Far-infrared spectra in the range from 600 to 20 cm-1 of two hydrophilic (1-ethyl-3-methylimidazolium tetrafluoroborate and 1-butyl-3-methylimidazolium tetrafluoroborate) and one hydrophobic (1-butyl-3-methylimidazolium hexafluorophosphate) ionic liquids and their mixtures with water at different concentrations are reported. Shifts of the librational water bands depending on the nature of the anion are found to be related to the strength of the interaction between the water molecules and the anions. For both hydrophilic ionic liquids, the librational band is centered around 460 cm-1, whereas for the hydrophobic ionic liquid, it is shifted to 388 cm-1, indicating less hindered rotation of single water molecules. Multivariate curve resolution, paying special attention to the spectral range from 50 to 350 cm-1, was used to investigate the presence of different species with increasing water concentration. For both hydrophilic ionic liquids, a band located at 153 cm-1 was resolved into two different contributions. A small contribution at 202 cm-1 can be attributed to intermolecular interactions between water molecules forming dimers. The major contribution (centered at 148 cm-1) corresponds to water molecules that do not bond to each other via H-bonding. It is therefore assigned to a hindered translation arising from the stretching of the hydrogen bond between BF4- anions and water molecules. Formation of water dimers in the hydrophobic ionic liquid does not occur. Furthermore, the spectral contribution of the stretching of H-bonds between water molecules and PF6- cannot be unambiguously detected, which indicates an extremely weak interaction between water molecules and this anion.

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A totally non-invasive in situ investigation in one of the main halls of the Palace of the Lions in the Alhambra (Granada, Spain) has been carried out. Analyses were made with a fiber-optic portable Raman microspectrometer placed on scaffolding platforms at a height of ca. 12 m above the ground level during the period of conservation works. The objects of this study are the decorated plasterworks in the seven vaults of the Hall of the Kings. Together with the results, the different practical problems related to the positioning of the instrumental setup and the influence of the local environment during the analysis are discussed. In general, high quality spectra were obtained despite difficulties for micro-probe head positioning and sometimes the vibrations of the corresponding scaffold. Different typical antiquity pigments have been identified: cinnabar, minium, carbon black and lapis lazuli. Furthermore, the luminescence pattern from lapis lazuli found in most blue decorations has allowed the establishment of the natural origin and provenance of the pigment. Apart from this natural lapis lazuli, synthetic ultramarine blue was also found in one of the vaults showing up a recent restoration. In addition, some degradation products of cinnabar and minium were identified, with the major advantage of providing real-time information to the conservators during their work.

FTIR spectroscopy has been used to monitor and determine the degree of crystallisation in a sample of polyhydroxybutyrate-co-14%valerate (PHB-co-14%HV). Time series spectra of solution-cast films of the polymer revealed spectral changes attributed to the onset of crystallisation. Curve fitting was used to obtain an absolute measure of crystallinity. Mean centred principal-component analysis (PCA) revealed that 99.9% of the spectral variance could be attributed to factor 1. The loadings plot for factor 1 contained features attributable to crystalline and amorphous phases. These features were opposite in sign, indicating that changes in the spectra with the onset of crystallisation are simultaneous and opposite in direction, i.e. as the crystalline band increases the amorphous band decreases. Cross-peaks in asynchronous 2D correlation maps indicate there are likely to be very minor components that are changing out of phase. The presence of these minor components is supported by examination of the loadings of higher factors in the PCA model. PCA has been shown to be suitable for determining the number of dynamic spectral features and has enabled relative and objective monitoring of crystallisation kinetics.

This work presents the results of the study of plasterwork decorations located on the stalactite vaults of the Hall of the Kings in the Alhambra (Granada, Spain) by means of Raman micro‐spectroscopy. Field investigations were carried out in situ using a portable Raman spectrometer during a conservation campaign in a completely non‐invasive manner. In addition, taking into account the results obtained, a well‐directed sampling was carried out to obtain complementary information by means of laboratory studies. Despite several practical problems during the non‐invasive field studies (like difficulties for probe positioning and vibrations of the scaffolding), almost all the pigments present in the decorations of the Hall were identified using excitation at 785 nm: cinnabar, minium, carbon black, natural lapis lazuli and synthetic ultramarine blue. In addition, evidence of different degradation mechanisms of the red pigments was obtained in situ. On the contrary, the identification of blue‐greenish and green pigments had to be performed on microsamples using a Raman microscope with excitation at 514 nm in the laboratory. In samples with blue and green areas, azurite severely degraded to clinoatacamite was identified. These were probably the remains of the oldest blue decorations. In addition, a technique for green decorations consisting on copper chlorides mixed with a small amount of lapis lazuli was identified. Other degradation products, identified in the laboratory regardless of the color of the pigment, were calcium oxalates. Finally, the laboratory studies also enabled the investigation of the stratigraphy of the pictorial layers. In this way, the presence of re‐decorations with overlaying layers of pigments even of different colors was revealed. Copyright © 2014 John Wiley & Sons, Ltd.

This work explores the application of chemometric techniques to Raman spectra to study aged lipidic paint binders. These binders, commonly known as drying oils, were widely used by artists throughout history both individually and in mixtures. We prepared various model samples of the pure binders (linseed, poppy‐seed and walnut oils and egg yolk) and of binary mixtures thereof. These model samples were left to age naturally for six years and further characterized by Raman spectroscopy. A comparative study of the Raman spectral features before and after ageing process was carried out. This showed changes mainly in the bands located at 1267, 1655 and 3011 cm–1, which correspond to vibrations in cis double bonds. Multivariate analysis was performed by applying principal component analysis and partial least‐squares discriminant analysis on the corresponding Raman spectra to test whether spectral differences allowed samples to be distinguished on the basis of their composition. The CH stretching region was found to be especially useful for discrimination between the different binders. Furthermore, good sensitivity and specificity were found in the discriminant analysis particularly for the identification of binders containing egg yolk. The results of these multivariate analyses demonstrated the potential use of both chemometric approaches in the field of Cultural Heritage for drying oil characterization and identification, and also for gaining a deeper insight into the ageing process. Copyright © 2011 John Wiley & Sons, Ltd.