X-ray diffraction studies of Pompeian wall paintings using synchrotron radiation and dedicated laboratory made systems

The full identification of artwork materials requires not only elemental analysis but also structural information of the compounds as provided by X-ray diffraction (XRD). This is easily done when taking samples (or micro-samples) from artworks. However, there is an increasing interest in performing non-destructive studies that require adapted XRD systems. Comparative study of synchrotron high-resolution X-ray powder diffraction (SR-HRPD) and laboratory non-destructive systems (portable XRD and micro-XRD) is the main objective of this work. There are no qualitative differences among the three systems as for detected phases in the Pompeian wall paintings that were studied, except in the case of minority phases which only were detected by SR-HRPD. The identified pigments were goethite, hematite, cinnabar, glauconite, Pompeian blue, together with calcite, dolomite and aragonite. Synchrotron XRD diagrams show better resolution than the others. In general, the peak widths in the diagrams obtained with the portable XRD system are similar to those obtained by micro-diffraction equipment. Factors such as residual divergence of X-ray sources, incidence angle and slit or collimator size are discussed in relation with the quality of XRD diagrams.     

Studies of LSO:Tb radio-luminescence properties using white beam hard X-ray synchrotron irradiation

A radio-luminescence set-up was installed at the synchrotron light source ANKA to characterise scintillators under the high X-ray photon flux density of white beam synchrotron radiation. The system allows for investigating the radio-luminescence spectrum of the material under study as well as analysing in situ changes of its scintillation behaviour (e.g. under heat load and/or intensive ionising radiation). In this work we applied the radio-luminescence set-up for investigating the radiation damage effects on the luminescence properties of a new kind of thin single crystal scintillator for high resolution X-ray imaging based on a layer of modified Lu₂SiO₅ grown by liquid phase epitaxy on a dedicated substrate within the framework of an EC project (SCIN^TAX).1 The project SCINTAX is funded by the European Community (STRP 033 427), see http://www.scintax.eu.      

Synthesis and fading of eighteenth‐century Prussian blue pigments: a combined study by spectroscopic and diffractive techniques using laboratory and synchrotron radiation sources

Prussian blue, a hydrated iron(III) hexacyanoferrate(II) complex, is a synthetic pigment discovered in Berlin in 1704. Because of both its highly intense color and its low cost, Prussian blue was widely used as a pigment in paintings until the 1970s. The early preparative methods were rapidly recognized as a contributory factor in the fading of the pigment, a fading already known by the mid‐eighteenth century. Herein two typical eighteenth‐century empirical recipes have been reproduced and the resulting pigment analyzed to better understand the reasons for this fading. X‐ray absorption and Mössbauer spectroscopy indicated that the early syntheses lead to Prussian blue together with variable amounts of an undesirable iron(III) product. Pair distribution functional analysis confirmed the presence of nanocrystalline ferrihydrite, Fe₁₀O₁₄(OH)₂, and also identified the presence of alumina hydrate, Al₁₀O₁₄(OH)₂, with a particle size of ～15 Å. Paint layers prepared from these pigments subjected to accelerated light exposure showed a tendency to turn green, a tendency that was often reported in eighteenth‐ and nineteenth‐century books. The presence of particles of hydrous iron(III) oxides was also observed in a genuine eighteenth‐century Prussian blue sample obtained from a polychrome sculpture.     

Preparation, characterization, and property of polyaniline/Prussian blue micro-composites in a low-temperature hydrothermal process

Polyaniline/Prussian blue micro-composites have been synthesized by a low-temperature hydrothermal process. Prussian blue is obtained using the single iron-source precursor K₃[Fe(CN)₆] in acidic aqueous solution. The composite was characterized by field-emission scanning electron microscopy (FE-SEM), Fourier transmission infrared spectroscopy (FT-IR), and X-ray diffractometer (XRD). The magnetic behavior of polyaniline/Prussian blue composites and the effect of the concentration of K₃[Fe(CN)₆] on the morphology of polyaniline/Prussian blue micro-composites have been investigated.     

Shades of green in 15th century paintings: combined microanalysis of the materials using synchrotron radiation XRD, FTIR and XRF

A representative selection of green paintings from fifteenth century Catalonia and the Crown of Aragon are analyzed by a combination of synchrotron radiation microanalytical techniques including FTIR, XRD, and XRF. The green pigments themselves are found to be a mixture of copper acetates/basic copper acetates and basic copper chlorides. Nevertheless, a broader range of green shades were obtained by mixing the green pigment with yellow, white, and blue pigments and applied forming a sequence of micrometric layers. Besides the nature of the pigments themselves, degradation and reaction products, such as carboxylates, formates and oxalates were also identified. Some of the copper based compounds, such as the basic copper chloride, may be either part of the original pigment or a weathering product. The high resolution, high brilliance, and small footprint of synchrotron radiation proved to be essential for the analysis of those submillimetric paint layers made of a large variety of compounds heterogeneous in nature and distribution and present in extremely low concentrations.     

Study of two large-dimension Murillo's paintings by means of macro X-ray fluorescence imaging,point X-ray fluorescence analysis,and stratigraphic studies

During the recent restoration of two large-dimension paintings by Murillo, entitled “Miracle of the loaves and fishes” and “Moses and the water from the rock of Horeb,” several studies about the materials employed for their execution were carried out. Macro X-ray fluorescence scanning technique was performed on both works complemented by point X-ray fluorescence and stratigraphic analyses, in order to characterize the different components of the paintings (i.e., ground layer, pigments, and binders). The results allowed us to better elucidate Murillo painting technique and his creative process. Ground layer was prepared in the usual fashion of the artist, using earths, calcium carbonate, iron oxide pigments, and white lead. The polichromy is composed of lead white mixed with various pigments, depending on the colour tone to be obtained in the pictorial composition: Red and yellow ochres, vermilion, azurite, smalt, and lead-tin yellow were the main pigments identified during our study. Finally, the presence of previous conservation treatments was evidenced by detecting pigments (zinc white, Prussian blue, etc.) not coeval with the artist palette.     

Effect of lateral fluorination in antiferroelectric and ferroelectric mesophases: synchrotron X-ray diffraction,dielectric spectroscopy and electro-optic study

Effect of lateral fluorination in the rigid core on several macroscopic and microscopic properties of a terphenyl based mesogenic chiral ester has been studied by synchrotron X-ray, dielectric and electro-optic techniques. Correlation lengths across the smectic planes, in para-, ferro- and antiferroelectric phases, are found to be significantly less in the fluorinated compound. Para to ferroelectric transition is found to be tricritical in nature in both the compounds. Fluorination resulted in slower response under a square pulse. Collective mode relaxation behaviour, with and without bias field, in all the phases are also found to be different in the fluorinated compound.     

Auger and direct electron spectra in X-ray photoelectron studies of zinc,zinc oxide,gallium and gallium oxide

Auger and direct electron spectra from Zn, ZnO, Ga and Ga₂O₃ have been studied with X-ray photoelectron spectroscopy (ESCA). The chemical shift between zinc electron binding energies in Zn and ZnO is very small, whereas the zinc Auger electron signals are separated by 4.3 eV. In gallium, the oxide and metal signals are separated by 1.9 eV, but the Auger electron energy shift is three times as large. Thus the Auger signals are more sensitive to the chemical environment than the direct electron signals, which is the same relation as earlier observed for copper and copper oxides.     

Radiation source for medical X-ray examination,based on the use of electron radiation during channeling in crystals

One of the possible applications of relativistic electron radiation during channeling in crystals, i.e., the use of radiation for medical visualization, is considered.A setup scheme is proposed, the results of numerical simulation of electron dynamics in crystals and radiation generation and the results of calculations of dose loads are presented.     

Disintegration of hydrogen phases in palladium and titanium during irradiation with a synchrotron radiation bunch in the X-ray spectral region

Data from measurements of the disintegration kinetics of hydrogen phases in palladium and titanium during annealing and irradiation with a synchrotron radiation bunch in the X-ray spectral region on the VEPP-3 LIGA Technology station are presented. The hydride phases in palladium and titanium remain stable at sample temperatures of 60°C and irradiation doses of up to 3000 J cm^?3 during irradiation with a synchrotron radiation bunch and start to decompose during sample heating to a temperature of 90–100°C.     

Observation of cation reordering during the olivine-spinel transition in fayalite by in situ synchrotron X-ray diffraction at high pressure and temperature

The olivine-spinel phase transition in fayalite at high pressure and temperature has been studied using time-resolved x-ray diffraction. Structure refinements show a delay of cation reordering relative to anions during the phase transformation and an increase in the cell volume while the cations reorder into their sites. A significant stress drop in the sample is observed. This experiment, for the first time, quantitatively demonstrates a pseudomartensitic transformation: a diffusionless anion sublattice transition coupled with short-range diffusional cation reordering.     

X-ray synchrotron study of liquid-vapor interfaces at short length scales: effect of long-range forces and bending energies

We have investigated the small-scale structure of the liquid-vapor interface using synchrotron x-ray scattering for liquids with different molecular structures and interactions. The effective momentum-dependent surface energy first decreases from its macroscopic value due to the effect of long-range forces, and then increases with increasing wave vector. The results are analyzed using a recent density functional theory. The large wave-vector increase is attributed to a bending energy for which local and nonlocal contributions are equally important.     

Nuclear Bragg X-ray scattering of synchrotron radiation by57Fe2O3: Methodology and studies of dynamical processes

A program of studies of nuclear Bragg X-ray scattering with⁵⁷Fe₂O₃ at the National Synchrotron Light Source at Brookhaven National Laboratory and at the Cornell University CHESS facility is reviewed. Two main areas, instrumentation development and studies of dynamical diffraction processes, are described. The latter area has included: measurements of the temporal behavior of nuclear collective decay mode and direct observation of polarization mixing. Research performed under the auspices of the U.S. Department of Energy under Contract DE-AC02-76CH00016.     

The vibrational spectra of the cyanide ligand revisited: the ν(CN) infrared and Raman spectroscopy of Prussian blue and its analogues

A careful analysis of the Raman spectra of the M′_x[M(CN)₆]_y Prussian blue species has enabled a general model for the interpretation of the ν(CN) vibrational spectra. The spectral patterns are derived from those of the metal ions with local O_h symmetry. Two limiting models are discussed. A ‘localized mode’ model, involving matrix‐isolated species, is in much better accord with the observations than a ‘factor group’ model. The use of the infrared feature as fingerprint of specific M CN M′ units arises from the axis‐specific nature of individual T_1u modes. The interpretation of the A_1g and E_g Raman features is done in terms of localized vibrations, with involvement of additional energy terms from the lattice motions. Copyright © 2011 John Wiley & Sons, Ltd.     

Chemical, morphological and chromatic behavior of mural paintings under Er:YAG laser irradiation

Several pigments (malachite CuCO₃⋅Cu(OH)₂, azurite 2CuCO₃⋅Cu(OH)₂, yellow ochre (goethite α-FeOOH, gypsum CaSO₄⋅2H₂O), St. John’s white CaCO₃ formed from slaked lime) and respective mural paintings specimens were subjected to the free-running Er:YAG laser radiation in order to study their damage thresholds, in a broad range of laser fluences, both in dry and wet conditions. The specimens’ damage thresholds were evaluated by spectroscopic methods, colorimetric measurements and microscopic observation. The pigments containing –OH groups were found to be more sensitive than St. John’s white; hence the most sensitive paint layers in dry conditions are those containing malachite, azurite (both 1.3 J/cm²) and yellow ochre (2.5 J/cm²) as compared to the ones containing St. John’s white (15.2 J/cm²). The presence of wetting agents (w.a.) attenuated the pigments chemical alteration. The damage thresholds of all the paint layers, in presence of w.a., were found to be around 2.5 J/cm². The alteration was caused by thermo-mechanical damage and by binding medium ablation of a fresco and a secco prepared specimens, respectively.     

Synthesis, crystal structure and blue electroluminescence of a new zinc complex based on 2,6-bis(benzimidazolyl)pyridine

A very stable and blue luminescent complex Zn(bbp)Cl₂ (bbp: 2,6-bis(benzimidazolyl)pyridine) was synthesized. X-ray crystal structural analysis for the complex revealed that there are intermolecular π?π interactions in the solid state. The fluorescence properties for this complex were studied. The similar devices with the structure of [ITO/CuPc(31 nm)/NPB(80 nm)/[Zn(bbp)Cl₂] (or L) (85 nm)/LiF15/Al] were constructed to investigate their electroluminescent performance. Both the complex and the ligand can be fabricated as blue-emitting materials. The complex shows emission peak at 555 nm, electroluminescent efficiency 0.017 cd A⁻¹ and turn-on voltage 7 V, compared to 470 nm, 0.036 cd A⁻¹ and 9 V for the ligand.     

Physicochemical characterization of an Indian traditional medicine, Jasada Bhasma: detection of nanoparticles containing non-stoichiometric zinc oxide

Herbs and minerals are the integral parts of traditional systems of medicine in many countries. Herbo-Mineral medicinal preparations called Bhasma are unique to the Ayurvedic and Siddha systems of Indian Traditional Medicine. These preparations have been used since long and are claimed to be the very effective and potent dosage form. However, there is dearth of scientific analytical studies carried out on these products, and even the existing ones suffer from incomplete analysis. Jasada Bhasma is a unique preparation of zinc belonging to this class. This particular preparation has been successfully used by traditional practitioners for the treatment of diabetes and age-related eye diseases. This work presents a first comprehensive physicochemical characterization of Jasada Bhasma using modern state-of-the-art techniques such as X-ray photoelectron spectroscopy (XPS), inductively coupled plasma (ICP), elemental analysis with energy dispersive X-ray analysis (EDAX), dynamic light scattering (DLS), and transmission electron microscopy (TEM). Our analysis shows that the Jasada Bhasma particles are in oxygen deficient state and a clearly identifiable fraction of particles are in the nanometer size range. These properties like oxygen deficiency and nanosize particles in Jasada Bhasma might impart the therapeutic property of this particular type of medicine. A. C. Joshi: Private Practitioner (Vaidya).     

The impact of infrared synchrotron radiation in biology: Past,present and future

The Synchrotron Radiation Center (SRC) at the University of Wisconsin-Madison was shut down permanently in March 2014. It began operation in 1968 as the world's first dedicated synchrotron radiation user facility. This revolutionary idea of using synchrotron radiation for broad support of science and technology proved a resounding success, and it subsequently led to worldwide development of ever more powerful light sources for R&;D in many major scientific and technical areas. With upgrades and groundbreaking initiatives, SRC remained a cutting-edge and cost-effective facility to the end. SRC filled an important niche for tough experiments that were not possible at the newer facilities, given their beam time constraints. The world of IR, VUV, and soft X-ray research has been diminished by its loss, but its closing was necessitated by higher priorities at the US NSF.     

Degradation of azurite in mural paintings: distribution of copper carbonate, chlorides and oxalates by SRFTIR

This article illustrates the analysis by synchrotron micro-analytical techniques of an azurite painting presenting greenish chromatic degradation. The challenge of the experiments was to obtain the spatial distribution of the degradation products of azurite. Copper hydroxychlorides, carbonates and copper oxalates have been mapped by SR FTIR imaging of cross sections in transmission mode. To complement the information, Py/GC/MS and GC/MS techniques were applied in order to characterize the binding media and organic materials present as well as their degradation products. Results contribute to a better understanding of the decay of blue areas in ancient paintings not only from the particular point of view of azurite weathering, but also by adding information regarding the oxalates’ formation and their distribution in painting samples. Synchrotron radiation demonstrates its capability for the mapping in painting cross sections.     

The integration of nanoscale porous silicon light emitters: materials science, properties, and integration with electronic circuitry

The stability, efficiency, speed, and spectral range of light-emitting devices (LEDs) made of nanoscale porous silicon is improving. The first part of this paper discusses the preparation and properties of nanoscale silicon, with emphasis on porous silicon. In the second part, the properties of LEDs made of porous silicon are reviewed. In the third part, the integration of PSi LEDs with silicon microelectronic circuits is discussed. The paper ends with a short discussion of the prospects for realistic optoelectronic devices.