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.     

Rapid outdoor non‐destructive detection of organic minerals using a portable Raman spectrometer

Raman spectral signatures have been obtained for a series of organic minerals using a compact portable Raman instrument equipped with 785‐nm laser excitation. Well‐resolved Raman spectra of crystalline salts of carboxylic acids, whewellite and mellite, as well as of the aromatic mineral idrialite were recorded. For comparative purposes, an amorphous fossil resin, baltic amber, was also investigated. The results obtained confirm that portable Raman instruments can be considered as excellent tools for field geological applications, including the detection of organic minerals in the frame of outcrops of sedimentary rocks or coal beds. Organic minerals can be added to the list of established biomarkers, including porphyrins, hydrocarbons and organic acids, which are important for the study with regard to future exobiological missions such as the ESA ExoMars mission to detect the presence of extinct or extant life on Mars. Copyright © 2009 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.     

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.     

New Developments and Applications of Handheld Raman,Mid-Infrared,and Near-Infrared Spectrometers

Abstract: Recently, miniaturization of Raman, mid-infrared (IR), and near-infrared (NIR) spectrometers has made substantial progress. Though mid-infrared systems are based exclusively on attenuated total reflection (ATR) measurements, near-infrared spectrometers operate in the diffuse reflection or transmission mode. The reduction in size, however, must not be accompanied by deterioration in measurement performance, and portable instrumentation will only have a real impact on quality and process control if Raman, IR, and NIR spectra of comparable quality to laboratory spectrometers can be obtained.

In the present communication, a short overview on the building principles of novel handheld systems will be provided and the results of qualitative and quantitative analyses of selected liquid and solid sample systems obtained with these Raman, Fourier transform infrared (FTIR), and NIR spectrometers will be evaluated in terms of their comparability with laboratory instruments and their suitability for on-site and field measurements.     

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.     

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.     

Raman and fluorescence lidar measurements of aircraft engine emissions

Laser induced Raman and fluorescent measurements were made in the exhaust of a gas turbine engine with a new field portable instrument devised specifically for gas turbine exhaust measurements. The gas turbine exhaust was analyzed by conventional instruments for CO, CO₂, NO, NO_x, total hydrocarbons, smoke and temperature, and these data were used as a ‘calibration’ standard for the evaluation of the laser Raman instrument. Results thus far indicate good correlations for CO₂, O₂, smoke, hydrocarbons and temperature. The instrument was not sensitive enough for NO detection but the data analysis indicates that 100 ppm may be detectable with instrument improvements. CO analysis was not attempted, but it is expected that CO could be detected with further research. NO₂ (or NO_x) was not attempted because theoretical and experimental laboratory analysis indicated severe interference with CO₂. The conclusion was that laser Raman shows a good potential for aircraft gas turbine emission analysis.     

Surface‐enhanced Raman spectra of melamine and other chemicals using a 1550 nm (retina‐safe) laser

Many trace chemical analyses are being transitioned from the lab to the field, among which is surface‐enhanced Raman spectroscopy. Although initial portable Raman analyzers primarily employ 785 nm laser excitation, recent studies suggest longer wavelengths, with an appropriate surface‐enhanced Raman‐active substrate, may provide equal sensitivity. Furthermore, 1550 nm excitation may provide added safety for the user, in that permanent retina damage does not occur. Here, we show that a reasonable enhancement factor can be obtained for melamine using 1550 nm laser excitation that is nearly equivalent to those obtained using 785 and 1064 nm laser excitation. We also demonstrate that a number of other chemicals of interest can be measured by 1550 nm surface‐enhanced Raman scattering, albeit only modest sensitivity is achieved because of instrument limitations, not enhancement factors. Copyright © 2011 John Wiley & Sons, Ltd.     

On‐and off‐site Raman study of rock‐shelter paintings at world‐heritage site of Bhimbetka

Rock‐shelter paintings of Bhimbetka world‐heritage site near Bhopal, India have been investigated using a portable Raman spectrometer. These paintings in the rock shelters belong to periods starting from pre‐historic to the 19th century AD (Gond period). In addition, tiny fragments of pigments (100–200 µm in size) extracted from some of the artworks were also studied in laboratory using a micro‐Raman spectrometer and analyzed using energy‐dispersive X‐ray analysis for elemental composition. Based on the Raman spectra and the elemental analysis mineral‐based pigments such as calcite, gypsum, hematite, whewellite, and goethite could be identified. A comparison of the spectra recorded on‐site using a light‐weight portable spectrometer with those using laboratory equipment is also made and discussed. Copyright © 2012 John Wiley & Sons, Ltd.     

Outdoor use of mobile Raman spectrometers to study the solutions and ices of amino acids

Selected amino acids (glycine, alanine, and threonine) were analysed in the form of water solutions, mixtures of these amino acids in solution, as well as their respective ices using two hand‐held instruments under outdoor and winter mountain conditions. The hand‐held instruments featured 785 and 532 nm excitations; the latter being one of the first using this wavelength on the market. The changes to the Raman spectra of the solutions and ices are discussed in relationship to the degree of ambiguity of the detection of the amino acids within the mixtures. The hand‐held instruments were able to detect two amino acids out of the three in solution. The results showed that the hand‐held instruments provide sufficient quality spectra when analysing ices prepared from the solutions; however, an unambiguous detection of these amino acids within mixtures still remains a challenge. Copyright © 2014 John Wiley & Sons, Ltd.     

Teaching Raman Spectroscopy in Both the Undergraduate Classroom and the Laboratory with a Portable Raman Instrument

We have evaluated a small portable Raman instrument on loan from B&W Tek, Inc., and have determined that it can successfully be used in the classroom both as a visual aid for teaching the fundamentals of Raman spectroscopy and for a variety of undergraduate experiments as a normal component of an instrumental analysis class. Having portable Raman instrumentation would allow the instructor to demonstrate the principles of Raman spectroscopy, as well as the concepts of calibration curves, blank subtraction, detection limits, and regression analysis. Both qualitative and quantitative types of experiments were done for solid Tylenol tablets, aqueous solutions of isopropyl alcohol, dimethyl sulfoxide, methanol, and ethanol, and gaseous CO₂ and N₂O₄. Additionally, surface‐enhanced resonance Raman spectra of Rhodamine 6G were obtained using a chloride ion–activated silver colloid. Spectra from the B&W Tek, Inc., instrument were comparable to literature Raman spectra.     

Non‐invasive approach in the study of polychrome terracotta sculptures: employment of the portable XRF to investigate complex stratigraphy

In the field of conservation science, in situ non‐invasive analytical techniques are widely used to investigate polychrome surfaces as frescoes, mural or easel paintings. Indeed, these techniques allow achieving information on materials composition and they often reduce the micro‐sampling. In this work, in situ non‐invasive techniques have been used to study a complex system, terracotta polychrome sculptures. The presence of the priming, the numerous painted layers and the ground layer spread on a porous material substrate are the main features of these sculptures; therefore, their study requires a scientific approach based on results obtained by different analytical techniques. In order to evaluate potentialities and limitations of the non‐invasive approach to this complex case, the results of energy‐dispersive X‐ray fluorescence (EDXRF), spectrophotometry and optical microscopy have been compared with the data achieved by laboratory analytical investigation as optical and scanning electron microscopy, energy‐dispersive X‐ray microanalysis and Raman spectroscopy. In particular, XRF data collected on several polychrome terracotta are here re‐examined on the basis of the results obtained by laboratory techniques. Even if, in some cases, portable XRF may induce to a wrong interpretation of the stratigraphy, it can be considered a suitable instrument for a preliminary diagnostic campaign of terracotta polychrome sculptures. Copyright © 2011 John Wiley & Sons, Ltd.     

A portable shifted excitation Raman difference spectroscopy system: device and field demonstration

In this paper, we present a portable shifted excitation Raman difference spectroscopy (SERDS) system applied in outdoor experiments. A dual‐wavelength diode laser emitting at 785 nm is used as excitation light source. The diode laser provides two individually controllable excitation lines at 785 nm with a spectral distance of about 10 cm⁻¹ for SERDS. This monolithic light source is implemented into a compact handheld Raman probe. Both components were developed and fabricated in‐house. SERDS measurements are performed in an apple orchard, and apples and green apple leafs are used as test samples. For each excitation wavelength, a single Raman spectrum is measured with 50 mW at the sample. Strong background interference from ambient daylight and laser‐induced fluorescence obscure the Raman signals. SERDS efficiently separates the wanted Raman signals from the disturbing background signals. For the Raman spectroscopic investigations of green leafs, one accumulation with an exposure time of 0.2 s was used for each excitation wavelength to avoid detector saturation. An 11‐fold improvement of the signal‐to‐background noise is achieved using SERDS. The results demonstrate the suitability of the portable SERDS system for rapid outdoor Raman investigations. Copyright © 2016 John Wiley & Sons, Ltd.     

Tentative differentiation between Iznik tiles and copies with Raman spectroscopy using both laboratory and portable instruments

Iznik tiles dated from the 16th century, copies of tiles and pottery of Théodore Deck from the 19th century and also tiles without any information on their origin were analyzed with both laboratory and portable Raman instruments. As the original tiles are generally fixed on the walls of historical buildings, the portable Raman spectrometer is more convenient for the analysis but the information obtained from the spectra is not very useful because of the medium resolution and complex baseline of the instrument in spite of its speed and ease of use. The Raman signature of the glazes is the most pertinent and easily accessible fingerprint of the artifacts. The differentiation between Iznik ceramics and other samples could be made with Raman spectrometers, according to the specific signature of Si O stretching and bending bands of Iznik glazes. Copyright © 2009 John Wiley & Sons, Ltd.     

In situ study of stones adorning a silver Torah shield using portable Raman spectrometers

A silver Torah shield fitted with a set of precious stones and glass imitations crafted in Poland in the first half of the 19th century was investigated using two of the currently distributed portable and relatively low‐cost Raman spectrometers in situ at the Jewish Museum in Prague. Observed Raman peaks corresponded well (+/− 3 cm⁻¹) to the reference values. The hand‐held instruments operated at 785‐ and 532‐nm laser excitations showed good performance in the fast and unambiguous identification of nearly 60 stones which were fitted on the shield: one blue aquamarine, three purple amethysts, thirteen red garnets (all classified as high‐percentage almandines), three white pearls, fifteen pieces of red coral and five chalcedonies (one white and four red). All of the other stones were identified as colored glass. The rather chaotic mixture of stones of various colors, cuts and sizes and the total volume of imitation glass support the theory that the mounted stones were gathered from Jewish households and donated for the adornment of the shield. The common portable Raman instruments represent an ideal tool for the quick and accurate identification of gemstones mounted in historical artifacts in situ in the framework of museum or collection sites in a non‐destructive way. Copyright © 2014 John Wiley & Sons, Ltd.     

Assessment of robustness and transferability of classification models built for cancer diagnostics using Raman spectroscopy

Over recent years, Raman spectroscopy has been demonstrated as a prospective tool for application in cancer diagnostics. The use of Raman spectroscopy for this purpose relies on pattern recognition methods that have been developed to perform well on data achieved under laboratory conditions. However, the application of Raman spectroscopy as a routine clinical tool is likely to result in imperfect data due to instrument‐to‐instrument variation. Such corruption to the pure tissue spectral data is expected to negatively impact the classification performance of the diagnostic model. In this paper, we present a thorough assessment of the robustness of the Raman approach. This was achieved by perturbing a set of spectra in different ways, including various linear shifts, nonlinear shifts and random noise and using previously optimised classification models to predict the class membership of each spectrum in a testing set. The loss of predictive power with increased corruption was used to calculate a score, which allows an easy comparison of the model robustness. For this approach, three different types of classification models, including linear discriminant analysis (LDA), partial least square discriminant analysis (PLS‐DA) and support vector machine (SVM), built for lymph node diagnostics were the subject of the robustness testing. The results showed that a linear perturbation had the highest impact on the performance of all classification models. Among all linear corruption methods, a gradient y‐shift resulted in the highest performance loss. Thus, the factor most likely to affect the predictive outcome of models when using different systems is a gradient y‐shift. Copyright © 2010 John Wiley & Sons, Ltd.     

Fast single-photon avalanche diode arrays for laser Raman spectroscopy

We incorporate newly developed solid-state detector technology into time-resolved laser Raman spectroscopy, demonstrating the ability to distinguish spectra from Raman and fluorescence processes. As a proof of concept, we show fluorescence rejection on highly fluorescent mineral samples willemite and spodumene using a 128×128 single-photon avalanche diode (SPAD) array with a measured photon detection efficiency of 5%. The sensitivity achieved in this new instrument architecture is comparable to the sensitivity of a technically more complicated system using a traditional photocathode-based imager. By increasing the SPAD active area and improving coupling efficiency, we expect further improvements in sensitivity by over an order of magnitude. We discuss the relevance of these results to in situ planetary instruments, where size, weight, power, and radiation hardness are of prime concern. The potential large-scale manufacturability of silicon SPAD arrays makes them prime candidates for future portable and in situ Raman instruments spanning numerous applications where fluorescence interference is problematic.     

Grating-Stabilized External Cavity Diode Lasers for Raman Spectroscopy—A Review

Abstract: Conventional Raman techniques require a continuous-wave laser with stabilized wavelength, narrow line width, and sufficient output power. Due to their miniature size and low cost, diode lasers are good choice as light sources for Raman spectroscopy, especially when compact and portable instruments are needed. However, a solitary multimode diode laser has certain drawbacks that limit its use for Raman application. To circumvent these drawbacks, an external cavity can be coupled to the active gain medium of the diode to enhance the laser performance. A grating-based external cavity allows the laser to operate in a single longitudinal mode with greatly reduced line width and stabilized wavelength. This article examines the fundamentals of semiconductor lasers to show the necessity of operating diode lasers in an external cavity for Raman applications. Two feedback grating-based external cavity diode laser (ECDL) designs, viz. Littrow and Littman-Metcalf configurations, are explained. Historic and recent progress in the development of ECDL devices is reported. An updated summary of ECDL-equipped Raman systems applied to fields such as in vivo biomedical studies and in situ process/quality control is provided. Topics on mode-hop-free continuous scanning, wavelength stabilization, and dealing with ambient conditions are discussed.