Printer Friendly

Vibrational Spectroscopies and Chemometry for Nondestructive Identification and Differentiation of Painting Binders.

1. Introduction

The chemical nature of the materials used in painting as binding media is usually very diverse and complex, which makes their characterization a challenging task. A greater knowledge of the original binders used by the artist is of great interest to art historians because it allows them to distinguish between different painting techniques, which are often directly associated with the geographical, social, and chronological contexts in which the artist lived and worked. Information about the class of binders is also important for restorers, who often use solvents during the cleaning and restoration of artworks [1].

The identification and chemical characterization of various painting binders (protein-, polysaccharide-, and lipid-based) has been frequently addressed in published research, mainly using techniques such as gas chromatography/mass spectrometry (GC/MS) in combination with various offline or online derivatization procedures [2, 3]. Recent authors have proposed the use of spectroscopic techniques, as vibrational and electronic spectroscopic methods, coupled with multivariate analysis for the discrimination of different painting binders (animal glue, whole egg, and linseed oil) [2, 4-6] and also of organic compounds of the same class, like lipidic binders [7-10], subjected to natural ageing.

Separation methods (like gas chromatography, capillary electrophoresis, and liquid chromatography) and mass spectrometry present limitations for their application, such as large sample consumption, long experimental times, complex sample preparation, and multiparameter operating conditions. These are obvious problems for the analysis of samples of historical interest [4, 11, 12]. Spectroscopic techniques have the potential to overcome these limitations, as they allow nondestructive and contactless measurements, giving molecular information on complex macromolecules, and could be performed in situ by means of portable devices.

The work presented here explores the application of chemometric tools, such as principal component analysis (PCA) to combined FT-NIR and Raman data in order to enable us to distinguish among organic compounds of the same and different classes. With this aim in mind, we prepared 13 model samples containing traditional organic materials, commonly used by artists throughout history as binding media. These models samples were ageing naturally for three months at room temperature, without controlled environmental conditions, and then were further characterized by Raman and FT-NIR spectroscopy. The present model is not a realistic presentation of fully aged artworks, because the ageing processes of these materials last a much longer time. Nevertheless these models are useful for assessing the possibility of our data analysis.

Because these two vibrational spectroscopies obey different selection rules and provide often complementary information, combining the two could permit a greater amount of spectroscopic information to be extracted from each sample. Nevertheless, there are several different causes that can lead to random noise in Raman and FT-NIR spectra, thus making the identification of spectral bands more difficult, particularly in computational analyses, as in the present work. To identify small differences in the original spectra, first derivatives of the spectral data were used for PCs extraction [4, 6, 8, 9, 13]. As a result, an increase in sensitivity/specificity for differentiation capability and classification can be expected, due to the new dimensions added to the dataset [8, 9]. Principal Component Analysis (PCA) can be used to explain the variance-covariance structure of a set of data by the original variables' linear combination that form a new set of independent coordinates, called principal components (PC). The PCs are hierarchically ordered to describe the largest variance of the dataset, so that a smaller number of variables can account for most of the information from the original dataset [14]. The purpose of all multivariate data analysis is to decompose the data in order to detect and model the "hidden phenomena" or better to define the set of natural coordinates for these variables that show more clearly the similitudes and differences between the various samples [14, 15]. Therefore, the application of PCA to large spectral datasets can be exploited to extract meaningful information from spectral differences, allowing us to discriminate among different samples based on their composition [14, 15].

The results clearly show the potential of this methodology to extract the information needed to identify the painting materials that is contained in the FT-NIR and Raman spectra.

2. Materials and Methods

2.1. Materials. All neat binding media analyzed in this work, along with corresponding symbols, are listed in Table 1.

Each drying oil, as supplied, was applied as film on four microscope glass slides. Proteinaceous and polysaccharide binding media were prepared according to recipes from original treatises and artists' accounts [16-18]. Rabbit skin glue, strong glue, and fish glue were swollen and dissolved in warm demineralized water to give a solution of 5% (w/w). Egg white was beaten to form stiff peaks and left for 24 h; foam was skimmed and removed and then a solution of 50% (w/w) clear egg white in demineralized water was prepared. Egg yolk was extracted from egg by piercing the yolk and allowing the liquid to drip from the encasing film; the yolk was diluted in demineralized water to give a 50% (w/w) emulsion. Whole egg was prepared by mixing one part of egg white solution and two parts on egg yolk emulsion along with one part of vinegar. Casein was swollen in water for 24 h to give a 1.5% (w/w) solution; dilute ammonia solution was added until the swollen gel dissolved and excess ammonia was left to evaporate. Arabic gum was dissolved in warm demineralized water with a ratio of 1 to 2 (w/w), heating in a double boiler; the mixture was left to soak 48 h for a full absorption and finally, the obtained solution was strained through two layers of cheesecloth into a clean jar. Tragacanth gum was added to demineralized water in a ratio 1: 30 (w/w) and left to swell in a mucilaginous suspension. Then, this suspension was strain in a similar way to that previously described for Arabic gum.

All these organic binders and oils were individually applied as film on four microscope glass slides and left to dry on a shelf (T: ~20[degrees]C; RH: ~50-55%; light: solar light through a window). Hence, sixty-eight model samples for neat binders were prepared.

These materials were analyzed after an ageing of three months. As regards drying oils, they should be treated as "fresh" binding media because the drying process has not already been completed (according to previous studies, an oil paint can be regarded as aged only one year after its preparation [17, 19]).

2.2. Fourier Transform-Near Infrared (FT-NIR) Measurements. FT-NIR reflectance spectra were acquired by using a portable ALPHA FT-IR spectrometer (Bruker Optics) equipped with an external reflection module. Total reflection spectra (including both the specular and diffuse reflection contributions) were collected in situ, in the spectral range 7500-3900 [cm.sup.-1], with a resolution of 4 [cm.sup.-1], averaging over 128 scans. The spectral sampling distance used for each scan was 2 [cm.sup.-1]. The background was acquired using a gold mirror as reference sample. In total, 272 spectra were recorded, at four different positions for each sample (16 spectra for each binder).

2.3. Micro-Raman Spectroscopy. Micro-Raman analysis was performed using a micro-Raman spectrometer (Renishaw 2000) equipped with a 785 nm diode laser, operating at 1.1 mW laser power on the sample. The laser was focused onto the sample using a 50x objective lens, so that an area of about 2 [micro]m in diameter was analyzed. Spectra were recorded in the 2000-200 [cm.sup.-1] spectral range, with a spectral resolution of 4 [cm.sup.-1]. The integration time and the spectral sampling distance used for each scan were 25 s and 1 [cm.sup.-1], respectively. Each spectrum was the average of three acquisitions. The spectrometer was frequency calibrated at the beginning of each measurement session by using the Raman signal from a silicon wafer at 520 [cm.sup.-1]. No changes related to photochemical damage were observed on the samples after the Raman measurements. In total, 272 spectra were recorded, at four different positions for each sample (16 spectra for each binder).

2.4. Data Analysis. Micro-Raman and FT-NIR spectral datasets were preprocessed using the PCA method by means of The Unscrambler X version 10.3 software (CAMO).

Although micro-Raman spectra were registered between 2000 and 200 [cm.sup.-1], data analysis was performed in the 1800-750 [cm.sup.-1] range, since the most important bands of binding media are located in this spectral region. The FT-NIR spectra were analyzed in the 6000 and 3900 [cm.sup.-1] range, where the signal was well defined and not much affected by noise.

The FT-NIR and micro-Raman datasets were preprocessed separately to discern variability in the original spectra. In detail, the FT-NIR spectra were subjected to the Savitzky-Golay derivative algorithm [20] (2nd order polynomial, 15 data points) without any other preprocessing. The micro-Raman spectra were, instead, subjected to baseline subtraction, average reduction of variables (factor two), and first derivative calculation by applying the Savitzky-Golay algorithm (2nd order polynomial, 15 data points). Then, both the FT-NIR and micro-Raman spectra were vector normalized, as the use of absolute band heights could lead to erroneous sample classifications [7]. The combined spectra were obtained as follows: the first derivative Raman and FT-NIR spectra were joined, generating the new combined Raman-FT-NIR spectrum, 16 for each typology of sample.

Each new combined spectrum includes 1575 data points, with the first 1050 derived from the FT-NIR spectrum abscissa, related to the spectral region 6000-3900 [cm.sup.-1], and the remaining 525 points taken from the micro-Raman spectrum abscissa in the 1800-750 [cm.sup.-1] spectral region. Each combined spectrum is characterized by both fundamental and combination-overtone modes, as have been previously described in the FT-NIR and micro-Raman sections.

The Uncertainty Test was always performed to estimate the significance of variables. Then, PCA was performed by applying a mean centering onto data column-wise, and the Nonlinear Iterative Partial Least Squares (NIPALS) algorithm. Each model was always validated by Leave One Out (LOO) cross-validation and by a projection of evaluated sets of spectral data acquired by the same samples (four spectra for each type of sample).

3. Results and Discussion

This study involves the application of the Principal Component Analysis (PCA) on FT-NIR and micro-Raman spectroscopic data in order to characterize the spectral differences, in frequency and intensity, among various classes of binding media. The following discussion is divided into two main sections dealing with an initial characterization of FT-NIR and Raman spectra of each binder and a successive evaluation of results obtained from the statistical model.

3.1. FT-NIR and Micro-Raman Spectra of Different Binders. First, we discuss the proteinaceous binders such as casein, egg white, and glues; following, we analyze the egg yolk and whole egg, which differ from the other protein-based binding media for the lipid content [6, 18]. Finally we discuss the spectra of the other materials.

We report in Figure 1 the FT-NIR spectra (Figure 1(a)) and the Raman spectra (Figure 1(b)) of casein, egg white, and glues. The raw FT-NIR spectra of these proteinaceous binding media do not show significant spectral differences. The combination band of amide III (C-N stretching/N-H in plane bending), the first overtone of carbonyl stretching (~4600 [cm.sup.-1]), and the combination band of the stretching and bending modes of NH (~4880 [cm.sup.-1]) represent the characteristic signals of proteins. Furthermore, a weak absorption band, located at about 3988 [cm.sup.-1] and ascribed to the first CN-C stretching overtone in amides, can be observed [6, 21]. For all these binders, the methylenic overtones and combination bands result to be broad and weak (Figure 1(a)). Nevertheless, some differences can be highlighted: in the spectra of the glues, the combination band of asymmetric methylenic C-H stretching and bending is located at 4376 [cm.sup.-1], while in the spectra related to casein and egg white, this absorption band is located at about 4340 [cm.sup.-1]. Furthermore, this absorption band results to be more intense than the symmetric one, always for the case of glues.

The micro-Raman spectra of casein, egg white, and glues (Figure 1(b)) are characterized by the vibrations related to amide I (at about 1665 [cm.sup.-1]), C[H.sub.2] scissoring (at about 1450 [cm.sup.-1]), and amide III (at about 1245 [cm.sup.-1]). A sharp band due to the aromatic ring breathing is present in all these spectra, which arises from phenylalanine amino acid residues (at about 1002 [cm.sup.-1]) [6, 18]. This last peak is especially pronounced in egg white and casein, for which phenylalanine is present in higher concentrations than in collagen-based glues [18].

Furthermore, contributions due to tyrosine amino acid are present in all these protein-based binders (826-850, 1210, and 1605-1610 [cm.sup.-1]) [18]. Moreover, in the spectra of casein and egg white, peaks ascribable to tryptophan amino acid (at approximately 1550 and 880 [cm.sup.-1]) and to phosphoproteins (-954 [cm.sup.-1]) can be found [18].

The FT-NIR spectra related to egg yolk and whole egg, shown in Figure 2(a), are characterized by the methylenic combination bands and their overtones, in the ranges 42504350 [cm.sup.-1] and 5600-5800 [cm.sup.-1], more intense with respect to the other protein-based binders, due to the lipid content of yolk [6, 21]. The shape and position of the methylenic combination bands from the lipid component in egg yolk/whole egg are different with respect to those from drying oils, thus providing distinctive features for their recognition [6, 21]. However, the main proteinaceous bands are all detectable, as can be seen in Figure 2(a).

Concerning the corresponding Raman spectra (Figure 2(b)), due to the presence of fatty acid esters, the characteristic carbonyl vibration at 1740 [cm.sup.-1] is present. Furthermore, bands due to the following vibrations are predominant: 1302 [cm.sup.-1] (in-phase methylene twist) [18], 1442 [cm.sup.-1] (scissoring mode of methylene) [18], and 1655 [cm.sup.-1] , (cis-double bond stretching) [22]. This last band has a frequency close to the usual value at which the amide I band is observed (1665 [cm.sup.-1]) [18, 22]. Egg yolk and whole egg have the lowest values for polyunsaturated fatty acids in comparison with drying oils [2, 8]. Nevertheless, characteristic proteinaceous bands are present, as can be seen in Figure 2(b). The phenylalanine ring breathing (~1002 [cm.sup.-1]) [18, 22] results to be more intense in whole egg spectrum, because it presents a major proteinaceous content for the preparation (it was prepared mixing one part of egg white with two parts of egg yolk and one part of vinegar).

FT-NIR spectra of drying oils are shown in Figure 3(a). As regards drying oils, the main near infrared absorption bands are represented by the combination of methylenic C-H stretching and bending (between 4250 and 4350 [cm.sup.-1]) and first C[H.sub.2] stretching overtone bands (in the 5700-5800 [cm.sup.-1] spectral range). The second overtone of ester carbonyl stretching mode is observed at 5176 [cm.sup.-1], whereas the combination of ester C=O and methylenic C-H stretching modes occurs at about 4690 [cm.sup.-1] [6, 8]. Raw FT-NIR spectra of drying oils do not show significant spectral differences between each other. In addition, the FT-NIR spectrum related to stand-oil does not show any information that could be ascribed to the effect of the heating process used during its preparation.

On the other hand, the major Raman bands (shown in Figure 3(b)) are represented by symmetric rock in cisdouble bond (~1265 [cm.sup.-1]), in-phase methylene twist mode (~1302 [cm.sup.-1]), scissoring mode of methylene (~1442 [cm.sup.-1]), cis-double bound stretching mode (~1655 [cm.sup.-1]), and ester stretching (~1745 [cm.sup.-1]), as discussed by different authors [2, 8]. Therefore, the drying oils Raman spectra predominantly contain bands arising from vibrations of the hydrocarbon chains. As can be seen in Figure 3(b), the major difference between the different drying oils is located at the band 1655 [cm.sup.-1] that is more intense for linseed oil and stand-oil. Linseed oil, indeed, contains around 52-55% of linolenic acid in its chemical composition, whereas poppy-seed oil contains 0.4-0.6% and walnut oil contains 10-15% [2, 22]. Concerning stand-oil, the heating process generates a complex set of reactions leading to different products, including systems with conjugated double bonds [23].

Broad bands characterize the FT-NIR spectra of gums, as shown in Figure 4(a). The characteristic signals of polysaccharides are represented by the combination bands of O-H stretching and bending (~5140 [cm.sup.-1]), of O-H bending and C-O stretching (~4800 [cm.sup.-1]) and of C-H and C-C/C-O-C stretching modes (~4010 [cm.sup.-1]) [21]. In addition, a very broad band ascribed to combination band of C-H stretching and bending, at about 4270 [cm.sup.-1], can be observed [21].

As regards the near infrared region, the combination band of O-H stretching and bending represents the main difference between two gums. In the spectrum of tragacanth gum, this band is shifted of around 20 [cm.sup.-1] towards longer wavenumbers in comparison with Arabic gum.

The Raman spectra, shown in Figure 4(b), do not present intense peaks in the 1800-1500 [cm.sup.-1] spectral range. This feature already differentiates the gums from the other binding media previously described. These materials, indeed, do not contain aromatic or aliphatic C=C double bonds. In addition, no amide I and amide III bands are present, in contrast to proteinaceous binders [22, 24]. The rather broad peaks in the 1500-1200 [cm.sup.-1] region are ascribed to CH deformations, whereas the peaks at lower wavenumbers are associated with C-C and C-O symmetrical stretching modes (1200-950 [cm.sup.-1]) and C-O-C sugar ring vibrations (950-800 [cm.sup.-1]) [22, 24]. The Raman spectrum of Arabic gum shows a doublet at around 850 [cm.sup.-1] (882 [cm.sup.-1] and 841 [cm.sup.-1]), whereas tragacanth gum has a singlet (857 [cm.sup.-1]). This feature allows distinguishing between the two gums.

3.2. PCA Applied on Combined First Derivative FT-NIR and Micro-Raman Spectra. In this section, the potentialities of PCA to improve the description of each class of binders are evaluated and discussed.

The application of a multivariate analytical tool, such as PCA, to the combined first derivative FT-NIR and Raman spectra allows the concomitant extraction of important information. The obtained statistical model explains a significant percentage (83%) of the cumulative variability by means of the first four PCs. In detail, PC1 explains 49% of the total variance contained in the data, whereas PC2, PC3, and PC4 explain 19, 11, and 4% of the total variance, respectively. Focusing on the two-dimensional score plot in the space defined by PC1 and PC2 (Figure 5) four different data groups can be individuated: (1) gums; (2) drying oils; (3) egg yolk and whole egg; (4) glues, casein, and egg white.

In Figures 6(a), 6(b), and 6(c), the loading plots of PC1 and PC2 are reported, highlighting the contributions that can be ascribed to polysaccharide-, lipid-, and protein-based binding media, respectively. In all loading plots, the "plus" symbol is associated with a first derivative contribution concordant with the starting combined spectra, while a "minus" sign is used when its behavior is reversed. Gums dataset displays a negative score value for PC1, whereas it has a positive score value for PC2 (Figure 5). As can be seen in Figure 6(a), the greatest contributions to PC1 related to polysaccharide-based binding media are represented by the combination band of O-H stretching and bending (~5140 [cm.sup.-1]) [21], the combination band of C-H and C-C/CO-C stretching modes (~4010 [cm.sup.-1]) [21], and the C-O-C sugar ring vibrations (950-800 [cm.sup.-1]) [22, 24]. As regards PC2, the main highlighted polysaccharide vibrations are the combination band of O-H stretching and bending and the C-O-C sugar ring vibrations (Figure 6(a)). So, the first two PCs allow describing polysaccharide materials, immediately focusing on their principal spectral properties in NIR and Raman regions but do not allow any further differentiation.

Focusing, instead, on drying oils, these binders datasets contribute with a positive score value to PC1, whereas they result to be very close to a zero value for PC2 (Figure 5). PC1, shown in Figure 6(b), is characterized by bands associated with drying oils, such as the C[H.sub.2] stretching first overtone band (in the 5700-5800 [cm.sup.-1] spectral range) [6, 8], combination band of methylenic C-H stretching and bending (between 4250 and 4350 [cm.sup.-1]) [6, 8], scissoring mode of methylene (1442 [cm.sup.-1]) [2, 8], and in-phase methylene twist mode (~1302 [cm.sub.-1]) [2, 8]. In PC2, their main contributions are related to combination band of methylenic C-H stretching and bending, in NIR region, and scissoring mode of methylene, in Raman region. These contributions cause a very low score value for PC2, because they are opposed: the former is positive, while the latter is negative (Figure 6(b)). Also, for drying oils this statistical model immediately allows to highlight their characteristic spectral bands. Nevertheless, no differentiation between various drying oils is obtained.

Concerning glues, C, and EW display a negative score value for PC1 and a negative one for PC2 (Figure 5). As regards proteinaceous binders, in the loading plot of PC1 (Figure 6(c)), specific contributions due to amide I (~1665 [cm.sup.-1]), C[H.sub.2] scissoring (~1450 [cm.sup.-1]), and phenylalanine ring breathing (1002 [cm.sup.-1]) vibrations can be observed [18, 22]. Nevertheless, PC2 better describes protein-based binding media. Indeed, in the corresponding loading plot (Figure 6(c)) intense contributions related to the combination band of the stretching and bending modes of NH at about 4880 [cm.sup.-1], amide I mode, C[H.sub.2] scissoring vibration, and phenylalanine ring breathing mode can be highlighted [6, 21]. Instead, EY and WE are located at an intermediate position between drying oils and the other protein-based binding media (Figure 5). These binders are characterized by a lipid content that is completely absent in C, EW, and glues.

As previously discussed, the purpose of all multivariate data analysis is to decompose the data in order to detect and model the "hidden phenomena." Taking into mind this principle/precept, the PC4 results to be notably interesting. As we can observe in the space defined by the score plot of PC2 and PC4 (Figure 7(a)) a clear separation between AG and TG can be observed as well as between EW, C, and glues. Indeed, the loading plot of PC4, reported in Figure 7(b), is characterized by two main contributions: phenylalanine ring breathing and C-O-C ring vibration. Concerning phenylalanine ring breathing vibration, PC4 defines a trend that describes the different content of this amino acid in proteinaceous binding media. The peak at 1002 [cm.sup.-1], as previously described, is especially pronounced in EW and C Raman spectra, for which phenylalanine is present in higher concentrations than in collagen-based glues (a total of approximately 12% of tyrosine plus phenylalanine is detected in egg and casein, compared to approximately 4% total in animal glue) [18].

On the other hand, C-O-C ring vibration, also described by PC4, shows the specific frequency related to TG: the characteristic singlet at 857 [cm.sup.-1] [22, 24]. Additionally, another minor contribution, ascribable to gums, is the combination band of OH stretching and bending. In this case, the corresponding frequency is 5180 [cm.sup.-1], which is close to that observed for AG near infrared spectrum (Figure 4(a)).

In Table 2 a summary of the main spectral properties highlighted by this statistical model for the different classes of binding media is reported.

4. Conclusions

In this work, we have analyzed model films of protein-, polysaccharide-, and lipid-based binding media after a natural ageing of three months, highlighting the applicability of FT-NIR and Raman spectroscopies for their characterization. Assignment of main near infrared and Raman bands revealed significant differences between spectra related to various classes of binders. These differences are emphasized by PCA applied on the corresponding combined first derivative spectra. The application of PCA on combined first derivative spectra has allowed immediately visualizing the main spectral properties, in both regions investigated, of these materials. The proposed method represents a novel noninvasive and nondestructive approach for their identification and differentiation.

Additionally, the results described highlighted the capability of this methodology to extract information related to hidden variance. Therefore, we differentiated egg white and casein between each other and from glues, based on different content in the amino acid phenylalanine. It has been also possible to distinguish between Arabic gum and tragacanth gum. Nevertheless, we did not observe any differentiation within drying oils or glues groups. This result indicates and suggests the need for further PCA modelling of each such group in order to fine-tune the analysis and to understand the characteristic features of the different classes of binders.

This work represents a contribution to the development of nondestructive, optical methods that could provide knowledge of the binder media used by artists. Their identification is often quite difficult due to their complex molecular nature. The development of these methods, which could act without detriment of the sample, helps not only in complementing historical research, but also in the process of conservation and restoration of artworks. 10.1155/2017/3475659

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this article.


Authors wish to thank Dr. M. Picollo, IFAC-CNR, Italy, for making available the ALPHA-FTIR spectrometer for this research. This work was supported by Italian MIUR (PRIN, Grant 2010329WPF_007) and by University of Florence (ex60%). Support from Ente Cassa di Risparmio di Firenze (Grant no. 2014.0405A2202.8044) is also kindly acknowledged.


[1] B. H. Stuart, Analytical Techniques in Materials Conservation, John Wiley & Sons, New York, NY, USA, 2007.

[2] E. Manzano, J. Garcia-Atero, A. Dominguez-Vidal, M. J. Ayora-Canada, L. F. Capitan-Vallvey, and N. Navas, "Discrimination of aged mixtures of lipidic paint binders by Raman spectroscopy and chemometrics," Journal of Raman Spectroscopy, vol. 43, no. 6, pp. 781-786, 2012.

[3] M. P. Colombini, A. Andreotti, I. Bonaduce, F. Modugno, and E. Ribechini, "Analytical strategies for characterizing organic paint media using gas chromatography/mass spectrometry," Accounts of Chemical Research, vol. 43, no. 6, pp. 715-727, 2010.

[4] N. Navas, J. Romero-Pastor, E. Manzano, and C. Cardell, "Raman spectroscopic discrimination of pigments and tempera paint modelsamples by principal component analysis on first-derivative spectra," Journal of Raman Spectroscopy, vol. 41, no. 11, pp. 1486-1493, 2010.

[5] N. Navas, J. Romero-Pastor, E. Manzano, and C. Cardell, "Benefits of applying combined diffuse reflectance FTIR spectroscopy and principal component analysis for the study of blue tempera historical painting," Analytica Chimica Acta, vol. 630, no. 2, pp. 141-149, 2008.

[6] M. Vagnini, C. Miliani, L. Cartechini, P. Rocchi, B. G. Brunetti, and A. Sgamellotti, "FT-NIR spectroscopy for non-invasive identification of natural polymers and resins in easel paintings," Analytical and Bioanalytical Chemistry, vol. 395, no. 7, pp. 2107-2118, 2009.

[7] A. Pallipurath, J. Skelton, P. Ricciardi, S. Bucklow, and S. Elliott, "Multivariate analysis of combined Raman and fibre-optic reflectance spectra for the identification of binder materials in simulated medieval paints," Journal of Raman Spectroscopy, vol. 44, no. 6, pp. 866-874, 2013.

[8] S. Carlesi, M. Ricci, C. Cucci et al., "Multivariate analysis of combined fourier transform near-infrared spectrometry (FT-NIR) and Raman datasets for improved discrimination of drying oils," Applied Spectroscopy, vol. 69, no. 7, pp. 865-876, 2015.

[9] S. Carlesi, M. Ricci, C. Cucci, C. Lofrumento, M. Picollo, and M. Becucci, "Multivariate analysis of combined reflectance FT-NIR and micro-Raman spectra on oil-paint models," Microchemical Journal, vol. 124, pp. 703-711, 2016.

[10] J. Bueno and I. K. Lednev, "Advanced statistical analysis and discrimination of gunshot residue implementing combined Raman and FT-IR data," Analytical Methods, vol. 5, no. 22, pp. 6292-6296, 2013.

[11] A. Zoppi, C. Lofrumento, M. Ricci, E. Cantisani, T. Fratini, and E. M. Castellucci, "A novel piece of Minoan art in Italy: the first spectroscopic study of the wall paintings from Phaistos," Journal of Raman Spectroscopy, vol. 43, no. 11, pp. 1663-1670, 2012.

[12] J. Romero-Pastor, N. Navas, S. Kuckova, A. Rodriguez-Navarro, and C. Cardell, "Collagen-based proteinaceous binder-pigment interaction study under UV ageing conditions by MALDITOF-MS and principal component analysis," Journal of Mass Spectrometry, vol. 47, no. 3, pp. 322-330, 2012.

[13] C. Pasquini, "Near infrared spectroscopy: fundamentals, practical aspects and analytical applications," Journal of the Brazilian Chemical Society, vol. 14, no. 2, pp. 198-219, 2003.

[14] M. Otto, Chemometrics: Statistics and Computer Application in Analytical Chemistry, John Wiley & Sons, 2007.

[15] K. H. Esbensen, "Multivariate Data Analysis-In Practice," CAMO Software AS., 2009.

[16] C. Cennini and F. Frezzato, "Il Libro Dell'arte," N. Pozza, 2003.

[17] L. Masschelein-Kleiner, Ancient Binding Media, Varnishes and Adhesives, ICCROM, Rome, Italy, 2nd edition, 1995.

[18] A. Nevin, I. Osticioli, D. Anglos, A. Burnstock, S. Cather, and E. Castellucci, "Raman spectra of proteinaceous materials used in paintings: a multivariate analytical approach for classification and identification," Analytical Chemistry, vol. 79, no. 16, pp. 6143-6151, 2007.

[19] I. Bonaduce, L. Carlyle, M. P. Colombini et al., "New insights into the ageing of linseed oil paint binder: a qualitative and quantitative analytical study," PLoS ONE, vol. 7, no. 11, Article ID e49333, 2012.

[20] A. Savitzky and M. J. E. Golay, "Smoothing and differentiation of data by simplified least squares procedures," Analytical Chemistry, vol. 36, no. 8, pp. 1627-1639, 1964.

[21] D. A. Burns and E. W. Ciurczak, Handbook of Near-infrared Analysis, CRC Press, Boca Raton, Fla, USA, 2008.

[22] P. Vandenabeele, B. Wehling, L. Moens, H. Edwards, M. De Reu, and G. Van Hooydonk, "Analysis with micro-Raman spectroscopy of natural organic binding media and varnishes used in art," Analytica Chimica Acta, vol. 407, no. 1-2, pp. 261-274, 2000.

[23] O. Zovi, L. Lecamp, C. Loutelier-Bourhis, C. M. Lange, and C. Bunel, "Stand reaction of linseed oil," European Journal of Lipid Science and Technology, vol. 113, no. 5, pp. 616-626, 2011.

[24] L. Brambilla, C. Riedo, C. Baraldi et al., "Characterization of fresh and aged natural ingredients used in historical ointments by molecular spectroscopic techniques: IR, Raman and fluorescence," Analytical and Bioanalytical Chemistry, vol. 401, no. 6, pp. 1827-1837, 2011.

Serena Carlesi, (1) Maurizio Becucci, (1,2) and Marilena Ricci (1)

(1) Department of Chemistry "Ugo Schiff', University of Florence, Via della Lastruccia 3-13, 50019 Sesto Fiorentino, Italy

(2) The European Laboratory for Non-Linear Spectroscopy (LENS), Via N. Carrara 1, 50019 Sesto Fiorentino (FI), Italy

Correspondence should be addressed to Marilena Ricci;

Received 1 February 2017; Accepted 15 March 2017; Published 25 May 2017

Academic Editor: Ewa Schab-Balcerzak

Caption: FIGURE 1: FT-NIR (a) and Raman (b) spectra of casein-C, egg white-EW, fish glue-FG, strong glue-SG, and rabbit glue-RG. Raman spectra are presented after background subtraction. Star symbols point to some specific spectral features discussed in the text. The assignments of the FT-NIR and Raman spectra are reported in Tables S1 and S2 in Supplementary Material available online at

Caption: FIGURE 2: FT-NIR (a) and Raman (b) spectra of eggyolk-EY and whole egg- WE. Raman spectra are presented after background subtraction. Star symbols point to some specific spectral features discussed in the text. The assignments of the FT-NIR and Raman spectra are reported in Tables S3 and S4.

Caption: FIGURE 3: FT-NIR (a) and Raman (b) spectra of drying oils. Raman spectra are presented after background subtraction. Star symbols point to some specific spectral features discussed in the text. Symbols for each drying oil are taken from Table 1. The assignments of the FT-NIR and Raman spectra are reported in Tables S5 and S6.

Caption: FIGURE 4: FT-NIR (a) and Raman (b) spectra of tragacanth gum-TG and Arabic gum-AG. Raman spectra are presented after background subtraction. Star symbols point to some specific spectral features discussed in the text. The assignments of the FT-NIR and Raman spectra are reported in Tables S7 and S8.

Caption: FIGURE 5: PCA applied to combined FT-NIR and Raman first derivative spectra, taking into account all neat binding media: score plot of PC1-PC2.

Caption: FIGURE 6: PCA applied to combined FT-NIR and Raman first derivative spectra, taking into account all neat binding media: score plot of PC1-PC2 (a); loading plots of PC1 and PC2, highlighting in the different panels the bands associated with different materials: polysaccharides (a), lipids (b), and proteinaceous materials (c).

Caption: FIGURE 7: PCA applied to combined FT-NIR and Raman spectra, taking into account all neat binding media: score plot of PC2-PC4 (a) and loading plot of PC4 (b), highlighting proteinaceous and polysaccharide contributions.
TABLE 1: The neat binding media analyzed with reporting the
manufacturer and the corresponding identification symbol.

Neat binder              Producer/manufacturer     Symbol

Proteinaceous binders

Rabbit skin glue                Zecchi               RG
Strong glue                     Zecchi               SG
Fish glue                       Zecchi               FG
Egg white                    Local market            EW
Egg yolk                     Local market            EY
Whole egg                    Local market            WE
Casein                          Zecchi               C

Drying oils

Linseed oil                     Zecchi              LOZ
Linseed oil                     Maimeri             LOM
Linseed oil                    Ferrario             LOF
Poppy-seed oil                  Zecchi              POZ
Poppy-seed oil                  Talens              POT
Walnut oil                      Zecchi              WOZ
Walnut oil                     Ferrario             WOF
Stand-oil                       Zecchi              SOLZ

Polysaccharide media

Arabic gum                      Zecchi               AG
Tragacanth gum                  Zecchi               TG

TABLE 2: Main near infrared and Raman bands, characteristic for
different classes of binding media, highlighted by PCA applied on
combined spectra referred to all neat binders.

Class of binders                      FT-NIR

Polysaccharide-based           v(OH) + [delta](OH)
                                  v(CH) + v(COC)
Lipid-based                  1st overtone C[H.sub.2]
                       v(C[H.sub.2]) + [delta](C[H.sub.2])
                                 [v(OH) + v(OH)]
Protein-based                  v(NH) + [delta](NH)
                                  v(OH) + v(OH)

Class of binders                    Micro-Raman

Polysaccharide-based           [delta](COC) sugar ring
Lipid-based                      [delta](C[H.sub.2])

Protein-based                          Amide I
                                 Phe ring breathing
COPYRIGHT 2017 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2017 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Research Article
Author:Carlesi, Serena; Becucci, Maurizio; Ricci, Marilena
Publication:Journal of Chemistry
Article Type:Technical report
Date:Jan 1, 2017
Previous Article:Adsorption of Cr(VI) onto Hybrid Membrane of Carboxymethyl Chitosan and Silicon Dioxide.
Next Article:Geochemistry of Aquatic Sediments.

Terms of use | Privacy policy | Copyright © 2022 Farlex, Inc. | Feedback | For webmasters |