Micro‐Raman innovative methodology to identify Ag–Cu mixed sulphides as tarnishing corrosion products

Mixed Cu–Ag alloys with different compositions have been produced and subjected to an accelerated sulphidation process which causes the development of a mixed sulphide‐rich corroded film on their surface. It was called tarnishing, that is, the formation of a blue‐brownish patina when Cu–Ag alloys are exposed in a sulfur‐containing atmosphere. The structures of the pristine alloys have been determined by the combined analytical techniques as scanning electron microscopy energy dispersive X‐ray microanalysis and X‐ray diffraction. The experimental conclusions confirmed the occurrence of micro phase separation with the formation of different dendritic domains of about 10 µm in width. The sulphidized samples were firstly investigated by optical microscopy and X‐ray diffraction in order to verify the homogeneity of the patina and to identify the different AgCuS phases appearing on the alloy surfaces. It was observed that, despite the inherent micro‐heterogeneity of the alloys, the sulphide layer was throughout uniform in composition at the micro‐scale. The complex scenario of the relative stability of all the various mixed sulphides involved was then explored by micro‐Raman spectroscopy (μ‐RS), pointing out that the Cu‐for‐Ag substitution in the crystal lattice of the mixed Ag–Cu sulphides caused a monotonous blue shift of the vibrational wavenumbers in Raman spectra. This study has unveiled microscopic details of the tarnishing process, furnishing an innovative, cheap and non‐destructive methodology based on μ‐Raman spectroscopy for the evaluation of the silver‐copper artefacts via the compositions of their corroded products. Copyright © 2016 John Wiley & Sons, Ltd.     

Subsurface analysis of painted sculptures and plasters using micrometre‐scale spatially offset Raman spectroscopy (micro‐SORS)

A recently developed variant of spatially offset Raman spectroscopy (SORS) for the non‐invasive analysis of thin painted layers, micro‐SORS, has been applied, for the first time, to real objects of Cultural Heritage – namely painted sculptures and plasters. Thin layers of paint originating from multiple restoration processes often applied over many centuries have been analysed non‐destructively using micro‐SORS to depths inaccessible to, or unresolvable into separate layers, by conventional confocal Raman microscopy. The concept has been demonstrated on several artistic artefacts of historical significance originating from Italy and dating from the medieval to the 18th century. The technique extends the depth applicability of Raman spectroscopy and with its inherently high chemical specificity that expands the portfolio of existing non‐destructive analytical tools in Cultural Heritage permitting to avoid cross‐sectional analysis often necessitated with this type of samples with conventional Raman microscopy. Currently, the method is non‐invasive only for artworks that can be placed under Raman microscope although there is a prospect for its use in a mobile system with largely removed restrictions on sample dimensions. © 2015 The Authors Journal of Raman Spectroscopy Published by John Wiley & Sons Ltd.     

New insight into the nature and properties of pale green surfaces of outdoor bronze monuments

The present study concerns the chemical–physical and electrochemical characterisations of the pale green surfaces formed on outdoor bronzes exposed in urban conditions. In the first part, results from investigations performed on the equestrian statue of the French king Louis XIV exposed in the Palace of Versailles (France) are given. Analyses by energy-dispersive spectrometry and Raman spectroscopy, coupled with scanning electron microscopy, show that the external layer is characterised by a marked selective dissolution of copper and zinc of the alloy leading to an important relative enrichment in tin compounds. The same phenomenon with the same magnitude, determined from dissolution factors f_Cu and f_Zn, has also been evidenced on other bronze monuments used for comparison. Proportionality between the amount of dissolved copper and zinc cations to their respective initial content in the alloy is evidenced independently of the tin content. The pale green patina appears to be a complex mixture of copper and tin compounds whose structure still needs to be more precisely characterised. In the second part, the electrochemical reactivity of tin compound enriched patina was investigated by cyclic voltammetry from a Cu10Sn electrode in sulfate solution at pH=2 and 5.6. This patina is stable at pH 5.6 but reactive at pH 2 in relation to the modification of properties of tin species in the patina. Mott–Schottky application in pH 5.6 solution revealed that the bronze patina exhibits two types of semiconducting properties according to the potential domains, similar to what has been observed for pure tin in aqueous solutions. The destabilisation of bronze patinas in outdoor conditions and consequently the cyclic erosion due to rainfall have been attributed to the modification of tin species properties rather than to the transformation of copper compounds. PACS  07.78.+s; 81.05.-t; 81.15.-z; 81.65.Kn     

Large scale investigation of chemical composition, structure and corrosion mechanism of bronze archeological artefacts from Mediterranean basin

A large number of Cu-based archaeological artefacts from the Mediterranean basin have been selected for investigation of their chemical composition, metallurgical features and corrosion products (i.e. the patina).The guidelines for the selection of the Cu-based artefacts have taken into account the representativeness of the Mediterranean archaeological context, the manufacturing technique, the degradation state and the expected chemical composition and structure of the objects.The results show wide variation of the chemical composition of the alloys that include all kinds of ancient Cu-based alloys such as low and high tin, and also leaded bronzes, copper and copper-iron alloys.The examination of the alloy matrix shows largely different metallurgical features thus indicating the use of different manufacturing techniques for producing the artefacts. The results of the micro-chemical investigation of the patina show the structures and the chemical composition of the stratified corrosion layers where copper or tin depletion phenomenon are commonly observed with a remarkably surface enrichment of some soil elements such as P, S, Ca, Si, Fe, Al and Cl. This information indicates the strict interaction between soil components and corrosion reactions and products. In particular, the ubiquitous and near constant presence of chlorine in the corrosion layers is observed in the patina of the archaeological Cu-based artefacts found in different contexts in Italy, Turkey, Jordan, Egypt, Spain and Tunisia. This latter occurrence is considered dangerous because it could induce a cyclic corrosion reaction of copper that could disfigure the artefact.The micro-chemical and micro-structural results also show that another source of degradation of the bronze archaeological artefacts, are their intrinsic metallurgical features whose formation is induced during the manufacturing of the objects, carried out in ancient times by repeated cycles of cold or hot mechanical work and thermal treatments. These combined treatments induce crystallisation and segregation phenomena of the impurities along the grain boundaries and could cause mechanical weakness and increase the extent of the inter-granular corrosion phenomena. PACS 68.55.Jk; 68.35.Dv; 68.37.Hk; 68.55.Nq; 81.05.Bx     

Analysis of the Hoard of Beçin using X‐ray‐based techniques

Four hundred and sixteen silver coins stemming from the Ottoman Empire (16th and 17th centuries) were analyzed to confirm the fineness of the coinage as well as to study the provenance of the alloy used for the coins. As most of the coins showed the typical green patina on their surfaces due to corrosion processes that have led to the depletion of copper in the near surface domains of the silver coins in comparison to their core composition, small samples had to be taken, embedded in synthetic resin, and cross sectioned to investigate the true‐heart metal composition. μ‐synchrotron micro X‐ray fluorescence analysis and μ‐proton‐induced X‐ray emission were applied to determine the silver contents as well as the minor and trace elements. The type of the alloy was investigated as well as if coins minted in different locations demonstrated homogeneous traits concerning the predominant impurities (Au and Bi), which could suggest a common ore. Finally, energy‐dispersive microanalysis in a scanning electron microscope was applied to study the homogeneity/heterogeneity of the coins and the presence of surface enrichments and to explain differences between the μ‐synchrotron micro X‐ray fluorescence analysis and μ‐proton‐induced X‐ray emission measurements concerning the main component. In general, the silver content of the analyzed specimen varies between 90 and 95%. These outcomes have not supported the historical interpretations, which predict that during the period studied, a debasement of approximately 44% of the silver content of the coins should have occurred. Copyright © 2012 John Wiley & Sons, Ltd.     

Micro‐Raman and infrared analysis of medieval pottery findings from Braničevo,Serbia

A selection of Byzantine table pottery (17 samples) dating from the period between the beginning of the 12th century and the first half of the 13th century, discovered at Braničevo in Serbia, were analysed by Fourier transform infrared, micro‐Raman and scanning electron microscopy with energy dispersive spectroscopy and petrography analysis. The aim of the investigation was to determine the chemical and mineralogical composition of the body and of the glaze and thus to determine the production technology. Fourier transform infrared spectroscopy provided data for estimating the firing temperature and the basic mineralogical composition, and micro‐Raman spectroscopy was applied to study and characterise both the glaze and the body of the analysed sherds. It was found that noncalcareous clays, characterised by a rich mineral assemblage, were fired at temperatures between 700 and 900 °C. Oxidizing atmosphere was applied in the production of the red colour pottery. The dark and grey coloured paste of one group of sherds was produced by firing organic matter‐rich clays in a reducing environment. The main type of transparent glaze was identified as lead‐rich, and two samples were alkali–lime glazed. Copyright © 2011 John Wiley & Sons, Ltd.     

Characterization of colorants and opacifiers in roman glass mosaic tesserae through spectroscopic and spectrometric techniques

Several glass mosaic tesserae were recovered during the archeological excavation of the thermal baths at the ‘Villa dei Quintili’ in Rome and dated to the second century ad . This work reports the results of an archeometrical investigation performed, through a multi‐technique approach, on 19 colored opaque tesserae. The aims of the study were (1) the characterization of coloring and opacifying agents used for the production of the glass tesserae and (2) the definition of the technological processes involved. Colorimetric measurements allowed us to classify the tesserae in color groups, while the glassy matrix and the dispersed crystallites were characterized in detail through micro‐Raman spectroscopy, field emission scanning electron microscopy with energy dispersive X‐ray spectroscopy, laser ablation‐inductively coupled plasma‐mass spectrometry, and X‐ray powder diffraction analyses. Most of the glass shows the typical soda‐lime‐silicate composition (except for the orange and red tesserae). Raman results and elemental analysis prove the use of Sn–Pb antimonates to create yellow glass and of Ca‐antimonates for the white tesserae. A mixture of Sn–Pb antimonates and copper ions was used to obtain the emerald green color, while Ca‐antimonates were employed in both copper‐colored and cobalt‐colored blue glass to obtain different shades (blue‐green, dark, and light blue). X‐ray powder diffraction analyses reveal the presence of metallic copper (Cu⁰) and Cu₂O particles (cuprite) in red and orange tesserae, respectively. These results confirm the high technological level reached by the glassmakers of the Imperial Age. Copyright © 2014 John Wiley & Sons, Ltd.     

Influence of seawater and its aerosols on copper patina composition

X-ray diffraction analysis was used to monitor patina composition on copper samples exposed during one-year period to different seawater zones (splash, tidal and full immersion) and marine atmospheric aerosols. Two phases contributed most to patina formation: cuprite (copper oxide) and atacamite (copper chloride compound). Their relative XRD spectra intensities were very similar in patina formed in the tidal sea zone, but atacamite became the sole majority phase in the full immersion zone. The cuprite phase decreased over time, and two minority copper sulfates phases appeared: posnjakite and chalcanthite (CuSO₄). The results revealed that copper patina composition is strongly influenced by chloride pollution and specific zone conditions. Additional factors, such as wind-blown sand, continuous dredging in coastal areas and vessel docking, influenced degree of pollutant compound adherence to patinas and consequently their structure (porous or compact).     

Nanomechanics of single silkworm and spider fibres: a Raman and micro‐mechanical in situ study of the conformation change with stress

The combination of micro‐Raman spectroscopy and an advanced universal fibre tester (UFT) made it possible to probe at the nanoscale (through monitoring the modification of chemical bonds) the change in conformation (α‐helix, β‐sheet, etc.), macromolecular fibroin chain orientation and coupling during the application of stress, quantitatively. Different single fibres of silkworms (Bombyx mori, Gonometa rufobrunea, Gonometa postica) and a spider (Nephila madagascariensis) were tested in a dry environment and compared with the behaviour of keratin fibre. As observed previously for single keratin fibres, a direct relationship is observed between nano‐ and micro‐mechanical tensile behaviour. The phase transition plateau, well defined for some pristine B. mori fibres, disappears in degummed fibres, which indicates a structural modification and increasing disorder with chemical treatments. Stress‐controlled micro‐Raman analysis shows that a few modes involving CH₂ and/or amide groups of β‐conformation chains undergo a wavenumber softening during the elastic behaviour (∼0–3%), although most of the modes are not affected. A different behaviour is observed for modes associated with ‘ordered’ and ‘disordered’ β‐sheets and helical chains. Larger softening is observed for lattice modes with increasing stress/strain, as expected. Structural changes and relationships with mechanical behaviour are discussed. Copyright © 2008 John Wiley & Sons, Ltd.     

Raman and infrared analysis of glues used for pottery conservation treatments

The conservation of ceramics and glass involves the repair or the restoration of broken and fragmented artefacts with polymer adhesives and gap fillers. In the past, many different adhesives had been used. Re‐restoration is often required and the fast identification of adhesive residues on objects would be very useful to define the best of way to remove them, in particular to avoid the use of noxious chemicals. Sixteen pottery artefacts restored during the 19th and 20th centuries at the Musée National de Céramique in Sèvres have been analysed by non‐destructive Raman microspectroscopy. For comparison purposes, the artefacts were also sampled in order to acquire infrared (IR) absorption spectra in KBr pellets. Modern adhesives (methyl metacrylate/acrylate, vinyl acetate, polychloroprene, methyl 2‐cyanoacrylate and diglycidylether biphenol) were also characterised with the same methods. IR and Raman spectra were obtained for all ancient glue residues, but among the 16 analysed items, only 7 adhesives have been identified unambiguously, and an assignment proposed for 4 others solely on the basis of the Raman signature. Copyright © 2009 John Wiley & Sons, Ltd.     

Study of both fingerprint and high wavenumber Raman spectroscopy of pathological nasopharyngeal tissues

High wavenumber (HW) Raman spectroscopy has weaker fluorescence background compared with fingerprint (FP) region. This study aims to evaluate the discrimination feasibility of nasopharyngeal non‐cancerous and nasopharyngeal cancer (NPC) tissue with both FP and HW Raman spectroscopy. HW Raman spectra of nasopharyngeal tissue were obtained for the first time. Raman spectra were collected to differentiate nasopharyngeal non‐cancerous (n = 37) from NPC (n = 41) tissues in FP (800–1800cm⁻¹), HW (2700–3100cm⁻¹), and integrated FP/HW region. First, to assess the utility of this method, the averaged Raman spectral intensities and intensity ratios of corresponding Raman bands were analyzed in HW and FP regions, respectively. The results show that intensities as well as the ratios of specific Raman peaks might be helpful in distinguishing nasopharyngeal non‐cancerous from NPC tissue with the HW Raman spectroscopy, as with FP Raman reported before. The multivariate statistical method based on the combination of principal component analysis–liner discriminant analysis (PCA‐LDA), together with leave‐one‐patient‐out, cross‐validation diagnostic algorithm, was used for discriminating nasopharyngeal non‐cancerous from NPC tissue, generating sensitivities of 87.8%, 85.4%, and 95.1% and specificities of 86.5%, 91.9%, and 89.2%, respectively, with Raman spectroscopy in the FP, HW, and integrated FP/HW regions. The posterior probability of classification results and receiver operating characteristic curves were utilized to evaluate the discrimination of PCA‐LDA algorithm, verifying that HW Raman spectroscopy has a positive effect on the differentiation for the diagnosis of NPC tissue by integrated FP/HW Raman spectroscopy. What's more, the potential of Raman spectroscopy used for differentiating different pathology NPC tissues was also discussed. The results demonstrate that both FP and HW Raman spectroscopy have the potential for diagnosis and detection in early nasopharyngeal carcinoma, and HW Raman spectroscopy may improve the discrimination of NPC tissue compared with FP region alone, providing a promising diagnostic tool for the diagnosis of NPC tissue. Copyright © 2015 John Wiley & Sons, Ltd.     

In situ monitoring of solid‐state transition of p‐aminobenzoic acid polymorphs using Raman spectroscopy

The purpose of this study is to investigate the mechanism of solid‐state polymorphic transition of p‐aminobenzoic acid (PABA) using in situ Raman spectroscopy measurement. The polymorphic transition experiments were conducted on a micro quartz vessel mounted on a microscope, hot and cold stage, under isothermal conditions. The temperature was precisely controlled by a standalone temperature controller equipped with liquid nitrogen cooling system. The Raman spectroscopy probe was positioned on the surface of the solid sample in the micro vessel. The polymorphic transition progression was in situ monitored and recorded by Raman spectroscopy. Based on the polymorphic transition rate resulted from the quantitative analysis of Raman spectra, the mechanism of solid‐state polymorphic transition of PABA was examined by various empirical kinetic models. An Arrhenius analysis was also performed to calculate activation energies from 134.7 kJ mol⁻¹ to 137.7 kJ mol⁻¹ for the transition. The results demonstrated that in situ Raman spectroscopy is a valuable and accurate technique to probe polymorphic transition process. Copyright © 2009 John Wiley & Sons, Ltd.     

Raman microscopy of prehistoric paintings in French megalithic monuments

Remains of pictorial decorations in a series of six representative megalithic monuments of Brittany (France) and two French stelae have been studied by micro‐Raman spectroscopy for the first time. Fungal colonies on the painted orthostats made it difficult to obtain in situ Raman spectra of the paint components. Nevertheless, paint micro‐specimens studied in the laboratory by micro‐Raman spectroscopy, X‐ray photoelectron spectroscopy and scanning electronic microscopy combined with energy dispersive X‐ray spectroscopy have made possible to characterise the materials present. The minerals α‐quartz, albite, microcline, muscovite, phlogopite, celadonite, beryl and anatase have been identified in the granitic rocks supporting the paintings, while dolomite and calcite are dominant in the calcareous rocky substrata. Haematite is the main component of the red pictographs, whereas amorphous carbon and manganese oxides/oxihydroxides have been used in the black ones. Calcite, gypsum and amorphous carbon have been detected as additional components of the paint in some cases. Contamination with modern tracing materials (polystyrene and ε‐copper‐phthalocyanine blue) has been detected in several cases. The presence of pigments as decorative elements in megalithic monuments of Western France and its possible relation with those of the Iberian Peninsula create interesting expectations for the knowledge of the European megalithic culture. Copyright © 2015 John Wiley & Sons, Ltd.     

Assessment of ex vivo perfused liver health by Raman spectroscopy

Raman spectroscopy was applied in this research to monitor the overall health and degradation of porcine livers perfused ex vivo using the VasoWaveW® perfusion system. A novel Raman‐based diagnostic analysis was developed that enables near real‐time and label‐free monitoring of organ health during ex vivo perfusion designed to extend the useful life of the organ for transplantation. Multivariate statistical analysis of Raman spectra of organ perfusate fluid, using a combination of principal component analysis and linear discriminant analysis, proved to be an effective technique to assess the degradation properties of the livers. Three livers (with replicates) were perfused ex vivo under different pressures and temperatures and were compared with a 24‐h time‐course. Results indicated that perfusion pressure was a more significant factor in organ degradation than was temperature. In addition, a non‐linear degradation profile was identified for all three perfused livers, and this profile was different for individual livers, demonstrating the time‐dependent transition from its initial ‘healthy’ state towards a more ‘unhealthy’ degenerative state at 24 h. The Raman spectroscopy‐based approach described here has potential applications in perfusion and diagnostic instrumentation that can be used in near real‐time during organ transit and in operating rooms to help identify appropriately healthy organs for transplantation. Copyright © 2015 John Wiley & Sons, Ltd.     

Temperature‐dependent,micro‐Raman spectroscopic study of barium titanate nanoparticles

A comparative, temperature‐dependent (80–500 K at 5 K intervals), micro‐Raman spectroscopic study of 300 and 50 nm diameter ceramic BaTiO₃ nanoparticles was carried out with the purpose of elucidating the nanoparticle size effect on the temperature dependence of the polar and non‐polar phonons. A method for calibrating Raman intensities, along with an iterative spectral fitting algorithm, is proposed for concurrent Raman band position and intensity analysis, increasing the analytical abilities of single temperature point Raman spectroscopy. The 300 nm particles exhibit all three phase transitions, whereas the 50 nm particles do not show evidence of these phase transitions in the same temperature range. The Curie temperature appears to be a phonon converging point, irrespective of the phonon symmetry. An attempt was made to qualitatively relate the temperature‐dependent Raman spectra to complimentary non‐spectroscopic methods, such as heat capacity and X‐ray diffraction studies. The study proves that the temperature‐dependent behavior of the polar phonon, 265 cm⁻¹, can be utilized as a sensitive phase transition probe. Copyright © 2014 John Wiley & Sons, Ltd.     

Complementary use of X‐ray methods to study ancient production remains and metals from Northern Portugal

Archaeological artefacts recovered at Castanheiro do Vento (Northern Portugal) were characterised by integrating macro and micro‐energy dispersive X‐ray fluorescence spectrometry (EDXRF) and scanning electron microscopy with X‐ray microanalysis. The collection includes metallurgical remains (ceramic crucibles, a metallic nodule and a vitrified fragment) and metals (tools and ornaments) whose chronology spans from the Chalcolithic to the Roman Age. The study of production remains was able to identify distinct copper‐based metallurgical operations including the smelting of copper ores, the melting of copper and tin and/or the melting of bronze scrap. Micro‐EDXRF identified copper and arsenical copper tools as well as bronze and leaded bronze ornaments. The composition of tools (Cu with varying As contents: 0.46–3.6%) reveals an incipient technology, typical of the Chalcolithic till the Middle Bronze Age. On the contrary, ornaments are composed by different alloys – low tin bronze (4.8% Sn), high tin bronze (14.9% Sn) and high tin‐leaded bronze (16.5% Sn and 2.4% Pb) ? evidencing technological and economic choices that clearly indicate a late period such as the Roman Age. In conclusion, this multiproxy approach was able to study those ancient artefacts with a minimum impact on their archaeological and museological significance while providing important answers to the interpretation of the archaeological settlement and to better understand the metallurgical evolution in the Portuguese territory. Copyright © 2014 John Wiley & Sons, Ltd.     

Rapid screening of sildenafil and tadalafil adulterated in healthcare products by Micro‐Raman spectroscopy

Sildenafil and tadalafil are inhibitors of phosphodiesterase type 5, which are frequently added into healthcare products. The objective of this study was to evaluate the possibility of using micro‐Raman spectroscopy as a non‐destructive technique to screen for sildenafil and tadalafil in adulterated healthcare products. Using a viewing microscope, the suspect area of healthcare products was selected, which had a discernable crystal form or shape from the surrounding zone. Optimization of instrumental parameters of the Raman spectrometer was chosen to reduce the background fluorescence, and the Raman spectra were collected. The spectra collected were compared with the standard Raman spectra of pure sildenafil and tadalafil. Samples with an identifiable Raman signature to that of sildenafil or tadalafil could be confirmed using liquid chromatography–mass spectrometry (LC/MS). Additionally, wavelet denoising combined with similarity calculation was used to establish an automated approach for discrimination of adulterated healthcare products. Correlation coefficient was chosen for similarity calculation based on the spectra collected and the standard Raman spectra of pure sildenafil and tadalafil. We compared ten samples, secured by administrative authorities in Shanghai, to analyse and demonstrate the capabilities of our proposed method. We established six samples containing sildenafil or tadalafil warranting analysis using LC/MS. Thus, the use of micro Raman spectroscopy provides a quick, convenient and non‐destructive method for screening adulterated chemicals in healthcare products. Raman spectroscopy combined with similarity calculation requires little training after spectra library is developed, thus showing great promise to identify the adulterated healthcare products in the future. Copyright © 2012 John Wiley & Sons, Ltd.     

Micro‐Raman analysis of GaAs Schottky barrier solar cell

Gallium arsenide (GaAs) cells have been in the race with silicon single‐crystal cells for the highest efficiency photovoltaic devices. The annealed, irradiated Schottky barrier (SB) solar cells were characterised using micro‐Raman spectroscopy at three different regions: namely, at the (1) ohmic contact region, (2) unirradiated region and (3) irradiated region. We also present a micro‐Raman study of the damage process in annealed GaAs SB solar cells bombarded by high‐energy ions. A Gaussian line shape was fitted to the Raman spectra of the longitudinal optical phonon A₁(LO), and parameters such as intensity, full width at half maximum (FWHM) and the area under the peak were obtained for the different annealing temperatures. Biaxial stress (σ), carrier concentration (n), depletion length (L_d), dislocation velocity (ν) and life time of the first‐order optical phonon (τ) of the A₁(LO) mode of the irradiated region of the samples annealed at different temperatures were calculated. Copyright © 2010 John Wiley & Sons, Ltd.     

Micro‐Raman spectroscopy and VP‐SEM/EDS applied to the identification of mineral particles and fibres in histological sections

Histological sections of a patient affected by an important respiratory disease were analysed firstly by optical microscope(OM)—crossed polarisers—to identify the presence of incorporated inorganic particles, with particular attention to the fibrous ones. Then, the particles/fibres that were found were studied both with micro‐Raman spectroscopy and variable‐pressure scanning electron microscopy with energy‐dispersive spectroscopy (VP‐SEM/EDS). The two techniques allowed the in situ characterisation of the inorganic phases without disintegration of the organic matter. Micro‐Raman spectroscopy was able to identify the vibrating chemical groups of the mineral phase associated with the inorganic grain while the crystalline structure was preserved by the biological system. The VP‐SEM/EDS characterisation, defining the elemental chemical composition of the analysed particle/fibre, allowed confirmation of the mineral phase deducible from spectroscopic data or its identification with certainty when the spectroscopic data were not exhaustive. Copyright © 2009 John Wiley & Sons, Ltd.