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Sample records for spectrophotometry technique desenvolvimento

  1. Spectrophotometry of comets at optical wavelengths

    NASA Technical Reports Server (NTRS)

    Ahearn, M. F.

    1982-01-01

    Techniques for spectrophotometry of comets are discussed, and results are reviewed for line and continuum spectrophotometry of comets at optical wavelengths. The techniques considered include photographic spectroscopy and spectrophotometry, photoelectric spectrophotometry, and methods based on the use of image dissector scanners, Fourier-transform instruments, and Fabry-Perot spectrometers. Results are summarized for the study of cometary emission features due to C2, CN, CH, OH, NH, C3, NH2, O, H, CO(plus), and H2O(plus). Relative abundances of various species in comets are examined, along with continuum spectrophotometry of the nuclei, comas, and tails of comets.

  2. Multi-filter spectrophotometry simulations

    NASA Technical Reports Server (NTRS)

    Callaghan, Kim A. S.; Gibson, Brad K.; Hickson, Paul

    1993-01-01

    To complement both the multi-filter observations of quasar environments described in these proceedings, as well as the proposed UBC 2.7 m Liquid Mirror Telescope (LMT) redshift survey, we have initiated a program of simulated multi-filter spectrophotometry. The goal of this work, still very much in progress, is a better quantitative assessment of the multiband technique as a viable mechanism for obtaining useful redshift and morphological class information from large scale multi-filter surveys.

  3. Determination of the reduced sulfur species in the anoxic zone of the Black Sea: A comparison of the spectrophotometry and iodometry techniques

    NASA Astrophysics Data System (ADS)

    Dubinin, A. V.; Demidova, T. P.; Kremenetskii, V. V.; Kokryatskaya, N. M.; Rimskaya-Korsakova, M. N.; Yakushev, E. V.

    2012-04-01

    The report presents the results of the studies of the reduced sulfur species in the water of the anoxic zone of the Black Sea. The content of hydrogen sulfide was determined by means of spectrophotometry using dilution with oxygen-free distilled water. The detection limit of the H2S amounted to 0.3 μM with the method's precision below 3%. The accuracy of the spectrophotometric determination was verified by iodometry after the fixation of the hydrogen sulfide in zinc acetate under the distillation with argon from the acidified seawater sample.

  4. Spectrophotometry: Past and Present

    NASA Astrophysics Data System (ADS)

    Adelman, Saul J.

    2009-01-01

    I describe the rise of optical region spectrophotometry in the 1960's and 1970's when it achieved a status as a major tool in stellar research through its decline and near demise at present. With absolutely calibrated fluxes and Balmer profiles usually of H-gamma, astronomers used model atmospheres predictions to find both the effective temperatures and surface gravities of many stars. Spectrophotometry as I knew it was photometrically calibrated low dispersion spectroscopy with a typical resolution of order 25 A. A typical data set consists of 10 to 15 values covering most of the optical spectral region. The strengths and shortcomings of the rotating grating scanners are discussed. The accomplishments achieved using spectrophotometric data, which were obtained with instruments using photomultipliers, are reviewed. Extensions to other spectral regions are noted and attempts to use observations from space to calibrate the optical region will be discussed. There are two steps to fully calibrate flux data. The first requires the calibration of the fluxes of one or more standard stars against sources calibrated absolutely in a laboratory. The use of Vega as the primary standard has been both a blessing as it is so bright and a curse especially as modeling it correctly requires treating it as a fast rotating star seen nearly pole-on. At best its calibration has errors of about 1%. The other step is to apply extinction corrections for the Earth's atmosphere and then calibrate the fluxes using the fluxes of standard stars. Now the ASTRA Spectrophotometer promises a revitalization of the use and availability of optical flux data. Its design specifications included solutions to the problems of past optical spectrophotometric instruments.

  5. Computer programs for absorption spectrophotometry.

    PubMed

    Jones, R N

    1969-03-01

    Brief descriptions are given of twenty-two modular computer programs for performing the basic numerical computations of absorption spectrophotometry. The programs, written in Fortran IV for card input and output, are available from the National Research Council of Canada. The input and output formats are standardized to permit easy interfacing to yield more complex data processing systems. Though these programs were developed for ir spectrophotometry, they are readily modified for use with digitized visual and uv spectrophotometers. The operations covered include ordinate and abscissal unit and scale interconversions, ordinate addition and subtraction, location of band maxima and minima, smoothing and differentiation, slit function convolution and deconvolution, band profile analysis and asymmetry quantification, Fourier transformation to time correlation curves, multiple overlapping band separation in terms of Cauchy (Lorentz), Gauss, Cauchy-Gauss product, and Cauchy-Gauss sum functions and cell path length determination from fringe spacing analysis. PMID:20072266

  6. Optical Region Spectrophotometry: Past and Present

    NASA Astrophysics Data System (ADS)

    Adelman, Saul J.

    In the 1960s and 1970s optical region spectrophotometry achieved the status of a major tool in stellar research. New instrumentation, rotating grating scanners using photomultiplier tubes as detectors, and improved absolute calibrations of Vega made this possible. After this period the use of this technique declined to its near demise at present. The use of Vega as the primary standard has been both a blessing as it is so bright and a curse especially as modeling it correctly requires treating it as a fast rotating star seen nearly pole-on. It may be better to use several stars to define any future absolute calibration. With absolutely calibrated fluxes and Balmer profiles, often Hγ, investigators used the predictions of model atmospheres to find both the effective temperatures and the surface gravities of stars. The fluxes were photometrically calibrated low dispersion spectra with a typical resolution of order 25 Å. A typical data set consisted of 10-15 values covering most of the optical spectral region. At present two instrumental projects ACCESS and the ASTRA Spectrophotometer promise, respectively, a new substantially improved absolute calibration of the optical fluxes of several targets and the availability of a considerable amount of well-calibrated optical flux data for use in studies concerned with stellar properties. They jointly promise to revive optical region spectrophotometric studies.

  7. PMAS - Faint Object 3D Spectrophotometry

    NASA Astrophysics Data System (ADS)

    Roth, M. M.; Becker, T.; Kelz, A.

    2002-01-01

    will describe PMAS (Potsdam Multiaperture Spectrophotometer) which was commissioned at the Calar Alto Observatory 3.5m Telescope on May 28-31, 2001. PMAS is a dedicated, highly efficient UV-visual integral field spectrograph which is optimized for the spectrophotometry of faint point sources, typically superimposed on a bright background. PMAS is ideally suited for the study of resolved stars in local group galaxies. I will present results of our preliminary work with MPFS at the Russian 6m Telescope in Selentchuk, involving the development of new 3D data reduction software, and observations of faint planetary nebulae in the bulge of M31 for the determination of individual chemical abundances of these objects. Using this data, it will be demonstrated that integral field spectroscopy provides superior techniques for background subtraction, avoiding the otherwise inevitable systematic errors of conventional slit spetroscopy. The results will be put in perspective of the study of resolved stellar populations in nearby galaxies with a new generation of Extremely Large Telescopes.

  8. Absolute Spectrophotometry of 237 Open Cluster Stars

    NASA Astrophysics Data System (ADS)

    Clampitt, L.; Burstein, D.

    1994-12-01

    We present absolute spectrophotometry of 237 stars in 7 nearby open clusters: Hyades, Pleiades, Alpha Persei, Praesepe, Coma Berenices, IC 4665, and M 39. The observations were taken using the Wampler single-channel scanner (Wampler 1966) on the Crossley 0.9m telescope at Lick Observatory from July 1973 through December 1974. 21 bandpasses spanning the spectral range 3500 Angstroms to 7780 Angstroms were observed for each star, with bandwiths ranging from 32Angstroms to 64 Angstroms. Data are standardized to the Hayes--Latham (1975) system. Our measurements are compared to filter colors on the Johnson BV, Stromgren ubvy, and Geneva U V B_1 B_2 V_1 G systems, as well as to spectrophotometry of a few stars published by Gunn, Stryker & Tinsley and in the Spectrophotometric Standards Catalog (Adelman; as distributed by the NSSDC). Both internal and external comparisons to the filter systems indicate a formal statistical accuracy per bandpass of 0.01 to 0.02 mag, with apparent larger ( ~ 0.03 mag) differences in absolute calibration between this data set and existing spectrophotometry. These data will comprise part of the spectrophotometry that will be used to calibrate the Beijing-Arizona-Taipei-Connecticut Color Survey of the Sky (see separate paper by Burstein et al. at this meeting).

  9. Limitation of fluorescence spectrophotometry in the measurement of naphthenic acids in oil sands process water.

    PubMed

    Lu, Weibing; Ewanchuk, Andrea; Perez-Estrada, Leonidas; Sego, Dave; Ulrich, Ania

    2013-01-01

    Fluorescence spectrophotometry has been proposed as a quick screening technique for the measurement of naphthenic acids (NAs). To evaluate the feasibility of this application, the fluorescence emission spectra of NAs extracted from three oil sands process water sources were compared with that of commercial NAs. The NAs resulting from the bitumen extraction process cannot be differentiated because of the similarity of the fluorescence spectra. Separation of the fluorescent species in NAs using high performance liquid chromatography with fluorescence detector proved unsuccessful. The acidic fraction of NAs is fluorescent but the basic fraction of NAs is not fluorescent, implying that aromatic acids in NAs give rise to the fluorescent signals. The concentrations of NAs in oil sands process water were measured by Fourier transform infrared spectroscopy (FTIR), fluorescence spectrophotometry and ultra high performance liquid chromatography-time of flight/mass spectrometry (UPLC-TOF/MS). Commercial Merichem and Kodak NAs are the best standards to use when measuring NAs concentration with FTIR and fluorescence spectrophotometry. In addition, the NAs concentrations measured by fluorescence spectrophotometry are about 30 times higher than those measured by FTIR and UPLC-TOF/MS. The findings in this study underscore the limitation of fluorescence spectrophotometry in the measurement of NAs. PMID:23379948

  10. Identification of Organic Colorants in Art Objects by Solution Spectrophotometry: Pigments.

    ERIC Educational Resources Information Center

    Billmeyer, Fred W., Jr.; And Others

    1981-01-01

    Describes solution spectrophotometry as a simple, rapid identification technique for organic paint pigments. Reports research which includes analytical schemes for the extraction and separation of organic pigments based on their solubilities, and the preparation of an extensive reference collection of spectral curves allowing their identification.…

  11. Spectrophotometry B, A, and F stars. III

    NASA Astrophysics Data System (ADS)

    Adelman, S. J.; Pyper, D. M.

    1983-03-01

    Optical region energy distributions of 13 bright normal B, A, and F stars consistent with the Hayes-Latham calibration of Vega are presented. These scans contain more wavelength values than those given in previous papers in this series. The procedure of synthesizing u-b and b-y values from spectrophotometry is improved. Effective temperatures are found using the empirical calibration of Code and his colleagues and the fully line-blanketed solar composition model atmospheres of Kurucz.

  12. Fast spectrophotometry with compressive sensing

    NASA Astrophysics Data System (ADS)

    Starling, David; Storer, Ian

    2015-03-01

    Spectrophotometers and spectrometers have numerous applications in the physical sciences and engineering, resulting in a plethora of designs and requirements. A good spectrophotometer balances the need for high photometric precision, high spectral resolution, high durability and low cost. One way to address these design objectives is to take advantage of modern scanning and detection techniques. A common imaging method that has improved signal acquisition speed and sensitivity in limited signal scenarios is the single pixel camera. Such cameras utilize the sparsity of a signal to sample below the Nyquist rate via a process known as compressive sensing. Here, we show that a single pixel camera using compressive sensing algorithms and a digital micromirror device can replace the common scanning mechanisms found in virtually all spectrophotometers, providing a very low cost solution and improving data acquisition time. We evaluate this single pixel spectrophotometer by studying a variety of samples tested against commercial products. We conclude with an analysis of flame spectra and possible improvements for future designs.

  13. Spectrophotometry of Io - Preliminary Voyager 1 results

    NASA Technical Reports Server (NTRS)

    Soderblom, L.; Johnson, T.; Kupferman, P.; Pieri, D.; Morrison, D.; Danielson, E.; Smith, B.; Veverka, J.; Sagan, C.; Cook, A.

    1980-01-01

    Multispectral images of Io acquired with the Voyager 1 narrow-angle camera agree with earth-based spectrophotometry to better than 10%. Although the surface materials have general spectral properties similar to various allotropes of sulfur, their ultraviolet (UV) reflectances are much higher. It is likely that varying amounts of SO2 frost mixed with or absorbed on sulfur-rich materials raises the UV reflectance. The possible association with large amounts of SO2 with low temperature forms of sulfur in the white patches on Io is consistent with Io surface models in which SO2 and S exist in thermally stable stratified zones.

  14. Spectrophotometry of Planetary Nebulae in the Bulge of M31

    NASA Astrophysics Data System (ADS)

    Roth, Martin M.; Becker, Thomas; Kelz, Andreas; Schmoll, Jürgen

    2004-03-01

    We introduce crowded-field integral field (3D) spectrophotometry as a useful technique for the study of resolved stellar populations in nearby galaxies. The spectroscopy of individual extragalactic stars, which is now feasible with efficient instruments and large telescopes, is confronted with the observational challenge of accurately subtracting the bright, spatially and wavelength-dependent nonuniform background of the underlying galaxy. As a methodological test, we present a pilot study with selected extragalactic planetary nebulae (XPNe) in the bulge of M31, demonstrating how 3D spectroscopy is able to improve the limited accuracy of background subtraction that one would normally obtain with classical slit spectroscopy. It is shown that because of the absence of slit effects, 3D spectroscopy is a most suitable technique for spectrophometry. We present spectra and line intensities for five XPNe in M31, obtained with the MPFS instrument at the Russian 6 m Bolshoi Teleskop Azimutal'nij, INTEGRAL at the William Herschel Telescope , and PMAS at the Calar Alto 3.5 m telescope. The results for two of our targets, for which data are available in the literature, are compared with previously published emission-line intensities. The three remaining PNe have been observed spectroscopically for the first time. One object is shown to be a previously misidentified supernova remnant. Our monochromatic Hα maps are compared with direct Fabry-Pérot and narrowband filter images of the bulge of M31, verifying the presence of filamentary emission of the interstellar medium in the vicinity of our objects. We present an example of a flux-calibrated and continuum-subtracted filament spectrum and demonstrate how the interstellar medium component introduces systematic errors in the measurement of faint diagnostic PN emission lines when conventional observing techniques are employed. It is shown how these errors can be eliminated with 3D spectroscopy, using the full two

  15. The role of spectrophotometry in the diagnosis of melanoma

    PubMed Central

    2010-01-01

    Background Spectrophotometry (SPT) could represent a promising technique for the diagnosis of cutaneous melanoma (CM) at earlier stages of the disease. Starting from our experience, we further assessed the role of SPT in CM early detection. Methods During a health campaign for malignant melanoma at National Cancer Institute of Naples, we identified a subset of 54 lesions to be addressed to surgical excision and histological examination. Before surgery, all patients were investigated by clinical and epiluminescence microscopy (ELM) screenings; selected lesions underwent spectrophotometer analysis. For SPT, we used a video spectrophotometer imaging system (Spectroshade® MHT S.p.A., Verona, Italy). Results Among the 54 patients harbouring cutaneous pigmented lesions, we performed comparison between results from the SPT screening and the histological diagnoses as well as evaluation of both sensitivity and specificity in detecting CM using either SPT or conventional approaches. For all pigmented lesions, agreement between histology and SPT classification was 57.4%. The sensitivity and specificity of SPT in detecting melanoma were 66.6% and 76.2%, respectively. Conclusions Although SPT is still considered as a valuable diagnostic tool for CM, its low accuracy, sensitivity, and specificity represent the main hamper for the introduction of such a methodology in clinical practice. Dermoscopy remains the best diagnostic tool for the preoperative diagnosis of pigmented skin lesions. PMID:20707921

  16. Complex noninvasive spectrophotometry in examination of patients with vibration disease

    NASA Astrophysics Data System (ADS)

    Tchernyi, V. V.; Rogatkin, D. A.; Gorenkov, R. V.; Karpov, V. N.; Shumskiy, V. I.; Lubchenko, P. N.

    2006-02-01

    A lot of industry workers all over the world have dealings with a strong mechanical vibration as with daily technology processes. Very often such long-time professional vibration causes the so-called professional "vibration disease", in English literature "white fingers syndrome", caused by a local vibration of hands. Among different clinical features of the vibration disease a leader's part of them consists of different cardiovascular and trophic disorders of tissues. The objects of the present study were the peripheral blood microcirculation, peripheral blood oxygenation and tissues hypoxia state in a finger skin under vibration disease. For this purpose we have used a combined noninvasive spectrophotometry diagnostic technique consisting of Laser-Doppler Flowmetry (LDF), Laser Fluorescent Diagnostics (LFD) and Tissues Reflectance Oximetry (TRO). The results show good possibilities of all mentioned above diagnostic methods in estimation of different vascular disorders. A good correlation between persistent microcirculation disorders and trophic disturbances revealed in tissues of distal ends of upper extremities of the patients with vibration disease was estimated. Additionally, in present study with the use of real and long-time TRO and LDF methods a good correlation between LDF and TRO data including correlation in detected rhythms of blood microcirculation was estimated as well.

  17. Characterising the atmospheres of transiting exoplanets using narrowband spectrophotometry

    NASA Astrophysics Data System (ADS)

    Wilson, Paul Anthony; Sing, David; Nikolov, Nikolay; Lecavelier des Etangs, Alain; Pont, Frédéric; Fortney, Jonathan; Ballester, Gilda; Lopez-Morales, Mercedes; Desert, Jean-Michel; Vidal-Madjar, Alfred

    2015-08-01

    Transiting hot-Jupiters provide an excellent opportunity to detect and characterise exoplanetary atmospheres. However, to be able to perform a wide scale comparative exoplanetology we have to observe targets which are too faint for the Hubble Space Telescope (HST). To do this, we use the the 10.4 m Gran Telescopio Canarias (GTC) telescope together with unique tunable filters capable of precision narrowband photometry at specific wavelengths. This technique coupled with the use of the world’s largest optical telescope allows us to obtain photon-limited sub-mmag narrowband transit spectrophotometry, capable of detecting Na, K, TiO and other important atmospheric species. The detection (and non-detection) of such key species can provide information on the temperature profile of the atmosphere determine the presence and extent of condensate clouds and give us insight into the chemical processes at play. This information is vital to be able to discern different exoplanet atmospheres and will in the future allow us to categorise exoplanets into different sub-classes.In this talk I will present the ground based detection of potassium in HAT-P-1b and describe the techniques used to deal with the systematics present in the data. I will discuss, in context of HST observations, the effects resolution has on the measurements and how atmospheric signatures could be missed if the resolution is not sufficiently high. Tunable filters allow the atmosphere to be probed higher up, where the pressures are lower and where the temperatures may be higher. Such conditions could cause the dissociation of molecular hydrogen into atomic hydrogen by the EUV flux from the host star. This will have important effects on the amplitude of the detection of alkali metals. With studies such as this one, we are well on our way to performing comparative exoplanetology using statistical methods.

  18. Cell effects on high-resolution transmission spectrophotometry

    NASA Astrophysics Data System (ADS)

    Soares, Oliverio D.

    1998-12-01

    Liquids molecular transmission spectrophotometry has a broad area of applications including spectrophotometry. The measurement of the spectral transmission factor could require levels of accuracy in the order of 10-3 to 10-4. This implies the need for detailed analysis of the corrections to compensate measuring cell unpairing, differences in refractive index between reference liquid (water or solvent) and corresponding spectral non-flatness as well as the multiple inter-reflection at the various dielectric interfaces. Procedures for self-correction of optical measuring cells unpairing and compensation of further effects are presented.

  19. Electrothermal atomic absorption spectrophotometry of nickel in tissue homogenates

    SciTech Connect

    Sunderman, F.W. Jr.; Marzouk, A.; Crisostomo, M.C.; Weatherby, D.R.

    1985-01-01

    A method for analysis of Ni concentrations in tissues is described, which involves (a) tissue dissection with metal-free obsidian knives, (b) tissue homogenization in polyethylene bags by use by a Stomacher blender, (c) oxidative digestion with mixed nitric, sulfuric, and perchloric acids, and (d) quantitation of Ni by electrothermal atomic absorption spectrophotometry with Zeeman background correction. The detection limit for Ni in tissues is 10 ng per g, dry weight; the coefficient of variation ranges from 7 to 15%, depending on the tissue Ni concentration; the recovery of Ni added in concentration of 20 ng per g, dry weight, to kidney homogenates averages 101 +/- 8% (mean +/-SD). In control rats, Ni concentrations are highest in lung (102 +/- 39 ng per g, dry weight) and lowest in spleen (35 +/- 16 ng per g, dry wt.). In descending order of Ni concentrations, the tissues of control rats rank as follows: lung > heart > bone > kidney > brain > testis > fat > liver > spleen. In rats killed 24 h after sc injection of NiCl/sub 2/ (0.125 mmol per kg, body weight) Ni concentrations are highest in kidney (17.7 +/- 2.5 ..mu..g per g, dry weight) and lowest in brain (0.38 +/- 0.14 ..mu..g per g, dry weight). In descending order of Ni concentrations, the tissues of NiCl/sub 2/-treated rats rank as follows: kidney >> lung > spleen > testis > heart > fat > liver > bone > brain. The present method fills the need for an accurate, sensitive, and practical technique to determine tissue Ni concentrations, with stringent precautions to minimize Ni contamination during tissue sampling and processing. 35 references, 5 figures, 1 table.

  20. Evolution of Instrumentation for UV-Visible Spectrophotometry. Part I.

    ERIC Educational Resources Information Center

    Altemose, Ines R.

    1986-01-01

    Traces the development of instruments used in spectrophotometry. Discusses how spectrophotometric measurements are made. Describes the color comparator, the filter photometer, and the spectrophotometer. Outlines the evolution of optical systems, including light sources, the monochromator, the photodetector, double-beam optics, and split-beam…

  1. Ion Exchange Chromatography and Spectrophotometry: An Introductory Undergraduate Laboratory Experiment.

    ERIC Educational Resources Information Center

    Foster, N.; And Others

    1985-01-01

    Describes an experiment in which students use ion exchange chromatography to separate a mixture of chloro complexes of transition metal ions and then use spectrophotometry to define qualitatively the efficiency of the ion exchange columns. Background information, materials needed, and procedures used are included. (JN)

  2. Preparation of Ion Exchange Films for Solid-Phase Spectrophotometry and Solid-Phase Fluorometry

    NASA Technical Reports Server (NTRS)

    Hill, Carol M.; Street, Kenneth W.; Tanner, Stephen P.; Philipp, Warren H.

    2000-01-01

    Atomic spectroscopy has dominated the field of trace inorganic analysis because of its high sensitivity and selectivity. The advantages gained by the atomic spectroscopies come with the disadvantage of expensive and often complicated instrumentation. Solid-phase spectroscopy, in which the analyte is preconcentrated on a solid medium followed by conventional spectrophotometry or fluorometry, requires less expensive instrumentation and has considerable sensitivity and selectivity. The sensitivity gains come from preconcentration and the use of chromophore (or fluorophore) developers and the selectivity is achieved by use of ion exchange conditions that favor the analyte in combination with speciative chromophores. Little work has been done to optimize the ion exchange medium (IEM) associated with these techniques. In this report we present a method for making ion exchange polymer films, which considerably simplify the solid-phase spectroscopic techniques. The polymer consists of formaldehyde-crosslinked polyvinyl alcohol with polyacrylic acid entrapped therein. The films are a carboxylate weak cation exchanger in the calcium form. They are mechanically sturdy and optically transparent in the ultraviolet and visible portion of the spectrum, which makes them suitable for spectrophotometry and fluorometry.

  3. Spectrophotometry of 237 Stars in 7 Open Clusters

    NASA Astrophysics Data System (ADS)

    Clampitt, Lori; Burstein, David

    1997-08-01

    Spectrophotometry is presented for 237 stars in 7 nearby open clusters: Hyades, Pleiades, Alpha Persei, Praesepe, Coma Berenices, IC 4665, and M39. The observations were taken by Lee McDonald and David Burstein using the Wampler single-channel scanner on the Crossley 0.9m telescope at Lick Observatory from July 1973 through December 1974. Sixteen bandpasses spanning the spectral range 3500 Angstroms to 7780 Angstroms were observed for each star, with bandwidths 32Angstroms, 48 Angstroms or 64 Angstroms. Data are standardized to the Hayes-Latham system to mutual accuracy of 0.016 mag per passband. The accuracy of the spectrophotometry is assessed in three ways on a star-by-star basis. First, comparisons are made with previously published spectrophotometry for 19 stars observed in common. Second, (B-V) colors and uvby colors are compared for 236 stars and 221 stars, respectively. Finally, comparsions are made for 200 main sequence stars to the spectral synthesis models of Kurucz, fixing log g = 4.0 and [Fe/H] = 0.0, and only varying effective temperature. The accuracy of tests using uvby colors and the Kurucz models are shown to track each other closely, yielding an accuracy estimate (1 sigma ) of 0.01 mag for the 13 colors formed from bandpasses longward of the Balmer jump, and 0.02 mag for the 3 colors formed from the three bandpasses below the Balmer jump. In contrast, larger scatter is found relative to the previously published spectrophotometry of Bohm-Vitense & Johnson (16 stars in common) and Gunn & Stryker (3 stars). We also show that the scatter in the fits of the spectrophotometric colors and the uvby filter colors is a reasonable way to identify the observations of which specific stars are accurate to 1 sigma , 2 sigma , .... As such, the residuals from both the filter color fits and the Kurucz model fits are tabulated for each star where it was possible to make a comparison, so users of these data can choose stars according to the accuracy of the data

  4. [Are ultraviolet and visible spectroscopy and spectrophotometry obsolete methods in pharmaceutical analysis?].

    PubMed

    Görög, S; Babják, M; Gazdag, M; Horváth, P; Osztheimer, E; Rényei, M; Varga, K

    1999-04-01

    It has been investigated if UV-VIS spectroscopy and spectrophotometry can be regarded to be obsolete methods in pharmaceutical analysis. The conclusions are as follows. As a consequence of the introduction and spreading of highly efficient spectroscopic methods in the structural analysis of organic compounds the importance of UV-VIS spectroscopy as a structure elucidation tool has greatly decreased. At the same time, however, diode-array UV spectrophotometers used as HPLC detectors have created very convenient possibilities for the identification of minor components (impurities, degradation products, etc.) in drugs. This statement is illustrated by several practical examples. On the basis of some data taken from the British Pharmacopoeia 1998 it is stated that UV spectrophotometry as a quantitative analytical method still belongs to the most frequently used analytical techniques in pharmaceutical analysis. At the same time, however, the authors are of negative opinion about the up-to-dateness and usefulness of colorimetric methods still very often published for the determination of drug substances. PMID:10389299

  5. Derivative spectrophotometry in the analysis of mixtures of phenols and herbicides.

    PubMed

    Baranowska, I; Pieszko, C

    2000-12-01

    Derivative spectrophotometry (zero-crossing technique) was applied to the determination of selected phenols and herbicides in two-component mixtures. Methyl- and chlorophenols (3-methylphenol, 2,3- and 3,4-dimethylphenol, 2,5-, 2,6- and 3,4-dichlorophenol and 2,4,5-trichlorophenol) and triazine, uracil and urea herbicides (simazine, propazine, hexazinone, bromacil and metoxuron) were examined. The RSD values ranged between 0.05 and 4% and the recoveries obtained were between 97 and 110%. The developed derivative spectrophotometric method was also applied as a complementary technique for the separation of overlapping peaks of sample compounds obtained by HPLC with diode-array detection. Metoxuron and 3-methylphenol, metoxuron and 2,5-dichlorophenol and simazine and 2,6-dichlorophenol were determined simultaneously by this method at the level of 1 x 10(-3) g l-1. PMID:11219078

  6. Absolute spectrophotometry of Neptune - 3390 to 7800 A

    NASA Astrophysics Data System (ADS)

    Bergstralh, J. T.; Neff, J. S.

    1983-07-01

    Absolute spectrophotometry of Neptune from 3390 to 7800 Å, with spectral resolution of 10 Å in the interval 3390 - 6055 and 20 Å in the interval 6055 - 7800 Å, is reported. The results are compared with filter photometry (Appleby, 1973; Wamsteker, 1973; Savage et al., 1980) and with synthetic spectra computed on the basis of a parameterization proposed by Podolak and Danielson (1977) for aerosol scattering and absorption. A CH4/H2 ratio is derived for the convectively mixed part of Neptune's atmosphere, and constrains optical properties of hypothetical aerosol layers.

  7. A sensitive, spatially uniform photodetector for broadband infrared spectrophotometry

    SciTech Connect

    Iglesias, Enrique J.; Smith, Allan W.; Kaplan, Simon G

    2008-05-01

    We describe the design and performance of a liquid helium-cooled As:Si blocked-impurity-band photodetector system intended for spectrophotometry in the thermal infrared (2 to 30 {mu}m) spectral region. The system has been characterized for spectral sensitivity, noise, thermal stability, and spatial uniformity, and optimized for use with a Fourier-transform infrared spectrophotometer source for absolute goniometric reflectance measurements. Its performance is evaluated and compared to more common detector systems used in this spectral region, including room-temperature pyroelectric and liquid-N2-cooled photoconductive devices.

  8. Method for rapidly determining a pulp kappa number using spectrophotometry

    DOEpatents

    Chai, Xin-Sheng; Zhu, Jun Yong

    2002-01-01

    A system and method for rapidly determining the pulp kappa number through direct measurement of the potassium permanganate concentration in a pulp-permanganate solution using spectrophotometry. Specifically, the present invention uses strong acidification to carry out the pulp-permanganate oxidation reaction in the pulp-permanganate solution to prevent the precipitation of manganese dioxide (MnO.sub.2). Consequently, spectral interference from the precipitated MnO.sub.2 is eliminated and the oxidation reaction becomes dominant. The spectral intensity of the oxidation reaction is then analyzed to determine the pulp kappa number.

  9. Noninvasive detection of plant nutrient stress using fiber optic spectrophotometry

    NASA Astrophysics Data System (ADS)

    Chen, Jun-Wei; Asundi, Anand K.; Liew, Oi Wah; Boey, William S. L.

    2001-05-01

    In a previous paper, we described the use of fiber optic spectrophotometry as a non-destructive and sensitive method to detect early symptoms of plant nutrient deficiency. We report further developments of our work on Brassica chinensis var parachinensis (Bailey) showing reproducibility of our data collected at a different seasonal period. Plants at the mid-log growth phase were subjected to nutrient stress by transferring them to nitrate- and calcium- deficient nutrient solution in a standing aerated hydroponic system. After tracking changes in leaf reflectance by FOSpectr for nine days, the plants were returned to complete nutrient solution and their recovery was monitored for a further nine days. The responses of nutrient stressed plants were compared with those grown under complete nutrient solution over the 18-day trial period. We also compared the sensitivity of FOSpectr detection against plant growth measurements vis-a-vis average leaf number and leaf width and show that the former method gave an indication of nutrient stress much earlier than the latter. In addition, this work indicated that while normal and nutrient-stressed plants could not be distinguished within the first 7 days by tracking plant growth indicators, stressed plants did show a clear decline in average leaf number and leaf width in later stages of growth even after the plants were returned to complete nutrient solution. The results further reinforce the need for early detection of nutrient stress, as late remedial action could not reverse the loss in plant growth in later stages of plant development.

  10. Voyager absolute far-ultraviolet spectrophotometry of hot stars

    NASA Technical Reports Server (NTRS)

    Holberg, J. B.; Forrester, W. T.; Shemansky, D. E.; Barry, D. C.

    1982-01-01

    Voyager observations in the 912-1200 A spectral region are used to indirectly intercompare absolute stellar spectrophotometry from previous experiments. Measurements of hot stars obtained by the Voyager 1 and 2 ultraviolet spectrometers show considerably higher 912-1200 A continuum fluxes than the recent observations of Brune et al. (1979) and Carruthers et al. (1981). The intercomparisons show all observations in basic agreement near 1200 A. The Carruthers et al. flux measurements are preferred down to 1050 A at which point the Voyager and Brune et al. values are respectively 60% higher and 60% lower. Below 1050 A the diasgreement among the observations becomes very large and the fluxes predicted by model atmospheres have been adopted. The pure hydrogen line-blanketed model atmosphere calculations of Wesemael et al. 1980) in comparison with Voyager observations of HZ 43 are used to adjust the Voyager calibration below 1050 A. This adjusted Voyager calibration, which is in good agreement with current model atmosphere fluxes for both early-type stars and DA white dwarfs, will be used for Voyager astronomical observations.

  11. Automated measurement of urinary creatinine by multichannel kinetic spectrophotometry.

    PubMed

    Ohira, Shin-Ichi; Kirk, Andrea B; Dasgupta, Purnendu K

    2009-01-15

    Urinary creatinine analysis is required for clinical diagnosis, especially for evaluation of renal function. Creatinine adjustment is also widely used to estimate 24-h excretion from spot samples. Few convenient validated approaches are available for in-house creatinine measurement for small- to medium-scale studies. Here we apply the Jáffe reaction to creatinine determination with zone fluidic multichannel kinetic spectrophotometry. Diluted urine sample and reagent, alkaline picric acid, were mixed by a computer-programmed dispenser and rapidly delivered to a four-channel detection cell. The absorbance change was monitored by a flow-through light-emitting diode-photodiode-based detector. Validation results against high-performance liquid chromatography-ultraviolet (HPLC-UV)/mass spectrometry (MS) are presented. Responses for 10-fold diluted samples were linear within clinically relevant ranges (0-250 mg/L after dilution). The system can analyze 70 samples per hour with a limit of detection of 0.76 mg/L. The relative standard deviation was 1.29% at 100 mg/L creatinine (n=225). Correlation with the HPLC (UV quantitation/MS confirmation) system was excellent (linear, r2=0.9906). The developed system allows rapid, simple, cost-effective, and robust creatinine analysis and is suitable for the analysis of large numbers of urine samples. PMID:18977332

  12. HUBBLE SPACE TELESCOPE SPECTROPHOTOMETRY AND MODELS FOR SOLAR ANALOGS

    SciTech Connect

    Bohlin, R. C.

    2010-04-15

    Absolute flux distributions for seven solar analog stars are measured from 0.3 to 2.5 {mu}m by Hubble Space Telescope (HST) spectrophotometry. In order to predict the longer wavelength mid-IR fluxes that are required for James Webb Space Telescope calibration, the HST spectral energy distributions are fit with Castelli and Kurucz model atmospheres; and the results are compared with fits from the MARCS model grid. The rms residuals in 10 broadband bins are all <0.5% for the best fits from both model grids. However, the fits differ systematically: the MARCS fits are 40-100 K hotter in T {sub eff}, 0.25-0.80 higher in log g, 0.01-0.10 higher in log z, and 0.008-0.021 higher in the reddening E(B - V), probably because their specifications include different metal abundances. Despite these differences in the parameters of the fits, the predicted mid-IR fluxes differ by only {approx}1%; and the modeled flux distributions of these G stars have an estimated ensemble accuracy of 2% out to 30 {mu}m.

  13. A new method for rapid determination of carbohydrate and total carbon concentrations using UV spectrophotometry.

    PubMed

    Albalasmeh, Ammar A; Berhe, Asmeret Asefaw; Ghezzehei, Teamrat A

    2013-09-12

    A new UV spectrophotometry based method for determining the concentration and carbon content of carbohydrate solution was developed. This method depends on the inherent UV absorption potential of hydrolysis byproducts of carbohydrates formed by reaction with concentrated sulfuric acid (furfural derivatives). The proposed method is a major improvement over the widely used Phenol-Sulfuric Acid method developed by DuBois, Gilles, Hamilton, Rebers, and Smith (1956). In the old method, furfural is allowed to develop color by reaction with phenol and its concentration is detected by visible light absorption. Here we present a method that eliminates the coloration step and avoids the health and environmental hazards associated with phenol use. In addition, avoidance of this step was shown to improve measurement accuracy while significantly reducing waiting time prior to light absorption reading. The carbohydrates for which concentrations and carbon content can be reliably estimated with this new rapid Sulfuric Acid-UV technique include: monosaccharides, disaccharides and polysaccharides with very high molecular weight. PMID:23911443

  14. Influence of medium and temperature on the hydrolysis kinetics of propacetamol hydrochloride: determination using derivative spectrophotometry.

    PubMed

    Barcia, Emilia; Martin, Alicia; Azuara, Ma Luz; Negro, Sofia

    2005-03-01

    Propacetamol hydrochloride (PRO) is a water-soluble prodrug of paracetamol (PA) which can be parenterally administered as analgesic for the treatment of postoperative pain, acute trauma, and gastric and/or intestinal disorders where oral administration is not possible. In these circumstances, PRO can be administered in physiologic or glucose solutions since it is rapidly and quantitatively hydrolyzed into PA by plasma estearases. We have studied the degradation kinetics of PRO in 5% glucose and 0.9% saline solutions at 4 degrees C and 25 degrees C (storage and room temperatures, respectively). The analytic technique used to determine PRO and PA quantitatively was first-derivative spectrophotometry. The degradation process of PRO can be best fitted to a second-order kinetics with independence of the medium used (saline or glucose solution). The hydrolysis kinetics of PRO conversion into PA depends on the temperature but not on the assay medium (saline or glucose solution). The degradation rate constants obtained for PRO were approximately 4.5 times higher at 25 degrees C than at 4 degrees C. The values of t(90%) for PRO were 3.17 h and 3.61 h at 25 degrees C, and 13.42 h and 12.36 h at 4 degrees C when the tests were performed in 5% glucose and 0.9% saline solutions, respectively. PMID:15744097

  15. Electrothermal atomic absorption spectrophotometry of nickel in tissue homogenates.

    PubMed

    Sunderman, F W; Marzouk, A; Crisostomo, M C; Weatherby, D R

    1985-01-01

    A method for analysis of Ni concentrations in tissues is described, which involves (a) tissue dissection with metal-free obsidian knives, (b) tissue homogenization in polyethylene bags by use of a "Stomacher" blender, (c) oxidative digestion with mixed nitric, sulfuric, and perchloric acids, and (d) quantitation of Ni by electrothermal atomic absorption spectrophotometry with Zeeman background correction. The detection limit for Ni in tissues is 10 ng per g, dry weight; the coefficient of variation ranges from 7 to 15 percent, depending on the tissue Ni concentration; the recovery of Ni added in concentration of 20 ng per g, dry weight, to kidney homogenates averages 101 +/- 8 percent (mean +/- SD). In control rats, Ni concentrations are highest in lung (102 +/- 39 ng per g, dry weight) and lowest in spleen (35 +/- 16 ng per g, dry wt.). In descending order of Ni concentrations, the tissues of control rats rank as follows: lung greater than heart greater than bone greater than kidney greater than brain greater than testis greater than fat greater than liver greater than spleen. In rats killed 24 h after sc injection of NiCl2 (0.125 mmol per kg, body weight) Ni concentrations are highest in kidney (17.7 +/- 2.5 micrograms per g, dry weight) and lowest in brain (0.38 +/- 0.14 micrograms per g, dry weight). In descending order of Ni concentrations, the tissues of NiCl2-treated rats rank as follows: kidney much greater than lung greater than spleen greater than testis greater than heart greater than fat greater than liver greater than bone greater than brain.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:4037701

  16. FTIR (Fourier transform infrared) spectrophotometry for thin film monitors: Computer and equipment integration for enhanced capabilities

    SciTech Connect

    Cox, J.N.; Sedayao, J.; Shergill, G.; Villasol, R. ); Haaland, D.M. )

    1990-01-01

    Fourier transform infrared spectrophotometry (FTIR) is a valuable technique for monitoring thin films used in semiconductor device manufacture. Determinations of the constituent contents in borophosphosilicate (BPSG), phosphosilicate (PSG), silicon oxynitride (SiON:H,OH), and spin-on-glass (SOG) thin films are a few applications. Due to the nature of the technique, FTIR instrumentation is one of the most extensively computer-dependent pieces of equipment that is likely to be found in a microelectronics plant. In the role of fab monitor or reactor characterization tool, FTIR instruments can rapidly generate large amounts of data. By linking a local FTIR data station to a remote minicomputer its capabilities are greatly improved. We discuss three caused of enhancement. First, the FTIR in the fab area communicates and interacts in real time with the minicomputer: transferring data segments to it, instructing it to perform sophisticated processing, and returning the result to the operator in the fab. Characterizations of PSG thin films by this approach are discussed. Second, the spectra of large numbers of samples are processed locally. The large database is then transmitted to the minicomputer for study by statistical/graphics software. Results of CVD-reactor spatial profiling experiments for plasma SiON are presented. Third, processing of calibration spectra is performed on the minicomputer to optimize the accuracy and precision of a Partial Least Squares'' analysis mode. This model is then transferred to the data station in the fab. The analysis of BPSG thin films is discussed in this regard. The prospects for fully automated at-line monitoring and for real-time, in-situ monitoring will be discussed. 10 refs., 4 figs.

  17. Comparison of liposome entrapment parameters by optical and atomic absorption spectrophotometry.

    PubMed

    Yoss, N L; Popescu, O; Pop, V I; Porutiu, D; Kummerow, F A; Benga, G

    1985-01-01

    Methods for the complete characterization of liposomes prepared by ether-injection are described in detail. The validity of atomic absorption spectrophotometry for measuring markers of trapped volume was checked by comparative determinations of markers with established optical spectrophotometrical methods. The favorable results using atomic absorption spectrophotometry to quantitate the marker Mn2+ are of particular relevance as manganese ion is also the paramagnetic probe in n.m.r. measurements of water permeability of liposomes; our results indicate that in such measurements no other marker need be incorporated. PMID:3986305

  18. UV-Visible First-Derivative Spectrophotometry Applied to an Analysis of a Vitamin Mixture

    NASA Astrophysics Data System (ADS)

    Aberásturi, F.; Jiménez, A. I.; Jiménez, F.; Arias, J. J.

    2001-06-01

    A simple new experiment that uses UV-vis spectrophotometry to introduce undergraduate chemistry students to multicomponent analysis is presented and a method for the simultaneous determination of three vitamins using derivative spectrophotometry (zero-crossing method) is described. The methodology is simple and easy to apply and allows the determination of folic acid, pyridoxine, and thiamine over the concentration ranges 1.02-14.28, 1.00-16.00, and 6.00-20.00 mg mL-1, respectively. The resulting errors were nearly always less than 5%.

  19. UV spectrophotometry for monitoring the performance of a yeast-based deoxygenation process to treat ships' ballast water.

    PubMed

    Veilleux, Éloïse; de Lafontaine, Yves; Thomas, Olivier

    2016-04-01

    This study assessed the usefulness of UV spectrophotometry for the monitoring of a yeast-based deoxygenation process proposed for ships' ballast water treatment to prevent the transfer of aquatic invasive species. Ten-day laboratory experiments using three treatment concentrations and different water types were conducted and resulted in complete oxygen depletion of treated waters. The treatment performance and quality of treated waters were determined by measuring the UV-visible absorbance spectra of water samples taken over time. Samples were also used for laboratory analysis of water quality properties. The UV absorbance spectra values were strongly correlated (r = 0.96) to yeast cell density in treated waters. The second-order derivative (D (2)) of the spectra varied greatly over time, and the spectrum profiles could be divided into two groups corresponding to the oxygenated and anoxic phases of the treatment. The D (2) value at 215 nm was strongly correlated (r = 0.94) to ammonia levels, which increased over time. The D (2) value at 225 nm was strongly correlated (r > 0.97) to DO concentration. Our results showed that UV spectrophotometry may provide a rapid assessment of the behavior and performance of the yeast bioreactor over time by quantifying (1) the density of yeast cells, (2) the time at which anoxic conditions were reached, and (3) a water quality index of the treated water related to the production of ammonia. We conclude that the rapidity of the technique confers a solid advantage over standard methods used for water quality analysis in laboratory and would permit the direct monitoring of the treatment performance on-board ships. PMID:26944435

  20. Determination of astaxanthin in Haematococcus pluvialis by first-order derivative spectrophotometry.

    PubMed

    Liu, Xiao Juan; Juan, Liu Xiao; Wu, Ying Hua; Hua, Wu Ying; Zhao, Li Chao; Chao, Zhao Li; Xiao, Su Yao; Yao, Xiao Su; Zhou, Ai Mei; Mei, Zhou Ai; Liu, Xin; Xin, Liu

    2011-01-01

    A highly selective, convenient, and precise method, first-order derivative spectrophotometry, was applied for the determination of astaxanthin in Haematococcus pluvialis. Ethyl acetate and ethanol (1:1, v/v) were found to be the best extraction solvent tested due to their high efficiency and low toxicity compared with nine other organic solvents. Astaxanthin coexisting with chlorophyll and beta-carotene was analyzed by first-order derivative spectrophotometry in order to optimize the conditions for the determination of astaxanthin. The results show that when detected at 432 nm, the interfering substances could be eliminated. The dynamic linear range was 2.0-8.0 microg/mL, with a correlation coefficient of 0.9916. The detection threshold was 0.41 microg/mL. The RSD for the determination of astaxanthin was in the range of 0.01-0.06%; the results of recovery test were 98.1-108.0%. The statistical analysis between first-order derivative spectrophotometry and HPLC by T-testing did not exceed their critical values, revealing no significant differences between these two methods. It was proved that first-order derivative spectrophotometry is a rapid and convenient method for the determination of astaxanthin in H. pluvialis that can eliminate the negative effect resulting from the coexistence of astaxanthin with chlorophyll and beta-carotene. PMID:22320081

  1. Teaching Beer's Law and Absorption Spectrophotometry with a Smart Phone: A Substantially Simplified Protocol

    ERIC Educational Resources Information Center

    Kuntzleman, Thomas S.; Jacobson, Erik C.

    2016-01-01

    A very simple protocol for teaching Beer's Law and absorption spectrophotometry using a smart phone is described. Materials commonly found in high school chemistry laboratories or even around the house may be used. Data collection and analysis is quick and easy. Despite the simple nature of the experiment, excellent results can be achieved.

  2. Uranium isotopes quantitatively determined by modified method of atomic absorption spectrophotometry

    NASA Technical Reports Server (NTRS)

    Lee, G. H.

    1967-01-01

    Hollow-cathode discharge tubes determine the quantities of uranium isotopes in a sample by using atomic absorption spectrophotometry. Dissociation of the uranium atoms allows a large number of ground state atoms to be produced, absorbing the incident radiation that is different for the two major isotopes.

  3. Noise analysis for CCD-based ultraviolet and visible spectrophotometry.

    PubMed

    Davenport, John J; Hodgkinson, Jane; Saffell, John R; Tatam, Ralph P

    2015-09-20

    We present the results of a detailed analysis of the noise behavior of two CCD spectrometers in common use, an AvaSpec-3648 CCD UV spectrometer and an Ocean Optics S2000 Vis spectrometer. Light sources used include a deuterium UV/Vis lamp and UV and visible LEDs. Common noise phenomena include source fluctuation noise, photoresponse nonuniformity, dark current noise, fixed pattern noise, and read noise. These were identified and characterized by varying light source, spectrometer settings, or temperature. A number of noise-limiting techniques are proposed, demonstrating a best-case spectroscopic noise equivalent absorbance of 3.5×10(-4)  AU for the AvaSpec-3648 and 5.6×10(-4)  AU for the Ocean Optics S2000 over a 30 s integration period. These techniques can be used on other CCD spectrometers to optimize performance. PMID:26406516

  4. Spectrophotometry of planetary atmosphere from the X-15 rocket airplane

    NASA Technical Reports Server (NTRS)

    Murcray, W. B.

    1973-01-01

    Nike-Apache and Nike-Tomahawk rocket flights using spectrophotometric techniques to investigate auroral activity are reported. The specific objectives were to obtain data relative to typical auroral situations, including quiet pre-breakup auroras, westward traveling surges, breakup auroras, and post-breakup auroras. It was found that excited atoms move considerable distances between excitation and emission owing to the high velocity wind conditions prevailing above 200 km. Based on the results of these observations, recommendations are made for future studies of ionized atmospheric activity at higher altitudes.

  5. Near infrared quadruple wavelength spectrophotometry of the rat head.

    PubMed

    Hazeki, O; Tamura, M

    1989-01-01

    A quadruple wavelength method to monitor the changes in concentration of oxygenated and deoxygenated hemoglobin and the redox state of cytochrome oxidase within a living tissue is presented. The expected advantages of this technique over the triple wavelength method are (i) that it can compensate for the light scattering change of tissue itself or for instabilities of light source and photomultiplier, (ii) that it can treat the optical properties of the red blood cell in a tissue in the same way as in an in vitro model system, and (iii) that it requires no estimation of the absorption coefficient of cytochrome oxidase in situ. PMID:2551140

  6. Detection of tallow adulteration in cow ghee by derivative spectrophotometry

    PubMed Central

    Jirankalgikar, Nikhil M.; De, Subrata

    2014-01-01

    Context: Ghee is a widely consumed dairy product in India and that prepared from cow milk is mentioned in ayurvedic texts as an ingredient of many formulations/additive as well. Detection of cow ghee adulteration with vegetable oils/fats and animal body fats is a key concern. Indicated values for commonly used parameters to differentiate pure and adulterated ghee materials are many a times overlapping. Among reported techniques, ultraviolet fluorescence and paper chromatography technique are not that much sensitive while other methods require sophisticated instrumental facilities (such as gas chromatography, mass spectrometry) and costly analytical processes. Aims: The present paper deals with a promising spectroscopic method to determine the tallow adulteration in cow ghee. Materials and Methods: Ghee and tallow (taken in chloroform) as such and mixed in different proportions were scanned by spectrophotometer and their second order spectra were analyzed. Results: The value of the ratio of the absorbance of peaks at about 238 nm and 297 nm steadily decreases with the increasing proportion of tallow. This decrease shows consistent linearity suggesting its applicability for quantitative estimation of tallow in cow ghee. Conclusion: The developed derivative spectroscopic method is a rapid, sensitive, cost-effective method for detection of tallow adulteration in cow ghee. PMID:25097406

  7. Determination of Iron in Milk Powdermicrowave Digestion and Flame Atomicabsorption Spectrophotometry

    NASA Astrophysics Data System (ADS)

    Zhao, Guangyuan; Li, Bo

    To investigate the conditions of microwave digestion for determining Iron in milk powder by flame atomic absorption spectrophotometry(FAAS), the content of iron in milk powder was determined by flame atomic absorption spectrophotometry after the samples were microwavely digested under different conditions. The optimum parameters for microwave digestion were obtained by the orthogonal test at last. The best optimum parameters for microwave digestion was that, the volume of digestion solution was 8mL, the reagent proportion for HNO3 and H2O2 was 4:1, the digestion time was 8min, the digestion pressure was 2.6 Mpa and the digestion power was 1000 W. The content of Iron in assayed milk powder was 0.0560mg/g. Microwave digestion was a time-saving and practical pretreatment of samples.

  8. Monitoring of monosaccharides, oligosaccharides, ethanol and glycerol during wort fermentation by biosensors, HPLC and spectrophotometry.

    PubMed

    Monošík, Rastislav; Magdolen, Peter; Stredanský, Miroslav; Šturdík, Ernest

    2013-05-01

    The aim of the present study was to analyze sugar levels (namely maltose, maltotriose, glucose and fructose) and alcohols (ethanol and glycerol) during the fermentation process in wort samples by amperometric enzymatic biosensors developed by our research group for industrial application, HPLC and spectrophotometry, and to compare the suitability of the presented methods for determination of individual analytes. We can conclude that for the specific monitoring of maltose or maltotriose only the HPLC method was suitable. On the other hand, biosensors and spectrophotometry reflected a decrease in total sugar concentration better and were able to detect both glucose and fructose in the later stages of fermentation, while HPLC was not. This can be attributed to the low detection limits and good sensitivity of the proposed methods. For the ethanol and glycerol analysis all methods proved to be suitable. However, concerning the cost expenses and time analysis, biosensors represented the best option. PMID:23265480

  9. Spectrophotometry of Dust in Comet Hale-Bopp

    NASA Technical Reports Server (NTRS)

    Witteborn, Fred C. (Technical Monitor)

    1997-01-01

    Comets, such as Hale-Bopp (C/1995 O1), are frozen reservoirs of primitive solar nebula dust grains and ices. Analysis of the composition of cometary dust grains from infrared spectroscopic techniques permits an estimation of the types of organic and inorganic materials that constituted the early primitive solar nebula. In addition, the cometary bombardment of the Earth (approximately 3.5 Gy ago) supplied the water for the oceans and brought organic materials to Earth which may have been biogenic. Spectroscopic observations of comet Hale-Bopp suggest the possible presence of organic hydrocarbon species, silicate and olivine dust grains, and water ice. Spectroscopy near 3 microns obtained in Nov 1996 r=2.393 AU, delta=3.034 AU) shows a feature which we attribute to PAH emission. The spatial morphology of the 3.28 microns PAH feature is also presented. Optical and infrared spectrophotometric observations of comets convey valuable information about the spatial distribution and properties of dust and gas within the inner coma. In the optical and NIR shortward of 2 microns, the observed light is primarily scattered sunlight from the dust grains. At longer wavelengths, particularly in the 10 gm window, thermal emission from these grains dominates the radiation allowing an accurate estimate of grain sizes and chemical composition. Here we present an initial analysis of spectra taken with the NASA HIFOGS at 7-14 microns as part of a multiwavelength temporal study of the "comet of the century".

  10. Quantification of minerals and trace elements in raw caprine milk using flame atomic absorption spectrophotometry and flame photometry.

    PubMed

    Singh, Mahavir; Yadav, Poonam; Garg, V K; Sharma, Anshu; Singh, Balvinder; Sharma, Himanshu

    2015-08-01

    This study reports minerals and trace elements quantification in raw caprine milk of Beetal breed, reared in Northern India and their feed, fodder & water using flame atomic absorption spectrophotometry and flame photometry. The mineral and trace elements' concentration in the milk was in the order: K > Ca > Na > Fe > Zn > Cu. The results showed that minerals concentration in caprine milk was lesser than reference values. But trace elements concentration (Fe and Zn) was higher than reference values. Multivariate statistical techniques, viz., Pearsons' correlation, Cluster analysis (CA) and Principal component analysis (PCA) were applied to analyze the interdependences within studied variables in caprine milk. Significantly positive correlations were observed between Fe - Zn, Zn - K, Ca - Na and Ca - pH. The results of correlation matrix were further supported by Cluster analysis and Principal component analysis as primary cluster pairs were found for Ca - pH, Ca - Na and Fe - Zn in the raw milk. No correlation was found between mineral & trace elements content of the milk and feed. PMID:26243956

  11. SUMMARY REPORT: EVALUATION OF A NEW FLUOROMETRIC TECHNIQUE THAT USES HIGHLY SELECTIVE INTERFERENCE FILTERS FOR MEASURING CHLOROPHYLL IN THE PRESENCE OF CHLOROPHYLL B AND PHEOPIGMENTS

    EPA Science Inventory

    A new fluorometric technique was compared to conventional fluorometry with and without pheophytin a (pheo a) correction and to spectrophotometry using Lorenzen's modified monochromatic equations and Jeffrey and Humphrey's trichromatic equation to calculate chlorophyll a (chl a). ...

  12. Comparative study between derivative spectrophotometry and multivariate calibration as analytical tools applied for the simultaneous quantitation of Amlodipine, Valsartan and Hydrochlorothiazide

    NASA Astrophysics Data System (ADS)

    Darwish, Hany W.; Hassan, Said A.; Salem, Maissa Y.; El-Zeany, Badr A.

    2013-09-01

    Four simple, accurate and specific methods were developed and validated for the simultaneous estimation of Amlodipine (AML), Valsartan (VAL) and Hydrochlorothiazide (HCT) in commercial tablets. The derivative spectrophotometric methods include Derivative Ratio Zero Crossing (DRZC) and Double Divisor Ratio Spectra-Derivative Spectrophotometry (DDRS-DS) methods, while the multivariate calibrations used are Principal Component Regression (PCR) and Partial Least Squares (PLSs). The proposed methods were applied successfully in the determination of the drugs in laboratory-prepared mixtures and in commercial pharmaceutical preparations. The validity of the proposed methods was assessed using the standard addition technique. The linearity of the proposed methods is investigated in the range of 2-32, 4-44 and 2-20 μg/mL for AML, VAL and HCT, respectively.

  13. Comparative study between derivative spectrophotometry and multivariate calibration as analytical tools applied for the simultaneous quantitation of Amlodipine, Valsartan and Hydrochlorothiazide.

    PubMed

    Darwish, Hany W; Hassan, Said A; Salem, Maissa Y; El-Zeany, Badr A

    2013-09-01

    Four simple, accurate and specific methods were developed and validated for the simultaneous estimation of Amlodipine (AML), Valsartan (VAL) and Hydrochlorothiazide (HCT) in commercial tablets. The derivative spectrophotometric methods include Derivative Ratio Zero Crossing (DRZC) and Double Divisor Ratio Spectra-Derivative Spectrophotometry (DDRS-DS) methods, while the multivariate calibrations used are Principal Component Regression (PCR) and Partial Least Squares (PLSs). The proposed methods were applied successfully in the determination of the drugs in laboratory-prepared mixtures and in commercial pharmaceutical preparations. The validity of the proposed methods was assessed using the standard addition technique. The linearity of the proposed methods is investigated in the range of 2-32, 4-44 and 2-20 μg/mL for AML, VAL and HCT, respectively. PMID:23727675

  14. Near-infrared and ultraviolet spectrophotometry of the young planetary nebula Hubble 12

    NASA Technical Reports Server (NTRS)

    Rudy, Richard J.; Rossano, George S.; Erwin, Peter; Puetter, R. C.; Feibelman, Walter A.

    1993-01-01

    The young planetary nebula Hubble 12 is observed using near-IR and UV spectrophotometry. The brightness of the O I lines, which is greater than in any other planetary nebula yet measured, indicates that fluorescent excitation by stellar continuum is the principal mechanism generating these lines. Extinction, electron density, and electron temperature are determined using infrared measurements combined with UV data and published optical observations. The range in extinction, density, and temperature implies that, within the ionized region, pockets of emission with distinctly different conditions exist. Logarithmic abundances for helium, oxygen, and sulfur are presented.

  15. Absolute spectrophotometry of Wolf-Rayet stars from 1200 to 7000 A - A cautionary tale

    NASA Technical Reports Server (NTRS)

    Garmany, C. D.; Conti, P. S.; Massey, P.

    1984-01-01

    It is demonstrated that absolute spectrophotometry of the continua of Wolf-Rayet stars may be obtained over the wavelength range 1200-7000 A using IUE and optical measurements. It is shown that the application of a 'standard' reddening law to the observed data gives spurious results in many cases. Additional UV extinction is apparently necessary and may well be circumstellar in origin. In such hot stars, the long-wavelength 'tail' of the emergent stellar continuum are measured. The inadequacy of previous attempts to determine intrinsic continua and effective temperatures of Wolf-Rayet stars is pointed out.

  16. Directly suspended droplet microextraction in combination with microvolume UV-vis spectrophotometry for determination of phosphate.

    PubMed

    Pena-Pereira, Francisco; Cabaleiro, Noelia; de la Calle, Inmaculada; Costas, Marta; Gil, Sandra; Lavilla, Isela; Bendicho, Carlos

    2011-08-15

    A miniaturized methodology for the determination of phosphate in waters has been developed by combining directly suspended droplet microextraction (DSDME) with microvolume spectrophotometry. The method is based on the extraction of the ion pair formed between 12-molybdophosphate and malachite green onto a microdrop of methyl isobutyl ketone and subsequent spectrophotometric determination with no dilution. An enrichment factor of 325 was obtained after 7.5 min of microextraction. The detection limit was 6.1 nM phosphate and the repeatability, expressed as relative standard deviation, was 2.7% (n=6). The method was successfully applied to the determination of dissolved reactive phosphorus in different freshwater samples. PMID:21726744

  17. Documentation for the machine-readable version of the Absolute Calibration of Stellar Spectrophotometry

    NASA Technical Reports Server (NTRS)

    Warren, W. H., Jr.

    1982-01-01

    The machine-readable data file of The Absolute Calibration of Stellar Spectrophotometry as distributed by the Astronomical Data Center is described. The data file contains the absolute fluxes for 16 stars published in Tables 1 and 2 of Johnson (1980). The absolute calibrations were accomplished by combining the 13-color photometry calibrations of Johnson and Mitchell (1975) with spectra obtained with a Michelson spectrophotometer and covering the wavelength range 4000 to 10300 A (Johnson 1977). The agreement between this absolute calibration and another recent one based upon data for a Lyr and 109 Vir by Tug, White and Lockwood (1977) is shown by Johnson (1980) to be quite good.

  18. Rocket instrument for far-UV spectrophotometry of faint astronomical objects

    NASA Technical Reports Server (NTRS)

    Hartig, G. F.; Fastie, W. G.; Davidsen, A. F.

    1980-01-01

    A sensitive sounding rocket instrument for moderate (about 10-A) resolution far-UV (1160-1750-A) spectrophotometry of faint astronomical objects has been developed. The instrument employes a photon-counting microchannel plate imaging detector and a concave grating spectrograph behind a 40-cm Dall-Kirkham telescope. A unique remote-control pointing system, incorporating an SIT vidicon aspect camera, two star trackers, and a tone-encoded command telemetry link, permits the telescope to be oriented to within 5 arc sec of any target for which suitable guide stars can be found. The design, construction, calibration, and flight performance of the instrument are discussed.

  19. Rocket instrument for far-UV spectrophotometry of faint astronomical objects.

    PubMed

    Hartig, G F; Fastie, W G; Davidsen, A F

    1980-03-01

    A sensitive sounding rocket instrument for moderate (~10-A) resolution far-UV (lambda1160-lambda1750-A) spectrophotometry of faint astronomical objects has been developed. The instrument employs a photon-counting microchannel plate imaging detector and a concave grating spectrograph behind a 40-cm Dall-Kirkham telescope. A unique remote-control pointing system, incorporating an SIT vidicon aspect camera, two star trackers, and a tone-encoded command telemetry link, permits the telescope to be oriented to within 5 arc sec of any target for which suitable guide stars can be found. The design, construction, calibration, and flight performance of the instrument are discussed. PMID:20220923

  20. CVF spectrophotometry of Pluto - Correlation of composition with albedo. [Circularly variable filter

    SciTech Connect

    Marcialis, R.L.; Lebofsky, L.A. Arizona Univ., Tucson )

    1991-02-01

    The present time-resolved, 0.96-2.65-micron spectrophotometry for the Pluto-Charon system indicates night-to-night variations in the depths of the methane absorptions such that the bands' equivalent width is near minimum light. The interpretation of these data in terms of a depletion of methane in dark regions of the planet, relative to bright ones, is consistent with the Buie and Fink (1987) observations. The near-IR spectrum of Pluto seems to be dominated by surface frost. It is suggested that the dark equatorial regions of Pluto are redder than those of moderate albedo. 28 refs.

  1. Verification of terahertz-wave spectrophotometry by Compton backscattering of coherent synchrotron radiation

    NASA Astrophysics Data System (ADS)

    Sei, Norihiro; Takahashi, Toshiharu

    2014-01-01

    We developed a continuous-spectrum light beam from Compton backscattering by using coherent synchrotron radiation in an L-band linac at the Kyoto University Research Reactor Institute. The ratio of Compton backscattered photons to background photons when coherent synchrotron radiation was used was three times larger than when coherent transition radiation was used. The transmission spectrum of a polystyrene film in the terahertz-wave region was evaluated by measuring the spectrum of the Compton backscattered photons and it roughly agreed with that measured by a Martin-Puplett-type interferometer. The spectrophotometry using Compton backscattering shows promise as a new tool for investigations in terahertz-wave science.

  2. Determination of traces of silver in waters by anion exchange and atomic absorption spectrophotometry

    USGS Publications Warehouse

    Chao, T.T.; Fishman, M. J.; Ball, J.W.

    1969-01-01

    A method has been developed for the accurate determination of 0.1-1 ??g of silver per liter of water. The method permits stabilization of silver in water without loss to container walls. Optimum conditions have been established for the complete recovery of silver from water with an anion-exchange column, for quantitative elution of silver from the resin, and for measurement of silver by atomic absorption spectrophotometry after chelation with ammonium pyrrolidine dithiocarbamate and extraction of the chelate with MIBK. Silver in the 1-10 ??g 1 range can be determined by extraction without pre-concentration on an ion-exchange resin. ?? 1969.

  3. Recent Developments in the Speciation and Determination of Mercury Using Various Analytical Techniques

    PubMed Central

    Suvarapu, Lakshmi Narayana; Baek, Sung-Ok

    2015-01-01

    This paper reviews the speciation and determination of mercury by various analytical techniques such as atomic absorption spectrometry, voltammetry, inductively coupled plasma techniques, spectrophotometry, spectrofluorometry, high performance liquid chromatography, and gas chromatography. Approximately 126 research papers on the speciation and determination of mercury by various analytical techniques published in international journals since 2013 are reviewed. PMID:26236539

  4. Ultraviolet spectrophotometry of comet Giacobini-Zinner during the ICE encounter. [International Cometary Explorer (ICE)

    NASA Technical Reports Server (NTRS)

    Ahearn, Michael F.; Mcfadden, Lucy A.; Feldman, Paul D.; Boehnhardt, Hermann; Rahe, Juergen; Festou, Michael; Brandt, John C.; Maran, Stephen P.; Niedner, Malcom B.; Smith, Andrew M.

    1986-01-01

    The IUE spectrophotometry of Comet P/Giacobini-Zinner was acquired in support of the International Cometary Explorer (ICE) mission. The abundances (or upper limits) of UV-active species were calculated. During the ICE encounter the H2O production rate was 3 times 10 to the 28th power/sec, + or - 50%, consistent with values derived from the ICE experiments. Comparison of the abundance of CO2(+) ions with the total electron density measured by the plasma electron experiment on ICE indicates a deficiency of ions relative to electrons indicating a population of ions not detected by remote sensing. The absence of detectable Mg(+) rules out this species as a possible ion of M/Q = 24 detected by the Ion Composition Instrument, part of the ICE complement of instruments.

  5. Do GSM 900MHz signals affect cerebral blood circulation? A near-infrared spectrophotometry study

    NASA Astrophysics Data System (ADS)

    Wolf, Martin; Haensse, Daniel; Morren, Geert; Froehlich, Juerg

    2006-06-01

    Effects of GSM 900MHz signals (EMF) typical for a handheld mobile phone on the cerebral blood circulation were investigated using near-infrared spectrophotometry (NIRS) in a three armed (12W/kg, 1.2W/kg, sham), double blind, randomized crossover trial in 16 healthy volunteers. During exposure we observed borderline significant short term responses of oxyhemoglobin and deoxyhemoglobin concentration, which correspond to a decrease of cerebral blood flow and volume and were smaller than regular physiological changes. Due to the relatively high number of statistical tests, these responses may be spurious and require further studies. There was no detectable dose-response relation or long term response within 20min. The detection limit was a fraction of the regular physiological changes elicited by functional activation. Compared to previous studies using PET, NIRS provides a much higher time resolution, which allowed investigating the short term effects efficiently, noninvasively, without the use of radioactive tracers and with high sensitivity.

  6. Indirect determination of trace phenol in water by atomic-absorption spectrophotometry.

    PubMed

    Bo-Xing, X; Tong-Ming, X; Ming-Neng, S; Yu-Zhi, F

    1985-03-01

    An indirect method for determination of trace phenol in water by atomic-absorption spectrophotometry (AAS) is described. The phenol is brominated in acidic solution with KBrO(3)-KBr solution at room temperature. The excess of bromine is reacted with KI and the I(2) produced is extracted into cyclohexane and then reduced back to I(-) with ascorbic acid. The I(-) is then complexed with Cd(2+) in sulphuric acid medium and the complex extracted into MIBK. The extract is analysed by flame AAS for Cd (and hence indirectly for phenol). The linear concentration range for determination of phenol is 6 x 10(-7)-0.9 x 10(-5)M in aqueous solution. Several foreign ions and organic substances do not interfere. PMID:18963829

  7. Spatially Multiplexed Micro-Spectrophotometry in Bright Field Mode for Thin Film Characterization.

    PubMed

    Pini, Valerio; Kosaka, Priscila M; Ruz, Jose J; Malvar, Oscar; Encinar, Mario; Tamayo, Javier; Calleja, Montserrat

    2016-01-01

    Thickness characterization of thin films is of primary importance in a variety of nanotechnology applications, either in the semiconductor industry, quality control in nanofabrication processes or engineering of nanoelectromechanical systems (NEMS) because small thickness variability can strongly compromise the device performance. Here, we present an alternative optical method in bright field mode called Spatially Multiplexed Micro-Spectrophotometry that allows rapid and non-destructive characterization of thin films over areas of mm² and with 1 μm of lateral resolution. We demonstrate an accuracy of 0.1% in the thickness characterization through measurements performed on four microcantilevers that expand an area of 1.8 mm² in one minute of analysis time. The measured thickness variation in the range of few tens of nm translates into a mechanical variability that produces an error of up to 2% in the response of the studied devices when they are used to measure surface stress variations. PMID:27338398

  8. Determination of butyltin metabolites in the mouse liver by flameless atomic absorption spectrophotometry.

    PubMed

    Uneo, S; Susa, N; Furukawa, Y

    1995-08-01

    A new analytical method for observation of the metabolic status of butyltin compounds in the mouse liver was devised by a combination of extraction, purification and separation followed by quantitative analysis of each butyltin compound. After the extraction of all tin compounds from liver homogenate with ethyl acetate, these compounds were purified by combination of the fractional extract with organic solvents and column chromatography. The purified fraction was also analyzed by thin-layer chromatography, identifying each tin compound from differences in mobility on a silica gel plate. The tin content in the each separated spot on the plates was measured by flameless atomic absorption spectrophotometry after extraction by acid treatment. About 90% of tin was recovered by this method from the liver of mice which had been administered tri- or dibutyltin compound orally. This method will be useful for quantification of each metabolic product formed from butyltin compounds in vivo. PMID:8519922

  9. Near-infrared spectrophotometry of four Seyfert 1 galaxies and NGC 1275

    NASA Technical Reports Server (NTRS)

    Rudy, R. J.; Jones, B.; Levan, P. D.; Puetter, R. C.; Smith, H. E.; Willner, S. P.; Tokunaga, A. T.

    1982-01-01

    Low-resolution spectrophotometry from 2 to 4 microns is reported for the four Seyfert 1 galaxies Mrk 335, 3C 120, Mrk 509, NGC 7469, and the peculiar emission-line galaxy NGC 1275. The spectrum of NGC 7469 exhibits a strong 3.3-micron dust feature, indicating a thermal origin for the bulk of its considerable nonstellar infrared emission. NGC 1275 has a large stellar contribution to its infrared flux at wavelengths shortward of 3 microns. The spectrum from 3 to 4 microns fits a power law which fits the 10-micron and 20-micron broad bands, as well. A thermal model which can explain the spectrum of NGC 1275 is discussed. Mrk 335 displays a complex spectrum suggestive of thermal dust emission. 3C 120 and Mrk 509 have nonstellar infrared emission shortward of 2 microns, but the data are ambiguous as to whether this emission is thermal or nonthermal in origin.

  10. Analysis of lithium in deep basalt groundwaters using graphite furnace atomic absorption spectrophotometry

    SciTech Connect

    Dill, J.A.; Marcy, A.D.

    1986-05-01

    Lithium is under consideration for use as a reactive (sorptive) tracer in experiments designed to provide information regarding natural attenuation processes in a basalt-groundwater environment. In support of these activities, background lithium concentrations in samples obtained from a variety of test horizons have been determined using graphite furnace atomic absorption spectrophotometry. Significant interference was observed in these determinations and was found to be due to the presence of silicate in the samples. It was found that these problems could be circumvented through the use of alkaline silicate or synthetic groundwater matrix modifiers. This matrix effect was examined in some detail. Results obtained using the graphite furnace were compared to results obtained using inductively coupled plasma atomic emission spectroscopy.

  11. Spatially Multiplexed Micro-Spectrophotometry in Bright Field Mode for Thin Film Characterization

    PubMed Central

    Pini, Valerio; Kosaka, Priscila M.; Ruz, Jose J.; Malvar, Oscar; Encinar, Mario; Tamayo, Javier; Calleja, Montserrat

    2016-01-01

    Thickness characterization of thin films is of primary importance in a variety of nanotechnology applications, either in the semiconductor industry, quality control in nanofabrication processes or engineering of nanoelectromechanical systems (NEMS) because small thickness variability can strongly compromise the device performance. Here, we present an alternative optical method in bright field mode called Spatially Multiplexed Micro-Spectrophotometry that allows rapid and non-destructive characterization of thin films over areas of mm2 and with 1 μm of lateral resolution. We demonstrate an accuracy of 0.1% in the thickness characterization through measurements performed on four microcantilevers that expand an area of 1.8 mm2 in one minute of analysis time. The measured thickness variation in the range of few tens of nm translates into a mechanical variability that produces an error of up to 2% in the response of the studied devices when they are used to measure surface stress variations. PMID:27338398

  12. Fiber optic spectrophotometry monitoring of plant nutrient deficiency under hydroponic culture conditions

    NASA Astrophysics Data System (ADS)

    Liew, Oi Wah; Boey, William S. L.; Asundi, Anand K.; Chen, Jun-Wei; He, Duo-Min

    1999-05-01

    In this paper, fiber optic spectrophotometry (FOSpectr) was adapted to provide early detection of plant nutrient deficiency by measuring leaf spectral reflectance variation resulting from nutrient stress. Leaf reflectance data were obtained form a local vegetable crop, Brassica chinensis var parachinensis (Bailey), grown in nitrate-nitrogen (N)- and calcium (Ca)- deficient hydroponics nutrient solution. FOSpectr analysis showed significant differences in leaf reflectance within the first four days after subjecting plants to nutrient-deficient media. Recovery of the nutrient-stressed plants could also be detected after transferring them back to complete nutrient solution. In contrast to FOSpectr, plant response to nitrogen and calcium deficiency in terms of reduced growth and tissue elemental levels was slower and less pronounced. Thus, this study demonstrated the feasibility of using FOSpectr methodology as a non-destructive alternative to augment current methods of plant nutrient analysis.

  13. Determination of dry sludge in heavy oil by dual wavelength spectrophotometry

    SciTech Connect

    Fukui, Y.; Nakai, S.; Yamazoe, S. )

    1989-04-01

    Contents of dry sludge in heavy oils have been usually determined by the gravimetric methods. These methods involve complicated operations and require much time. Therefore, a simplified and rapid method for the determination of dry sludge has been awaited both for process control and quality control in a petroleum refinery. Recently, some spectrophotometric methods have been reported by Ono, Mirsayapova, et al., Kaibara, et al, and Fukui for the determination of asphaltene in residual oils. However, no spectrometric method for the determination of dry sludge has ever been reported. A novel method for the rapid determination of dry sludge has been achieved by dual wavelength spectrophotometry. Dry sludge can be determined directly without any solvent, using a thin-walled cell. The method is available for high viscosity oils up to 20,000 cSt {at}50{degree}C, and the time required for the determination is much reduced, compared with the conventional gravimetric methods.

  14. Removal of iron interferences by solvent extraction for geochemical analysis by atomic-absorption spectrophotometry

    USGS Publications Warehouse

    Zhou, L.; Chao, T.T.; Sanzolone, R.F.

    1985-01-01

    Iron is a common interferent in the determination of many elements in geochemical samples. Two approaches for its removal have been taken. The first involves removal of iron by extraction with methyl isobutyl ketone (MIBK) from hydrochloric acid medium, leaving the analytes in the aqueous phase. The second consists of reduction of iron(III) to iron(II) by ascorbic acid to minimize its extraction into MIBK, so that the analytes may be isolated by extraction. Elements of interest can then be determined using the aqueous solution or the organic extract, as appropriate. Operating factors such as the concentration of hydrochloric acid, amounts of iron present, number of extractions, the presence or absence of a salting-out agent, and the optimum ratio of ascorbic acid to iron have been determined. These factors have general applications in geochemical analysis by atomic-absorption spectrophotometry. ?? 1985.

  15. A quantitative and qualitative method to control chemotherapeutic preparations by Fourier transform infrared-ultraviolet spectrophotometry.

    PubMed

    Dziopa, Florian; Galy, Guillaume; Bauler, Stephanie; Vincent, Benoit; Crochon, Sarah; Tall, Mamadou Lamine; Pirot, Fabrice; Pivot, Christine

    2013-06-01

    Chemotherapy products in hospitals include a reconstitution step of manufactured drugs providing an adapted dosage to each patient. The administration of highly iatrogenic drugs raises the question of patients' safety and treatment efficiency. In order to reduce administration errors due to faulty preparations, we introduced a new qualitative and quantitative routine control based on Fourier Transform Infrared (FTIR) and UV-Visible spectrophotometry. This automated method enabled fast and specific control for 14 anticancer drugs. A 1.2 mL sample was used to assay and identify each preparation in less than 90 sec. Over a two-year period, 9370 controlled infusion bags showed a 1.49% nonconformity rate, under 15% tolerance from the theoretical concentration and 96% minimum identification matching factor. This study evaluated the reliability of the control process, as well as its accordance to chemotherapy deliverance requirements. Thus, corrective measures were defined to improve the control process. PMID:23014899

  16. Determination of glucosinolates in 19 Chinese medicinal plants with spectrophotometry and high-pressure liquid chromatography.

    PubMed

    Hu, Ye; Liang, Hao; Yuan, Qipeng; Hong, Yuancheng

    2010-08-01

    Glucosinolates were evaluated in 19 traditional Chinese medicinal plants involved in seven different families: Brassicaceae, Capparaceae, Euphorbiaceae, Phytolaccaceae, Tropaeolaceae, Caricaceae and Rubiaceae. The total glucosinolate contents were determined by spectrophotometry. Results showed that the high contents of total glucosinolates were found in some herbs of Brassicaceae, Capparaceae and Euphorbiaceae families, while low total glucosinolate contents were observed in two Rubiaceae herbs. In addition, eight glucosinolates (glucoraphanin, glucoraphenin, sinalbin, sinigrin, progoitrin, 4-hydroglucobrassicin, glucoiberin and glucoibervirin) in these herbs were measured using HPLC, and the data showed that individual glucosinolates and their contents varied at different degrees among the distinct species. The highest contents of cancer-protective compounds were found in the seeds of Raphanus sativus L. (glucoraphenin), Sinapis alba (sinalbin) and Phyllanthus emblica L. (sinigrin). PMID:20645206

  17. Developments of Si-PIN detectors for Continuous Spectro-photometry of Black Holes (CSPOB)

    SciTech Connect

    Bhoumik, Debashis; Mondal, Shyamal; Chakrabarti, S. K.

    2008-10-08

    The goal of the proposed small-satellite mission named Continuous Spectro-Photometry of Black holes (CSPOB) is to observe a given galactic black hole candidate for several months continuously or almost continuously. In the former case, two identical satellites are required, while one satellite is sufficient if we employ one satellite. Such an observation from 0.5keV to 30keV should answer several questions regarding the spectral and timing properties of accretion processes. In particular, on the origin of the sub-Keplerian component of the accretion flow which is observed in many black hole candidates. We present preliminary results on the development of X-ray detectors based on Hamamatsu made Si-PIN Photodiodes at our laboratory.

  18. Regional variations of skin blood flow response to histamine: evaluation by spectrophotometry and laser Doppler flowmetry

    NASA Astrophysics Data System (ADS)

    Tur, Ethel; Aviram, Guy; Zeltser, D.; Brenner, Sarah; Maibach, Howard I.

    1996-01-01

    To study inherent differences in skin function related to regional variation, we tested the hypothesis that different reactivities of small blood vessels via their direct and indirect activation by histamine play an important role in the observed regional variation of processes. Histamine was administered to three cutaneous regions in 20 volunteers, and the induced response was quantified utilizing spectrophotometry and laser Doppler flowmetry. The back exhibited the greatest response, followed by the forearm and ankle in decreasing order of responsiveness. We suggest that the intensity of the wheal and flare response may partly be related to the local reactivity of the blood vessels once the histamine actually reached them, and to their indirect dilatation via the axonal reflex. These blood vessel response observations may provide initial insight into inherent functional differences influencing cutaneous manifestations of endogenous and exogenous diseases.

  19. Spectrophotometry of Wolf-Rayet stars - Intrinsic colors and absolute magnitudes

    NASA Technical Reports Server (NTRS)

    Torres-Dodgen, Ana V.; Massey, Philip

    1988-01-01

    Absolute spectrophotometry of about 10-A resolution in the range 3400-7300 A have been obtained for southern Wolf-Rayet stars, and line-free magnitudes and colors have been constructed. The emission-line contamination in the narrow-band ubvr systems of Westerlund (1966) and Smith (1968) is shown to be small for most WN stars, but to be quite significant for WC stars. It is suggested that the more severe differences in intrinsic color from star to star of the same spectral subtype noted at shorter wavelengths are due to differences in atmospheric extent. True continuum absolute visual magnitudes and intrinsic colors are obtained for the LMC WR stars. The most visually luminous WN6-WN7 stars are found to be located in the core of the 30 Doradus region.

  20. Microcirculation Under an Elastic Bandage During Rest and Exercise - Preliminary Experience With the Laser-Doppler Spectrophotometry System O2C

    PubMed Central

    Sommer, Björn; Berschin, Gereon; Sommer, Hans-Martin

    2013-01-01

    There is an abundace of studies on the influence of rest and exercise as well as external compression on cutaneous, subcutaneous and muscle tissue blood flow using different measurement techniques. As a novel approach, we simultaneously examined the influence of a custom- made elastic thigh bandage on cutaneous and subcutaneous venous blood oxygenation (SO2), postcapillary venous filling pressures (rHb) and blood flow (flow) using the non-invasive laser- Doppler spectrophotometry system “Oxygen-to-see(O2C)”. Parameters were obtained in 20 healthy volunteers in 2 mm and 8 mm tissue depth during rest, 5 and 10 minutes of moderate bicycle exercise following a 10-minute recovery period. Without the bandage, results matched the known physiological changes indicating higher blood backflow from superficial and deep veins. Underneath the elastic bandage, we observed lower post-capillary filling pressures during exercise. However, after the bandage was removed in the post-exercise period, all obtained parameters of microcirculation remained increased, indicating a higher amount of local venous blood volume in this area. Our observations might be the result of external compression, thermoregulatory and exercise-dependent vascular mechanisms. With the O2C device, a promising new non- invasive technique of measuring local microcirculation in soft tissue exists. This study gives new insights in the field of non-invasive diagnostics with special regard to the influence of elastic bandages on local microcirculation. Key Points It can be demonstrated that a novel non-invasive laser-Doppler spectrophotometry system allows the determination of capillary-venous microcirculation in an in-vivo study during exercise-rest cycles. The results received with this technique indicate that a) without an elastic thigh bandage, turnover rates of capillary and post-capillary microperfusion in skin and subcutaneous fat tissue increase under physical exertion, b) skin blood flow decreases while

  1. Non-invasive monitoring and quantitative analysis of patch test reactions by reflectance spectrophotometry, laser Doppler flowmetry and transepidermal water loss

    NASA Astrophysics Data System (ADS)

    Eikje, Natalja Skrebova; Arase, Seiji

    2008-02-01

    Reflectance spectrophotometry (RS), laser Doppler flowmetry (LDF) and transepidermal water loss (TEWL) techniques were simultaneously used to non-invasively monitor skin colour (SC), skin blood flow (SBF) and barrier function damage (BFD) in routinely patch-tested Japanese patients in dermatology clinic. The analytical quality, reliability and reproducibility of each technique were compared and analyzed in correlated to visual scoring patch test (PT) reactions as negative (-), doubtful (+?), weak (+) and strong (++/+++) at 48- and 72-hour monitoring. An attempt was made to quantify predominant in the clinic "+?"- and "+'"-PT-reactions. The relationship between 48 h and 72 h measurements in different reaction groups was poor for TEWL, LDF showed a tendency to decrease at 72 h, but good for RS. A correlation between visual scorings and instrumental mean values was poor for TEWL, good for LDF and excellent for RS. So, measurements by RS were the most statistically significant to non-invasively monitor and quantify doubtful, weak and strong PT reactions, accordingly providing continuous data grading of reaction intensity suitable in the clinic. Moreover, monitoring of SC changes was the most reliable parameter for the quantitative distinguishing of doubtful and weak reactions in pigmented skin.

  2. Direct UV Spectrophotometry and HPLC Determination of Triton X-100 in Split Virus Influenza Vaccine.

    PubMed

    Pavlović, Bojana; Cvijetić, Nataša; Dragačević, Luka; Ivković, Branka; Vujić, Zorica; Kuntić, Vesna

    2016-03-01

    One of the most commonly used surfactants in the production of split virus influenza vaccine is nonionic surfactant Triton X-100. After splitting of the virus is accomplished, Triton X-100 is removed from the vaccine by subsequent production steps. Because of toxicity of Triton X-100, which remains in the vaccine in residual amounts, a sufficiently sensitive method for its detection and quantification needs to be defined. Two methods for determination of Triton X-100 residuals were developed: the UV-spectrophotometry and HPLC methods. For both methods, preparation of vaccine samples and removal of proteins and virus particles were crucial: samples were treated with methanol (1:1) and then centrifuged at 25 000 × g for 30 min. After such treatment, the majority of vaccine components that interfered in the UV region were removed, and diluted samples could be directly measured. The chromatographic system included C18 column, step methanol gradient, and detection at 225 nm with a single peak of Triton X-100 at 12.6 min. Both methods were validated and gave satisfactory results for accuracy, precision, specificity, linearity, and robustness. LOQ was slightly lower for the HPLC method. Hence, it was shown that both methods are suitable for analysis of residual amounts of Triton X-100, with the advantages of the UV method being its simplicity and availability in most laboratories. PMID:26960682

  3. Binding study of tetracyclines to human serum albumin using difference spectrophotometry.

    PubMed

    Zia, H; Price, J C

    1976-02-01

    The binding of several tetracyclines to human serum albumin was studied using difference spectrophotometry and a spectrophotometric probe, 2-(4'-hydroxybenzeneazo)benzoic acid. Difference spectra observed for the interaction between the probe and human serum albumin were similar to probe-bovine serum albumin spectra but were less intense for a given concentration of probe and did not reach saturation as quickly. Difference spectra for the tetracyclines were dependent on the characteristics of the ring substituents. More hydrophobic substituents on the D and C rings tended to give more intense difference spectra, but charge-transfer complexing may also have been involved since methacycline with a methylene group in the 6-position showed the most intense spectra of the compounds studied. Solvent perturbation, pH, and urea studies tended to confirm that something other than hydrophobic binding of the tetracyclines was involved. Drug-probe displacement studies showed that methacycline gave the greatest probe displacement followed by doxycycline, chlortetracycline, oxytetracycline, and tetracycline. This order of displacement of the anionic probe indicates that both hydrophobic and charge-transfer binding are involved. Experiments with calcium ion and ethylenediaminetetraacetic acid showed that the difference spectra obtained with the tetracyclines and human serum albumin were not the result of metallic bridge-chelate formation. PMID:3641

  4. Spectrophotometry of the galaxies and nebulosity associated with the quasar III Zw 2

    NASA Technical Reports Server (NTRS)

    Green, R. F.; Williams, T. B.; Morton, D. C.

    1978-01-01

    Results are presented for spectrophotometry of the object III Zw 2, the faint nebulosity to the NW of its nucleus, and two associated galaxies (a normal elliptical and a more luminous late-type spiral). The object III Zw 2 is defined to be a quasar on the basis of its dominant starlike nucleus, redshift, and optical and radio variability. The spectrophotometrically measured redshifts of the two associated galaxies are shown to place III Zw 2 as a member of Zwicky Cluster 0007.7+1056, thus establishing the cosmological origin of the quasar's emission-line redshift of 0.089. It is found that the nebulosity to the NW of the quasar exhibits an emission-line spectrum at the same redshift as the nucleus with an underlying red continuum, that the strength of the forbidden lines relative to the permitted lines is 3 to 4 times greater than in the nucleus, and that the data for the nebulosity are not well fitted by a bremsstrahlung emission spectrum, but are consistent with a spectrum of starlight from an underlying galaxy at the system redshift of 0.089.

  5. Application of response surface methodology for determination of methyl red in water samples by spectrophotometry method

    NASA Astrophysics Data System (ADS)

    Khodadoust, Saeid; Ghaedi, Mehrorang

    2014-12-01

    In this study a rapid and effective method (dispersive liquid-liquid microextraction (DLLME) was developed for extraction of methyl red (MR) prior to its determination by UV-Vis spectrophotometry. Influence variables on DLLME such as volume of chloroform (as extractant solvent) and methanol (as dispersive solvent), pH and ionic strength and extraction time were investigated. Then significant variables were optimized by using a Box-Behnken design (BBD) and desirability function (DF). The optimized conditions (100 μL of chloroform, 1.3 mL of ethanol, pH 4 and 4% (w/v) NaCl) resulted in a linear calibration graph in the range of 0.015-10.0 mg mL-1 of MR in initial solution with R2 = 0.995 (n = 5). The limits of detection (LOD) and limit of quantification (LOQ) were 0.005 and 0.015 mg mL-1, respectively. Finally, the DLLME method was applied for determination of MR in different water samples with relative standard deviation (RSD) less than 5% (n = 5).

  6. Optical and infrared spectrophotometry of the symbiotic system V1016 Cygni

    NASA Technical Reports Server (NTRS)

    Rudy, Richard J.; Rossano, George S.; Cohen, Ross D.; Puetter, R. C.

    1990-01-01

    Spectrophotometry from 0.46 to 1.3 micron of the peculiar emission-line object V1016 Cyg is presented. The optical region displays a weak continuum underlying the rich emission-line spectrum detailed in past studies. The infrared spectrum consists of prominent emission lines of H I, He I, He II, forbidden Ni, O I, and forbidden S III overlying a strong stellar continuum. The latter displays bands at 0.94 micron and 1.13 micron characteristic of a late-type, oxygen-rich giant as well as an absorption at 1.05 micron which is due to VO. The presence of these molecular features indicates a spectral class of M6 or later for the cool secondary. The reddening of the secondary does not appear to be much different from that of the emission lines. Among the infrared emission features is the rarely seen permitted transition of neutral oxygen at 1.1287 micron. Its presence at a strength comparable to O I 8446 A, together with the absence of O I 13164 A, confirms the result of Strafella that the strong O I lines arise primarily from fluorescent excitation by Ly-beta.

  7. Feasibility of spectro-photometry in X-rays (SPHINX) from the moon

    NASA Astrophysics Data System (ADS)

    Sarkar, Ritabrata; Chakrabarti, Sandip Kumar

    2010-08-01

    Doing space Astronomy on lunar surface has several advantages. We present here feasibility of an All Sky Monitoring Payload for Spectro-photometry in X-rays (SPHINX) which can be placed on a lander on the moon or in a space craft orbiting around the moon. The Si-PIN photo-diodes and CdTe crystals are used to detect solar flares, bright gamma bursts, soft gamma-ray repeaters from space and also X-ray fluorescence (XRF) from lunar surface. We present the complete Geant4 simulation to study the feasibility of such an instrument in presence of Cosmic Diffused X-Ray Background (CDXRB). We find that the signal to noise ratio is sufficient for moderate to bright GRBs (above 5 keV), for the quiet sun (up to 100 keV), solar flares, soft gamma-ray repeaters, X-ray Fluorescence (XRF) of lunar surface etc. This is a low-cost system which is capable of performing multiple tasks while stationed at the natural satellite of our planet.

  8. Stability of low concentration calibration standards for graphite furnace atomic absorption spectrophotometry

    SciTech Connect

    Bass, D A; TenKate, L B

    1993-11-01

    Graphite furnace atomic absorption spectrophotometry (GFAAS) is used for determination of ultra-trace metals in environmentally important samples. In the generation of GFAAS calibration curves for many environmental applications, low concentration calibration standards must be prepared dally, as required by the Statement of Work (SOW) for the US Environmental Protection Agency (EPA) Contract Laboratory Program (CLP). This results in significant time and work for the analyst and significant cost to the Analytical Chemistry Laboratory (ACL) for chemicals and waste management. While EPA SW 846 is less prescriptive than the CLP SOW, ACL has been following the CLP guidelines because in-house criteria regarding the stability of GFAAS standards have not been established. A study was conducted to determine the stability of GFAAS standards for analytes commonly used in the ACL (single and mixed) as a function of time. Data were collected over nine months. The results show that GFAAS standards for Sb, Pb, Se, Ag, and TI are stable for a longer period of time than currently assumed by the CLP SOW. Reducing the frequency of preparing these standards will increase efficiency, decrease the handling of hazardous the quantity of hazardous waste generated, and decrease the quantity of hazardous substances to be ordered and stocked by the laboratory. These benefits will improve GFAAS analysis quality, reduce costs, enhance safety, and lower environmental concerns.

  9. Determination of attapulgite and nifuroxazide in pharmaceutical formulations by sequential digital derivative spectrophotometry.

    PubMed

    Toral, M Inés; Paine, Maximiliano; Leyton, Patricio; Richter, Pablo

    2004-01-01

    A new method for the sequential determination of attapulgite and nifuroxazide in pharmaceutical formulations by first- and second-derivative spectrophotometry, respectively, has been developed. In order to obtain the optimal conditions for nifuroxazide stability, studies of solvent, light, and temperature effects were performed. The results show that a previous hydrolysis of 2 h in 1.0 x 10(-1)M NaOH solution is necessary in order to obtain stable compounds for analytical purposes. Subsequently, the first- and second-derivative spectra were evaluated directly in the same samples. The sequential determination of the drugs can be performed using the zero-crossing method; the attapulgite determination was carried out using the first derivative at 278.0 nm and the nifuroxazide determination, using the second derivative at 282.0 nm. The determination ranges were 5.7 x 10(-6)-1.0 x 10(-4) and 3.7 x 10(-8) -1.2 x 10(-4)M for attapulgite and nifuroxazide, respectively. Repeatability (relative standard deviation) values of 1.2 and 3.0% were observed for attapulgite and nifuroxazide, respectively. The ingredients commonly found in commercial pharmaceutical formulations do not interfere. The proposed method was applied to the determination of these drugs in tablets. Further, infrared spectroscopy and cyclic voltammetry studies were carried out in order to obtain knowledge of the decomposition products of nifuroxazide. PMID:15675443

  10. A New Concept for Spectrophotometry of Exoplanets with Space-borne Telescopes

    NASA Astrophysics Data System (ADS)

    Matsuo, Taro; Itoh, Satoshi; Shibai, Hiroshi; Sumi, Takahiro; Yamamuro, Tomoyasu

    2016-06-01

    We propose a new concept for the spectral characterization of transiting exoplanets with future space-based telescopes. This concept, called densified pupil spectroscopy, allows us to perform high, stable spectrophotometry against telescope pointing jitter and deformation of the primary mirror. This densified pupil spectrometer comprises the following three roles: division of a pupil into a number of sub-pupils, densification of each sub-pupil, and acquisition of the spectrum of each sub-pupil with a conventional spectrometer. Focusing on the fact that the divided and densified sub-pupil can be treated as a point source, we discovered that a simplified spectrometer allows us to acquire the spectra of the densified sub-pupils on the detector plane‑an optical conjugate with the primary mirror‑by putting the divided and densified sub-pupils on the entrance slit of the spectrometer. The acquired multiple spectra are not principally moved on the detector against low-order aberrations such as the telescope pointing jitter and any deformation of the primary mirror. The reliability of the observation result is also increased by statistically treating them. Our numerical calculations show that because this method suppresses the instrumental systematic errors down to 10 ppm under telescopes with modest pointing accuracy, next generation space telescopes with more than 2.5 m diameter potentially provide opportunities to characterize temperate super-Earths around nearby late-type stars through the transmission spectroscopy and secondary eclipse.

  11. Determination of uranium(IV) by derivative spectrophotometry of its complexes with hydroethylidenediphosphomic acid

    SciTech Connect

    Perfil'ev, V.A.; Mishchenko, V.T.; Poluektov, N.S.

    1985-05-20

    This paper reports on a study of the spectral characteristics of complex compounds of uranium-(IV) with a ligand containing the phosphonic groups - hydroxyethyllidenediphosphonic acid (HEDPA) - and its possible use for analysis. The method of derivative spectrophotometry has been used since absorption bands corresponding to a mixture of compounds can thus be resolved into absorption bands of the individual components, and their fine structure can be studied. The method ensures accuracy and reproducibility of the analysis of the mixture of compounds. It was found that, depending on the ratio of the components in the solution, compounds with composition of U(IV) . HEDPA . and U(IV) . 2 HEDPA are formed. It is shown that the complexes studied can be used for the determination of uraniun(IV) in pure salts (C /SUB min/ = 0.05 ..mu..g/ml) and also in the presence of iron (II) ions. In this latter case, the second derivatives of the absorption spectra were used.

  12. Fiber optic spectrophotometry for monitoring dissolved oxygen in a tropical ornamental fish tank environment

    NASA Astrophysics Data System (ADS)

    Asundi, Anand K.; Chen, Jun-Wei; He, Duo-Min

    1999-05-01

    Using Fiber Optic Spectro-Photometry (FOSP) methodology, a set of high sensitivity fiber optic oxygen monitoring system performing NDT is developed for fish farming environment. The working principle of the sensor is based on the detection signal at a particular wavelength due to the fluorescence and quenching of coated dye (ruthenium complex) in response to oxygen concentration at the tip of the probe. This paper looks into the application of fiber optics oxygen sensor in an aquatic environment. A comparison study of the optical probe was made with a conventional electrochemical oxygen sensor. Both sensors were setup to monitor the dissolved oxygen of an aquatic system for a period of time. This new methodology offers an alternative choice for monitoring dissolved oxygen. Apart from the possibility to miniaturize the monitoring equipment for aquatic environment, it is also feasible to 'bundle' other chemical sensors together into one single cable, thus achieving compactness, effectiveness and yet without forgoing whatever the traditional electrochemical sensors could offer.

  13. Partitioning of organophosphorus pesticides into phosphatidylcholine small unilamellar vesicles studied by second-derivative spectrophotometry

    NASA Astrophysics Data System (ADS)

    Takegami, Shigehiko; Kitamura, Keisuke; Ohsugi, Mayuko; Ito, Aya; Kitade, Tatsuya

    2015-06-01

    In order to quantitatively examine the lipophilicity of the widely used organophosphorus pesticides (OPs) chlorfenvinphos (CFVP), chlorpyrifos-methyl (CPFM), diazinon (DZN), fenitrothion (FNT), fenthion (FT), isofenphos (IFP), profenofos (PFF) and pyraclofos (PCF), their partition coefficient (Kp) values between phosphatidylcholine (PC) small unilamellar vesicles (SUVs) and water (liposome-water system) were determined by second-derivative spectrophotometry. The second-derivative spectra of these OPs in the presence of PC SUV showed a bathochromic shift according to the increase in PC concentration and distinct derivative isosbestic points, demonstrating the complete elimination of the residual background signal effects that were observed in the absorption spectra. The Kp values were calculated from the second-derivative intensity change induced by addition of PC SUV and obtained with a good precision of R.S.D. below 10%. The Kp values were in the order of CPFM > FT > PFF > PCF > IFP > CFVP > FNT ⩾ DZN and did not show a linear correlation relationship with the reported partition coefficients obtained using an n-octanol-water system (R2 = 0.530). Also, the results quantitatively clarified the effect of chemical-group substitution in OPs on their lipophilicity. Since the partition coefficient for the liposome-water system is more effective for modeling the quantitative structure-activity relationship than that for the n-octanol-water system, the obtained results are toxicologically important for estimating the accumulation of these OPs in human cell membranes.

  14. Determination of myoglobin based on its enzymatic activity by stopped-flow spectrophotometry

    NASA Astrophysics Data System (ADS)

    Zheng, Qi; Liu, Zhihong; Cai, Ruxiu

    2005-04-01

    A new method has been developed for the determination of myoglobin (Mb) based on its enzymatic activity for the oxidation of o-phenylenediamine (OPDA) with hydrogen peroxide. Stopped-flow spectrophotometry was used to study the kinetic behavior of the oxidation reaction. The catalytic activity of Mb was compared to other three kinds of catalyst. The time dependent absorbance of the reaction product, 2,3-diamimophenazine (DAPN), at a wavelength of 426 nm was recorded. The initial reaction rate obtained at 40 °C was found to be proportional to the concentration of Mb in the range of 1.0 × 10 -6 to 4.0 × 10 -9 mol L -1. The detection limit of Mb was found to be 9.93 × 10 -10 mol L -1. The relative standard deviations were within 5% for the determination of different concentrations of Mb. Excess of bovine serum albumin (BSA), Ca(II), Mg(II), Cu(II), glucose, caffeine, lactose and uric acid did not interfere.

  15. Determination of Oxytetracycline from Salmon Muscle and Skin by Derivative Spectrophotometry.

    PubMed

    Toral, M Inés; Sabay, Tamara; Orellana, Sandra L; Richter, Pablo

    2015-01-01

    A method was developed for the identification and quantification of oxytetracycline residues present in salmon muscle and skin using UV-Vis derivative spectrophotometry. With this method, it was possible to reduce the number of steps in the procedure typically required for instrumental analysis of a sample. The spectral variables, order of the derivative, scale factor, smoothing factor, and analytical wavelength were optimized using standard solutions of oxytetracycline dissolved in 900 mg/L oxalic acid in methanol. The matrix effect was significant; therefore, quantification for oxytetracycline residues was carried out using drug-free salmon muscle and skin samples fortified with oxytetracycline. The LOD and LOQ were found to be 271 and 903 μg/kg, respectively. The precision and accuracy of the method were validated using drug-free salmon muscle and skin tissues fortified at three different concentrations (8, 16, and 32 mg/kg) on 3 different days. The recoveries at all fortified concentrations were between 90 and 105%, and RSDs in all cases were less than 6.5%. This method can be used to screen out compliant samples and thereby reduce the number of suspect positive samples that will require further confirmatory analysis. PMID:26025109

  16. Preliminary Results from the Array Camera for Optical to Near-IR Spectrophotometry (ARCONS)

    NASA Astrophysics Data System (ADS)

    Mazin, Benjamin A.; O'Brien, K.; Bumble, B.; Strader, M.; Meeker, S.; Stoughton, C.; Marsden, D.; Walter, A.; Szypyrt, P.; Ulbricht, G.

    2013-01-01

    In September 2012, the ARray Camera for Optical to Near-IR Spectrophotometry (ARCONS) was deployed at the 120" Shane telescope at Lick Observatory. ARCONS is a photon conuting integral field unit (IFU) that utilizes Microwave Kinetic Inductance Detectors (MKIDs), which are an emerging superconducting detector technology. MKIDs measure the energy (to within several percent) and arrival time (to within a microsecond) of detected photons. ARCONS contains a 2024 (46x44) pixel MKID array and has an operational bandwidth of 400 to 1100 nm. At the Shane telescope's Coudé focus, the array had a field of view of 22"x23". A variety of observations were made to demonstrate the potential applications of ARCONS's ability to do time-resolved low resolution spectro-imaging. Observations were made of short period compact binaries to look for spectral orbital variations. Observations of eclipsing white dwarfs were made to look for transit timing variations in orbital periods that would indicate the presence of additional companions. Observations were also made of faint galaxies to determine their redshifts, and observations of Low-Mass X-ray Binaries were made to probe the IR-emitting region of their jets. In another use of ARCONS's timing resolution, simultaneous optical and radio observations of the Crab pulsar were made, with the help of collaborators. In this talk I will discuss the preliminary results of a subset of these observations.

  17. Determination of chromium and molybdenum in medical foods by graphite furnace atomic absorption spectrophotometry.

    PubMed

    Phifer, E C

    1995-01-01

    Graphite furnace atomic absorption spectrophotometry was used to determine chromium and molybdenum in 7 medical foods from 5 manufacturers. Linear standard curves were obtained for both elements for concentrations between 5 and 25 ng/mL. Detection limits were 0.24 ng/mL for Cr and 0.67 ng/mL for Mo. Characteristic masses were 3.1 and 14.7 pg for Cr and Mo, respectively. No difference was detected between wet and dry ashing methods, and dry ashing was used to complete the study. The method was validated by assaying various National Institute of Standards and Technology standard reference materials. Analysis of these products for Cr and Mo were within certified values. One product was evaluated by this method for reproducibility (n = 5). Relative standard deviations were 6.8 and 4.8% for Cr and Mo, respectively. This product contained 0.31 +/= 0.02 micrograms Cr/g and 0.63 +/- 0.03 micrograms Mo/g. The remaining products contained 0.09-1.28 micrograms Cr/g and 0.07-2.3 micrograms Mo/g. Mean recovery values were 98 +/- 14% (n = 14) for Cr at spike levels of 0.20-1.89 micrograms/g and 102 +/- 24% (n = 10) for Mo at spike levels of 0.30-1.89 micrograms/g. PMID:8664588

  18. Cold-induced aggregation microextraction based on ionic liquids and fiber optic-linear array detection spectrophotometry of cobalt in water samples.

    PubMed

    Gharehbaghi, Maysam; Shemirani, Farzaneh; Farahani, Malihe Davudabadi

    2009-06-15

    A new simple and rapid cold-induced aggregation microextraction (CIAME) method was applied to preconcentrate cobalt(II) ions from water samples as a prior step to its determination by fiber optic-linear array detection spectrophotometry (FO-LADS). In this method, very small amounts of 1-hexyl-3-methylimidazolium hexafluorophosphate [Hmim][PF(6)] and 1-hexyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imide [Hmim][Tf(2)N] as hydrophobic ionic liquids (ILs) and extractant solvents were dissolved in the sample solution containing Triton X-114 (anti-sticking agent). 1-(2-Pyridylazo)-2-naphthol (PAN) was chosen as the complexing agent. After dissolving, the solution was cooled in the ice bath and a cloudy solution was formed of IL fine droplets due to the decrease of IL solubility. After centrifuging, the fine droplets of extractant phase were settled to the bottom of the conical-bottom centrifuge tube. Analysis was carried out by a fiber optic-linear array detector spectrophotometer at 570 nm. In this method, which is robust against high content of salt and water-miscible organic solvents, various parameters were investigated and optimized. The applicability of the technique was evaluated by the determination of trace amounts of cobalt in several water samples. Under the optimum conditions, the limit of detection (LOD) of the method was 0.14 ng mL(-1) and the relative standard deviation (R.S.D.) for 30 ng mL(-1) cobalt was 2.32%. PMID:19095354

  19. Preparation of dry extract of Mikania glomerata Sprengel (Guaco) and determination of its coumarin levels by spectrophotometry and HPLC-UV.

    PubMed

    Soares e Silva, Luciana Soares E; da Santos da Silva, Luciane Santos; Brumano, Larissa; Stringheta, Paulo César; Aparecida de Oliveira Pinto, Miriam; Moreira Dias, Leticia Oliveira; de Sá Martins Muller, Camila; Scio, Elita; Fabri, Rodrigo Luiz; Castro, Helena C; da Penha Henriques do Amaral, Maria

    2012-01-01

    Guaco (Mikania glomerata Sprengel) syrup is one of the most popular herbal medicines used to treat the symptoms of asthmatic bronchitis, cough and hoarseness. The coumarin 2H-1-benzopyran-2-one, is one of the major constituents of Guaco and contributes to its pharmacological effects. The pharmaceutical capsule form of dry extract of Guaco is recommended by the Brazilian Program of Medicinal Plants and Herbal Medicines and used in primary health care. In order to identify a new protocol to obtain the raw material for Guaco capsule production we evaluated two methods, including a freezedrying process (lyophilization) and the spray-dryer technique, as well as the use of two adjuvants, Maltodextrins and Aerosil®, in different concentrations. The coumarin levels of the dried extracts were analyzed by UV-spectrophotometry and HPLC-UV/DAD. The adjuvant Aerosil® 8% showed better dry powder physical appearance. Lyophilization was observed to be the best process to obtain the dry extract of Guaco based on the measured coumarin levels. PMID:22932215

  20. Application of first-derivative, ratio derivative spectrophotometry, TLC-densitometry and spectrofluorimetry for the simultaneous determination of telmisartan and hydrochlorothiazide in pharmaceutical dosage forms and plasma.

    PubMed

    Bebawy, Lories I; Abbas, Samah S; Fattah, Laila A; Refaat, Heba H

    2005-10-01

    Four sensitive methods are described for the direct determination of telmisartan (TELM) and hydrochlorothiazide (HCT) in combined dosage forms without prior separation. The first method is a first derivative spectophotometry (1D) using a zero- crossing technique of measurement at 241.6 and 227.6 nm for TELM and HCT, respectively. The second method is the first derivative of ratio spectrophotometry (1DD) where the amplitudes were measured at 242.7 nm for TELM and 274.9 nm for HCT. The third method is based on TLC separation of the two drugs followed by the densitometric measurements of their spots at 295 and 225 nm for TELM and HCT, respectively. The separation was carried out on silica gel 60 F254 using butanol: ammonia 25% (8:2 v/v) as mobile phase. The fourth method is spectrofluorimetric determination of TELM, depending on measuring the native fluorescence of the drug in 1 M sodium hydroxide at lambda excitation 230 nm and emission at 365 nm. The proposed methods were applied successfully for the determination of the two drugs in bulk powder and in pharmaceutical formulations. The spectrofluorimetric method was utilized for the analysis of TELM in human plasma. PMID:16129437

  1. Estimation of nitrite in source-separated nitrified urine with UV spectrophotometry.

    PubMed

    Mašić, Alma; Santos, Ana T L; Etter, Bastian; Udert, Kai M; Villez, Kris

    2015-11-15

    Monitoring of nitrite is essential for an immediate response and prevention of irreversible failure of decentralized biological urine nitrification reactors. Although a few sensors are available for nitrite measurement, none of them are suitable for applications in which both nitrite and nitrate are present in very high concentrations. Such is the case in collected source-separated urine, stabilized by nitrification for long-term storage. Ultraviolet (UV) spectrophotometry in combination with chemometrics is a promising option for monitoring of nitrite. In this study, an immersible in situ UV sensor is investigated for the first time so to establish a relationship between UV absorbance spectra and nitrite concentrations in nitrified urine. The study focuses on the effects of suspended particles and saturation on the absorbance spectra and the chemometric model performance. Detailed analysis indicates that suspended particles in nitrified urine have a negligible effect on nitrite estimation, concluding that sample filtration is not necessary as pretreatment. In contrast, saturation due to very high concentrations affects the model performance severely, suggesting dilution as an essential sample preparation step. However, this can also be mitigated by simple removal of the saturated, lower end of the UV absorbance spectra, and extraction of information from the secondary, weaker nitrite absorbance peak. This approach allows for estimation of nitrite with a simple chemometric model and without sample dilution. These results are promising for a practical application of the UV sensor as an in situ nitrite measurement in a urine nitrification reactor given the exceptional quality of the nitrite estimates in comparison to previous studies. PMID:26340062

  2. Determination of ibuprofen in combined dosage forms and cream by direct UV spectrophotometry after solid-phase extraction.

    PubMed

    Sunaric, Slavica; Petkovic, Milica; Denic, Marko; Mitic, Snezana; Pavlovic, Aleksandra

    2013-01-01

    Solid-phase extraction method followed by direct UV spectrophotometry at 264 nm was developed and applied for the selective ibuprofen determination in two-component formulation of ibuprofen and pseudoephedrine-HCl, combined powder which contains ibuprofen in the form of salt with L-arginine and 10% ibuprofen cream. Procedures for ibuprofen determination in complex pharmaceutical preparations by direct UV spectrophotometry lack selectivity because of interferences of other active substances and fat components. A limited number of spectrophotometric methods applicable to these samples are based on derivative (first and second-order) UV spectroscopy. Common HPLC procedures are more selective but more expensive and for creams also require some type of extraction because the large amount of oily excipients would clog up the column. The proposed solid-phase extraction method proved to be suitable for analysis of ibuprofen in combined tablets, powders and creams by direct UV spectrophotometry. Also the method provides an effective clean-up of the cream and allows ibuprofen determination by HPLC analysis. For the extraction three different commercial sorbents were tested: anion exchange Oasis MAX, hydrophilic-lipophilic balanced Oasis HLB and reverse-phase Chromabond C18ec. The optimization of the SPE method was first done on standard ibuprofen solutions and then the suitability of the method was checked on solutions of commercial pharmaceutical samples. The method yields good results for all three types of commercial preparations on the anion-exchange Oasis MAX cartridges, with recoveries of 90-100.2%. The interferences in UV analysis were not registered and good precision (RSD < 6%) was obtained. The present method has been verified as accurate as the reference HPLC with the great advantage of less expensive instrumentation. For this reason, the method would be suitable for a routine and rapid drug quality control. PMID:23757930

  3. [Use of solubilization for the preparation of samples for determination of heavy metals in biological materials using atomic absorption spectrophotometry].

    PubMed

    Pfüller, U; Fuchs, V; Golbs, S; Ebert, E; Pfeifer, D

    1980-01-01

    Solubilisation was tested for its suitability to prepare organic samples for metal determination. Flameless atomic-absorption spectrophotometry was used as test method. Copper, manganese, zinc, and chromium levels were determined from various organ systems of Wistar rat, in response to "normal" feeding of pelletised standard feed. A comparison between experimentally established concentrations, on the one hand, and literature data, on the other, suggested that solubilisation was applicable with good success to the preparation of samples from which to determine reliable values, in ppm and ppb, of the above elements. PMID:7436671

  4. Determination of silver in soils, sediments, and rocks by organic-chelate extraction and atomic absorption spectrophotometry

    USGS Publications Warehouse

    Chao, T.T.; Ball, J.W.; Nakagawa, H.M.

    1971-01-01

    A useful method for the determination of silver in soil, sediment, and rock samples in geochemical exploration has been developed. The sample is digested with concentrated nitric acid, and the silver extracted with triisooctyl thiophosphate (TOTP) in methyl isobutyl ketone (MIBK) after dilution of the acid digest to approximately 6 M. The extraction of silver into the organic extractant is quantitative and not affected by the nitric acid concentration from 4 M to 8 M, or by different volumes of TOTP-MIBK. The extracted silver is stable and remains in the organic phase up to several days. The silver concentration is determined by atomic absorption spectrophotometry. ?? 1971.

  5. Detecting estrogenic activity in water samples withestrogen-sensitive yeast cells using spectrophotometry and fluorescencemicroscopy

    SciTech Connect

    Wozei, E.; Holman, H-Y.N.; Hermanowicz, S.W.; Borglin S.

    2006-03-15

    Environmental estrogens are environmental contaminants that can mimic the biological activities of the female hormone estrogen in the endocrine system, i.e. they act as endocrine disrupters. Several substances are reported to have estrogen-like activity or estrogenic activity. These include steroid hormones, synthetic estrogens (xenoestrogens), environmental pollutants and phytoestrogens (plant estrogens). Using the chromogenic substrate ortho-nitrophenyl-{beta}-D-galactopyranoside (ONPG) we show that an estrogen-sensitive yeast strain RMY/ER-ERE, with human estrogen receptor (hER{alpha}) gene and the lacZ gene which encodes the enzyme {beta}-galactosidase, is able to detect estrogenic activity in water samples over a wide range of spiked concentrations of the hormonal estrogen 17{beta}-estradiol (E2). Ortho-nitrophenol (ONP), the yellow product of this assay can be detected using spectrophotometry but requires cell lysis to release the enzyme and allow product formation. We improved this aspect in a fluorogenic assay by using fluorescein di-{beta}-D-galactopyranoside (FDG) as a substrate. The product was visualized using fluorescence microscopy without the need to kill, fix or lyse the cells. We show that in live yeast cells, the uptake of E2 and the subsequent production of {beta}-galactosidase enzyme occur quite rapidly, with maximum enzyme-catalyzed fluorescent product formation evident after about 30 minutes of exposure to E2. The fluorogenic assay was applied to a selection of estrogenic compounds and the Synchrotron-based Fourier transform infrared (SR-FTIR) spectra of the cells obtained to better understand the yeast whole cell response to the compounds. The fluorogenic assay is most sensitive to E2, but the SR-FTIR spectra suggest that the cells respond to all the estrogenic compounds tested even when no fluorescent response was detected. These findings are promising and may shorten the duration of environmental water screening and monitoring regimes using

  6. Sensitive determination of total particulate phosphorus and particulate inorganic phosphorus in seawater using liquid waveguide spectrophotometry.

    PubMed

    Ehama, Makoto; Hashihama, Fuminori; Kinouchi, Shinko; Kanda, Jota; Saito, Hiroaki

    2016-06-01

    Determining the total particulate phosphorus (TPP) and particulate inorganic phosphorus (PIP) in oligotrophic oceanic water generally requires the filtration of a large amount of water sample. This paper describes methods that require small filtration volumes for determining the TPP and PIP concentrations. The methods were devised by validating or improving conventional sample processing and by applying highly sensitive liquid waveguide spectrophotometry to the measurements of oxidized or acid-extracted phosphate from TPP and PIP, respectively. The oxidation of TPP was performed by a chemical wet oxidation method using 3% potassium persulfate. The acid extraction of PIP was initially carried out based on the conventional extraction methodology, which requires 1M HCl, followed by the procedure for decreasing acidity. While the conventional procedure for acid removal requires a ten-fold dilution of the 1M HCl extract with purified water, the improved procedure proposed in this study uses 8M NaOH solution for neutralizing 1M HCl extract in order to reduce the dilution effect. An experiment for comparing the absorbances of the phosphate standard dissolved in 0.1M HCl and of that dissolved in a neutralized solution [1M HCl: 8M NaOH=8:1 (v:v)] exhibited a higher absorbance in the neutralized solution. This indicated that the improved procedure completely removed the acid effect, which reduces the sensitivity of the phosphate measurement. Application to an ultraoligotrophic water sample showed that the TPP concentration in a 1075mL-filtered sample was 8.4nM with a coefficient of variation (CV) of 4.3% and the PIP concentration in a 2300mL-filtered sample was 1.3nM with a CV of 6.1%. Based on the detection limit (3nM) of the sensitive phosphate measurement and the ambient TPP and PIP concentrations of the ultraoligotrophic water, the minimum filtration volumes required for the detection of TPP and PIP were estimated to be 15 and 52mL, respectively. PMID:27130091

  7. [Study on determination of eight metal elements in Hainan arecanut leaf by flame atomic absorption spectrophotometry].

    PubMed

    Liu, Li-yun; Wang, Ping; Feng, Mei-li; Dong, Zhi-guo; Li, Jie

    2008-12-01

    Arecanut is a sort of palm that is important economic crop for the farmers in Hainan province of China, wherein there are many kinds of metal elements such as K, Ca, Na, Mg, Fe, Mn, Cu, Zn etc. These elements are important nutrition for the growth of arecanut. It is very valuable to study on the content of these metal elements in arecanut leaf in terms of plant nutriology of arecanut. The arecanut leaf in Wangling county, Hainan province of China was sampled by diagonal-field-sampling method. Refering to other plant sample determination by FAAS, the detailed studies are done with different digestion and determination methods. In the present paper the effects of mixed acid of HNO3-HClO4 digestion method on determining the amount of metal elements in the arecanut leaf by FAAS is reported, and another one is incineration digestion method. FAAS method was established for the determination of K, Ca, Mg, Na, Fe, Mn, Cu and Zn The samples were incinerated or heated with HNO3-HClO4 (4:1). In the meantime, the optimum parameters of FAAS and effects of different digestion methods on the results were discussed. The recovery rate of standard addition is 98.36%-102.38% in the first method; RSD is 0.42%-2.328% (n=6); The recovery rate of standard addition is 99.22%-103.72% in the second method; RSD is 0.58%-1.283 (n=6). The metal amount determined by the first method is lower than the second method, the ratio is 0.9703-0.9934. The two methods are satisfied, but the latter is better. It is precise enough to common experiment to use flame atomic absorption spectrophotometry with digestion by incineration If the especially precise experiment is required, the digestion methods with mixed acid of HNO3-HClO4 may be introduced. The paper introduced methods dependable for determination of some metal elements in order to study on some nutrient effects of these metal elements in arecanut. PMID:19248529

  8. [Determination of nine mineral elements in hulless barley by ultraviolet spectrophotometry and flame atomic absorption spectrometry].

    PubMed

    Liu, Jin; Zhang, Huai-Gang

    2010-04-01

    The contents of nine mineral elements, including sulphur, zinc, calcium, magnesium, potassium, sodium, iron, copper and manganese in five hulless barley (Hordeum vulgare L. var. nudum Hook. f.) lines were determined by ultraviolet spectrophotometry and flames atomic absorption spectrometry (FAAS). For the determination of sulphur, the samples were dissolved by magnesia and anhydrous sodium carbonate at 250 degrees C for 0. 5 h and at 550 degrees C for 3 h in the muffle furnace, and then a certain amount of barium chloride was put into the sample solution for colorimetry of the UV-Vs spectrophotometer. For the determination of other eight mineral elements, all of the samples were dissolved by a kind of incinerating method: first, the sample was put into the muffle furnace at 250 degrees C for 0. 5 h and at 550 degrees C for 2.5 h, then two droplets of 50%HNO3 were distributed into each sample, and the last step was putting the sample into the muffle furnace at 550 degrees C for 0.5 h. And then all of the ash was dissolved by 50%HNO3 to 50 milliliter and determined by flames atomic absorption spectrometry. The precision, accuracy, repeatability and stability of the method were discussed too. The results showed that the relative standard deviations (RSD) were between 1.2% and 3.7%; The average recoveries were 97.44%-101.52% and the relative standard deviations (RSD) of sample determination were 1.3%-3.8%. The repeatability experiment showed that the relative standard deviations (RSD) were 2.6%-6.1%. And the content of each mineral element was the same after 24 hours; All these showed that the method has a good precision, accuracy, repeatability and stability. In all the hulless barley samples, the average contents were in the order of K > S > Mg > Ca > Fe > Na > Zn > Mn > Cu, and the contents of zinc, iron and manganese closely related to people's health were relatively higher than other crops. The data of the experiment could provide an accurate and credible evidence

  9. Derivative spectrophotometry for the determination of faropenem in the presence of degradation products: an application for kinetic studies.

    PubMed

    Cielecka-Piontek, Judyta

    2013-07-01

    A simple and selective derivative spectrophotometric method was developed for the quantitative determination of faropenem in pure form and in pharmaceutical dosage. The method is based on the zero-crossing effect of first-derivative spectrophotometry (λ = 324 nm), which eliminates the overlapping effect caused by the excipients present in the pharmaceutical preparation, as well as degradation products, formed during hydrolysis, oxidation, photolysis, and thermolysis. The method was linear in the concentration range 2.5-300 μg/mL (r = 0.9989) at λ = 341 nm; the limits of detection and quantitation were 0.16 and 0.46 μg/mL, respectively. The method had good precision (relative standard deviation from 0.68 to 2.13%). Recovery of faropenem ranged from 97.9 to 101.3%. The first-order rate constants of the degradation of faropenem in pure form and in pharmaceutical dosage were determined by using first-derivative spectrophotometry. A statistical comparison of the validation results and the observed rate constants for faropenem degradation with these obtained with the high-performance liquid chromatography method demonstrated that both were compatible. PMID:23816120

  10. Comparison of four methods for digesting food samples for determination of trace levels of cadmium by flameless atomic absorption spectrophotometry

    SciTech Connect

    Cabanis, M.T.; Cassanas, G.; Cabanis, J.C.; Brun, S.

    1988-01-01

    The authors compared 4 digestion procedures, namely, sulfuric-nitric acid in an open flask, nitric acid under pressure, sulfuric-nitric acid with refluxing, and nitric-hydrochloric-peroxide with refluxing, for the determination of cadmium by flameless atomic absorption spectrophotometry in 3 foodstuffs: rice, beef, and cream cheese. The foodstuffs were homogenized and divided into several batches for analysis. The results were evaluated using a 2-way cross analysis of variance. The study revealed that the digestion procedure was a highly significant factor (P < 10/sup -4/) in the analysis of the 3 foods; whereas the nature of the foodstuffs was not significant for rice and meat and only slightly significant (P < 10/sup -2/) for cream cheese. When the foodstuffs were spiked with a known amount of cadmium, they observed a loss of the metal when the sulfuric-nitric acid procedure in an open flask and the nitric-hydrochloric-peroxide digestion procedure were used. Taken together, the results of the present study indicate that the choice of the reagents used for digestion of foodstuffs is a crucial factor for cadmium determination by flameless atomic absorption spectrophotometry.

  11. Spectrophotometric Determination of the Dissociation Constant of an Acid-Base Indicator Using a Mathematical Deconvolution Technique

    ERIC Educational Resources Information Center

    Alter, Krystyn P.; Molloy, John L.; Niemeyer, Emily D.

    2005-01-01

    A laboratory experiment reinforces the concept of acid-base equilibria while introducing a common application of spectrophotometry and can easily be completed within a standard four-hour laboratory period. It provides students with an opportunity to use advanced data analysis techniques like data smoothing and spectral deconvolution to…

  12. Simple spectrophotometry method for the determination of sulfur dioxide in an alcohol-thionyl chloride reaction.

    PubMed

    Zheng, Jinjian; Tan, Feng; Hartman, Robert

    2015-09-01

    Thionyl chloride is often used to convert alcohols into more reactive alkyl chloride, which can be easily converted to many compounds that are not possible from alcohols directly. One important reaction of alkyl chloride is nucleophilic substitution, which is typically conducted under basic conditions. Sulfur dioxide, the by-product from alcohol-thionyl chloride reactions, often reacts with alkyl chloride to form a sulfonyl acid impurity, resulting in yield loss. Therefore, the alkyl chloride is typically isolated to remove the by-products including sulfur dioxide. However, in our laboratory, the alkyl chloride formed from alcohol and thionyl chloride was found to be a potential mutagenic impurity, and isolation of this compound would require extensive safety measures. As a result, a flow-through process was developed, and the sulfur dioxide was purged using a combination of vacuum degassing and nitrogen gas sweeping. An analytical method that can quickly and accurately quantitate residual levels of sulfur dioxide in the reaction mixture is desired for in-process monitoring. We report here a simple ultraviolet (UV) spectrophotometry method for this measurement. This method takes advantage of the dramatic change in the UV absorbance of sulfur dioxide with respect to pH, which allows for accurate quantitation of sulfur dioxide in the presence of the strong UV-absorbing matrix. Each sample solution was prepared using 2 different diluents: 1) 50 mM ammonium acetate in methanol +1% v/v hydrochloric acid, pH 1.3, and 2) 50 mM ammonium acetate in methanol +1% glacial acetic acid, pH 4.0. The buffer solutions were carefully selected so that the UV absorbance of the sample matrix (excluding sulfur dioxide) at 276 nm remains constant. In the pH 1.3 buffer system, sulfur dioxide shows strong UV absorbance at 276 nm. Therefore, the UV absorbance of sample solution is the sum of sulfur dioxide and sample matrix. While in the pH 4.0 buffer system, sulfur dioxide has

  13. Review of uranium bioassay techniques

    SciTech Connect

    Bogard, J.S.

    1996-04-01

    A variety of analytical techniques is available for evaluating uranium in excreta and tissues at levels appropriate for occupational exposure control and evaluation. A few (fluorometry, kinetic phosphorescence analysis, {alpha}-particle spectrometry, neutron irradiation techniques, and inductively-coupled plasma mass spectrometry) have also been demonstrated as capable of determining uranium in these materials at levels comparable to those which occur naturally. Sample preparation requirements and isotopic sensitivities vary widely among these techniques and should be considered carefully when choosing a method. This report discusses analytical techniques used for evaluating uranium in biological matrices (primarily urine) and limits of detection reported in the literature. No cost comparison is attempted, although references are cited which address cost. Techniques discussed include: {alpha}-particle spectrometry; liquid scintillation spectrometry, fluorometry, phosphorometry, neutron activation analysis, fission-track counting, UV-visible absorption spectrophotometry, resonance ionization mass spectrometry, and inductively-coupled plasma mass spectrometry. A summary table of reported limits of detection and of the more important experimental conditions associated with these reported limits is also provided.

  14. Assessment of cosmetic ingredients in the in vitro reconstructed human epidermis test method EpiSkin™ using HPLC/UPLC-spectrophotometry in the MTT-reduction assay.

    PubMed

    Alépée, N; Hibatallah, J; Klaric, M; Mewes, K R; Pfannenbecker, U; McNamee, P

    2016-06-01

    Cosmetics Europe recently established HPLC/UPLC-spectrophotometry as a suitable alternative endpoint detection system for measurement of formazan in the MTT-reduction assay of reconstructed human tissue test methods irrespective of the test system involved. This addressed a known limitation for such test methods that use optical density for measurement of formazan and may be incompatible for evaluation of strong MTT reducer and/or coloured chemicals. To build on the original project, Cosmetics Europe has undertaken a second study that focuses on evaluation of chemicals with functionalities relevant to cosmetic products. Such chemicals were primarily identified from the Scientific Committee on Consumer Safety (SCCS) 2010 memorandum (addendum) on the in vitro test EpiSkin™ for skin irritation testing. Fifty test items were evaluated in which both standard photometry and HPLC/UPLC-spectrophotometry were used for endpoint detection. The results obtained in this study: 1) provide further support for Within Laboratory Reproducibility of HPLC-UPLC-spectrophotometry for measurement of formazan; 2) demonstrate, through use a case study with Basazol C Blue pr. 8056, that HPLC/UPLC-spectrophotometry enables determination of an in vitro classification even when this is not possible using standard photometry and 3) addresses the question raised by SCCS in their 2010 memorandum (addendum) to consider an endpoint detection system not involving optical density quantification in in vitro reconstructed human epidermis skin irritation test methods. PMID:26891813

  15. Determination of Pb in Biological Samples by Graphite Furnace Atomic Absorption Spectrophotometry: An Exercise in Common Interferences and Fundamental Practices in Trace Element Determination

    ERIC Educational Resources Information Center

    Spudich, Thomas M.; Herrmann, Jennifer K.; Fietkau, Ronald; Edwards, Grant A.

    2004-01-01

    An experiment is conducted to ascertain trace-level Pb in samples of bovine liver or muscle by applying graphite furnace atomic absorption spectrophotometry (GFAAS). The primary objective is to display the effects of physical and spectral intrusions in determining trace elements, and project the usual methods employed to minimize accuracy errors…

  16. SINGLE-LABORATORY EVALUATION OF SW-846 METHODS 7090/7091 DETERMINATION OF BERYLLIUM BY FLAME AND FURNACE ATOMIC ABSORPTION SPECTROPHOTOMETRY

    EPA Science Inventory

    The results of a single-laboratory study of the 'Determination of Beryllium by Flame and Furnace Atomic Absorption Spectrophotometry', are described. The study examined the application of these two powerful beryllium detection methods to the analysis of selected liquid and solid ...

  17. Determination of cobalt and zinc in highpurity niobium, tantalum, molybdenum and tungsten metals by atomicabsorption spectrophotometry after separation by extraction.

    PubMed

    Donaldson, E M; Charette, D J; Rolko, V H

    1969-09-01

    A method for determining 0.0005-0.05% of cobalt and zinc in high-purity niobium, tantalum, molybdenum and tungsten metals by atomic-absorption spectrophotometry is described. After sample dissolution, cobalt and zinc are separated simultaneously from the matrix materials by chloroform extraction of their thiocyanatediantipyrylmethane ion-association complexes, at pH 3.25, from a citric acid medium approximately 1.2M in sodium thiocyanate. Interference from copper is eliminated with thiourea. Large amounts of iron interfere under the recommended conditions, but moderate amounts may be present in the sample solution without causing appreciable error in the results. Phosphorus (as orthophosphate) interferes in the extraction of cobalt from tungsten solutions. Moderate amounts of other impurities do not interfere in the proposed method. PMID:18960635

  18. Coupling laser ablation and atomic fluorescence spectrophotometry: an example using mercury analysis of small sections of fish scales.

    PubMed

    Beaudin, Luc; Johannessen, Sophia C; Macdonald, Robie W

    2010-11-01

    Mercury is a toxic element that exchanges among air, water, and sediments and biomagnifies into high trophic level organisms. Here, we present a novel combination of laser ablation with relatively low-cost cold vapor atomic fluorescence spectrophotometry to analyze Hg vaporized from targeted patches of fish scale 300-500 μm square. This method permits the analysis of multiple samples from the same scale, which is useful, because fish scale growth rings may provide an archive from which spatial and temporal trends in environmental Hg can be inferred at fine resolution. The detection limit of the method is 1.5 pg Hg, with a precision of 0.1 pg/μL. Developed using fish scales, the method could be adapted to other media, such as baleen, shells, nails, hair, teeth, wood and, possibly, varved sediments. PMID:20942426

  19. Comparison of HPLC, UV spectrophotometry and potentiometric titration methods for the determination of lumefantrine in pharmaceutical products.

    PubMed

    da Costa César, Isabela; Nogueira, Fernando Henrique Andrade; Pianetti, Gérson Antônio

    2008-09-10

    This paper describes the development and evaluation of a HPLC, UV spectrophotometry and potentiometric titration methods to quantify lumefantrine in raw materials and tablets. HPLC analyses were carried out using a Symmetry C(18) column and a mobile phase composed of methanol and 0.05% trifluoroacetic acid (80:20), with a flow rate of 1.0ml/min and UV detection at 335nm. For the spectrophotometric analyses, methanol was used as solvent and the wavelength of 335nm was selected for the detection. Non-aqueous titration of lumefantrine was carried out using perchloric acid as titrant and glacial acetic acid/acetic anhydride as solvent. The end point was potentiometrically determined. The three evaluated methods showed to be adequate to quantify lumefantrine in raw materials, while HPLC and UV methods presented the most reliable results for the analyses of tablets. PMID:18571353

  20. Combination of fluorescence imaging and local spectrophotometry in fluorescence diagnostics of early cancer of larynx and bronchi

    SciTech Connect

    Sokolov, Vladimir V; Filonenko, E V; Telegina, L V; Boulgakova, N N; Smirnov, V V

    2002-11-30

    The results of comparative studies of autofluorescence and 5-ALA-induced fluorescence of protoporphyrin IX, used in the diagnostics of early cancer of larynx and bronchi, are presented. The autofluorescence and 5-ALA-induced fluorescence images of larynx and bronchial tissues are analysed during the endoscopic study. The method of local spectrophotometry is used to verify findings obtained from fluorescence images. It is shown that such a combined approach can be efficiently used to improve the diagnostics of precancer and early cancer, to detect a primary multiple tumours, as well as for the diagnostics of a residual tumour or an early recurrence after the endoscopic, surgery or X-ray treatment. The developed approach allows one to minimise the number of false-positive results and to reduce the number of biopsies, which are commonly used in the white-light bronchoscopy search for occult cancerous loci. (laser biology and medicine)

  1. The Kinetics of Mo(Co)6 Substitution Monitored by Fourier Transform Infrared Spectrophotometry.

    ERIC Educational Resources Information Center

    Suslick, Kenneth S.; And Others

    1987-01-01

    Describes a physical chemistry experiment that uses Fourier transform (FTIR) spectrometers and microcomputers as a way of introducing students to the spectral storage and manipulation techniques associated with digitized data. It can be used to illustrate FTIR spectroscopy, simple kinetics, inorganic mechanisms, and Beer's Law. (TW)

  2. Application of portable fluorescence spectrophotometry for integrity testing of recycled water dual distribution systems.

    PubMed

    Hambly, Adam C; Henderson, Rita K; Baker, Andy; Stuetz, Richard M; Khan, Stuart J

    2015-01-01

    Water utilities supplying recycled water to households via a "third-pipe" or "dual reticulation" system have a need for a rapid, portable method to detect cross-connections within potable water reticulation networks. This study evaluates portable fluorimetry as a technique for cross-connection detection in the field. For the first time, an investigation of a full-scale dual reticulation water-recycling network has been carried out to identify cross-connections using a portable fluorimeter. We determined that this can be carried out with a 3 mL water sample, and unlike methods that are currently in use for cross-connection detection, can be achieved quickly without disruption to water flow or availability within the network. It was also revealed that fluorescence trigger values could be established with high levels of confidence by sampling less than 2.5% of the network. Fluorescence analysis was also able to uncover a single, real cross-connection event. As such, this paper is a fundamental demonstration of fluorescence as a reliable, highly portable technique for cross-connection detection within dual reticulation water recycling networks and further establishes the abilities of fluorescence devices as valuable field instruments for water quality monitoring. PMID:25506735

  3. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; determination of antimony by automated-hydride atomic absorption spectrophotometry

    USGS Publications Warehouse

    Brown, G.E.; McLain, B.J.

    1994-01-01

    The analysis of natural-water samples for antimony by automated-hydride atomic absorption spectrophotometry is described. Samples are prepared for analysis by addition of potassium and hydrochloric acid followed by an autoclave digestion. After the digestion, potassium iodide and sodium borohydride are added automatically. Antimony hydride (stibine) gas is generated, then swept into a heated quartz cell for determination of antimony by atomic absorption spectrophotometry. Precision and accuracy data are presented. Results obtained on standard reference water samples agree with means established by interlaboratory studies. Spike recoveries for actual samples range from 90 to 114 percent. Replicate analyses of water samples of varying matrices give relative standard deviations from 3 to 10 percent.

  4. Spectrophotometry of Peculiar B-Stars and A-Stars - Part Nine - HD5797 HD12288 9-TAURI HD81009 HD111133 33-LIBRAE and HD216533

    NASA Astrophysics Data System (ADS)

    Adelman, S. J.

    1981-02-01

    Optical region spectrophotometry of λλ3300-7100 is presented for seven sharp-lined peculiar A stars: HD 5797, HD 12288, 9 Tauri, HD 81009, HD 111133, 33 Librae, and HD 216533. Many of proposed periods in the literature are questioned. Some of the deviations from the predictions of normal stellar atmospheres suggest that such continua are only remotely related to those of peculiar A stars.

  5. Mode identification based on time-series spectrophotometry for the bright rapid sdB pulsator EC 01541-1409

    NASA Astrophysics Data System (ADS)

    Randall, S. K.; Fontaine, G.; Geier, S.; Van Grootel, V.; Brassard, P.

    2014-03-01

    We present an analysis of time-resolved spectrophotometry gathered with FORS/VLT for the rapidly pulsating hot B subdwarf EC 01541-1409 with the aim of identifying the degree index ℓ of the larger amplitude modes. This mode identification can be extremely useful in detailed searches for viable asteroseismic models in parameter space, and can be crucial for testing the validity of a solution a posteriori. To achieve it, we exploit the ℓ-dependence of the monochromatic amplitude, phase, and velocity-to-amplitude ratio of a mode as a function of wavelength. We use the ℓ-sensitive phase lag between the flux perturbation and the radial velocity as an additional diagnostic tool. On this basis, we are able to unambiguously identify the dominant 140.5 s pulsation of our target as a radial mode, and the second-highest amplitude periodicity at 145.8 s as an ℓ = 2 mode. We further exploit the exceptionally high-sensitivity data that we gathered for the dominant mode to infer modal properties that are usually quite difficult to estimate in sdB pulsators, namely the physical values of the dimensionless radius, temperature, and surface gravity perturbations. Based on observations collected at the European Organisation for Astronomical Research in the Southern Hemisphere, Chile (proposal ID 087.D-0047).Appendix A is available in electronic form at http://www.aanda.org

  6. A New Method for Accurate Signal Processing in Measurements of Elemental Mercury Vapor by Atomic Fluorescence Spectrophotometry

    NASA Astrophysics Data System (ADS)

    Ambrose, J. L., II; Jaffe, D. A.

    2015-12-01

    The most widely used method for quantifying atmospheric Hg is gold amalgamation pre-concentration, followed by thermal desorption (TD) and detection via atomic fluorescence spectrophotometry (AFS). Most AFS-based atmospheric Hg measurements are carried out using commercial analyzers manufactured by Tekran® Instruments Corp. (instrument models 2537A and 2537B). A generally overlooked and poorly characterized source of analytical uncertainty in these measurements is the method by which the raw Hg AFS signal is processed. In nearly all applications of Tekran® analyzers for atmospheric Hg measurements, researchers rely upon embedded software which automatically integrates the Hg TD peaks. However, Swartzendruber et al. (2009; doi:10.1016/j.atmosenv.2009.02.063) demonstrated that the Hg TD peaks can be more accurately defined, and overall measurement precision increased, by post-processing the raw Hg AFS signal; improvements in measurement accuracy and precision were shown to be more significant at lower sample loadings. Despite these findings, a standardized method for signal post-processing has not been presented. To better characterize uncertainty associated with Tekran® based atmospheric Hg measurements, and to facilitate more widespread adoption of an accurate, standardized signal processing method, we developed a new, distributable Virtual Instrument (VI) which performs semi-automated post-processing of the raw Hg AFS signal from the Tekran® analyzers. Here we describe the key features of the VI and compare its performance to that of the Tekran® signal processing method.

  7. Rapid determination of trace thiabendazole in apple juice utilizing dispersive liquid-liquid microextraction combined with fluorescence spectrophotometry.

    PubMed

    Li, Wei; Wang, Yuning; Huang, Limin; Wu, Ting; Hu, Huilian; Du, Yiping

    2015-09-01

    Food safety has become a large concern and prompts an urgent need for the development of rapid, simple and sensitive analytical methods that can monitor pesticide residues in foods. This study aimed to provide a method for quantitative determination of trace thiabendazole in apple juice. Due to its high sensitivity and selectivity, fluorescence spectrophotometry was utilized as a front end to dispersive liquid-liquid microextraction (DLLME). The experimental parameters that influenced the extraction were systematically investigated. Under optimum conditions, the whole procedure, including DLLME and analysis of one sample, was carried out within 5 min, and linearity was found in the 5-50 µg/L range with a correlation coefficient (r) of 0.9987. The limit of detection value was 2.2 µg/L. Good reproducibility was achieved based with a less than 4.5% relative standard deviation (RSD) for five replicates at different sample concentrations. This method was shown to be suitable for rapid and sensitive quantification of thiabendazole in apple juice. PMID:25645350

  8. Quantitative analysis of Eu 2+ and Eu 3+ in LiCl-KCl eutectic melt by spectrophotometry and electrochemistry

    NASA Astrophysics Data System (ADS)

    Kim, Tack-Jin; Uehara, Akihiro; Nagai, Takayuki; Fujii, Toshiyuki; Yamana, Hajimu

    2011-02-01

    The redox behavior of Eu 2+ and Eu 3+ in the LiCl-KCl eutectic at 773 K was investigated. Since the equilibrium potential of the melt is very close to the redox potential of the Eu 3+|Eu 2+ couple, the Eu 2+ and Eu 3+ species coexist. Quantitative analysis of Eu 2+ and Eu 3+ was performed by spectrophotometry and by potentiometry. Under the coexistence of Eu 2+ and Eu 3+, potentiometric titration of Eu ion using a yttria-stabilized zirconia membrane electrode (YSZME) was performed by changing the concentration of O 2-. The formation of the europium oxychloride, EuOCl, was confirmed by X-ray diffraction analysis, whiles no precipitation of the oxides, EuO and Eu 2O 3, was found. The equivalent point of the EuOCl formation ( x = [O 2-] added/[Eu] total) was shifted to a smaller value from the theoretical value ( x = 1) due to the coexisting Eu 2+. The contribution of the coexisting Eu 2+ to the formation of EuOCl was estimated by using [Eu 2+]/[Eu 3+] as determined by potentiometry and this was subtracted from the titration data. The solubility product of EuOCl was determined to be p ks(EuOCl) = 7.81 ± 0.10.

  9. Formaldehyde in Alcoholic Beverages: Large Chemical Survey Using Purpald Screening Followed by Chromotropic Acid Spectrophotometry with Multivariate Curve Resolution

    PubMed Central

    Jendral, Julien A.; Monakhova, Yulia B.; Lachenmeier, Dirk W.

    2011-01-01

    A strategy for analyzing formaldehyde in beer, wine, spirits, and unrecorded alcohol was developed, and 508 samples from worldwide origin were analyzed. In the first step, samples are qualitatively screened using a simple colorimetric test with the purpald reagent, which is extremely sensitive for formaldehyde (detection limit 0.1 mg/L). 210 samples (41%) gave a positive purpald reaction. In the second step, formaldehyde in positive samples is confirmed by quantitative spectrophotometry of the chromotropic acid-formaldehyde derivative combined with Multivariate Curve Resolution-Alternating Least Squares (MCR-ALS). Calculation of UV-VIS and 13C NMR spectra confirmed the monocationic dibenzoxanthylium structure as the product of the reaction and disproved the widely cited para,para-quinoidal structure. Method validation for the spectrophotometric procedure showed a detection limit of 0.09 mg/L and a precision of 4.2–8.2% CV. In total, 132 samples (26%) contained formaldehyde with an average of 0.27 mg/L (range 0–14.4 mg/L). The highest incidence occurred in tequila (83%), Asian spirits (59%), grape marc (54%), and brandy (50%). Our survey showed that only 9 samples (1.8%) had formaldehyde levels above the WHO IPCS tolerable concentration of 2.6 mg/L. PMID:21760790

  10. Rapid determination of polysaccharides in BianTi Soft Extract by spectrophotometry coupled with gas chromatography-mass spectrometry.

    PubMed

    Zheng, Minxia; Shen, Jie; Yang, Kai; Qian, Songxiang; Feng, Sujuan

    2010-04-01

    A simple approach for the rapid determination of polysaccharides in BianTi Soft Extract using spectrophotometry coupled with gas chromatography-mass spectrometry (GC-MS) was developed. The mixed standard solution composed of D-glucose, D-mannose, galactose and D-xylose in different proportions (1.00: 1.01: 0.12: 0.05) was prepared according to the monosaccharide composition analysis of the polysaccharides by GC-MS. The determination of polysaccharides by UV-Vis spectrophotometer was performed after 35-min color reaction, in which 1 ml 5% phenol and 4 ml sulfate was used. The assay of the method validation has shown that the method was stable, reliable and feasible. Furthermore, the proposed method was successfully applied in the preparation procedure of BianTi Soft Extract, selecting out optimal decoction conditions and suitable decoction container. It suggests that the convenient method could be useful for the quality control of BianTi Soft Extract. Meanwhile, it may be an alternative for polysaccharides determination of other formulations. PMID:20668575

  11. The H-band emitting region of the luminous blue variable P Cygni: Spectrophotometry and interferometry of the wind

    SciTech Connect

    Richardson, N. D.; Gies, D. R.; Baron, F.; Parks, J. R.; Matson, R. A.; Touhami, Y.; Aldoretta, E. J.; McAlister, H. A.; Schaefer, G. H.; Ten Brummelaar, T. A.; Sturmann, J.; Sturmann, L.; Chesneau, O.; Monnier, J. D.; Che, X.; Clemens, D. P.; Taylor, B.; Morrison, N. D.; Kraus, S.; Ridgway, S. T.; and others

    2013-06-01

    We present the first high angular resolution observations in the near-infrared H band (1.6 μm) of the luminous blue variable star P Cygni. We obtained six-telescope interferometric observations with the CHARA Array and the MIRC beam combiner. These show that the spatial flux distribution is larger than expected for the stellar photosphere. A two-component model for the star (uniform disk) plus a halo (two-dimensional Gaussian) yields an excellent fit of the observations, and we suggest that the halo corresponds to flux emitted from the base of the stellar wind. This wind component contributes about 45% of the H-band flux and has an angular FWHM = 0.96 mas, compared to the predicted stellar diameter of 0.41 mas. We show several images reconstructed from the interferometric visibilities and closure phases, and they indicate a generally spherical geometry for the wind. We also obtained near-infrared spectrophotometry of P Cygni from which we derive the flux excess compared to a purely photospheric spectral energy distribution. The H-band flux excess matches that from the wind flux fraction derived from the two-component fits to the interferometry. We find evidence of significant near-infrared flux variability over the period from 2006 to 2010 that appears similar to the variations in the Hα emission flux from the wind.

  12. Episodes of apnea and bradycardia in the preterm newborn: impact on cerebral oxygenation measured by near-infrared spectrophotometry

    NASA Astrophysics Data System (ADS)

    Van Huffel, Sabine; Craemers, Johan; Lenaerts, Bart; Daniels, Hans; Naulaers, Gunnar; Casaer, Paul

    1998-12-01

    The objective of this study is to evaluate the effect of episodes of apneas and/or mild bradycardia (heart rate decreases of 10 to 20% or more) on cerebral oxyhemoglobin (HbO2) and reduced hemoglobin (Hb) concentration as measured by Near Infrared Spectrophotometry (NIRS). Measurements were carried out on 7 preterm infants who experienced apneic and bradycardiac events. It is shown how to characterize these events using time-frequency analysis. In addition to NIRS (performed with a NIRO-500 from Hamamatsu, Japan), the heart rate, ECG, peripheral arterial oxygen saturation (measured at the foot) and respiration (abdominal and thoracic pressure, and nasal airflow) were continuously recorded. The impact of apneic events and periodic breathing on these measurements reveals the clinical relevance of NIRS. In particular, we investigate whether these changes in heart rate and respiration also influence HbO2 and reduced Hb concentration in neonatal brain. These changes are characterized, as well as their relationships with the other simultaneously recorded signals such as peripheral arterial oxygen saturation.

  13. Retinopathy of prematurity and induced changes in arterial oxygen saturation with near infrared spectrophotometry: a retrospective cohort study

    NASA Astrophysics Data System (ADS)

    von Siebenthal, K.; Keel, M.; Dietz, V.; Fauchere, J. C.; Martin, X.; Wolf, Martin; Duc, G.; Bucher, H. U.

    1996-10-01

    Near-infrared spectrophotometry (NIRS) is a noninvasive method for measuring oxygenated and deoxygenated hemoglobin in the neonatal brain. Using oxygen as a tracer, it is possible to calculate cerebral blood flow (cbf) and hemoglobin concentration (cHbc), which corresponds to cerebral blood volume, by inducing small changes in arterial oxygen saturation. Variability of tcpO2 is considered to be associated with severe retinopathy of prematurity (ROP). A preliminary analysis without control found a 51 percent incidence of ROP in infants subjected to NIRS measurements whereas among infants who were not exposed to oxygen changes, only 29 percent developed ROP. A controlled study with matched pairs was performed. Thirty-nine premature newborns who had received NIRS recordings were matched with 39 out of 172 infants who had not received NIRS. Using this controlled study design there was no difference in the incidence and severity of ROP between the two groups. The conclusions are that: 1) small changes in oxygen saturation of 3 to 10 percent to measure cbf and cHbc did not increase the incidence or the degree of severity of ROP. 2) A controlled study design is important. Analyses of uncontrolled data would have led to the conclusion that oxygen changes as used with NIRS increase the risk of ROP.

  14. Determination of thallium at ultra-trace levels in water and biological samples using solid phase spectrophotometry

    NASA Astrophysics Data System (ADS)

    Amin, Alaa S.; El-Sharjawy, Abdel-Azeem M.; Kassem, Mohammed A.

    2013-06-01

    A new simple, very sensitive, selective and accurate procedure for the determination of trace amounts of thallium(III) by solid-phase spectrophotometry (SPS) has been developed. The procedure is based on fixation of Tl(III) as quinalizarin ion associate on a styrene-divinylbenzene anion-exchange resin. The absorbance of resin sorbed Tl(III) ion associate is measured directly at 636 and 830 nm. Thallium(I) was determined by difference measurements after oxidation of Tl(I) to Tl(III) with bromine. Calibration is linear over the range 0.5-12.0 μg L-1 of Tl(III) with relative standard deviation (RSD) of 1.40% (n = 10). The detection and quantification limits are 150 and 495 ng L-1 using 0.6 g of the exchanger. The molar absorptivity and Sandell sensitivity are also calculated and found to be 1.31 × 107 L mol-1 cm-1 and 0.00156 ng cm-2, respectively. The proposed procedure has been successfully applied to determine thallium in water, urine and serum samples.

  15. UV-visible scanning spectrophotometry and chemometric analysis as tools for carotenoids analysis in cassava genotypes (Manihot esculenta Crantz).

    PubMed

    Moresco, Rodolfo; Uarrota, Virgílio Gavicho; Pereira, Aline; Tomazzoli, Maíra Maciel; Nunes, Eduardo da C; Peruch, Luiz Augusto Martins; Gazzola, Jussara; Costa, Christopher; Rocha, Miguel; Maraschin, Marcelo

    2015-01-01

    In this study, the metabolomics characterization focusing on the carotenoid composition of ten cassava (Manihot esculenta) genotypes cultivated in southern Brazil by UV-visible scanning spectrophotometry and reverse phase-high performance liquid chromatography was performed. Cassava roots rich in β-carotene are an important staple food for populations with risk of vitamin A deficiency. Cassava genotypes with high pro-vitamin A activity have been identified as a strategy to reduce the prevalence of deficiency of this vitamin. The data set was used for the construction of a descriptive model by chemometric analysis. The genotypes of yellow-fleshed roots were clustered by the higher concentrations of cis-β-carotene and lutein. Inversely, cream-fleshed roots genotypes were grouped precisely due to their lower concentrations of these pigments, as samples rich in lycopene (red-fleshed) differed among the studied genotypes. The analytical approach (UV-Vis, HPLC, and chemometrics) used showed to be efficient for understanding the chemodiversity of cassava genotypes, allowing to classify them according to important features for human health and nutrition. PMID:26673931

  16. Measurement of aluminum in neuronal tissues using electrothermal atomization atomic absorption spectrophotometry

    SciTech Connect

    Pierson, K.B.; Evenson, M.A.

    1986-07-01

    Studies characterizing aluminum complexes isolated from neuronal tissues require accurate and precise techniques for aluminum measurement. A solution of 0.01 M nitric acid containing 0.2% Triton X-100 was the optimal diluent for aluminum measurement under the experimental conditions used. Three National Bureau of Standards Standard Reference Materials (SRM) were digested, and the aluminum concentration of each was measured with a Perkin-Elmer 503 atomic absorption spectrophotometer equipped with a Perkin-Elmer HGA 2100 controller. The calculated detection limit of aluminum was 120 pg using 15-..mu..L sample injections (8 ..mu..g/L). Aluminum concentrations present in citrus leaves (SRM 1572), pine needles (SRM 1575), and tomato leaves (SRM 1573) were 100 +- 12 (certified value, 92 +- 15), 522 +- 45 (certified value, 454 +- 30), and 1273 +- 112 (provisional value, 1200) ..mu..g/g, respectively. The within- and between-day precision had coefficients of variation for citrus leaves, pine needles, and tomato leaves of 18 and 12%, 6.3 and 8.6%, and 3.7 and 8.7%, respectively. Aluminum absorbance was enhanced at high pH values and by zinc.

  17. Simultaneous determination of moxifloxacin and cefixime by first and ratio first derivative ultraviolet spectrophotometry

    PubMed Central

    2012-01-01

    Background The new combination of moxifloxacin HCl and cefixime trihydrate is approved for the treatment of lower respiratory tract infections in adults. At initial formulation development and screening stage a fast and reliable method for the dissolution and release testing of moxifloxacin and cefixime were highly desirable. The zero order overlaid UV spectra of moxifloxacin and cefixime showed >90% overlapping. Hence, simple, accurate precise and validated two derivative spectrophotometric methods have been developed for the determination of moxifloxacin and cefixime. Methods In the first derivative spectrophotometric method varying concentration of moxifloxacin and cefixime were prepared and scanned in the range of 200 to 400 nm and first derivative spectra were calculated (n = 1). The zero crossing wavelengths 287 nm and 317.9 nm were selected for determination of moxifloxacin and cefixime, respectively. In the second method the first derivative of ratio spectra was calculated and used for the determination of moxifloxacin and cefixime by measuring the peak intensity at 359.3 nm and 269.6 nm respectively. Results Calibration graphs were established in the range of 1–16 μg /mL and 1–15 μg /mL for both the drugs by first and ratio first derivative spectroscopic methods respectively with good correlation coefficients. Average accuracy of assay of moxifloxacin and cefixime were found to be 100.68% and 98 93%, respectively. Relative standard deviations of both inter and intraday assays were less than 1.8%. Moreover, recovery of moxifloxacin and cefixime was more than 98.7% and 99.1%, respectively. Conclusions The described derivative spectrophotometric methods are simple, rapid, accurate, precise and excellent alternative to sophisticated chromatographic techniques. Hence, the proposed methods can be used for the quality control of the cited drugs and can be extended for routine analysis of the drugs in formulations. PMID:22995678

  18. A simple vapour phase decomposition (VPD) of quartz powder in a polypropylene vessel and determination of phosphorus by spectrophotometry.

    PubMed

    Thangavel, S; Dash, K; Chaurasia, S C

    2001-09-13

    A simple, low pressure, low temperature vapour phase decomposition (VPD) of quartz powder has been developed for the determination of phosphorus. A platinum dish containing the quartz or silicon powder was placed inside a polypropylene vessel containing 40 ml of 1:1 mixture of HF and HNO(3). After capping the vessel, the entire assembly was heated on a water bath at approximately 90 degrees C for 8 h. The platinum dish was removed from the vessel, the sample solution was treated with 0.5 ml of H(2)SO(4) and 0.5 ml of HClO(4) and was heated on a hot plate till HClO(4) fumed out. The resultant solution was diluted to 40 ml ( approximately 0.4N), analysed for phosphorus by spectrophotometry as an ion-pair of molybdophosphate with crystal violet. Phosphorus contamination by reagents has been drastically reduced (around 250 times) compared to the conventional dissolution procedure. The optimum reaction conditions were [H(+)]=0.42N, [H(+)]/Mo=62 for the formation of molybdophosphate and its extraction into n-butyl acetate. No interferences due to fluoride, silicate (active silica) and arsenic (V) upto 6.7x10(3),2.7x10(3) and 2.0x10(3) times the content of phosphorus, respectively were observed. The LOD was found to be 0.066 mug g(-1) (+/-3 s). RSD is 0.4-2.3% and the molar absorptivity is 2.7x10(5) l mole(-1) cm(-1). PMID:18968395

  19. In Vitro Spectrophotometry of Tooth Discoloration Induced by Tooth-Colored Mineral Trioxide Aggregate and Calcium-Enriched Mixture Cement

    PubMed Central

    Arman, Marjan; Khalilak, Zohreh; Rajabi, Moones; Esnaashari, Ehsan; Saati, Keyvan

    2015-01-01

    Introduction: There are numerous factors that can lead to tooth discoloration after endodontic treatment, such as penetration of endodontic materials into the dentinal tubules during root canal treatment. The aim of this in vitro study was to compare discoloration induced by tooth colored mineral trioxide aggregate (MTA) and calcium-enriched mixture (CEM) cement in extracted human teeth. Methods and Materials: Thirty two dentin-enamel cuboid blocks (7×7×2 mm) were prepared from extracted maxillary central incisors. Standardized cavities were prepared in the middle of each cube, leaving 1 mm of enamel and dentin on the labial surface. The specimens were randomly divided into two study groups (n=12) and two positive and negative control groups (n=4). In either study groups the cavities were filled with MTA or CEM cement. The positive and negative control groups were filled with blood or left empty, respectively. The cavities were sealed with composite resin and stored in normal saline. Color measurement was carried out by spectrophotometry at different time intervals including before (T0), and 1 week (T1), 1 month (T2) and 6 months (T3) after placement of materials. Repeated-measures ANOVA was used to compare the discoloration between the groups; the material type was considered as the inter-subject factor. The level of significance was set at 0.05. Results: No significant differences were detected between the groups in all time intervals (P>0.05). Conclusion: Tooth discoloration was similarly detectable with both of the two experimental materials. PMID:26576163

  20. Intercomparison and coupling of magnesium-induced co-precipitation and long-path liquid-waveguide capillary cell techniques for trace analysis of phosphate in seawater.

    PubMed

    Li, Qian P; Hansell, Dennis A

    2008-03-17

    Currently, two common techniques for nanomolar-level phosphate measurements in seawater are magnesium-induced co-precipitation (MAGIC) and long-path liquid-waveguide capillary cell (LWCC) spectrophotometry. These techniques have been applied in the open ocean, and our understanding of phosphate distributions in oligotrophic subtropical gyres is based on those data. However, intercomparison of these methods has not previously been performed at nanomolar levels. Here, we report experimental results directly comparing the MAGIC and LWCC techniques. We also evaluated the impact of various commonly employed filters on phosphate determinations, as well as interferences from dissolved organic phosphorus (DOP) and arsenate. Our results find agreement between these methods at phosphate concentrations <100nM. We found that filter selection is important for accurate determinations of phosphate, and that DOP hydrolysis affects both techniques similarly. Finally, we demonstrate the advantage of combining MAGIC preconcentration and LWCC spectrophotometry for analysis of very low nanomolar concentrations. PMID:18298969

  1. Identification and characterization of in vivo metabolites of asulacrine using advanced mass spectrophotometry technique in combination with improved data mining strategy.

    PubMed

    Afzal, Attia; Zhong, Yunxi; Sarfraz, Muhammad; Peng, Ying; Sheng, Longsheng; Wu, Zimei; Sun, Jianguo; Wang, Guangji

    2016-04-29

    Asulacrine (ASL) is a broad-spectrum, antitumor drug whose data are promising for the treatment of breast and lung cancers; however, a high incidence of phlebitis hampered its further development. Phlebitis is associated with generation of reactive species. Asulacrine donates electrons and produces oxidative stress in chemical reactions. It was expected that ASL would actively metabolize to oxidized products through reactive intermediates and produce more products in vivo than reported and thus cause phlebitis. A comprehensive study was planned to investigate in vivo metabolism of ASL, using high-resolution mass spectrometry LC/IT-TOF MS in positive mode. Metabolites were detected by different software by applying annotated detection strategy. The possible metabolites and their product ions were simultaneously detected by segmented data acquisition to get accurate mass values. Segmented data acquisition improved signal-to-noise (S/N) ratio, which was helpful to detect metabolites and their fragments even when present in trace amounts. A total of 21 metabolites were detected in gender-based biological fluids and characterized by comparing their accurate mass values, fragmentation patterns, and relative retention times with that of ASL. Among previously reported glucuronosylation metabolites, some oxidation, hydroxylation, carboxylation, demethylation, hydrogenation, glutamination, and acetylcysteine conjugation were detected for the first time. Twenty metabolites were tentatively identified by using the annotated strategy for data acquisition and post-data mining. PMID:27040513

  2. HPLC-DAD and UV-spectrophotometry for the determination of lychnopholide in nanocapsule dosage form: validation and application to release kinetic study.

    PubMed

    Branquinho, Renata Tupinambá; Mosqueira, Vanessa Carla Furtado; Kano, Eunice Kazue; de Souza, Jacqueline; Dorim, Diego Dias Ramos; Saúde-Guimarães, Dênia Antunes; de Lana, Marta

    2014-01-01

    Simple and sensitive methods using high-performance liquid chromatography-diode array detection (HPLC-DAD) and ultraviolet (UV)-spectrophotometry were developed and compared to quantify lychnopholide (LYC) in poly-ε-caprolactone nanocapsules and to study its release kinetics. Both methods were validated concerning their specificity, linearity, limits of detection and quantification, precision, accuracy and stability. HPLC-DAD analyses were conducted using an RP C18 column, isocratic elution with a methanol-water (60:40 v/v) mobile phase at 0.8 mL/min flow rate and detection at 265 nm. The linear response (r(2) > 0.999) was obtained within a concentration range of 2-25 µg/mL using HPLC-DAD and 5-40 µg/mL using spectrophotometry. Intra-day and inter-day precision were obtained with low relative standard deviation values. The accuracy of the methods was within the range 98-101% for HPLC-DAD and from 96-100% for UV-spectrophotometry. Both methods were suitable to be applied for the determination of drug loading percentage (>96%) and encapsulation efficiency (>90%). Furthermore, the sensitivity of HPLC-DAD method allows studies of LYC release/dissolution in sink conditions. LYC presented 100% dissolution after 24 h, whereas only 60% of LYC was released from the nanocapsule dosage form, with no burst effect. The methods fulfilled all validation parameters evaluated for LYC quantification in the polymeric nanocapsules and have proven to be accurate, selective and sensitive in the previously mentioned applications. PMID:23247030

  3. Studies on the oxidation reaction of tyrosine (Tyr) with H 2O 2 catalyzed by horseradish peroxidase (HRP) in alcohol-water medium by spectrofluorimetry and differential spectrophotometry

    NASA Astrophysics Data System (ADS)

    Tang, Bo; Wang, Yan; Liang, Huiling; Chen, Zhenzhen; He, Xiwen; Shen, Hanxi

    2006-03-01

    An oxidation reaction of tyrosine (Tyr) with H 2O 2 catalyzed by horseradish peroxidase (HRP) was studied by spectrofluorimetry and differential spectrophotometry in the alcohol(methanol, ethanol, 1-propanol and isopropanol)-water mutual solubility system. Compared with the enzymatic-catalyzed reaction in the water medium, the fluorescence intensities of the product weakened, even extinguished. Because the addition of alcohols made the conformation of HRP change, the catalytic reaction shifted to the side of polymerization and the polymer (A nH 2, n ≥ 3) exhibited no fluorescence. The four alcohols cannot deactivate HRP. Moreover isopropanol activated HRP remarkably.

  4. Probing potassium in the atmosphere of HD 80606b with tunable filter transit spectrophotometry from the Gran Telescopio Canarias

    NASA Astrophysics Data System (ADS)

    Colón, Knicole D.; Ford, Eric B.; Redfield, Seth; Fortney, Jonathan J.; Shabram, Megan; Deeg, Hans J.; Mahadevan, Suvrath

    2012-01-01

    We report observations of HD 80606 using the 10.4-m Gran Telescopio Canarias and the Optical System for Imaging and low Resolution Integrated Spectroscopy (OSIRIS) tunable filter imager. We acquired very high precision, narrow-band photometry in four bandpasses around the K I absorption feature during the 2010 January transit of HD 80606b and during out-of-transit observations conducted in 2010 January and April. We obtained differential photometric precisions of ˜2.08 × 10-4 for the in-transit flux ratio measured at 769.91 nm, which probes the K I line core. We find no significant difference in the in-transit flux ratio between observations at 768.76 and 769.91 nm. Yet, we find a difference of ˜8.09 ± 2.88 × 10-4 between these observations and observations at a longer wavelength that probes the K I wing (777.36 nm). While the presence of red noise in the transit data has a non-negligible effect on the uncertainties in the flux ratio, the 777.36-769.91 nm colour during transit shows no effects from red noise and also indicates a significant colour change, with a mean value of ˜8.99 ± 0.62 × 10-4. This large change in the colour is equivalent to a ˜4.2 per cent change in the apparent planetary radius with wavelength, which is much larger than the atmospheric scaleheight. This implies the observations probed the atmosphere at very low pressures as well as a dramatic change in the pressure at which the slant optical depth reaches unity between ˜770 and 777 nm. We hypothesize that the excess absorption may be due to K I in a high-speed wind being driven from the exoplanet's exosphere. We discuss the viability of this and alternative interpretations, including stellar limb darkening, star-spots and effects from Earth's atmosphere. We strongly encourage follow-up observations of HD 80606b to confirm the signal measured here. Finally, we discuss the future prospects for exoplanet characterization using tunable filter spectrophotometry.

  5. Infrared Spectrophotometry of PHOBOS

    NASA Astrophysics Data System (ADS)

    Rivkin, A. S.; Trilling, D. E.; Plassmann, J. H.; Brown, R. H.; Bell, J. F., III

    1999-09-01

    We have obtained multispectral images of both the leading and trailing sides of Phobos from the IRTF at 10 wavelengths in the 1.65--3.5 mu m region. The observations were made on 26 April 1999 (UT), with the Cold Coronagraph (CoCo) on NSFCAM. The coronagraph effectively removes the scattered light of Mars from our observations. We find no evidence for a 3-mu m absorption feature (indicative of water of hydration) to within 5-10% on either hemisphere. This finding increases the likelihood that the unexpectedly low density of Phobos found by Viking and the Phobos 2 spacecraft is due to macroporosity effects (as suggested by Avanesov et al. Plan. Space Sci. 1991), among others) rather than compositional effects, since the spectral signature of plausible lower-density materials such as hydrated minerals and water ice have not been found. This is similar to the situation for 253 Mathilde, where the NEAR spacecraft encounter found a low density (Yeomans et al. Science 1997) while Rivkin et al. (Icarus 1997) found an anhydrous surface mineralogy, leading to an interpretation that macroporosity effects were important. The work of Murchie and Erard (Icarus 1996), using data from the Phobos 2 spacecraft, showed that Phobos could be separated into different geological units, based on color and morphology. The fresher areas associated with Stickney crater are bluer in color than the ``background'' areas. For comparison with this work, the ``blue'' unit dominates the leading hemisphere, the ``red'' unit the trailing hemisphere. In the 1.65--3.5 mu m region, we find the two hemispheres to have virtually identical spectra. When connected to visible spectra of Phobos (Murchie and Erard, among others), the leading hemisphere has strong similarities to T-class asteroid spectra. The spectrum of the trailing hemisphere resembles mature lunar soils more closely than any asteroid class.

  6. Ultraviolet cometary spectrophotometry

    NASA Technical Reports Server (NTRS)

    Ahearn, M. F.

    1983-01-01

    During the 13 shifts dedicated to observations of Comet Bradfield (including the two European shifts), five high dispersion exposures were obtained with the LWR camera, 27 low dispersion images with the LWR camera, and 36 low dispersion images with the SWP camera of which 5 were observations of the geocoronal background and 4 were taken in a serendipity mode while the nucleus of the comet was centered on the large aperture of the LWR camera.

  7. High-Sensitivity Spectrophotometry.

    ERIC Educational Resources Information Center

    Harris, T. D.

    1982-01-01

    Selected high-sensitivity spectrophotometric methods are examined, and comparisons are made of their relative strengths and weaknesses and the circumstances for which each can best be applied. Methods include long path cells, noise reduction, laser intracavity absorption, thermocouple calorimetry, photoacoustic methods, and thermo-optical methods.…

  8. Micro solid phase spectrophotometry in a sequential injection lab-on-valve platform for cadmium, zinc, and copper determination in freshwaters.

    PubMed

    Santos, Inês C; Mesquita, Raquel B R; Rangel, António O S S

    2015-09-01

    This work describes the development of a solid phase spectrophotometry method in a μSI-LOV system for cadmium, zinc, and copper determination in freshwaters. NTA (Nitrilotriacetic acid) beads with 60-160 μm diameter were packed in the flow cell of the LOV for a μSPE column of 1 cm length. The spectrophotometric determination is based on the colourimetric reaction between dithizone and the target metals, previously retained on NTA resin. The absorbance of the coloured product formed is measured, at 550 nm, on the surface of the NTA resin beads in a solid phase spectrophotometry approach. The developed method presented preconcentration factors in the range of 11-21 for the metal ions. A LOD of 0.23 μg L(-1) for cadmium, 2.39 μg L(-1) for zinc, and 0.11 μg L(-1) for copper and a sampling rate of 12, 13, and 15 h(-1) for cadmium, zinc, and copper were obtained, respectively. The proposed method was successfully applied to freshwater samples. PMID:26388376

  9. White LEDs as broad spectrum light sources for spectrophotometry: demonstration in the visible spectrum range in a diode-array spectrophotometric detector.

    PubMed

    Piasecki, Tomasz; Breadmore, Michael C; Macka, Mirek

    2010-11-01

    Although traditional lamps, such as deuterium lamps, are suitable for bench-top instrumentation, their compatibility with the requirements of modern miniaturized instrumentation is limited. This study investigates the option of utilizing solid-state light source technology, namely white LEDs, as a broad band spectrum source for spectrophotometry. Several white light LEDs of both RGB and white phosphorus have been characterized in terms of their emission spectra and energy output and a white phosphorus Luxeon LED was then chosen for demonstration as a light source for visible-spectrum spectrophotometry conducted in CE. The Luxeon LED was fixed onto the base of a dismounted deuterium (D(2) ) lamp so that the light-emitting spot was geometrically positioned exactly where the light-emitting spot of the original D(2) lamp is placed. In this manner, the detector of a commercial CE instrument equipped with a DAD was not modified in any way. As the detector hardware and electronics remained the same, the change of the deuterium lamp for the Luxeon white LED allowed a direct comparison of their performances. Several anionic dyes as model analytes with absorption maxima between 450 and 600 nm were separated by CE in an electrolyte of 0.01 mol/L sodium tetraborate. The absorbance baseline noise as the key parameter was 5 × lower for the white LED lamp, showing clearly superior performance to the deuterium lamp in the available, i.e. visible part of the spectrum. PMID:21077241

  10. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; determination of chromium in water by graphite furnace atomic absorption spectrophotometry

    USGS Publications Warehouse

    McLain, B.J.

    1993-01-01

    Graphite furnace atomic absorption spectrophotometry is a sensitive, precise, and accurate method for the determination of chromium in natural water samples. The detection limit for this analytical method is 0.4 microg/L with a working linear limit of 25.0 microg/L. The precision at the detection limit ranges from 20 to 57 percent relative standard deviation (RSD) with an improvement to 4.6 percent RSD for concentrations more than 3 microg/L. Accuracy of this method was determined for a variety of reference standards that was representative of the analytical range. The results were within the established standard deviations. Samples were spiked with known concentrations of chromium with recoveries ranging from 84 to 122 percent. In addition, a comparison of data between graphite furnace atomic absorption spectrophotometry and direct-current plasma atomic emission spectrometry resulted in suitable agreement between the two methods, with an average deviation of +/- 2.0 microg/L throughout the analytical range.

  11. Mass spectrometry and UV-VIS spectrophotometry of ruthenium(II) [RuClCp(mPTA)2](OSO2CF3)2 complex in solution.

    PubMed

    Peña-Méndez, Eladia María; González, Beatriz; Lorenzo, Pablo; Romerosa, Antonio; Havel, Josef

    2009-12-01

    Ruthenium(II) complexes are of great interest as a new class of cancerostatics with advantages over classical platinum compounds including lower toxicity. The stability of the [RuClCp(mPTA)2](OSO2CF3)2 complex (I) (Cp cyclopentadienyl, mPTA N-methyl 1,3,5-triaza-7-phosphaadamantane) in aqueous solution was studied using spectrophotometry, matrix-assisted laser desorption/ionization (MALDI) and laser desorption/ionization (LDI) time-of-flight (TOF) mass spectrometry (MS). Spectrophotometry proves that at least three different reactions take place in water. Dissolution of I leads to fast coordination of water molecules to the Ru(II) cation and then slow hydrolysis and ligand exchange of chloride and mPTA with water, hydroxide or with trifluoromethane sulfonate itself. Via MALDI and LDI of the hydrolyzed solutions the formation of singly positively charged ions of general formula RuCl(p)(Cp)(q)(mPTA)(r)(H2O)(s)(OH)(t) (p = 0-1, q = 0-1, r = 0-2, s = 0-5, t = 0-2) and of some fragment ions was shown. The stoichiometry was determined by analyzing the isotopic envelopes and computer modelling. The [RuClCp(mPTA)2](OSO2CF3)2 complex can be stabilized in dilute hydrochloric acid or in neutral 0.15 M isotonic sodium chloride solution. PMID:19902414

  12. Use of HPLC/UPLC-spectrophotometry for detection of formazan in in vitro Reconstructed human Tissue (RhT)-based test methods employing the MTT-reduction assay to expand their applicability to strongly coloured test chemicals.

    PubMed

    Alépée, N; Barroso, J; De Smedt, A; De Wever, B; Hibatallah, J; Klaric, M; Mewes, K R; Millet, M; Pfannenbecker, U; Tailhardat, M; Templier, M; McNamee, P

    2015-06-01

    A number of in vitro test methods using Reconstructed human Tissues (RhT) are regulatory accepted for evaluation of skin corrosion/irritation. In such methods, test chemical corrosion/irritation potential is determined by measuring tissue viability using the photometric MTT-reduction assay. A known limitation of this assay is possible interference of strongly coloured test chemicals with measurement of formazan by absorbance (OD). To address this, Cosmetics Europe evaluated use of HPLC/UPLC-spectrophotometry as an alternative formazan measurement system. Using the approach recommended by the FDA guidance for validation of bio-analytical methods, three independent laboratories established and qualified their HPLC/UPLC-spectrophotometry systems to reproducibly measure formazan from tissue extracts. Up to 26 chemicals were then tested in RhT test systems for eye/skin irritation and skin corrosion. Results support that: (1) HPLC/UPLC-spectrophotometry formazan measurement is highly reproducible; (2) formazan measurement by HPLC/UPLC-spectrophotometry and OD gave almost identical tissue viabilities for test chemicals not exhibiting colour interference nor direct MTT reduction; (3) independent of the test system used, HPLC/UPLC-spectrophotometry can measure formazan for strongly coloured test chemicals when this is not possible by absorbance only. It is therefore recommended that HPLC/UPLC-spectrophotometry to measure formazan be included in the procedures of in vitro RhT-based test methods, irrespective of the test system used and the toxicity endpoint evaluated to extend the applicability of these test methods to strongly coloured chemicals. PMID:25701760

  13. Dismantling techniques

    SciTech Connect

    Wiese, E.

    1998-03-13

    Most of the dismantling techniques used in a Decontamination and Dismantlement (D and D) project are taken from conventional demolition practices. Some modifications to the techniques are made to limit exposure to the workers or to lessen the spread of contamination to the work area. When working on a D and D project, it is best to keep the dismantling techniques and tools as simple as possible. The workers will be more efficient and safer using techniques that are familiar to them. Prior experience with the technique or use of mock-ups is the best way to keep workers safe and to keep the project on schedule.

  14. Narrow-Band Spectrophotometry of Comet Hale-Bopp (C/1995 O1) Near Perihelion I.: Photometric Behavior of C2, C3, CN Molecular Bands

    NASA Astrophysics Data System (ADS)

    Sung, Eon-Chang; Kim, Ho-Il; Youn, Jae-Hyuk

    2000-12-01

    We present the results from narrow-band spectrophotometry of Comet Hale-Bopp (C/1995 O1) near perihelion obtained at Sobaeksan Optical Astronomy Observatory 61cm telescope equipped with PM 512 CCD camera (512 x 512, 0.5''/pixel) and narrow-band filter set for the comet on 19 nights from February 21 to May 1, 1997. We discuss molecular emission band morphology and photometric behavior of Comet Hale-Bopp. The morphology of CN band shows more symmetric light distributions than C2 or C3 bands. On other hand, C2 and C3 band have more compact light distributions than CN band. Similar to wide-band image, molecular band morphology shows spiral structures at the core of the comet. The CN surface brightness variation with changing heliocentric distance shows difference from those of C2 and C.3 The brightness, however, of these molecular bands near perihelion shows previously known 7day period light variations.

  15. Aqueous complexation of citrate with neodymium(III) and americium(III): a study by potentiometry, absorption spectrophotometry, microcalorimetry, and XAFS.

    PubMed

    Brown, M Alex; Kropf, A Jeremy; Paulenova, Alena; Gelis, Artem V

    2014-05-01

    The aqueous complexation of Nd(III) and Am(III) with anions of citrate was studied by potentiometry, absorption spectrophotometry, microcalorimetry, and X-ray absorption fine structure (XAFS). Using potentiometric titration data fitting the metal-ligand (L) complexes that were identified for Nd(III) were NdHL, NdL, NdHL2, and NdL2; a review of trivalent metal-citrate complexes is also included. Stability constants for these complexes were calculated from potentiometric and spectrophotometric titrations. Microcalorimetric results concluded that the entropy term of complex formation is much more dominant than the enthalpy. XAFS results showed a dependence in the Debye-Waller factor that indicated Nd(iii)-citrate complexation over the pH range of 1.56-6.12. PMID:24619154

  16. Ion pair-based liquid-phase microextraction combined with cuvetteless UV-vis micro-spectrophotometry as a miniaturized assay for monitoring ammonia in waters.

    PubMed

    Senra-Ferreiro, Sonia; Pena-Pereira, Francisco; Costas-Mora, Isabel; Romero, Vanesa; Lavilla, Isela; Bendicho, Carlos

    2011-09-15

    A miniaturized method based on liquid-phase microextraction (LPME) in combination with microvolume UV-vis spectrophotometry for monitoring ammonia in waters is proposed. The methodology is based on the extraction of the ion pair formed between the blue indophenol obtained according to the Berthelot reaction and a quaternary ammonium salt into a microvolume of organic solvent. Experimental parameters affecting the LPME performance such as type and concentration of the quaternary ammonium ion salt required to form the ion pair, type and volume of extractant solvent, effect of disperser solvent, ionic strength and extraction time, were optimized. A detection limit of 5.0 μg L(-1) ammonia and an enrichment factor of 30 can be attained after a microextraction time of 4 min. The repeatability, expressed as relative standard deviation, was 7.6% (n=7). The proposed method can be successfully applied to the determination of trace amounts of ammonia in several environmental water samples. PMID:21807208

  17. Quantification of Sunscreen Benzophenone-4 in Hair Shampoos by Hydrophilic Interactions Thin-Layer Chromatography/Densitometry or Derivative UV Spectrophotometry.

    PubMed

    Sobańska, Anna W; Kałębasiak, Katarzyna; Pyzowski, Jarosław; Brzezińska, Elżbieta

    2015-01-01

    Benzophenone-4 (BZ4) was separated from surfactants, dyes, preservatives, and other components of hair shampoos by thin-layer chromatography on silica gel 60 stationary phase, with ethyl acetate-ethanol-water-pH 6 phosphate buffer (15 : 7 : 5 : 1 v/v/v/v) as mobile phase. Densitometry scanning of chromatograms was performed at 285 nm. The densitometric calibration curve for BZ4 was nonlinear (second-degree polynomial), with R > 0.999. The limits of detection and quantification were ca. 0.03 and ca. 0.1 μg spot(-1), respectively. The results obtained by HPTLC-densitometry were compared to those obtained by zero and 2nd derivative UV spectrophotometry. In the case of spectrophotometric methods, calibration curves were linear with R > 0.9998. The chromatographic method was fully validated. PMID:25734022

  18. Simultaneous determination of benznidazole and itraconazole using spectrophotometry applied to the analysis of mixture: A tool for quality control in the development of formulations.

    PubMed

    Pinho, Ludmila A G; Sá-Barreto, Lívia C L; Infante, Carlos M C; Cunha-Filho, Marcílio S S

    2016-04-15

    The aim of this work was the development of an analytical procedure using spectrophotometry for simultaneous determination of benznidazole (BNZ) and itraconazole (ITZ) in a medicine used for the treatment of Chagas disease. In order to achieve this goal, the analysis of mixtures was performed applying the Lambert-Beer law through the absorbances of BNZ and ITZ in the wavelengths 259 and 321 nm, respectively. Diverse tests were carried out for development and validation of the method, which proved to be selective, robust, linear, and precise. The lower limits of detection and quantification demonstrate its sensitivity to quantify small amounts of analytes, enabling its application for various analytical purposes, such as dissolution test and routine assays. In short, the quantification of BNZ and ITZ by analysis of mixtures had shown to be efficient and cost-effective alternative for determination of these drugs in a pharmaceutical dosage form. PMID:26827177

  19. Ultrasound-assisted emulsification microextraction with simultaneous derivatization coupled to fibre optics-based cuvetteless UV-vis micro-spectrophotometry for formaldehyde determination in cosmetic samples.

    PubMed

    Lavilla, Isela; Cabaleiro, Noelia; Pena, Francisco; de la Calle, Inmaculada; Bendicho, Carlos

    2010-07-26

    In this work, ultrasound-assisted emulsification microextraction in combination with fibre optics-based cuvetteless UV-vis micro-spectrophotometry has been proposed as a novel method for the determination of formaldehyde in water-based cosmetics such as shampoo, conditioner and shower gel. The use of a powerful cup-horn sonoreactor allows simultaneous extraction and derivatization of the samples without any pre-treatment. The type and volume of organic extractant solvent, need for a disperser solvent, sonication conditions (sonication time and amplitude), ionic strength and centrifuging time have been carefully studied. Matrix effects were also evaluated. The European official method for quantification of formaldehyde in cosmetic products was used for comparison purposes. An important improvement in sensitivity and sample throughput as well as miniaturization was achieved. A limit of detection of 0.02 microg g(-1) of formaldehyde and a repeatability expressed as relative standard deviation of 5.9% were obtained. PMID:20638500

  20. Simultaneous determination of benznidazole and itraconazole using spectrophotometry applied to the analysis of mixture: A tool for quality control in the development of formulations

    NASA Astrophysics Data System (ADS)

    Pinho, Ludmila A. G.; Sá-Barreto, Lívia C. L.; Infante, Carlos M. C.; Cunha-Filho, Marcílio S. S.

    2016-04-01

    The aim of this work was the development of an analytical procedure using spectrophotometry for simultaneous determination of benznidazole (BNZ) and itraconazole (ITZ) in a medicine used for the treatment of Chagas disease. In order to achieve this goal, the analysis of mixtures was performed applying the Lambert-Beer law through the absorbances of BNZ and ITZ in the wavelengths 259 and 321 nm, respectively. Diverse tests were carried out for development and validation of the method, which proved to be selective, robust, linear, and precise. The lower limits of detection and quantification demonstrate its sensitivity to quantify small amounts of analytes, enabling its application for various analytical purposes, such as dissolution test and routine assays. In short, the quantification of BNZ and ITZ by analysis of mixtures had shown to be efficient and cost-effective alternative for determination of these drugs in a pharmaceutical dosage form.

  1. Spectrophotometry of peculiar B and A stars. XVIII - The helium rich variable stars HR 1890, Sigma Orionis E, and HD 37776

    NASA Technical Reports Server (NTRS)

    Adelman, S. J.; Pyper, D. M.

    1985-01-01

    Optical region spectrophotometry at 3300-7850 A has been obtained for three helium rich stars, HR 1890, Sigma Ori E, and HD 37776, of the Orion OB1 Association. New uvby-beta photometry of HR 1890 and HD 37776 as well as published data are also used to investigate the variability of these stars. A new period of 1.53862 days was determined for HD 37776. For all three stars H-beta varies in antiphase with strong He I lines. The spectrophotometric bandpass containing the strong He I line at 4471 A varies in phase with the R index of Pedersen and Thomsen (1977). Evidence is found for weak absorption features which appear to be an extension of the 5200 A feature seen in cooler CP stars.

  2. LASER BIOLOGY AND MEDICINE: Combination of fluorescence imaging and local spectrophotometry in fluorescence diagnostics of early cancer of larynx and bronchi

    NASA Astrophysics Data System (ADS)

    Sokolov, Vladimir V.; Filonenko, E. V.; Telegina, L. V.; Boulgakova, N. N.; Smirnov, V. V.

    2002-11-01

    The results of comparative studies of autofluorescence and 5-ALA-induced fluorescence of protoporphyrin IX, used in the diagnostics of early cancer of larynx and bronchi, are presented. The autofluorescence and 5-ALA-induced fluorescence images of larynx and bronchial tissues are analysed during the endoscopic study. The method of local spectrophotometry is used to verify findings obtained from fluorescence images. It is shown that such a combined approach can be efficiently used to improve the diagnostics of precancer and early cancer, to detect a primary multiple tumours, as well as for the diagnostics of a residual tumour or an early recurrence after the endoscopic, surgery or X-ray treatment. The developed approach allows one to minimise the number of false-positive results and to reduce the number of biopsies, which are commonly used in the white-light bronchoscopy search for occult cancerous loci.

  3. Simultaneous determination of nickel and copper by H-point standard addition method-first-order derivative spectrophotometry in plant samples after separation and preconcentration on modified natural clinoptilolite as a new sorbent.

    PubMed

    Roohparvar, Rasool; Taher, Mohammad Ali; Mohadesi, Alireza

    2008-01-01

    For the simultaneous determination of nickel(ll) and copper(ll) in plant samples, a rapid and accurate method was developed. In this method, solid-phase extraction (SPE) and first-order derivative spectrophotometry (FDS) are combined, and the result is coupled with the H-point standard addition method (HPSAM). Compared with normal spectrophotometry, derivative spectrophotometry offers the advantages of increased selectivity and sensitivity. As there is no need for carrying out any pretreatment of the sample, the spectrophotometry method is easy, but because of a high detection limit, it is not so practical. In order to decrease the detection limit, it is suggested to combine spectrophotometry with a preconcentration method such as SPE. In the present work, after separation and preconcentration of Ni(ll) and Cu(ll) on modified clinoptilolite zeolite that is loaded with 2-[1-(2-hydroxy-5-sulforphenyl)-3-phenyl-5-formaza-no]-benzoic acid monosodium salt (zincon) as a selective chromogenic reagent, FDS-HPSAM, which is a simple and selective spectrophotometric method, has been applied for simultaneous determination of these ions. With optimum conditions, the detection limit in original solutions is 0.7 and 0.5 ng/mL, respectively, for nickel and copper. The linear concentration ranges in the proposed method for nickel and copper ions in original solutions are 1.1 to 3.0 x 10(3) and 0.9 to 2.0 x 10(3) ng/mL, respectively. The recommended procedure is applied to successful determination of Cu(ll) and Ni(ll) in standard and real samples. PMID:18567311

  4. Stapedectomy technique.

    PubMed

    House, J W

    1993-06-01

    This article reviews the evolution of the author's stapedectomy technique from total footplate removal with single loop wire prosthesis and Gelfoam seal to small fenestra stapedectomy with platinum ribbon piston prosthesis and blood seal. The author concludes that the microdrill is effective, safe, and cost effective for performing this procedure. Since using this technique, the author has had no cases of sensorineural hearing loss and few complaints of dizziness or vertigo. PMID:8341570

  5. Spatial Techniques

    NASA Astrophysics Data System (ADS)

    Jabeur, Nafaa; Sahli, Nabil

    The environment, including the Earth and the immense space, is recognized to be the main source of useful information for human beings. During several decades, the acquisition of data from this environment was constrained by tools and techniques with limited capabilities. However, thanks to continuous technological advances,spatial data are available in huge quantities for different applications. The technological advances have been achieved in terms of hardware and software as well. They are allowing for better accuracy and availability, which in turn improves the quality and quantity of useful knowledge that can be extracted from the environment. They have been applied to geography, resulting in geospatial techniques. Applied to both science and technology, geospatial techniques resulted in areas of expertise, such as land surveying, cartography, navigation, remote sensing, Geographic Infor-mation Systems (GISs), and Global Positioning Systems (GPSs). They had evolved quickly with advances in computing, satellite technology and a growing demand to understand our global environment. In this chapter, we will discuss three important techniques that are widely used in spatial data acquisition and analysis: GPS and remote sensing techniques that are used to collect spatial data and a GIS that is used to store, manipulate, analyze, and visualize spatial data. Later in this book, we will discuss the techniques that are currently available for spatial knowledge discovery.

  6. Decomposition techniques

    USGS Publications Warehouse

    Chao, T.T.; Sanzolone, R.F.

    1992-01-01

    Sample decomposition is a fundamental and integral step in the procedure of geochemical analysis. It is often the limiting factor to sample throughput, especially with the recent application of the fast and modern multi-element measurement instrumentation. The complexity of geological materials makes it necessary to choose the sample decomposition technique that is compatible with the specific objective of the analysis. When selecting a decomposition technique, consideration should be given to the chemical and mineralogical characteristics of the sample, elements to be determined, precision and accuracy requirements, sample throughput, technical capability of personnel, and time constraints. This paper addresses these concerns and discusses the attributes and limitations of many techniques of sample decomposition along with examples of their application to geochemical analysis. The chemical properties of reagents as to their function as decomposition agents are also reviewed. The section on acid dissolution techniques addresses the various inorganic acids that are used individually or in combination in both open and closed systems. Fluxes used in sample fusion are discussed. The promising microwave-oven technology and the emerging field of automation are also examined. A section on applications highlights the use of decomposition techniques for the determination of Au, platinum group elements (PGEs), Hg, U, hydride-forming elements, rare earth elements (REEs), and multi-elements in geological materials. Partial dissolution techniques used for geochemical exploration which have been treated in detail elsewhere are not discussed here; nor are fire-assaying for noble metals and decomposition techniques for X-ray fluorescence or nuclear methods be discussed. ?? 1992.

  7. Solubility of Lead Sulfate in Water and in Sodium Sulfate Solutions: An Experiment in Atomic Absorption Spectrophotometry.

    ERIC Educational Resources Information Center

    Lehman, Thomas A.; Everett, Wayne W.

    1982-01-01

    Describes a set of undergraduate laboratory experiments which provide experience in deuteration and derivatization procedures applied to infrared spectroscopy. Basic skills in vacuum-line technique are also taught while measuring infrared spectra of deuterated solid samples and demonstrating the value of derivatization as an aid to interpreting…

  8. Determination of Copper by Graphite Furnace Atomic Absorption Spectrophotometry: A Student Exercise in Instrumental Methods of Analysis.

    ERIC Educational Resources Information Center

    Williamson, Mark A.

    1989-01-01

    Discusses a student exercise which requires the optimizing of the charring and atomization temperatures by producing a plot of absorbance versus temperature for each temperature parameter. Notes that although the graphite furnace atomic absorption spectroscopy technique has widespread industrial use, there are no published, structured experiments…

  9. Tracer Technique

    NASA Astrophysics Data System (ADS)

    Haba, H.; Motomura, S.; Kamino, S.; Enomoto, S.

    In radioactive tracer technique, radioactive nuclides are used to follow the behavior of elements or chemical species in chemical and other processes. This is realized by means of radioactivity measurement. In 1913, Hevesy and Paneth succeeded in determining the extremely low solubility of lead salts by using naturally occurring 210Pb as a radioactive tracer. As various radioactive nuclides became artificially available, this technique has been widely employed in studies of chemical equilibrium and reactions as well as in chemical analysis. It is also an essential technique in biochemical, biological, medical, geological, and environmental studies. Medical diagnosis and industrial process control are the fields of its most important practical application. In this chapter, fundamental ideas concerning radioactive tracers will be described followed by their application with typical examples. Detailed description on their application to life sciences and medicine is given in Vol. 4.

  10. Miscellaneous Techniques

    NASA Astrophysics Data System (ADS)

    Jha, Shyam N.

    Nondestructive way of determining the food quality is the need of the hour. Till now major methods such as colour measurements and their modeling; machine vision systems; X-ray, CT and MRI; NIR spectroscopy; electronic nose and tongue; and ultrasonic technology have been discussed in detail. These techniques, in general, are considered to be sophisticated and costly, and therefore probably are not being adopted as fast as it should be. I am however of the reverse opinion. While going through these techniques, it has been seen that majority of quality parameters have been measured and correlated with the signals obtained using different equipment.

  11. Titration Techniques

    NASA Astrophysics Data System (ADS)

    Jacobsen, Jerrold J.; Houston Jetzer, Kelly; Patani, Néha; Zimmerman, John; Zweerink, Gerald

    1995-07-01

    Significant attention is paid to the proper technique for reading a meniscus. Video shows meniscus-viewing techniques for colorless and dark liquids and the consequences of not reading a meniscus at eye level. Lessons are provided on approaching the end point, focusing on end point colors produced via different commonly used indicators. The concept of a titration curve is illustrated by means of a pH meter. Carefully recorded images of the entire range of meniscus values in a buret, pipet, and graduated cylinder are included so that you can show your students, in lecture or pre-lab discussion, any meniscus and discuss how to read the buret properly. These buret meniscus values are very carefully recorded at the rate of one video frame per hundredth of a milliliter, so that an image showing any given meniscus value can be obtained. These images can be easily incorporated into a computer-based multimedia environment for testing or meniscus-reading exercises. Two of the authors have used this technique and found the exercise to be very well received by their students. Video on side two shows nearly 100 "bloopers", demonstrating both the right way and wrong ways to do tasks associated with titration. This material can be used in a variety of situations: to show students the correct way to do something; to test students by asking them "What is this person doing wrong?"; or to develop multimedia, computer-based lessons. The contents of Titration Techniques are listed below: Side 1 Titration: what it is. A simple titration; Acid-base titration animation; A brief redox titration; Redox titration animation; A complete acid-base titration. Titration techniques. Hand technique variations; Stopcock; Using a buret to measure liquid volumes; Wait before reading meniscus; Dirty and clean burets; Read meniscus at eye level (see Fig. 1); Meniscus viewing techniques--light colored liquids; Meniscus viewing techniques--dark liquids; Using a magnetic stirrer; Rough titration

  12. Electrochemical Techniques

    SciTech Connect

    Chen, Gang; Lin, Yuehe

    2008-07-20

    Sensitive and selective detection techniques are of crucial importance for capillary electrophoresis (CE), microfluidic chips, and other microfluidic systems. Electrochemical detectors have attracted considerable interest for microfluidic systems with features that include high sensitivity, inherent miniaturization of both the detection and control instrumentation, low cost and power demands, and high compatibility with microfabrication technology. The commonly used electrochemical detectors can be classified into three general modes: conductimetry, potentiometry, and amperometry.

  13. Continuous Wavelet Transform, a powerful alternative to Derivative Spectrophotometry in analysis of binary and ternary mixtures: A comparative study.

    PubMed

    Elzanfaly, Eman S; Hassan, Said A; Salem, Maissa Y; El-Zeany, Badr A

    2015-12-01

    A comparative study was established between two signal processing techniques showing the theoretical algorithm for each method and making a comparison between them to indicate the advantages and limitations. The methods under study are Numerical Differentiation (ND) and Continuous Wavelet Transform (CWT). These methods were studied as spectrophotometric resolution tools for simultaneous analysis of binary and ternary mixtures. To present the comparison, the two methods were applied for the resolution of Bisoprolol (BIS) and Hydrochlorothiazide (HCT) in their binary mixture and for the analysis of Amlodipine (AML), Aliskiren (ALI) and Hydrochlorothiazide (HCT) as an example for ternary mixtures. By comparing the results in laboratory prepared mixtures, it was proven that CWT technique is more efficient and advantageous in analysis of mixtures with severe overlapped spectra than ND. The CWT was applied for quantitative determination of the drugs in their pharmaceutical formulations and validated according to the ICH guidelines where accuracy, precision, repeatability and robustness were found to be within the acceptable limit. PMID:26186613

  14. Determination of the complexation constants of Pb(II) and Cd(II) with thymol blue using spectrophotometry, SQUAD and the HSAB principle

    NASA Astrophysics Data System (ADS)

    Balderas-Hernández, P.; Rojas-Hernández, A.; Galván, M.; Romo, M. Romero; Palomar-Pardavé, M.; Ramírez-Silva, M. T.

    2007-01-01

    This paper presents the results concerning the determination of the formation constants of the complexes between thymol blue, TB, and the metal ions Pb(II) or Cd(II). The experimental procedure was carried out in the presence of a nitrogen atmosphere at 25 °C. The spectrophotometry data obtained were processed through the software SQUAD to calculate the complexation constants of the metal-indicator and to establish an adequate base of the models which considered the structure of the indicator, and the actual metal species in the aqueous solutions. For the Pb(II)-TB-H 2O system the log K value calculated for the PbTB complex was 5.591 ± 0.057 while for the Cd(II)-TB-H 2O system, the log K value of the CdTB complex was 5.099 ± 0.008. Also, supporting theoretical chemistry results on the chemical hardness of TB molecule were performed to enable establishment of a relative prediction scale of the TB complexation constants ranking in the framework of the Principle of Hard and Soft Acids and Bases or HSAB Principle.

  15. Determination of total iron in water and foods by dispersive liquid-liquid microextraction coupled with microvolume UV-vis spectrophotometry.

    PubMed

    Peng, Bo; Shen, Yingping; Gao, Zhuantao; Zhou, Min; Ma, Yongjun; Zhao, Shengguo

    2015-06-01

    A novel microvolume UV-vis spectrophotometry method was proposed for the rapid determination of total iron coupling with an efficient pretreatment method known as dispersive liquid-liquid microextraction (DLLME). The basis of the method is a quantitative colorimetric reaction between ferrous iron and 2-(5-bromo-2-pyridylazo)-5-(diethyl amino) phenol (5-Br-PADAP) after the reduction of Fe(III) to Fe(II) by using ascorbic acid as reducing agent. Parameters related to the efficiency of microextraction, such as pH, complexant concentration, the volume ratio of disperser solvent and extraction solvent were discussed and optimized in detail. Under the optimized conditions, the absorbance was in proportion to iron concentration in the range of 5-400μgL(-1) with a correlation coefficient (R) of 0.9993. The limit of detection (LOD) and limit of quantitation (LOQ) were 1.5μgL(-1) and 5.2μgL(-1), respectively. The relative standard deviation (RSD) for samples were 1.37- 4.42% (n=3). Good recoveries of iron were obtained in the range of 95.4-103.2% in food samples, 96.9-103.6% in water samples and 98.8-102.3% in Certified Reference Material. The proposed method was rapid, reliable and high-selective for the determination of total iron in food and water samples. PMID:25624235

  16. Selective determination of the holmium in rare earth mixtures by second derivative spectrophotometry with 2-isobutylformyl-1,3-dione-indan and octylphenol poly-(ethyleneglycol)ether

    SciTech Connect

    Wang Naixing; Si Zhikun; Jiang Wei

    1996-09-01

    In this paper the absorption spectra of 4f electron transitions of the system of holmium with 2-isobutylformyl-1,3-dione-indan and TX-100 have been studied by normal and derivative spectrophotometry. The molar absorptivities are 98 (at 450 nm) and 21 (at 460 nm) 1 {center_dot} mol{sup -1} {center_dot} cm{sup -1}, respectively. The use of the second derivative spectra, eliminates the interference by other lanthanides and improves the sensitivity for holmium determination. The derivative molar absorptivity is 558 1 {center_dot} mol{sup -1} {center_dot} cm{sup -1}. The calibration graph was linear up to 25{mu}g/ml of holmium. The relative standard deviation evaluated from ten independent determinations of 8.0 {mu}g/ml holmium is 1.0%. The detection limit, obtained from the sensitivity of the calibration graph and for 3 S{sub b} (S{sub b} = standard deviation of a blank without holmium, n = 11), was found to be 0.31 {mu}g/ml of holmium. The quantification limit, obtained for 10 S{sub b}, was 1.0 {mu}g/ml of holmium. A method has been developed for determining holmium in a mixture of lanthanides by means of the second derivative spectra and the analytical results obtained are satisfactory.

  17. Does the prior application of the field kit bullet hole testing kit 3 on a suspected bullet hole bias the analysis of atomic absorption spectrophotometry?

    PubMed

    Seltenhammer, Monika H; Fitzl, Christine; Wieser, Ingo; Binder, Reinhard; Paula, Pia; Risser, Daniele U

    2014-09-01

    Forensic ballistics is the study of bullet trajectory and consists of determining gunshot residue (GSR) to identify bullet holes. Among several highly sensitive methods, atomic absorption spectrophotometry (AAS) is employed to analyze GSR in the laboratory. However, it is sometimes necessary to identify bullet holes immediately at a crime scene. The purpose of this examination was to determine whether the use of the field test Bullet Hole Testing Kit 3 (BTK3) on a suspected bullet hole would influence the outcome of AAS-analysis: Three commonly encountered firearms (Glock17, Tokarev, and Colt) were fired at skin, wood, and cloth. AAS-analysis was performed with and without previous BTK3 application. The results clearly indicate that there is no significant interaction on the grounds of BTK3 use (BTK3 vs. no-BTK3 [kit_nokit] [Pb: p = 0.1309; Sb: p = 0.9111], material*kit_nokit [Pb: p = 0.5960; Sb: p = 0.9930], distance*kit_nokit [Pb: p = 0.4014; Sb: p = 0.9184], and firearm type*kit_nokit [Pb: p = 0.9662; Sb: p = 0.9885]); hence, applying this field kit does not falsify later AAS outcomes. PMID:25040851

  18. Determination of the complexation constants of Pb(II) and Cd(II) with thymol blue using spectrophotometry, SQUAD and the HSAB principle.

    PubMed

    Balderas-Hernández, P; Rojas-Hernández, A; Galván, M; Romo, M Romero; Palomar-Pardavé, M; Ramírez-Silva, M T

    2007-01-01

    This paper presents the results concerning the determination of the formation constants of the complexes between thymol blue, TB, and the metal ions Pb(II) or Cd(II). The experimental procedure was carried out in the presence of a nitrogen atmosphere at 25 degrees C. The spectrophotometry data obtained were processed through the software SQUAD to calculate the complexation constants of the metal-indicator and to establish an adequate base of the models which considered the structure of the indicator, and the actual metal species in the aqueous solutions. For the Pb(II)-TB-H2O system the logK value calculated for the PbTB complex was 5.591+/-0.057 while for the Cd(II)-TB-H2O system, the logK value of the CdTB complex was 5.099+/-0.008. Also, supporting theoretical chemistry results on the chemical hardness of TB molecule were performed to enable establishment of a relative prediction scale of the TB complexation constants ranking in the framework of the Principle of Hard and Soft Acids and Bases or HSAB Principle. PMID:16829173

  19. Speciation of selenium in environmental samples by solid-phase spectrophotometry using 2,3-dichloro-6-(2,7-dihydroxy-naphthylazo)quinoxaline.

    PubMed

    Amin, Alaa S

    2014-01-01

    Solid-phase spectrophotometry was applied to determination of trace amounts of selenium (Se) in water, soil, plant materials, human hair, and a cosmetic preparation (lipstick). Se(IV) was sorbed in a dextran type lipophilic gel as a complex with 2,3-dichloro-6-(2,7-dihydroxy-naphthylazo)quinoxaline (DCDHNAQ), whereas Se(VI) was determined after boiling in HCI for 10 min to convert Se(VI) to Se(IV). Resin phase absorbances at 588 and 800 nm were measured directly, which allowed the determination of Se in the range of 0.2-3.3 microg/L with an RSD of 1.22%. The influences of analytical parameters including pH of the aqueous solution, amounts of DCDHNAQ, and sample volume were investigated. The molar absorptivities were found to be 1.09 x 10(6), 4.60 x 10(6), and 1.23 x 10(7) L/mol cm for 100, 500, and 1000 mL, respectively. The LOD and LOQ of the 500 mL sample method were 110 and 360 ng/L, respectively, when using 50 mg dextran type lipophilic gel. For a 1000 mL sample, the LOD and LOQ were 60 and 200 ng/L, respectively, using 50 mg of the exchanger. Increasing the sample volume enhanced the sensitivity. No considerable interferences were observed from other investigated anions and cations on the Se determination. PMID:24830171

  20. Comparative study between univariate spectrophotometry and multivariate calibration as analytical tools for quantitation of Benazepril alone and in combination with Amlodipine.

    PubMed

    Farouk, M; Elaziz, Omar Abd; Tawakkol, Shereen M; Hemdan, A; Shehata, Mostafa A

    2014-04-01

    Four simple, accurate, reproducible, and selective methods have been developed and subsequently validated for the determination of Benazepril (BENZ) alone and in combination with Amlodipine (AML) in pharmaceutical dosage form. The first method is pH induced difference spectrophotometry, where BENZ can be measured in presence of AML as it showed maximum absorption at 237nm and 241nm in 0.1N HCl and 0.1N NaOH, respectively, while AML has no wavelength shift in both solvents. The second method is the new Extended Ratio Subtraction Method (EXRSM) coupled to Ratio Subtraction Method (RSM) for determination of both drugs in commercial dosage form. The third and fourth methods are multivariate calibration which include Principal Component Regression (PCR) and Partial Least Squares (PLSs). A detailed validation of the methods was performed following the ICH guidelines and the standard curves were found to be linear in the range of 2-30μg/mL for BENZ in difference and extended ratio subtraction spectrophotometric method, and 5-30 for AML in EXRSM method, with well accepted mean correlation coefficient for each analyte. The intra-day and inter-day precision and accuracy results were well within the acceptable limits. PMID:24424258

  1. Complex Refractive Index Spectra of CH3NH3PbI3 Perovskite Thin Films Determined by Spectroscopic Ellipsometry and Spectrophotometry.

    PubMed

    Löper, Philipp; Stuckelberger, Michael; Niesen, Bjoern; Werner, Jérémie; Filipič, Miha; Moon, Soo-Jin; Yum, Jun-Ho; Topič, Marko; De Wolf, Stefaan; Ballif, Christophe

    2015-01-01

    The complex refractive index (dielectric function) of planar CH3NH3PbI3 thin films at room temperature is investigated by variable angle spectroscopic ellipsometry and spectrophotometry. Knowledge of the complex refractive index is essential for designing photonic devices based on CH3NH3PbI3 thin films such as solar cells, light-emitting diodes, or lasers. Because the directly measured quantities (reflectance, transmittance, and ellipsometric spectra) are inherently affected by multiple reflections, the complex refractive index has to be determined indirectly by fitting a model dielectric function to the experimental spectra. We model the dielectric function according to the Forouhi-Bloomer formulation with oscillators positioned at 1.597, 2.418, and 3.392 eV and achieve excellent agreement with the experimental spectra. Our results agree well with previously reported data of the absorption coefficient and are consistent with Kramers-Kronig transformations. The real part of the refractive index assumes a value of 2.611 at 633 nm, implying that CH3NH3PbI3-based solar cells are ideally suited for the top cell in monolithic silicon-based tandem solar cells. PMID:26263093

  2. [Tracheostomy techniques].

    PubMed

    Mieth, M; Schellhaaß, A; Hüttner, F J; Larmann, J; Weigand, M A; Büchler, M W

    2016-01-01

    Due to the comprehensive establishment of modern techniques, tracheostomy has become a routine procedure in intensive care units (ICU). The negative effects of prolonged translaryngeal intubation on the laryngeal and tracheal mucosa up to tracheal stenosis can be reduced by tracheostomy. Furthermore, long-term ventilation is facilitated; however, there is no clear evidence on the optimal timing of tracheostomy in critically ill patients. The specific indications and contraindications of surgical as well as percutaneous tracheostomy must be strictly observed for a safe and successful intervention. Exchanging the tracheostomy tube may lead to potentially dangerous situations especially after percutaneous tracheostomy. A standardized and structured approach is therefore recommended. PMID:26643155

  3. Separation techniques.

    PubMed

    Duke, T

    1998-10-01

    The past two years have seen continued development of capillary electrophoresis methods. The separation performance of flowable sieving media now equals, and in some respects exceeds, that provided by gels. The application of microfabrication techniques to separation science is gaining pace. There is a continuing trend towards miniaturization and integration of separation with preparative or analytical steps. Innovative separation methods based on microfabrication technology include electrophoresis in purpose-designed molecular sieves, dielectric, trapping using microelectrodes, and force-free motion in Brownian ratchets. PMID:9818184

  4. Determination of trapidil in human serum and urine by derivative UV spectrophotometry after selective solid-phase extraction.

    PubMed

    Ragno, Gaetano; Risoli, Antonella; De Luca, Michele; Ioele, Giuseppina; Oliverio, Filomena

    2007-10-01

    A novel analytical technique able to determine the anti-ischemic drug trapidil in human serum and urine is proposed. In order to achieve satisfactory sensitivity and selectivity, an extraction procedure was required to isolate the drug from complex matrixes such as serum and urine. A solid-phase extraction procedure was investigated to both increase the analyte concentration and eliminate the interfering molecules present in large amounts in both matrixes. Optimization of the extraction step was realized by selecting a new polymeric sorbent based on a surface-modified styrene-divinylbenzene polymer which provided fast and efficient drug extraction. Drug quantification was performed by using the third-order derivative spectra of the SPE eluates. Absorbance specific signals at (3)D(335,316) and (3)D(316) nm for urine and serum, respectively, were demonstrated to be directly proportional to drug concentration and barely affected by residual matrix interferences. Under the optimized experimental conditions the calibration plots were linear over the concentration range 0.2-50 microg mL(-1). The method was validated by analysis of a series of spiked samples. Accuracy (recovery of 95 and 94% for serum and urine, respectively) and precision (RSD below 4%) were good. PMID:17676316

  5. Development of a novel mixed hemimicelles dispersive micro solid phase extraction using 1-hexadecyl-3-methylimidazolium bromide coated magnetic graphene for the separation and preconcentration of fluoxetine in different matrices before its determination by fiber optic linear array spectrophotometry and mode-mismatched thermal lens spectroscopy.

    PubMed

    Kazemi, Elahe; Haji Shabani, Ali Mohammad; Dadfarnia, Shayessteh; Abbasi, Amir; Rashidian Vaziri, Mohammad Reza; Behjat, Abbas

    2016-01-28

    This study aims at developing a novel, sensitive, fast, simple and convenient method for separation and preconcentration of trace amounts of fluoxetine before its spectrophotometric determination. The method is based on combination of magnetic mixed hemimicelles solid phase extraction and dispersive micro solid phase extraction using 1-hexadecyl-3-methylimidazolium bromide coated magnetic graphene as a sorbent. The magnetic graphene was synthesized by a simple coprecipitation method and characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM). The retained analyte was eluted using a 100 μL mixture of methanol/acetic acid (9:1) and converted into fluoxetine-β-cyclodextrin inclusion complex. The analyte was then quantified by fiber optic linear array spectrophotometry as well as mode-mismatched thermal lens spectroscopy (TLS). The factors affecting the separation, preconcentration and determination of fluoxetine were investigated and optimized. With a 50 mL sample and under optimized conditions using the spectrophotometry technique, the method exhibited a linear dynamic range of 0.4-60.0 μg L(-1), a detection limit of 0.21 μg L(-1), an enrichment factor of 167, and a relative standard deviation of 2.1% and 3.8% (n = 6) at 60 μg L(-1) level of fluoxetine for intra- and inter-day analyses, respectively. However, with thermal lens spectrometry and a sample volume of 10 mL, the method exhibited a linear dynamic range of 0.05-300 μg L(-1), a detection limit of 0.016 μg L(-1) and a relative standard deviation of 3.8% and 5.6% (n = 6) at 60 μg L(-1) level of fluoxetine for intra- and inter-day analyses, respectively. The method was successfully applied to determine fluoxetine in pharmaceutical formulation, human urine and environmental water samples. PMID:26755141

  6. New techniques

    NASA Astrophysics Data System (ADS)

    Pisacane, V. L.

    1983-04-01

    Equipment, operations, calibration, and accuracy of existing positioning, geodetic, and gravimetric equipment are explored. Radio navigation and positioning systems now include OMEGA, LORAN, VOR, DME, TACAN, and LONAR. Dedicated positioning satellites comprise the Transit and Navstar systems, with positioning accuracies of 8 m available with the GPS. Missile tracking, particularly for submarine launched rockets, is accomplished with the Satrack satellite, which furnishes position and velocity accuracy to within 40 ft and 0.08 ft/sec, respectively. VLBI techniques permit sighting of astronomical objects to obtain 20 cm accuracy for pole positioning and 1 m/sec for earth rotation speeds. Methods have been devised to use portable equipment which compensates for refraction when using lasers and masers in ranging trials. NASA has established a fixed and mobile global laser tracking network to provide a ranging accuracy of 100 cm when employed with satellite and lunar reflectors. Lasers are also used for terrain contouring, aircraft ranging, and satellite altimetry. A free-fall gravimeter has been developed which involves dropping one reflector of a two-beam Michelson interferometer, yielding an accuracy of 10 microgal. It is noted that new standards are needed for the NASA Deep Space Network.

  7. Simultaneous determination of Cu 2+, Zn 2+, Cd 2+, Hg 2+ and Pb 2+ by using second-derivative spectrophotometry method

    NASA Astrophysics Data System (ADS)

    Han, Yanyan; Li, Yan; Si, Wei; Wei, Dong; Yao, Zhenxing; Zheng, Xianpeng; Du, Bin; Wei, Qin

    2011-09-01

    A new method of simultaneous determination of Cu 2+, Zn 2+, Cd 2+, Hg 2+ and Pb 2+ is proposed here by using the second-derivative spectrophotometry method. In pH = 10.35 Borax-NaOH buffer, using meso-tetra (3-methoxyl-4-hydroxylphenyl) porphyrin ([T-(3-MO-4-HP)P]) as chromomeric reagent, micelle solution was formed after Tween-80 surfactant was added into the solution containing Cu 2+, Zn 2+, Cd 2+, Hg 2+ and Pb 2+ ions. The original absorption spectrum of the above complexes was obtained after heating in the boiling water for 25 min. The second-derivative absorption peaks of five metal-porphyrin complexes can be separated from the original absorption spectrum by using chemometric tool. In this way, Cu 2+, Zn 2+, Cd 2+, Hg 2+ and Pb 2+ ions can be determined simultaneously. Under the optimal conditions, the linear ranges of the calibration curve were 0-0.60, 0-0.60, 0-0.40, 0-0.80 and 0-0.48 μg mL -1 for Cu 2+, Zn 2+, Cd 2+, Hg 2+ and Pb 2+, respectively. The molar absorptivity of these color systems were 1.38 × 10 5, 1.01 × 10 5, 3.24 × 10 5, 1.07 × 10 5 and 1.29 × 10 5 L mol -1 cm -1. The method developed in this paper has advantages in selectivity, sensitivity, operation and can effectively resolve spectra overlapping problem. This method has been applied to determine the real samples with satisfactory results.

  8. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; determination of low-level silver by graphite furnace atomic absorption spectrophotometry

    USGS Publications Warehouse

    Damrau, D.L.

    1993-01-01

    Increased awareness of the quality of water in the United States has led to the development of a method for determining low levels (0.2-5.0 microg/L) of silver in water samples. Use of graphite furnace atomic absorption spectrophotometry provides a sensitive, precise, and accurate method for determining low-level silver in samples of low ionic-strength water, precipitation water, and natural water. The minimum detection limit determined for low-level silver is 0.2 microg/L. Precision data were collected on natural-water samples and SRWS (Standard Reference Water Samples). The overall percent relative standard deviation for natural-water samples with silver concentrations more than 0.2 microg/L was less than 40 percent throughout the analytical range. For the SRWS with concentrations more than 0.2 microg/L, the overall percent relative standard deviation was less than 25 percent throughout the analytical range. The accuracy of the results was determined by spiking 6 natural-water samples with different known concentrations of the silver standard. The recoveries ranged from 61 to 119 percent at the 0.5-microg/L spike level. At the 1.25-microg/L spike level, the recoveries ranged from 92 to 106 percent. For the high spike level at 3.0 microg/L, the recoveries ranged from 65 to 113 percent. The measured concentrations of silver obtained from known samples were within the Branch of Quality Assurance accepted limits of 1 1/2 standard deviations on the basis of the SRWS program for Inter-Laboratory studies.

  9. Simultaneous determination of Cu2+, Zn2+, Cd2+, Hg2+ and Pb2+ by using second-derivative spectrophotometry method.

    PubMed

    Han, Yanyan; Li, Yan; Si, Wei; Wei, Dong; Yao, Zhenxing; Zheng, Xianpeng; Du, Bin; Wei, Qin

    2011-09-01

    A new method of simultaneous determination of Cu2+, Zn2+, Cd2+, Hg2+ and Pb2+ is proposed here by using the second-derivative spectrophotometry method. In pH=10.35 Borax-NaOH buffer, using meso-tetra (3-methoxyl-4-hydroxylphenyl) porphyrin ([T-(3-MO-4-HP)P]) as chromomeric reagent, micelle solution was formed after Tween-80 surfactant was added into the solution containing Cu2+, Zn2+, Cd2+, Hg2+ and Pb2+ ions. The original absorption spectrum of the above complexes was obtained after heating in the boiling water for 25 min. The second-derivative absorption peaks of five metal-porphyrin complexes can be separated from the original absorption spectrum by using chemometric tool. In this way, Cu2+, Zn2+, Cd2+, Hg2+ and Pb2+ ions can be determined simultaneously. Under the optimal conditions, the linear ranges of the calibration curve were 0-0.60, 0-0.60, 0-0.40, 0-0.80 and 0-0.48 μg mL(-1) for Cu2+, Zn2+, Cd2+, Hg2+ and Pb2+, respectively. The molar absorptivity of these color systems were 1.38×10(5), 1.01×10(5), 3.24×10(5), 1.07×10(5) and 1.29×10(5)Lmol(-1)cm(-1). The method developed in this paper has advantages in selectivity, sensitivity, operation and can effectively resolve spectra overlapping problem. This method has been applied to determine the real samples with satisfactory results. PMID:21664176

  10. HST/COS FUV Spectrophotometry of the Key Binary Solar Twins 16 Cyg A&B: Astrophysical Laboratories for the Future Sun and Older Solar Analogs

    NASA Astrophysics Data System (ADS)

    Guinan, Edward

    2014-10-01

    The fortuitous location of the wide G1.5V/G2.5V binary 16 Cyg A&B as the brightest stars in the Kepler Field is a "game changer," permitting the determination of the stars' fundamental properties from asteroseismolgy analyses. Recent studies returned precise determinations of the stars' basic properties including masses and age (6.8+/-0.4 Gyr), along with the rotation periods. Thus, 16 Cyg A&B are now the oldest solar-mass analogs with reliable ages and physical properties. Only the Sun has better determined physical properties. 16 Cyg A&B now serve as old-age anchors for Rotation-Age-Activity-Irradiance relations (and Gyrochronology studies) for solar-type stars. Extensive Ca II HK spectrophotometry reveals low levels of chromospheric emission are below the lowest values for our Sun. These stars serve as critical test beds for studying solar/stellar dynamos for stars less active than the Sun. These advances have catapulted 16 Cyg A&B into a prominent place in solar/stellar astrophysics for studying the evolution, internal structure, magnetic dynamos, angular momentum loss, and FUV irradiances of old solar-mass stars. Although 16 Cyg has been observed from X-ray - IR, there are no observations in the FUV region where most of the crucial diagnostic chromospheric & transition region emissions occur. We request COS FUV medium resolution (G130M, G160M) spectra (six orbits/star). This permits the important FUV (1150-1750A) line emission strengths, profiles and Doppler shifts to be analyzed and compared with the Sun and other solar-analogs. This program is complemented by Ca II HK, high precision uvby observations, and by proposed Chandra X-ray coronal observations.

  11. First light of the VLT planet finder SPHERE. III. New spectrophotometry and astrometry of the HR 8799 exoplanetary system

    NASA Astrophysics Data System (ADS)

    Zurlo, A.; Vigan, A.; Galicher, R.; Maire, A.-L.; Mesa, D.; Gratton, R.; Chauvin, G.; Kasper, M.; Moutou, C.; Bonnefoy, M.; Desidera, S.; Abe, L.; Apai, D.; Baruffolo, A.; Baudoz, P.; Baudrand, J.; Beuzit, J.-L.; Blancard, P.; Boccaletti, A.; Cantalloube, F.; Carle, M.; Cascone, E.; Charton, J.; Claudi, R. U.; Costille, A.; de Caprio, V.; Dohlen, K.; Dominik, C.; Fantinel, D.; Feautrier, P.; Feldt, M.; Fusco, T.; Gigan, P.; Girard, J. H.; Gisler, D.; Gluck, L.; Gry, C.; Henning, T.; Hugot, E.; Janson, M.; Jaquet, M.; Lagrange, A.-M.; Langlois, M.; Llored, M.; Madec, F.; Magnard, Y.; Martinez, P.; Maurel, D.; Mawet, D.; Meyer, M. R.; Milli, J.; Moeller-Nilsson, O.; Mouillet, D.; Origné, A.; Pavlov, A.; Petit, C.; Puget, P.; Quanz, S. P.; Rabou, P.; Ramos, J.; Rousset, G.; Roux, A.; Salasnich, B.; Salter, G.; Sauvage, J.-F.; Schmid, H. M.; Soenke, C.; Stadler, E.; Suarez, M.; Turatto, M.; Udry, S.; Vakili, F.; Wahhaj, Z.; Wildi, F.; Antichi, J.

    2016-03-01

    Context. The planetary system discovered around the young A-type HR 8799 provides a unique laboratory to: a) test planet formation theories; b) probe the diversity of system architectures at these separations, and c) perform comparative (exo)planetology. Aims: We present and exploit new near-infrared images and integral-field spectra of the four gas giants surrounding HR 8799 obtained with SPHERE, the new planet finder instrument at the Very Large Telescope, during the commissioning and science verification phase of the instrument (July-December 2014). With these new data, we contribute to completing the spectral energy distribution (SED) of these bodies in the 1.0-2.5 μm range. We also provide new astrometric data, in particular for planet e, to further constrain the orbits. Methods: We used the infrared dual-band imager and spectrograph (IRDIS) subsystem to obtain pupil-stabilized, dual-band H2H3 (1.593 μm, 1.667 μm), K1K2 (2.110 μm, 2.251 μm), and broadband J (1.245 μm) images of the four planets. IRDIS was operated in parallel with the integral field spectrograph (IFS) of SPHERE to collect low-resolution (R ~ 30), near-infrared (0.94-1.64 μm) spectra of the two innermost planets HR 8799 d and e. The data were reduced with dedicated algorithms, such as the Karhunen-Loève image projection (KLIP), to reveal the planets. We used the so-called negative planets injection technique to extract their photometry, spectra, and measure their positions. We illustrate the astrometric performance of SPHERE through sample orbital fits compatible with SPHERE and literature data. Results: We demonstrated the ability of SPHERE to detect and characterize planets in this kind of systems, providing spectra and photometry of its components. The spectra improve upon the signal-to-noise ratio of previously obtained data and increase the spectral coverage down to the Y band. In addition, we provide the first detection of planet e in the J band. Astrometric positions for planets

  12. In vitro DNA binding studies of anticancer drug idarubicin using spectroscopic techniques.

    PubMed

    Ozluer, Can; Kara, Hayriye Eda Satana

    2014-09-01

    The interaction between idarubicin and double stranded deoxyribonucleic acid (ds-DNA) was investigated by UV-VIS spectrophotometry, fluorescence and Raman spectroscopy techniques. The absorption spectra of idarubicin with ds-DNA showed a slight red shift and hypochromic effect. In the fluorescence experiments, emission peaks were decreased by adding ds-DNA. Using ethidium bromide (ETB) as a fluorescence probe, fluorescence quenching of the emission peak was observed in the ETB-DNA system when idarubicin was added. Moreover, similar results were obtained in Raman spectroscopy. Binding constants of idarubicin with ds-DNA were determined as 5.14×10(5) M(-1) and 5.8×10(5) M(-1) for UV-VIS spectrophotometry and fluorescence spectroscopy, respectively. The large binding constant indicated that idarubicin has a high affinity with ds-DNA. All the evidences indicated that the binding mode of idarubicin with DNA was an intercalative binding. Furthermore, quantitative determination of idarubicin in pharmaceutical formulation was done. PMID:24911270

  13. Classification of commercial wines from the Canary Islands (Spain) by chemometric techniques using metallic contents.

    PubMed

    Frías, Sergio; Conde, José E; Rodríguez-Bencomo, Juan J; García-Montelongo, Francisco; Pérez-Trujillo, Juan P

    2003-02-01

    Eleven elements, K, Na, Ca, Mg, Fe, Cu, Zn, Mn, Sr, Li and Rb, were determined in dry and sweet wines bearing the denominations of origin of El Hierro, La Palma and Lanzarote islands (Canary Islands, Spain). Analyses were performed by flame atomic absorption spectrophotometry, with the exceptions of lithium and rubidium for which flame atomic emission spectrophotometry was used. Sweet wines from La Palma were elaborated as naturally sweet with over-ripe grapes and significant differences were found in all the analysed elements with the exceptions of sodium, iron and rubidium with regard to dry wines from the same island. Contrarily, sweet wines from Lanzarote elaborated with grapes in a similar ripening state to dry wines did not present significant differences between them with the exception of strontium, the content of which was greater in dry wines. Among the three islands, significant differences in mean content were found with the exceptions of iron and copper. Cluster analysis and principal component analysis show differences in wines according to the island of origin and the ripening state of the grapes. Linear discriminant analysis using rubidium, sodium, manganese and strontium, the four most discriminant elements, gave 100% recognition ability and 95.6% prediction ability. The sensitivity and specificity obtained using soft independent modelling of class analogy (SIMCA) as a modelling multivariate technique were both 100% for El Hierro and Lanzarote, and 100 and 95%, respectively, for La Palma. The modelling and discriminant capacities of the different metals were also studied. PMID:18968916

  14. SPECTROPHOTOMETRY OF THE HUYGENS REGION OF THE ORION NEBULA, THE EXTENDED ORION NEBULA, AND M 43: SCATTERED LIGHT SYSTEMATICALLY DISTORTS CONDITIONS DERIVED FROM EMISSION LINES

    SciTech Connect

    O'Dell, C. R.; Harris, Jessica A. E-mail: jessica.a.harris@vanderbilt.ed

    2010-10-15

    We report on medium resolution spectrophotometry of the Orion Nebula region, including for the first time the Extended Orion Nebula (EON) and the nearby M 43. The 49 long-slit observations were divided into 99 smaller samples, which have allowed determinations of the amount of extinction, extinction-corrected H{beta} surface brightness, electron temperatures (from [S II], [N II], and [O III]), and electron densities (from [S II] and [Cl III]) throughout much of this complex region. We verify an earlier conclusion from a radio/optical study that beyond about 5' from {theta}{sup 1}Ori C local emission begins to be contaminated by scattering of light from the much brighter central Huygens region of M 42, and this scattered light component becomes dominant at large distances. This contamination means that the derived properties for the outer regions are not accurate. From comparison of the light from the dominant star in M 43 with the continuum of that nebula (which is almost entirely scattered starlight), it is determined that scattered light is enhanced in the blue, which can lead to observed Balmer line ratios that are theoretically impossible and erroneous electron temperatures. This blue scattering of emission lines is important even in the Huygens region because it means that at anything except very high spectroscopic resolution the observed lines are a blend of the original and scattered light, with shorter wavelength lines being artificially enhanced. This can lead to overestimates of the electron temperatures derived from the nebular and auroral line ratios of forbidden lines. This phenomenon is probably applicable to many other H II regions. We have been able to use extinction-insensitive line ratios, the extinction-corrected surface brightness in H{beta}, and the equivalent width of the continuum to create for the first time a three-dimensional model of the entire M 42, EON, and M 43 region. This is an irregular concave blister of ionized gas bounded on the

  15. Spectrophotometry of the Huygens Region of the Orion Nebula, the Extended Orion Nebula, and M 43: Scattered Light Systematically Distorts Conditions Derived from Emission Lines

    NASA Astrophysics Data System (ADS)

    O'Dell, C. R.; Harris, Jessica A.

    2010-10-01

    We report on medium resolution spectrophotometry of the Orion Nebula region, including for the first time the Extended Orion Nebula (EON) and the nearby M 43. The 49 long-slit observations were divided into 99 smaller samples, which have allowed determinations of the amount of extinction, extinction-corrected Hβ surface brightness, electron temperatures (from [S II], [N II], and [O III]), and electron densities (from [S II] and [Cl III]) throughout much of this complex region. We verify an earlier conclusion from a radio/optical study that beyond about 5' from θ1Ori C local emission begins to be contaminated by scattering of light from the much brighter central Huygens region of M 42, and this scattered light component becomes dominant at large distances. This contamination means that the derived properties for the outer regions are not accurate. From comparison of the light from the dominant star in M 43 with the continuum of that nebula (which is almost entirely scattered starlight), it is determined that scattered light is enhanced in the blue, which can lead to observed Balmer line ratios that are theoretically impossible and erroneous electron temperatures. This blue scattering of emission lines is important even in the Huygens region because it means that at anything except very high spectroscopic resolution the observed lines are a blend of the original and scattered light, with shorter wavelength lines being artificially enhanced. This can lead to overestimates of the electron temperatures derived from the nebular and auroral line ratios of forbidden lines. This phenomenon is probably applicable to many other H II regions. We have been able to use extinction-insensitive line ratios, the extinction-corrected surface brightness in Hβ, and the equivalent width of the continuum to create for the first time a three-dimensional model of the entire M 42, EON, and M 43 region. This is an irregular concave blister of ionized gas bounded on the outside by apparent

  16. Photoelectric spectrophotometry of radio galaxies

    NASA Technical Reports Server (NTRS)

    Yee, H. K. C.; Oke, J. B.

    1978-01-01

    The absolute energy distributions from 3200 to 10,000 A of 26 3CR radio galaxies are determined on the basis of spectrophotometric observations with the multichannel spectrometer of the Hale 5-m telescope. It is found that there is a continuous range of emission-line characteristics and UV excess in the sample and that a strong correlation exists between the nonthermal component luminosity and hydrogen emission, which favors the hypothesis that direct photoionization by the nuclear radiation is responsible for the emission lines observed. Calculations are performed which show that in almost all cases the power-law component model provides sufficient UV photons to produce the observed H-beta line. Indications are obtained that the optical nuclear component is related to the radio emission in some complex manner and that strong radio galaxies tend to be accompanied by UV excess and emission lines.

  17. Ultraviolet spectrophotometry of three LINERs

    NASA Technical Reports Server (NTRS)

    Goodrich, R. W.; Keel, W. C.

    1986-01-01

    Three galaxies known to be LINERs were observed spectroscopically in the ultraviolet in an attempt to detect the presumed nonthermal continuum source thought to be the source of photoionization in the nuclei. NGC 4501 was found to be too faint for study with the IUE spectrographs, while NGC 5005 had an extended ultraviolet light profile. Comparison with the optical light profile of NGC 5005 indicates that the ultraviolet source is distributed spatially in the same manner as the optical starlight, probably indicating that the ultraviolet excess is due to a component of hot stars in the nucleus. These stars contribute detectable absorption features longward of 2500 A; together with optical data, the IUE spectra suggest a burst of star formation about 1 billion yr ago, with a lower rate continuing to produce a few OB stars. In NGC 4579, a point source contributing most of the ultraviolet excess is found that is much different than the optical light distribution. Furthermore, the ultraviolet to X-ray spectral index in NGC 4579 is 1.4, compatible with the UV to X-ray indices found for samples of Seyfert galaxies. This provides compelling evidence for the detection of the photoionizing continuum in NGC 4579 and draws the research fields of normal galaxies and active galactic nuclei closer together. The emission-line spectrum of NGC 4579 is compared with calculations from a photoionization code, CLOUDY, and several shock models. The photoionization code is found to give superior results, adding to the increasing weight of evidence that the LINER phenomenon is essentially a scaled-down version of the Seyfert phenomenon.

  18. Ultraviolet spectrophotometry of degenerate stars

    NASA Technical Reports Server (NTRS)

    Greenstein, J. L.; Oke, J. B.

    1979-01-01

    Observations of one helium- and three hydrogen-atmosphere degenerates made with the International Ultraviolet Explorer are discussed. Fluxes in the UV give temperatures in good accordance with those determined from the ground and from the ANS satellite data. Profiles of the strong L-alpha absorption in two DA's fit predictions for the expected temperatures. Gravity determination is vitiated by their steep temperature dependence. If one accepts that theoretical predictions should be correct, corrections to the absolute IUE calibration derived are an upward shift of 3-5%, with irregular residuals attaining + or - 7%.

  19. Submillimeter spectrophotometry in the Pamirs

    NASA Astrophysics Data System (ADS)

    Maslow, I. A.; Soglasnova, V. A.; Sholomitskij, G. B.; Gromov, V. D.; Nikolskij, U. V.; Maslennikov, K. L.

    1989-07-01

    Observations of planets, interstellar molecular-dust clouds (zones of active star formation), and galaxies were carried out at several submillimeter-range wavelengths mainly in the 0.34 mm 'transparency window'. The brightness temperatures were measured and the parameters of the brightness distribution of the radiation in the extended sources were estimated. For the brightest sources, the results are in agreement with measurements obtained earlier.

  20. Multichannel spectrophotometry of stellar flares

    NASA Technical Reports Server (NTRS)

    Mochnacki, S. W.; Zirin, H.

    1980-01-01

    Stellar flares have been observed using the 32 channel spectrophotometer on the 5 m telescope. Net flare fluxes in the region 3200-7000 A are presented. A simple model of blackbody radiation and hydrogen recombination emission appears to fit the continuum points well. Owing to vignetting problems, only the region between 4200 and 7000 A was used for a detailed fit to the Planck function to obtain apparent temperatures and effective areas. The rise of each flare was associated with an increase of the area, while the initial steep decline of the light was associated with a similar decrease of the blackbody temperature. The maximum temperatures, coincident with maximum light, were 7500-9500 K, similar to values for solar flares. The hydrogen line emission rose simultaneously with the continuum but declined more slowly. The ratio of H sub gamma to H sub alpha was about 1.5 at the peak, declining to about 1.0 after the peak.

  1. Synoptic Spectrophotometry Enabled by SMARTS

    NASA Astrophysics Data System (ADS)

    Walter, Frederick M.

    2011-05-01

    The photometric record for many types of astrophysical objects is remarkably fecund, due to a growing body of synoptic photometric surveys. The same cannot be said for the spectroscopic record, despite the fact that much of the astrophysics requires spectroscopy, rather than photometry, to decipher. I shall report on selected topics I've been studying over the past 7 years, using the SMARTS/CTIO 1.5m telescope to obtain long time series on interesting stars. The venerable RC spectrograph offers resolutions from 300 to 3000 km/s, and can obtain useful spectra from magnitudes 0 to 18 (for emission line objects) in less than an hour. The capabilities of the echelle spectrograph greatly expand the scope of the science. I shall touch on science topics ranging from long term evolution of classical and recurrent novae, the accretion-induced activity in T Tauri stars and cataclysmic variables, to the orbits of O stars.

  2. Quantitative estimation of diacerein in bulk and in capsule formulation using hydrotropic solubilizing agents by UV-spectrophotometry and the first order derivative using the area under curve method

    PubMed Central

    Pandey, Ramchandra; Patil, Pravin O.; Patil, Manohar U.; Deshmukh, Prashant K.; Bari, Sanjay B.

    2012-01-01

    Purpose: This study was designed to develop and validate two simple, rapid, and economical UV-spectrophotometric and the first-order derivative methods using the area under curve method for estimation of diacerein in bulk and in capsule formulation. Materials and Methods: In this study, hydrotrophic solution of 8 M urea and 0.5 M potassium citrate were employed as the solubilizing agent to solubilize a poorly water-soluble drug, diacerein. In the UV-spectrophotometry method, two wavelengths 252.0 nm and 266.2 nm and in the first-order derivative spectrophotometric methods two wavelengths 259.4 nm and 274.2 nm in 8 M urea and two wavelengths 247.8 nm and 267.4 nm in the UV-spectrophotometry method and in the first-order derivative spectrophotometric methods two wavelengths 259.2 nm and 274.2 nm in 0.5 M potassium citrate were selected for determination of areas. Results: Hydrotrophic agents used did not interfere in spectrophotometric analysis of diacerein. Diacerein followed linearity in the concentration range of 2–12 μg/mL with a coefficient correlation of 0.999 for both methods. Conclusion: The amount of drugs estimated by both proposed methods are in good accord with label claim. The % RSD value in recovery, precision, and ruggedness studies are found to be less than 2 indicate that the method is accurate, precise, and rugged. PMID:23781470

  3. Analytical techniques: A compilation

    NASA Technical Reports Server (NTRS)

    1975-01-01

    A compilation, containing articles on a number of analytical techniques for quality control engineers and laboratory workers, is presented. Data cover techniques for testing electronic, mechanical, and optical systems, nondestructive testing techniques, and gas analysis techniques.

  4. Spectrophotometry of (32) Pomona, (145) Adeona, (704) Interamnia, (779) Nina, (330825) 2008 XE3, and 2012 QG42 and laboratory study of possible analog samples

    NASA Astrophysics Data System (ADS)

    Busarev, Vladimir V.; Barabanov, Sergey I.; Rusakov, Vyacheslav S.; Puzin, Vasiliy B.; Kravtsov, Valery V.

    2015-12-01

    Six asteroids including two NEAs, one of which is PHA, accessible for observation in September 2012 were investigated using a low-resolution (R ≈ 100) spectrophotometry in the range 0.35-0.90 μm with the aim to study features of their reflectance spectra. A high-altitude position of our Terskol Observatory (3150 m above sea level) favorable for the near-UV and visible-range observations of celestial objects allowed us to probably detect some new spectral features of the asteroids. Two subtle absorption bands centered at 0.53 and 0.74 μm were found in the reflectance spectra of S-type (32) Pomona and interpreted as signs of presence of pyroxenes in the asteroid surface matter and its different oxidation. Very similar absorption bands centered at 0.38, 0.44 and 0.67-0.71 μm have been registered in the reflectance spectra of (145) Adeona, (704) Interamnia, and (779) Nina of primitive types. We performed laboratory investigations of ground samples of known carbonaceous chondrites, Orguel (CI), Mighei (CM2), Murchison (CM2), Boriskino (CM2), and seven samples of low-iron Mg serpentines as possible analogs of the primitive asteroids. In the course of this work, we discovered an intense absorption band (up to ∼25%) centered at 0.44 μm in reflectance spectra of the low-Fe serpentine samples. As it turned out, the equivalent width of the band has a high correlation with content of Fe3+ (octahedral and tetrahedral) in the samples. It may be considered as a confirmation of the previously proposed mechanism of the absorption due to electronic transitions in exchange-coupled pairs (ECP) of Fe3+ neighboring cations. It means that the absorption feature can be used as an indicator of ferric iron in oxidized and hydrated low-Fe compounds on the surface of asteroids and other atmosphereless celestial bodies. Moreover, our measurements showed that the mechanism of light absorption is partially or completely blocked in the case of intermediate to high iron contents. Therefore

  5. Spectrophotometry, colors, and photometric properties of the 67P/Churyumov-Gerasimenko nucleus from the OSIRIS instrument onboard the ROSETTA mission

    NASA Astrophysics Data System (ADS)

    Fornasier, Sonia; Hasselmann, Pedro; Feller, Clement; Barucci, Maria Antonietta; Lara, Luisa; Oklay, Nilda; Tubiana, Cecilia; Besse, Sebastien; Scholten, Frank; Sierks, Holger; Leyrat, Cedric; La Forgia, Fiorangela; Lazzarin, Monica; Pajola, Maurizio; Thomas, Nick; Pommerol, Antoine; Massironi, Matteo

    2015-04-01

    between the two lobes of the comet, and is both the most active and brightest surface on the comet. This region has a bluer spectral slope than the darker regions that we interpret being caused by a higher abundance of water ice in the surface composition, although we note that no water ice absorption bands have been detected with the VIRTIS infrared imaging spectrometer during the August-September observations at resolutions of 15-25 m/px (Capaccioni et al. 2015). The absence of large areas of water ice rich mixtures in VIRTIS data may be attributed to their lower spatial resolution than the OSIRIS images, together with the presence of non-volatile materials that may mask the water ice spectral absorptions. We will present the results of the global photometric properties in several filters, derived using the Hapke model, together with the analysis of the local colors spectrophotometry, and albedo variations of the 67P nucleus. This unique data set places further constraints on the origin and distribution of cometary activity on the surface. References: Capaccioni et al, 2015, Science, in press Sierks et al, 2015, Science, in press Thomas et al., 2015, Science, in press

  6. Comparison of Hydrogen Sulfide Analysis Techniques

    ERIC Educational Resources Information Center

    Bethea, Robert M.

    1973-01-01

    A summary and critique of common methods of hydrogen sulfide analysis is presented. Procedures described are: reflectance from silver plates and lead acetate-coated tiles, lead acetate and mercuric chloride paper tapes, sodium nitroprusside and methylene blue wet chemical methods, infrared spectrophotometry, and gas chromatography. (BL)

  7. Electrooptical remote sensing methods as nondestructive testing and measuring techniques in agriculture.

    PubMed

    Myers, V I; Allen, W A

    1968-09-01

    Characteristics of plants that influence reflectance and emission of electromagnetic energy are discussed. Four main spectral regions are influenced by plants. These wavelength bands include the visible region of chlorophyll absorption, very near ir wavelengths, where plant structure is of major importance, the near and middle ir wavelengths, where water and CO(2) absorption predominate, and the far ir region of thermal ir emission. Soil characteristics that influence reflectance and emission of energy are discussed. Nondestructive testing techniques described include laboratory spectrophotometry, field spectrometry, color photography, radiometry, and generation of line scan imagery. Spectrophotometer and spectrometer reflectance data obtained in the laboratory and field are related to interpretation of remote sensing imagery. Model studies that permit predictions of reflectance from plant canopies are described. The principle of multispectral sensing which permits utilization of multiple wavelength channels for establishing unique plant and soil signature is reviewed. PMID:20068888

  8. Aerodynamic measurement techniques. [laser based diagnostic techniques

    NASA Technical Reports Server (NTRS)

    Hunter, W. W., Jr.

    1976-01-01

    Laser characteristics of intensity, monochromatic, spatial coherence, and temporal coherence were developed to advance laser based diagnostic techniques for aerodynamic related research. Two broad categories of visualization and optical measurements were considered, and three techniques received significant attention. These are holography, laser velocimetry, and Raman scattering. Examples of the quantitative laser velocimeter and Raman scattering measurements of velocity, temperature, and density indicated the potential of these nonintrusive techniques.

  9. Aquisição de Estreptococos Mutans e Desenvolvimento de Cárie Dental em Primogênitos

    PubMed Central

    NOCE, Erica; RUBIRA, Cassia Maria Fischer; da Silva ROSA, Odila Pereira; da SILVA, Salete Moura Bonifácio; BRETZ, Walter Antonio

    2011-01-01

    Objetivo Avaliar o momento de aquisição de estreptococos mutans (EM), desenvolvimento de cárie dental e as variáveis a eles associadas no decorrer de 23 meses, em primogênitos de famílias de baixo nível socioeconômico, desde os sete meses de idade. Método A amostra foi selecionada com base em mães densamente colonizadas por EM, incluindo todos os membros de 14 famílias que conviviam na mesma casa. Foram envolvidos no estudo 14 mães, pais e primogênitos e 8 parentes, na maioria avós. Exames clínicos e radiográficos iniciais determinaram os índices de cárie e condição periodontal dos adultos. Contagens de EM foram feitas em todos os adultos nas duas primeiras visitas. Nas crianças foram avaliados os níveis de EM, o número de dentes e de cáries, em quatro visitas. Resultados A prevalência de EM nos adultos foi alta, estando ausente em apenas um dos pais. EM foram detectados em 1, 2, 3 e 10 crianças, respectivamente nas visitas #1, 2, 3 e 4. A cárie dental foi detectada em apenas três crianças na última visita (aos 30 meses de idade), as quais apresentaram escores de EM significantemente maiores que as crianças sem cárie, na mesma visita. Conclusão Exclusivamente a condição social de baixa renda e mães densamente colonizadas por EM não são sinônimo de colonização precoce e alta atividade de cárie em crianças cuidadas em casa. O desenvolvimento de cárie está significantemente associado a escores elevados de EM nas crianças. PMID:22022218

  10. Color alteration in teeth subjected to different bleaching techniques

    NASA Astrophysics Data System (ADS)

    Briso, A. L. F.; Fonseca, M. S. M.; de Almeida, L. C. A. G.; Mauro, S. J.; Dos Santos, P. H.

    2010-12-01

    This study evaluated the color alteration of teeth subjected to the action of different bleaching agents and the influence of light sources commonly used in association with these products, In GI, the specimens remained immersed in artificial saliva. The specimens in GII were bleached with a 10% carbamide peroxide gel 4 hours/day during 3 weeks; the teeth in the other three groups were subjected to three sessions of three 10-min applications of 35% hydrogen peroxide gel at 7-day intervals. In GIII, no light was used, while in GIV and GV the gel was associated with a quartz-tungsten-halogen light and a LED/laser source, respectively. The teeth color was evaluated before and 7 days after the bleaching sessions by reflectance spectrophotometry. Data were analyzed statistically by ANOVA and Fisher's test (α = 0.05), and showed that a significant color change was obtained in all treated groups. After the first week of treatment and at the end of it, the bleaching protocols showed similar results. The results of the present study indicate that association of a light source is not necessary to obtain the bleaching effect and that optimal bleaching can be achieved with all techniques tested.

  11. Ultrasound-assisted ionic liquid-based dispersive liquid-liquid microextraction for preconcentration of patent blue V and its determination in food samples by UV-visible spectrophotometry.

    PubMed

    Unsal, Yunus Emre; Soylak, Mustafa; Tuzen, Mustafa

    2015-04-01

    Ultrasound-assisted ionic liquid-based dispersive liquid-liquid microextraction procedure (UA-IL-DLLME) was developed for determination of trace levels of patent blue V prior to its determination by UV-visible spectrophotometry. Patent blue V was extracted from 25-mL sample into a 100-μL volume of ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]), with the aid of sonication in an ultrasonic bath. Several variables affecting microextraction efficiency were optimized. Under the optimum experimental conditions, the detection limit (3 s) was 0.68 μg L(-1), and the preconcentration factor was 100. The relative standard deviation for six replicate determinations of patent blue V was 4.5%. The method was applied to the determination of patent blue V in food samples. The proposed procedure is effective, very simple, and fast. PMID:25800367

  12. O que bilíngues bimodais têm a nos dizer sobre desenvolvimento bilíngue?

    PubMed Central

    de Quadros, Ronice Müller; Lillo-Martin, Diane; Pichler, Deborah Chen

    2013-01-01

    O objetivo deste trabalho é apresentar o que as pesquisas que estamos desenvolvendo com crianças ouvintes, filhas de pais surdos, adquirindo Língua Brasileira de Sinais (Libras) e Português e Língua de Sinais Americana (ASL) e Inglês (Lillo-Martin et al. 2010) têm a nos dizer sobre desenvolvimento bilíngue. Os dados deste estudo fazem parte de um banco de dados de interações espontâneas coletadas longitudinalmente, alternando contextos de aquisição da Libras e do português como língua alvo, no Brasil e dados coletados longitudinalmente. nos mesmos contextos, de crianças adquirindo ASL e inglês1. Além disso, há também dados do estudo experimental com testes aplicados nos dois pares de línguas que se agregam ao presente estudo. Uma visão geral dos estudos desenvolvidos sobre a aquisição bilíngue bimodal por crianças ouvintes, filhas de pais surdos, será apresentada e, então, serão expostos alguns aspectos linguísticos deste tipo de aquisição, considerando as discussões sobre aquisição bilíngue a partir da pesquisa realizada. PMID:24431480

  13. Kinetics, Reaction Orders, Rate Laws, and Their Relation to Mechanisms: A Hands-On Introduction for High School Students Using Portable Spectrophotometry

    ERIC Educational Resources Information Center

    Carraher, Jack M.; Curry, Sarah M.; Tessonnier, Jean-Philippe

    2016-01-01

    Teaching complex chemistry concepts such as kinetics using inquiry-based learning techniques can be challenging in a high school classroom setting. Access to expensive laboratory equipment such as spectrometers is typically limited and most reaction kinetics experiments have been designed for advanced placement (AP) or first-year undergraduate…

  14. Optical microscopy as a comparative analytical technique for single-particle dissolution studies.

    PubMed

    Svanbäck, Sami; Ehlers, Henrik; Yliruusi, Jouko

    2014-07-20

    Novel, simple and cost effective methods are needed to replace advanced chemical analytical techniques, in small-scale dissolution studies. Optical microscopy of individual particles could provide such a method. The aim of the present work was to investigate and verify the applicability of optical microscopy as an analytical technique for drug dissolution studies. The evaluation was performed by comparing image and chemical analysis data of individual dissolving particles. It was shown that the data obtained by image analysis and UV-spectrophotometry produced practically identical dissolution curves, with average similarity and difference factors above 82 and below 4, respectively. The relative standard deviation for image analysis data, of the studied particle size range, varied between 1.9% and 3.8%. Consequently, it is proposed that image analysis can be used, on its own, as a viable analytical technique in single-particle dissolution studies. The possibility for significant reductions in sample preparation, operational cost, time and substance consumption gives optical detection a clear advantage over chemical analytical methods. Thus, image analysis could be an ideal and universal analytical technique for rapid small-scale dissolution studies. PMID:24751345

  15. The radiocarbon hydroxyl technique

    NASA Technical Reports Server (NTRS)

    Campbell, Malcolm J.; Sheppard, John C.

    1994-01-01

    The Radiocarbon Technique depends upon measuring the rate of oxidation of CO in an essentially unperturbed sample of air. The airborne technique is slightly different. Hydroxyl concentrations can be calculated directly; peroxyl concentrations can be obtained by NO doping.

  16. Nondestructive evaluation technique guide

    NASA Technical Reports Server (NTRS)

    Vary, A.

    1973-01-01

    A total of 70 individual nondestructive evaluation (NDE) techniques are described. Information is presented that permits ease of comparison of the merits and limitations of each technique with respect to various NDE problems. An NDE technique classification system is presented. It is based on the system that was adopted by the National Materials Advisory Board (NMAB). The classification system presented follows the NMAB system closely with the exception of additional categories that have been added to cover more advanced techniques presently in use. The rationale of the technique is explained. The format provides for a concise description of each technique, the physical principles involved, objectives of interrogation, example applications, limitations of each technique, a schematic illustration, and key reference material. Cross-index tabulations are also provided so that particular NDE problems can be referred to appropriate techniques.

  17. Seals and Sealing Techniques

    NASA Technical Reports Server (NTRS)

    1972-01-01

    Developments by the aerospace industry in seals and sealing techniques are announced for possible use in other areas. The announcements presented are grouped as: sealing techniques for cryogenic fluids, high pressure applications, and modification for improved performance.

  18. Comparison of inert-gas-fusion and modified Kjeldahl techniques for determination of nitrogen in niobium alloys

    NASA Technical Reports Server (NTRS)

    Merkle, E. J.; Graab, J. W.; Davis, W. F.

    1974-01-01

    This report compares results obtained for the determination of nitrogen in a selected group of niobium-base alloys by the inert-gas-fusion and the Kjeldahl procedures. In the inert-gas-fusion procedure the sample is heated to approximately 2700 C in a helium atmosphere in a single-use graphite crucible. A platinum flux is used to facilitate melting of the sample. The Kjeldahl method consisted of a rapid decomposition with a mixture of hydrofluoric acid, phosphoric acid, and potassium chromate; distillation in the presence of sodium hydroxide; and highly sensitive spectrophotometry with nitroprusside-catalyzed indophenol. In the 30- to 80-ppm range, the relative standard deviation was 5 to 7 percent for the inert-gas-fusion procedure and 2 to 8 percent for the Kjeldahl procedure. The agreement of the nitrogen results obtained by the two techniques is considered satisfactory.

  19. Two-dimensional and 3-D images of thick tissue using time-constrained times-of-flight and absorbance spectrophotometry

    NASA Astrophysics Data System (ADS)

    Benaron, David A.; Lennox, M.; Stevenson, David K.

    1992-05-01

    Reconstructing deep-tissue images in real time using spectrophotometric data from optically diffusing thick tissues has been problematic. Continuous wave applications (e.g., pulse oximetry, regional cerebral saturation) ignore both the multiple paths traveled by the photons through the tissue and the effects of scattering, allowing scalar measurements but only under limited conditions; interferometry works poorly in thick, highly-scattering media; frequency- modulated approaches may not allow full deconvolution of scattering and absorbance; and pulsed-light techniques allow for preservation of information regarding the multiple paths taken by light through the tissue, but reconstruction is both computation intensive and limited by the relative surface area available for detection of photons. We have developed a picosecond times-of-flight and absorbance (TOFA) optical system, time-constrained to measure only photons with a narrow range of path lengths and arriving within a narrow angel of the emitter-detector axis. The delay until arrival of the earliest arriving photons is a function of both the scattering and absorbance of the tissues in a direct line between the emitter and detector, reducing the influence of surrounding tissues. Measurement using a variety of emitter and detector locations produces spatial information which can be analyzed in a standard 2-D grid, or subject to computer reconstruction to produce tomographic images representing 3-D structure. Using such a technique, we have been able to demonstrate the principles of tc-TOFA, detect and localize diffusive and/or absorptive objects suspended in highly scattering media (such as blood admixed with yeast), and perform simple 3-D reconstructions using phantom objects. We are now attempting to obtain images in vivo. Potential future applications include use as a research tool, and as a continuous, noninvasive, nondestructive monitor in diagnostic imaging, fetal monitoring, neurologic and cardiac

  20. Multiple imaging techniques demonstrate the manipulation of surfaces to reduce bacterial contamination and corrosion.

    PubMed

    Arnold, J W; Boothe, D H; Suzuki, O; Bailey, G W

    2004-12-01

    Surface imaging techniques were combined to determine appropriate manipulation of technologically important surfaces for commercial applications. The complementarity of the microscopy methods, scanning electron microscopy, electron probe microanalysis and atomic force microscopy assessed and correlated form and function of the surface modifications. Stainless steel disks (1 cm in diameter) were laser-cut from the same sheets of stainless steel and treated by electropolishing or left untreated for controls. Each treatment was analysed separately using each technique. First, the disks were examined by visual inspection and electron probe microanalysis for surface characteristics and elemental composition, respectively. Aliquots of bacterial suspensions (saline rinses of poultry carcasses from a commercial broiler processing plant) were then diluted in broth and monitored for growth by spectrophotometry. Stainless steel disks (1 cm in diameter) were added and the cultures were grown to sufficient density to allow attachment of bacterial cells to test surfaces. Relative differences in the surface morphology shown by atomic force microscopy, including Z ranges, roughness and other measurements, corresponded by treatment with the differences in reduction of bacterial counts shown by scanning electron microscopy. A model of wet-processing conditions tested the effects of corrosive treatment of surfaces. Less bacterial attachment occurred after corrosive treatment on controls and electropolished samples. Electropolishing significantly reduced bacterial numbers and the effects of corrosive action compared to the controls. Thus, the multiple imaging techniques showed that engineered changes on stainless steel surfaces improved the resistance of the surface finish to bacterial attachment, biofilm formation, and corrosive action. PMID:15566492

  1. Development of a cloud point extraction and spectrophotometry-based microplate method for the determination of nitrite in human urine and blood

    NASA Astrophysics Data System (ADS)

    Zhao, Jiao; Lu, Yunhui; Fan, Chongyang; Wang, Jun; Yang, Yaling

    2015-02-01

    A novel and simple method for the sensitive determination of trace amounts of nitrite in human urine and blood has been developed by combination of cloud point extraction (CPE) and microplate assay. The method is based on the Griess reaction and the reaction product is extracted into nonionic surfactant Triton-X114 using CPE technique. In this study, decolorization treatment of urine and blood was applied to overcome the interference of matrix and enhance the sensitivity of nitrite detection. Multi-sample can be simultaneously detected thanks to a 96-well microplate technique. The effects of different operating parameters such as type of decolorizing agent, concentration of surfactant (Triton X-114), addition of (NH4)2SO4, extraction temperature and time, interfering elements were studied and optimum conditions were obtained. Under the optimum conditions, a linear calibration graph was obtained in the range of 10-400 ng mL-1 of nitrite with limit of detection (LOD) of 2.5 ng mL-1. The relative standard deviation (RSD) for determination of 100 ng mL-1 of nitrite was 2.80%. The proposed method was successfully applied for the determination of nitrite in the urine and blood samples with recoveries of 92.6-101.2%.

  2. Imaging (NIRI) and quantitation (NIRS) in tissue using time-resolved spectrophotometry: the impact of statistically and dynamically variable optical path lengths

    NASA Astrophysics Data System (ADS)

    Benaron, David A.; Ho, David C.; Rubinsky, Boris; Shannon, Mark

    1993-09-01

    Near-infrared spectroscopy (NIRS) and near-infrared optical imaging (NIRI) are two medical techniques under development, respectively offering the ability to use light to noninvasively quantitate metabolite concentration and to image structure within the human body. Due to the dual effects of scattering and absorbance, quantitative measurement using NIRS and reconstruction of deep-tissue structure using NIRI have been problematic. Significant advances have occurred, however, over the past few years that have brought these measurements closer to reality. In this paper, we present several of the areas in which our laboratory has made progress, and discuss the relevance of these contributions in the light of work by other laboratories. With regard to NIR spectroscopy, it now appears both practical and necessary to take into account the length of the paths taken by light in order to derive deep-tissue estimates of pigment concentrations such as hemoglobin. With regard to NIR imaging, path corrected approaches offer improved resolution, and have been used successfully by our group and others to image phantoms, animals, and now humans. Different simplifications have been used in order to accomplish separately spectroscopy and imaging, but it is hoped that a common method will allow combination of the two techniques in order to achieve spatially resolved quantitative optical measurements.

  3. Development of a cloud point extraction and spectrophotometry-based microplate method for the determination of nitrite in human urine and blood.

    PubMed

    Zhao, Jiao; Lu, Yunhui; Fan, Chongyang; Wang, Jun; Yang, Yaling

    2015-02-01

    A novel and simple method for the sensitive determination of trace amounts of nitrite in human urine and blood has been developed by combination of cloud point extraction (CPE) and microplate assay. The method is based on the Griess reaction and the reaction product is extracted into nonionic surfactant Triton-X114 using CPE technique. In this study, decolorization treatment of urine and blood was applied to overcome the interference of matrix and enhance the sensitivity of nitrite detection. Multi-sample can be simultaneously detected thanks to a 96-well microplate technique. The effects of different operating parameters such as type of decolorizing agent, concentration of surfactant (Triton X-114), addition of (NH4)2SO4, extraction temperature and time, interfering elements were studied and optimum conditions were obtained. Under the optimum conditions, a linear calibration graph was obtained in the range of 10-400 ng mL(-1) of nitrite with limit of detection (LOD) of 2.5 ng mL(-1). The relative standard deviation (RSD) for determination of 100 ng mL(-1) of nitrite was 2.80%. The proposed method was successfully applied for the determination of nitrite in the urine and blood samples with recoveries of 92.6-101.2%. PMID:25448978

  4. Surgical forceps techniques.

    PubMed

    Malden, N

    2001-01-01

    This paper considers two new elevator and dental forceps techniques for the atraumatic removal of teeth to avoid a surgical procedure where possible. The techniques described should be applicable in relatively well defined but commonly occurring situations. The two techniques involve the unconventional use of conventional dental extraction forceps, with the aim of facilitating removal of the retained roots of certain teeth: the first for incisors, canines and premolars and the second for lower first molars. The term 'surgical forceps technique's is tentatively put forward as a description of these hybrid procedures. PMID:11819949

  5. Ultrasensitive, simple and solvent-free micro-assay for determining sulphite preservatives (E220-228) in foods by HS-SDME and UV-vis micro-spectrophotometry.

    PubMed

    Gómez-Otero, E; Costas, M; Lavilla, I; Bendicho, C

    2014-03-01

    A new method based on headspace single-drop microextraction in combination with UV-vis micro-spectrophotometry has been developed for the ultrasensitive determination of banned sulphite preservatives (E220-228) in fruits and vegetables. Sample acidification was used for SO2 generation, which is collected onto a 5,5'-dithiobis-(2-nitrobenzoic acid) microdrop for spectrophotometric measurement. A careful study of this reaction was necessary, including conditions for SO2 generation from different sulphating salts, drop pH, 5,5'-dithiobis-(2-nitrobenzoic acid) concentration and potential interference effects. Variables influencing mass transfer (stirring, sample volume and addition of salt) and microextraction time were also studied. A simple sulphite extraction was carried out, and problems caused by oxidation during the extraction process were addressed. A high enrichment factor (380) allows the determination of low levels of free SO2 in fruits and vegetables (limit of detection 0.06 μg g(-1), limit of quantification 0.2 μg g(-1)) with an adequate precision (repeatability, relative standard deviation 5 %). In addition, the sulphiting process was studied through the monitoring of residual SO2 in a vegetal sample, thus showing the importance of a sensitive tool for SO2 detection at low levels. PMID:23995438

  6. New NO donor ligands and complexes containing furfuryl or crown ether moiety: Syntheses, crystal structures and tautomerism in ortho-hydroxy substituted compounds as studied by UV-vis spectrophotometry

    NASA Astrophysics Data System (ADS)

    Şahin, Duygu; Koçoğlu, Serhat; Şener, Öznur; Şenol, Cemal; Dal, Hakan; Hökelek, Tuncer; Hayvalı, Zeliha

    2015-12-01

    NO donor ligands were prepared by the condensation of methoxy substituted salicylaldehyde with 5-methylfurfurylamine (1 and 2) and 4‧-aminobenzo-15-crown 5 (3-5). New crown ether ligands of Schiff base type (3-5) containing recognition sites for alkali metal and transition guest cations. Ni(II) complexes (1a-5a) have been synthesized with bidentate NO donor Schiff base ligands (1-5) with Ni(CH3COO)2.·4H2O. Monotopic crystalline 1:1 (Na+:ligand) sodium complexes (3b-5b) of the crown ether ligands were also prepared. Schiff bases (1-5) and complexes (1a-5a, 3b-5b) were characterized by elemental analyses, FT-IR, 1H-, 13C-NMR and mass spectroscopies. The crystal structures of 1, 1a and 2 were verified by X-ray diffraction analysis. The tautomeric equilibria (phenol-imine, O-H⋯N and keto-amine, O⋯H-N forms) have been systematically studied by using UV-vis spectrophotometry for the o-hydroxy substituted compounds (1-5). The UV-visible spectra of these ligands (1-5) were recorded and commented in polar, non-polar, acidic and basic media.

  7. Desenvolvimento das câmeras de raios-X duros do satélite MIRAX

    NASA Astrophysics Data System (ADS)

    Braga, J.; Rothschild, R.; Staubert, R.; Heise, J.; Remillard, R.; D'Amico, F.; Jablonski, F.; Mejía, J.; Carvalho, H.; Heindl, B.; Matteson, J.; Kendziorra, E.; Wilms, J.; in't Zand, J.; Kuulkers, E.

    2003-08-01

    O MIRAX (Monitor e Imageador de RAios-X) é um projeto de desenvolvimento de um pequeno satélite astronômico de raios-X (~200 kg, ~240 W). A estratégia básica da missão será observar continuamente (~9 meses por ano) a região central (~1000 graus2) do plano Galáctico e realizar estudos espectroscópicos de banda larga (2-200 keV) e alta sensibilidade de um grande conjunto de fontes através de imagens com resolução de ~6'. Isso proporcionará uma cobertura inédita do "espaço de descobertas" através da detecção, localização, identificação e estudo detalhado de fenômenos imprevisíveis, tais como transientes fracos de raios-X, novas rápidas de raios-X e bursts de raios gama, assim como o estudo de fontes com emissão persistente. Neste trabalho apresentamos o projeto das duas câmeras de raios-X duros (CXDs) do MIRAX, que irão operar na faixa de 10 a 200 keV. Cada CXD consistirá de um plano de detectores CZT (Cd0,9Zn0,1Te) de 0,5 mm de resolução espacial e 370 cm2 de área total, e de uma máscara codificada com elementos quadrados de 1,3 mm de lado e 0,5 cm de espessura. A máscara terá dimensões de 315 cm ´ 275 cm e será montada a 700 cm de distância dos detectores. Com essa configuração as CXDs terão 6' de resolução angular e, quando colocadas a um ângulo de 29° entre si, as duas câmeras propiciam um campo totalmente codificado de 39° ´ 6°12' e um campo total de 76° ´ 44°. Serão apresentadas simulações de observações da região do plano Galáctico com o conjunto formado pelas duas CXDs.

  8. Emerging optical nanoscopy techniques

    PubMed Central

    Montgomery, Paul C; Leong-Hoi, Audrey

    2015-01-01

    To face the challenges of modern health care, new imaging techniques with subcellular resolution or detection over wide fields are required. Far field optical nanoscopy presents many new solutions, providing high resolution or detection at high speed. We present a new classification scheme to help appreciate the growing number of optical nanoscopy techniques. We underline an important distinction between superresolution techniques that provide improved resolving power and nanodetection techniques for characterizing unresolved nanostructures. Some of the emerging techniques within these two categories are highlighted with applications in biophysics and medicine. Recent techniques employing wider angle imaging by digital holography and scattering lens microscopy allow superresolution to be achieved for subcellular and even in vivo, imaging without labeling. Nanodetection techniques are divided into four subcategories using contrast, phase, deconvolution, and nanomarkers. Contrast enhancement is illustrated by means of a polarized light-based technique and with strobed phase-contrast microscopy to reveal nanostructures. Very high sensitivity phase measurement using interference microscopy is shown to provide nanometric surface roughness measurement or to reveal internal nanometric structures. Finally, the use of nanomarkers is illustrated with stochastic fluorescence microscopy for mapping intracellular structures. We also present some of the future perspectives of optical nanoscopy. PMID:26491270

  9. Contamination Control Techniques

    SciTech Connect

    EBY, J.L.

    2000-05-16

    Welcome to a workshop on contamination Control techniques. This work shop is designed for about two hours. Attendee participation is encouraged during the workshop. We will address different topics within contamination control techniques; present processes, products and equipment used here at Hanford and then open the floor to you, the attendees for your input on the topics.

  10. Techniques for Teachers Section

    ERIC Educational Resources Information Center

    Tait, A., Ed.

    1973-01-01

    Includes a simple technique to demonstrate Millikan's oil drop experiment, an environmental studies experiment to measure dissolved oxygen in water samples, and a technique to demonstrate action-reaction. Science materials described are the Pol-A-Star Tomiscope, Nuffield chemistry film loops, air pucks and pH meters. (JR)

  11. TECHNIQUES FOR EFFECTIVE TEACHING.

    ERIC Educational Resources Information Center

    HASTINGS, GERALDINE; AND OTHERS

    A COMPENDIUM OF WORKABLE AND REASONABLE TECHNIQUES TO PROVIDE TEACHERS WITH ALTERNATIVES IN SELECTING LEARNING EXPERIENCES IS PRESENTED. MATERIALS ARE DESIGNED TO AID TEACHERS AND LEARNERS IN ALL SUBJECT MATTER AREAS. TEACHING TECHNIQUES DESCRIBED ARE (1) THE CASE STUDY, (2) DISCUSSIONS SUCH AS SYMPOSIUM, COLLOQUIUM, BUZZ SESSIONS, AND…

  12. Emerging Imaging Techniques

    PubMed Central

    McVeigh, Elliot R.

    2007-01-01

    This article reviews recent developments in selected imaging technologies focused on the cardiovascular system. The techniques covered are: ultrasound biomicroscopy (UBM), microSPECT, microPET, near infrared imaging, and quantum dots. For each technique, the basic physical principles are explained and recent example applications demonstrated. PMID:16614313

  13. Simulation verification techniques study

    NASA Technical Reports Server (NTRS)

    Schoonmaker, P. B.; Wenglinski, T. H.

    1975-01-01

    Results are summarized of the simulation verification techniques study which consisted of two tasks: to develop techniques for simulator hardware checkout and to develop techniques for simulation performance verification (validation). The hardware verification task involved definition of simulation hardware (hardware units and integrated simulator configurations), survey of current hardware self-test techniques, and definition of hardware and software techniques for checkout of simulator subsystems. The performance verification task included definition of simulation performance parameters (and critical performance parameters), definition of methods for establishing standards of performance (sources of reference data or validation), and definition of methods for validating performance. Both major tasks included definition of verification software and assessment of verification data base impact. An annotated bibliography of all documents generated during this study is provided.

  14. [Fe₃O₄-β-Cyclodextrin Polymer Nano Composites Solid-Phase Extraction-UV-Vis Spectrophotometry for Separation Analysis Malachite Green].

    PubMed

    Feng, Gang; Ping, Wen-hui; Zhu, Xia-shi

    2016-02-01

    In this paper, carboxymethyl-hydroxypropyl-β-cyclodextrin polymer modified magnetic particles Fe₃O₄ (CM-HP-β-CD- CP-MNPs) were prepared and applied to magnetic solid phase extraction of malachite green combined with UV-Visible spectrom- etry detection. The synthesized magnetic particles were characterized by element analysis, Fourier transform infrared spectra and transmission electron microscopy. Several variables affecting the extraction and desorption of malachite green such as pH, the amount of adsorbent, the type and volume of eluent, extraction and desorption time, and temperature were investigated. Under the optimum conditions, malachite green could be adsorbed by CM-HP-β-CDCP-MNPs (RE% = 92), and elution by C₂H₅OH (EE% = 90). the preconcentration factor of the proposed method was approximately 7.5, the CM-HP-β-CDCP-MNPs could be used repeatedly for 5 times and offered better recovery. The linear range and detection limit (DL) were found to be 0.08~8.00 µg · mL⁻¹ and 5.6 ng · mL⁻¹ respectively. This technique had been successfully applied to the determination of malachite green in real samples. The inclusion interaction of CM-HP--CDCP-MNPs with malachite green was studied through FTIR. PMID:27209745

  15. Electrical termination techniques

    NASA Technical Reports Server (NTRS)

    Oakey, W. E.; Schleicher, R. R.

    1976-01-01

    A technical review of high reliability electrical terminations for electronic equipment was made. Seven techniques were selected from this review for further investigation, experimental work, and preliminary testing. From the preliminary test results, four techniques were selected for final testing and evaluation. These four were: (1) induction soldering, (2) wire wrap, (3) percussive arc welding, and (4) resistance welding. Of these four, induction soldering was selected as the best technique in terms of minimizing operator errors, controlling temperature and time, minimizing joint contamination, and ultimately producing a reliable, uniform, and reusable electrical termination.

  16. Active cleaning technique device

    NASA Technical Reports Server (NTRS)

    Shannon, R. L.; Gillette, R. B.

    1973-01-01

    The objective of this program was to develop a laboratory demonstration model of an active cleaning technique (ACT) device. The principle of this device is based primarily on the technique for removing contaminants from optical surfaces. This active cleaning technique involves exposing contaminated surfaces to a plasma containing atomic oxygen or combinations of other reactive gases. The ACT device laboratory demonstration model incorporates, in addition to plasma cleaning, the means to operate the device as an ion source for sputtering experiments. The overall ACT device includes a plasma generation tube, an ion accelerator, a gas supply system, a RF power supply and a high voltage dc power supply.

  17. Interpretation Techniques Development

    NASA Technical Reports Server (NTRS)

    Alford, W. L.

    1973-01-01

    The processes, algorithms and procedures for extraction and interpretation of ERTS-1 data are discussed. Analysis of data acquired temporally is possible through geometric correction, correlation, and registration techniques. The powerful techniques in image enhancement developed for the lunar and planetary programs are valuable for Earth Resources Survey programs. There is evidence that both optical and digital methods of spatial information extraction can provide valuable sources of data information the ERTS system. The techniques available, even for a limited number of bands and limited resolution can be effectively used to extract much of the information required by resource managers.

  18. Application of derivative and derivative ratio spectrophotometry to simultaneous trace determination of rhodamine B and rhodamine 6G after dispersive liquid-liquid microextraction.

    PubMed

    Xiao, Ni; Deng, Jian; Huang, Kaihui; Ju, Saiqin; Hu, Canhui; Liang, Jun

    2014-07-15

    Two novel methods, first derivative spectrophotometric method ((1)D) and first derivative ratio spectrophotometric method ((1)DR), have been developed for the simultaneous trace determination of rhodamine B (RhB) and rhodamine 6G (Rh6G) in food samples after dispersive liquid-liquid microextraction (DLLME). The combination of derivative spectrophotometric techniques and DLLME procedure endows the presented methods with enhanced sensitivity and selectivity. Under optimum conditions, the linear calibration curves ranged from 5 to 450 ng mL(-1), with the correlation coefficients (r) of 0.9997 for RhB and 0.9977 for Rh6G by (1)D method, and 0.9987 for RhB and 0.9958 for Rh6G by (1)DR method, respectively. The calculated limits of detection (LODs) based on the variability of the blank solutions (S/N = 3 criterion) for 11 measurements were in the range of 0.48-1.93 ng mL(-1). The recoveries ranged from 88.1% to 111.6% (with RSD less than 4.4%) and 91.5-110.5% (with RSD less than 4.7%) for (1)D and (1)DR method, respectively. The influence of interfering substances such as foreign ions and food colorants which might be present in the food samples on the signals of RhB and Rh6G was examined. The developed methods have been successfully applied to the determination of RhB and Rh6G in black tea, red wine and chilli powder samples with the characteristics of simplicity, cost-effectiveness, environmental friendliness, and could be valuable for routine analysis. PMID:24691361

  19. Application of derivative and derivative ratio spectrophotometry to simultaneous trace determination of rhodamine B and rhodamine 6G after dispersive liquid-liquid microextraction

    NASA Astrophysics Data System (ADS)

    Xiao, Ni; Deng, Jian; Huang, Kaihui; Ju, Saiqin; Hu, Canhui; Liang, Jun

    2014-07-01

    Two novel methods, first derivative spectrophotometric method (1D) and first derivative ratio spectrophotometric method (1DR), have been developed for the simultaneous trace determination of rhodamine B (RhB) and rhodamine 6G (Rh6G) in food samples after dispersive liquid-liquid microextraction (DLLME). The combination of derivative spectrophotometric techniques and DLLME procedure endows the presented methods with enhanced sensitivity and selectivity. Under optimum conditions, the linear calibration curves ranged from 5 to 450 ng mL-1, with the correlation coefficients (r) of 0.9997 for RhB and 0.9977 for Rh6G by 1D method, and 0.9987 for RhB and 0.9958 for Rh6G by 1DR method, respectively. The calculated limits of detection (LODs) based on the variability of the blank solutions (S/N = 3 criterion) for 11 measurements were in the range of 0.48-1.93 ng mL-1. The recoveries ranged from 88.1% to 111.6% (with RSD less than 4.4%) and 91.5-110.5% (with RSD less than 4.7%) for 1D and 1DR method, respectively. The influence of interfering substances such as foreign ions and food colorants which might be present in the food samples on the signals of RhB and Rh6G was examined. The developed methods have been successfully applied to the determination of RhB and Rh6G in black tea, red wine and chilli powder samples with the characteristics of simplicity, cost-effectiveness, environmental friendliness, and could be valuable for routine analysis.

  20. Determination of Se in soil samples using the proton induced X-ray emission technique

    NASA Astrophysics Data System (ADS)

    Cruvinel, Paulo E.; Flocchini, Robert G.

    1993-04-01

    An alternative method for the direct determination of total Se in soil samples is presented. A large number of trace elements is present in soil at concentration values in the range of part per billion and tenths of parts of million. The most common are the trace elements of Al, Si, K, Ca, Ti, V, Cr, Fe, Cu, Zn, Br, Rb, Mo, Cd and Pb. As for biological samples many of these elements are of great importance for the nutrition of plants, while others are toxic and others have an unknown role. Selenium is an essential micronutrient for humans and animals but it is also known that in certain areas Se deficiency or toxicity has caused endemic disease to livestock and humans through the soil-plant-animal linkage. In this work the suitability of the proton induced X-ray emission (PIXE) technique as a fast and nondestructive technique useful to measure total the Se content in soil samples is demonstrated. To validate the results a comparison of data collected using the conventional atomic absorption spectrophotometry (AAS) method was performed.

  1. Small Scale Organic Techniques

    ERIC Educational Resources Information Center

    Horak, V.; Crist, DeLanson R.

    1975-01-01

    Discusses the advantages of using small scale experimentation in the undergraduate organic chemistry laboratory. Describes small scale filtration techniques as an example of a semi-micro method applied to small quantities of material. (MLH)

  2. Relaxation techniques for stress

    MedlinePlus

    ... fall. There are also many other types of breathing techniques you can learn. In many cases, you do ... These sensors measure your skin temperature, brain waves, ... time, you can learn to change them without using the monitor.

  3. Pattern recognition technique

    NASA Technical Reports Server (NTRS)

    Hong, J. P.

    1971-01-01

    Technique operates regardless of pattern rotation, translation or magnification and successfully detects out-of-register patterns. It improves accuracy and reduces cost of various optical character recognition devices and page readers and provides data input to computer.

  4. "Techniques for Teachers" Section

    ERIC Educational Resources Information Center

    Tait, A.

    1972-01-01

    A series of short articles describe a method of combined developing/fixing for monochrome film, techniques for thin layer chromatography, experiments with lasers, and safety precautions to be used with lasers in school laboratories. (AL)

  5. Renal Tumor Biopsy Technique

    PubMed Central

    Zhang, Lei; Li, Xue-Song; Zhou, Li-Qun

    2016-01-01

    Objective: To review hot issues and future direction of renal tumor biopsy (RTB) technique. Data Sources: The literature concerning or including RTB technique in English was collected from PubMed published from 1990 to 2015. Study Selection: We included all the relevant articles on RTB technique in English, with no limitation of study design. Results: Computed tomography and ultrasound were usually used for guiding RTB with respective advantages. Core biopsy is more preferred over fine needle aspiration because of superior accuracy. A minimum of two good-quality cores for a single renal tumor is generally accepted. The use of coaxial guide is recommended. For biopsy location, sampling different regions including central and peripheral biopsies are recommended. Conclusion: In spite of some limitations, RTB technique is relatively mature to help optimize the treatment of renal tumors. PMID:27174334

  6. The MST Radar Technique

    NASA Technical Reports Server (NTRS)

    Balsley, B. B.

    1985-01-01

    The past ten year have witnessed the development of a new radar technique to examine the structure and dynamics of the atmosphere between roughly 1 to 100 km on a continuous basis. The technique is known as the MST (for Mesosphere-Stratosphere-Troposphere) technique and is usable in all weather conditions, being unaffected by precipitation or cloud cover. MST radars make use of scattering from small scale structure in the atmospheric refractive index, with scales of the order of one-half the radar wavelength. Pertinent scale sizes for middle atmospheric studies typically range between a fraction of a meter and a few meters. The structure itself arises primarily from atmospheric turbulence. The technique is briefly described along with the meteorological parameters it measures.

  7. Exemplary Management Techniques

    ERIC Educational Resources Information Center

    School Business Affairs, 1977

    1977-01-01

    Featured in the third article of the series are management techniques for school insurance record management and for reducing the amount of time school maintenance personnel spend driving from school to school. (Author/MLF)

  8. Nondestructive testing techniques

    NASA Astrophysics Data System (ADS)

    Bray, Don E.; McBride, Don

    A comprehensive reference covering a broad range of techniques in nondestructive testing is presented. Based on years of extensive research and application at NASA and other government research facilities, the book provides practical guidelines for selecting the appropriate testing methods and equipment. Topics discussed include visual inspection, penetrant and chemical testing, nuclear radiation, sonic and ultrasonic, thermal and microwave, magnetic and electromagnetic techniques, and training and human factors. (No individual items are abstracted in this volume)

  9. Apollo Onboard Navigation Techniques

    NASA Technical Reports Server (NTRS)

    Interbartolo, Michael

    2009-01-01

    This viewgraph presentation reviews basic navigation concepts, describes coordinate systems and identifies attitude determination techniques including Primary Guidance, Navigation and Control System (PGNCS) IMU management and Command and Service Module Stabilization and Control System/Lunar Module (LM) Abort Guidance System (AGS) attitude management. The presentation also identifies state vector determination techniques, including PGNCS coasting flight navigation, PGNCS powered flight navigation and LM AGS navigation.

  10. Techniques for colorectal anastomosis

    PubMed Central

    Ho, Yik-Hong; Ashour, Mohamed Ahmed Tawfik

    2010-01-01

    Colorectal anastomotic leak remains one of the most feared post-operative complications, particularly after anterior resection of the rectum with, the shift from abdomino-peritoneal resections to total mesorectal excision and primary anastomosis. The literature fails to demonstrate superiority of stapled over hand-sewn techniques in colorectal anastomosis, regardless of the level of anastomosis, although a high stricture rate was noted in the former technique. Thus, improvements in safety aspects of anastomosis and alternatives to hand-sewn and stapled techniques are being sought. Here, we review alternative anastomotic techniques used to fashion bowel anastomosis. Compression anastomosis using compression anastomotic clips, endoluminal compression anastomotic rings, AKA-2, biofragmental anastomotic rings, or Magnamosis all involve the concept of creating a sutureless end-to-end anastomosis by compressing two bowel ends together, leading to a simultaneous necrosis and healing process that joins the two lumens. Staple line reinforcement is a new approach that reduce the drawbacks of staplers used in colorectal practice, i.e. leakage, bleeding, misfiring, and inadequate tissue approximation. Various non-absorbable, semi or fully absorbable materials are now available. Two other techniques can provide alternative anastomotic support to the suture line: a colorectal drain and a polyester stent, which can be utilized in ultra-low rectal excision and can negate the formation of a defunctioning stoma. Doxycycline coated sutures have been used to overcome the post-operative weakness in anastomosis secondary to rapid matrix degradation mediated by matrix metalloproteinase. Another novel technique, the electric welding system, showed promising results in construction of a safe, neat, smooth sutureless bowel anastomosis. Various anastomotic techniques have been shown to be comparable to the standard techniques of suturing and stapling. However, most of these alternatives need