The first Raman spectroscopic study of San rock art in the Ukhahlamba Drakensberg Park,South Africa

San rock art sites are found throughout southern Africa; unfortunately this unique heritage is rapidly being lost through natural weathering processes, which have been the focus of various studies conducted in the uKhahlamba Drakensberg Park since 1992. It has recently been shown that the ability of Raman spectroscopy to identify salts on rock faces on a micro, as well as nano scale, can make a contribution to these projects. In order to test the feasibility of undertaking on‐site analyses, a small rock fragment with red and white pigments still attached, which had weathered off the rock face, was analysed with Raman spectroscopy under laboratory conditions, using a Dilor XY Raman instrument and a DeltaNu Inspector Raman portable instrument. A small sample of black pigment (<1 mm²), collected from a badly deteriorated painting and a few relevant samples collected on site, were analysed as well. It was possible to identify most of the inorganic pigments and minerals detected with previous XRD and EDX measurements including whewellite and weddellite coatings, which could be a tool for carbon dating purposes. Two carotenoid pigments were detected for the first time in San rock art pigments. Animal fat was also observed for the first time on both red and white pigments, on the rock face adjacent to the paintings and in highest concentrations on the back of the rock fragment. The spectra quality makes successful on‐site measurements a good prospect. Copyright © 2008 John Wiley & Sons, Ltd.     

Application of field portable EDXRF spectrometry to analysis of pigments of Levantine rock art

The results of the analyses of elemental composition of red and black pigments of Levantine rock art from La Saltadora rock shelters (Valltorta gorge, Castellón, Spain) are presented in this paper. Nondestructive analyses were carried out using a portable energy dispersive X‐ray fluorescence (EDXRF) spectrometer developed for in situ analysis. The results revealed the strong presence of calcium in all the analyzed locations due to the contribution of the underlying calcareous bedrock and the overlying crust. Iron is the main element detected in red pigments and manganese in black pigments. Iron and calcium ratios have been found indicative of the degree of preservation of the pictorial layer. Trace elements detected in the pigment composition confirm the use of different raw materials. Therefore, this work illustrates the potential of the portable EDXRF spectrometers for in situ analysis of rock art paintings. Copyright © 2010 John Wiley & Sons, Ltd.     

Raman spectroscopic study of medieval Indian art of 17th century

We report the first Raman spectroscopic investigations of medieval Indian art of 17th century. Three miniature paintings, belonging to Mogul and Rajput schools from the collections of the Madras Museum, were investigated by micro‐Raman spectroscopy using different excitation wavelengths. Many areas in the paintings exhibited rich spectra containing several intense Raman bands. The Raman bands were assigned on the basis of the reported reference spectra of the pigments. Evidences for the presence of massicot, red‐lead, lead‐white, vermilion, litharge, Indian yellow and anatase are found. In addition, tentative assignments of some of the Raman bands to atacamite and orpiment are also made. The present studies suggest that several mineral‐based unique pigments were popular among the Indian artists of this period. Copyright © 2010 John Wiley & Sons, Ltd.     

Three fabricated pigments (Han purple,indigo and emerald green) in ancient Chinese artifacts studied by Raman microscopy,energy‐dispersive X‐ray spectrometry and polarized light microscopy

In this study, we analyzed three fabricated pigments from ancient artifacts in China. The purple pigment was obtained from a painted pottery figurine unearthed from the Chu Tombs group of the Western Han dynasty in Xuzhou, Jiangsu Province. The dark blue dye was from silk textiles in the Palace Museum. The green pigment was from decorative paintings on ancient architectures in the Palace Museum. These pigments were analyzed with Raman microscopy (RM), energy‐dispersive X‐ray (EDX) analytic spectroscopy and polarized light microscopy (PLM). By comparing their Raman spectra with standard samples, the primary ingredients of the purple pigment and the dark blue dye were found to be Han purple and indigo, respectively. However, the green pigment could not be identified by RM because of strong fluorescence. It was then confirmed to be emerald green by using EDX analytic microscopy and PLM. We also describe the traditional manufacturing methods of these pigments and their applications on artifacts in Chinese history. Copyright © 2007 John Wiley & Sons, Ltd.     

Rapid detection of 2,2′,4,4′‐tetrabromodiphenyl ether (BDE‐47) using a portable Au‐colloid SERS sensor

In situ rapid detection and identification of polybrominated diphenyl ethers, a group of well‐known persistent organic pollutants, present a great challenge. To develop a portable and sensitive surface‐enhanced Raman scattering (SERS) sensor for rapid 2,2′,4,4′‐tetrabromodiphenyl ether (BDE‐47) detection, we adopted the most commonly used Au nanoparticles, which are effective in the analysis of hydrophobic BDE‐47 with a simple optimization in citrate content and sampling technique. Qualitative and quantitative determination of BDE‐47 was achieved using a portable Raman spectrometer. The SERS response exhibited a linear dependence on the BDE‐47 concentration up to 1000 nM with a detection limit of 75 nM. The density function theory‐calculated Raman spectra agreed well with the experimental observations, and the results justified the existence of electromagnetic enhancement and charge transfer mechanism. This in situ SERS platform allows easy and reliable detection of hydrophobic molecules such as BDE‐47 in complex matrices. Copyright © 2014 John Wiley & Sons, Ltd.     

The first in situ Raman spectroscopic study of San rock art in South Africa: procedures and preliminary results

Southern Africa has a rich heritage of hunter‐gatherer, herder and farmer rock art traditions made by using both painted and engraved techniques. Until now, there have been only a handful of studies on the chemical analysis of the paint, as all previous types of analysis required the removal of pigment samples from the sites a practice which has been avoided. Raman spectroscopy is an ideal techniques to analyse the paint non‐destructively and also offers the possibility of in situ work with portable instruments. This article describes the procedures and reports the preliminary results of the first in situ Raman spectroscopic study of rock art in South Africa (also a first worldwide), where we, first, evaluate the capability of a Raman portable instrument in very difficult conditions, second, analyse the paints in order to contribute to a better knowledge of the technology used and, third, evaluate the possible contribution of in situ analyses in conservation studies. The paintings from two different rock art sites were studied. The instrument proved to be highly suitable for in situ analyses in physically very challenging conditions. Most of the pigments and alteration products previously detected under laboratory conditions were identified, thereby giving information on both the pigments and conservation state of the paintings. A layered structure of alteration products and pigment was identified in situ for the first time by controlling the laser power, thereby obtaining the same results as in mapping experiments of cross sections of paint. Copyright © 2010 John Wiley & Sons, Ltd.     

Pigment analysis of Portuguese portrait miniatures of 17th and 18th centuries by Raman Microscopy and SEM‐EDS

Seventeen Portuguese miniature portraits on copper support from the Évora Museum collection (Portugal) were analyzed in situ and nondestructively by Raman microscopy (RM), SEM‐EDS, and stereomicroscopy. This work constitutes a great breakthrough in the study of miniature paintings from the 17^th and 18^th centuries, since the chemical information known about this unique kind of paintings are still scarce, and in particular, this exclusive collection was never been subjected to any physicochemical study. In this work, each portrait was examined in detail in order to characterize the pigments palette used by the miniaturists. The μ‐Raman analysis, in particular, guaranteed an exceptional visualization and good individual identification of small grains of pigments and other constituents of the pictorial layer. Using this technique, 19 compounds were identified, including bluish black covellite, a pigment rarely found in oil paintings. SEM‐EDS was used as an important complementary technique to confirm the chemical nature of some pigments and to identify shell gold (gold dust) in some portraits. Overall, the pigments identified in this large set of old paintings are broadly consistent with those mentioned in the painting treatises of that time or reported in other more modern bibliographic sources. Copyright © 2014 John Wiley & Sons, Ltd.     

Development of a portable x‐ray fluorescence spectrometer equipped with two monochromatic x‐ray sources and silicon drift detector and field analysis of Islamic glasses at an excavation site in Egypt

A portable x‐ray fluorescence spectrometer equipped with a silicon drift detector (SDD) and a digital signal processor (DSP) was developed for in‐field analysis of archeological samples at an excavation site. This spectrometer allows us to carry out highly sensitive analyses of various elements with atomic numbers down to Na in air by using two monochromatic x‐ray sources obtained by doubly bent toroidal monochromators of graphite (0002) (Pd Kα for medium–heavy elements) and PET (200) (Pd Lα for light elements) and white x‐rays with a Zr filter excited at 40 kV for heavy elements. The detection limit was 0.31% for Al and 4 ppm for Sr in a standard cement sample. The spectrometer was set in a room of the excavation laboratory at al‐Tūr Sinai in the Sinai Peninsula in Egypt in the summer of 2001. The Middle Eastern Culture Center has been conducting an excavation of the sites in al‐Tūr al‐Kilani and Rāya, which were important port cities of Red Sea trade from early Islamic periods: al‐Tūr (A.D. 14–20) and Rāya (A.D. 8–12). The instrument was operated without any problems and 222 glass objects, 26 pottery sherds, seven pigments and 88 metallic objects were analyzed non‐destructively during a 1 month stay. Since this was the first chemical analysis done at the sites, many important archaeological findings were obtained in the present study. Glass objects were successfully classified based on their chemical compositions. Characterization of stained (luster) glasses was conducted. Copyright © 2004 John Wiley & Sons, Ltd.     

Raman spectra of nitrogen‐containing organic compounds obtained using a portable instrument at −15 °C at 2860 m above sea level

Well‐resolved Raman spectra of samples of nitrogen‐containing compounds were detected using a portable Raman instrument (Ahura First Defender XL) outdoors at a low ambient temperature of −15 °C and at an altitude of 2860 m (Pitztall, Austria). The portable Raman spectrometer tested here is equipped with a 785‐nm diode laser and a fixed frontal probe. Solid form of formamide, urea, 3‐methylpyridine, aniline, indene, 1‐(2‐aminoethyl)piperazine, indoline and benzofuran were detected unambiguously under high‐mountain field conditions. The main Raman features (strong, medium and partially weak bands) were observed at the correct wavenumber positions (with a spectral resolution 7–10 cm⁻¹) in the wavenumber range 200–1600 cm⁻¹. The results obtained demonstrate the possibility of employing a miniaturised Raman spectrometer as a key instrument for investigating the presence of nitrogen‐containing organic compounds and biomolecules outdoors under low temperature conditions. Within the payload designed by European Space Agency (ESA) and National Aeronautics and Space Administration (NASA) for future missions, focussing not only on Mars, Raman spectroscopy represents an important instrumentation for the detection of organic nitrogen‐containing compounds relevant to life detection on planetary surfaces or near sub‐surfaces. Copyright © 2009 John Wiley & Sons, Ltd.     

In situ energy dispersive X‐ray fluorescence analysis of rock art pigments from the ‘Abrigo dos Gaivões’ and ‘Igreja dos Mouros’ caves (Portugal)

A portable energy dispersive X‐ray fluorescence spectrometer was used to obtain the elemental composition of Neolithic rock art paintings of the ‘Abrigo dos Gaivões’ and ‘Igreja dos Mouros’ caves. These caves, located in the Esperança parish, Arronches' county, in the San Mamede's mountains (Portugal), belong to a group of spread shelters just next to the western Spanish border. Results show the strong presence of iron in bare rock, and this element can be clearly detected as the main component of the red paintings. No evidence of manganese was detected in either the brownish or the black paintings, contrary to other Neolithic paintings in the Mediterranean area. Copyright © 2011 John Wiley & Sons, Ltd.     

Discrimination of carotenoid and flavonoid content in petals of pansy cultivars (Viola x wittrockiana) by FT‐Raman spectroscopy

Fourier Transform Raman spectroscopy (FT‐Raman) has been applied for the non‐destructive in‐situ analysis of pigments on differently colored flower petals of pansy cultivars (Viola x wittrockiana). The main target of the present study was to investigate how far the Raman mapping technique through FT‐Raman spectroscopy and cluster analysis of the Raman spectra is a potential method for the direct, in‐situ discrimination of flavonoids (flavonols against anthocyanins) and of carotenoids occurring in flowers, using intact and differently colored flower petal of Viola x wittrockiana for this case study. In order to get more information about the reliability of the direct in‐situ flavonoid detection by the Raman method, pigments extracts of the petals were separated by thin‐layer chromatography (TLC) and investigated by Raman spectroscopy. Hierarchical cluster analysis (HCA) of the Raman spectra from reference pigments (carotenoids, anthocyanins and flavonols), from areas of the flower petals, and from the TLC extracts allowed discriminating the various pigments, in particular flavonoids (flavonols against anthocyanins) and carotenoids. With a two‐dimensional Raman mapping technique, which provides a chemical image of the sample under investigation, we determined by cluster analysis the distribution of carotenoids, anthocyanins and flavonols from the outer layer of the petals, and by integrating through suitable spectral regions selected as characteristic markers for particular pigments their relative concentration could approximately be determined. We found a satisfactory correlation between the patterns seen on the visible images and the patterns on the chemical images obtained by Raman mapping. Copyright © 2011 John Wiley & Sons, Ltd.     

Near‐infrared surface‐enhanced Raman spectroscopy (NIR‐SERS) studies on oxyheamoglobin (OxyHb) of liver cancer based on PVA‐Ag nanofilm

A near‐infrared surface‐enhanced Raman spectroscopy (NIR‐SERS) method was employed for oxyheamoglobin (OxyHb) detection to develop a simple blood test for liver cancer detection. Polyvinyl alcohol protected silver nanofilm (PVA‐Ag nanofilm) used as the NIR‐SERS active substrate to enhance the Raman scattering signals of OxyHb. High quality NIR‐SERS spectrum from OxyHb adsorbed on PVA‐Ag nanofilm can be obtained within 16 s using a portable Raman spectrometer. NIR‐SERS measurements were performed on OxyHb samples of healthy volunteers (control subjects, n = 30), patients (n = 40) with confirmed liver cancer (stage I, II and III) and the liver cancer patients after surgery (n = 30). Meanwhile, the tentative assignments of the Raman bands in the measured NIR‐SERS spectra were performed, and the results suggested cancer specific changes on molecule level, including a decrease in the relative concentrations and the percentage of aromatic amino acids of OxyHb, changes of the vibration modes of the C_aH_m group and pyrrole ring of OxyHb of liver cancer patients. In this paper, principal component analysis (PCA) combined with independent sample T test analysis of the measured NIR‐SERS spectra separated the spectral features of the two groups into two distinct clusters with the sensitivity of 95.0% and the specificity of 85.7%. Meanwhile, the recovery situations of the liver cancer patients after surgery were also assessed using the method of discriminant analysis‐predicting group membership based on PCA. The results show that 26.7% surgeried liver cancer patients were distinguished as the normal subjects and 63.3% were distinguished into the cancer. Our study demonstrated great potentials for developing NIR‐SERS OxyHb analysis into a novel clinical tool for non‐invasive detection of liver cancers. Copyright © 2013 John Wiley & Sons, Ltd.     

Quantitative or semi‐quantitative?–laboratory‐based WD‐XRF versus portable ED‐XRF spectrometer: results obtained from measurements on nickel‐base alloys

‘Semi‐quantitative’ analytical procedures are becoming more and more popular. Using such procedures, the question of the accuracy of results arises. The accuracy of an analytical procedure depends to a great extent on spectral resolution, counting statistics and matrix correction. Two ‘semi‐quantitative’ procedures are compared with a quantitative analytical program. Using a laboratory‐based wavelength‐dispersive x‐ray fluorescence (WD‐XRF) spectrometer and a portable energy‐dispersive x‐ray fluorescence (ED‐XRF) spectrometer, 28 different nickel‐base alloy Certified Reference Materials (CRMs) were analyzed. Line interferences and inaccurate matrix correction are reasons for deviations from the reference value. As the comparison shows, ‘semi‐quantitative’ analyses on the WD‐XRF spectrometer can be accepted as quantitative determinations. The investigations show that the results obtained with the portable ED‐XRF spectrometer do not meet the quality requirements of laboratory analysis, but they are good enough for field investigations. Copyright © 2004 John Wiley & Sons, Ltd.     

On‐site detection of phosgene agents by surface‐enhanced Raman spectroscopy coupled with a chemical transformation approach

Phosgene and its analogs are greatly harmful to the public health, environmental safety and homeland security as widely used industrial substances with extremely high toxicity. In order to rapidly evaluate the emergency risk caused by these chemicals, a new highly sensitive method based on surface‐enhanced Raman spectroscopy (SERS) technique for measurement of phosgene agents was developed for the first time. Coupled with a chemical transformation approach, the highly toxic phosgene was conveniently converted to a SERS‐sensitive probe, i.e. iodine (I₂), with low toxicity or non‐toxicity. The characteristic SERS peak in 459 cm⁻¹ was used for quantitation and was presumed as a formation of triiodide anion (I₃⁻), which was induced in an iodide (I⁻)‐aggregation Au NPs system. The total measurement can be completed in ~20 min with the limits of detection of ~60 µg/l (phosgene) and ~30 µg/l (diphosgene), respectively, on a portable Raman spectrometer. This work is the first report of SERS measurement on phosgene and diphosgene in a quantitative level. This method is expected to meet the requirements of on‐site detection of phosgene agents, promote emergency responses and raise more opportunities for the portable SERS applications. Copyright © 2015 John Wiley & Sons, Ltd.     

Raman spectra of organic acids obtained using a portable instrument at −5 °C in a mountain area at 2000 m above sea level

Well‐resolved Raman spectra of organic acids were obtained with 785 nm excitation using a portable Raman instrument (Ahura First Defender XL) under low temperature −5 °C atmospheric conditions at an altitude of 2000 m (Axamer Lizum, Innental, Austria). The portable Raman spectrometer tested in this setting permits fast and unambiguous detection of solid forms of these organic acids (formic, acetic, valeric, hexanoic, heptanoic, isophthalic, ascorbic and mellitic) under field conditions. This demonstrates the possibility to use a miniaturized Raman spectrometer as a key instrument for investigating the presence of organic compounds and biomolecules under low temperature conditions. These results are important for future missions focusing not only on Mars, where Raman spectroscopy will be a key non‐destructive analytical tool for the in situ identification of organic compounds relevant to life detection on planetary surfaces or near sub‐surfaces. Copyright © 2009 John Wiley & Sons, Ltd.     

In situ detection of cocaine hydrochloride in clothing impregnated with the drug using benchtop and portable Raman spectroscopy

This study describes the application of benchtop and portable Raman spectroscopy for the in situ detection of cocaine hydrochloride in clothing impregnated with the drug. Raman spectra were obtained from a set of undyed natural and synthetic fibres and dyed textiles impregnated with the drug. The spectra were collected using three Raman spectrometers: one benchtop dispersive spectrometer coupled to a fibre‐optic probe and two portable spectrometers. Despite the presence of some spectral bands arising from the natural and synthetic polymer and dyed textiles, the drug could be identified by its characteristic Raman bands. High‐quality spectra of the drug could be acquired in situ within seconds and without any sample preparation or alteration of the evidential material. A field‐portable Raman spectrometer is a reliable technique that can be used by emergency response teams to rapidly identify unknown samples. Copyright © 2009 John Wiley & Sons, Ltd.     

Microanalysis of clay‐based pigments in painted artworks by the means of Raman spectroscopy

FT Raman spectroscopy and micro‐Raman spectroscopy with lasers of three different wavelengths (1064 nm, 785 nm and 532 nm) were used for analysis of reference samples of natural clay pigments including white clay minerals (kaolinite, illite, montmorillonite), green earths (glauconite and celadonite) and red earths (natural mixtures of white clay minerals with hematite). In addition, eight micro‐samples obtained from historical paintings containing clay pigments in ground and colour layers have been examined. Powder X‐ray diffraction and micro‐diffraction were used as supplementary methods. It was found that laser operating at 1064 nm provided the best quality Raman spectra for distinguishing different white clay minerals, but the spectra of green and red earths were affected by strong fluorescence caused by the presence of iron. Green earth minerals could be easily distinguished by 532 or 785 nm excitation lasers, even in small concentrations in the paint layers. On the other hand, when anatase (TiO₂) or iron oxides (such as hematite) were present as admixtures (both are quite common, particularly in red earths), the collection of characteristic spectra of clay minerals which form the main component of the layer was hindered or even prevented. Another complicating factor was the fluorescence produced by organic binders when analysing the micro‐samples of artworks. In those cases, it is always necessary to use powder X‐ray micro‐diffraction to avoid misleading interpretations of the pigment's composition. Copyright © 2013 John Wiley & Sons, Ltd.     

Raman studies of Japanese art objects by a portable Raman spectrometer using liquid crystal tunable filters

Raman spectroscopic studies of a few Japanese art objects have been performed by using a portable Raman spectrometer constructed with liquid crystal tunable filters as dispersive elements. Interesting information has been obtained from the Raman spectra observed from ukiyo‐e's (Japanese woodblock prints) and their woodblocks. The performance data and the imaging capabilities of the constructed spectrometer are presented. Copyright © 2011 John Wiley & Sons, Ltd.     

Comparison of near infrared laser excitation wavelengths and its influence on the interrogation of seized drugs‐of‐abuse by Raman spectroscopy

The laser excitation wavelength is an important parameter in obtaining Raman spectra from drugs‐of‐abuse. This article compares the effect of near infrared wavelengths, 785 nm, using both benchtop and portable instrumentation and benchtop 1064 nm on the Raman spectra of seized drugs‐of‐abuse, including cocaine hydrochloride, cocaine freebase (crack), methylenedioxymethamphetamine (‘ecstasy’), amphetamine, diamorphine (heroin) and cannabis. The significant benefit of using 1064 nm for the interrogation of this type of sample is highlighted. Copyright © 2009 John Wiley & Sons, Ltd.