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Although many prominent artists have experimented with pastels, this technique has been the subject of very limited scientific research. The first known recipes of pastels date back to the 16th century, but only during the 18th century did the pastel technique become more common. Identifying and characterising the organic constituents in pastels materials is challenging given that they are present in extremely low concentrations and could be produced using many organic substances, whose chemical composition alters during ageing. The chemical-physical behaviour of organic media in artworks is often crucial in causing the degradation problems, which need to be addressed by conservation. We evaluated the applicability of an analytical approach based on chromatography and mass spectrometry to investigate the composition of the pastels used by Umberto Boccioni in a drawing dated 1908 and conserved at the Museo del Novecento in Milan (Italy). The investigation of the formulation of artists’ pastels used in the first decade of the 20th century is particularly important in order to improve the knowledge of this technique. The analysis highlighted the presence of proteins and plant gums in the artwork samples, with differences in the composition for the different samples.

We investigated the cedar wood doors of the Bahia Palace in Marrakesh (Morocco), which are richly decorated with geometric motifs. A gas chromatographic mass spectrometric analytical procedure (GC/MS) was used to characterize the organic binders in micro samples collected from one of the doors. In order to examine the artist's palette, X-ray fluorescence (XRF), Raman and Fourier transform infrared spectroscopy (FTIR) and high performance liquid chromatography (HPLC-DAD), were applied to samples in fragments or on cross-sections of the embedded samples. This multi analytical approach effectively identified the polychrome decoration technique, mainly based on the use of animal glue as a proteinaceous binder, and characterized the superficial varnishes. Lastly many of the different pigments used for the creation of these works of art were identified. We believe that this study contributes significantly to the knowledge of Moroccan art from a material and technological point of view.

In this paper we present a new analytical GC/MS method for the analysis of mixtures of free fatty acids and metal soaps in paint samples. This approach is based on the use of two different silylating agents: N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) and 1,1,1,3,3,3-hexamethyldisilazane (HMDS). Our experimentation demonstrated that HMDS does not silylate fatty acid carboxylates, so it can be used for the selective derivatization and GC/MS quantitative analysis of free fatty acids. On the other hand BSTFA is able to silylate both free fatty acids and fatty acids carboxylates. The reaction conditions for the derivatization of carboxylates with BSTFA were thus optimized with a full factorial 32 experimental design using lead stearate and lead palmitate as model systems. The analytical method was validated following the ICH guidelines. The method allows the qualitative and quantitative analysis of fatty acid carboxylates of sodium, calcium, magnesium, aluminium, manganese, cobalt, copper, zinc, cadmium, and lead and of lead azelate. In order to exploit the performances of the new analytical method, samples collected from two reference paint layers, from a gilded 16th century marble sculpture, and from a paint tube belonging to the atelier of Edvard Munch, used in the last period of his life (1916–1944), were characterized.

In this paper we present the technical study of protein-drying oil mixtures in the paint formulation of original manufacturers paint tubes from Fabbrica di colori per Belle Arti Maimeri dating back to the 1950s. The study is part of a wider research project aimed at understanding the chemistry of protein-drying oil mixtures, and how the oil curing in the presence of proteins may affects the protein analysis with mass spectrometric based techniques. Tempera grassa, according to traditional Late Medieval and Renaissance painting techniques, entails the use, as paint binder, of a mixture of a drying oil with a water miscible medium, commonly egg. The paints analysed in this study were, according to technical documentation available at the manufacturer, based on a mixture of linseed oil, ovalbumin and mastic resin. All the components of the paints were detected but proteins proved very challenging. They could not be detected by pyrolysis coupled to gas chromatography-mass spectrometry, nor by using classical procedures for gas chromatography – mass spectrometry analysis of amino acids after hydrolysis. A new analytical procedure based on two subsequent hydrolysis steps assisted by microwaves was implemented and proved to be successful. The first step with trifluoroacetic acid was aimed at a partial hydrolysis of proteins into peptides, for their efficient extraction. The second with hydrochloric acid in the vapour phase was used for a complete hydrolysis of peptides into amino acids for the GC–MS analysis. Linking experimental results on the tempera grassa paints to data obtained on the curing of oil/protein mixtures in paint mock-ups, the hypothesis that copolymerisation of proteins and the oil has taken place is proposed, and a discussion on how this may affect protein detection is carried out.

International audience; The huge number of complex formulations of synthetic dyes and pigments commercialized in the 19th century makes their comprehensive characterization both difficult and fundamental for their successful identifications in artworks. The description of the exact starting composition of a wide collection of reference materials is preliminary to the study of the challenging photo-degradation processes in which most of the early synthetic dyes and pigments are involved. In this paper, four eosin-based lakes, all containing eosin Y, and one also containing eosin B, but differing in the organic and inorganic materials used as fillers, were fully characterized. These formulations were reconstructed on the base of historical recipes from the extensive Wiesel's collection, dated to the 19th century and bought by Dr Kremer (Kremer Pigmente, Germany) in the 1990s. The composition of each formulation was characterized by Fourier transform infrared spectroscopy (FT-IR) and luminescence spectroscopy was used as a probe for their inert-distinction. Reference paint layers were then prepared by casting the lakes in linseed oil, and their ageing and impact on color change was monitored for one year by analyzing two sets of paint model systems by colorimetry. For each system, two sets were prepared and one was stored in the dark while the other exposed to natural light. The material distribution and homogeneity of the samples were tested by Synchrotron Radiation based micro infrared spectroscopy (SR-μ-FT-IR). Finally, an ultra-sensitive method based on Liquid Chromatography coupled with High Resolution Mass Spectrometry (LC-HRMS) allowed us to characterize eosin degradation products detected but never identified before, and to evaluate their kinetics of formation.

For more than a century, the analyses of painting fragments have been carried out mainly through the preparation of thick resin-embedded cross-sections. Taking into account the development of innovative micro-analytical imaging techniques, alternatives to this standard preparation method are considered. Consequently, dedicated efforts are required to develop preparation protocols limiting the risks of chemical interferences (solubilisation, reduction/oxidation or other reactions) which modify the sample during its preparation, as well as the risks of analytical interferences (overlap of detected signals coming from the sample and from materials used in the preparation). This study focuses particularly on the preparation of thin-sections (1–20 μm) for single or combined fourier transform infrared (FTIR) spectroscopy and X-ray 2D micro-analysis. A few strategies specially developed for the μFTIR analysis of painting cross-sections have already been reported and their potential extrapolation to the preparation of thin-sections is discussed. In addition, we propose two new specific methods: (i) the first is based on a free-embedding approach, ensuring a complete chemical and analytical neutrality. It is illustrated through application on polymeric design objects corpus; (ii) the second is based on a barrier coating approach which strengthens the sample and avoids the penetration of the resin into the sample. The barrier coating investigated is a silver chloride salt, an infrared transparent material, which remains malleable and soft after pellet compression, enabling microtoming. This last method was successfully applied to the preparation of a fragment from a gilded Chinese sculpture (15th C.) and was used to unravel a unique complex stratigraphy when combining μFTIR and μXRF.

In the Comment by Dr. I. Rabin from Bundesanstalt fur Materialforschung und -prufung in Berlin are stated many conjectures and apparent guesses contradicting several of our interpretations. Most of Rabin's ‘guesses’ and interpretations are unwarranted. Below we rebut some of the misinterpretations under separate headings.

This paper presents the results of an investigation of organic binding media detected in samples from the Mycenaean wall-paintings at the “Palace of Nestor” in Pylos (Western Messenia, Greece): samples dated from the Late Bronze Age (ca. 1200 BC). This is the first scientific study to be conducted on organic binding media in Mycenanean painting, and it is a study that aims to contribute significantly towards our understanding of the original painting techniques used during the Bronze Age. The analytical procedures employed for the detection and characterization of the organic substances preserved within the paint layers (proteinaceous materials, lipids and plant gums), were based on chromatography/mass spectrometry techniques (PY–GC/MS, GC/MS). The most significant results, highlighting an a secco painting technique, are herein reported and discussed.

This paper presents an analytical GC-MS procedure to study the chemical composition of plant gums, determining aldoses and uronic acids in one step. The procedure is based on the silylation of aldoses and uronic acids, released from plant gums by microwave assisted hydrolysis, and previously converted into the corresponding diethyl-dithioacetals and diethyl-dithioacetal lactones. Using this method only one peak for each compound is obtained, thus providing simple and highly reproducible chromatograms. The analytical procedure was optimised using reference samples of raw plant gums (arabic, karaya, ghatti, guar, locust bean and tragacanth, cherry, plum and peach gums), commercial watercolours and paint layers prepared according to ancient recipes at the Opificio delle Pietre Dure of Florence (Italy). To identify gum media in samples of unknown composition, a decisional schema for the gum identification and the principal component analysis of the relative sugar percentage contents were employed. The procedure was used to study samples collected from wall paintings from Macedonian tombs (4th-3rd centuries bc) and from the Mycenaean "Palace of Nestor" (13th century bc) in Pylos, Greece. The presence of carbohydrates was ascertained and plant gum binders (fruit and a mixture of tragacanth and fruit tree gums) were identified in some of the samples.

Journal of cultural heritage - In Press.Proof corrected by the author Available online since lundi 18 mars 2013