Spectral Database Systems: A Review

Abstract: Spectroscopy has been demonstrated to be an important method of analysis and detection. A spectral database system (SDBS) can not only satisfy the traditional requirements for spectral management but also provides several new functions, including spectra sharing on the website and web-based and real-time analysis and detection. Chemists and spectroscopists could analyze and detect pure materials and some mixtures rapidly with the help of standard SDBS, and now they are trying to improve these systems to fulfill rapid analysis for complex mixtures, even those as complex as agro-products. Overall, SDBS make it possible to analyze and detect unknown samples rapidly and nondestructively. This article focuses on significant progress in research on infrared (IR), near-infrared (NIR), and Raman SDBSs. Additionally, the drawbacks and obstacles of SDBSs are summarized and trends are discussed.     

Vibrational Spectroscopy in Clinical Analysis

Abstract: Vibrational spectroscopy includes several different techniques, the most important of which are mid-infrared (IR), near-IR, and Raman spectroscopy. Raman and mid-IR spectroscopy are complementary techniques and usually both are required to completely measure the vibrational modes of a molecule. Vibrational spectrometry covers a series of well-established analytical methodologies suitable to be employed for both qualitative and quantitative purposes. In the first part of this review, we will focus on theoretical aspects related to vibrational techniques; in the second part, the most important papers, published during the period 2005–2014, related to clinical analysis performed with vibrational spectroscopy techniques will be critically discussed.     

Wavenumber Calibration of CCD Detector Raman Spectrometers Controlled by a Sinus Arm Drive

Abstract

The calibration procedures needed for use of dispersive Raman spectrometers have been reviewed. Like other high‐precision spectrometers incorporating moving gratings, Raman spectrometers are subject to problems with wavenumber scale accuracy. Commercially available Raman spectrometers of types DILOR‐HORIBA LabRam and RENISHAW System 1000 have been examined for wavenumber scale stability, linearity, and reproducibility. For reliable use of the wavenumber data, daily calibration is a necessity. A procedure to examine the linearity of such mechanical drive systems is presented. A new finding was that the examined spectrometers give wavenumber calibration errors that were quite reproducible from day to day at a given temperature in the laboratory but depended markedly on the selected setting of the gratings. Knowledge of this linearity problem is essential for obtaining a reliable calibration. The most correct calibration was obtained by the use of certain “golden” settings of the sinus drive at a constant temperature of the laboratory. In this way, the examined spectrometers could be used with better precision, without daily calibration, provided the temperature of the room was constant or corrected for. A procedure for correction of these errors by the software is suggested.     

Fast detection of sulphate minerals (gypsum,anglesite, baryte) by a portable Raman spectrometer

Well‐resolved Raman spectra of gypsum, anglesite and baryte were detected using a portable Raman instrument (Ahura First Defender XL) in the laboratory and outdoor under atmospheric conditions. Spectra were obtained using a 785‐nm excitation. The portable spectrometers display generally lower spectral resolution compared with the laboratory confocal instrument but permit the fast, unambiguous detection of minerals under field conditions. Portable Raman instruments can be advocated as excellent tools for field geological, environmental as well as exobiological applications. A miniaturized Raman instrument will be included in the Pasteur analytical package of the ESA ExoMars mission and interesting research applications can now be proposed for in situ field planetary studies. Additionally, portable Raman instruments represent an ideal tool for demonstrating possible applications of Raman spectroscopic techniques outdoor. In geosciences this approach represents a new field which could completely change classical field work. Copyright © 2009 John Wiley & Sons, Ltd.     

Application of Vibrational Spectroscopy in Combination with Chemometrics Techniques for Authentication of Herbal Medicine

Abstract: One of the emerging issues in herbal medicine is its authenticity. The substitution of highly valuable materials in herbal medicine with lower ones is common practice in the herbal medicine industry. This practice can cause serious effects or be harmful to human health; therefore, the authentication of herbal medicine using analytical techniques is necessary. Due to its capability as fingerprint technique, vibrational spectroscopy (infrared and Raman), especially in combination with several chemometrics techniques, is the method of choice for authentication purposes. This review highlights the use of mid-infrared, near-infrared, and Raman spectroscopy for authentication of herbal medicine, either in raw materials or in final products.     

Raman scattering by hot and thermal polaritons in crystal quartz

Summary Nonlinear mixing of IR and visible radiation,i.e. coherent Raman scattering by polaritons driven by a CO₂ laser, has been used to obtain the dispersion curve and its width inq-space of the polariton associated to theE-phonon at 1065 cm⁻¹ in crystal quartz. It is shown in this paper that a direct method to determine indipendently, with high precision, the refractive index and absorbance of a crystal can be obtained in this way. The results are compared with accurate data obtained from Raman scattering by polaritions in thermal equilibrium and very good agreement is found between the two measurements. It is finally shown that nonlinear-mixing techniques turn out to be completely consistent with the simple picture of scattering of light by hot polaritons. This work was supported by the Italian Consiglio Nazionale delle Ricerche del Ministero della Pubblica Istruzione.     

Rapid near-infrared Raman spectroscopy system for real-time in vivo skin measurements

A rapid dispersive-type near-infrared (NIR) Raman spectroscopy system and a Raman probe were developed to facilitate real-time, noninvasive, in vivo human skin measurements. Spectrograph image aberration was corrected by a parabolic-line fiber array, permitting complete CCD vertical binning, thereby yielding a 3.3-16-fold improvement in signal-to-noise ratio. Good quality in vivo cutaneous NIR Raman spectra free of interference from fiber fluorescence and silica Raman scattering can be acquired in less than 1 s, which greatly facilitates practical noninvasive tissue characterization and clinical diagnosis.     

Quantitative analysis of the content of deltamethrin in agrochemicals by near-infrared, attenuated total reflectance infrared and raman spectroscopy

The method of near-infrared, attenuated total reflectance infrared and Raman spectroscopy was used for the rapid determination of the content of deltamethrin in agrochemicals. The quantitative models were established by PLS (partial least squares) method and optimized. The independent validation sets were used to evaluate the model accuracy. The determination coefficient R2 and RMSECV of the near-infrared model and mid-infrared model were 0.9999, 0.022 and 0.9996 and 0.056, respectively. The accuracy of both was similar. The determination coefficient R2 and RMSECV of Raman were 0. 996 7 and 0.172, which exhibits the lower accuracy. The result indicated that near-infrared, mid-infrared and Raman spectroscopy can be applied to the rapid determination of the content of the active ingredients precisely, which has an important significance in the on-line determination, analysis on site in the enterprise and the rapid quantitative analysis of agrichemicals in the department of quality monitoring.     

EFFECTS OF APODIZATION FUNCTION,ZERO FILLING,BACKGROUND SPECTRA,AND ABSORBANCE TRANSFORMATION ON MID-INFRARED CALIBRATIONS FOR FEED COMPOSITION

ABSTRACT

Research has demonstrated that diffuse reflectance mid-infrared spectroscopy can, like near-infrared diffuse reflectance, be used to quantitatively determine the composition of ground samples of forages and soils without the need for KBr dilution. While it has been demonstrated that the accuracy of calibrations developed using mid-infrared spectra can be equal to or better than that achieved using near-infrared spectra, the influence of factors such as apodization function has not been determined. Results based on the spectra of 173 treated forage samples obtained using a DigiLab FTS-60 spectrometer have demonstrated that many parameters associated with mid-infrared spectra have little or no effect on partial least squares calibrations. Additional zero filling of spectra had little effect other than to increase the derivative gaps found to produce optimal calibrations, but calibrations developed using Kubelka-Munk transformed data, as opposed to absorbance data, were not as accurate. Choice of apodization function also had little effect, although slightly better results were found using triangular or weak Norton-Beer. Likewise, the frequency of taking a background spectrum did not seem to have any great effect on calibrations, although results were slightly better with hourly or daily acquisitions as opposed to one for each sample as is done in the near-infrared.     

Assignments of Carbon-Sulphur Vibrations by Selenation: An FT-IR and FT-Raman Study on 1, 3, 5-Trithiacyclohexane

Abstract

The IR and Raman spectra of 1, 3, 5-trithiacyclohexane (1) and 1, 3, 5-triselenocyclohexane (2) have been recorded with FT-instrumentation within 3500–100 cm^?l, and the C-S vibrations of 1 have been reviewed by comparing its spectra with those of 2. The IR and Raman spectra slightly differ from those previously reported and some vibrations, previously assigned to C-H modes in 1on the basis of NCT calculations, are reassigned to C-S modes on the basis of the selenation effect. “Selenation” has proved to be a very simple and effective tool in recognizing carbon-sulfur vibrations both in IR and Raman. The Raman peaks due to carbon-chalcogen vibrations are less intense in 1 than in 2, according to the higher polarizability of the selenium atom.     

A comprehensive spectroscopic study of synthetic Fe2+, Fe3+, Mg2+ and Al3+ copiapite by Raman,XRD, LIBS,MIR and vis–NIR

The identification of iron sulfates on Mars by the Mars Exploration Rovers (MERs) and the Mars Reconnaissance Orbiter emphasized the importance of studying iron sulfates in laboratory simulation experiments. The copiapite group of minerals was suggested as one of the potential iron sulfates occurring on the surface and subsurface on Mars, so it is meaningful to study their spectroscopic features, especially the spectral changes caused by cation substitutions. Four copiapite samples with cation substitutions (Fe³⁺, Al³⁺, Fe²⁺, Mg²⁺) were synthesized in our laboratory. Their identities were confirmed by powder X‐ray diffraction (XRD). Spectroscopic characterizations by Raman, mid‐IR, vis‐NIR and laser‐induced‐breakdown spectroscopy (LIBS) were conducted on those synthetic copiapite samples, as these technologies are being (and will be) used in current (and future) missions to Mars. We have found a systematic ν₁peak shift in the Raman spectra of the copiapite samples with cation substitutions, a consistent atomic ratio detection by LIBS, a set of systematic XRD line shifts representing structural change caused by the cation substitutions and a weakening of selection rules in mid‐IR spectra caused by the low site symmetry of (SO₄)²⁻ in the copiapite structures. The near‐infrared (NIR) spectra of the trivalent copiapite species show two strong diagnostic water features near 1.4 and 1.9 µm, with two additional bands near 2.0 µm. In the vis‐NIR spectra, the position of an electronic band shifts from 0.85 µm for ferricopiapite to 0.866 µm for copiapite, and this shift suggests the appearance of a Fe²⁺ electronic transition band near 0.9 µm. Copyright © 2010 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.     

A Review of the State of the Art,Limitations, and Perspectives of Infrared Spectroscopy for the Analysis of Wine Grapes,Must, and Grapevine Tissue

Abstract

As a fast and easy-to-operate technique, infrared (IR) spectroscopy has gained wide industrial acceptance for routine wine analysis. Considering the continuing improvements in hardware and software design and the analytical requirements of real-time or multiparametric analysis by the modern grape and wine industry, it is anticipated that in the near future IR spectroscopy will progressively become a routine method for process monitoring and process control in different stages of grape and wine production. This review highlights recent developments and applications of IR spectroscopy (near- and mid-infrared) to measure compositional parameters in wine grapes, grape juice, and grapevine tissues (e.g., leaves, stems, grapevine wood). In addition, some critical aspects and limitations in instrument availability, type of application, and overall understanding of the technology, which can be barriers for adoption of IR technologies by the grape and wine industry, will be discussed.     

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.     

Trace-gas analysis using diode lasers in the near-IR and long-path techniques

Room-temperature, near-infrared, semiconductor diode lasers continue to gain importance for gas monitoring applications owing to their compactness, ease of use, reasonable cost and compatibility with telecommunications-grade optical fiber components. They may probe overtone or combination vibrational bands for a large variety of atmospheric relevant molecular species. These spectral bands exhibit line strengths orders of magnitude lower than those of fundamental vibrations, occurring in the mid-infrared. As a consequence, they are often used in conjunction with long-path techniques, enabling one to perform high sensitivity local measurements through long absorption path-lengths. At this purpose, resonant optical cavities can be fruitfully employed. This paper is devoted to a discussion of the main features of cavity-enhanced absorption spectrometers, operating with near-infrared diode lasers. We report on the operating principle as well as the achievable performance of these devices, also compared to more traditional apparatus, based on the multiple reflection cells. Experimental results on water vapour and oxygen detection are reported.     

Improved diode properties in zinc telluride thin film-silicon nanowire heterojunctions

In this study, structural and optoelectronic properties and photodedection characteristics of diodes constructed from p-zinc telluride (ZnTe) thin film/n-silicon (Si) nanowire heterojunctions are reported. Dense arrays of vertically aligned Si nanowires were successfully synthesized on (1 1 0)-oriented n-type single crystalline Si wafer using simple and inexpensive metal-assisted etching (MAE) process. Following the nanowire synthesis, p-type ZnTe thin films were deposited onto vertically oriented Si nanowires via radio frequency magnetron sputtering to form three-dimensional heterojunctions. A comparative study of the structural results obtained from X-ray diffraction and Raman spectroscopy measurements showed the improved crystallinity of the ZnTe thin films deposited onto the Si nanowire arrays. The fabricated nanowire-based heterojunction devices exhibited remarkable diode characteristics and enhanced optoelectronic properties and photosensitivity in comparison to the planar reference. The electrical measurements revealed that the diodes with nanowires had a well-defined rectifying behaviour with a rectification ratio of 10⁴ at ±2 V and a relatively small ideality factor of n = 1.8 with lower reverse leakage current and series resistance at room temperature in dark condition. Moreover, an open-circuit voltage of 100 mV was also observed under illumination. Based on spectral photoresponsivity measurements, the nanowire-based device exhibited a distinct responsivity and high detectivity in visible and near-infrared (NIR) wavelength regions. The device characteristics observed here offer that the fabricated ZnTe thin film/Si nanowire-based p–n heterojunction structures will find important applications in future and will be a promising candidate for high-performance and low-cost optoelectronic device applications, NIR photodedectors in particular.     

A Review of Recent Near-Infrared Research for Wood and Paper (Part 2)

Abstract: This review article introduces recent technical and scientific reports on near-infrared (NIR) spectroscopy in the wood and paper industry, which have increased during the last decade. Many researchers have reported that the NIR technique is useful for detection of both chemical and physical properties of wood materials and has been widely used in cases where the characteristic cellular structure of the material is retained. With regard to application of NIR spectroscopy to pulp and paper, many publications have reported its potential as an on-line measurement technique during paper-making process control. NIR spectroscopy is considered fundamental in applied research on wood and paper. Utilization of NIR spectroscopy in the wood and paper industry should take into account its applicability and limitations as a nondestructive technique.     

Use of Infrared Spectroscopy for In-Field Measurement and Phenotyping of Plant Properties: Instrumentation,Data Analysis,and Examples

Abstract: Recent developments in agricultural technology have led to a demand for a new era of nondestructive methods of plant analysis in the field rather than in the laboratory. The combination of fundamental science (e.g., plant physiology, biochemistry, and other disciplines), multivariate data analysis, and spectroscopy will enable the development of technologies for reliable and rapid on-farm or in-field low-cost testing. This will enable both farmers and scientist to maximize sales in existing markets and to target new markets with differentiated products or select new varieties, better soil management, among other issues. Infrared (IR) spectroscopy has been successfully applied for the determination of composition analysis in several fields (e.g., agriculture, pharmaceutical, etc.) and in product quality assessment and production control. The IR spectrum can give a global signature of composition (fingerprint), which, with the application of chemometric techniques, can be used to elucidate particular compositional characteristics not easily detected by traditional targeted chemical analyses. This article highlights the principles of IR spectroscopy, commercially available instruments and software, and calibration issues including calibration development, networking, and transfer. In addition, recent and potential applications of IR spectroscopy in grains, fruits, and other plant tissues are presented and discussed.     

In‐situ and laboratory Raman analysis in the field of cultural heritage: the case of a mural painting

The present work exemplifies, over a mural painting from the 14th century, the advantages of an initial exhaustive research using latest generation hand‐held spectrometers (Raman mainly) in order to perform the characterization of valuable objects of cultural heritage. These in‐situ techniques (meaning on‐site and non‐destructive) are very useful to study the pigments and materials, to identify the nature and causes of some of the main sources of deterioration and to examine past repaints. In addition, the in‐situ measurements are of great importance in the selection of micro‐samples for the laboratory analyses. In this particular case, the combination of these results with the chemical imaging analyses in the laboratory (such as Raman and energy dispersive X‐ray spectrometry imaging) allowed the characterization of the mural painting, including, the identification of all restoration works applied in the past. Copyright © 2014 John Wiley & Sons, Ltd.     

一种新的多元校正模型分子光谱传递方法

无论是近红外还是红外光谱,多元校正模型的传递问题都尚未解决。为了实现模型和光谱的传递,提出了一种改进的PDS算法——SA-PDS算法,论方法通过PDS算法进行模型传递,使用光谱间的夹角大小作为判定准则来选择传递参数,使得模型传递过程不受到样品性质参考值的影响,也不再依赖于模型,并且可以双向传递。该方法分别通过在近红外数据和中红外数据中应用来证明模型传递的可行性,实验收集烟叶样本测得其近红外光谱,沥青样本测得其中红外光谱,将烟叶总糖会计师和沥青蜡含量作为模型预测对象。使用光谱夹角作为PDS参数选择标准与使用预测标准偏差作为判定准则相比,实验表明：对于近红外光谱的从机向主机的传递,其验证集预测精密度RMSEP从5.257 4降低至1.337 1,优于RMSEP(1.350 3)方法,预测偏差也同样被改善。对于中红外光谱从机向主机的传递,新方法验证集预测精密度RMSEP从0.525 1降低至0.186 9,优于RMSEP(0.219)方法。主机向从机的传递也取得了满意的传递结果。