Nagore Prieto-Taboada

Raman spectra of the different phases in the CaSO4-H2O system.

Although it is known that the CaSO4/H2O system is formed by at least five different phases, this fact is not correctly documented in Raman spectroscopy studies. The main problem detected in the literature was the incorrect definition of the anhydrite, which produced the assignation of different spectra for a single compound. In this sense, two different spectra were clearly identified from the bibliography, which showed different main Raman bands at 1017 or 1025 cm(-1), although anhydrite could be present even as three different polymorphous species with different structures. A better understanding of the whole system obtained from a review of the literature allowed new conclusions to be established. Thanks to that revision and the development of different thermodynamical experiments by Raman spectroscopy, the Raman spectra of each phase were successfully identified for the first time. In this way, the main Raman bands of gypsum, bassanite, anhydrite III, anhydrite II and anhydrite I were identified at 1008, 1015, 1025, 1017 and 1017 cm(-1), respectively. To conclude this work, the contradictions found in literature were critically summarized.

Buildings as repositories of hazardous pollutants of anthropogenic origin.

In the present work the pollutant content of diverse building materials was evaluated by the combination of spectrometric and chromatographic techniques. A first non-destructive analysis carried out by μ-XRF and Raman spectroscopy revealed a high impact of pollutants, which reached depths higher than 6mm. The quantitative analyses pointed out that black crust as accumulation nucleus where concentration values up to 3408 mg/kg of lead, 752 mg/kg of chromium or 220 mg/kg of arsenic, high amounts of diverse sulphates and nitrates as well as substantial amounts of polycyclic aromatic hydrocarbons (PAHs) of a clear pyrolytic source were determined. On the other hand, samples without black crust showed also a surprising soluble salt content up to 5%. Polychlorinated biphenyls (PCB) were found to be absent in all material types. The chemometric analysis of the quantitative results revealed that the accumulation capacity and the subsequent pollutant content depends on the type of construction materials, being mortars the most susceptible.

Spectroscopic evaluation of the environmental impact on black crusted modern mortars in urban–industrial areas

AbstractA multianalytical characterisation of black crusted modern construction materials from buildings located in the Bilbao Metropolitan area (North Spain) was carried out. According to the mineral composition determined by Raman spectroscopy, calcite and hematite were the major compounds found while aragonite, limonite, rutile, quartz and some aluminosilicates such as obsidian or amazonite (KAlSi3O8) were also present in minor percentages. As deterioration products, gypsum and anhydrite were widely found not only in the surface but also in the inner part of strongly deteriorated samples. Coquimbite (Fe2(SO4)3·9H2O) was identified as well in the most protected facade where high amounts of Fe, having probably an anthropogenic origin, were measured by micro X-ray fluorescence (μ-XRF). Zn was found to be in high amounts while Cu, Pb, Ti, Mn, Sr and K were identified as minor elements. Considering the non-expected concentrations found for some anthropogenic elements, a sequential extraction was carried out in order to determine their chemical form by means of ion chromatography and inductively coupled plasma mass spectrometry. The orientation of the facades, which had a different influence from rain washing and industrial and traffic impact, was shown to affect the accumulation of different compounds in the black crust. Finally, the MEDUSA software was used to simulate the reactions among the original compounds, deposited pollutants and the atmospheric acid gases in order to explain the presence of the decaying species found. FigureMultianalytical Speciation protocol applied on the analysis of modern mortars

Optimization of two methods based on ultrasound energy as alternative to European standards for soluble salts extraction from building materials.

The Italian recommendation NORMAL 13/83, later replaced by the UNI 11087/2003 norm, were used as standard for soluble salts extraction from construction materials. These standards are based on long-time stirring (72 and 2h, respectively) of the sample in deionized water. In this work two ultrasound based methods were optimized in order to reduce the extraction time while efficiency is improved. The instrumental variables involved in the extraction assisted by ultrasound bath and focused ultrasounds were optimized by experimental design. As long as it was possible, the same non-instrumental parameters values as those of standard methods were used in order to compare the results obtained on a mortar sample showing a black crust by the standards and the optimized methods. The optimal extraction time for the ultrasounds bath was found to be of two hours. Although the extraction time was equal to the standard UNI 11087/2003, the obtained extraction recovery was improved up to 119%. The focused ultrasound system achieved also better recoveries (up to 106%) depending on the analyte in 1h treatment time. The repeatabilities of the proposed ultrasound based methods were comparables to those of the standards. Therefore, the selection of one or the other of the ultrasound based methods will depend on topics such as laboratory facilities or number of samples, and not in aspects related with their quality parameters.

In situ X-ray fluorescence-based method to differentiate among red ochre pigments and yellow ochre pigments thermally transformed to red pigments of wall paintings from Pompeii

Most of the magnificent wall paintings from the ancient city of Pompeii are decorated with red and yellow colors coming from the ochre pigments used. The thermal impact of the pyroclastic flow from the eruption of Vesuvius, in AD 79, promoted the transformation of some yellow painted areas to red. In this work, original red ochre, original yellow ochre, and transformed yellow ochre (nowadays showing a red color) of wall paintings from Pompeian houses (House of Marcus Lucretius and House of Gilded Cupids) were analyzed by means of a handheld energy-dispersive X-ray fluorescence spectrometer to develop a fast method that allows chemical differentiation of the original red ochre and the transformed yellow ochre. Principal component analysis of the multivariate obtained data showed that arsenic is the tracer element to distinguish between both red colored ochres. Moreover, Pompeian raw red and yellow ochre pigments recovered from the burial were analyzed in the laboratory with use of a benchtop energy-dispersive X-ray fluorescence spectrometer to confirm the elemental composition and the conclusions drawn from the in situ analysis according to the yellow ochre pigment transformation in real Pompeian wall paintings.

Biodeterioration of Pompeian mural paintings: fungal colonization favoured by the presence of volcanic material residues

This work was focused on the study of the biodegradation processes jeopardizing a mural painting conserved in the basement of Ariadne House (archaeological site of Pompeii, Italy). The fresco stood out for its peculiar state of preservation: the upper part, recovered in 1988, was just barely colonized by microorganisms. On the contrary, the lower part (excavated in 2005) was almost completely covered by extensive biological patinas. The genomic characterization carried out by polymerase chain reaction (PCR) highlighted the presence of seven different fungi strains on the mural surface. Beside, in situ and laboratory analyses were performed with the purpose of identifying the causes of the heterogeneous spatial distribution of the biopatinas. The in situ Raman spectroscopy and energy dispersive X-ray fluorescence (ED-XRF) spectroscopy measurements excluded any link between the heterogeneous colonization and the original materials present in the wall. On the other side, X-ray diffraction (XRD) and scanning electron microscopy (SEM) on microsamples proved the presence of a thin volcanic material layer overlying the lower part of the fresco. Considering that most of the biofilms of the studied mural painting only growth over these residues, it was confirmed the role of volcanic material as a suitable support for biological colonization. Thanks to the obtained results, this research helped to understand more in depth an important degradation pathway threatening the artworks from one of the most important archaeological sites in the world.

Analytical study to evaluate the origin and severity of damage caused by salt weathering in a historical Palace House: the attack of infiltration water

The attack of acid infiltration water on a historical building was thoroughly studied by a combination of ion chromatography, chemometric and thermodynamic chemical modelling. The treatment of the quantitative data points out the formation and damage mechanisms of degradation compounds (salts of nitrates, sulfates and chlorides). The soluble salts content was evaluated by comparison with current guides in order to advise on the required actions of restoration. The results also revealed that the salts followed the Arnold and Zehnders model distribution, by capillarity effect. Using this multianalytical methodology, the principal mechanisms of decay were established.

In situ DRIFT, Raman, and XRF implementation in a multianalytical methodology to diagnose the impact suffered by built heritage in urban atmospheres

AbstractThis work addresses the evaluation of an innovative mutianalytical method to assess the conservation state of a fifteenth century palace house. With the goal of reducing the handicaps of field analysis, the in situ spectroscopic assessment, often based on the use of X-ray fluorescence and Raman spectrometers, was complemented by the use of diffuse reflectance infrared Fourier transform spectroscopy. In this manner, its usefulness as a diagnostic tool to discover the origin and mechanisms of the damage caused by atmospheric and infiltration water attacks were thoroughly examined. Moreover, the study was extended in the laboratory to increase the information obtained by nondestructive techniques. The results revealed a severe material loss caused by soluble salts. Thus, a noninvasive sampling method using cellulose patches was tested to study the amount and mobility of salts by means of ion chromatography. Finally, to establish the chemical degradation processes that are occurring in the palace, a chemometric analysis of the quantitative data as well as the construction of thermodynamic models was done to advise on the required restorative actions. Graphical AbstractThe different phases of the multianalytical method to assess the conservation state of built heritage

Relevance of cross-section analysis in correct diagnosis of the state of conservation of building materials as evidenced by spectroscopic imaging.

In the present work the need to use cross-section analysis as a routine procedure to characterize physiochemical damage on building materials was evaluated using a combination of spectroscopic imaging techniques based on Raman spectroscopy, X-ray fluorescence spectroscopy (XRF), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX). First, samples for cross-section analysis required special preparation to avoid the loss of soluble and weakly anchored compounds and thereby ensure the representativeness of the analysis. To this end, samples were dry drilled and fractured with a single blow rather than cut to avoid friction. Cross-section analysis allowed surface deposition (crusts and patinas) to be differentiated from penetrating pollution and the affected depth to be determined. Elemental and molecular distributions were obtained to establish the origin of the compounds/elements found. Moreover, establishing the depth reached by the pollutant, which depends on the material porosity, can help to determine the physicochemical form of the pollutant. Finally, SEM-EDX images allowed surface and internal cracks, as well as the causes of these physical stresses, to be identified. As a result, surface analysis alone was shown to lead to incomplete or even incorrect conclusions that can be avoided by using cross-section analysis as a routine procedure when assessing the state of conservation of building materials.

Study of the soluble salts formation in a recently restored house of Pompeii by in-situ Raman spectroscopy

The walls and mural paintings of Pompeii exposed directly to the rainfalls are the most impacted in view of the observed decay. However, there are also wall paintings in protected rooms showing evidences of decaying. The aim of this research was to study the salts formed in such protected wall paintings only by non-invasive and in-situ Raman spectroscopy to understand their decaying processes. The perystile of the House of the Gilded Cupids (Regio VI, Insula 16), one of the most important houses of Pompeii was studied. Although an exhaustive restoration was carried out in 2004, a new conservation treatment was needed in 2013 and only two years later, extensive crystallizations of soluble salts were again threatening several of the restored surfaces, thus, the presence of an unsolved degradation pathway was deduced. Thank to the proposed methodology, it was pointed out that the key is the acidified rainfall impact in the non-protected backside of the walls containing the wall paintings. Thus, a new concept in the preservation of the houses of Pompeii is provided, in which the need of the protection of those walls from both sides is suggested to avoid the movement of water through the pores of the walls.