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  • SAGE Publications  (11)
  • Chemistry/Pharmacy  (11)
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  • SAGE Publications  (11)
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  • Chemistry/Pharmacy  (11)
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  • 1
    Online Resource
    Online Resource
    SAGE Publications ; 2017
    In:  Applied Spectroscopy Vol. 71, No. 6 ( 2017-06), p. 1231-1241
    In: Applied Spectroscopy, SAGE Publications, Vol. 71, No. 6 ( 2017-06), p. 1231-1241
    Abstract: Classical least squares (CLS) regression is a popular multivariate statistical method used frequently for quantitative analysis using Fourier transform infrared (FT-IR) spectrometry. Classical least squares provides the best unbiased estimator for uncorrelated residual errors with zero mean and equal variance. However, the noise in FT-IR spectra, which accounts for a large portion of the residual errors, is heteroscedastic. Thus, if this noise with zero mean dominates in the residual errors, the weighted least squares (WLS) regression method described in this paper is a better estimator than CLS. However, if bias errors, such as the residual baseline error, are significant, WLS may perform worse than CLS. In this paper, we compare the effect of noise and bias error in using CLS and WLS in quantitative analysis. Results indicated that for wavenumbers with low absorbance, the bias error significantly affected the error, such that the performance of CLS is better than that of WLS. However, for wavenumbers with high absorbance, the noise significantly affected the error, and WLS proves to be better than CLS. Thus, we propose a selective weighted least squares (SWLS) regression that processes data with different wavenumbers using either CLS or WLS based on a selection criterion, i.e., lower or higher than an absorbance threshold. The effects of various factors on the optimal threshold value (OTV) for SWLS have been studied through numerical simulations. These studies reported that: (1) the concentration and the analyte type had minimal effect on OTV; and (2) the major factor that influences OTV is the ratio between the bias error and the standard deviation of the noise. The last part of this paper is dedicated to quantitative analysis of methane gas spectra, and methane/toluene mixtures gas spectra as measured using FT-IR spectrometry and CLS, WLS, and SWLS. The standard error of prediction (SEP), bias of prediction (bias), and the residual sum of squares of the errors (RSS) from the three quantitative analyses were compared. In methane gas analysis, SWLS yielded the lowest SEP and RSS among the three methods. In methane/toluene mixture gas analysis, a modification of the SWLS has been presented to tackle the bias error from other components. The SWLS without modification presents the lowest SEP in all cases but not bias and RSS. The modification of SWLS reduced the bias, which showed a lower RSS than CLS, especially for small components.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2017
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 2
    Online Resource
    Online Resource
    SAGE Publications ; 2018
    In:  Applied Spectroscopy Vol. 72, No. 8 ( 2018-08), p. 1234-1243
    In: Applied Spectroscopy, SAGE Publications, Vol. 72, No. 8 ( 2018-08), p. 1234-1243
    Abstract: Raman spectroscopy has been applied to the quantitative analysis of the concentration of bisulfate in acid-sulfate fluids at different temperatures. The quantitative analysis method is based on the peak area ratios of [Formula: see text](ν 1 ) and H 2 O (ν 2 ), where PA([Formula: see text]/H 2 O) = [[Formula: see text]] × (0.0066 × T + 1.3070) at a temperature range of 0–100 ℃. We found that the molal scattering coefficient of bisulfate increases slightly at the elevated temperature may be due to the changes of fraction of water molecules that are hydrogen-bonded. The method can also be applied to analyze physicochemical parameters of other acid fluids, such as hydrogen phosphate, bicarbonate, etc., and especially to the in situ detection of deep sea acid-sulfate hydrothermal fluids in the future.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2018
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 3
    In: Applied Spectroscopy, SAGE Publications, Vol. 72, No. 1 ( 2018-01), p. 48-59
    Abstract: Deep-sea carbon dioxide (CO 2 ) plays a significant role in the global carbon cycle and directly affects the living environment of marine organisms. In situ Raman detection technology is an effective approach to study the behavior of deep-sea CO 2 . However, the Raman spectral characteristics of CO 2 can be affected by the environment, thus restricting the phase identification and quantitative analysis of CO 2 . In order to study the Raman spectral characteristics of CO 2 in extreme environments (up to 300 ℃ and 30 MPa), which cover most regions of hydrothermal vents and cold seeps around the world, a deep-sea extreme environment simulator was developed. The Raman spectra of CO 2 in different phases were obtained with Raman insertion probe (RiP) system, which was also used in in situ Raman detection in the deep sea carried by remotely operated vehicle (ROV) “Faxian”. The Raman frequency shifts and bandwidths of gaseous, liquid, solid, and supercritical CO 2 and the CO 2 –H 2 O system were determined with the simulator. In our experiments (0–300 ℃ and 0–30 MPa), the peak positions of the symmetric stretching modes of gaseous CO 2, liquid CO 2 , and supercritical CO 2 shift approximately 0.6 cm –1 (1387.8–1388.4 cm –1 ), 0.7 cm –1 (1385.5–1386.2 cm –1 ), and 2.5 cm –1 (1385.7–1388.2 cm –1 ), and those of the bending modes shift about 1.0 cm –1 (1284.7–1285.7 cm –1 ), 1.9 cm –1 (1280.1–1282.0 cm –1 ), and 4.4 cm –1 (1281.0–1285.4 cm –1 ), respectively. The Raman spectral characteristics of the CO 2 –H 2 O system were also studied under the same conditions. The peak positions of dissolved CO 2 varied approximately 4.5 cm –1 (1282.5–1287.0 cm –1 ) and 2.4 cm –1 (1274.4–1276.8 cm –1 ) for each peak. In comparison with our experiment results, the phases of CO 2 in extreme conditions (0–3000 m and 0–300 ℃) can be identified with the Raman spectra collected in situ. This qualitative research on CO 2 can also support the further quantitative analysis of dissolved CO 2 in extreme conditions.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2018
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 4
    Online Resource
    Online Resource
    SAGE Publications ; 1991
    In:  Applied Spectroscopy Vol. 45, No. 5 ( 1991-06), p. 874-882
    In: Applied Spectroscopy, SAGE Publications, Vol. 45, No. 5 ( 1991-06), p. 874-882
    Abstract: Fourier transform infrared (FT-IR) emission spectroscopy has been used to study both molybdenum oxide and supported molybdenum oxide catalysts. An infrared emission cell was specially designed to treat the samples in vacuo or in various gases over a wide temperature range (25–700°C). The experimental conditions including sample preparation, effects of temperature, and sample thickness on the emission spectrum are detailed. The infrared emission spectrum of pure MoO 3 was nearly identical to the spectrum obtained by the KBr disc transmission method. An infrared emission study on the reduction and the oxidation of molybdenum oxide is presented. In situ infrared emission spectra were recorded for supported molybdena on Al 2 O 3 , SiO 2 , ZrO 2 , and TiO 2 at elevated temperatures, and the nature of the molybdenum-containing species on these supports is discussed on the basis of the infrared emission results.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1991
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 2021
    In:  Applied Spectroscopy Vol. 75, No. 5 ( 2021-05), p. 531-544
    In: Applied Spectroscopy, SAGE Publications, Vol. 75, No. 5 ( 2021-05), p. 531-544
    Abstract: Many spectra have a polynomial-like baseline. Iterative polynomial fitting is one of the most popular methods for baseline correction of these spectra. However, the baseline estimated by iterative polynomial fitting may have a substantial error when the spectrum contains significantly strong peaks or have strong peaks located at the endpoints. First, iterative polynomial fitting uses temporary baseline estimated from the current spectrum to identify peak data points. If the current spectrum contains strong peaks, then the temporary baseline substantially deviates from the true baseline. Some good baseline data points of the spectrum might be mistakenly identified as peak data points and are artificially re-assigned with a low value. Second, if a strong peak is located at the endpoint of the spectrum, then the endpoint region of the estimated baseline might have a significant error due to overfitting. This study proposes a search algorithm-based baseline correction method (SA) that aims to compress sample the raw spectrum to a dataset with small number of data points and then convert the peak removal process into solving a search problem in artificial intelligence to minimize an objective function by deleting peak data points. First, the raw spectrum is smoothened out by the moving average method to reduce noise and then divided into dozens of unequally spaced sections on the basis of Chebyshev nodes. Finally, the minimal points of each section are collected to form a dataset for peak removal through search algorithm. SA selects the mean absolute error as the objective function because of its sensitivity to overfitting and rapid calculation. The baseline correction performance of SA is compared with those of three baseline correction methods, the Lieber and Mahadevan-Jansen method, adaptive iteratively reweighted penalized least squares method, and improved asymmetric least squares method. Simulated and real Fourier transform infrared and Raman spectra with polynomial-like baselines are employed in the experiments. Results show that for these spectra the baseline estimated by SA has fewer error than those by the three other methods.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2021
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 6
    Online Resource
    Online Resource
    SAGE Publications ; 1994
    In:  Applied Spectroscopy Vol. 48, No. 8 ( 1994-08), p. 977-984
    In: Applied Spectroscopy, SAGE Publications, Vol. 48, No. 8 ( 1994-08), p. 977-984
    Abstract: The fluorescence lifetimes of a series of crude oils at various concentrations have been measured for UV-visible excitation and emission wavelengths. The lifetime results are compared with fluorescence spectra and quantum yields for these solutions. The concentration effects of energy transfer and quenching are large and result in a significant decrease in fluorescence lifetimes for high concentrations and for heavy crude oils. Thus, radiationless processes dominate in energy transfer. At high concentrations, energy transfer produces large red shifts in fluorescence emission spectra, while quenching produces a large reduction in quantum yields. Stern-Volmer analyses of lifetime and quenching data show a linear dependence of energy transfer and quenching rates on concentration. The rate constants are consistent with collisions which are very efficient at energy transfer and quenching, and the rates of these two processes are comparable.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1994
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 7
    In: Applied Spectroscopy, SAGE Publications, Vol. 64, No. 3 ( 2010-03), p. 268-274
    Abstract: Attenuated total reflection (ATR) Fourier transform infrared (FT-IR) spectroscopy has been applied to study the short and long term postmortem metabolic processes in rat and human kidney cortexes. The goals of this project were as follows: (1) to investigate the changes of ATR spectra in different rat and human tissues after death, (2) to explore the best mathematical model with different band absorption ratio changes to determine the postmortem interval (PMI), and (3) to establish a preliminary human postmortem ATR spectra database. There were three different types of metabolic changes after death based on the spectral results: (1) the intensities of some bands increased continuously (e. g., C–H stretching region), (2) the intensities of other bands decreased continuously (e.g., PO 2 − symmetric stretching), and (3) other bands remained relatively stable (e.g., C–OH bending, CO–O–C antisymmetric stretching). The band absorbance ratios for rats were found to display either a significant increase or decrease with increasing time after death. Of the absorbance ratios of the various bands investigated to find the best fit with the cubic model function in rats, the A 1652 / A 1396 ratio showed the strongest correlation ( R 2 = 0.937). Comparison of the rat kidney cortex spectra with selected human postmortem cases showed similar postmortem metabolic changes. In conclusion, ATR FT-IR spectroscopy was shown to be a convenient and reliable method of determining short and long term postmortem intervals by simultaneously monitoring several specific parameters, although these observations have yet to be applied at forensic scenes by further field studies.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2010
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 8
    In: Applied Spectroscopy, SAGE Publications, Vol. 72, No. 11 ( 2018-11), p. 1621-1631
    Abstract: The OH stretching band of water is very sensitive to temperature and salinity for the existence of hydrogen bonds between H 2 O molecules. In this study, the OH stretching band was deconvoluted into two Gaussian peaks, with peak 1 at approximately 3450 cm −1 and peak 2 at approximately 3200 cm −1 . The positions of peaks 1 and 2 both shifted to higher wavenumbers with increasing temperature from 50 ℃ to 300 ℃. The effects of salinity in the range of 0–2 mol/kg NaCl on the OH stretching band were also studied. Linearity for the relationship between Raman shift of peak 1 and temperature increased as the salt concentration increased from 0 to 2 mol/kg, while peak 2 displayed an opposing trend. Two temperature calibration models were developed based on the temperature-dependent changes in the Raman frequency shifts of peaks 1 and 2 (precision of 0.9 ℃ and 1.0 ℃, respectively). The calibration models for temperature were successfully applied to determining the temperatures of deep-sea hydrothermal fluids in the Okinawa Trough hydrothermal field. The degree of mixing of hydrothermal fluids and ambient seawater during in situ Raman measurements was estimated by the difference in temperatures determined through these calibration models and those measured through thermocouple sensors.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2018
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 9
    In: Applied Spectroscopy, SAGE Publications, Vol. 77, No. 6 ( 2023-06), p. 636-651
    Abstract: Probes such as carbon dots (C-dots) have extensive and important applications in the quantitative analysis of complex biological and environmental systems. However, the development of probes is often hindered by incomplete selectivity, i.e., a probe that responds to one substance is also prone to respond to coexisting structurally similar substances. Therefore, the above dilemma often leads to be developed as semi-selective probes, so that the development of probes is abandoned halfway. This work shows how a semi-selective probe can enhance selectivity by combining a proper multivariate calibration model. Primarily, we developed a semi-selective fluorescent probe that responded to tetracyclines (TCs) with discarded tobacco leaves. Then, we introduced the multivariate quantitative fluorescence model (QFM) to enhance its selectivity and solve the problem of fluorescence spectral shift. For the determination of chlortetracycline (CTC) with this semi-selective C-dots probe in mineral and lake water samples and compared to the traditional quantitative model, the introduced QFM resulted in an average relative predictive error (ARPE) in mineral water spiked samples decreased from 57.1 to 5.6%, which reduced the ARPE in the lake water spiked samples from 18.1 to 4.7%. The above results show that the QFM-assisted semi-selective probe C-dots strategy (QFM C−dots ) can enhance selectivity, and QFM C−dots achieved high-selective and accurate determination of CTC in interfering mineral and lake water samples, with the limit of detection and limit of quantitation of 0.55 and 1.66 μM, respectively. The proposed strategy of enhancing selectivity by introducing a proper multivariate calibration model can reduce the difficulty and increase success rate of developing probes, which can be expected to provide an interesting alternative for the development of probes, especially when encountering semi-selective problems.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2023
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 10
    Online Resource
    Online Resource
    SAGE Publications ; 2023
    In:  Applied Spectroscopy Vol. 77, No. 7 ( 2023-07), p. 753-763
    In: Applied Spectroscopy, SAGE Publications, Vol. 77, No. 7 ( 2023-07), p. 753-763
    Abstract: Turquoise is one of the key ingredients in some magical Tibetan medicines, and its quality and content directly affect the medicine's effectiveness. In this paper, laser-induced breakdown spectroscopy (LIBS) technology was first applied to detect the raw materials of Tibetan medicine. The traditional data analysis methods could not meet the practical requirements of modern Tibetan medicine factories due to matrix effects. The concept of correlation coefficient (ρ) in pattern recognition technique was introduced as an evaluation index, and the model was established based on the intensities of the four characteristic Al and Cu spectral lines of the samples for different contents of turquoise, which was applied to estimate the contents of turquoise in the samples to be tested. We detected the LIBS on 126 samples of raw ore from 42 areas in China and evaluated the turquoise content using self-developed software with an error of 〈 10%. This paper's technical testing process and methods can also be applied to test other mineral compositions and provide technical support for modernizing and standardizing Tibetan medicines.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2023
    detail.hit.zdb_id: 1474251-2
    SSG: 11
    Location Call Number Limitation Availability
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