (Slovenia). All the isotopic data can be represented by a "field" ranging from Huelva, to Almeria Spanish provinces. This trend could be due to the mixing of cinnabar products treated in Rome.     

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 Roman age wall paintings found in Pordenone, Trieste and Montegrotto

The aim of the present work is the study of many fragments of wall painting from archaeological excavations in three different Roman age sites dating back to the I Century before Common Era: Pordenone (località Torre); Trieste (Crosada) and Padova (Montegrotto). The techniques used were optical microscopy, scanning electron microscopy (SEM), equipped with a EDS microanalysis detector, X-rays powder diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Fourier transform Raman spectroscopy (FT-Raman) and electron paramagnetic resonance (EPR) spectroscopy. The identified pigments were: cinnabar, hematite, celadonite, glauconite, cuprorivaite (Egyptian blue), yellow and red ochre, calcite, limonite, coal black.In general, the mortar preparation did not correspond to the complex procedure suggested by Vitruvius (De Architectura), but generally showed a porous layer, with crushed grains under the pigment layer. In some cases, two superimposed pigment layers were found: yellow superimposed on both red and pink, black on pink, green on black.The slight differences we found in the use of the pigments in the three studied sites might show that the same technology, culture and taste spread all over the Roman Empire in North Eastern Italy (X^a Regio Venetia et Histria).     

Analysis of pigments from Roman wall paintings found in Vicenza

The analysis of about 60 samples of wall paintings was carried out using different chemicophysical techniques: optical microscopy, scanning electron microscopy (SEM) equipped with an EDS microanalysis detector, X-ray powder diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The identified pigments were cinnabar, hematite, red ochre, celadonite, cuprorivaite (Egyptian blue), yellow ochre, goethite and carbon. Only in one case some lead white was found instead. In general, the mortar preparation did not correspond to the complex structure suggested by Vitruvius (De Architectura), but it generally showed a porous layer, with crushed grains under the pigment layer. In certain cases two superposed pigment layers were found: yellow superimposed on both red and pink, black on pink, green on black.     

Analysis of pigments from Roman wall paintings found in the "agro centuriato" of Julia Concordia (Italy)

The analysis of wall painting fragments recovered in the "agro centuriato" of Julia Concordia has been carried out by using Scanning Electron Microscopy equipped with an EDS microanalysis detector (SEM-EDS), Infrared Spectroscopy (FTIR) and X-Ray powder Diffraction (XRD). The pigments used have been identified and the data obtained suggest the presence of three rustic villas richly decorated also with Egyptian blue. The presence of white of aragonite suggest that these villas were decorated during the Imperial Age, in agreement with the recovery of high quality materials and a bronze statue.     

Aragonite Formation in the Chiton (Mollusca) Girdle

In the chitons (Polyplacophora, Mollusca), the body is not entirely protected by the shell. Mineralized spicules or scales often, but not always, decorate the exposed part of the girdle. Here, we report a study on the composition and ultrastructural organization of these mineralized skeletal parts in four different chiton species. In all specimens, the mineral component (97–98 wt‐%) is aragonite, and the organic matrix (2–3 wt‐%) consists of highly glycosylated proteins. X‐Ray diffraction and scanning electron microscopy show that the organic matrix fibers are aligned, morphologically and crystallographically, with the prismatic aragonite crystals. Matrix and mineral are thus clearly related. The matrix–mineral composite bundles are, however, assembled in the various skeletal parts examined with widely different degrees of alignment and order. In the same organism, the crystals are aligned within a range of ±15° in one type of spicule, while they are randomly oriented in another type. The wide heterogeneity in shape, density, and ultrastructure suggests that the girdle mineralized tissues do not fulfill a fundamental role necessary for the survival of the organism. This, together with the lack of chitin in the organic matrix, supports the hypothesis that they evolved separately from the other chiton mineralized tissues, namely the shell plates and teeth.     

Raman spectroscopic analysis of the Maya wall paintings in Ek'Balam, Mexico

Raman spectroscopy has been applied to the examination of wall painting fragments from the archaeological site of Ek'Balam (Yucatán, Mexico). Thirty-three samples have been studied, all originating from room 23 of the Acropolis, and being representative of the painting technique at Ek'Balam during the late Classic Maya period. Several pigments such as haematite, calcite, carbon, cinnabar and indigo were identified in these samples. The latter pigment was presumed to be present as 'Maya blue', which is an intercalation product of indigo and palygorskite clay. The observed Raman spectra are reported and some band assignments have been made. This survey is the first Raman spectroscopic examination of a whole set of pigments in archaeological Maya wall painting fragments.     

Byzantine wall paintings from Mani (Greece): microanalytical investigation of pigments and plasters

The present case study concerns the technology of Byzantine wall paintings from the Mani Peninsula, Greece. An assemblage of 12 Byzantine churches, constructed in the tenth to fifteenth century, was included in an initial analytical survey. Two random samples of wall paintings were taken in each monument in order to study their micro stratigraphy and the composition of pigment and plaster layers. Polished sections were fabricated for examination with optical microscopy and scanning electron microscopy (SEM). Furthermore, selected samples were powdered and analysed with Fourier-transformed infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The analytical results achieved in this case study provided general conclusions concerning painting techniques for wall paintings in a rather provincial area of the Byzantine Empire. The palette comprised mainly earthen pigments like ochres and carbon black but occasionally also other pigments like cinnabar, minium and ultramarine. In view of future studies, a portable X-ray fluorescence analysis (XRF) set-up was tested.     

TG,DTA and X-ray thermodiffraction study of wall paintings from the fifteenth century

Journal of Thermal Analysis and Calorimetry - In this work, it is reported that thermal analysis techniques such as TG, DTA and X-ray thermodiffraction, performed in air or nitrogen atmosphere, are...     

Study of prehispanic wall paintings from Xochicalco, Mexico, using PIXE, XRD, SEM and FTIR

The characterization of samples of painted plasters obtained from the archaeological site of Xochicalco, in Central Mexico, is presented. Elemental concentrations of the painted layers were obtained by using proton induced X-ray emission (PIXE). The main crystalline structures of the samples are identified with the help of X-ray diffraction (XRD), while the microstructure is studied by scanning electron microscopy (SEM). The information resulting from the application of these three techniques is used to achieve more accurate values for the elemental concentrations. Additional data regarding organic components of the paintings was obtained through Fourier transform infrared spectrometry (FTIR). Although the latter results only provided reliable data on inorganic components, they help to clarify the results from XRD and confirm those of SEM.     

The degradation of wall paintings and stone: Specific ion effects

Salts are ubiquitous both on the surface and in the porous network of works of art such as wall paintings and stone. Cyclic solubilization and crystallization takes place with fluctuating environmental conditions, inducing mechanical stress in the pores and the flaking of the artistic surface. The preventive conservation of precious cultural heritage would thus benefit from models able to describe quantitatively the behavior of electrolyte solutions. Besides the pore size distribution of the wall, cyclic crystallization depends on relative humidity and temperature. Whereas the behavior of single salts' solutions is known, that of mixed solutions (commonly found on artifacts) is still an open issue, owing to the specific interactions of counterions and coions. Classical theories of electrolytes need many fitting parameters to provide predictive and quantitative information, and research focuses on matching phenomenological set of rules with models that take into account quantum mechanical dispersion forces. Classical models have been used so far to describe the behavior of some mixed salts' solutions commonly found on murals and stone, in terms of their RH_eq, which is the relative humidity of air in equilibrium with the saturated solution. Results indicate that environmental conditions deemed safe in the presence of single salts, represent indeed a threat to artifacts in the presence of mixed solutions, with other deviations due to the fact that the crystallization of salts takes place within mesoporous networks. We hope that the reviewed results might contribute a stimulus for further reanalysis of the degradation of works of art, where the synergistic effect of counterions and coions are taken into account. Such interpretation of the artifacts' degradation has been so far overlooked in preservation studies.     

Experimental and computational studies of the metal-metal stretching vibration in X(3)MMX(3) compounds (X = alkoxide, alkyl, amide)

Raman spectra of a number of triply bonded M(2)X(6) (M = Mo, W; X = alkoxide, alkyl) compounds have been obtained. Several exhibit a band assignable to the metal-metal stretching vibration nu(M)(M). This band was not identified in earlier studies of the M(2)(NMe(2))(6) compounds. We have attempted to correlate the Raman vibrational data with structural data from single-crystal X-ray diffraction studies. Diffraction studies of the M(2)(O-1-4-pentyl[2.2.2]bicyclooctyl)(6) species show a crowded environment around the dimetal core, but the M-M-O angles differ substantially from 90 degrees. Thus, this angle does not solely determine the extent to which the metal-metal and ligand-based vibrational modes couple and, in turn, our ability to observe nu(M)(M). Computational studies of model systems confirm the assignment of the band as being nu(M)(M), although the predicted vibrational energies are consistently too high by ca. 7%. The computational results suggest that a nu(M)(M) band may be present in the published spectra of the M(2)(NMe(2))(6) pair.     

Highly Dispersed X/SiO(2) and C/X/SiO(2) (X=Alumina, Titania, Alumina/Titania) in the Gas and Liquid Media

Fumed oxides, such as silica, alumina, titania, and mixed X/silicas (X=Al₂O₃ (AS), TiO₂ (TS), CVD-TiO₂, Al₂O₃/TiO₂ (AST)), pristine or covered by carbon deposits formed due to pyrolysis of cyclohexene, were studied using nitrogen adsorption–desorption, photon correlation spectroscopy particle sizing, and electrophoresis. A significant influence of the nature of surface-active sites and structural features of oxides (individual silica, mixed fumed, or prepared using chemical vapor deposition (CVD)) on the pyrolysis of cyclohexene is observed with respect to the pore size distributions due to differences between primary particles in aggregates and on their outer surfaces in the filling of channels by pyrocarbon, resulting also in a decrease in fractal dimension. Structural characteristics and dependences of the particle size distribution and electrokinetic potential of X/SiO₂ and C/X/SiO₂ on the pH of aqueous suspensions suggest that the carbon deposit covers mainly acidic sites at the X/SiO₂ interfaces and X phase patches possessing catalytic activity in pyrolysis, as the negative charge of particles is reduced by pyrocarbon grafting.     

Ultrafast photochemical dissociation of an equatorial CO ligand from trans(X,X)-[Ru(X)2(CO)2(bpy)] (X = Cl, Br, I): a picosecond time-resolved infrared spectroscopic and DFT computational study

Ultrafast photochemistry of the complexes trans(X,X)-[Ru(X)(2)(CO)(2)(bpy)] (X = Cl, Br, I) was studied in order to understand excited-state reactivity of equatorial CO ligands, coordinated trans to the 2,2'-bipyridine ligand (bpy). TD-DFT calculations have identified the lowest electronic transitions and singlet excited states as mixed X -->bpy/Ru --> bpy ligand to ligand/metal to ligand charge transfer (LLCT/MLCT). Picosecond time-resolved IR spectroscopy in the region of nu(CO) vibrations has revealed that, for X = Cl and Br, subpicosecond CO dissociation is accompanied by bending of the X-Ru-X moiety, producing a pentacoordinated intermediate trans(X,X)-[Ru(X)(2)(CO)(bpy)]. Final movement of an axial halide ligand to the vacant equatorial position and solvent (CH(3)CN) coordination follows with a time constant of 13-15 ps, forming the photoproduct cis(X,X)-[Ru(X)(2)(CO)(CH(3)CN)(bpy)]. For X = I, the optically populated (1)LLCT/MLCT excited state undergoes a simultaneous subpicosecond CO dissociation and relaxation to a triplet IRuI-localized excited state which involves population of an orbital that is sigma-antibonding with respect to the axial I-Ru-I bonds. Vibrationally relaxed photoproduct cis(I,I)-[Ru(I)(2)(CO)(CH(3)CN)(bpy)] is formed with a time constant of ca. 55 ps. The triplet excited state is unreactive, decaying to the ground state with a 155 ps lifetime. The experimentally observed photochemical intermediates and excited states were assigned by comparing calculated (DFT) and experimental IR spectra. The different behavior of the chloro and bromo complexes from that of the iodo complex is caused by different characters of the lowest triplet excited states.     

Byzantine wall paintings from Kastoria, northern Greece: spectroscopic study of pigments and efflorescing salts

This study concerns the investigation of pigments and efflorescence phenomena on the wall paintings of Kastoria, a rural, non-metropolitan Byzantine town. A large number of representative samples were collected from the murals of three churches, dated to post-Byzantine era (14th-17th c. AD). The identified pigments for the red colour were hematite (Fe2O3), cinnabar (HgS) and minium (Pb3O4), while brown and yellow colours were attributed to mixtures of ochres (Fe-oxides and hydroxides) and lime. The utilization of admixtures of iron, lead and mercury compounds was also attested in order to render specific tones on the painted surfaces. Black and dark blue hues were prepared using black carbon and Mn in some cases. Grey colours were assigned to a mixture of black carbon and lime. Green colour is rather attributed to admixtures of Fe-rich minerals and lime and not to the commonly used green earths. Baryte (BaSO4) was also evidenced as a filler or extender. Phosphorous was detected and connected to proteinaceous material and Mo and Sb were traced which are probably affiliated to Fe-oxides. Regarding efflorescing salts, the determined compounds are: calcite, dolomite, gypsum, halite, nitratine, natron and mirabilite, all of which are related to temperature and humidity changes and moisture fluctuations inside the wall paintings.     

Polysulfur nitride, (SN)X,the first example of a polymeric metal

Summary Polymeric sulfur nitride, (SN) _x , is an unusual substance, which although composed of non-metallic elements exhibits metallic properties and even becomes superconducting at very low. temperatures (0.3 K). The bonds between the polymeric chains are much weaker than within the chains. Therefore all electrical and mechanical properties are highly anisotropic. The preparation and crystal structure is described and a review is given of the physical investigations, especially of the electrical and optical properties and of the lattice dynamics. Parallels are drawn to the properties of organic polymers.

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Zusammenfassung Polyschwefelnitrid, (SN) _x , ist eine ungewöliche Substanz, die, obwohl aus zwei Nichtmetallen aufgebaut, metallische Eigenschaften besitzt und bei sehr tiefen Temperaturen (0.3 K) sogar supraleitend wird. Die Bindungen zwischen den Ketten sind viel schwächer als die innerhalb der Ketten. Deshalb sind alle elektrischen und mechanischen Eigenschaften stark anisotrop. Es werden die Herstellung und die Struktur der Kristalle beschrieben und ein Überblick über die vorliegenden physikalischen Untersuchungen gegeben, insbesondere zu den elektrischen und optischen Eigenschaften und zur Gitterdynamik. Vergleiche werden gezogen zu den Eigenschaften organischer Polymere.

     

Three-coordinate [Cu(II)X(3)](-) (X=Cl, Br), trapped in a molecular crystal

Mixtures of [Ph(3)PNPPh(3)](+)Cl(-) with CuBr(2) (or CuBr(2)+CuCl(2)) in ethanol/dichloromethane yield crystals containing three-coordinate copper(II) with mixed chloride and bromide ligands, namely [Ph(3)PNPPh(3)](+)[CuCl(0.9)Br(2.1)](-) (1) and [Ph(3)PNPPh(3)](+)[CuCl(2.4)Br(0.6)](-) (2). The trigonal-planar coordination of copper(II) is angularly distorted but unambiguous, as there is no other halide ligand within 6.7 A of the copper atom. Density functional theory (DFT) calculations on planar [CuClBr(2)](-) show that the energy surface for angle bending is very soft. Crystallisation in the presence of CH(3)CN yields [Ph(3)PNPPh(3)](+)[CuCl(0.7)Br(2.3)(NCCH(3))](-) (3), in which there is additional secondary coordination by NCCH(3) (Cu-N 2.44 A). DFT calculations of the potential energy surface for this secondary coordination show that it is remarkably flat (<3 kcal mol(-1) for a variation of Cu-N by 0.8 A). The crystal packing in 1, 2 and 3, which involves multiple phenyl embraces between [Ph(3)PNPPh(3)](+) ions and numerous C-H...Cl and C-H...Br motifs, is associated with intermolecular energies that are larger than the variations in intramolecular energies. For reference, the crystal structures of [Ph(3)PNPPh(3)(+)](2)[Cu(2)Cl(6)](2-) (4) and [Ph(3)PNPPh(3)(+)](2)[Cu(2)Br(6)](2-) (5) are described. We conclude 1) that three-coordinate copper(II) with monatomic halide ligands, although uncommon, can be regarded as normal, 2) that steric control by ligands is not necessary to enforce three-coordination, 3) that a hydrophobic aryl environment stabilises [Cu(Cl/Br)(3)](-), and 4) that the energy change in the transition from three- to four-coordinate copper(II) is very small (ca 5 kcal mol(-1)).     

A vibrational analysis of the (X2O)2(g) (X=H,D, T) isotopomeric species

Harmonic vibrational analysis is carried out for the water dimer (¹H or natural isotopic mixture) and its²D and³T isotopomers in the gas phase, using the recently designed flexible potential energy functions. The results represent the most complete and reliable theoretical evaluation of the vibrational frequencies, directly applicable to various observation interpretations. The complete data set can also be useful for a more general isotopomeric reasoning.     

Initial Stage of Mechanical Alloying in Fe(80)X(20) (X = Mo, W) Systems

The kinetics of an initial stage of mechanical alloying in Fe/Mo and Fe/W (80 : 20, at. %) systems was studied by X-ray diffraction and Mössbauer spectroscopy. It was established that, upon mechanical treatment, X (Mo, W) passes into the Fe lattice to form an -Fe(X) solid solution, and a phase of pure iron exists in the systems for a long time together with the forming solution. The reverse dissolution (Fe in the X lattice) did not occur. Quantitatuve characteristics of the process (work of formation of intergrain surface and energy yields of the consumption of initial components and formation of a solid solution) were estimated in the energy units. It was shown that, upon annealing, a supersaturated solid solution separates into a solution with the equilibrium concentration X, an intermetallic compound Fe₇X₆, and an amorphous phase (the effect of inverse melting).