Micro‐Raman study of PET single fibres under high hydrostatic pressure: phase/conformation transition and amorphization

The micro/nano structural evolution of a PET single fibre under hydrostatic pressure has been studied by Raman micro spectroscopy in a diamond anvil cell (DAC). Different bands in the Raman spectra were used as probes: the low wavenumber collective modes (<250 cm⁻¹) representative of the long‐range chain organization, as well as the stretching and bending amide and aromatic ring modes representative of the local chain behaviour. The in situ analysis at different pressures shows an evolution from an axial oriented trans‐conformation to an amorphous, isotropic material, i.e. the reverse transformation observed during the process of drawing the fibre from an isotropic amorphous precursor. Copyright © 2007 John Wiley & Sons, Ltd.     

Origin of the variability of the mechanical properties of silk fibres: 2 The nanomechanics of single silkworm and spider fibres

The variability in mechanical stress–strain behaviour of various silks obtained from Bombyx mori silkworm and Nephila madagascarensis spider fibres has been studied by high resolution Raman analysis using the Raman shift induced by application of a controlled strain on the νN–H mode as a probe. Silk fibres exhibiting typical 1, 2, 3 and 4 Types have been selected from their characteristic tensile stress–strain behaviour. A perfect relationship between the nanomechanic (at the scale of the chemical bond) and macroscopic (silk single fibre) behaviour is observed as in the case of other polyamide fibres (natural keratin and synthetic PA66). Copyright © 2012 John Wiley & Sons, Ltd.     

Nanomechanics of single keratin fibres: A Raman study of the α‐helix →β‐sheet transition and the effect of water

The use of micro‐Raman spectroscopy, through chemical‐bond, nano‐scale probes, allows the changes in conformations (α‐helix →β‐sheet), chain orientation, breakage of disulfide bonds (20%) and the increase of intra‐ and inter‐chain distances during the application of stress to be distinguished. The combination of micro‐Raman spectroscopy and a Universal Fibre Tester allows a quantitative measurement of the extension of chemical bonds in the peptide chain during loading. The nano‐structural transformations of keratin during strain of human hair in a dry environment (40–60% relative humidity) and saturated with water have been studied. Water permits the sliding of the chains and decreases the bond energy of the hair. Spectral analyses and 2D correlation are two coherent and independent methods to follow the structural nano‐mechanical (Raman) and micro‐mechanical (strain/stress) analyses, and confirm the validity of the experimental results, tools and principles used, as well as the agreement with the structural model of keratin fibres described by Chapman and Hearle. Copyright © 2006 John Wiley & Sons, Ltd.     

Microfocus X‐ray scattering and micro‐Raman spectroscopy: Transcrystallinity in isotactic polypropylene

Microfocus X‐ray scattering and micro Raman spectroscopy have been applied to study the β‐transcrystalline morphology in isotactic polypropylene. The transformation from the α‐ to the β‐form through the so‐called bifurcation of growth mechanism has been investigated with high spatial resolution. We found that the mixed α–β region does not present spatial correlation along the shearing direction, implying that there is no cooperative crystallization from the different β‐nucleation centres. In addition, a strong change in the lamellar orientation of the α‐form thin layer that induces the growth of the β‐crystallites has been observed for the first time. Finally, changes in the relative intensities of some selected Raman bands allowed the observation of the α–β transformation process at the molecular level.

     

On the noise limit of stress and temperature measurements with micro‐Raman spectroscopy

We report for the first time on the thorough experimental and theoretical assessment of the noise limit of mechanical stress and temperature measurements with micro‐Raman spectroscopy. A comprehensive study has been performed in which, for different incident laser light intensities and acquisition times, 1000 Raman spectra of mono‐crystalline silicon were acquired per setting. Curve fitting was employed to obtain the peak positions of all the spectra, from which the standard deviations of the measured peak positions were obtained versus the total accumulated amount of laser light incident on the sample during one measurement. It has been found that the noise in the obtained peak position decreases as 1/sqrt(n) over more than three decades of the incident amount of laser light. At very low light conditions, the noise decreases as 1/n. By comparing the experimental results obtained to recent theoretical work, we show that the acquisition is limited by photon shot noise over most of the range and is limited by electronic detector noise at very low light conditions only. Pixelation errors do not play a role. It is concluded that the low electronic noise of typical Raman spectroscope detectors is overkill for the investigation of mechanical stress and temperature in silicon and other materials with comparable peaks, as it has absolutely no influence on the noise level of such an experiment. Maximum Raman signal intensity on the detector and high quantum efficiency detection are more important. Copyright © 2013 John Wiley & Sons, Ltd.     

Imaging of internal stress around a mineral inclusion in a sapphire crystal: application of micro‐Raman and photoluminescence spectroscopy

We developed a micro‐Raman and photoluminescence imaging technique for visualizing the internal stress fields in a sapphire crystal. The technique was applied to an Australian sapphire gemstone with a zircon inclusion. Considering piezospectroscopic effects on Raman and photoluminescence spectra, the Raman shifts of sapphire around the zircon inclusion were converted to hydrostatic pressure and deviatoric components of stress tensor. The internal stress was highly concentrated at the tips of the zircon crystal, where the deviatoric stress and the hydrostatic pressure component reached 700 and 470 MPa, respectively. Generation of compressive stress on the crystal surface of zircon can be explained by the difference in thermal expansion coefficients and elastic constants between sapphire and zircon. In general, internal stress fields induced by mineral inclusions reflect the pressure and temperature conditions at which the host sapphire gemstones were crystallized. Thus, the present technique can be utilized to identify the origin of gemstones. Copyright © 2012 John Wiley & Sons, Ltd.     

Estimation of spectra sample size for characterizing single cells using micro‐Raman spectroscopy

Single‐cell micro‐Raman spectroscopy has the potential to become a powerful, new cytometric approach for discriminating between cell types and identifying subpopulations of cells based on differences in the intrinsic, molecular content of the cells. Despite the considerable progress in demonstrating many biomedical applications of single‐cell Raman spectroscopy, an unresolved issue with this method is the inconsistent manner in which the technique has been applied experimentally to acquire spectra from a cell, which can potentially lead to irreproducible and inconsistent results from study to study. Specifically, the problem pertains to the validity of using micro‐Raman spectroscopy to sample an arbitrary fraction of the cell volume and to claim that the resulting spectrum represents the entire cell volume. In this study, we investigate the effect of sample size (i.e. the number of Raman spectra acquired from distinct locations in a cell) on the ability to generate a Raman spectrum that accurately describes the total molecular content of the cell. Furthermore, we demonstrate that a minimum sample size of Raman spectra acquired from a cell can be used in place of a full hyperspectral Raman image to achieve the same degree of discrimination between different cell populations. Lymphocytes exposed to the chemotherapy drug, doxorubicin, at different concentrations and exposure times are used as a model biological system in this study. This work demonstrates the importance of adequate spectral sampling and presents an approach for determining the minimum sample size needed to reproduce a Raman spectrum of a whole cell, which are expected to impact future single‐cell Raman spectroscopy studies. Copyright © 2015 John Wiley & Sons, Ltd.     

Origin of the variability of the mechanical properties of silk fibres: 3. Order and macromolecule orientation in Bombyx mori bave,hand‐stretched strings and Nephila madagascarensis spider fibres

The comparison of the low wavenumber of polarized Raman spectra (50–300 cm^–1) from Bombyx mori (fresh cocoons fibres, hand‐stretched ‘Crins de Florence’ strings from the gland content, dried gland, regenerated silk films) and Nephila madagascarensis silks reveals the high polarisation of fibre modes and the absence of polarisation for dried gland and regenerated silk films. This is consistent with X‐ray diffraction measurements. The orientation of the fibroin/spidroin chains is due to the stretching during production, as for advanced synthetic fibres. The bandwidth of the ‘ordered chains’ signature is almost the same for the different fibres. However, the degree of polarisation seems to be higher in the case of spider fibre. The huge bandwidth of low wavenumber components of regenerated films indicates high disorder. Measurements along the fibre point out conformation changes with a periodicity (~20 mm) related to the silkworm head motion during the fabrication of the cocoon. Copyright © 2012 John Wiley & Sons, Ltd.     

Effect of Al content on the structure of Al‐substituted goethite: a micro‐Raman spectroscopic study

The characterization of X‐ray diffraction, X‐ray fluorescence, and field emission scanning electron microscope were used to confirm the successful preparation of Al‐substituted goethite with different Al content. The micro‐Raman spectroscopy was utilized to investigate the effect of Al content on the goethite lattice. The results show that all the feature bands of goethite shifted to high wavenumbers after the occurrence of Al substitution for Fe in the structure of goethite. The shift of wavenumber shows a good linear relationship as a function of increasing Al content especially for the band at 299 cm⁻¹ (R² = 0.9992). The in situ Raman spectroscopy of thermally treated goethite indicated that the Al substitution not only hinders the transformation of goethite, but also retarded the crystallization of thermally formed hematite. All the results indicated that Raman spectrum displayed an excellent performance in characterizing Al‐substituted goethite, which implied the promising application in other substituted metal oxides or hydroxides. Copyright © 2013 John Wiley & Sons, Ltd.     

Della Robbia blue glaze: micro‐Raman temperature study and X‐ray fluorescence spectroscopy characterization

Micro‐Raman temperature study and X‐ray fluorescence (XRF) spectroscopy were used for characterization of the blue glaze on Saint John the Baptist—majolica terracotta relief attributed to Andrea Della Robbia and Saint John the Baptist with Cross—majolica terracotta statue attributed to Giovanni Della Robbia. Both objects are on permanent exhibition in the John and Mable Ringling Museum of Art in Sarasota, FL. This study proves that the detection of the 548 cm⁻¹ Raman band alone cannot serve as evidence for presence of lazurite crystallites in the pigment in the glaze. It was established that the famous Della Robbia blue is due to the combined effect of Co Ni Cu Zn atoms and S₃⁻ ions embedded in a lead silicate matrix. It is proposed that the Della Robbia family used Co‐containing sulfide ores as a source for manufacturing their blue pigments. Copyright © 2009 John Wiley & Sons, Ltd.     

Ageing of calcium silicate cements for endodontic use in simulated body fluids: a micro‐Raman study

To evaluate bioactivity properties, a calcium silicate experimental cement (wTC) and a phosphate‐doped wTC cement (wTC‐TCP) were aged for different times (1–180 days) at 37 °C in two simulated body fluids, i.e. Dulbecco's phosphate buffered saline (DPBS) and Hank's balanced salt solution (HBSS). The cements were analyzed by micro‐Raman spectroscopy to investigate the presence of calcium phosphate deposits and the composition changes as a function of the storage time (hydration of anhydrite/gypsum and formation of ettringite; hydration of belite/alite and formation of hydrated silicates). After 1 day of ageing in DPBS, the two cements already showed a different behavior: only the surface of wTC‐TCP cement showed the band at 965 cm⁻¹, suggesting the formation of a detectably thick calcium phosphate deposit. The trend of the I₉₆₅/I₉₉₀ Raman intensity ratio indicated the formation of a meanly thicker apatite deposit on the wTC‐TCP cement until 90 days. After 60 days of ageing in DPBS, the thickness of the apatite deposit on wTC and wTC‐TCP was about 200 and 500 µm, respectively, whereas at 180 days, the two cements did not appear significantly different (thickness of about 900 µm). The bioactivity of both cements in HBSS was less pronounced than in DPBS, according to the lower phosphate concentration of HBSS; at the same time, higher amounts of calcite were found on the surface of both cements. The wTC‐TCP cement showed a higher bioactivity in this medium also; after 180 days, the thickness of the apatite deposit on wTC and wTC‐TCP was < 50 µm and about 100 µm, respectively. Copyright © 2009 John Wiley & Sons, Ltd.     

In situ chemical analysis of modern organic tattooing inks and pigments by micro‐Raman spectroscopy

The chemical composition of tattooing pigments has varied greatly over time according to available technologies and materials. Beginning with naturally derived plant and animal extracts, to coloured inorganic oxides and salts, through to the modern industrial organic pigments favoured in today's tattooing studios. The demand for tattooing is steadily growing as it gains cultural popularity and acceptance in today's society, but ironically, increasing numbers of individuals are seeking laser removal of their tattoos for a variety of reasons. Organic pigments are favoured for tattooing because of their high tinting strength, light fastness, enzymatic resistance, dispersion and relatively inexpensive production costs. Adverse reactions have been reported for some organic inks, as well as potential complications, during laser removal procedures stemming from the unintentional creation of toxic by‐products. Currently, regulatory bodies such as the US Food and Drug Administration have not approved any coloured inks to be injected into the skin, and tattoo ink manufacturers often do not disclose the ingredients in their products to maintain proprietary knowledge of their creations. A methodology was established using micro‐Raman spectroscopy on an animal model to correctly identify the constituents of a selection of modern, organic tattoo inks in situ or post procedure, within the skin. This may serve as a preliminary tool prior to engaging in Q‐switched laser removals to assess the risks of producing potentially hazardous compounds. Likewise, the pigments responsible for causing adverse reactions in some patients may be quickly identified to hasten any corresponding treatment. Copyright © 2008 John Wiley & Sons, Ltd.     

Characterization of archeological glasses by micro‐Raman spectroscopy

The method based on the deconvolution of the Raman spectra of glasses, proposed for the investigation of glazed ceramics by Colomban, is applied to archeological samples of glass of two different origins in an attempt to characterize the glass composition and the fictive temperature using a contactless, nondestructive spectroscopic technique. The samples investigated are glassy mosaic tesserae of Roman times from Massa Lubrense, Napoli, Italy, and medieval rosary grains found during the excavations in the church of San Martino di Rivosecco, Parma, Italy. The polymerization index, obtained as the ratio of the bending and stretching band amplitudes, suggests firing temperatures not less than 1000–1100 °C for both Roman and medieval glasses. From the wavenumber shift of some stretching bands at about 1050–1100 cm⁻¹, the content of lead was estimated. The medieval samples show a lower Pb content, a result confirmed by elementary energy dispersive X‐ray spectral data. Copyright © 2010 John Wiley & Sons, Ltd.     

Thermal micro‐Raman spectroscopic study of polymorphic transformation of famotidine under different compression pressures

The objective of this study was to investigate the effect of pressure and/or temperature on the polymorphic transformation of famotidine from form B to form A by using a thermal confocal Raman microspectroscopy. A compact with a wide transparent zone in the center and an opaque zone surrounding it was prepared by compressing a conical mass of famotidine form B. Two unique Raman peaks at 2897 and 2920 cm⁻¹ for famotidine forms B and A, respectively, were used as markers. The result indicates that the opaque zone in each compact was composed of famotidine from B, and it did not undergo any polymorphic transformation by preparing with higher compression pressure and/or by heating. The Raman peak intensity ratio of the 2920 cm⁻¹ and 2897 cm⁻¹ bands markedly increased starting from 120 °C for the transparent zone prepared by compressing with 19.61 × 10⁴ kPa pressure, but increased from 100 °C with 49.03 × 10⁴ kPa pressure, indicating the occurrence of thermally induced polymorphic transformation of famotidine from form B to form A. However, the transparent zone prepared by 9.81 × 10⁴ kPa compression pressure retained the same Raman spectrum as that of the famotidine form B, revealing that the thermally induced polymorphic transformation of famotidine was dependent on the pressure applied. There was no polymorphic transformation of famotidine in the transparent zone when it was prepared by a higher compression pressure at a lower temperature or by a lower pressure at a higher temperature. The combined effect of compression and temperature was found to accelerate the polymorphic transformation from form B to form A in the transparent zone of famotidine. Copyright © 2006 John Wiley & Sons, Ltd.     

Origin of the variability of the mechanical properties of silk fibers: 4. Order/crystallinity along silkworm and spider fibers

The poor crystallinity of proteic fibers has fuelled an ongoing debate over their exact organization. We present a full‐range Raman comparison of Nephila madagascariensis spider and Bombyx mori silkworm silks that sheds some new light on that matter. On the one hand, a large variability is observed along the fibers in the −200 to 200 cm⁻¹ spectral window, which is sensitive to the long‐range order signature of polyamide chains. This questions the validity of previous literature data considering silk fiber as a homogeneous material. On the other hand, the ‘amide I’ band is almost independent of the targeted point, which sets a limit to this widely used structure probe. In‐line mapping of the fibers showed that the extension of the ordered zones ranges between 1 and 3 µm. The correlation between the macromechanical behavior (the stress–strain curves) and the nanomechanics (Raman low wavenumber signatures) under controlled tensile strain demonstrates a Prevorsek's type microstructure: the macromolecular chains belong to both ordered and amorphous ‘regions’. Copyright © 2014 John Wiley & Sons, Ltd.     

Deterioration of iron archaeological artefacts: micro‐Raman investigation on Cl‐containing corrosion products

Deterioration after excavation of archaeological iron artefacts buried in soil is often associated with the presence of chlorinated phases in corrosion products, leading to serious problems for conservation of metallic objects of cultural heritage. Therefore, in order to better understand the corrosion process related to the presence of chlorine, some high‐resolution techniques of material characterisation are implemented. The analyses are realised on cross sections of corroded iron objects excavated from archaeological sites dated from the 12th to the 16th century A.D. Cl‐containing phases appear even when the Cl level in the water is low. In addition to the common oxy‐hydroxide‐containing chloride, akaganeite (β–FeOOH) often mentioned in the literature, a ferrous hydroxychloride β–Fe₂(OH)₃Cl was also found in the corrosion layers. Moreover, part of the study is based on the preparation and desalinisation of pure akaganeite powder in order to characterise the influence of the chloride content on its crystalline structure as characterised by Raman spectroscopy. Copyright © 2007 John Wiley & Sons, Ltd.     

Pigment identification and decoration analysis of a 5th century Chinese lacquer painting screen: a micro‐Raman and FTIR study

To investigate the pigments and decoration applied to a wood‐based lacquer painting screen from the tomb of Si‐ma Jin‐long, Shanxi Province, central China, made by Chinese craftsmen in the 5th century, a combination of micro‐Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), wavelength dispersive X‐ray fluorescence (WDXRF), and microscopic examination was used. The obtained results are as follows: (1) the black, yellow, and red colors are identified as carbon black, orpiment and realgar, and cinnabar, respectively, by using micro‐Raman spectroscopy. The FTIR result shows that the white pigment filled in the leaves is not lead white, as assumed in the literature, but gypsum. Whether lead white was used at other locations remains unanswered and requires more samples for further work; (2) the thickness of each discernable pigment layer, as observed under the microscope, is approximately equal and the differences among them are small, suggesting a superfine painting skill; besides, a noticeable smooth interface between wood and the red grounding substance indicates that a polishing process might have been applied before the painting; (3) the red background was proved to contain cinnabar, but further FTIR analyses found no evidence for the presence of Chinese wood oil; and (4) the most interesting finding, rarely reported before, is that white grains of different sizes are found in both pigment layers and the grounding substance, which are perhaps an intentional addition. Further, in situ XRF and Raman analyses indicate that they are sourced from hydroxyapatite, coming probably from the intentional addition of animal bone ash to the lacquer. But how such a process could be finished and what purpose it served have not yet been answered. Copyright © 2009 John Wiley & Sons, Ltd.     

UV‐resonance Raman micro‐spectroscopy to assess residual chromophores in cellulosic pulps

Ultraviolet‐resonance Raman (UV‐RR) micro‐spectroscopy is an appropriate and sensitive tool to assess the chromophore structures in bleached cellulosic pulps used for papermaking. The particular selectivity in detection and identification of chromophores in pulps is achieved by acquiring the UV‐RR spectra in the solid state with laser excitation at 325 nm. This wavelength corresponds to absorption of poly‐unsaturated chromophore structures in partially bleached/fully bleached pulps, and linearly correlated with the signal at ca 1600 cm⁻¹ in the UV‐RR spectra. The characteristic vibrations from particular pulp chromophore structures have been assigned from experiments with model compounds, thus allowing the establishment of a UV‐RR database. Among the components of bleached pulp, the xylan–lignin complex was suggested to be an important source of chromophores. The monitoring of pulp bleaching by UV‐RR allowed us to suggest that it is the formation of new polysaccharide‐derived chromophores upon bleaching that hinders development of further brightness and is co‐responsible for the brightness reversion of fully bleached pulps. Copyright © 2010 John Wiley & Sons, Ltd.     

An analysis of bivalve larval shell pigments using micro‐Raman spectroscopy

Micro‐Raman spectroscopy has been used on adult bivalve shells to investigate organic and inorganic shell components but has not yet been applied to bivalve larvae. It is known that the organic matrix of larval shells contains pigments, but less is known about the presence or source of these molecules in larvae. We investigated Raman spectra of seven species of bivalve larvae to assess the types of pigments present in shells of each species and how the ratio of inorganic : organic material changes in a dorso‐ventral direction. In laboratory experiments, we reared larvae of three clam species in waters containing different organic signatures to determine if larvae incorporated compounds from source waters into their shells. We found differences in spectra and pigments between most species but found less intraspecific differences. A neural network classifier for Raman spectra classified five out of seven species with greater than 85% accuracy. There were slight differences between the amount and type of pigment present along the shell, with the prodissoconch I and shell margin areas being the most variable. Raman spectra of 1‐day‐old larvae were found to be differentiable when larvae were reared in waters with different organic signatures. With micro‐Raman spectroscopy, it may be possible to identify some unknown species in the wild and trace their natal origins, which could enhance identification accuracy of bivalve larvae and ultimately aid management and restoration efforts. Copyright © 2014 John Wiley & Sons, Ltd.