Computer tomography of the brain and spectrophotometry of the CSF in cerebral concussion and contusion

International Nuclear Information System (INIS)

Bergvall, U.; Kjellin, K.G.; Levander, B.; Svendsen, P.; Soederstroem, C.E.

1978-01-01

Computer tomography (CT) and spectrophotometry of CSF were performed in 30 patients with the clinical diagnosis of cerebral concussion or contusion. The patients with concussion all had normal CT-findings. Spectrophotometry of CSF was sometimes positive for cerebral contusion with normal CT-findings, but the two methods were complementary so that the extent of the lesion was determined by CT and spectrophotometry of CSF indicated the cause. (Auth.)

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

Science.gov (United States)

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.

An important improvement in Ferron-timed spectrophotometry

NARCIS (Netherlands)

Zhang, Jing; Chang, Fang; Ren, Yijin; Shi, Qiuyi

Ferron dosage ([Ferron]) is key to ferron-timed spectrophotometry (ferron assay). In order to clarify some important questions, the following studies were conducted: (1) The effect of [Ferron] on the sensitivity of total aluminum (AlT) determination was experimentally investigated and ²⁷Al nuclear

A Computer-aided Learning Exercise in Spectrophotometry.

Science.gov (United States)

Pamula, Frederick

1994-01-01

Discusses the use of a computer simulation program in teaching the concepts of spectrophotometry. Introduces several parts of the program and program usage. Presents an assessment activity to evaluate students' mastery of material. Concludes with the advantages of this approach to the student and to the assessor. (ASK)

Evaluation of atomic absorption Spectrophotometry (ashing, non ...

African Journals Online (AJOL)

Three commonly used techniques, namely atomic absorption spectrophotometry (AAS-Ashing and AAS-Non Ashing) and titrimetry (potassium permanganate titration) have been evaluated in this study to determine the calcium content in six food samples whose calcium levels ranged from 0 to more than 250mg/100g ...

On image tube spectrophotometry of weak emission lines

International Nuclear Information System (INIS)

Duflot, R.

1979-01-01

The usual precision of image tube spectrophotometry measures relative to low intensity lines can be improved by the 'method of two lines'. This operating process tested on H II galactic regions leads to a precision of 13%. (Auth.)

Photochemical reaction monitoring by ultra-violet spectrophotometry.

Science.gov (United States)

Roig, B; Touraud, E; Thomas, O

2002-11-01

Within the framework of the monitoring of the trichloroacetylchloride (TCAC) photosynthesis, ultra-violet (UV) spectrophotometry is proposed as a simple and rapid tool allowing, in real time, the control of the process efficiency. A good correlation has been obtained between the results acquired by this alternative method and the standard gas chromatography.

PRECISION SPECTROPHOTOMETRY AT THE LEVEL OF 0.1%

International Nuclear Information System (INIS)

Yan Renbin

2011-01-01

Accurate relative spectrophotometry is critical for many science applications. Small wavelength-scale residuals in the flux calibration can significantly impact the measurements of weak emission and absorption features in the spectra. Using Sloan Digital Sky Survey data, we demonstrate that the average spectra of carefully selected red-sequence galaxies can be used as a spectroscopic standard to improve the relative spectrophotometry precision to 0.1% on small wavelength scales (from a few to hundreds of Angstroms). We achieve this precision by comparing stacked spectra across tiny redshift intervals. The redshift intervals must be small enough that any systematic stellar population evolution is minimized and is less than the spectrophotometric uncertainty. This purely empirical technique does not require any theoretical knowledge of true galaxy spectra. It can be applied to all large spectroscopic galaxy redshift surveys that sample a large number of galaxies in a uniform population.

Spectrophotometry of the QSO NRAO 530

International Nuclear Information System (INIS)

Junkkarinen, V.

1984-01-01

Spectrophotometry of the QSO NRAO 530 with the KPNO Cryogenic Camera is reported. A redshift of 0.902 is determined from the H-beta, H-gamma, and 3727 A forbidden O II emission lines, confirming a redshift that had been based on a single line, the 2798 A Mg II. The H-beta equivalent is smaller than in normal QSOs, which may be characteristic of optically variable QSOs. 16 references

Automation of plutonium spectrophotometry

International Nuclear Information System (INIS)

Perez, J.J.; Boisde, G.; Goujon de Beauvivier, M.; Chevalier, G.; Isaac, M.

1980-01-01

Instrumentation was designed and constructed for automatic control of plutonium by molecular absorption spectrophotometry, on behalf of the reprocessing facilities, to meet two objectives: on-line measurement, of the valency state of plutonium, on by-pass, with the measured concentration covering the process concentration range up to a few mg.l -1 ; laboratory measurement of plutonium adjusted to valency VI, with operation carried out using a preparative system meeting the required containment specifications. For this two objectives, the photometer, optical cell connections are made by optical fibers resistant to β, γ radiation. Except this characteristic the devices are different according to the quality required for result [fr

Fourier transform infrared spectrophotometry and X-ray powder ...

African Journals Online (AJOL)

This study aimed at demonstrating complementary roles offered by both Fourier transform infrared (FTIR) spectrophotometry and x-ray powder diffraction (XRPD) techniques in characterizing clay size fraction of kaolins. The clay size fraction of kaolin samples obtained from Kgwakgwe, Makoro, Lobatse and Serule kaolin ...

Process for neptunium analysis by absorption spectrophotometry

International Nuclear Information System (INIS)

Wagner, J.F.

1987-01-01

An aqueous solution of a neptunium compounds is treated by a reagent, preferentially a vanadyl sulfate oxidized by cerium IV ions, to obtain neptunium V by oxidation of neptunium IV and reduction of neptunium VI. The reagent is chosen for a negligible absorption at the wavelength used for neptunium V absorption spectrophotometry for instance 981 nm [fr

Absolute spectrophotometry of the β Lyr

International Nuclear Information System (INIS)

Burnashev, V.I.; Skul'skij, M.Yu.

1978-01-01

In 1974 an absolute spectrophotometry of β Lyr was performed with the scanning spectrophotometer in the 3300-7400 A range. The energy distribution in the β Lyr spectrum is obtained. The β Lyr model is proposed. It is shown, that the continuous spectrum of the β Lyr radiation can be presented by the total radiation of the B8 3 and A5 3 two stars and of the gaseous envelope with Te =20000 K

Zirconium determination in rocks by solid-phase spectrophotometry

International Nuclear Information System (INIS)

Brykina, G.D.; Lebedeva, G.G.; Agapova, G.F.; AN SSSR, Moscow

1990-01-01

A method was developed for determination of zirconium in rocks by solid-phase spectrophotometry using AV-17x8-Cl anion exchanger modified with xylenol orange. Relative standard deviation at the level of (2-4.9)x10 -3 % ZrO 2 was about 0.245

Comparative determination of phenytoin by spectrophotometry, gas chromatography, liquid chromatography, enzyme immunoassay, and radioimmunoassay

International Nuclear Information System (INIS)

Castro, A.; Ibanez, J.; DiCesare, J.L.; Adams, R.F.; Malkus, H.

1978-01-01

Sera from patients being treated with phenytoin were analyzed for the drug by spectrophotometry, gas chromatography, radioimmunoasay, enzyme immunoassay, and liquid chromatography. The assay values obtained were intercompared statistically. Enzyme immunoassay and liquid chromatography appear to be attractive alternatives to the more traditional methods of spectrophotometry and gas chromatography. Our radioimmunoassay data correlated poorly with results by the four other methods

Uranium determination by UV-Vis spectrophotometry in organic matrix

International Nuclear Information System (INIS)

Iwaki, Leonardo E.O.; Silva, Ieda S.; Oliveira, Luis C.

2013-01-01

Concentrations of uranium in the process samples provide essential information required for nuclear process monitoring. A large number of techniques have been developed to allow uranium determination, but each technique possesses some advantages and disadvantages and cannot be applied without difficulty to all samples. The ultraviolet visible spectrophotometry (UV-Vis) is widely method used in analytical industrial processes due to its simplicity, rapidity, low costs, low generation of analytical waste, easy calibration and operation. In this study, we describe a simple and fast quantification method to determination of a high amount of uranium in organic phase (TBP/kerosene) using UV-Vis spectrophotometry. The process sample was analyzed in UV-Vis and compared with inductively coupled plasma optical emission spectrometry (ICP OES) showing similar results in both methods. The statistical tests (Student-t and Fischer) showed that the both techniques they are equivalent. (author)

Two-dimensional spectrophotometry of planetary nebulae by CCD imaging

International Nuclear Information System (INIS)

Jacoby, G.H.; Africano, J.L.; Quigley, R.J.; Western Washington Univ., Bellingham, WA)

1987-01-01

The spatial distribution of the electron temperature and density and the ionic abundances of O(+), O(2+), N(+), and S(+) have been derived from CCD images of the planetary nebulae NGC 40 and NGC 6826 taken in the important emission lines of forbidden O II, forbidden O III, H-beta, forbidden N II, and forbidden S II. The steps required in the derivation of the absolute fluxes, line, ratios, and ionic abundances are outlined and then discussed in greater detail. The results show that the CCD imaging technique for two-dimensional spectrophotometry can effectively compete with classical spectrophotometry, providing the added benefits of complete spatial coverage at seeing-disk spatial resolution. The multiplexing in the spatial dimension, however, results in a loss of spectral information, since only one emission line is observed at any one time. 37 references

Spectrophotometry of the Seyfert galaxy NGC 4593

International Nuclear Information System (INIS)

MacAlpine, G.M.; Williams, G.A.; Lewis, D.W.

1979-01-01

Spectrophotometry of the bright class 1 Seyfert galaxy NGC 4593 is presented. The emission-line characteristics are briefly discussed and compared with those of other Seyfert galaxies. The measured hydrogen Balmer-line ratios are reasonably consistent with expected recombination values, and the emission intensities of Fe II, He I 5876, and forbidden O III 4363 relative to other lines are stronger than average in NGC 4593

Spectrophotometry of four galaxies of high surface brightness

International Nuclear Information System (INIS)

Arakelyan, M.A.; Magtesyan, A.P.

1982-01-01

Spectrophotometry has been performed for the emission lines in the nuclei of Arakelyan galaxies Nos. 428, 449, 454, 532. In the first two objects, H II clouds occur roughly-equal2 kpc out from the nucleus. No. 449 may contain another cloud moving at roughly-equal1500 km/sec radial velocity. radial

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

Science.gov (United States)

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…

The determination of zirconium by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Rodriguez, E.R.; Cunha, M.T.C. da

1975-01-01

The interference of iron in the determination of zirconium by atomic absorption spectrophotometry was studied. Attempts were made to emininate this interference by complexing the iron with EDTA, ascorbic acid and hydrazine; also by the addition of ammonium fluoride to the solution. Some experiments were carried out in order to explain the results obtained [pt

Studies of selected transuranium and lanthanide tri-iodides under pressure using absorption spectrophotometry

International Nuclear Information System (INIS)

Haire, R.G.; Young, J.P.; Peterson, J.R.; Tennessee Univ., Knoxville; Benedict, U.

1987-01-01

The anhydrous tri-iodides of plutonium, americium and curium under pressure have been investigated using absorption spectrophotometry. These initial studies on plutonium and curium tri-iodides together with the published data for americium tri-iodide show that the rhombohedral form of these compounds (BiI 3 -type structure) can be converted to the orthorhombic form (PuBr 3 -type structure) by applying pressure at room temperature. Absorption spectrophotometry can often differentiate between two crystallographic forms of a material and has been used in the present high-pressure studies to monitor the effects of pressure on the tri-iodides. A complication in these studies of the tri-iodides is a significant shift of their absorption edges with pressure from the near UV to the visible spectral region. With curium tri-iodide this shift causes interference with the major f-f absorption peaks and precludes identification by absorption spectrophotometry of the high pressure phase of CmI 3 . (orig.)

Determination of micro amounts of samarium and europium by analogue derivative spectrophotometry

International Nuclear Information System (INIS)

Ishii, H.; Satoh, K.

1982-01-01

Derivative spectrophotometry using the analogue differentiation circuit was applied to the determination of samarium and europium at ppm levels. By measuring the second or the fourth derivative spectra of the characteristic absorption bands of both the rare earth ions around 400 nm, they can be determined directly and selectively in the presence of large amounts of most other rare earths without any prior separation. Further, aptly selecting conditions for the measurement of the derivative spectra, the simultaneous determination of both the rare earth elements was feasible. The principle and the characteristics of analogue derivative spectrophotometry are also described. (orig.) [de

Spectrophotometry of CRL 2688 from 2 to 24 microns

International Nuclear Information System (INIS)

Forrest, W.J.; Merrill, K.M.; Russell, R.W.; Soifer, B.T.

1975-01-01

Medium-resolution spectrophotometry (Δlambda/lambdaapprox. =0.01) of CRL 2688 from 2 μ to 24 μ are reported. No significant features are found from 3 μ to 24 μ, although the spectral flux distribution is broader than that of a single-temperature blackbody

8-13μm spectrophotometry of galaxies

International Nuclear Information System (INIS)

Roche, P.F.; Aitken, D.K.; Whitmore, B.

1983-01-01

Spectrophotometry at 8-13 μm of Mkn 231 confirms that the 10 μm minimum is due to large columns of silicate dust in the line-of-sight to the nucleus. Fits to the detailed spectral shape demonstrate that the cool absorbing grains are at the emission (z=0.042) rather than the absorption (z approx.= 0.025) redshift and are located within the nuclear region. (author)

Improving the submicro determination of vanadium in natural water using primary-secondary wavelength spectrophotometry

International Nuclear Information System (INIS)

Khongven Gao

1999-01-01

In acidic solution and in the presence of ammonium persulfate, the conventional reaction of vanadium(5) with gallic acid to form an orange complex has been used for the improvement of the determination of trace amounts of vanadium in water by the updated method named primary-secondary wavelength spectrophotometry. The results show that the analytical precision and accuracy were improved and gave higher determination sensitivity than ordinary spectrophotometry. The relative standard deviations were less than 5.6 % [ru

Spectrophotometry or visual inspection to most reliably detect xanthochromia in subarachnoid hemorrhage: systematic review.

Science.gov (United States)

Chu, Kevin; Hann, Angus; Greenslade, Jaimi; Williams, Julian; Brown, Anthony

2014-09-01

We assess the sensitivity and specificity of xanthochromia as adjudicated by visual inspection and spectrophotometry at predicting the presence of cerebral aneurysm in patients with suspected subarachnoid hemorrhage who have a normal computed tomography (CT) head scan result. A systematic review was performed. MEDLINE and EMBASE databases were searched. Relevant studies with clinical data on the diagnostic accuracy of visual inspection or spectrophotometry were considered. Patients who had a normal CT head scan result followed by a lumbar puncture were included in this review. Sensitivities, specificities, and heterogeneity (I(2)) were calculated. Subgroup analyses were performed to explore reasons for the heterogeneity. There were major methodological limitations in the studies found. Twenty-two relevant articles were heterogeneous in regard to time to lumbar puncture, spectrophotometry methods, and follow-up of patients not undergoing cerebral angiography. Twelve of the 22 studies selected patients on the basis of a cerebral aneurysm or subarachnoid hemorrhage on imaging, or a positive lumbar puncture result. These studies were excluded from our initial analysis, which included only patients with clinically suspected subarachnoid hemorrhage. In this initial analysis, pooled estimates of sensitivity and specificity for spectrophotometry were 87% (95% confidence interval [CI] 71% to 96%; I(2)=26%) and 86% (95% CI 84% to 88%; I(2)=96%), respectively. For visual inspection, pooled sensitivity and specificity were 83% (95% CI 59% to 96%; I(2)=52%) and 96% (95% CI 93% to 97%; I(2)=76%), respectively. Sensitivity estimates are difficult to interpret without knowing time to lumbar puncture. The heterogeneity in the underlying studies, combined with significant overlap in pooled confidence limits, makes it impossible to provide a definite conclusion about the diagnostic accuracy of spectrophotometry versus visual inspection. Copyright © 2014 American College of Emergency

Spectrophotometry of cerebrospinal fluid in subacute and chronic subdural haematomas

Science.gov (United States)

Kjellin, K. G.; Steiner, L.

1974-01-01

Spectrophotometric examinations were performed on cerebrospinal and subdural fluids in subacute (five patients) and chronic (20 patients) subdural haematomas, with special reference to the diagnostic aid of CSF spectrophotometry. Spectrophotometric xanthochromia of haemorrhagic origin was found in all CSFs examined, while definite visible xanthochromia was observed in only 28% and the CSF was judged as colourless in 52% of those cases. Characteristic bleeding patterns were found spectrophotometrically in all the 20 CSFs examined within 24 hours after lumbar puncture, haematoma patterns being detected in 90-95% of the cases. In many cases the electrophoretically separated protein fractions of CSF and subdural fluids were spectrophotometrically examined. In conclusion, CSF spectrophotometry is a simple, fast, and extremely sensitive method, which in our opinion should be used routinely in the diagnosis of suspected subdural haematomas, if lumbar puncture is not contraindicated. PMID:4140892

Surface composition of Mercury from reflectance spectrophotometry

Science.gov (United States)

Vilas, Faith

1988-01-01

The controversies surrounding the existing spectra of Mercury are discussed together with the various implications for interpretations of Mercury's surface composition. Special attention is given to the basic procedure used for reducing reflectance spectrophotometry data, the factors that must be accounted for in the reduction of these data, and the methodology for defining the portion of the surface contributing the greatest amount of light to an individual spectrum. The application of these methodologies to Mercury's spectra is presented.

Dynamic range broadening for photomultipliers in kinetic spectrophotometry

International Nuclear Information System (INIS)

Rumas, V.K.

1983-01-01

The circuit of switching on a photomultiplier with prestage modulation developed for kinetic spectrophotometry purposes is described. Distinguishing features of the scheme are wide range of control pulse duration (40 nc - 2.5 mc) and direct transistor photostart by laser light pulse. In the case of PM prestage modulation for the second dynode modulation depth attains 400 while PM opening time constitutes 40 nc

Solid-phase spectrophotometry

International Nuclear Information System (INIS)

Brykina, G.D.; Marchenko, D.Yu.; Shpigun, O.A.

1995-01-01

Solid-phase spectrophotometry (SPS), which is based on the direct measurement of light absorption of an ion exchanger containing a substance of interest, was reviewed. Since 1976, it has been known that aborbance of an ion exchanger is directly proportional to the concentration of a particular ion in solution. A similar dependence can also be followed for other sorbents, as well as for foams, membranes, films, etc., which do not exhibit ion exchange properties. One can use absorption, diffuse reflection, and luminescence spectra parameters as an analytical signal. Thus, SPS of ion exchangers is among the analytical techniques that combine the sorption concentration and surface determination of the substance of interest. This review summarizes the advancements in SPS over the last six years and demonstrates the prospects for its development. Special attention is paid to experimental methods for measuring solid-phase absorption and to the basic procedures of sample preparation, including new ones. These two facets are of great importance for obtaining precise results and extending the capabilities of SPS

A comparison of hair colour measurement by digital image analysis with reflective spectrophotometry.

Science.gov (United States)

Vaughn, Michelle R; van Oorschot, Roland A H; Baindur-Hudson, Swati

2009-01-10

While reflective spectrophotometry is an established method for measuring macroscopic hair colour, it can be cumbersome to use on a large number of individuals and not all reflective spectrophotometry instruments are easily portable. This study investigates the use of digital photographs to measure hair colour and compares its use to reflective spectrophotometry. An understanding of the accuracy of colour determination by these methods is of relevance when undertaking specific investigations, such as those on the genetics of hair colour. Measurements of hair colour may also be of assistance in cases where a photograph is the only evidence of hair colour available (e.g. surveillance). Using the CIE L(*)a(*)b(*) colour space, the hair colour of 134 individuals of European ancestry was measured by both reflective spectrophotometry and by digital image analysis (in V++). A moderate correlation was found along all three colour axes, with Pearson correlation coefficients of 0.625, 0.593 and 0.513 for L(*), a(*) and b(*) respectively (p-values=0.000), with means being significantly overestimated by digital image analysis for all three colour components (by an average of 33.42, 3.38 and 8.00 for L(*), a(*) and b(*) respectively). When using digital image data to group individuals into clusters previously determined by reflective spectrophotometric analysis using a discriminant analysis, individuals were classified into the correct clusters 85.8% of the time when there were two clusters. The percentage of cases correctly classified decreases as the number of clusters increases. It is concluded that, although more convenient, hair colour measurement from digital images has limited use in situations requiring accurate and consistent measurements.

Indirect determination of uranium by atomic-absorption spectrophotometry using an air-acetylene flame

International Nuclear Information System (INIS)

Alder, J.F.; Das, B.C.

1977-01-01

An indirect method has been developed for the determination of uranium by atomic-absorption spectrophotometry using an air-acetylene flame. Use is made of the reduction of copper(II) by uranium(IV) followed by complex formation of the copper(I) ions so produced with neocuproine (2,9-dimethyl-1,10-phenanthroline) and finally the determination of copper in this complex by atomic-absorption spectrophotometry. The results show that the method can be recommended, provided that care is taken to ensure the complete reduction of uranium(VI) to uranium(IV). The sensitivity of the method is 4.9 μg of uranium and the upper limit 500 μg without dilution. (author)

Free radicals in irradiated unstabilized polypropylene, as seen by diffuse reflection absorption-spectrophotometry

International Nuclear Information System (INIS)

Zagorski, Z.P.; Rafalski, A.

1998-01-01

The introduction of UV-Vis absorption spectrophotometry to the study of radiation chemistry of polymers has opened the possibility to investigate even very opaque samples. The virgin powder polypropylene, as obtained from the industrial production line, shows after irradiation unstable products of radiolysis. Until now they were investigated mainly by EPR method. Optical absorption spectra (by diffuse reflection spectrophotometry) contribute to better identification and study of changes in time, temperature and diffusion of reactive gases. Studying the formation of stable compounds, which do not produce EPR signal, we are able to examine these species on the basis of their electronic spectra. The most important results concern the peroxides in irradiated polypropylene

Ultraviolet Spectrophotometry of VV Cephei

Directory of Open Access Journals (Sweden)

Young Woon Kang

1992-06-01

Full Text Available The IUE archival spectra of VV Cephei were collected to investigate the eclipse nature in the ultraviolet. The temperature of the B star has been determined, as approximately 30000K, based on the flux distributions during egress. Light curves of VV Cephei were reduced from the spectrophotometry of the IUE archival spectra. Three light curves at the center wavelengths of 3250 Å, 2550 Å and 2850 Å have been analyzed by the modified Wilson and Devinney light curve program. The radii of the B star and M star were deduced to 0.05 and 0.22 of unit separation, respectively. The UV light curves show an evidence that the light was attenuated by the highly opaque atomsphere of the M star.

Spectrophotometry of Symbiotic Stars (Abstract)

Science.gov (United States)

Boyd, D.

2017-12-01

(Abstract only) Symbiotic stars are fascinating objects - complex binary systems comprising a cool red giant star and a small hot object, often a white dwarf, both embedded in a nebula formed by a wind from the giant star. UV radiation from the hot star ionizes the nebula, producing a range of emission lines. These objects have composite spectra with contributions from both stars plus the nebula and these spectra can change on many timescales. Being moderately bright, they lend themselves well to amateur spectroscopy. This paper describes the symbiotic star phenomenon, shows how spectrophotometry can be used to extract astrophysically useful information about the nature of these systems, and gives results for three symbiotic stars based on the author's observations.

Determination of tantalum in standard steels by INAA and absorption spectrophotometry

Energy Technology Data Exchange (ETDEWEB)

Obrusnik, I; Posta, S [Ustav Jaderneho Vyzkumu, Rez (Czechoslovakia)

1978-02-14

Two analytical methods, instrumental neutron activation analysis (INAA) and absorption spectrophotometry with malachite green, have been used for the determination of tantalum in standard steels produced by the Research Institute of CKD Prague - steels No. 167 and No. 169 with expected concentrations of Ta 0.01% and 0.03%, respectively. INAA method consisted of irradiation of steel samples (chips) in a nuclear reactor and Ge(Li) ..gamma..-ray spectrometry after a cooling period of one month. A spectrophotometric determination is based on the extraction of ionic associate of TaF/sub 6//sup -/ with malachite green into Oenzene from a solution of diluted sulphuric acid and hydrofluoric acid. The results obtained by the two methods are in a good agreement. However, INAA method is more sensitive and precise then spectrophotometry for the determination of tantalum in steels in the above-mentioned concentration ranges.

Determination of tantalum in standard steels by INAA and absorption spectrophotometry

International Nuclear Information System (INIS)

Obrusnik, I.; Posta, S.

1978-01-01

Two analytical methods, instrumental neutron activation analysis (INAA) and absorption spectrophotometry with malachite green, have been used for the determination of tantalum in standard steels produced by the Research Institute of CKD Prague - steels No. 167 and No. 169 with expected concentrations of Ta 0.01% and 0.03%, respectively. INAA method consisted of irradiation of steel samples (chips) in a nuclear reactor and Ge(Li) γ-ray spectrometry after a cooling period of one month. A spectrophotometric determination is based on the extraction of ionic associate of TaF 6 - with malachite green into Oenzene from a solution of diluted sulphuric acid and hydrofluoric acid. The results obtained by the two methods are in a good agreement. However, INAA method is more sensitive and precise then spectrophotometry for the determination of tantalum in steels in the above-mentioned concentration ranges. (author)

Spectrophotometry-based detection of carbapenemase producers among Enterobacteriaceae.

Science.gov (United States)

Bernabeu, Sandrine; Poirel, Laurent; Nordmann, Patrice

2012-09-01

Carbapenem-hydrolyzing ß-lactamases are the most powerful ß-lactamases being able to hydrolyse almost all ß-lactams. They are mostly of the KPC, VIM, IMP, NDM, and OXA-48 type. A spectrophotometry technique based on analysis of the imipenem hydrolysis has been developed that differentiated carbapenemase- from noncarbapenemase producers. This inexpensive technique adapted to screening of carbapenemase producers may be implemented in any reference laboratory worldwide. Copyright © 2012 Elsevier Inc. All rights reserved.

Estimation of nitrate and nitrogen forms of vegetables by UV-spectrophotometry after photo-oxydation.

Science.gov (United States)

Ribeiro, T; Depres, S; Couteau, G; Pauss, A

2003-01-01

An alternative method for the estimation of nitrate and nitrogen forms in vegetables is proposed. Nitrate can be directly estimated by UV-spectrophotometry after an extraction step with water. The other nitrogen compounds are photo-oxidized into nitrate, and then estimated by UV-spectrophotometry. An oxidative solution of sodium persulfate and a Hg-UV lamp is used. Preliminary assays were realized with vegetables like salade, spinachs, artichokes, small peas, broccolis, carrots, watercress; acceptable correlations between expected and experimental values of nitrate amounts were obtained, while the detection limit needs to be lowered. The optimization of the method is underway.

[Noninvasive total hemoglobin monitoring based on multiwave spectrophotometry in obstetrics and gynecology].

Science.gov (United States)

Pyregov, A V; Ovechkin, A Iu; Petrov, S V

2012-01-01

Results of prospective randomized comparative research of 2 total hemoglobin estimation methods are presented. There were laboratory tests and continuous noninvasive technique with multiwave spectrophotometry on the Masimo Rainbow SET. Research was carried out in two stages. At the 1st stage (gynecology)--67 patients were included and in second stage (obstetrics)--44 patients during and after Cesarean section. The standard deviation of noninvasive total hemoglobin estimation from absolute values (invasive) was 7.2 and 4.1%, an standard deviation in a sample--5.2 and 2.7 % in gynecologic operations and surgical delivery respectively, that confirms lack of reliable indicators differences. The method of continuous noninvasive total hemoglobin estimation with multiwave spectrophotometry on the Masimo Rainbow SET technology can be recommended for use in obstetrics and gynecology.

Discovery and spectrophotometry of high-redshift quasars

International Nuclear Information System (INIS)

MacAlpine, G.M.; Feldman, F.R.

1982-01-01

We report on the discovery and spectrophotometry of 30 new high-redshift quasars, which were detected using the Curtis Schmidt technique. We also discuss new follow-up spectrophotometry for 23 quasar candidates from University of Michigan Lists I--IV. Our program sample contains eight quasars with z>3, at least five objects exhibiting broad absorption troughs, and a pair of quasars which are 1' apart on the sky and nearly identical in redshift, at z near 2.13. The redshift distribution for the majority of quasars in UM List IV suggests that most of the single-line quasar candidates in the UM List have low to moderate redshifts, with the reported line often being Mg II lambda2798 or C III] lambda1909. For 17 high-redshift quasars where lambda912 at the emission-line redshift could be examined, we did not find any definite Lyman limit cutoffs. Although three objects show a decline of the continuum within 100 A of lambda912, we do not believe them to be unambiguous examples for emission-line clouds situated in the line of sight. When our O I lambda1304 measurements are combined with the data of others to yield a composite spectrum, we obtain O I lambda1304/lambda8446 = 1.35. This suggests reddening with E/sub B/-Vroughly-equal0.23. Finally, our data exhibit a correlation between Lyα emission line velocity widths and redshift. The higher z quasars in the sample tend to have narrower lines, due, at least in part, to bias in the detection technique

Determination of losartan potassium, quinapril hydrochloride and hydrochlorothiazide in pharmaceutical preparations using derivative spectrophotometry and chromatographic-densitometric method.

Science.gov (United States)

Stolarczyk, Mariusz; Maślanka, Anna; Apola, Anna; Krzek, Jan

2013-01-01

Two methods, spectrophotometric and chromatographic-densitometric ones, were developed for determination of losartan potassium, quinapril hydrochloride and hydrochlorothiazide in pharmaceutical preparations. Spectrophotometric method involved derivative spectrophotometry and zero order spectrophotometry. The measurements were carried out at lambda = 224.0 nm for quinapril, lambda = 261.0 nm for hydrochlorothiazide and lambda = 270.0 nm for losartan when the derivative spectrophotometry was applied and lambda = 317.0 nm when zero order spectrophotometry was applied for the determination of hydrochlorothiazide. In chromatographic-densitometric studies high performance thin layer chromatography (HPTLC) plates were used as stationary phase and a mixture of solvents n-butanol : acetic acid : water (15 : 5 : 1, v/v/v) as mobile phase. Under the established conditions good resolution of examined constituents was obtained. Retardation factor for quinapril hydrochloride was R(f) - 0.70, for losartan potassium R(f) - 0.85 and for hydrochlorothiazide R(f) - 0.78. The developed methods are characterized by high sensitivity and accuracy. For quantitative analysis, densitometric measurements were carried out at lambda = 218.0 nm for quinapril, lambda = 275.0 nm for hydrochlorothiazide and = 232.0 nm for losartan.

Combined spectrophotometry and tensile measurements of human connective tissues: potentials and limitations.

Science.gov (United States)

Ernstberger, Markus; Sichting, Freddy; Baselt, Tobias; Hartmann, Peter; Aust, Gabriela; Hammer, Niels

2013-06-01

Strain-dependent transmission data of nine iliotibial tract specimens are determined using a custom-built optical setup with a halogen light source and an industrial norm material testing machine. Polarized light microscopy and hematoxylin-eosin staining indicated that lateral contraction of collagen structures is responsible for total intensity variations during a 20-cycle preconditioning and a 5-cycle tensile test. Tensile force progress is opposite to total transmission progress. Due to dehydration, wavelength-specific radiation intensity shifting is determined during the test, primarily noticeable in a water absorption band between 1400 and 1500 nm. The results show the capability of integrating spectrophotometry technology into biomechanics for determining structural alterations of human collagen due to applied strain. Being more sensitive to drying, spectrophotometry may likely serve as a quality control in stress-strain testing of biological structures.

Tunable Diode Laser Heterodyne Spectrophotometry of Ozone

Science.gov (United States)

Fogal, P. F.; McElroy, C. T.; Goldman, A.; Murcray, D. G.

1988-01-01

Tunable diode laser heterodyne spectrophotometry (TDLHS) has been used to make extremely high resolution (less than 0.0005/ cm) solar spectra in the 9.6 micron ozone band. Observations have shown that a signal-to-noise ratio of 95 : 1 (35% of theoretical) for an integration time of 1/8 second can be achieved at a resolution of 0.0005 wavenumbers. The spectral data have been inverted to yield a total column amount of ozone, in good agreement with that. measured at the nearby National Oceanographic and Atmospheric Administration (NOAA) ozone monitoring facility in Boulder, Colorado.

Kombineret laser Doppler flowmetri og spectrophotometri som metode til vurdering af mikrocirculation

DEFF Research Database (Denmark)

Berggren Olsen, Mette; Sørensen, Hanne Birke; Houlind, Kim Christian

Kombineret laser Doppler flowmetri og spectrophotometri som metode til vurdering af mikrocirculation Berggren, MB, reservelæge, Karkirurgisk Afdeling, Kolding, mette.marie.berggren.olsen@slb.regionsyddanmark.dk; Houlind, K, lektor, afdelingslæge, Ph.d., Karkirurgisk afdeling, Kolding, kim...

An application of micelle solubilization spectrophotometry in the determination of thorium

International Nuclear Information System (INIS)

Peng Changhai; Zeng Xiaoming

1988-01-01

In this review article the characteristics of the analytical method of Th by means of micelle solubilization spectrophotometry are described and the mechanism of the solubilization and chemical reactions involved is discussed. Also the various color-developing reagents that have been used for this determination are described and compared

The determination of copper in biological materials by flame spectrophotometry

Science.gov (United States)

Newman, G. E.; Ryan, M.

1962-01-01

A method for the determination of the copper content of biological materials by flame spectrophotometry is described. The effects of interference by ions such as sodium and phosphate were eliminated by isolating copper as the dithizonate in CCl4. Results obtained for the urinary excretion of copper by a patient with Wilson's disease before and after treatment with penicillamine are reported. PMID:14479334

Determination of gadolinium by the method of derivative spectrophotometry

International Nuclear Information System (INIS)

Aleksandrova, N.N.; Mishchenko, V.T.; Poluehktov, N.S.; Mukomel', V.L.

1988-01-01

Technique for gadolinium determination at the presence of interfering rare earth elements, which is based on the derivative spectrophotometry method, is suggested. The technique is of increased selectivity and allows to determine gadolinium in the mixtures with elements, which presence in solution makes impossible to determine gadolinium directly. At binary mixtures analysis Sr relative standard deviation does not exceed 0.03, while at the analysis of more complex mixtures Sr increases up to 0.06

Determination of piroxicam in pharmaceutical preparations by ultraviolet direct spectrophotometry, ultraviolet difference spectrophotometry and high performance liquid chromatography

Energy Technology Data Exchange (ETDEWEB)

Hackmann, E.R.M.; Santos Gianotto, E.A. dos; Miritello Santoro, M.I.R. (Universidade de Sao Paulo (Brazil))

1993-02-01

Piroxicam in pharmaceutical preparations (capsules (C), tablets (T), oral drops (OD), suppositories (S) and simulated sample (SS)) was determined by UV direct spectrophotometry (UVS) at 333 nm, by UV difference spectrophotometry (UVDS) at 327 nm, and in C and T, by high performance liquid chromatography (HPLC). For UVS, Beer's law was obeyed in the range 3.0-8.5 [mu]g/mL. The coefficient of correlation (CC), absolute precision (AP) and relative precision (RP) were 0.9999, 0.02 and 0.33%, respectively. The coefficient of variation (CV) for C, T, OD, S and SS were 0.48%, 0.35%, 0.48% and 0.19%, respectively. The recovery average (RA) was 100.22%. For UVDS, Beer's law was obeyed in the range 5.0-15.0 [mu]g/mL. The CC, AP and RP were respectively 0.9999, 0.05 and 0.47%. The CV for C, T, OD, S and SS were 0.64%, 0.84%, 0.62%, 0.54% and 0.15%, respectively. The RA was 99.02%. In HPLC determination, a LiChrospher[reg sign] 100 RP-18 (5 [mu]m) in LiChroCART[reg sign] 125-4 column at ambient temperature with a mobile phase consisting of methanol: (buffer solution citric acid-dibasic sodium phosphate pH 3.0) (55:45) and UV detection at 254 nm enabled the determination of piroxicam in C and T. The response peak area versus concentration presented linearity in the range 10.0-100.0 [mu]g/mL. The CC, AP and RP were 0.9997, 0.45 and 0.90%, respectively. The CV was 0.51%-0.82% and the RA, 97.13%. 14 refs., 1 fig., 5 tabs.

Neutron dosimetry by UV and IR spectrophotometry of the newly developed dyed ECE tracks

International Nuclear Information System (INIS)

Sohrabi, M.; Sadeghi Bajd, S.

1990-01-01

New, large and high-contrasted dyed ECE recoil tracks have been successfully developed. The chief reason for this development has been the provision of large photon-absorbing sites on a non-absorbing unaffected polymer surface for UV and IR spectrophotometry. In this approach, ECE recoil tracks in polycarbonate were dyed using our optimised conditions; sensitisation in 20% by weight acrylic acid at 75 0 C for 3.5 h and dyeing in 3% by weight eosin at 95 0 C for 4 h. Spectrophotometry by UV and IR, track counting and optical densitometry were applied to the samples. These preliminary studies showed some promise for UV absorbance measurements for routine large-scale applications. the results of which are presented and discussed. (author)

Measurement of uranium concentration by molecular absorption spectrophotometry by means optical fibers

International Nuclear Information System (INIS)

Gauna, Alberto C.; Pascale, Ariel A.

1996-01-01

An on-line method for measuring the concentration of uranium in uranyl nitrate-nitric acid aqueous solutions is described. The method is based on molecular absorption spectrophotometry with transmission of light by means of optical fibers. It is ideally suited for control and processes development applications. (author)

Spectrophotometric and potentiometric study of uranyl hydrolysis in perchlorate medium. Is derivative spectrophotometry suitable for search of the chemical model?

International Nuclear Information System (INIS)

Lubal, P.; Havel, J.

1997-01-01

Uranyl hydrolysis (I = 3.00 mol dm -3 NaClO 4 , T = 298.15 K) was studied by potentiometry and spectrophotometry. Numerical analysis of experimental data yielded the logarithmic values of hydrolytic constants for (UO 2 ) p (OH) q (2p-q) species with (p, q) indices: (2, 2) - 6.24 ± 0.02, (3, 5) - 16.80 ± 0.04, and (3, 4) - 12.8 ± 0.1 (potentiometry) and (2, 2) - 6.13 ± 0.02, (3, 5) - 16.81 ± 0.02, and (32, 4) - 12.57 ± 0.02 (average values obtained by derivative spectrophotometry from the first to the fourth order). The spectra of hydrolytic species were deconvoluted and the use of derivative spectrophotometry in equilibria studies has been discussed. (authors)

Water contentwater of determination of cationic polystyrene sulfonate resins by infrared spectrophotometry

International Nuclear Information System (INIS)

Noki, V.

1987-01-01

A method of the determination of water content in polystyrene sulfonate ion-exchange resins in the presence of alkaline earth counter-ions by I.R. spectrophotometry is proposed. This method does not hold in the case of transition metal due to the formation of coordinated complexes with water molecules.

Collection/concentration of trace uranium for spectrophotometric detection using activated carbon and first-derivative spectrophotometry

International Nuclear Information System (INIS)

El-Sayed, A.A.; Hamed, M.M.; El-Reefy, S.; Hmmad, H.A.

2007-01-01

The need exists for preconcentration of trace and ultratrace amounts of uranium from environmental, geological and biological samples. The adsorption of uranium on various solids is important from the purification, environmental, and radioactivity waste disposal points of view. A method is described for the determination of traces of uranium using first-derivative spectrophotometry after adsorptive preconcentration of uranium on activated carbon. Various parameters that influence the adsorptive preconcentration of uranium on activated carbon, viz., pH, amounts of activated carbon and time of stirring and interference of metals have been studied. First-derivative spectrophotometry in conjunction with adsorptive preconcentration of uranium on activated carbon is used for determining uranium at concentration levels down to 20 ppb (w/v). (orig.)

Analysis of nifedipine content in transdermal drug delivery system using non-destructive visible spectrophotometry technique

International Nuclear Information System (INIS)

Normaizira Hamidi; Normaizira Hamidi; Normaizira Hamidi; Mohd Nasir Taib; Mohd Nasir Taib; Wui, Wong Tin; Wui, Wong Tin

2008-01-01

The applicability of visible spectrophotometry technique as a tool to determine the drug content of polymeric film for use as a transdermal drug delivery system was investigated. Hydroxypropylmethycellulose (HPMC) was selected as the matrix polymer and nifedipine as the model drug. Blank and nifedipine-loaded HPMC films were prepared using the solvent evaporation method. The absorbance spectra of these films under the visible wavelengths between 400 and 800 nm were assessed and compared against the drug content values obtained by means of the conventional destructive UV- spectrophotometry technique. The latter required the use of a solvent system which contained methanol, a harmful organic component in pharmaceutical applications. The results indicated that the absorbance values, attributed to nifedipine, at the wavelengths of 545, 585, 638 and 755nm were significantly correlated to the drug content values obtained using the chemical assay method (Pearson correlation value: r = 0.990 and p < 0.01). The visible spectrophotometry technique is potentially suitable for use to determine the nifedipine content of films owing to its nature of characterization of transdermal drug delivery system which does not require sample destruction during the process of measurement. The samples are recoverable from test and analysis of the entire batch of samples is possible without the need of solvents and chemical reagents. (author)

Spectrophotometry of peculiar B and A stars

International Nuclear Information System (INIS)

Adelman, S.J.

1980-01-01

Spectrophotometry of the optical region lambda lambda 3300-7100 is presented for seven magnetic Ap stars: HD 32650, 84 Ursa Majoris, HD 149822, 19 Lyrae, 4 Cygni, HD 196178, and 108 Aquarii. The energy distributions of all seven stars show definite lambda 4200 and lambda 5200 broad, continuum features as well as other more subtle deviations from the predictions of normal stellar atmospheres. The observations of HD 32650 violate the general rule for the Ap stars that the temperature found by comparing the Balmer jump regions with the predictions of normal stalle atmospheres with log g = 4.0 are systematically greater than those found from fitting the slopes of the Paschen continua. (orig.)

Spectrophotometry of the shell around AG Carinae

Science.gov (United States)

Mitra, P. Mila; Dufour, Reginald J.

1990-01-01

Spatially-resolved long-slit spectrophotometry are presented for two regions of the shell nebula around the P-Cygni variable star AG Carinae. The spectra cover the 3700-6800 A wavelength range. Emission-line diagnostics are used to derive extinction, electron temperatures, and densities for various positions in the nebula. The chemical abundances and ionization structure are calculated and compared with other types of planetary nebulae and shells around other luminous stars. It is found that the N/O and N/S ratios of Ag Car are high compared to solar neighborhood ISM values. The O/H depletion found for the AG Car shell approaches that found in the condensations of the Eta Car system.

Using UV-VIS spectrophotometry for determining ecotoxicity of selected non-steroidal anti-inflammatory drugs

Czech Academy of Sciences Publication Activity Database

Čapka, Lukáš; Zlámalová Gargošová, H.; Vávrová, M.

2015-01-01

Roč. 24, 12C (2015), s. 4758-4762 ISSN 1018-4619 Institutional support: RVO:68081715 Keywords : ecotoxicity * NSAIDs * UV-VIS spectrophotometry Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 0.372, year: 2015

Identification and spectrophotometry of faint southern radio galaxies

International Nuclear Information System (INIS)

Spinrad, H.; Kron, R.G.; Hunstead, R.W.

1980-01-01

We have observed a mixed sample of southern radio sources, identified on the Palomar sky survey or on previous direct plates taken with medium-aperture reflectors. At CIO we obtained a few deep 4m photographs and SIT spectrophotometry for redshift and continuum-color measurement. Almost all our sources were faint galaxies; the largest redshift measured was for 3C 275, with z=0.480. The ultraviolet continuum of PKS 0400--643, a ''thermal'' galaxy with z=0.476, closely resembles that of 3C 295 and shows some color evolution in U--B compared to nearby giant ellipticals

Fully-differential spectrophotometry determination of trace thorium in uranium-containing waste water separated by CL-TBP levextrel resin

International Nuclear Information System (INIS)

You Jiannan

2000-01-01

A method for separation by CL-TBP levextrel resin and determination of trace thorium in uranium-containing waste water by fully-differential spectrophotometry is developed. In 4 mol/L HNO 3 medium, in presence of tartaric acid, CL-TBP levextrel resin is used for adsorption of thorium and separating from other elements. The thorium on the resin is stripped by 4 mol/L HCl, with oxalic acid and urea as screening agent, thorium forms red complex with arsenazo III. The maximum absorption of the complex is at 668 nm, and the molar absorptivity is 1.27 x 10 5 L/(mol·cm) . The complex can be steady for 2.5 h. By regulating micro-current of differential spectrophotometry, the method can realize determination with high precision. Sensitivity of this method increase 10 times than usual spectrophotometry. The relative standard deviation is better than +- 5% and recovery of thorium is 99%-107%

Estratégias para aumento de sensibilidade em espectrofotometria UV-VIS Strategies to increase sensitivity in UV-VIS spectrophotometry

Directory of Open Access Journals (Sweden)

Fábio R. P. Rocha

2004-10-01

Full Text Available Spectrophotometry is one of the most widespread analytical techniques due to its simplicity, reliability, and low-cost instrumentation for both direct measurements and coupled to other techniques or processes such as chromatography, electrophoresis and flow analysis. However, the application is often limited by sensitivity. This article describes some advances that greatly improve the performance of spectrophotometric measurements, especially in order to increase sensitivity, including the employment of liquid-core waveguides and solid-phase spectrophotometry.

Determination of macro nickel, vanadium and iron in crude oil and residues by derivative spectrophotometry

International Nuclear Information System (INIS)

Liu, W.; Wang, L.; Li, X.

1992-01-01

In this paper, a new method with derivative spectrophotometry and 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol as the chromogenic reagent in buffer solution of different pH developed for determining micro amounts of nickel. Vanadium and iron in crude oil and residues is reported. Forth-, Second- and Third-, Fourth-order derivative spectrophotometry were applied to determine nickel, nickel and vanadium, nickel and iron in crude oil and residues, respectively. The derivative maximums chosen for the measurement were at 556 nm for nickel, 540 nm and 643 nm for nickel and vanadium, 524 nm and 604 nm for nickel and iron. Beer's law is valid for the range 1.0 x 10 -6 to 2.5 x 10 -5 M

Determination of rare earth element content in yttrium aluminium garnet crystals by absorption spectrophotometry method

International Nuclear Information System (INIS)

Mejl'man, M.L.; Kolomijtsev, A.I.; Baskakova, Z.M.; Bagdasarov, Kh.S.; Kevorkov, A.M.

1985-01-01

Possibility of determination of relative and absolute contents of impurity trivalent REE ions in yttrium aluminium garnet of (YAG) monocrystals has been studied by the absorption spectrophotometry method. Absorption spectra in UV and visible regions YAG monocrystals doped by REE are studied. For each admixture the characteristic lines or absorption bands not overlapping with lines of other admixtures are defined and investigated. The extinction coefficients of characteristic lines are determined which allow one to measure absolute REE admixture concentrations in garnet crystals. A conclusion is drawn that the absorption spectrophotometry method permits to measure REE admixture content in YAG monocrystals within the concentration range of approximately 1x10sup(-3)-5 mas. % with an accuracy not less than 20% (with sample thickness of approximately 1 cm)

The Use of Self-scanned Silicon Photodiode Arrays for Astronomical Spectrophotometry

Science.gov (United States)

Cochran, A. L.

1984-01-01

The use of a Reticon self scanned silicon photodiode array for precision spectrophotometry is discussed. It is shown that internal errors are + or - 0.003 mag. Observations obtained with a photodiode array are compared with observations obtained with other types of detectors with agreement, from 3500 A to 10500 A, of 1%. The photometric properties of self scanned photodiode arrays are discussed. Potential pitfalls are given.

Spectrophotometry of the nucleus of the Sy 2 galaxy Markarian 308

International Nuclear Information System (INIS)

Popov, V.N.; Khachikyan, Eh.E.

1980-01-01

The results of spectrophotometry of the Sy2 galaxy Markarian 308 are presented. The profiles of the emission lines [N II] lambda lambda 6583, 6548 A, Hsub(α), [O III] lambda lambda 5007, 4959 A and Hsub(β) are drawn. The electron density, electron temperature, mass and effective volume of the emitting gas are estimated. Markarian 308 shows now less activity compared with other Sy2 galaxies

Ultraviolet spectrophotometry from Gemini 11 of stars in Orion

International Nuclear Information System (INIS)

Morgan, T.H.; Spear, G.G.; Kondo, Y.; Henize, K.G.

1975-01-01

Ultraviolet spectrophotometry in the wavelength region 2600--3600 A is reported for the bright early-type stars β, eta, γ, delta, iota, epsilon, sigma, xi, and kappa Ori. The results are in good agreement with other observations, and with the possible exception of the supergiants, are in good agreement with recent line-blanketed model atmospheres. There is evidence that the supergiants possess a small ultraviolet deficiency shortward of 3000 A relative to main-sequence stars of similar spectral type. The most extreme example of this phenomenon is the star kappa Ori

Spectrophotometry of comets Giacobini-Zinner and Halley

International Nuclear Information System (INIS)

Tegler, S.C.; O'dell, C.R.

1987-01-01

Optical window spectrophotometry was performed on comets Giacobini-Zinner and Halley over the interval 300-1000 nm. Band and band-sequence fluxes were obtained for the brightest features of OH, CN, NH, and C2, special care having been given to determinations of extinction, instrumental sensitivities, and corrections for Fraunhofer lines. C2 Swan band-sequence flux ratios were determined with unprecedented accuracy and compared with the predictions of the detailed equilibrium models of Krishna Swamy et al. (1977, 1979, 1981, and 1987). It is found that these band sequences do not agree with the predictions, which calls into question the assumptions made in deriving the model, namely resonance fluorescence statistical equilibrium. Suggestions are made as to how to resolve this discrepancy. 16 references

Spectrophotometry of comets Giacobini-Zinner and Halley

Science.gov (United States)

Tegler, Stephen C.; O'Dell, C. R.

1987-01-01

Optical window spectrophotometry was performed on comets Giacobini-Zinner and Halley over the interval 300-1000 nm. Band and band-sequence fluxes were obtained for the brightest features of OH, CN, NH, and C2, special care having been given to determinations of extinction, instrumental sensitivities, and corrections for Fraunhofer lines. C2 Swan band-sequence flux ratios were determined with unprecedented accuracy and compared with the predictions of the detailed equilibrium models of Krishna Swamy et al. (1977, 1979, 1981, and 1987). It is found that these band sequences do not agree with the predictions, which calls into question the assumptions made in deriving the model, namely resonance fluorescence statistical equilibrium. Suggestions are made as to how to resolve this discrepancy.

Comparative studies of method for determining total mercury in fish. Dithizone and flameless atomic absorption spectrophotometry techniques

International Nuclear Information System (INIS)

Protasowicki, M.; Ociepa, A.; Chodyniecki, A.

1977-01-01

Two methods for determining total mercury in fish were compared: the dithizone and flameless atomic absorption spectrophotometry techniques. The studies involved determination of recovery when 1μg of mercury as solutions of HgCl 2 or CH 3 HgC were added to each sample of herring flesh. Mean recoveries in the dithizone method were found to be 91.4+-7.47% and 90.25+-4.73% for the two solutions respectively, while the recoveries obtained with the flameless atomic absorption spectrophotometry were 95.00+-9.13% and 98.70+-7.14%, respectively. Both techniques were used to determine the mercury content in the same herring flesh sample. The first technique showed the content of 0.050+-0.018μg Hg g -1 while the result obtained with the other one was 0.062+-0.013μg Hg g -1 . The statistical treatment of the results obtained showed no difference between the two techniques, the significance level being α=0.05. Therefore, the results obtained with the dithizone method are comparable with those obtained with the flameless atomic absorption spectrophotometry for mercury contents of the magnitude order of 0.050 ug.g -1 . (author)

The quantification of spermatozoa by real-time quantitative PCR, spectrophotometry, and spermatophore cap size.

Science.gov (United States)

Doyle, Jacqueline M; McCormick, Cory R; DeWoody, J Andrew

2011-01-01

Many animals, such as crustaceans, insects, and salamanders, package their sperm into spermatophores, and the number of spermatozoa contained in a spermatophore is relevant to studies of sexual selection and sperm competition. We used two molecular methods, real-time quantitative polymerase chain reaction (RT-qPCR) and spectrophotometry, to estimate sperm numbers from spermatophores. First, we designed gene-specific primers that produced a single amplicon in four species of ambystomatid salamanders. A standard curve generated from cloned amplicons revealed a strong positive relationship between template DNA quantity and cycle threshold, suggesting that RT-qPCR could be used to quantify sperm in a given sample. We then extracted DNA from multiple Ambystoma maculatum spermatophores, performed RT-qPCR on each sample, and estimated template copy numbers (i.e. sperm number) using the standard curve. Second, we used spectrophotometry to determine the number of sperm per spermatophore by measuring DNA concentration relative to the genome size. We documented a significant positive relationship between the estimates of sperm number based on RT-qPCR and those based on spectrophotometry. When these molecular estimates were compared to spermatophore cap size, which in principle could predict the number of sperm contained in the spermatophore, we also found a significant positive relationship between sperm number and spermatophore cap size. This linear model allows estimates of sperm number strictly from cap size, an approach which could greatly simplify the estimation of sperm number in future studies. These methods may help explain variation in fertilization success where sperm competition is mediated by sperm quantity. © 2010 Blackwell Publishing Ltd.

THE DETERMINATION OF BUPROPION HYDROCHLORIDE IN PHARMACEUTICAL DOSAGE FORMS BY ORIGINAL UV- AND SECOND DERIVATIVE UV SPECTROPHOTOMETRY, POTENTIOMETRIC AND CONDUCTOMETRIC METHODS

Directory of Open Access Journals (Sweden)

Duygu YENİCELİ

2010-08-01

Full Text Available Spectrophotometric, potentiometric and conductometric methods are developed for the determination of bupropion hydrochloride (BLIP in pharmaceutical tablets. For the first method, original UV-spectrophotometry, 252 nm was determined as the optimum wavelength and used for the determinations. For the other method, second derivative UV spectrophotometry, the absorbances were measured at 217.4 and 221.8 nm and the distance between these extremum values was determined according to peak to peak method. Two spectrophotometric methods were validated over the concentration range of 5.72 - 20.03 ug/mL. The limit of detection and limit of quantitation values of original UV-spectrophotometry were 0.75 ug/mL and 2.28 jug/mL. Also, these parameters were determined as 0.23 ug/mL and 0.68 ug/mL respectively, for the second derivative UV spectrophotometry. Developed methods were fully validated and the applicability of the methods for the determination of BUP in pharmaceuticals were demonstrated. Also, simple potentiometric and conductometric methods were developed and the applicability of these methods were demonstrated. The results of four analytical methods were compared with ANOVA test and no significant difference was found statistically. As a result, the developed methods could be proposed to the rutin content analysis to be simple, cheap, accurate, and precise

Spectrophotometry of Artemisia tridentata to quantitatively determine subspecies

Science.gov (United States)

Richardson, Bryce; Boyd, Alicia; Tobiasson, Tanner; Germino, Matthew

2018-01-01

Ecological restoration is predicated on our abilities to discern plant taxa. Taxonomic identification is a first step in ensuring that plants are appropriately adapted to the site. An example of the need to identify taxonomic differences comes from big sagebrush (Artemisia tridentata). This species is composed of three predominant subspecies occupying distinct environmental niches, but overlap and hybridization are common in ecotones. Restoration of A. tridentata largely occurs using wildland collected seed, but there is uncertainty in the identification of subspecies or mix of subspecies from seed collections. Laboratory techniques that can determine subspecies composition would be desirable to ensure that subspecies match the restoration site environment. In this study, we use spectrophotometry to quantify chemical differences in the water-soluble compound, coumarin. Ultraviolet (UV) absorbance of A. tridentata subsp. vaseyana showed distinct differences among A.t. tridentata and wyomingensis. No UV absorbance differences were detected between A.t. tridentata and wyomingensis. Analyses of samples from > 600 plants growing in two common gardens showed that UV absorbance was unaffected by environment. Moreover, plant tissues (leaves and seed chaff) explained only a small amount of the variance. UV fluorescence of water-eluted plant tissue has been used for many years to indicate A.t. vaseyana; however, interpretation has been subjective. Use of spectrophotometry to acquire UV absorbance provides empirical results that can be used in seed testing laboratories using the seed chaff present with the seed to certify A. tridentata subspecies composition. On the basis of our methods, UV absorbance values 3.1 would indicate either A.t. tridentata or wyomingensis. UV absorbance values between 2.7 and 3.1 would indicate a mixture of A.t. vaseyana and the other two subspecies.

Blood volume measurement with indocyanine green pulse spectrophotometry: dose and site of dye administration

NARCIS (Netherlands)

Germans, Menno R.; de Witt Hamer, Philip C.; van Boven, Leonard J.; Zwinderman, Koos A. H.; Bouma, Gerrit J.

2010-01-01

(1) To determine the optimal administration site and dose of indocyanine green (ICG) for blood volume measurement using pulse spectrophotometry, (2) to assess the variation in repeated blood volume measurements for patients after subarachnoid hemorrhage and (3) to evaluate the safety and efficacy of

Spectrophotometry with optical fibers applied to nuclear product processing

International Nuclear Information System (INIS)

Boisde, G.; Perez, J.J.; Velluet, M.T.; Jeunhomme, L.B.

1988-01-01

Absorption spectrophotometry is widely used in laboratories for composition analysis and quality control of chemical processes. Using optical fibers for transmitting the light between the instrument and the process line allows to improve the safety and productivity of chemical processes, thanks to real time measurements. Such applications have been developed since 1975 in CEA for the monitoring of nuclear products. This has led to the development of fibers, measurement cells, and optical feedthrough sustaining high radiation doses, of fiber/spectrophotometer couplers, and finally of a photodiode array spectrophotometer optimized for being used together with optical fibers [fr

The analysis of coal-and coke ashes by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Coutinho, C.A.; Prates, H.T.; Pereira, C.P.

1977-01-01

In order to provide better conditions for the control of the chemical composition of the load in the USIMINAS blast furnaces, a method of analysis for sodium, potassium, iron, aluminium, calcium, magnesium and maganese in coal-and coke ash by atomic absorption spectrophotometry was developed. The precision of the calibration curves and the reproducibility of the results are given, together with an estimate of the speed compared with conventional methods of chemical analysis [pt

Determination of mercury, lead and cadmium in water by the CRA-atomic absorption spectrophotometry with solvent extraction

International Nuclear Information System (INIS)

Shim, Y.B.; Won, M.S.; Kim, C.J.

1980-01-01

The method of CRA-atomic absorption spectrophotometer with solvent extraction for the determination of mercury, lead and cadmium in water was studied. The optimum extracting conditions for CRA-atomic absorption spectrophotometry were the following: the complexes of mercury, lead and cadmium with dithizone were separated from the aqueous solution and concentrated into the 10 ml chloroform solution. Back extraction was performed; the concentrated mercury, lead and cadmium was extracted from the chloroform solution into the 10 ml 6-normal aqueous hydrochloric acid solution. In this case, recovery ratios were the following: mercury was 94.7%, lead 97.7% and cadmium 103.6%. The optimum operating conditions for the determination of mercury, lead and cadmium by the CRA-atomic absorption spectrophotometry also were investigated to test the dry step, ash step and atomization step for each metal. The experimental results of standard addition method were the following: the determination limit of each metal within 6% relative deviation was that lead was 0.04 ppb, and cadmium 0.01 ppb. Especially, mercury has been known impossible to determine by CRA-atomic absorption spectrophotometry until now. But in this study, mercury can be determined with CRA-atomic absorption spectrophotometer. Its determination limit was 4 ppb within 8% relative deviation. (author)

On a variant of the first derivative technique in spectrophotometry

International Nuclear Information System (INIS)

Kvaratskheli, Yu.K.; Pchelkin, V.A.; Demin, Yu.V.; Kukushkin, G.R.

1981-01-01

A variant of the first derivative technique in spectrophotometry is suggested which is based on continuous sinusoidal sweep of the wavelength within a narrow spectral region. A spectrophotometer has been designed which records the first derivative (dA/dlambda). A method has been developed of determining uranium (6) with arsenazo 3 in the presence of 20 times its amounts of zirconium thorium or iron (3). The method can be used for spectrophotometric determination of some other elements with different reagents, particularly in the analysis of elements with overlapped absorption spectra [ru

The nature of C-class asteroids from 3-micron spectrophotometry

Science.gov (United States)

Feierberg, M. A.; Lebofsky, L. A.; Tholen, D. J.

1985-01-01

Narrowband spectrophotometry between 2.3 and 3.5 micrometers is presented for 14 main-belt C asteroids greater than 100 km in diameter. Absorption features at 3 micrometers due to water of hydration are present in the spectra of nine of the asteroids, with intensities ranging from 6 to 23 percent. The other five asteroids have no such absorption greater than 2 percent in intensity. The present C-asteroid population may be fragments of larger parent bodies with anhydrous C3-like cores and hydrated C1I- or C2M-like mantles.

Method for rapidly determining a pulp kappa number using spectrophotometry

Science.gov (United States)

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.

Infrared spectrophotometry and radiative transfer in optically thick circumstellar dust envelopes

International Nuclear Information System (INIS)

Merrill, K.M.

1976-01-01

The Two-Micron Sky Survey of Neugebauer and Leighton and, more recently, the AFCRL Infrared Sky Survey of Walker and Price have detected numerous compact, isolated, bright infrared sources which are not identified with previously cataloged stars. Observations of many such objects suggest that extensive circumstellar dust envelopes modify the flux from a central source. The present investigations employ broad bandpass photometry at lambda lambda 1.65 μm to 12.5 μm and narrow bandpass spectrophotometry (Δ lambda/lambda approximately 0.015) at lambda lambda 2-4 μm and lambda lambda 8-13 μm to determine the properties of a large sample of such infrared sources. Infrared spectrophotometry can clearly differentiate between normal stars of spectral types M(''oxygen-rich'') and C (''carbon-rich'') on the basis of characteristic absorption bands arising in cool stellar atmospheres. Most of the 2 μ Sky Survey and many of the AFCRL Sky Survey sources appear to be stars of spectral types M and C which are differentiated from normal cool comparison stars only by the presence of extensive circumstellar dust envelopes. Due to the large optical depth of the envelopes, the flux from the star and from the dust cannot be simply separated. Hence solutions of radiative transfer through spherically symmetric envelopes of arbitrary optical depth were generated by a generalized computer code which employed opacities of real dust

Detection of silver nanoparticles in seawater at ppb levels using UV-visible spectrophotometry with long path cells.

Science.gov (United States)

Lodeiro, Pablo; Achterberg, Eric P; El-Shahawi, Mohammad S

2017-03-01

Silver nanoparticles (AgNPs) are emerging contaminants that are difficult to detect in natural waters. UV-visible spectrophotometry is a simple technique that allows detection of AgNPs through analysis of their characteristic surface plasmon resonance band. The detection limit for nanoparticles using up to 10cm path length cuvettes with UV-visible spectrophotometry is in the 0.1-10ppm range. This detection limit is insufficiently low to observe AgNPs in natural environments. Here we show how the use of capillary cells with an optical path length up to 200cm, forms an excellent technique for rapid detection and quantification of non-aggregated AgNPs at ppb concentrations in complex natural matrices such as seawater. Copyright © 2016 Elsevier B.V. All rights reserved.

Liquid-phase microextraction and fibre-optics-based cuvetteless CCD-array micro-spectrophotometry for trace analysis

International Nuclear Information System (INIS)

Sharma, Nisha; Pillai, Aradhana K.K.V.; Pathak, Neeraj; Jain, Archana; Verma, Krishna K.

2009-01-01

Liquid-phase microextraction (LPME) has been investigated for trace analysis in the present work in conjunction with fibre-optic-based micro-spectrophotometry which accommodates sample volume of 1 μL placed between the two ends of optical fibres. Methods have been evolved for the determination of (i) 1-100 μM and 0.5-20 μM of thiols by single drop microextraction (SDME) and LPME in 25 μL of the organic solvent, respectively, involving their reaction with the Ellman reagent and ion pair microextraction of thiolate ion formed; (ii) 70 μg to 7 mg L -1 of chlorine/chlorine dioxide by headspace in-drop reaction with alternative reagents, viz., mixed phenylhydrazine-4-sulphonic acid and N-(1-naphthyl)ethylenediamine dihydrochloride, o-dianisidine, o-tolidine, and N,N-diethyl-p-phenylenediamine; (iii) 0.2-4 mg L -1 of ammonia by reaction with 2,4-dinitro-1-fluorobenzene to give 2,4-dinitroaniline which was diazotized and coupled with 1-naphthylamine, the resulting dye was subjected to preconcentration by solid-phase extraction and LPME; and (iv) 25-750 μg L -1 of iodide/total iodine by oxidation of iodide by 2-iodosobenzoate, microextraction of iodine in organic solvent, and re-extraction into aqueous starch-iodide reagent drop held in the organic phase. LPME using 25-30 μL of organic solvent was found to produce more sensitive results than SDME. The cuvetteless spectrophotometry as used in combination with sample handling techniques produced limits of detection of analytes which were better than obtained by previously reported spectrophotometry.

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

Science.gov (United States)

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.

Comparison of gas chromotography, spectrophotometry and near infrared spectroscopy to quantify prussic acid potential in forages.

Science.gov (United States)

Goff, Ben M; Moore, Kenneth J; Fales, Steven L; Pedersen, Jeffery F

2011-06-01

Sorghum [Sorghum bicolor (L.) Moench] has been shown to contain the cyanogenic glycoside dhurrin, which is responsible for the disorder known as prussic acid poisoning in livestock. The current standard method for estimating hydrogen cyanide (HCN) uses spectrophotometry to measure the aglycone, p-hydroxybenzaldehyde (p-HB), after hydrolysis. Errors may occur due to the inability of this method to solely estimate the absorbance of p-HB at a given wavelength. The objective of this study was to compare the use of gas chromatography (GC) and near infrared spectroscopy (NIRS) methods, along with a spectrophotometry method to estimate the potential for prussic acid (HCNp) of sorghum and sudangrasses over three stages maturities. It was shown that the GC produced higher HCNp estimates than the spectrophotometer for the grain sorghums, but lower concentrations for the sudangrass. Based on what is known about the analytical process of each method, the GC data is likely closer to the true HCNp concentrations of the forages. Both the GC and spectrophotometry methods yielded robust equations with the NIRS method; however, using GC as the calibration method resulted in more accurate and repeatable estimates. The HCNp values obtained from using the GC quantification method are believed to be closer to the actual values of the forage, and that use of this method will provide a more accurate and easily automated means of quantifying prussic acid. Copyright © 2011 Society of Chemical Industry.

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

Science.gov (United States)

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. Copyright © 2012 Elsevier Ltd. All rights reserved.

Thin film thickness measurement error reduction by wavelength selection in spectrophotometry

International Nuclear Information System (INIS)

Tsepulin, Vladimir G; Perchik, Alexey V; Tolstoguzov, Victor L; Karasik, Valeriy E

2015-01-01

Fast and accurate volumetric profilometry of thin film structures is an important problem in the electronic visual display industry. We propose to use spectrophotometry with a limited number of working wavelengths to achieve high-speed control and an approach to selecting the optimal working wavelengths to reduce the thickness measurement error. A simple expression for error estimation is presented and tested using a Monte Carlo simulation. The experimental setup is designed to confirm the stability of film thickness determination using a limited number of wavelengths

Determination of serum albumin with tribromoarsenazo by spectrophotometry

Directory of Open Access Journals (Sweden)

Qing-Zhou Zhai

2007-08-01

Full Text Available The reaction of tribromoarsenazo(TB-ASA with serum albumin in the presence of emulgent OP was studied by spectrophotometry. In a Britton-Robinson buffer solution at pH 2.9, tribromoarsenazo and bovine serum albumin can immediately form a red compound in the presence of emulgent OP with a maximum absorption wavelength at 354 nm. The presence of emulgent OP can increase the reaction sensitivity and the compound stability. The molar absorptivity of the compound is ε354 nm = 6.13 x 105 M-1•cm-1. Beer's law is obeyed over the range of 5.0-75.0 mg•L-1 for bovine serum albumin. The present method was applied to the determination of the total proteins in human serums with satisfactory results.

Quantitation of heparosan with heparin lyase III and spectrophotometry.

Science.gov (United States)

Huang, Haichan; Zhao, Yingying; Lv, Shencong; Zhong, Weihong; Zhang, Fuming; Linhardt, Robert J

2014-02-15

Heparosan is Escherichia coli K5 capsule polysaccharide, which is the key precursor for preparing bioengineered heparin. A rapid and effective quantitative method for detecting heparosan is important in the large-scale production of heparosan. Heparin lyase III (Hep III) effectively catalyzes the heparosan depolymerization, forming unsaturated disaccharides that are measurable using a spectrophotometer at 232 nm. We report a new method for the quantitative detection of heparosan with heparin lyase III and spectrophotometry that is safer and more specific than the traditional carbazole assay. In an optimized detection system, heparosan at a minimum concentration of 0.60 g/L in fermentation broth can be detected. Copyright © 2013 Elsevier Inc. All rights reserved.

Direct imaging and spectrophotometry of Comet P/Tempel 2

International Nuclear Information System (INIS)

Boehnhardt, H.; Beisser, K.; Vanysek, V.; Mueller, B.E.A.; Weiss, M.

1990-01-01

Both direct imaging and spectrophotometry of Comet P/Tempel 2 during May-November 1988 have led to a nuclear diameter determination of the order of about 10 km. Sekanina's (1987) spin-vector model for this comet is judged capable of qualitatively accounting for both the visual light curve of the comet during this period, which exhibited a steep increase perihelion despite the normal, moderate-decrease perihelion, and an asymmetric extension of the fanlike coma in the solar direction. The late activity onset, the possible constant visual brightness immediately afterward, and the deviation of the fan axis orientation from the predicted value in May 1988, may all furnish additional constraints for P/Tempel 2 nucleus modeling. 24 refs

Practical application of solid phase spectrophotometry in analysis of materials and goods of mining and metallurgy

International Nuclear Information System (INIS)

Duan Qunzhang

1999-01-01

The author reviewed recent development and practical application of solid phase spectrophotometry in analysis of materials and goods of mining-metallurgy. Separation and preconcentration and conditions of coloring determination, sensitivity and range of detection, as well as interference of corresponding method are discussed

Rapid and Sensitive Determination of Lipid Oxidation Using the Reagent Kit Based on Spectrophotometry (FOODLABfat System

Directory of Open Access Journals (Sweden)

Chang Woo Kwon

2016-01-01

Full Text Available The reliability and availability of FOODLABfat system for determining acid value (AV and peroxide value (POV were assessed during the hydrolytic rancidification and lipid oxidation of edible oils. This reagent kit based on spectrophotometry was compared to the official methods (ISO 660 and 3960 protocols based on manual titration employing the standard mixture for the simulated oxidation models and edible oils during the thermally induced oxidation at 180°C. The linear regression line of standard mixture and the significant difference of thermally oxidized time course study determined between them showed high correlations (R2=0.998 and p<0.05 in both AVs and POVs. Considering ISO protocols with a probability of human error in manual titration, the rapidness and simplicity of the reagent kit based on spectrophotometry make it a promising alternative to monitor the lipid oxidation of edible oils and lipid-containing foods.

Optical imagery and spectrophotometry of CTB 80

Science.gov (United States)

Hester, J. Jeff; Kulkarni, Shrinivas R.

1989-01-01

Narrow-band imagery and spectrophotometry of the central region of CTB 80 are presented. The images show weak forbidden O III and ubiquitous filamentary forbidden S II and H-alpha emission from the extended radio lobes in which the core is embedded. The data indicate that the extended component is shock heated. Balmer line-dominated emission is observed around the perimeter of the core. Assuming that the volume of the radio shell is similar to the volume of the thermal shell, it is found that a magnetic field of about 600 microG and a cosmic-ray proton-to-electron ratio of about 200 are required to explain the pressure and synchrotron volume emissivity in the radio shell. It is suggested that the optical emission form the core of CTB 80 arises behind shocks which are being driven into a magnetized thermal plasma by the confined relativistic wind from PSR 1951+32.

Symbiotic stars: spectrophotometry at 3-4 and 8-13 μm

International Nuclear Information System (INIS)

Roche, P.F.; Aitken, D.K.

1983-01-01

Infrared spectrophotometry of 20 symbiotic stars, mostly of dust-rich variety, is presented. HDE 330036 is unique in showing an emission feature at 11.3 μm. The remainder combine a hot grey component and/or optically thin silicate emission. A model in which the grey component is due to optically thick silicate dust is not consistent with the spectra. It is proposed instead that iron-based grains, expected to form in the ejecta of cool stars, are heated by the ultraviolet radiation field of the hot companion. (author)

Optical fiber couplers for spectrophotometry. Perspectives for in-situ on-line and remote measurements

International Nuclear Information System (INIS)

Boisde, G.; Linger, C.; Chevalier, G.; Perez, J.J.

1983-01-01

Optical fiber couplers have been developed specially for nuclear chemical spectrophotometric applications. Coupling devices are described for TELEPHOT industrial photometers and some commercial spectrophotometer, together with the probes and measurement cells employed. The value of optical multiplexing is mentioned. Non nuclear applications in medical analysis are also mentioned, together with the possibilities offered by these devices for uses other than spectrophotometry [fr

Determination of micro amounts of praseodymium by analogue derivative spectrophotometry

International Nuclear Information System (INIS)

Ishii, Hajime; Satoh, Katsuhiko.

1986-01-01

Derivative spectrophotometry using the analogue differentiation circuit was applied to the determination of praseodymium at the ppm level. By the proposed method, in which the second or fourth derivative spectrum of the characteristic absorption band of praseodymium(III) at 444 nm is measured, as little as 3 ppm of praseodymium can be determined directly and easily even in the presence of large amounts of other rare earths without any prior separation. Interferences from neodymium, samarium, dysprosium, holmium and erbium ions which have characteristic absorption bands around 444 nm can easily be removed by utilizing the isosbestic point in the derivative spectra of praseodymium(III) and the interfering rare earth(III). (author)

8- to 13-micron spectrophotometry of Comet IRAS-Araki-Alcock

Science.gov (United States)

Feierberg, M. A.; Witteborn, F. C.; Johnson, J. R.; Campins, H.

1984-01-01

Spectrophotometry between 8.0 and 13.0 microns at 2 percent spectral resolution is presented for areas in and near the nuclear condensation of Comet IRAS-Araki-Alcock (1983d) on May 11 and 12, 1983. All the spectra can be fit very well by blackbody curves, and no 10-micron silicate emissions are seen. The temperature structure of the coma suggests the presence of small (radii less than 5 microns) dust particles within 150 km of the nucleus and larger ones further out. The change in the spatial distribution of the infrared flux between the two nights suggests that an outburst may have occurred sometime on May 11.

Analysis of impurities in silver matrix by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Hussain, R.; Ishaque, M.; Mohammad, D.

1999-01-01

A procedure for the analysis of aluminium, chromium, copper, lead, mercury, nickel and zinc mainly using flame lens atomic absorption spectrophotometry has been described. The results depict that the presence of silver does not introduce any significant interference, when standards are prepared in matching silver matrix solutions. The calibration curves obey the straight-line equations passing through the origin. Thus the separation of silver matrix from the analyte solutions is not necessary. The method has successfully been applied for the analysis of silver foils, wires, battery grade silver oxides and silver nitrate samples containing analyte elements in the concentration range 2 to 40 ppm. (author)

Optical properties of orthodontic aligners--spectrophotometry analysis of three types before and after aging.

Science.gov (United States)

Lombardo, Luca; Arreghini, Angela; Maccarrone, Roberta; Bianchi, Anna; Scalia, Santo; Siciliani, Giuseppe

2015-01-01

The aim was to assess and compare absorbance and transmittance values of three types of clear orthodontic aligners before and after two cycles of in vitro aging. Nine samples of orthodontic aligners from three different manufacturers (Invisalign, Align Technology, Santa Clara, CA, USA; All-In, Micerium, Avegno, GE, Italy; F22 Aligner, Sweden & Martina, Due Carrare, PD, Italy) were selected, and each sample was subjected to spectrophotometry analysis of both its transmittance and absorbance a total of 27 times. Samples were subsequently aged in vitro at a constant temperature in artificial saliva supplemented with food colouring for two cycles of 14 days each. The spectrophotometry protocol was then repeated, and the resulting data were analysed and compared by means of ANOVA (p < 0.05). All types of aligners tested yielded lower transmittance and higher absorbance values after aging, but the difference was not significant in any case. That being said, the F22 aligners were found to be most transparent, both before and after aging, followed by Invisalign and All-In, and these differences were statistically significant. Commercial aligners possess significantly different optical, and therefore aesthetic, properties, both as delivered and following aging.

KAJIAN ADSORPSI ION LOGAM Cr(VI OLEH ADSORBEN KOMBINASI ARANG AKTIF SEKAM PADI DAN ZEOLIT MENGGUNAKAN METODE SOLID-PHASE SPECTROPHOTOMETRY (SPS

Directory of Open Access Journals (Sweden)

Sulistyo Saputro

2016-10-01

  This study aims to study the use of activated rice husk charcoal and zeolite as combination adsorbents to adsorb Cr(VI metal ions; the effect of the combination adsorbents of activated rice husk charcoal and zeolite’s compositions to adsorb Cr(VI metal ions; and the sensitivity of solid-phase spectrophotometry (SPS as a method to determine the reduced levels of Cr(VI metal ions in the level of 15μ"> g/L. The activated rice husk charcoal used were obtained through the activation process by soaking in a solution of ZnCl2 10% while the zeolite with a solution of H2SO4 10%. The contacting process of the adsorbents with Cr(VI metal ions was done by varying the compositions of the activated rice husk charcoal and zeolite adsorbent, 1:1, 1:2, 1:3, and 2:1. The data analysis of the Cr(VI level used solid-phase spectrophotometry (SPS method. Characterization of activated rice husk charcoal and zeolite used FTIR. The results showed that: (1 a combination of activated rice husk charcoal and zeolite can be used as adsorbent to adsorb Cr(VI metal ions with the adsorption capacity was 0,28 15μ"> g/g; (2 the optimum composition of adsorbents was 1:2 with the percentage of absorption was 40,99%; (3 solid-phase spectrophotometry (SPS is a sensitive method to determine the reduced levels of Cr(VI in the level of 15μ"> g/L with the limit of detection (LOD was 0,021 15μ"> g/L.   Keywords: adsorption, Cr(VI,  activated  rice husk charcoal,  zeolite, solid-phase spectrophotometry

Determination of uranium and plutonium in high active solutions by extractive spectrophotometry

International Nuclear Information System (INIS)

Subba Rao, R.V.; Damodaran, K.; Santosh Kumar, G.; Ravi, T.N.

2000-01-01

Plutonium and uranium was extracted from nitric acid into trioctyl phosphine oxide in xylene. The TOPO layer was analysed by spectrophotometry. Thoron was used as the chromogenic agent for plutonium. Pyridyl azoresorcinol was used as chromogenic agent for uranium. The molar absorption coefficient for uranium and plutonium was found to be 19000 and 19264 liter/mole-cm, respectively. The correlation coefficient for plutonium and uranium was found to be 0.9994. The relative standard deviation for the determination of plutonium and uranium was found to be 0.96% and 1.4%, respectively. (author)

Determination of silica in silicates by differential spectrophotometry as α-molybdosilicic acid

International Nuclear Information System (INIS)

Ohlweiler, O.A.; Meditsch, J.O.; Silva, S.

1980-01-01

A method for determining silica in silicates by differential spectrophotometry, using β-molybdosilic acid, is described. The sample is attacked by a mixture of boron trioxide and lithium carbonate (10:1). α-molydbosilicic acid is developed in a buffered solution (pH approximatelly 3.9) containing acetic acid and sodium acetate. The analytical procedure involves a series of preliminary steps which were previously elaborated for the gravimetric determination of silica as oxine molybdosilicate and which account for the removal of phosphorus, titanium and zirconium through ion exchange resins. (C.L.B.) [pt

Rapid measurement of indocyanine green retention by pulse spectrophotometry: a validation study in 70 patients with Child-Pugh A cirrhosis before hepatectomy for hepatocellular carcinoma.

Science.gov (United States)

Cheung, Tan To; Chan, See Ching; Chok, Kenneth S H; Chan, Albert C Y; Yu, Wan Ching; Poon, Ronnie T P; Lo, Chung Mau; Fan, Sheung Tat

2012-06-01

The indocyanine green (ICG) retention test is the most popular liver function test for selecting patients for major hepatectomy. Traditionally, it is done using spectrophotometry with serial blood sampling. The newly-developed pulse spectrophotometry is a faster alternative, but its accuracy on Child-Pugh A cirrhotic patients undergoing hepatectomy for hepatocellular carcinoma has not been well documented. This study aimed to assess the accuracy of the LiMON(®), one of the pulse spectrophotometry systems, in measuring preoperative ICG retention in these patients and to devise an easy formula for conversion of the results so that they can be compared with classical literature records where ICG retention was measured by the traditional method. We measured the liver function of 70 Child-Pugh A cirrhotic patients before hepatectomy for hepatocellular carcinoma from September 2008 to January 2009. ICG retention at 15 minutes measured by traditional spectrophotometry (ICGR15) was compared with ICG retention at 15 minutes measured by the LiMON (ICGR15(L)). The median ICGR15 was 14.7% (5.6%-32%) and the median ICGR15(L) was 10.4% (1.2%-28%). The mean difference between them was -4.3606. There was a strong correlation between ICGR15 and ICGR15(L) (correlation coefficient, 0.844; 95% confidence interval, 0.762-0.899). The following formula was devised: ICGR15=1.16XICGR15(L)+2.73. The LiMON provides a fast and repeatable way to measure ICG retention at 15 minutes, but with constant underestimation of the real value. Therefore, when comparing results obtained by traditional spectrophotometry and the LiMON, adjustment of results from the latter is necessary, and this can be done with a simple mathematical calculation using the above formula.

Technical note: comparing von Luschan skin color tiles and modern spectrophotometry for measuring human skin pigmentation.

Science.gov (United States)

Swiatoniowski, Anna K; Quillen, Ellen E; Shriver, Mark D; Jablonski, Nina G

2013-06-01

Prior to the introduction of reflectance spectrophotometry into anthropological field research during the 1950s, human skin color was most commonly classified by visual skin color matching using the von Luschan tiles, a set of 36 standardized, opaque glass tiles arranged in a chromatic scale. Our goal was to establish a conversion formula between the tile-based color matching method and modern reflectance spectrophotometry to make historical and contemporary data comparable. Skin pigmentation measurements were taken on the forehead, inner upper arms, and backs of the hands using both the tiles and a spectrophotometer on 246 participants showing a broad range of skin pigmentation. From these data, a second-order polynomial conversion formula was derived by jackknife analysis to estimate melanin index (M-index) based on tile values. This conversion formula provides a means for comparing modern data to von Luschan tile measurements recorded in historical reports. This is particularly important for populations now extinct, extirpated, or admixed for which tile-based measures of skin pigmentation are the only data available. Copyright © 2013 Wiley Periodicals, Inc.

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

Science.gov (United States)

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. Copyright © 2016 Elsevier Ltd. All rights reserved.

Optical properties of orthodontic aligners?spectrophotometry analysis of three types before and after aging

OpenAIRE

Lombardo, Luca; Arreghini, Angela; Maccarrone, Roberta; Bianchi, Anna; Scalia, Santo; Siciliani, Giuseppe

2015-01-01

Background The aim was to assess and compare absorbance and transmittance values of three types of clear orthodontic aligners before and after two cycles of in vitro aging. Methods Nine samples of orthodontic aligners from three different manufacturers (Invisalign, Align Technology, Santa Clara, CA, USA; All-In, Micerium, Avegno, GE, Italy; F22 Aligner, Sweden & Martina, Due Carrare, PD, Italy) were selected, and each sample was subjected to spectrophotometry analysis of both its transmittanc...

Selenium determination in biological material by atomic absorption spectrophotometry in graphite furnace and using vapor generation

International Nuclear Information System (INIS)

Carvalho Vidal, M. de F. de.

1984-01-01

The applicability of the atomic absorption spectrophotometry to the determination of selenium in biological material using vapor generation and electrothermal atomization in the graphite furnace was investigated. Instrumental parameters and the analytical conditions of the methods were studied. Decomposition methods for the samples were tested, and the combustion in the Wickbold apparatus was chosen. (author) [pt

Emission flame spectrophotometry of chromium, cobalt, nickel trace amounts

International Nuclear Information System (INIS)

Prudnikov, Y.D.; Shapkina, Y.S.

1976-01-01

Chromium, cobalt, and nickel were determined in a flame spectrophotometer with a dual diffraction monochromator, DFS-12, in a high-temperature nitrogen-acetylene flame. The effect of ionization and the elements in the oxidizing flame was small. The lower limit of detection for the three elements is 1x10 -2 to 1 x10 -3 μg/ml, and the high selectivity of the analysis permits determining down to 10 -4 % Cr and Ni and to 10 -3 % Co. These elements may be determined in rocks and minerals from solutions prepared for analysis for alkali and alkali-earth elements. The possibilities of emission flame spectrophotometry are as great as those of atomic-absorption analysis, and it may be used for determining Cr, Co, and Ni in rocks and minerals, especially pure substances, metals, and other materials

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

Science.gov (United States)

Marcialis, Robert L.; Lebofsky, Larry A.

1991-01-01

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.

A new hydride generator for the determination of volatile elements by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Kersabiec, A.M. de

1979-01-01

The production of hydrides in order to use them for analysis by atomic absorption spectrophotometry depends on many parameters. A new apparatus has been designed for this specific operation. It is characterized by a reaction chamber with variable size and by appliances for regulation and control of the physical conditions of operation. Properties are both methodological studies and utilization in large scale analysis. The entire description of the apparatus is completed by an analytical study [fr

A laboratory manual for the determination of metals in water and wastewater by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Smith, R.

1983-01-01

This guide presents, in addition to a brief discussion of the basic principles and practical aspects of atomic absorption spectrophotometry, a scheme of analysis for the determination of 19 metals in water and wastewater, 16 by flame atomic absorption and 3 by vapour generation techniques. Simplicity, speed and accuracy were the main criteria considered in the selection of the various methods

HPLC determination of flavonoid glycosides in Mongolian Dianthus versicolor Fisch. (Caryophyllaceae) compared with quantification by UV spectrophotometry.

Science.gov (United States)

Obmann, Astrid; Purevsuren, Sodnomtseren; Zehl, Martin; Kletter, Christa; Reznicek, Gottfried; Narantuya, Samdan; Glasl, Sabine

2012-01-01

Dianthus versicolor is used in traditional Mongolian medicine against liver impairment. Fractions enriched in flavone-di- and triglycosides were shown to enhance bile secretion. Therefore, reliable and accurate analytical methods are needed for the determination of these flavonoids in the crude drug and extracts thereof. To provide a validated HPLC-DAD (diode array detector) method especially developed for the separation of polar flavonoids and to compare the data obtained with those evaluated by UV spectrophotometry. Separations were carried out on an Aquasil® C₁₈-column (4.6 mm × 250.0 mm, 5 µm) with a linear gradient of acetonitrile and water (adjusted to pH 2.8 with trifluoroacetic acid) as mobile phase. Rutoside was employed as internal standard with linear behavior in a concentration range of 0.007-3.5 mg/mL. Accuracy was determined by spiking the crude drug with saponarin resulting in recoveries between 92% and 102%. The method allows the quantification of highly polar flavonoid glycosides and the determination of their total content. For saponarin a linear response was evaluated within the range 0.007-3.5 mg/mL (R²  > 0.9999). It was proven that threefold sonication represents a time-saving, effective and cheap method for the extraction of the polar flavonoid glycosides. The contents determined by HPLC were shown to be in agreement with those obtained employing UV spectrophotometry. The study has indicated that the newly developed HPLC method represents a powerful technique for the quality control of D. versicolor. Ultraviolet spectrophotometry may be used alternatively provided that the less polar flavonoids are removed by purification. Copyright © 2011 John Wiley & Sons, Ltd.

Acid-Base Properties of Azo Dyes in Solution Studied Using Spectrophotometry and Colorimetry

Science.gov (United States)

Snigur, D. V.; Chebotarev, A. N.; Bevziuk, K. V.

2018-03-01

Colorimetry and spectrophotometry with chemometric data processing were used to study the acid-base properties of azo dyes in aqueous solution. The capabilities of both methods were compared. Ionization constants of all the functional groups of the azo compounds studied could be determined relative to the change in the specific color difference depending on the acidity of the medium. The colorimetric functions of ion-molecular forms of azo compounds used as an analytical signal allow us to obtain complete information on the acid-base equilibrium in a wide acidity range.

Chemometrics-assisted spectrophotometry method for the determination of chemical oxygen demand in pulping effluent.

Science.gov (United States)

Chen, Honglei; Chen, Yuancai; Zhan, Huaiyu; Fu, Shiyu

2011-04-01

A new method has been developed for the determination of chemical oxygen demand (COD) in pulping effluent using chemometrics-assisted spectrophotometry. Two calibration models were established by inducing UV-visible spectroscopy (model 1) and derivative spectroscopy (model 2), combined with the chemometrics software Smica-P. Correlation coefficients of the two models are 0.9954 (model 1) and 0.9963 (model 2) when COD of samples is in the range of 0 to 405 mg/L. Sensitivities of the two models are 0.0061 (model 1) and 0.0056 (model 2) and method detection limits are 2.02-2.45 mg/L (model 1) and 2.13-2.51 mg/L (model 2). Validation experiment showed that the average standard deviation of model 2 was 1.11 and that of model 1 was 1.54. Similarly, average relative error of model 2 (4.25%) was lower than model 1 (5.00%), which indicated that the predictability of model 2 was better than that of model 1. Chemometrics-assisted spectrophotometry method did not need chemical reagents and digestion which were required in the conventional methods, and the testing time of the new method was significantly shorter than the conventional ones. The proposed method can be used to measure COD in pulping effluent as an environmentally friendly approach with satisfactory results.

Use of reflectance spectrophotometry to predict the response of port wine stains to pulsed dye laser.

Science.gov (United States)

Halachmi, Shlomit; Azaria, Ron; Inbar, Roy; Ad-El, Dean; Lapidoth, Moshe

2014-01-01

Reflectance spectroscopy can be used to quantitate subtle differences in color. We applied a portable reflectance spectrometer to determine its utility in the evaluation of pulsed dye laser treatment of port wine stains (PWS) and in prediction of clinical outcome, in a prospective study. Forty-eight patients with PWS underwent one to nine pulsed dye laser treatments. Patient age and skin color as well as PWS surface area, anatomic location, and color were recorded. Pretreatment spectrophotometric measurements were performed. The subjective clinical results of treatment and the quantitative spectrophotometry results were evaluated by two independent teams, and the findings were correlated. The impact of the clinical characteristics on the response to treatment was assessed as well. Patients with excellent to good clinical results of laser treatments had pretreatment spectrophotometric measurements which differed by more than 10%, whereas patients with fair to poor results had spectrophotometric measurements with a difference of of less than 10%. The correlation between the spectrophotometric results and the clinical outcome was 73% (p Spectrophotometry has a higher correlation with clinical outcome and a better predictive value than other nonmeasurable, nonquantitative, dependent variables.

The Assessment of Liver Reserve Function by Spectrophotometry based on Determination of Phenacetin and Paracetamol.

Science.gov (United States)

Ren, Rui; Ma, Yongmei; Ma, Wanshan; Lu, Sumei

2015-01-01

To establish a technical system for assessing liver reserve function based on spectrophotometry by detection of phenacetin and paracetamol in blood samples. Taking detected contents of phenacetin and paracetamol by high performance liquid chromatography (HPLC) as standard, which was proved to be able to detect drug concentrations with high resolution and accuracy, we established a technical system based on the spectrophotometric technique to assay phenacetin and paracetamol, including the color system, the maximum absorption wavelength, the influence factors of color system, and the optimal conditions for hydrolysis. Then we verified our established system compared with that under HPLC by recovery test. This study established a technical system to detect phenacetin and paracetamol in blood samples using spectrophotometry. Mainly, 3 mol/L hydrochloric acid (HCl) was added to samples for hydrolysis for 30 minutes, then, adding 0.02% 1,2-naphthoquinone-4-sulfonate (NQS), 1% cetyltrimethyl ammonium bromide (CTA) and 2% sodium hydroxide (or 3% sodium carbonate) (ratio of 1:6:1:2 or 3), and the absorbance was measured at 500 nm and 570 nm to calculate their concentrations. Using an established spectrophotometric system to detect phenacetin and paracetamol in blood samples could assess liver reserve function, which was proved comparable with HPLC in resolution and repeatability.

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

Science.gov (United States)

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.

Airborne spectrophotometry of Comet Halley from 5 to 9 microns

Science.gov (United States)

Campins, H.; Bregman, J. D.; Witteborn, F. C.; Wooden, D. H.; Rank, D. M.; Cohen, M.; Allamandola, Louis J.; Tielens, Alexander G. G. M.

1986-01-01

Spectrophotometry from 5 to 9 microns (resolution = 0.02) of comet Halley was obtained from the Kuiper Airborne Observatory on 1985 Dec. 12.1 and 1986 April 8.6 and 10.5 UT. Two spectral features are apparent in all the observations, one from 5.24 to 5.6 microns, and the silicate emission feature which has an onset between 7 and 8 microns. There is no evidence for the 7.5 microns feature observed by the Vega 1 spacecraft; the large difference between the areal coverage viewed from the spacecraft and the airplane may explain the discrepancy. Color temperatures significantly higher than a blackbody indicate that small particles are abundant in the coma. Significant spatial and temporal variations in the spectrum show trends similar to those observed from the ground.

Determination of Lead in Blood by Atomic Absorption Spectrophotometry1

Science.gov (United States)

Selander, Stig; Cramér, Kim

1968-01-01

Lead in blood was determined by atomic absorption spectrophotometry, using a wet ashing procedure and a procedure in which the proteins were precipitated with trichloroacetic acid. In both methods the lead was extracted into isobutylmethylketone before measurement, using ammonium pyrrolidine dithiocarbamate as chelator. The simpler precipitation procedure was shown to give results identical with those obtained with the ashing technique. In addition, blood specimens were examined by the precipitation method and by spectral analysis, which method includes wet ashing of the samples, with good agreement. All analyses were done on blood samples from `normal' persons or from lead-exposed workers, and no additions of inorganic lead were made. The relatively simple protein precipitation technique gave accurate results and is suitable for the large-scale control of lead-exposed workers. PMID:5663425

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.

Science.gov (United States)

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. Copyright © 2015 Elsevier Ltd. All rights reserved.

On line spectrophotometry with optical fibers. Application to uranium-plutonium separation in a spent fuel reprocessing plant

International Nuclear Information System (INIS)

Boisde, G.; Mus, G.; Tachon, M.

1985-06-01

Optimization of mixer-settler operation for uranium-plutonium separation in the Purex process can be obtained by remote spectrophotometry with optical fibers. Data acquisition on uranium VI, uranium IV and plutonium III is examined in function of acidity and nitrate content of the solution. Principles for on line multicomponent monitoring and mathematical modelization of the measurements are described [fr

Study of Biological Pigments by Single Specimen Derivative Spectrophotometry

Science.gov (United States)

Goldstein, Jack M.

1970-01-01

The single specimen derivative (SSD) method provides an absolute absorption spectrum of a substance in the absence of a suitable reference. Both a reference and a measuring monochromatic beam pass through a single sample, and the specimen itself acts as its own reference. The two monochromatic beams maintain a fixed wavelength difference upon scanning, and the difference in absorbance of the two beams is determined. Thus, the resulting spectrum represents the first derivative of the conventional type absorption spectrum. Tissues and cell fractions have been examined at room and liquid N2 temperature and chromophoric molecules such as the mitochondrial cytochromes and blood pigments have been detectable in low concentrations. In the case of isolated cellular components, the observed effects of substrates and inhibitors confirm similar studies by conventional spectrophotometry. The extension of the SSD concept to the microscopic level has permitted the study of the tissue compartmentalization and function of cytochromes and other pigments within layered tissue. PMID:4392452

On-line photolithography modeling using spectrophotometry and Prolith/2

Science.gov (United States)

Engstrom, Herbert L.; Beacham, Jeanne E.

1994-05-01

Spectrophotometry has been applied to optimizing photolithography processes in semiconductor manufacturing. For many years thin film measurement systems have been used in manufacturing for controlling film deposition processes. The combination of film thickness mapping with photolithography modeling has expanded the applications of this technology. Experimental measurements of dose-to-clear, the minimum light exposure dose required to fully develop a photoresist, are described. It is shown how dose-to-clear and photoresist contrast may be determined rapidly and conveniently from measurements of a dose exposure matrix on a monitor wafer. Such experimental measurements may underestimate the dose-to- clear because of thickness variations of the photoresist and underlying layers on the product wafer. Online modeling of the photolithographic process together with film thickness maps of the entire wafer can overcome this problem. Such modeling also provides maps of dose-to- clear and resist linewidth that can be used to estimate and optimize yield.

Alternative set of conditions for molybdenum determination by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Edgar, R.M.

1975-01-01

In comparing a newly developed procedure with that recommended by Perkin--Elmer, et al., (Analytical Methods for Atomic Absorption Spectrophotometry, Perkin--Elmer Corp., Norwalk, Conn. 1973) two areas were found in which the new procedure appeared more suitable for Mo determination. If Cr is present in concentrations greater than 100 ppM, the recommended procedure results in an enhancement effect on Mo absorption. This erroneously high result is eliminated when the new procedure is followed. In the recommended procedure, when the sample has to be dissolved in hydrofluoric acid and Al is added to help eliminate interferences, the acid combines with the Al to form insoluble aluminum fluoride. The part that Al plays in eliminating interferences is lessened, because it is no longer in solution

Improvement of precision method of spectrophotometry with inner standardization and its use in plutonium solutions analysis

International Nuclear Information System (INIS)

Stepanov, A.V.; Stepanov, D.A.; Nikitina, S.A.; Gogoleva, T.D.; Grigor'eva, M.G.; Bulyanitsa, L.S.; Panteleev, Yu.A.; Pevtsova, E.V.; Domkin, V.D.; Pen'kin, M.V.

2006-01-01

Precision method of spectrophotometry with inner standardization is used for analysis of pure Pu solutions. Improvement of the spectrophotometer and spectrophotometric method of analysis is done to decrease accidental constituent of relative error of the method. Influence of U, Np impurities and corrosion products on systematic constituent of error of the method, and effect of fluoride-ion on completeness of Pu oxidation in sample preparation are studied [ru

A simple and cost-effective method, as an appropriate alternative for visible spectrophotometry: development of a dopamine biosensor.

Science.gov (United States)

Abbaspour, Abdolkarim; Khajehzadeh, Abdolreza; Ghaffarinejad, Ali

2009-08-01

In this study, a new, simple, fast and inexpensive method as an alternative to visible spectrophotometry is developed. In this method the cells containing the sample solution were scanned with a scanner, then the color of each cell was analyzed with software written in visual basic (VB 6) media to red, green and blue values. The cells were built by creating holes in the Plexiglas sheet. The dimensions of identical cells were examined by Cr (III) solution with known concentrations. The validity of this new method was studied by determination of dopamine (DA) without using any other reagent. The parameters which affect the system were optimized. The comparison between the current and traditional UV-Vis spectrophotometry methods was studied and the results revealed similar trends in both methods. The developed method was successfully applied to the determination of dopamine in serum and urine without using any pretreatment. Finally comparing the results obtained in the developed method showed that microwave irradiation of the solution can decrease the experimental time, increase sensitivity and improve the limit of detection.

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

Science.gov (United States)

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.

Use of reflectance spectrophotometry and colorimetry in a general linear model for the determination of the age of bruises.

Science.gov (United States)

Hughes, Vanessa K; Langlois, Neil E I

2010-12-01

Bruises can have medicolegal significance such that the age of a bruise may be an important issue. This study sought to determine if colorimetry or reflectance spectrophotometry could be employed to objectively estimate the age of bruises. Based on a previously described method, reflectance spectrophotometric scans were obtained from bruises using a Cary 100 Bio spectrophotometer fitted with a fibre-optic reflectance probe. Measurements were taken from the bruise and a control area. Software was used to calculate the first derivative at 490 and 480 nm; the proportion of oxygenated hemoglobin was calculated using an isobestic point method and a software application converted the scan data into colorimetry data. In addition, data on factors that might be associated with the determination of the age of a bruise: subject age, subject sex, degree of trauma, bruise size, skin color, body build, and depth of bruise were recorded. From 147 subjects, 233 reflectance spectrophotometry scans were obtained for analysis. The age of the bruises ranged from 0.5 to 231.5 h. A General Linear Model analysis method was used. This revealed that colorimetric measurement of the yellowness of a bruise accounted for 13% of the bruise age. By incorporation of the other recorded data (as above), yellowness could predict up to 32% of the age of a bruise-implying that 68% of the variation was dependent on other factors. However, critical appraisal of the model revealed that the colorimetry method of determining the age of a bruise was affected by skin tone and required a measure of the proportion of oxygenated hemoglobin, which is obtained by spectrophotometric methods. Using spectrophotometry, the first derivative at 490 nm alone accounted for 18% of the bruise age estimate. When additional factors (subject sex, bruise depth and oxygenation of hemoglobin) were included in the General Linear Model this increased to 31%-implying that 69% of the variation was dependent on other factors. This

Spectrophotometry and chemical composition of the oxygen-poor bipolar nebula NGC 6164-5

International Nuclear Information System (INIS)

Dufour, R.J.; Parker, R.A.R.; Henize, K.G.

1988-01-01

The paper presents new ground-based and IUE spectrophotometry of several positions in NGC 6164-5 surrounding the Population I Of star HD 148937. Electron temperatures, densities, and abundances are derived for the various positions in the nebula using spectral line information. For all of the regions observed, Ne/H is depleted by an amount comparable to O/H, while S/H and Ar/H have normal values. The results suggest that the nebula consists partly of material ejected from inner shell-burning regions of the Of star. In effect, HD 148937 is older and more advanced than what was previously thought. 34 references

Magnetic resonance cell-tracking studies: spectrophotometry-based method for the quantification of cellular iron content after loading with superparamagnetic iron oxide nanoparticles.

Science.gov (United States)

Böhm, Ingrid

2011-08-01

The purpose of this article is to present a user-friendly tool for quantifying the iron content of superparamagnetic labeled cells before cell tracking by magnetic resonance imaging (MRI). Iron quantification was evaluated by using Prussian blue staining and spectrophotometry. White blood cells were labeled with superparamagnetic iron oxide (SPIO) nanoparticles. Labeling was confirmed by light microscopy. Subsequently, the cells were embedded in a phantom and scanned on a 3 T magnetic resonance tomography (MRT) whole-body system. Mean peak wavelengths λ(peak) was determined at A(720 nm) (range 719-722 nm). Linearity was proven for the measuring range 0.5 to 10 μg Fe/mL (r  =  .9958; p  =  2.2 × 10(-12)). The limit of detection was 0.01 μg Fe/mL (0.1785 mM), and the limit of quantification was 0.04 μg Fe/mL (0.714 mM). Accuracy was demonstrated by comparison with atomic absorption spectrometry. Precision and robustness were also proven. On T(2)-weighted images, signal intensity varied according to the iron concentration of SPIO-labeled cells. Absorption spectrophotometry is both a highly sensitive and user-friendly technique that is feasible for quantifying the iron content of magnetically labeled cells. The presented data suggest that spectrophotometry is a promising tool for promoting the implementation of magnetic resonance-based cell tracking in routine clinical applications (from bench to bedside).

Magnetic Resonance Cell-Tracking Studies: Spectrophotometry-Based Method for the Quantification of Cellular Iron Content after Loading with Superparamagnetic Iron Oxide Nanoparticles

Directory of Open Access Journals (Sweden)

Ingrid Böhm

2011-07-01

Full Text Available The purpose of this article is to present a user-friendly tool for quantifying the iron content of superparamagnetic labeled cells before cell tracking by magnetic resonance imaging (MRI. Iron quantification was evaluated by using Prussian blue staining and spectrophotometry. White blood cells were labeled with superparamagnetic iron oxide (SPIO nanoparticles. Labeling was confirmed by light microscopy. Subsequently, the cells were embedded in a phantom and scanned on a 3 T magnetic resonance tomography (MRT whole-body system. Mean peak wavelengths Λpeak was determined at A720nm (range 719–722 nm. Linearity was proven for the measuring range 0.5 to 10 μg Fe/mL (r = .9958; p = 2.2 × 10−12. The limit of detection was 0.01 μg Fe/mL (0.1785 mM, and the limit of quantification was 0.04 μg Fe/mL (0.714 mM. Accuracy was demonstrated by comparison with atomic absorption spectrometry. Precision and robustness were also proven. On T2-weighted images, signal intensity varied according to the iron concentration of SPIO-labeled cells. Absorption spectrophotometry is both a highly sensitive and user-friendly technique that is feasible for quantifying the iron content of magnetically labeled cells. The presented data suggest that spectrophotometry is a promising tool for promoting the implementation of magnetic resonance-based cell tracking in routine clinical applications (from bench to bedside.

Likelihood of aneurysmal subarachnoid haemorrhage in patients with normal unenhanced CT, CSF xanthochromia on spectrophotometry and negative CT angiography.

Science.gov (United States)

Rana, A K; Turner, H E; Deans, K A

2013-01-01

Patients with suspected subarachnoid haemorrhage, a normal noncontrast computed tomography (CT) and cerebrospinal fluid (CSF) evidence of haemoglobin breakdown products often undergo CT angiography (CTA). If this is normal, then invasive catheter angiography may be offered. In current clinical practice, haemoglobin breakdown products are detected by spectrophotometry rather than visible xanthochromia, and CTA is performed on multidetector scanners. The aim of this study was to determine if such patients should still have a catheter angiography, given the associated risks. Patients positive for CSF spectrophotometry (n=26) were retrospectively identified from the clinical biochemistry information system and imaging data from the electronic radiology records were reviewed. Discharge letters were consulted to relate the biochemistry and radiology results to the final diagnosis. 15 patients with CT angiography were found. Nine patients had normal CT angiography. No causative aneurysms had been missed. One patient had small, coincidental aneurysms missed on initial reading of the CTA. The likelihood of a clinically significant aneurysm in a patient who is CT negative, lumbar puncture positive and CTA negative is low. Double reporting of negative CT angiograms may be advisable.

8-13 μm spectrophotometry of V1016 Cyg and the shape of the 'silicate' feature

International Nuclear Information System (INIS)

Aitken, D.K.; Roche, P.F.; Spenser, P.M.

1980-01-01

8 to 13μm spectrophotometry of V1016 Cyg shows a broad emission feature attributed to radiation from silicate grains. This emission feature more closely resembles that of the circumstellar shells of oxygen-rich supergiants than the more dilute feature, typical of the interstellar medium, which is observed from the Trapezium source in the Orion nebula. It appears to be possible to distinguish the evolutionary status of an object from the form of its silicate excess. (author)

Spectrophotometry of the double QSO, 0957+561

International Nuclear Information System (INIS)

Wills, B.J.; Wills, D.

1980-01-01

We report new spectrophotometry of the double QSO, 0957+561, and show that the absorption line region in each light path is very similar in redshift (Δv +- 14 km s -1 rms), in column density of Fe + (approx.3 x 10 14 cm -2 ), and in velocity dispersion (approx.40 km s -1 ). The simplest interpretation of these results is a very massive object deflecting the light from a more distant QSO. Based on this hypothesis we find that the differences between the emission line and continuum spectra may be explained by differential reddening, implying a reddening-corrected flux ratio B/Aapprox. =2--4. This ratio is different from that found at radio wavelengths (0.7 at 6 cm), but can be explained, based on the gravitational lens hypothesis, by different flux variability at radio and optical wavelengths; however, we have found no evidence for optical variability. Another difficulty may be that a point-mass gravitational lens would need to have a mass-to-light ratio greater than 1000, if it is closer than z=0.4; at larger distances its mass would be very large (approx.10 14 M/sub sun/ at z=1.2). Observations obtained so far might be explained if two massive QSOs are actually closer together than appear to be, as a result of mutual gravitational deflection of the light. 1

Quantitative determination of praesodymium(III)-neodymium(III)-holmium(III)-erbium(III) four-component systems by matrix-fourth derivative spectrophotometry

International Nuclear Information System (INIS)

Wu Yang; Jinzhang Gao; Jingwan Kang; Guangbi Bai; Cunxiong Li

1994-01-01

A new approach is developed through a combination of matrix representation and higher derivative spectrophotometry and can be used to analyse seven four-component mixtures of lanthanide ions, simultaneously, with a recovery of between 92.0 and 107.1%. The method is rapid, sensitive and accurate and is suitable for a large number of samples. (Author)

The spectrophotometry and chemical composition of the oxygen-poor bipolar nebula NGC 6164-5

Science.gov (United States)

Dufour, Reginald J.; Parker, Robert A. R.; Henize, Karl G.

1988-01-01

The paper presents new ground-based and IUE spectrophotometry of several positions in NGC 6164-5 surrounding the Population I Of star HD 148937. Electron temperatures, densities, and abundances are derived for the various positions in the nebula using spectral line information. For all of the regions observed, Ne/H is depleted by an amount comparable to O/H, while S/H and Ar/H have normal values. The results suggest that the nebula consists partly of material ejected from inner shell-burning regions of the Of star. In effect, HD 148937 is older and more advanced than what was previously thought.

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

Science.gov (United States)

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.

Colour characteristics of the blunt egg pole: cues for recognition of parasitic eggs as revealed by reflectance spectrophotometry

Czech Academy of Sciences Publication Activity Database

Polačiková, Lenka; Honza, Marcel; Procházka, Petr; Topercer, J.; Stokke, B. G.

2007-01-01

Roč. 74, č. 3 (2007), s. 419-427 ISSN 0003-3472 R&D Projects: GA ČR(CZ) GD524/05/H536; GA AV ČR IAA600930605; GA MŠk LC06073 Institutional research plan: CEZ:AV0Z60930519 Keywords : blackcap * brood parasitism * recognition cues * reflectance spectrophotometry * rejection behaviour Subject RIV: EH - Ecology, Behaviour Impact factor: 2.752, year: 2007

Modification of the Fitzpatrick system of skin phototype classification for the Indian population, and its correlation with narrowband diffuse reflectance spectrophotometry.

Science.gov (United States)

Sharma, V K; Gupta, V; Jangid, B L; Pathak, M

2018-04-01

The Fitzpatrick classification for skin phototyping is widely used, but its usefulness in dark-skinned populations has been questioned by some researchers. Recently, skin colour measurement has been proposed for phototyping skin colour objectively. To modify the Fitzpatrick system of skin phototyping for the Indian population and to study its correlation with skin colour using narrowband diffuse reflectance spectrophotometry METHODS: Answer choices for three items (eye colour, hair colour, colour of unexposed skin) out of 10 in the original Fitzpatrick questionnaire were modified, followed by self-administration of the original and the modified Fitzpatrick questionnaire by 70 healthy Indian volunteers. Skin colour (melanin and erythema indices) was measured from two photoexposed and two photoprotected sites using a narrowband reflectance spectrophotometer. The mean ± SD scores for the original and modified Fitzpatrick questionnaires were 25.40 ± 4.49 and 23.89 ± 4.82, respectively (r = 0.97, P Spectrophotometry can be a useful objective tool for skin phototyping. © 2018 British Association of Dermatologists.

Far-ultraviolet and optical spectrophotometry of X-ray selected Seyfert galaxies

International Nuclear Information System (INIS)

Clarke, J.T.; Bowyer, S.; Grewing, M.; California Univ., Berkeley; Tuebingen Universitaet, West Germany)

1986-01-01

Five X-ray selected Seyfert galaxies were examined via near-simultaneous far-ultraviolet and optical spectrophotometry in an effort to test models for excitation of emission lines by X-ray and ultraviolet continuum photoionization. The observed Ly-alpha/H-beta ratio in the present sample averages 22, with an increase found toward the high-velocity wings of the H lines in the spectrum of at least one of the Seyfert I nuclei. It is suggested that Seyfert galaxies with the most high-velocity gas exhibit the highest Ly-alpha/H-beta ratios at all velocities in the line profiles, and that sometimes this ratio may be highest for the highest velocity material in the broad-line clouds. Since broad-lined objects are least affected by Ly-alpha trapping effects, they have Ly-alpha/H-beta ratios much closer to those predicted by early photoionization calculations. 21 references

Intraoperative Vascular Neuromonitoring in Patients with Subarachnoid Hemorrhage: A Pilot Study Using Combined Laser-Doppler Spectrophotometry.

Science.gov (United States)

Schmitz, Emilija; Bischoff, Barbara; Wolf, Dennis; Schmitt, Hubert J; Eyupoglu, Ilker Y; Roessler, Karl; Buchfelder, Michael; Sommer, Björn

2017-11-01

Intraoperative monitoring of cerebral microcirculation in patients with subarachnoid hemorrhage (SAH) may predict the postoperative neurologic outcome. In this pilot study, we examined the value of a novel noninvasive real-time measurement technique for detecting changes in local microcirculation. We used the O2C (Oxygen to see) laser-Doppler spectrophotometry system in 14 patients with Hunt & Hess grade 2-5 SAH who underwent microsurgical cerebral aneurysm clipping. A subdural probe recorded capillary venous oxygenation (SO 2 ), relative hemoglobin concentration, blood cell velocity, and blood flow at a tissue depth of 7 mm. Data were recorded immediately before dural closure. We also recorded somatosensory evoked potentials (SEPs) with median and tibial nerve stimulation. Results were compared with neurologic performance, as measured on the modified Rankin Scale, at the day of discharge from the hospital and 12 months thereafter. Patient functional outcomes after discharge and 12 months were correlated with pathological decreased flow and increased SO 2 values. In 6 of 8 patients, microcirculatory monitoring parameters indicated ischemia during surgery, as shown by electrophysiological SEP changes and infarction detected on the postoperative computed tomography (CT) scan. Pathological SEP results correlated closely with infarct demarcation as seen on CT. Our results indicate the potential benefit of intraoperative combined laser-Doppler flowmetry and spectrophotometry for predicting postoperative clinical outcomes in this small patient sample. Larger-cohort testing is needed to verify our findings and show the possible merits of this novel method. Copyright © 2017 Elsevier Inc. All rights reserved.

Diagnosis of Smith-Lemli-Opitz syndrome by ultraviolet spectrophotometry

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F.B. Scalco

2003-10-01

Full Text Available Smith-Lemli-Opitz syndrome (SLOS is an autosomal recessive disorder due to an inborn error of cholesterol metabolism, characterized by congenital malformations, dysmorphism of multiple organs, mental retardation and delayed neuropsychomotor development resulting from cholesterol biosynthesis deficiency. A defect in 3ß-hydroxysteroid-delta7-reductase (delta7-sterol-reductase, responsible for the conversion of 7-dehydrocholesterol (7-DHC to cholesterol, causes an increase in 7-DHC and frequently reduces plasma cholesterol levels. The clinical diagnosis of SLOS cannot always be conclusive because of the remarkable variability of clinical expression of the disorder. Thus, confirmation by the measurement of plasma 7-DHC levels is needed. In the present study, we used a simple, fast, and selective method based on ultraviolet spectrophotometry to measure 7-DHC in order to diagnose SLOS. 7-DHC was extracted serially from 200 µl plasma with ethanol and n-hexane and the absorbance at 234 and 282 nm was determined. The method was applied to negative control plasma samples from 23 normal individuals and from 6 cases of suspected SLOS. The method was adequate and reliable and 2 SLOS cases were diagnosed.

The analysis, by atomic-absorption spectrophotometry, of matte-leach residues

International Nuclear Information System (INIS)

Mallett, R.C.; Ring, E.J.; Middleton, H.R.; Dubois, M.

1973-01-01

Alternative methods for the analysis of matte-leach residues by atomic-absorption spectrophotometry were investigated. For the determination of the platinum-group metals, gold, and certain of the base metals, a fusion with sodium peroxide, followed by the separation of gold by reverse-phase chromatography and of the platinum-group metals by ion-exchange, is proposed. The noble metals are then determined in a solution that is free of most base metals including the sodium present as a result of the fusion. Copper, nickel, iron, calcium, magnesium, and aluminium can be determined after they have been removed from the ion-exchange column. Arsenic, selenium, tellurium, bismuth, tin, silver, lead, manganese, zinc, and cobalt can be determined in a separate sample after dissolution by a sealed-tube method. This is also an alternative method for the determination of copper, nickel, and iron. Chromium is determined separately after fusion with sodium peroxide, and silver can also be determined in this way. The laboratory method for these procedures is given as an appendix [af

Quality control of test iodine in urine by spectrophotometry UV-Vis

Science.gov (United States)

Huda, Thorikul; Nafisah, Durotun; Kumorowulan, Suryati; Lestari, Sri

2017-12-01

A quality control of iodine test in with UV-Vis spectrophotometry has been done. The purpose of this research is to find out whether the test results of samples conducted by Clinical Office of Research and Development Of GAKI (BP2GAKI) laboratory are still controlled, feasible and reliable, and still consistent over time, as indicated by the control chart. Quality control parameters are linearity, precision, accuracy, limit of detection, and limit of quantification. Based on the quality control that has been done, obtained linearity (r)= -0.9974, the detection limit and the limit of quantitation are respectively 2.26 µg/L and 7.54 µg/L, while the accuracy is calculated by %recovery and precision with value % RSD are 97.4161% and 1.7136% respectively. The quality control of iodine test in urine using the control chart shows excellent or stable results for 30 days and no variation of the results is very different for each day.

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

Science.gov (United States)

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.

Zero crossing and ratio spectra derivative spectrophotometry for the dissolution tests of amlodipine and perindopril in their fixed dose formulations

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Maczka Paulina

2014-06-01

Full Text Available Dissolution tests of amlodipine and perindopril from their fixed dose formulations were performed in 900 mL of phosphate buffer of pH 5.5 at 37°C using the paddle apparatus. Then, two simple and rapid derivative spectrophotometric methods were used for the quantitative measurements of amlodipine and perindopril. The first method was zero crossing first derivative spectrophotometry in which measuring of amplitudes at 253 nm for amlodipine and 229 nm for perindopril were used. The second method was ratio derivative spectrophotometry in which spectra of amlodipine over the linearity range were divided by one selected standard spectrum of perindopril and then amplitudes at 242 nm were measured. Similarly, spectra of perindopril were divided by one selected standard spectrum of amlodipine and then amplitudes at 298 nm were measured. Both of the methods were validated to meet official requirements and were demonstrated to be selective, precise and accurate. Since there is no official monograph for these drugs in binary formulations, the dissolution tests and quantification procedure presented here can be used as a quality control test for amlodipine and perindopril in respective dosage forms.

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

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

2015-09-03

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. Copyright © 2015 Elsevier B.V. All rights reserved.

Europium determination in oxide and oxysulfide luminophors and their wastes by the method of direct and derivative spectrophotometry

International Nuclear Information System (INIS)

Mishchenko, V.T.; Aleksandrova, N.N.

1989-01-01

Spectrophotometric methods for europium determination in luminophors are proposed. Application of standard and derivative spectrophotometry allows one to determine europium in oxide and oxysulfide luminophors, their wastes and raffinates produced during waste reprocessing quite accurately and reliably. When determining Eu 2 O 3 (Eu 2 O 2 S) mass shares within 4-8 % limits absolute deviation from the mean result makes up to more than ± 0.2 %, relative standard deviation does not exceed 0.02

Determination of Ca, Cu, Fe and Pb in sugarcane raw spirits by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Lorenzo, Magdalena; Reyes, Arlyn; Blanco, Idania; Vasallo, Maria C

2010-01-01

The determination of Ca, Cu, Fe and Pb in sugarcane raw spirits by atomic absorption spectrophotometry was carried out. For 20 μL injected sample, calibration within the 0,5-25,0 mg. L -1 Ca; 0,25-5,0 mg. L -1 Cu, Pb and Cu intervals were established using the ratios Cu, Ca, Fe and Pb absorbance versus analyte concentration, respectively. Typical linear correlations of r = 0,999 were obtained. The proposed method was applied for the direct determination of Ca, Cu, Fe and Pb in sugar cane spirits, and in samples. The results obtained were in accordance to those obtained at 95% confidence level

Determination of Uranium In UO2 And U3O8 Powder Using UV-VIS Spectrophotometry

International Nuclear Information System (INIS)

Natalia Adventini; Diah Dwiana Lestiani; Muhayatun; Endah Damastuti

2009-01-01

Lab. TAR PTNBR BATAN - Bandung has been accredited by National Accreditation Committee on May 2 nd , 2006 as a test laboratory with number LP-311-ID, has to maintain its laboratory performance by participating in a proficiency test. In this activity, the determination of uranium in 2 samples of UO 2 with A1 and A2 codes and other 2 samples of U 3 O 8 with B1 and B2 codes using UV-Vis spectrophotometry was carried out. Colouring method was used by reacting thiocyanate ion with the uranyl ion in acidic solution to develop a stable yellow colour of uranyl thiocyanate complex solution and measured at wavelength of 380 nm. The result gave that concentration of uranium in A1, A2, B1 and B2 samples were 77.95; 75.29; 64.58 and 63.69% respectively. The Z-score value for A samples was - 1.99, meanwhile for B samples the Z score value of between laboratory was −1.29 with intra laboratory was -1,09. It meant that Z-score values for both samples were in good category. From this result, it showed that UV-Vis spectrophotometry is one of the several methods that can be used to determine uranium in UO 2 and U 3 O 8 powder. The Lab. TAR’s proficiency test for determination of uranium in UO 2 and U 3 O 8 gave a good result and it was hoped to support BATAN's program in the nuclear fuel field. (author)

[Wavelength Selection in Hemolytic Evaluation Systems with Spectrophotometry Detection].

Science.gov (United States)

Zhang, Hong; Su, Baochang; Ye, Xunda; Luo, Man

2016-04-01

Spectrophotometry is a simple hemolytic evaluation method commonly used in new drugs,biomedical materials and blood products.It is for the quantitative analysis of the characteristic absorption peaks of hemoglobin.Therefore,it is essential to select the correct detection wavelength when the evaluation system has influences on the conformation of hemoglobin.Based on the study of changes in the characteristic peaks over time of the hemolysis supernatant in four systems,namely,cell culture medium,phosphate buffered saline(PBS),physiological saline and banked blood preservation solution,using continuous wavelength scanning,the selections of detection wavelength were proposed as follows.In the cell culture medium system,the wavelength of 415 nm should be selected within 4h;,near 408 nm should be selected within 4~72h.In PBS system,within 4h,541 nm,577nm or 415 nm should be selected;4~72h,541 nm,577nm or near 406 nm should be selected.In physiological saline system,within 4h,414 nm should be selected;4~72h,near 405 nm should be selected;within 12 h,541nm or 577 nm could also be selected.In banked blood preservation solution system,within 72 h,415nm,540 nm or 576 nm should be selected.

Spectrophotometry of the Hα region in the spectrum of HR 1099 during the February 1978 radio flare

International Nuclear Information System (INIS)

Fraquelli, D.A.

1978-01-01

Spectrophotometry of the Hα emission line in the spectrum of HR 1099 (=HD 22468=V711 Tauri) was obtained during the radio flare of February 1978. The profiles observed during the flare have higher peak intensities and larger equivalent widths than profiles obtained outside of the flare at approximately the same orbital phases. Both the general shapes of the profiles and the equivalent widths appear to correlate with the radio flux. A preflare profile exhibits a flare-type profile, suggesting that radio outbursts in RS CVn systems may be preceded by Hα enhancement

Determination of radial peculiar velocities of galaxy clusters by means of the submillimeter spectrophotometry

International Nuclear Information System (INIS)

Sholomitskij, G.B.

1984-01-01

The possibility is considered to obtain from the extraatmospheric submillimeter spectrophotometry of galaxy clusters the ratios vsub(r)/Tsub(e) for clusters intergalactic gas that permits, together with the X-ray measurements of electronic temperature Tsub(e) in the case of hot scattering gas to determine absolute radial peculiar velocities vsub(r) of galaxy clusters relative to the relic radiation. By simulating such peculiar velocities as an example for the system of bandpass filters in the wavelength range 300 μm - 2 mm the accuracy of vsub(r) estimates is proved to be about 300 km/s (not taking into account the errors in Tsub(e)) the sensitivity of deeply cooled submillimeter bolometers being 1x10 -15 W/Hzsup(1/2)

A high-throughput screening strategy for nitrile-hydrolyzing enzymes based on ferric hydroxamate spectrophotometry.

Science.gov (United States)

He, Yu-Cai; Ma, Cui-Luan; Xu, Jian-He; Zhou, Li

2011-02-01

Nitrile-hydrolyzing enzymes (nitrilase or nitrile hydratase/amidase) have been widely used in the pharmaceutical industry for the production of carboxylic acids and their derivatives, and it is important to build a method for screening for nitrile-hydrolyzing enzymes. In this paper, a simple, rapid, and high-throughput screening method based on the ferric hydroxamate spectrophotometry has been proposed. To validate the accuracy of this screening strategy, the nitrilases from Rhodococcus erythropolis CGMCC 1.2362 and Alcaligenes sp. ECU0401 were used for evaluating the method. As a result, the accuracy for assaying aliphatic and aromatic carboxylic acids was as high as the HPLC-based method. Therefore, the method may be potentially used in the selection of microorganisms or engineered proteins with nitrile-hydrolyzing enzymes.

Determination of Lead in Urine by Atomic Absorption Spectrophotometry1

Science.gov (United States)

Selander, Stig; Cramé, Kim

1968-01-01

A method for the determination of lead in urine by means of atomic absorption spectrophotometry (AAS) is described. A combination of wet ashing and extraction with ammonium pyrrolidine dithiocarbamate into isobutylmethylketone was used. The sensitivity was about 0·02 μg./ml. for 1% absorption, and the detection limit was about 0·02 μg./ml. with an instrumental setting convenient for routine analyses of urines. Using the scale expansion technique, the detection limit was below 0·01 μg./ml., but it was found easier to determine urinary lead concentrations below 0·05 μg./ml. by concentrating the lead in the organic solvent by increasing the volume of urine or decreasing that of the solvent. The method was applied to fresh urines, stored urines, and to urines, obtained during treatment with chelating agents, of patients with lead poisoning. Urines with added inorganic lead were not used. The results agreed well with those obtained with a colorimetric dithizone extraction method (r = 0·989). The AAS method is somewhat more simple and allows the determination of smaller lead concentrations. PMID:5647975

H II region in NGC 6744: Spectrophotometry and chemical abundances

International Nuclear Information System (INIS)

Talent, D.L.

1982-01-01

Spectrophotometry of emission lines in the lambdalambda3700--6800 spectral range is presented for An H II region in an outer arm of NGC6744, a southern hemisphere galaxy of type SAB(r)bc II. The electron temperature, derived from the [O III] lines and assuming N/sub e/ = 100 cm -3 , was found to be 9,630 +- 450 K. Ionic abundances, derived in the usual fashion from the measured line strengths, were corrected to total relative number abundances by application of the standard ionization correction factor (ICF) scheme and by comparison to models. The derived abundances, relative to log Hequivalent12.00, are log He = 10.96 +- 0.06, log N = 7.34 +- 0.26, log O log O = 8.44 +- 0.10, log Ne = 7.80 +- 0.16, and log S = 6.75 +- 0.28. The NGC 6744 H II region abundances, and various ratios, are compared to similar data for H II regions in the SMC, LMC, and the Perseus arm of the Galaxy,. From the comparison it is suggested that the histories of nucleosynthesis in the outer regions of NGC 6744 and the Galaxy could have been quite similar

Spectroscopic studies of Wolf-Rayet stars. V - Optical spectrophotometry of the emission lines in Small Magellanic Cloud stars

International Nuclear Information System (INIS)

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

1989-01-01

Spectrophotometry of the strongest emission-line features for the eight known WR stars in the SMC is presented. Seven are relatively early WN types; and one is a WO. These are compared to stars of similar spectral types in the Galaxy and the LMC. The hydrogen-burning CNO cycle equilibrium nitrogen abundance with respect to helium appears to be similar to that in WN stars of the Galaxy and LMC even though the SMC objects presumably began their lives with appreciably smaller CNO content. 28 refs

Analysis of trace metals in sodium by flameless atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Mahalingam, T.R.; Geetha, R.; Thiruvengadasamy, A.; Mathews, C.K.

1981-01-01

The estimation of trace metallic impurities in sodium is normally carried out by distilling off the sodium in vacuuum and analysing the residue by atomic absorption spectrophotometry (AAS). This paper describes the direct determination of the following impurities (viz.) Fe, Co, Ni, Cr, Mn, Ca, and Cu in sodium without going through the distillation step. Here sodium is simply dissolved and the solution is subjected to analysis by AAS using flameless atomisation in a graphite furnace. The method of standard additions is employed. Preliminary experiments were carried out to study the matrix effect of sodium on the atomic absorption of cobalt. It has been found that if pyrolysis is done at 1250 0 C for 20 seconds prior to atomisation, the bulk of the sodium nitrate matrix could be successfully removed. The use of the optimum pyrolysis temperatures for the various elements listed above and the matrix interference on the absorbances of these analytes are discussed in this paper. The precision and accuracy of our analytical procedure is also presented. (orig.)

The determination, by atomic-absorption spectrophotometry, of impurities in manganese dioxide

International Nuclear Information System (INIS)

Balaes, G.E.E.; Robert, R.V.D.

1981-01-01

This report describes various methods for the determination of impurities in electrolytic manganese dioxide by atomic-absorption spectrophotometry (AAS). The sample is dissolved in a mixture of acids, any residue being ignited and retreated with acid. Several AAS methods were applied so that the analysis required to meet the specifications could be attained. These involved conventional flame AAS, AAS with electrothermal atomization (ETA), hydride generation coupled with AAS, and cold-vapour AAS. Of the elements examined, copper, iron, zinc, and lead can be determined direct with confidence with or without corrections based on recoveries obtained from spiked solutions. Nickel can be determined direct by use of the method of standard additions, and copper, nickel, and lead by ETA with the method of standard additions. Arsenic and antimony are determined by hydride generation coupled with AAS, and mercury by cold-vapour AAS. The precision of analysis (relative standard deviation) is generally less than 0,050. Values were obtained for aluminium, molybdenum, magnesium, sodium, copper, chromium, and cadmium, but the accuracy of these determinations has not been fully established

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

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Valerio Pini

2016-06-01

Full Text Available 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.

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

Science.gov (United States)

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.

Can the Assessment of Spontaneous Oscillations by Near Infrared Spectrophotometry Predict Neurological Outcome of Preterm Infants?

Science.gov (United States)

Stammwitz, André; von Siebenthal, Kurt; Bucher, Hans U; Wolf, Martin

2016-01-01

The aim was to assess the correlation between cerebral autoregulation and outcome. Included were 31 preterm infants, gestational age 26 1/7 to 32 2/7 and <24 h life. Coherence between cerebral total haemoglobin (tHb) or oxygenation index (OI) measured by near-infrared spectrophotometry (NIRS) and systemic heart rate (HR) or arterial blood pressure (MAP) was calculated as a measure of autoregulation. In contrast to previous studies, low coherences in the first 24 h were significantly associated with intraventricular haemorrhage, death or abnormal neurodevelopmental outcome at 18 months or later. We suggest that our results can be explained by the concept of a multi-oscillatory-functions-order.

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

Science.gov (United States)

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.

The role of spectrophotometry in the diagnosis of melanoma

Science.gov (United States)

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

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

Science.gov (United States)

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.

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

Science.gov (United States)

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).

Uranium determination by spectrophotometry, in chloride solutions, using titanium (III) as reducer; Determinacao de uranio por espectrofotometria, em solucoes cloridricas, utilizando titanio (III) como redutor

Energy Technology Data Exchange (ETDEWEB)

Bastos, E T.R.; Bastos, M B.R.

1986-08-01

A simple method for determining uranium in uranium (VI) solutions with the presence of uranium (IV), iron (II), and titanium (IV) in chloridic solution is described. The method comprises in uranium (VI) reduction with titanium (III), acidity adjustment and uranium (IV) spectrophotometry in hydrochloric acid 2 M. (C.G.C.).

Measurement of uranium concentration by molecular absorption spectrophotometry by means optical fibers; Medicion continua de concentracion de uranio por espectrofotometria de absorcion molecular mediante fibras opticas

Energy Technology Data Exchange (ETDEWEB)

Gauna, Alberto C.; Pascale, Ariel A. [Comision Nacional de Energia Atomica, Buenos Aires (Argentina). Centro Atomico Ezeiza. Agencia Minipost

1996-07-01

An on-line method for measuring the concentration of uranium in uranyl nitrate-nitric acid aqueous solutions is described. The method is based on molecular absorption spectrophotometry with transmission of light by means of optical fibers. It is ideally suited for control and processes development applications. (author)

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

Science.gov (United States)

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.

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

Science.gov (United States)

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.

Atomic absorption spectrophotometry for the determination of metallic impurities in coal

International Nuclear Information System (INIS)

Silva, M.J.S.F. da.

1983-06-01

The Brazilian Energetic Alternative Program expects the reduction of our dependence on foreign energy sources, through replacing fuel oil by mineral coal. Its gasification by means of nuclear energy must be also considered. However, the intensive burning of coal leads to serious environmental problems. During its combustion the release, to atmosphere, of toxic elements such as As, Hg, Pb, Sb, Se, Cd, Zn and others is of great concern. Increase in atmospheric pollution will take place by burning increased amounts of coal. In addition, some of those elements are concentrated in fly ashes. The determination of impurities in coal is also important for the Figueiras Project in the Nuclebras Mineral Prospection Program. Hence, it is important to have reliable analytical methods which can monitor inorganic constituents at various stages of coal production and utilization. The atomic absorption spectrophotometry is a suitable analytical technique to determine pollutants in coal because it is sensitive, simple, economic and cover a large range of concentrations. The need of a previous treatment of the sample is overcome by using an acid attack (HNO 3 + HClO 4 + HF) which has proved to be rapid and efficient. (Author) [pt

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

Science.gov (United States)

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.

Evaluation of Biologically Active Compounds from Calendula officinalis Flowers using Spectrophotometry

Directory of Open Access Journals (Sweden)

Butnariu Monica

2012-04-01

Full Text Available Abstract Background This study aimed to quantify the active biological compounds in C. officinalis flowers. Based on the active principles and biological properties of marigolds flowers reported in the literature, we sought to obtain and characterize the molecular composition of extracts prepared using different solvents. The antioxidant capacities of extracts were assessed by using spectrophotometry to measure both absorbance of the colorimetric free radical scavenger 2,2-diphenyl-1-picrylhydrazyl (DPPH as well as the total antioxidant potential, using the ferric reducing power (FRAP assay. Results Spectrophotometric assays in the ultraviolet-visible (UV-VIS region enabled identification and characterization of the full range of phenolic and flavonoids acids, and high-performance liquid chromatography (HPLC was used to identify and quantify phenolic compounds (depending on the method of extraction. Methanol ensured more efficient extraction of flavonoids than the other solvents tested. Antioxidant activity in methanolic extracts was correlated with the polyphenol content. Conclusions The UV-VIS spectra of assimilator pigments (e.g. chlorophylls, polyphenols and flavonoids extracted from the C. officinalis flowers consisted in quantitative evaluation of compounds which absorb to wavelengths broader than 360 nm.

Spectrophotometry of peculiar B and A stars. II. Eleven mercury-manganese stars

International Nuclear Information System (INIS)

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

1979-01-01

Spectrophotometry of eleven HgMn stars is presented for the optical region. As found in Paper I, the HgMn stars have systematically larger Δiota* and Δa values than the normal main sequence stars due to differences with respect to the mean continuum particularly of the lambda4464 values and the lambda5200 region, respectively. The HgMn stars exhibit a continuous range in the behavior of both the lambda4200 and lambda5200 regions between those stars that have index values larger than the appropriate criterion of presence and present definite evidence for the features to those stars with only a slight possibility of such features. The strengths of the lambda4200 and lambda5200 features appear not to be correlated. In the HgMn stars, both features may be due to differential line blocking. In the energy distribution of all eleven stars, the Balmer jump regions best fit the predictions of slightly hotter solar composition, log g=4.0, fully line blanketed model atmospheres than do the corresponding Paschen continua

[Mutual Effect on Determination of Gibberellins and Glyphosate in Groundwater by Spectrophotometry].

Science.gov (United States)

Zhang, Li; Chen, Liang; Liu, Fei

2015-04-01

In the present study, a spectrophotometry method for the simultaneous determination of gibberellins (GA3) and glyphosate in groundwater was established and optimized. In addition, the mutual effect on simultaneous determination of GA3 and glyphosate was studied. Based on the experiment, good linearity (R2 > 0.99) was obtained for GA3 in the range of 0-20 and 0-100 µg and for glyphosate in the range of 0-8 and 5-15 µg. The method's detection limit (MDL) of GA3 and glyphosate was 0.48 and 0.82 µg, respectively; and the recovery rates of 15 to 150 µg GA3 and 3 to 10 µg glyphosate in all samples at a spiked level were 71.3% ± 1.9% and 98.4% ± 8.1%, respectively. No obvious influence of glyphosate (0-100 mg · L(-1)) on the recovery rates of GA3 was observed, but the presence of glyphosate could cause slight determination precision decrease of GA3. Meanwhile, adding 2 mg · L(-1) GA3 can increase the recovery rate of glyphosate.

A Research on Determination of Lecithin in Eggs by Applying Microwave Digestion Techniques and Spectrophotometry

International Nuclear Information System (INIS)

Wu, M.; Ge, Q.L.; Gao, Y. Sh.; Chen, K. W.

2012-01-01

A method to quick detect concentration of lecithin in eggs, namely microwave digestion spectrophotometry, was established in this research. The homogenate of eggs was treated with absolute ethanol to eliminate phosphate protein in eggs which could possibly affect concentration of lecithin examined. A sample then received a new way of pre-treatment, called microwave digestion, before UV-Vis spectrometry was applied to examine the concentration of phosphate at 400 nm. The linear equation was A = 0.08628X (μg), the corresponding coefficient of correlation was 0.9998, the detection limit of phosphorous was 0.2μg (n=11). The content of lecithin in eggs was then obtained. According to the result, the recovery of 90% was secured; therefore the conclusion of high degree of accuracy was reached.

UV SPECTROPHOTOMETRY APPLICATION FOR QUANTITATIVE DETERMINATION OF VINPOCETINE IN DRUG FORMULATIONS

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J. V. Monaykina

2014-12-01

Full Text Available Introduction. In this paper simple, rapid and sensitive assay methods for quantitative determination of vinpocetine in two new drug formulations (suppositories and nasal cream are proposed. Analysis has been performed directly by using zero-order UV spectrophotometry. It is known from the special literature that the chromatographic techniques used for vinpocetine assay require expensive equipment and are rather time consuming. Therefore UV spectrophotometry is preferable due to its accuracy and simplicity. The object of this study was to develop new, simple, rapid, precise and accurate UV spectrophotometric procedure for the quantitative determination of vinpocetine in suppositories and nasal cream and evaluation of some validation characteristics of the methods. Materials and methods. The objects of the study were the new drug formulations of vinpocetine, namely 0,01 suppositories and 0,5% nasal cream developed by the scientists of The Chair of Technology of Drugs of Zaporizhzhia State Medical University. Distilled water and 0.05M HCl were used as the solvents, working standard sample of vinpocetine was used as a reference standard. Analytical equipment: spectrophotometer Specord 200, electronic balance ABT-120-5DM, measuring glassware of class A. Assay procedure: An accurately weighed sample of cream (1,200 – 2,000 g or one suppository was dissolved in 0.05M HCl and filtered into a 50,00 ml volumetric flask. Then the solution was brought to the mark with the same solvent and stirred. 3,00 ml or 4,00 ml of the resulting solutions (for suppositories or cream respectively were transferred into a 25,00 ml volumetric flask and brought to the mark with distilled water. Absorbance was measured at a wavelength of 272 nm on the blank of distilled water. The parallel measurement with 1,00 ml of 0,064% vinpocetine standard solution was carried out. The content of active substance was calculated according to standard formulas. Results. The suggested

APPLICATION OF UV-SPECTROPHOTOMETRY FOR THE QUANTITATIVE DETERMINATION OF CAPTOPRIL IN DRUG

Directory of Open Access Journals (Sweden)

Yu. V. Monaykina

2015-04-01

Full Text Available Introduction. In this paper the simple, rapid and sensitive assay method for the quantitative determination of captopril in two new pharmaceutical formulations (suppositories and nasal gel is proposed. Analysis was performed directly by using zero-order UV spectrophotometry. It is known from the special literature that the chromatographic techniques used for captopril assay require the expensive equipment and are rather time consuming. Therefore UV spectrophotometry is preferable due to its accuracy, sensitivity and simplicity. The aim of this study was to develop and validate a new, simple, rapid, precise and accurate UV spectrophotometric method for the quantitative determination of captopril in suppositories and nasal gel. Materials and methods. The objects of the study were the new drug formulations of captopril, namely 0,05 suppositories and 2,5% nasal gel developed by the scientists of The Chair of Technology of Drugs ofZaporozhye State Medical University. Distilled water was used as the solvent, working standard sample of captopril was used as a reference standard. Analytical equipment: spectrophotometer Specord 200, electronic balance ABT-120-5DM, measuring glassware of class A. Assay procedure: An accurately weighed sample of gel (0,4000 –0,8000 g or one suppository was dissolved in distilled water and filtered into a volumetric flask (50,00 ml for gel and 250,0 ml for suppository . Then the solution was brought to the mark with the same solvent and stirred. 1,00 ml of the resulting solution was transferred into a 25,00 ml volumetric flask and brought to the mark with distilled water. Absorbance was measured at a wavelength of 203 nm on the blank of a solvent. The parallel measurement with 1,00 ml of 0,03% captopril standard solution was carried out. The content of active substance was calculated according to standard formulas. Results. The suggested procedure was successfully applied for the analysis of two new pharmaceutical

Sensitivity and accuracy of atomic absorption spectrophotometry for trace elements in marine biological samples

International Nuclear Information System (INIS)

Fukai, R.; Oregioni, B.

1976-01-01

During the course of 1974-75 atomic absorption spectrophotometry (AAS) has been used extensively in our laboratory for measuring various trace elements in marine biological materials in order to conduct homogeneity tests on the intercalibration samples for trace metal analysis as well as to obtain baseline data for trace elements in various kinds of marine organisms collected from different locations in the Mediterranean Sea. Several series of test experiments have been conducted on the current methodology in use in our laboratory to ensure satisfactory analytical performance in measuring a number of trace elements for which analytical problems have not completely been solved. Sensitivities of the techniques used were repeatedly checked for various elements and the accuracy of the analyses were always critically evaluated by analyzing standard reference materials. The results of these test experiments have uncovered critical points relevant to the application of the AAS to routine analysis

Determination of molybdenum in flotation concentrates by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Ise, Kazuo

1978-01-01

Molybdenum was determined by atomic absorption spectrophotometry in 0.05 N ammoniacal solution after the decomposition of the concentrate with aqua regia. Negros ore from Philippines was used as a flotation feed, which contained chalcopyrites and calcium-magnesium minerals. Among the metals tested copper, iron and the alkaline earths interfered. Less than 50 ppm of copper yielded lower results for molybdenum. Higher results came out with more than 50 ppm of copper. In the presence of iron and citric acid (0.4 g/100 ml) which is a suppressor for hydroxide formation, a lower estimation resulted for molybdenum. Calcium interfered, lower results by 2 and >10% being obtained with respective 2.5 and 20 ppm of calcium. More than 20 ppm of magnesium behaved similarly. Sodium sulfate (0.5 g/100 ml) served as the suppressor for copper, iron and citric acid; 100 ppm each of copper and iron did not interfere in this way. Interferences due to calcium and magnesium (less than 60 ppm) was able to be masked by the addition of sodium silicate (200 ppm as silica). The analysis of flotation products and synthetic samples consisting of molybdenite, chalcopyrite, calcium chloride and magnesium sulfate revealed that the atomic absorption method can be applied to the analysis of the concentrates for molybdenum with an error of about 2%. (auth.)

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

International Nuclear Information System (INIS)

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

2015-01-01

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. - Highlights: • Multi-parametric determination of cadmium, zinc, and copper at the μg L"−"1 level. • In-line metal ions preconcentration using NTA resin. • Minimization of matrix interferences by performing solid phase spectrometry in a SI-LOV platform. • Successful application to metal ions determination in freshwaters.

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

Energy Technology Data Exchange (ETDEWEB)

Santos, Inês C. [CBQF–Centro de Biotecnologia e Química Fina – Laboratório Associado, Escola Superior de Biotecnologia, Universidade Católica Portuguesa/Porto, Rua Arquiteto Lobão Vital, Apartado 2511, 4202-401 Porto (Portugal); Mesquita, Raquel B.R. [CBQF–Centro de Biotecnologia e Química Fina – Laboratório Associado, Escola Superior de Biotecnologia, Universidade Católica Portuguesa/Porto, Rua Arquiteto Lobão Vital, Apartado 2511, 4202-401 Porto (Portugal); Laboratório de Hidrobiologia, Instituto de Ciências Biomédicas Abel Salazar (ICBAS), Universidade do Porto, Rua de Jorge Viterbo Ferreira no. 228, 4050-313 Porto (Portugal); Rangel, António O.S.S., E-mail: arangel@porto.ucp.pt [CBQF–Centro de Biotecnologia e Química Fina – Laboratório Associado, Escola Superior de Biotecnologia, Universidade Católica Portuguesa/Porto, Rua Arquiteto Lobão Vital, Apartado 2511, 4202-401 Porto (Portugal)

2015-09-03

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{sup −1} for cadmium, 2.39 μg L{sup −1} for zinc, and 0.11 μg L{sup −1} for copper and a sampling rate of 12, 13, and 15 h{sup −1} for cadmium, zinc, and copper were obtained, respectively. The proposed method was successfully applied to freshwater samples. - Highlights: • Multi-parametric determination of cadmium, zinc, and copper at the μg L{sup −1} level. • In-line metal ions preconcentration using NTA resin. • Minimization of matrix interferences by performing solid phase spectrometry in a SI-LOV platform. • Successful application to metal ions determination in freshwaters.

Ion-exclusion/cation-exchange chromatography with dual detection of the conductivity and spectrophotometry for the simultaneous determination of common inorganic anionic species and cations in river and wastewater.

Science.gov (United States)

Nakatani, Nobutake; Kozaki, Daisuke; Mori, Masanobu; Hasebe, Kiyoshi; Nakagoshi, Nobukazu; Tanaka, Kazuhiko

2011-01-01

Simultaneous determinations of common inorganic anionic species (SO(4)(2-), Cl(-), NO(3)(-), phosphate and silicate) and cations (Na(+), NH(4)(+), K(+), Mg(2+) and Ca(2+)) were conducted using an ion-chromatography system with dual detection of conductivity and spectrophotometry in tandem. The separation of ionic species on a weakly acidic cation-exchange resin was accomplished using a mixture of 100 mM ascorbic acid and 4 mM 18-crown-6 as an acidic eluent (pH 2.6), after which the ions were detected using a conductivity detector. Subsequently, phosphate and silicate were analyzed based on derivatization with molybdate and spectrophotometry at 700 nm. The detection limits at S/N = 3 ranged from 0.11 to 2.9 µM for analyte ionic species. This method was applied to practical river water and wastewater with acceptable criteria for the anion-cation balance and comparisons of the measured and calculated electrical conductivity, demonstrating the usefulness of the present method for water quality monitoring.

Heterodyne spectrophotometry of ozone in the 9.6-micron band using a tunable diode laser

Science.gov (United States)

Mcelroy, C. T.; Goldman, A.; Fogal, P. F.; Murcray, D. G.

1990-01-01

Tunable diode laser heterodyne spectrophotometry (TDLHS) has been used to make extremely high resolution (0.0003/cm) solar spectra in the 9.6-micron ozone band. Observations have shown that a signal-to-noise ratio of 120:1 (about 30 percent of theoretical) for an integration time of 1/8 s can be achieved at a resolution of 0.0013 wave numbers. The spectral data have been inverted to yield a total column amount of ozone, in good agreement with that measured at the nearby NOAA ozone monitoring facility in Boulder, Colorado. Line positions for several ozone lines in the spectral region 996-997/cm are reported. Recent improvements have produced a signal-to-noise ratio of 95:1 (about 40 percent of theoretical) at 0.0003/cm and extended the range of wavelengths which can be observed.

Review of recent applications of flow injection spectrophotometry to pharmaceutical analysis

International Nuclear Information System (INIS)

Tzanavaras, Paraskevas D.; Themelis, Demetrius G.

2007-01-01

Pharmaceutical analysis is one of the most important fields in analytical chemistry. The discovery of new drugs and the on-going update of international regulations for the safety and efficacy of pharmaceutical formulations demand the continuous development of new analytical methods. Inevitably, automation plays an important role, especially when a lot of samples have to be analyzed in the minimum of time. The present study reviews the applications of flow injection (FI) spectrophotometry to the determination of active pharmaceutical ingredients (APIs) in their respective formulations. However, the topic covered in this study is important not only to pharmaceutical analytical scientists. The principles, figures of merit and 'chemistry' of the presented methods can be of interest to bio-analytical and clinical chemists as well for the analysis of biological samples, to environmental analysts that study the up-to-date demand of the determination of the fate of pharmaceuticals in the environment and even to toxicologists and forensic scientists. This review covers scientific contributions published later than 2000. A variety of FI procedures based on homogeneous (direct UV measurements, colour-forming reactions, metal-drug interactions) and heterogeneous (optical sensors and solid-phase reactors) systems are discussed. A third section covers on-line sample pretreatment (solid-phase extraction, liquid-liquid extraction, on-line digestion, etc.)

Objective evaluation by reflectance spectrophotometry can be of clinical value for the verification of blanching/non blanching erythema in the sacral area.

Science.gov (United States)

Sterner, Eila; Fossum, Bjöörn; Berg, Elisabeth; Lindholm, Christina; Stark, André

2014-08-01

Early detection of non blanching erythema (pressure ulcer category I) is necessary to prevent any further skin damage. An objective method to discriminate between blanching/non blanching erythema is presently not available. The purpose of this investigation was to explore if a non invasive objective method could differentiate between blanching/non blanching erythema in the sacral area of patients undergoing hip fracture surgery. Seventy-eight patients were included. The sacral area of all patients was assessed using (i) conventional finger-press test and (ii) digital reading of the erythema index assessed with reflectance spectrophotometry. The patients were examined at admission and during 5 days postsurgery. Reflectance spectrophotometry measurements proved able to discriminate between blanching/non blanching erythema. The reliability, quantified by the intra-class correlation coefficient, was excellent between repeated measurements over the measurement period, varying between 0·82 and 0·96, and a significant change was recorded in the areas from day 1 to day 5 (P < 0·0001). The value from the reference point did not show any significant changes over the same period (P = 0·32). An objective method proven to identify early pressure damage to tissue can be a valuable tool in clinical practice. © 2013 The Authors. International Wound Journal © 2013 Medicalhelplines.com Inc and John Wiley & Sons Ltd.

Spectrophotometry of white dwarfs as observed at high signal-to-noise ratio. II

International Nuclear Information System (INIS)

Greenstein, J.L.; Liebert, J.W.

1990-01-01

CCD spectrophotometry is presented of 140 white dwarfs at high SNR and is analyzed in detail. Energy distributions at 14,000 A are given at bandpasses from 3571 to 8300 A, and equivalent widths of lines of H, He I, metals, and atomic and molecular carbon are given as functions of color for DB, DQ, DZ, and DA stars. New forbidden H I transitions at 6068 A and 6632 A are found in at least the two hottest DB stars, new metallic features are found in cooler DZ stars, and the presence of Ca I in vMa 2 is confirmed. The spectrum of the hot DQAB star G227 - 5 and the pressure-shifted carbon bands seen in 0038-226 are discussed in detail. Comparison of the optical energy distribution of the latter with published IR fluxes shows that the 1-2 micron region is strongly depressed, with extensive blanketing. Equivalent widths, central depths, and width parameters are presented for H-alpha in 73 DA stars in the sample, and their dependences on color are studied. 64 refs

Application of neutron activation analysis and spectrophotometry for the determination of copper level in sera and cerebrospinal fluids of schizophrenic patients

International Nuclear Information System (INIS)

Lipcsey, A.; Fekete, J.; Oerdoegh, M.; Szabo, E.

1985-01-01

Neutron activation analysis and spectrophotometry were used for the determination of copper content in sera and cerebrospinal fluids of schizophrenic patients against control persons. Comparison of the results of copper determination by both methods is tabulated. From the data the following conclusions can be drawn: for copper determinations in sera the results of the two methods agree excellently. At small copper concentrations in the cerebrospinal fluids the deviations are rather high. It can also be seen that the copper contents determined from cerebrospinal fluids taken at different times are nearly equal. (author)

Simultaneous determination of dysprosium, holmium and erbium in high purity rare earth oxides by second order derivative spectrophotometry

International Nuclear Information System (INIS)

Anbu, M.; Prasada Rao, T.; Iyer, C. S. P.; Damodaran, A. D.

1996-01-01

High purity individual rare earth oxides are increasingly used as major components in lasers (Y 2 O 3 ), phosphors (YVO 3 , Eu 2 O 3 ), magnetic bubble memory films (Gd 2 O 3 ) and refractive-index lenses and fibre optics (La 2 O 3 ). The determination of individual lanthanides in high purity rare earth oxides is a more important and difficult task. This paper reports the utilization of higher order derivative spectrophotometry for the simultaneous determination of dysprosium, holmium and erbium in high purity rare earth oxides. The developed procedure is simple, reliable and allows the determination of 0.001 to 0.2% of dysprosium, holmium and erbium in several rare earth. (author). 9 refs, 2 figs, 2 tabs

Determination of the Np(IV)-Np(III) normal potential in fused LiCl-CsCl (55-45%) by absorption spectrophotometry

International Nuclear Information System (INIS)

Lysy, R.; Duyckaerts, G.

1977-01-01

The following reaction Np 4+ + 1/2 H 2 + Cl - reversible Np 3+ + HCl has been studied quantitatively in fused LiCl-CsCl (55-45 mol %) in the temperature range of 450-600 0 C, by visible and near IR absorption spectrophotometry. At 450 deg C, the equilibrium constant equals K = 7.4 atmsup(1/2). The mean values of ΔH and ΔS in the temperature range of 450-600 deg C are: ΔH = (35.6+-10.3) kJ mol -1 , ΔS=(65.5+-13.0)J mol -1 K -1 [fr

Single-laboratory evaluation of SW-846 Methods 7090/7091 determination of beryllium by flame and furnace atomic absorption spectrophotometry. Summary report January-August 1987

International Nuclear Information System (INIS)

Hodge, V.F.; Darby, D.A.; Thompson, W.E.; Jones, C.L.

1988-02-01

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 samples after digestion by appropriate SW-846 methods. Method performance data including detection limits, optimum concentration ranges (linearity), spike recoveries, interferences, precision, accuracy, and optimum operating parameters are presented and discussed

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

Science.gov (United States)

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. Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Benefit of cerebrospinal fluid spectrophotometry in the assessment of CT scan negative suspected subarachnoid haemorrhage: a diagnostic accuracy study.

Science.gov (United States)

Hann, Angus; Chu, Kevin; Greenslade, Jaimi; Williams, Julian; Brown, Anthony

2015-01-01

This study aimed to determine if performing cerebrospinal fluid spectrophotometry in addition to visual inspection detects more ruptured cerebral aneurysms than performing cerebrospinal fluid visual inspection alone in patients with a normal head CT scan but suspected of suffering an aneurysmal subarachnoid haemorrhage (SAH). We performed a single-centre retrospective study of patients presenting to the emergency department of a tertiary hospital who underwent both head CT scan and lumbar puncture to exclude SAH. The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of an approach utilising both spectrophotometry and visual inspection (combined approach) was compared to visual inspection alone. A total of 409 patients (mean age 37.8 years, 56.2% female) were recruited and six (1.5%) had a cerebral aneurysm on angiography. The sensitivity of visual inspection was 50% (95% confidence interval [CI]: 12.4-82.6%), specificity was 99% (95% CI: 97.5-99.7%), PPV was 42.9% (95% CI: 10.4-81.3%) and NPV was 99.2% (95% CI: 97.8-99.8%). The combined approach had a sensitivity of 100% (95% CI: 54.1-100%), specificity of 79.7% (95% CI: 75.4-83.5%), PPV of 6.8% (95% CI: 2.6-14.3%) and a NPV of 100% (95% CI: 98.8-100%). The sensitivity of the combined approach was not significantly different to that of visual inspection alone (p=0.25). Visual inspection had a significantly higher specificity than the combined approach (p<0.01). The combined approach detected more cases of aneurysmal SAH than visual inspection alone, however the difference in sensitivity was not statistically significant. Visual xanthochromia should prompt angiography because of a superior specificity and PPV. Due to its reduced sensitivity, caution should be applied when using only visual inspection of the supernatant. Crown Copyright © 2014. Published by Elsevier Ltd. All rights reserved.

Quantitative analysis of trivalent uranium and lanthanides in a molten chloride by absorption spectrophotometry

International Nuclear Information System (INIS)

Toshiyuki Fujii; Akihiro Uehara; Hajimu Yamana

2013-01-01

As an analytical application for pyrochemical reprocessing using molten salts, quantitative analysis of uranium and lanthanides by UV/Vis/NIR absorption spectrophotometry was performed. Electronic absorption spectra of LiCl-KCl eutectic at 773 K including trivalent uranium and eight rare earth elements (Y, La, Ce, Pr, Nd, Sm, Eu, and Gd as fission product elements) were measured in the wavenumber region of 4,500-33,000 cm -1 . The composition of the solutes was simulated for a reductive extraction condition in a pyroreprocessing process for spent nuclear fuels, that is, about 2 wt% U and 0.1-2 wt% rare earth elements. Since U(III) possesses strong absorption bands due to f-d transitions, an optical quartz cell with short light path length of 1 mm was adopted in the analysis. The quantitative analysis of trivalent U, Nd, Pr, and Sm was possible with their f-f transition intensities in the NIR region. The analytical results agree with the prepared concentrations within 2σ experimental uncertainties. (author)

Environmental samples analysis by Atomic Absorption Spectrophotometry and Inductively Coupled Plasma-Optical Emission Spectroscopy

International Nuclear Information System (INIS)

Popescu, I.V.; Iordan, M.; Stihi, C.; Bancuta, A.; Busuioc, G.; Dima, G.; Ciupina, V.; Belc, M.; Vlaicu, Gh.; Marian, R.

2002-01-01

Biological samples are interesting from many aspects of environmental monitoring. By analyzing tree leaves conclusions can be drown regarding the metal loading in the growth medium. So that, starting from assumption that the pollution factors from environmental medium can modify the normal concentration of elements, we decided to control the presence of toxic elements and the deviation from normal state of elements in leaves of different trees from areas situated at different distances of pollution source. The aim of this work is to determine the elemental composition of tree leaves using Atomic Absorption Spectrophotometry (AAS) method and Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES) method. Using AAS spectrophotometer SHIMADZU we identified and determined the concentration of: Cd, Co, Cu, Zn, Mn, Cr, Fe, Se, Pb with an instrumental error less than 1% for most of the elements analyzed. The same samples were analyzed by ICP-OES spectrometer, BAIRD ICP2070-Sequential Plasma spectrometer. We identified and determined in leaves of different trees the concentration of Mg, Ca, and Sr with a precision less than 6%. (authors)

Application of infrared spectrophotometry to the identification of inorganic substances in dosage forms of Antacida group.

Science.gov (United States)

Umbreit, M H; Jedrasiewicz, A

2000-01-01

Powdered tablets from the Antacida group: Alusal, Milk of Magnesia, Alumag, Maalox, Magnosil, Alugastrin, Malugastrin, Rennie, and components deciding about their antiacidity like Al(OH)3, Mg(OH)2, Mg2Si3O8, NaAl(OH)2CO3, MgAl(OH)(SO4)2, CaCO3, MgCO3, were subjected to infrared spectrophotometric investigations. It was found that infrared spectra of each pharmaceutical compound are different and show a series of characteristic maxima, by which they can be identified with in the spectral range of 4000 cm-1-200 cm-1. Comparison of infrared spectra of finished products with spectra of their components it was showed that the application of infrared spectrophotometry methods enabled us to prove the presence of particular compounds used in formulations. Tablet mass and odorizing agents do not cause significant changes in spectra of the tablets studied, preparations from the Antacida group.

Simultaneous Determination of Cobalt (II and Nickel (II By First Order Derivative Spectrophotometry in Micellar Media

Directory of Open Access Journals (Sweden)

Rajni Rohilla

2012-01-01

Full Text Available A first-derivative spectrophotometry method for the simultaneous determination of Co (II and Ni (II with Alizarin Red S in presence of Triton X-100 is described. Measurements were made at the zero-crossing wavelengths at 549.0 nm for Co (II and 546.0 nm for Ni (II. The linearity is obtained in the range of 0.291- 4.676 μg/ml of Ni (II and 0.293- 4.124 μg/ml of Co (II in the presence of each other by using first derivative spectrophotometric method. The possible interfering effects of various ions were studied. The validity of the method was examined by using synthetic mixtures of Co (II and Ni (II. The developed derivative procedure, using the zero crossing technique, has been successfully applied for the simultaneous analysis of Co (II and Ni (II in spiked water samples.

A NEW CONCEPT FOR SPECTROPHOTOMETRY OF EXOPLANETS WITH SPACE-BORNE TELESCOPES

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Matsuo, Taro; Itoh, Satoshi; Shibai, Hiroshi; Sumi, Takahiro [Department of Earth and Space Science, Graduate School of Science, Osaka University, 1-1, Machikaneyamacho, Toyonaka, Osaka 560-0043 (Japan); Yamamuro, Tomoyasu [Optocraft, 3-16-8-101, Higashi Hashimoto, Midori-ku, Sagamihara, Kanagawa 252-0144 (Japan)

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.

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

Science.gov (United States)

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.

Antioxidant study of quercetin and their metal complex and determination of stability constant by spectrophotometry method.

Science.gov (United States)

Ravichandran, R; Rajendran, M; Devapiriam, D

2014-03-01

Quercetin found chelate cadmium ions, scavenge free radicals produced by cadmium. Hence new complex, quercetin with cadmium was synthesised, and the synthesised complex structures were determined by UV-vis spectrophotometry, infrared spectroscopy, thermogravimetry and differential thermal analysis techniques (UV-vis, IR, TGA and DTA). The equilibrium stability constants of quercetin-cadmium complex were determined by Job's method. The determined stability constant value of quercetin-cadminum complex at pH 4.4 is 2.27×10(6) and at pH 7.4 is 7.80×10(6). It was found that the quercetin and cadmium ion form 1:1 complex in both pH 4.4 and pH 7.4. The structure of the compounds was elucidated on the basis of obtained results. Furthermore, the antioxidant activity of the free quercetin and quercetin-cadmium complexes were determined by DPPH and ABTS assays. Copyright © 2013 Elsevier Ltd. All rights reserved.

Neutron activation analysis and atomic absorption spectrophotometry for the analysis of fresh, pasteurised and powder milk

International Nuclear Information System (INIS)

Wasim, M.; Rehman, S.; Arif, M.; Fatima, I.; Zaidi, J.H.

2012-01-01

This study shows the application of semi-absolute k 0 instrumental neutron activation analysis (k 0 -INAA), epithermal neutron activation analysis (ENAA) and atomic absorption spectrophotometry (AAS) for the determination of 21 elements (Br, Ca, Cl, Co, Cr, Cs, Cu, Fe, Hf, I, K, Mg, Mn, Na, Ni, P, Pb, Rb, Sc Sr, and Zn) in different types of milk samples. The ENAA was required for the determination of iodine, AAS for Cu, Ni and Pb and the rest of the elements were measured by k 0 -INAA. Thirteen elements (Br, Ca, Cl, Cs, Cu, Fe, K, Mg, Na, P, Rb, Sr and Zn) were identified in all milk samples. Ni was detected in eleven and Pb in two samples. Concentrations of most of the elements were within the ranges of the world reported data. The data was further explored by principal component analysis to find relationships between samples and elements. (orig.)

The UV-VIS spectrophotometry applied to color and stability study in colored mortars

Directory of Open Access Journals (Sweden)

Alejandre, F. J.

1999-06-01

Full Text Available In the field of methodologies for color studying, a research of it has been done on colored mortars by applying uv-vis spectrophotometry, instrumental technique which can be used for solid materials works, and previously applied to building materials study. Results obtained show that the mentioned technique permits to evaluate quantitatively and qualitatively colors in an easy and objective way, besides nowadays advantages of the instrumental analysis: digital color register, computerized data processing, and precision and exactness increment in chromatic comparisons.

Dentro de las metodologías existentes para el estudio del color, se ha realizado una investigación del mismo en morteros coloreados por medio de la espectrofotometría UV-VIS, técnica instrumental que es adaptable al trabajo con materiales sólidos, y que ha sido aplicada anteriormente en el estudio de diversos materiales de construcción. Los resultados obtenidos muestran cómo la citada técnica permite además de evaluar cualitativamente y cuantitativamente los colores de forma sencilla y objetiva, el disponer de las ventajas que conlleva actualmente el análisis instrumental: registro digital del color, tratamiento informatizado de datos y aumento de precisión y exactitud en las comparaciones cromáticas.

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

Science.gov (United States)

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. Copyright © 2013 Elsevier Ltd. All rights reserved.

Comments on a Method to Measure Sucralose Using UV Photodegradation Followed by UV Spectrophotometry.

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Fang, Te; Andrews, Susan A; Hofmann, Ron

2017-05-01

A simple and quick method to measure sucralose in aqueous solution at concentrations in the order of 0.1-1.2 g·L-1 proposed by Idris et al. uses UV irradiation prior to UV spectrophotometry. The photolysis of sucralose forms a photoactive compound characterized by maximum absorbance at approximately 270 nm. The conditions required for sucralose photolysis, however, had not been completely reported. In this work, the procedure described by Idris et al. was replicated using a low-pressure UV lamp to irradiate sucralose samples with a wider range of initial concentrations (0.04-10 g·L-1) with known fluences. It was determined that care must be taken to ensure that the same fluence is applied for both calibration and measurement steps because the absorbance of the sucralose photolysis product is a function of the applied fluence. The way the samples are irradiated also has an impact on the results in that the method exhibits a greater linear range if an apparatus is used that maximizes the fluence rate (e.g., by placing samples closer to the UV source or using a higher-intensity lamp).

Use of Dispersive Liquid-Liquid Microextraction and UV-Vis Spectrophotometry for the Determination of Cadmium in Water Samples

Directory of Open Access Journals (Sweden)

J. Pérez-Outeiral

2014-01-01

Full Text Available A simple and inexpensive method for cadmium determination in water using dispersive liquid-liquid microextraction and ultraviolet-visible spectrophotometry was developed. In order to obtain the best experimental conditions, experimental design was applied. Calibration was made in the range of 10–100 μg/L, obtaining good linearity (R2 = 0.9947. The obtained limit of detection based on calibration curve was 8.5 μg/L. Intra- and interday repeatability were checked at two levels, obtaining relative standard deviation values from 9.0 to 13.3%. The enrichment factor had a value of 73. Metal interferences were also checked and tolerable limits were evaluated. Finally, the method was applied to cadmium determination in real spiked water samples. Therefore, the method showed potential applicability for cadmium determination in highly contaminated liquid samples.

A novel UV-photolysis approach with acetone and isopropyl alcohol for the rapid determination of fluoride in organofluorine-containing drugs by spectrophotometry.

Science.gov (United States)

Mullapudi, Venkata Balarama Krishna; Dheram, Karunasagar

2018-01-01

A UV photolysis decomposition (UVPD) method for the determination of fluoride in fluorine containing pharmaceuticals by spectrophotometry is reported. It is based on the use of high intensity UV-irradiation in the presence of a digesting solution comprising a mixture of acetone and isopropanol. For the optimization of the UVPD procedure, three bulk drugs (levofloxacin, nebivolol and efavirenz) were chosen as representatives of three diverse compounds containing a single fluorine atom, two fluorine atoms, and trifluoromethyl groups respectively. Operational conditions of the UVPD method, such as concentration and volume of reagents (acetone and isopropyl alcohol), and UV irradiation time (1-6 minutes) were optimized. The efficiency of digestion was evaluated by the determination of fluoride in sample digests. Using the developed method, it was possible for complete conversion of the organofluoride to free fluoride ion for its subsequent determination by spectrophotometry based on bleaching of Zr-xylenol orange-color complex. Quantitative recovery (>98%) of the fluorine in the drug samples could be achieved using a mixture of 2% acetone + 2% isopropyl alcohol + 0.003% Na 2 CO 3 in just 5 minutes of UV irradiation, which can be considered an important aspect considering the difficulties involved in the cleavage of the CF bond. Accuracy was evaluated by comparison of results obtained by the UVPD method with the values estimated using formula weight of the compound and no statistical difference was observed between the results. Therefore, the proposed method is suitable for application in routine analysis of fluoride in organofluorine-containing drugs. Copyright © 2016. Published by Elsevier B.V.

Combination of rice husk and coconut shell activated adsorbent to adsorb Pb(II) ionic metal and it’s analysis using solid-phase spectrophotometry (sps)

Science.gov (United States)

Rohmah, D. N.; Saputro, S.; Masykuri, M.; Mahardiani, L.

2018-03-01

The purpose of this research was to know the effect and determine the mass comparation which most effective combination between rice husk and coconut shell activated adsorbent to adsorb Pb (II) ion using SPS method. This research used experimental method. Technique to collecting this datas of this research is carried out by several stages, which are: (1) carbonization of rice husk and coconut shell adsorbent using muffle furnace at a temperature of 350°C for an hour; (2) activation of the rice husk and coconut shell adsorbent using NaOH 1N and ZnCl2 15% activator; (3) contacting the adsorbent of rice husk and coconut shell activated adsorbent with liquid waste simulation of Pb(II) using variation comparison of rice husk and coconut shell, 1:0; 0:1; 1:1; 2:1; 1:2; (4) analysis of Pb(II) using Solid-Phase Spectrophotometry (SPS); (5) characterization of combination rice husk and coconut shell activated adsorbent using FTIR. The result of this research show that the combined effect of combination rice husk and coconut shell activated adsorbent can increase the ability of the adsorbent to absorb Pb(II) ion then the optimum adsorbent mass ratio required for absorbing 20 mL of Pb(II) ion with a concentration of 49.99 µg/L is a ratio of 2:1 with the absorption level of 97,06%Solid-Phase Spectrophotometry (SPS) is an effective method in the level of µg/L, be marked with the Limit of Detection (LOD) of 0.03 µg/L.

Headspace single-drop microextraction coupled to microvolume UV-vis spectrophotometry for iodine determination

International Nuclear Information System (INIS)

Pena-Pereira, Francisco; Lavilla, Isela; Bendicho, Carlos

2009-01-01

Headspace single-drop microextraction has been combined with microvolume UV-vis spectrophotometry for iodine determination. Matrix separation and preconcentration of iodide following in situ volatile iodine generation and extraction into a microdrop of N,N'-dimethylformamide is performed. An exhaustive characterization of the microextraction system and the experimental variables affecting iodine generation from iodide was carried out. The procedure employed consisted of exposing 2.5 μL of N,N'-dimethylformamide to the headspace of a 10 mL acidic (H 2 SO 4 2 mol L -1 ) aqueous solution containing 1.7 mol L -1 Na 2 SO 4 for 7 min. Addition of 1 mL of H 2 O 2 1 mol L -1 for in situ iodine generation was performed. The limit of detection was determined as 0.69 μg L -1 . The repeatability, expressed as relative standard deviation, was 4.7% (n = 6). The calibration working range was from 5 to 200 μg L -1 (r 2 = 0.9991). The large preconcentration factor obtained, ca. 623 in only 7 min, compensate for the 10-fold loss in sensitivity caused by the decreased optical path, which results in improved detection limits as compared to spectrophotometric measurements carried out with conventional sample cells. The method was successfully applied to the determination of iodine in water, pharmaceutical and food samples

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

Science.gov (United States)

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 1.31×10(7) 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. Copyright © 2013 Elsevier B.V. All rights reserved.

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

Science.gov (United States)

Khodadoust, Saeid; Ghaedi, Mehrorang

2014-12-10

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 (100μL of chloroform, 1.3mL of ethanol, pH 4 and 4% (w/v) NaCl) resulted in a linear calibration graph in the range of 0.015-10.0mgmL(-1) of MR in initial solution with R(2)=0.995 (n=5). The limits of detection (LOD) and limit of quantification (LOQ) were 0.005 and 0.015mgmL(-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). Copyright © 2014 Elsevier B.V. All rights reserved.

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

Science.gov (United States)

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.

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

Science.gov (United States)

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).

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

Science.gov (United States)

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. Copyright © 2015 Elsevier Ltd. All rights reserved.

Combination of solid phase extraction and dispersive liquid–liquid microextraction for separation/preconcentration of ultra trace amounts of uranium prior to its fiber optic-linear array spectrophotometry determination

International Nuclear Information System (INIS)

Dadfarnia, Shayessteh; Shabani, Ali Mohammad Haji; Shakerian, Farid; Shiralian Esfahani, Golnaz

2013-01-01

Graphical abstract: Pass the sample through the basic alumina column ⇒ elute retained uranium along with the cations ⇒ convert the uranium to its anionic benzoate complex ⇒ extract its ion pair with malachite green into small volume of chloroform by DLLME ⇒ measure its absorption at 621 nm using fiber optic-linear array detection spectrophotometry. -- Highlights: • By combination of SPE and DDLME a high preconcentration factor of 2500 was obtained. • Development of SPE-DDLME-Spectrophotometric method for det. of trace amounts of uranium. • Ultra trace amount of uranium in water samples was det. by the proposed method. • The detection limit of the proposed method is comparable to the most sensitive method. • The proposed method is a free interference spectrophotometric method for uranium det. -- Abstract: A simple and sensitive method for the separation and preconcentration of the ultra trace amounts of uranium and its determination by spectrophotometry was developed. The method is based on the combination of solid phase extraction and dispersive liquid–liquid microextraction. Thus, by passing the sample through the basic alumina column, the uranyl ion and some cations are separated from the sample matrix. The retained uranyl ion along with the cations are eluted with 5 mL of nitric acid (2 mol L −1 ) and after neutralization of the eluent, the extracted uranyl ion is converted to its anionic benzoate complex and is separated from other cations by extraction of its ion pair with malachite green into small volume of chloroform using dispersive liquid–liquid microextraction. The amount of uranium is then determined by the absorption measurement of the extracted ion pair at 621 nm using flow injection spectrophotometry. Under the optimum conditions, with 500 mL of the sample, a preconcentration factor of 1980, a detection limit of 40 ng L −1 , and a relative standard deviation of 4.1% (n = 6) at 400 ng L −1 were obtained. The method was

Evaluation of clinoptilolite for removal of ammoniacal nitrogen produced in aquaculture by Neutron activation analysis and UV-VIS spectrophotometry

International Nuclear Information System (INIS)

Bibiano C, L.; Iturbe G, J.L.; Lopez M, B.E.; Martinez M, V.

1997-01-01

In fish culture system, ammonia is excreted in the water as a metabolic by-product. In this work, sorption properties of clinoptilolite were determined and it was applied in culture of the rainbow trout Oncorhynchus mykiss for the removal of the ammoniacal nitrogen. The original clinoptilolite was treated with 1N NaCl solution from 24 to 192 h, for exchange NH 4 ions produced in fish culture. The content of Na in the clinoptilolite was determined by neutron activation analysis. The ammonium ion content in the exchange was analysed by UV-VIS spectrophotometry. Maximum uptake of sodium was reached between 24 and 48 hours at neutral pH with granules of the clinoptilolite from 14 to 24 mesh size. The adsorption capacity was from 3.28 to 6.8 mg of ammonium per gram of clinoptilolite. (Author)

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

Science.gov (United States)

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.

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

Science.gov (United States)

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.

Combination of solid phase extraction and dispersive liquid-liquid microextraction for separation/preconcentration of ultra trace amounts of uranium prior to its fiber optic-linear array spectrophotometry determination.

Science.gov (United States)

Dadfarnia, Shayessteh; Shabani, Ali Mohammad Haji; Shakerian, Farid; Shiralian Esfahani, Golnaz

2013-12-15

A simple and sensitive method for the separation and preconcentration of the ultra trace amounts of uranium and its determination by spectrophotometry was developed. The method is based on the combination of solid phase extraction and dispersive liquid-liquid microextraction. Thus, by passing the sample through the basic alumina column, the uranyl ion and some cations are separated from the sample matrix. The retained uranyl ion along with the cations are eluted with 5 mL of nitric acid (2 mol L(-1)) and after neutralization of the eluent, the extracted uranyl ion is converted to its anionic benzoate complex and is separated from other cations by extraction of its ion pair with malachite green into small volume of chloroform using dispersive liquid-liquid microextraction. The amount of uranium is then determined by the absorption measurement of the extracted ion pair at 621 nm using flow injection spectrophotometry. Under the optimum conditions, with 500 mL of the sample, a preconcentration factor of 1980, a detection limit of 40 ng L(-1), and a relative standard deviation of 4.1% (n=6) at 400 ng L(-1) were obtained. The method was successfully applied to the determination of uranium in mineral water, river water, well water, spring water and sea water samples. Copyright © 2013 Elsevier B.V. All rights reserved.

Determination of Alkaloid Contents in Various Tissues of Coptis Chinensis Franch. by Reversed Phase-High Performance Liquid Chromatography and Ultraviolet Spectrophotometry.

Science.gov (United States)

Yang, Yanfang; Peng, Jingling; Li, Fangping; Liu, Xin; Deng, Meng; Wu, Hezhen

2017-05-01

A simple and intuitive method for optimizing the chemical constituents of Coptis Chinensis Franch. is important to assess its quality and clinical efficacy. An high performance liquid chromatography and ultraviolet spectrophotometry method was developed for the determination of berberine hydrochloride, palmatine chloride, jatrorrhizine hydrochloride, epiberberine, coptisine, columbamine and magnoflorine in various tissues (i.e., phloem, xylem and medulla) and rizhome of C. Chinensis Franch. The transection of rhizome from outside-in includes cork layer, cortex, phloem, cambium, xylem and medulla. Cork layer consists of dead cells, and therefore is not of any research significance. Cortex, phloem and cambium were almost impossible to separate, therefore they were studied as a whole in our experiments. They were collectively referred to as "phloem". The analytes were separated on a Gemini-NX C18 (250 mm × 4.6 mm, 5 μm) reversed phase column using a gradient elution of acetonitrile-0.03 mol/L ammonium acetate solution (containing 0.1% triethylamine and 0.6% ammonium hydroxide) as the mobile phase at a flow rate of 1.0 mL/min and UV detection at 270 nm. The method allowing the simultaneous quantification of seven major active constituents was optimized and validated for linearity, precision, accuracy, limits of detection (LOD) and quantification. The LOD ranged from 0.102 to 0.651 mg/mL (r ≥ 0.9993). Accuracy, precision and recovery were all within the required limits. The average recovery was between 100.14% and 102.75% and the relative standard deviations were spectrophotometry at 345 nm wavelength. Based on contents of the seven constituents and clustering result, this investigation suggests that there are significant differences in the distribution of seven alkaloids in the tissues examined. Furthermore, the total alkaloid content in xylem is relatively lower than that in phloem, medulla and rhizome. © The Author 2017. Published by Oxford University Press. All

High-throughput screening assay used in pharmacognosy: Selection, optimization and validation of methods of enzymatic inhibition by UV-visible spectrophotometry

Directory of Open Access Journals (Sweden)

Graciela Granados-Guzmán

2014-02-01

Full Text Available In research laboratories of both organic synthesis and extraction of natural products, every day a lot of products that can potentially introduce some biological activity are obtained. Therefore it is necessary to have in vitro assays, which provide reliable information for further evaluation in in vivo systems. From this point of view, in recent years has intensified the use of high-throughput screening assays. Such trials should be optimized and validated for accurate and precise results, i.e. reliable. The present review addresses the steps needed to develop and validate bioanalytical methods, emphasizing UV-Visible spectrophotometry as detection system. Particularly focuses on the selection of the method, the optimization to determine the best experimental conditions, validation, implementation of optimized and validated method to real samples, and finally maintenance and possible transfer it to a new laboratory.

Application of wavelet and Fuorier transforms as powerful alternatives for derivative spectrophotometry in analysis of binary mixtures: A comparative study

Science.gov (United States)

Hassan, Said A.; Abdel-Gawad, Sherif A.

2018-02-01

Two signal processing methods, namely, Continuous Wavelet Transform (CWT) and the second was Discrete Fourier Transform (DFT) were introduced as alternatives to the classical Derivative Spectrophotometry (DS) in analysis of binary mixtures. To show the advantages of these methods, a comparative study was performed on a binary mixture of Naltrexone (NTX) and Bupropion (BUP). The methods were compared by analyzing laboratory prepared mixtures of the two drugs. By comparing performance of the three methods, it was proved that CWT and DFT methods are more efficient and advantageous in analysis of mixtures with overlapped spectra than DS. The three signal processing methods were adopted for the quantification of NTX and BUP in pure and tablet forms. The adopted methods were validated according to the ICH guideline where accuracy, precision and specificity were found to be within appropriate limits.

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

Science.gov (United States)

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. Copyright © 2013 Elsevier B.V. All rights reserved.

Simultaneous determination of sulphaquinoxaline and amprolium in veterinary mixture by HPLC and first derivative ultraviolet spectrophotometry

International Nuclear Information System (INIS)

El-Sattar, Osama Abd

2002-01-01

Two simple and reliable methods are described for the determination of sulphaquinoxaline (SQX) and amprolium (AMP) combined in veterinary powder. The first method depends on high performance liquid chromatography on a reversed phase column (Bondapak-C18) using mobile phase consisting of acetonitrile-methanol-water-phosphoric acid (30: 5: 55: 0.7, by volumes) at a flow rate of 1 ml min with UV detection at 254 nm. The detection limits were 0.2 ug ml and 0.35 ug ml and linearity ranges were 2-20 ug ml and 4-40ug ml for SQX and AMP, respectively. The second one deals with the first derivative (D) spectrophotometry with zero-crossing measurement at 253 nm and 226 nm for SQX and AMP respectively. The detection limits were 0.3 ug ml and linearity ranges were 1-18 ug ml and 4-32 ug-ml for SQX and AMP respectively. The proposed procedures were successfully applied to the determination of these drugs in laboratory prepared mixtures with mean percentage recovery ranged from 98.50 to 99.75 and in commercial preparation ranged from 103.85 to 104.85. (author)

Determination of calcium and magnesium in hydroethanolic extracts of propolis by atomic absorption flame spectrophotometry

Directory of Open Access Journals (Sweden)

E. Q. SANTANA

2009-01-01

Full Text Available

Propolis is a natural product collected by honeybees and has a large range of pharmacological activity, including antimicrobial, antitumoral, antioxidant and anti-inflammatory. Its use as a popular medicine is increasing all over the world, creating a need for quality control of the commercial products. In this study the levels of calcium and magnesium in commercial hydroalcoholic propolis extracts from varios states of Brazil were determined by atomic absorption flame spectrophotometry and different values were obtained for northern and southern states. This study can be extended to the analysis of metals that are harmful to health. The results showed that the calibration curves were linear over a wide concentration range (0.5-4.0 µg.mL^-1 for calcium and 0.05-0.4 µg.mL^-1 for magnesium with good correlation coefficients (0.999 and 0.988, respectively. Good analytical recovery (94% was obtained. The proposed method showed adequate precision and relative standard deviation lower than 2 %. The method is accurate and precise as well as having advantages such as simplicity and speed. Keywords: hydroalcoholic propolis extract; mineralization; analysis; calcium; magnesium.

Implementation of the method for the determination of lactulose (4-O-β-D-Galactopyranosyl-D-Fructofuranose) and HMF (5-hydroxymethyl-2-furaldehyde) in ultra-pasteurized milk (UHT) ultraviolet-visible spectrophotometry

International Nuclear Information System (INIS)

Cardenas Miranda, Jeisson Alberto

2015-01-01

Measurement methods of HMF concentrations and lactulose is implemented and evaluated in low-fat milk (2% fat), subjected to ultra pasteurization process in order to establish indicators of nutritional quality. A protocol is developed for the management of equipment and methodology of the analytical method. The determination methods of HMF and lactulose are validated by ultraviolet visible spectrophotometry. The content of HMF and lactulose is determined in different production batches for 4 months of storage at a temperature of 24 Celsius degrees [es

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

Science.gov (United States)

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

2015-12-01

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 (redfleshed) 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.

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

Science.gov (United States)

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

2015-06-15

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 (R(2)=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. Copyright © 2015 Elsevier B.V. All rights reserved.

Lead Quantification in Urine Samples of Athletes by Coupling DLLME with UV-Vis Spectrophotometry.

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Faraji, Hakim; Helalizadeh, Masoumeh

2017-04-01

Urine lead level is one of the most employed measures of lead exposure and risk. The urine samples used in this study were obtained from ten healthy male cyclists. Dispersive liquid-liquid microextraction combined with ultraviolet and visible spectrophotometry was utilized for preconcentration, extraction, and determination of lead in urine samples. Optimization of the independent variables was carried out based on chemometric methods in three steps. According to the screening and optimization study, 133 μL of CCl 4 (extracting solvent), 1.34 mL ethanol (dispersing solvent), pH 2.0, 0.00 % of salt, and 0.1 % O,O-diethyl dithiophosphoric (chelating agent) were used as the optimum independent variables for microextraction and determination of lead. Under the optimized conditions, R 2 was 0.9991, and linearity range was 0.01-100 μg L -1 . Precision was evaluated in terms of repeatability and intermediate precision, with relative standard deviations being <9.1 and <15.3 %, respectively. The accuracy was estimated using urine samples of cyclists as real samples and it was confirmed. The relative error of ≤5 % was considered significant in the method specificity study. The lead concentration mean for the cyclists was 3.79 μg L -1 in urine samples. As a result, the proposed method is a robust technique to quantify lead concentrations higher than 11.6 ng L -1 in urine samples.

Comparative study between optical densitometry and spectrophotometry for evaluation of PMMA dosimeters

International Nuclear Information System (INIS)

Louback, Luana Trevenzoli; Meira-Belo, Luiz C.

2011-01-01

The use of dosimetric systems based on color changes in PMMA is standardized by ISO/ASTM 51276:2002(E). In a general way, the evaluation of doses in these materials is done correlating the optical absorbance of the material and the absorbed dose. Usually, the absorbance is measured using a spectrophotometer at a wavelength suitably chosen. In the present work, it was performed a comparative study between the techniques of spectrophotometry and optical densitometry in dyed PMMA dosimeters type Harwell RED 4034 and PMMA samples commercially available in Brazil. The main results of this study were the determination of the radiochromic response for different samples of PMMA and the determination of the calibration conditions using a 60 Co beam. The studied materials are suitable for use as routine dosimeters, covering the range of the 500Gy to 100kGy. A direct comparison between the red dyed PMMA and the Harwell RED 4034 Perspex showed that the stabilization time and the fading of the radiochromic information in red dyed PMMA samples is higher than in RED 4034. However, both effects occur on period of weeks, which does not preclude its routine use. Furthermore, the increase in absorbance due to exposure to radiation, determined by the difference between specific absorbance of the irradiated sample and a non-irradiated one, is significantly higher in PMMA with red dyed that the RED 4034. In fact, the amplitude of absorbance peak of a sample irradiated with red dyed PMMA 2kGy and read at 602nm has the same order of magnitude from a peak of RED 4034 irradiated with 10 kGy and read at 640nm. A direct consequence of this fact is the real possibility of using simpler equipment (optical densitometer in this case) to measure the optical absorbance and evaluates the absorbed dose. (author)

The determination, by atomic-absorption spectrophotometry using electrothermal atomization, of platinum, palladium, rhodium, ruthenium, and iridium

International Nuclear Information System (INIS)

Haines, J.; Robert, R.V.D.

1982-01-01

A method that involves measurement by atomic-absorption spectrophotometry using electrothermal atomization has been developed for the determination of trace quantities of platinum, palladium, rhodium, ruthenium, and iridium in mineralogical samples. The elements are separated and concentrated by fusion, nickel sulphide being used as the collector, and the analyte elements are measured in the resulting acid solution. An organic extraction procedure was found to offer no advantages over the proposed method. Mutual interferences between the five platinum-group metals examined, as well as interferences from gold, silver, and nickel were determined. The accuracy of the measurement was established by the analysis of a platinum-ore reference material. The lower limits of determination of each of the analyte elements in a sample material are as follows: platinum 1,6μg/l, palladium 0,2μg/1, rhodium 0,5μg/l, ruthenium 3μg/l, and iridium 2,5μg/l. The relative standard deviations range from 0,05 for rhodium to 0.08 for iridium. The method, which is described in detail in the Appendix, is applicable to the determination of these elements in ores, tailings, and geological materials in which the total concentration of the noble metals is less than 1g/t

Can tissue spectrophotometry and laser Doppler flowmetry help to identify patients at risk for wound healing disorders after neck dissection?

Science.gov (United States)

Rohleder, Nils H; Flensberg, Sandra; Bauer, Florian; Wagenpfeil, Stefan; Wales, Craig J; Koerdt, Steffen; Wolff, Klaus D; Hölzle, Frank; Steiner, Timm; Kesting, Marco R

2014-03-01

Microcirculation and oxygen supply in cervical skin were measured with an optical, noninvasive method in patients with or without radiotherapy before neck dissection. The course of wound healing was monitored after the surgical procedure to identify predictive factors for postoperative wound healing disorders. Tissue spectrophotometry and laser Doppler flowmetry were used to determine capillary oxygen saturation, hemoglobin concentration, blood flow, and blood velocity at 2-mm and 8-mm depths in the cervical skin of 91 patients before neck dissection in a maxillofacial unit of a university hospital in Munich, Germany. Parameters were evaluated for differences between patients with irradiation (24) and without (67) and patients with wound healing disorders (25) and without (66) (univariate or multivariate statistical analyses). Velocity at 2 mm was lower in irradiated skin (P = .016). Flow at 2 mm was higher in patients with wound healing disorders (P = .018). High flow values could help to identify patients at risk for cervical wound healing disorders. Copyright © 2014 Elsevier Inc. All rights reserved.

SEM/EDX and vis spectrophotometry study of the stability of resin-bound mortars used for casting replicas and filling missing parts of historic stone fountains.

Science.gov (United States)

Roig-Salom, José-Luis; Doménech-Carbó, María-Teresa; de la Cruz-Cañizares, Juana; Bolívar-Galiano, Fernando; Pelufo-Carbonell, María-José; Peraza-Zurita, Yaiza

2003-04-01

A study by SEM/EDX and spectrophotometry in the visible region attempting to assess the stability of new resin-bound mortars used for casting replicas of marble historic fountains is presented in this paper. Different accelerating tests such as thermal ageing, UV light ageing, ageing in an SO(2) pollutant chamber, freezing cycles ageing, salt crystallisation ageing, natural ageing and biological attack have been applied to a series of test specimens prepared with polyester-, epoxy- and gel-coat-bound mortars. Examination of morphology, measurement of chemical composition and chromatic coordinates before and after ageing treatments establish the higher stability and resistance properties of these resin-bound mortars by comparison to those from the natural marbles.

Monitoring Pb in Aqueous Samples by Using Low Density Solvent on Air-Assisted Dispersive Liquid-Liquid Microextraction Coupled with UV-Vis Spectrophotometry.

Science.gov (United States)

Nejad, Mina Ghasemi; Faraji, Hakim; Moghimi, Ali

2017-04-01

In this study, AA-DLLME combined with UV-Vis spectrophotometry was developed for pre-concentration, microextraction and determination of lead in aqueous samples. Optimization of the independent variables was carried out according to chemometric methods in three steps. According to the screening and optimization study, 86 μL of 1-undecanol (extracting solvent), 12 times syringe pumps, pH 2.0, 0.00% of salt and 0.1% DDTP (chelating agent) were chosen as the optimum independent variables for microextraction and determination of lead. Under the optimized conditions, R = 0.9994, and linearity range was 0.01-100 µg mL -1 . LOD and LOQ were 3.4 and 11.6 ng mL -1 , respectively. The method was applied for analysis of real water samples, such as tap, mineral, river and waste water.

Evaluation of the acidity constants of the 4-hidroxy-5-6salicylideneamino9-2-7-naphthalenedisulfonic acid (Azomethine-H) using UV?vis spectrophotometry

Science.gov (United States)

Alarcón-Angeles, G.; Corona-Avendaño, S.; Rojas-Hernández, A.; Romero-Romo, M. A.; Ramírez-Silva, M. T.

2005-01-01

The time stability of the azomethine-H species was determined not to be better than 10 min in the absence of oxygen and light, however under phosphate buffered conditions the azomethine-H species remained stable for longer periods, as indicated by the spectrophotometric behaviour. Nevertheless, the analysis time still exceeded the stability allowance. Therefore, the determination of the acidity constants of the Azomethine-H species was studied by means of UV-vis spectrophotometry in buffered media by means of the point-by-point analysis and data processing with SQUAD to refine the resulting constants, which were: p Ka1=3.39, p Ka2 7.36 and p Ka3 8.73. The latter were associated to the corresponding acid-base equilibria of the amine and hydroxy groups constituting the molecule.

Determination of Tetracycline in Pharmaceutical Preparation by Molecular and Atomic Absorption Spectrophotometry and High Performance Liquid Chromatography via Complex Formation with Au(III) and Hg(II) Ions in Solutions

Science.gov (United States)

Abdulghani, Ahlam Jameel; Jasim, Hadi Hassan; Hassan, Abbas Shebeeb

2013-01-01

UV-visible and atomic spectrophotometry and HPLC techniques were applied for the determination of tetracycline (TC) in pharmaceutical preparations via complexation of the drug with Au(III) and Hg(II) ions in solutions. The mole ratio of TC to metal ions was 1 : 1. Maximum peak absorption at λ 425 and 320 nm for the two ions, respectively, was optimized at heating temperature 75°C for 15 minutes at pH = 4 followed by the extraction with ethyl acetate. The percentage of extraction and stability constants for the two complexes was 95.247, 95.335% and 2.518 × 104, 1.162 × 105 M−1, respectively. HPLC method was applied without extraction process. The analytical data obtained from direct calibration curves of UV-visible absorption, FAAS, and HPLC for Au(III) complexes were recovery (100.78, 104.85, and 101.777%, resp.); detection limits (0.7403, 0.0997, and 2.647 μg/ml, resp.); linearity (5–70, 5–30, and 10–150 μg/ml, resp.), and correlation coefficient (0.9991, 0.9967, and 0.9986, resp.). The analytical data obtained from direct calibration curves for Hg(II) complexes by UV-visible spectrophotometry and HPLC were recovery (100.95 and 102.000%, resp.); detection limits (0.5867 and 2.532 μg/ml, resp.); linearity (5–70 and 10–150 μg/ml, resp.); and correlation coefficients (0.9989 and 0.9997, resp.). PMID:23853607

Separation of Cu, In, Fe and Sn from nuclear grade thorium by tri-n-octyl amine-5 M HCI and their determination by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Moraes, S. de; Cipriani, M.; Abrao, A.

1976-01-01

The results of solvent extraction separation of a group of metal traces in high pure thorium with the aid of tri-n-octyl amine-benzene from ThCL 4 HCI are summarized. ThCl 4 HCI-KI solutions Cu,In,Fe and Sn are extracted together and determined by atomic absoprtion spectrophotometry, burning directly the organic phase. The behavior of Cu,In,Fe and Sn toward direct burn of the organic phase using hydrogen-air mixture was studied, and an absorption enhancement was observed. The procedure is being used ot perform the quality control of nuclear grade thorium and its compounds. The calibration curves have provided precisions in the range 1 to 10% in analysis of thorium

Simple and fast method for iron determination in white and red wines using dispersive liquid-liquid microextraction and ultraviolet-visible spectrophotometry.

Science.gov (United States)

Maciel, Juliana V; Soares, Bruno M; Mandlate, Jaime S; Picoloto, Rochele S; Bizzi, Cezar A; Flores, Erico M M; Duarte, Fabio A

2014-08-20

This work reports the development of a method for Fe extraction in white and red wines using dispersive liquid-liquid microextraction (DLLME) and determination by ultraviolet-visible spectrophotometry. For optimization of the DLLME method, the following parameters were evaluated: type and volume of dispersive (1300 μL of acetonitrile) and extraction (80 μL of C(2)Cl(4)) solvents, pH (3.0), concentration of ammonium pyrrolidinedithiocarbamate (APDC, 500 μL of 1% m/v APDC solution), NaCl concentration (not added), and extraction time. The calibration curve was performed using the analyte addition method, and the limit of detection and relative standard deviation were 0.2 mg L(-1) and below 7%, respectively. The accuracy was evaluated by comparison of results obtained after Fe determination by graphite furnace atomic absorption spectrometry, with agreement ranging from 94 to 105%. The proposed method was applied for Fe determination in white and red wines with concentrations ranging from 1.3 to 4.7 mg L(-1).

Study for the determination of samarium, europium,terbium, dysprosium and yttrium in gadolinium oxide matrix by means of atomic absorption spectrophotometry using a graphite furnace

International Nuclear Information System (INIS)

Caires, A.C.F.

1985-01-01

A study for determination of samarium, europium, terbium, dysprosium and yttrium in a gadolinium oxide matrix by atomic absorption spectrophotometry using a graphite furnace is presented. The best charrring and atomization conditions were estabilished for each element, the most convenient ressonance lines being selected as well. The study was carried out for the mentioned lanthanides both when pure and when in binary mixtures with gadolinium, besides those where all for them were together with gadolinium. The determination limits for pure lanthanides were found to be between 1.3 and 9.6 ng assuming a 20% relative standard deviation as acceptable. The detection limits were in the range 0.51 and 7.5 ng, assuming as positive any answer higher than twofold the standard deviation. (author) [pt

Inter-laboratory verification of European pharmacopoeia monograph on derivative spectrophotometry method and its application for chitosan hydrochloride.

Science.gov (United States)

Marković, Bojan; Ignjatović, Janko; Vujadinović, Mirjana; Savić, Vedrana; Vladimirov, Sote; Karljiković-Rajić, Katarina

2015-01-01

Inter-laboratory verification of European pharmacopoeia (EP) monograph on derivative spectrophotometry (DS) method and its application for chitosan hydrochloride was carried out on two generation of instruments (earlier GBC Cintra 20 and current technology TS Evolution 300). Instruments operate with different versions of Savitzky-Golay algorithm and modes of generating digital derivative spectra. For resolution power parameter, defined as the amplitude ratio A/B in DS method EP monograph, comparable results were obtained only with algorithm's parameters smoothing points (SP) 7 and the 2nd degree polynomial and those provided corresponding data with other two modes on TS Evolution 300 Medium digital indirect and Medium digital direct. Using quoted algorithm's parameters, the differences in percentages between the amplitude ratio A/B averages, were within accepted criteria (±3%) for assay of drug product for method transfer. The deviation of 1.76% for the degree of deacetylation assessment of chitosan hydrochloride, determined on two instruments, (amplitude (1)D202; the 2nd degree polynomial and SP 9 in Savitzky-Golay algorithm), was acceptable, since it was within allowed criteria (±2%) for assay deviation of drug substance, for method transfer in pharmaceutical analyses. Copyright © 2015 Elsevier B.V. All rights reserved.

Simultaneous determination of selenium and tellurium in native sulfur by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Arikawa, Yoshiko; Hirai, Shoji; Ozawa, Takejiro.

1979-01-01

A method for the determination of selenium and tellurium in native sulfur has been investigated by means of atomic absorption spectrophotometry. Native sulfur collected from around fumarole or volcanic crater is ground down into powder, a portion of which weighing 1 g is subjected to analysis. A 2.6% (w/v) sodium hydroxide solution is added by 10 ml to the sample in a teflon beaker, and the mixture is then heated on a hot plate. Sulfur is decomposed and dissolved in the form of disulfide and thiosulfate. A 30% hydrogenperoxide solution is added by 10 ml to oxidize them to sulfate. At the same time selenium and tellurium contained in the sulfur sample are also thought to be oxidized to Se(VI) and Te(VI) states. The solution is neutralized with hydrochloric acid and diluted with distilled water to 100 ml. The sample solution thus prepared is sprayed into the air-acetylene flame of the atomic absorption spectrophotometer. The absorbance is measured at 195.9 nm for selenium and 214.2 nm for tellurium. Calibration curve is prepared by measuring the absorbances of the solutions prepared as follows. One gram portions of pure sulfur (99.9999%) are decomposed as for the samples. After neutralization, standard solutions containing each same amount of selenium and tellurium (0 -- 1000 μg) are added to the sulfur solution and then diluted with water to 100 ml. The standard deviations were estimated to be 50.4 ppm for selenium at 756 ppm and 16.6 ppm for tellurium at 587 ppm. For the check of the reliability of the method, results were compared with those obtained by neutron activation analysis. Results obtained by both methods showed good agreement. (author)

Evaluating optimal superficial limb perfusion at different angles using non-invasive micro-lightguide spectrophotometry.

Science.gov (United States)

Darmanin, Geraldine; Jaggard, Matthew; Hettiaratchy, Shehan; Nanchahal, Jagdeep; Jain, Abhilash

2013-06-01

It is common practice to elevate the limbs postoperatively to reduce oedema and hence optimise perfusion and facilitate rehabilitation. However, elevation may be counterproductive as it reduces the mean perfusion pressure. There are no clear data on the optimal position of the limbs even in normal subjects. The optimal position of limbs was investigated in 25 healthy subjects using a non-invasive micro-lightguide spectrophotometry system "O2C", which indirectly measures skin and superficial tissue perfusion through blood flow, oxygen saturation and relative haemoglobin concentration. We found a reduction in skin and superficial tissue blood flow of 17% (p=0.0001) on arm elevation (180° shoulder flexion) as compared to heart level and an increase in skin and superficial tissue blood flow of 25% (p=0.02) on forearm elevation of 45°. Lower limb skin and superficial tissue blood flow decreased by 15% (p=0.004) on elevation to 47 cm and by 70% on dependency (p=0.0001) compared to heart level. However, on elevation of the lower limb there was also a 28% reduction in superficial venous pooling (p=0.0001) compared to heart level. In the normal limb, the position for optimal superficial perfusion of the upper limb is with the arm placed at heart level and forearm at 45°. In the lower limb the optimal position for superficial perfusion would be at heart level. However, some degree of elevation may be useful if there is an element of venous congestion. Copyright © 2013 British Association of Plastic, Reconstructive and Aesthetic Surgeons. Published by Elsevier Ltd. All rights reserved.

Noninvasive Measurement of Hemoglobin Using Spectrophotometry: Is it Useful for the Critically Ill Child?

Science.gov (United States)

Akyildiz, Basak

2018-01-01

This study compared the accuracy of noninvasively measuring hemoglobin using spectrophotometry (SpHb) with a pulse CO-oximeter and laboratory hemoglobin (Hb) measurements. A total of 345 critically ill children were included prospectively. Age, sex, and factors influencing the reliabilityof SpHb such as SpO2, heart rate, perfusion index (PI), and vasoactive inotropic score were recorded. SpHb measurements were recorded during the blood draw and compared with the Hb measurement. Thirteen patients (low PI in 9 patients and no available Hb in 4 patients) were excluded and 332 children were eligible for final analysis. The mean Hb was 8.71±1.49 g/dL (range, 5.9 to 12 g/dL) and the mean SpHb level was 9.55±1.53 g/dL (range, 6 to 14.2 g/dL). The SpHb bias was 0.84±0.86,with the limits of agreement ranging from -2.5 to 0.9 g/dL. The difference between Hb and SpHb was >1.5 g/dL for only 47 patients. Of these, 24 patients had laboratory Hb levels <7 g/dL. There was a weak positive correlation between differences and PI (r=0.349; P= 0.032). The pulse CO-oximeter is a promising tool for measuring SpHb and monitoring critically ill children. However, PI may affect these results. Additional studies investigating the reliability of the trend of continuous SpHb values compared with simultaneously measured laboratory Hb values in the same patient are warranted.

Separation of Cu, In, Fe and Sn from nuclear grade thorium by tri-n-octyl amine--5 M HCI and their determination by atomic absorption spectrophotometry

Energy Technology Data Exchange (ETDEWEB)

de Moraes, S; Cipriani, M; Abrao, A

1976-03-01

The results of solvent extraction separation of a group of metal traces in high pure thorium with the aid of tri-n-octyl amine-benzene from ThCl/sub 4/HCl are summarized. ThCl/sub 4/HCl-KI solutions of Cu, In, Fe and Sn are extracted together and determined by atomic absoprtion spectrophotometry and burning directly the organic phase. The behavior of Cu, In, Fe and Sn toward direct burn of the organic phase using hydrogen-air mixture was studied, and an absorption enhancement was observed. The procedure is being used to perform the quality control of nuclear grade thorium and its compounds. The calibration curves have provided precisions in the range 1 to 10% in analysis of thorium.

A rapid and accurate method for determining protein content in dairy products based on asynchronous-injection alternating merging zone flow-injection spectrophotometry.

Science.gov (United States)

Liang, Qin-Qin; Li, Yong-Sheng

2013-12-01

An accurate and rapid method and a system to determine protein content using asynchronous-injection alternating merging zone flow-injection spectrophotometry based on reaction between coomassie brilliant blue G250 (CBBG) and protein was established. Main merit of our approach is that it can avoid interferences of other nitric-compounds in samples, such as melamine and urea. Optimized conditions are as follows: Concentrations of CBBG, polyvinyl alcohol (PVA), NaCl and HCl are 150 mg/l, 30 mg/l, 0.1 mol/l and 1.0% (v/v), respectively; volumes of the sample and reagent are 150 μl and 30 μl, respectively; length of a reaction coil is 200 cm; total flow rate is 2.65 ml/min. The linear range of the method is 0.5-15 mg/l (BSA), its detection limit is 0.05 mg/l, relative standard deviation is less than 1.87% (n=11), and analytical speed is 60 samples per hour. Copyright © 2013 Elsevier Ltd. All rights reserved.

Operator care and eco-concerned development of a fast, facile and economical assay for basic nitrogenous drugs based on simplified ion-pair mini-scale extraction using safer solvent combined with drop-based spectrophotometry.

Science.gov (United States)

Plianwong, Samarwadee; Sripattanaporn, Areerut; Waewsa-nga, Kwanrutai; Buacheen, Parin; Opanasopit, Praneet; Ngawhirunpat, Tanasait; Rojanarata, Theerasak

2012-08-30

A fast, facile, and economical assay for basic nitrogenous drugs has been developed based on the mini-scale extraction of the drug-dye ion pair complex combined with the use of safe-for-analyst and eco-friendlier organic extractant and drop-based micro-spectrophotometry. Instead of using large volume devices, the extraction was simply carried out in typical 1.5 mL microcentrifuge tubes along with the use of micropipettes for accurate transfer of liquids, vortex mixer for efficient partitioning of solutes and benchtop centrifuge for rapid phase separation. In the last step, back-extraction was performed by using the microvolume of acidic solution in order to concentrate the colored species into a confined aqueous microdrop and to keep the analyst away from unwanted contact and inhalation of organic solvents during the quantitation step which was achieved by using cuvetteless UV-vis micro-spectrophotometry without any prior dilutions. Using chlorpheniramine maleate as a representative analyte and n-butyl acetate as a less toxic and non-ozone depleting extractant, the miniaturized method was less laborious and much faster. It was accurate, precise and insensitive to the interferences from common excipients. Notably, it gave the assay results of drug in tablets and oral solution comparable to the large-scale pharmacopeial method while the consumption of organic solvents and the release of wastes were lowered by 200-400 folds. Copyright © 2012 Elsevier B.V. All rights reserved.

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

Science.gov (United States)

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.

Simultaneous determination of polysaccharides and 21 nucleosides and amino acids in different tissues of Salvia miltiorrhiza from different areas by UV-visible spectrophotometry and UHPLC with triple quadrupole MS/MS.

Science.gov (United States)

Xiang, Xiang; Sha, Xiuxiu; Su, Shulan; Zhu, Zhenhua; Guo, Sheng; Yan, Hui; Qian, Dawei; Duan, Jin-Ao

2018-03-01

Salvia miltiorrhiza, a traditional Chinese medicine, is a widely used herbal medicine to treat cardiovascular and cerebrovascular diseases. In this study, ultraviolet (UV)-visible spectrophotometry and ultra-high performance liquid chromatography with triple quadrupole tandem mass spectrometry analytical methods were used for rapid quantification of polysaccharides and 21 nucleosides and amino acids in S. miltiorrhiza to determine 17 samples of different tissues from different areas. Based on the total contents, hierarchical clustering analysis and principal components analysis were performed to classify these samples. The established methods were validated with good linearity, precision, repeatability, stability, and recovery. Chemical analysis revealed a higher content of total analytes in the sample of inflorescence from Nanjing (34.17 mg/g), sample of root and rhizome from Shaanxi (34.13 mg/g) and sample of stem and leaf from Nanjing (31.14 mg/g), respectively, indicating that root and rhizome from Shaanxi and the aerial parts from Nanjing exhibited the highest quality due to their highest content. In addition, contents of nucleosides and amino acids in the aerial parts (14.67 mg/g) were much higher than that in roots and rhizomes (9.17 mg/g). This study suggested that UV-visible spectrophotometry and ultra-high performance liquid chromatography with triple quadrupole tandem mass spectrometry are effective techniques to analyze polysaccharides, nucleosides, and amino acids in plants, and they provided valuable information for the development and utilization value of the aerial parts of S. miltiorrhiza. This analysis would also provide useful information for the quality control of S. miltiorrhiza. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Comparative study of analytical methods by direct and first-derivative UV spectrophotometry for evaluation of losartan potassium in capsules

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Rudy Bonfilio

2010-03-01

Full Text Available Losartan potassium is an antihypertensive non-peptide agent, which exerts its action by specific blockade of angiotensin II receptors. The aim of the present study was the validation and application of analytical methods for the quality control of losartan potassium 50 mg in pharmaceutical capsules, using direct and first-derivative UV spectrophotometry. Based on losartan potassium spectrophotometric characteristics, a signal at 205 nm of the zero-order spectrum and a signal at 234 nm of the first-derivative spectrum, were found adequate for quantification. The results were used to compare these instrumental techniques. The linearity between the signals and concentrations of losartan potassium in the ranges of 3.0-7.0 mg L-1 and 6.0-14.0 mg L-1 for direct and first-derivative spectrophotometry in aqueous solutions, respectively, presented a correlation coefficient (r of 0.9999 in both cases. The methods were applied for losartan potassium in capsule dosage obtained from local pharmacies, and were shown to be efficient, easy to apply and low cost. These methods do not use polluting reagents and require relatively inexpensive equipment.O losartano potássico é um agente anti-hipertensivo não peptídico, que exerce sua ação por bloqueio específico dos receptores da angiotensina II. Este trabalho propôs a validação e aplicação de métodos analíticos orientados ao controle de qualidade de losartano potássico 50 mg na forma farmacêutica cápsula, utilizando a espectrofotometria direta e derivada de primeira ordem na região do UV. Baseado nas características espectrofotométricas de losartano potássico, um sinal a 205 nm do espectro de ordem zero e um sinal a 234 nm do espectro de primeira derivada foram adequados para a quantificação. Os resultados foram usados para comparar essas duas técnicas instrumentais. O coeficiente de correlação entre as respostas e as concentrações de losartano potássico na faixa de 3,0-7,0 mg L-1 e 6

Comparison of two novel in-syringe dispersive liquid-liquid microextraction techniques for the determination of iodide in water samples using spectrophotometry.

Science.gov (United States)

Kaykhaii, Massoud; Sargazi, Mona

2014-01-01

Two new, rapid methodologies have been developed and applied successfully for the determination of trace levels of iodide in real water samples. Both techniques are based on a combination of in-syringe dispersive liquid-liquid microextraction (IS-DLLME) and micro-volume UV-Vis spectrophotometry. In the first technique, iodide is oxidized with nitrous acid to the colorless anion of ICl2(-) at high concentration of hydrochloric acid. Rhodamine B is added and by means of one step IS-DLLME, the ion-pair formed was extracted into toluene and measured spectrophotometrically. Acetone is used as dispersive solvent. The second method is based on the IS-DLLME microextraction of iodide as iodide/1, 10-phenanthroline-iron((II)) chelate cation ion-pair (colored) into nitrobenzene. Methanol was selected as dispersive solvent. Optimal conditions for iodide extraction were determined for both approaches. Methods are compared in terms of analytical parameters such as precision, accuracy, speed and limit of detection. Both methods were successfully applied to determining iodide in tap and river water samples. Copyright © 2013 Elsevier B.V. All rights reserved.

A methodological approach to study the stability of selected watercolours for painting reintegration, through reflectance spectrophotometry, Fourier transform infrared spectroscopy and hyperspectral imaging

Science.gov (United States)

Pelosi, Claudia; Capobianco, Giuseppe; Agresti, Giorgia; Bonifazi, Giuseppe; Morresi, Fabio; Rossi, Sara; Santamaria, Ulderico; Serranti, Silvia

2018-06-01

The aim of this work is to investigate the stability to simulated solar radiation of some paintings samples through a new methodological approach adopting non-invasive spectroscopic techniques. In particular, commercial watercolours and iron oxide based pigments were used, these last ones being prepared for the experimental by gum Arabic in order to propose a possible substitute for traditional reintegration materials. Reflectance spectrophotometry in the visible range and Hyperspectral Imaging in the short wave infrared were chosen as non-invasive techniques for evaluation the stability to irradiation of the chosen pigments. These were studied before and after artificial ageing procedure performed in Solar Box chamber under controlled conditions. Data were treated and elaborated in order to evaluate the sensitivity of the chosen techniques in identifying the variations on paint layers, induced by photo-degradation, before they could be observed by eye. Furthermore a supervised classification method for monitoring the painted surface changes adopting a multivariate approach was successfully applied.

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

Science.gov (United States)

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.

Atomic absorption spectrophotometry of europium using an enhancing effect of ammonium perchlorate

International Nuclear Information System (INIS)

Oguro, Hiroshi

1976-01-01

In the atomic absorption spectrophotometry of europium in air-acetylene flame, ammonium perchlorate (NH 4 ClO 4 ) increases the absorption of europium. In the case of 0.5 M NH 4 ClO 4 , the increase is by about 1.5 times. In this paper, a method for eliminating the interferences of many coexisting compounds using an enhancing effect and a method for determining Eu 2 O 3 in La 2 O 3 were investigated. The working conditions using Nippon Jarrell-Ash model AA-1 atomic absorption/flame emission spectrophotometer were as follows; wavelength 4594 A, lamp current 15 mA, burner height 10 mm, air flow-rate 6.51/min, acetylene flow-rate 1.81/min. Though the enhancing or depressing effects of HCl, HNO 3 , HBr and HClO 4 in concentrations below 0.1 M were eliminated by 0.5 M NH 4 ClO 4 , the remarkable depressing effects of H 2 SO 4 and H 3 PO 4 on europium could not be eliminated. The interferences of Na + , K + , Cs + and Al 3+ in the concentration of 200 ppm were not eliminated, but those of other cations including rare earth elements were completely eliminated. Lanthanum in the range of (2000--10000) ppm increased the absorption of europium by about 1.4 times. But the effect of lanthanum in the range of (0--9000) ppm was also eliminated by NH 4 ClO 4 . The calibration curve for europium in the presence of NH 4 ClO 4 was linear in the range of (0--400) ppm with a sensitivity larger by about 1.5 times than that for europium alone. The analytical procedure is as follows. A sample is dissolved in HCl and NH 4 ClO 4 is added. Europium in the sample solution is determined by atomic absorption method using air-acetylene flame. For practical samples, the values obtained were in fair agreement with those by the flame emission method using a nitrous oxide-acetylene flame. The coefficients of variation by the present method were (3.7--2.4)% (Eu 2 O 3 content (1--3)%). (auth.)

Direct DOC and nitrate determination in water using dual pathlength and second derivative UV spectrophotometry.

Science.gov (United States)

Causse, Jean; Thomas, Olivier; Jung, Aude-Valérie; Thomas, Marie-Florence

2017-01-01

UV spectrophotometry is largely used for water and wastewater quality monitoring. The measurement/estimation of specific and aggregate parameters such as nitrate and dissolved organic carbon (DOC) is possible with UV spectra exploitation, from 2 to multi wavelengths calibration. However, if nitrate determination from UV absorbance is known, major optical interferences linked to the presence of suspended solids, colloids or dissolved organic matter limit the relevance of UV measurement for DOC assessment. A new method based on UV spectrophotometric measurement of raw samples (without filtration) coupling a dual pathlength for spectra acquisition and the second derivative exploitation of the signal is proposed in this work. The determination of nitrate concentration is carried out from the second derivative of the absorbance at 226 nm corresponding at the inflexion point of nitrate signal decrease. A short optical pathlength can be used considering the strong absorption of nitrate ion around 210 nm. For DOC concentration determination the second derivative absorbance at 295 nm is proposed after nitrate correction. Organic matter absorbing slightly in the 270-330 nm window, a long optical pathlength must be selected in order to increase the sensitivity. The method was tested on several hundred of samples from small rivers of two agricultural watersheds located in Brittany, France, taken during dry and wet periods. The comparison between the proposed method and the standardised procedures for nitrate and DOC measurement gave a good adjustment for both parameters for ranges of 2-100 mg/L NO3 and 1-30 mg/L DOC. Copyright © 2016 Elsevier Ltd. All rights reserved.

New development of spectrophotometric analysis of thorium

International Nuclear Information System (INIS)

Yang Xiangzhen

1992-01-01

This review covers new development of spectrophotometric determination of thorium since 1980's. The methods include general spectrophotometry, double wavelength spectrophotometry, catalytic spectrophotometry, total differential spectrophotometry, derivative spectrophotometry and fluorescent spectrophotometry, etc

Near-infrared spectrophotometry of eight 3CR radiogalaxies: the first detections of [O III]500.7 and [S III]953.2 emission lines in galaxies with z > 1

International Nuclear Information System (INIS)

Rawlings, Steve; Lacy, Mark

1991-01-01

We present the results of near-IR spectrophotometry of eight 3CR radiogalaxies with redshifts in the range 0.256≤z≤1.575. The narrow [O III]500.7 emission line was detected in 3C13 (z = 1.351), and the narrow [S III]953.2 emission line in 3C79 (z = 0.256), in the northern near-IR knot of 3C356 (z = 1.079) and marginally in 3C368 (z=1.132). We show that narrow-line emission can sometimes account for a substantial fraction of the broad-band near-IR flux arising from the substructures of high-z radiogalaxies, but that this fraction is strongly dependent on, and therefore a valuable probe of, physical conditions within the substructures. (author)

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

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Julien A. Jendral

2011-01-01

Full Text Available 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.

Evaluation of various techniques for the pretreatment of sewage sludges prior to trace metal analysis by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Smith, R.

1983-01-01

Six techniques were evaluated for their suitability for the pretreatment of dried sewage sludge prior to trace metal analysis by atomic absorption spectrophotometry. The evaluation comprised analysis of two prepared samples of dried sludge for aluminium, cadmium, chromium, copper, iron, lead, manganese, nickel and zinc, after the following pretreatment: dry ashing at 500 degrees Celsius followed by extraction with dilute hydrochloric acid; dry ashing at 500 degrees Celsius followed by extraction with aqua regia; nitric acid digestion followed by extraction with hydrochloric acid; extraction with aqua regia; ashing with magnesium nitrate solution at 550 degrees Celsius followed by digestion with hydrochloric acid and extraction with nitric acid; extraction with nitric acid. Procedures involving the use of perchloric acid, hydrofluoric acid and hydrogen peroxide were not considered for reasons of safety. Except in the case of aluminium the direct mineral acid digestion and/or extraction methods generally gave higher recoveries than the procedures incorporating an ashing step. Direct extraction of the sample with aqua regia was recommended as a rapid and simple general method of sample pretreatment prior to analysis for all the metals investigated except aluminium. For this metal, more drastic sample pretreatment will be required, for example fusion or hydrofluoric acid digestion

An optical investigation of dentinal discoloration due to commonly endodontic sealers, using the transmitted light polarizing microscopy and spectrophotometry.

Science.gov (United States)

Suciu, Ioana; Ionescu, Ecaterina; Dimitriu, Bogdan Alexandru; Bartok, Ruxandra Ioana; Moldoveanu, Georgiana Florentina; Gheorghiu, Irina Maria; Suciu, Ileana; Ciocîrdel, Mihai

2016-01-01

The aim of this study was to establish the degree of tooth crown staining by commonly used endodontic sealers. Crown discolorations by tooth canal sealers [AH Plus (Dentsply DeTrey Gmbh, Konstanz, Germany); Endofill (Produits Dentaires SA, Vevey, Switzerland); Apexit (Dentsply DeTrey Gmbh, Konstanz, Germany); and MTA Fillapex (Angelus, Londrina, Brazil)] were tested on extracted human premolars. The samples were divided into five groups of five samples each, after root canal sealing. Five teeth were used as control groups. The spectrophotometric method was performed in order to quantify in terms of color change of the coronal part (it was also recorded a track on how the color changes over time). For the microscopic study of the extracted dental specimens subjected to this study, polarized transmitted light microscopy was used. This method involves the development of special microscopic preparations, called "thin sections". In our case, the thin section was performed on 20 prepared and obturated recently extracted teeth. The degree of discoloration was determined after one week and three months using spectrophotometry and polarized light microscopy. All sealers usually cause some degree of discoloration on the cervical aspect of the crowns that increases in time. AH Plus and Endofill caused the greatest discoloration, followed by Apexit and MTA Fillapex.

Formaldehyde in alcoholic beverages: large chemical survey using purpald screening followed by chromotropic Acid spectrophotometry with multivariate curve resolution.

Science.gov (United States)

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 (13)C 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.

High-performance liquid chromatography and derivative spectrophotometry for simultaneous determination of pravastatin and fenofibrate in the dosage form

Directory of Open Access Journals (Sweden)

Hefnawy Mohamed M.

2014-12-01

Full Text Available High performance liquid chromatography (HPLC and second-order derivative spectrophotometry have been used for simultaneous determination of pravastatin (PS and fenofibrate (FF in pharmaceutical formulations. HPLC separation was performed on a phenyl HYPERSIL C18 column (125 mm × 4.6 mm i.d., 5 μm particle diameter in the isocratic mode using a mobile phase acetonitrile/0.1 % diethyl amine (50:50, V/V, pH 4.5 pumped at a flow rate of 1.0 mL min-1. Measurement was made at 240 nm. Both drugs were well resolved on the stationary phase, with retention times of 2.15 and 5.79 min for PS and FF, respectively. Calibration curves were linear (R = 0.999 for PS and 0.996 for FF in the concentration range of 5-50 and 20-200 µg mL-1 for PS and FF, respectively. Pravastatin and fenofibrate were quantitated in combined preparations also using the second-order derivative response at 237.6 and 295.1 nm for PS and FF, respectively. Calibration curves were linear, with the correlation coefficient R = 0.999 for pravastatin and fenofibrate, in the concentration range of 5-20 and 3-20 µg mL-1 for PS and FF, respectively. Both methods were fully validated and compared, the results confirmed that they were highly suitable for their intended purpose.

Determinação de cumarina em extrato fluido e tintura de guaco por espectrofotometria derivada de primeira ordem Determination of coumarin in fluid extract and tinture of "guaco" by first derivative spectrophotometry

Directory of Open Access Journals (Sweden)

Adriana de Carvalho Osório

2004-12-01

Full Text Available O objetivo do trabalho foi desenvolver um método de doseamento de cumarina (1,2-benzopirano em extrato fluido e tintura de guaco (Mikania glomerata Sprengel. O método desenvolvido foi por espectrofotometria derivada de primeira ordem, que se mostrou preciso, exato, reprodutível e de fácil execução.The objective of this work was to develop a method for coumarin(1,2-benzopyran dosage in fluid extract and tinture of "guaco" (Mikania glomerata Sprengel. First derivative spectrophotometry was developed and proved to be accurate, exact, reprodutive and of easy execution.

Preparation of Dry Extract of Mikania glomerata Sprengel (Guaco and Determination of Its Coumarin Levels by Spectrophotometry and HPLC-UV

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Maria da Penha Henriques do Amaral

2012-08-01

Full Text Available 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 freeze-drying 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.

Diagnosis of soils polluted by aromatic hydrocarbons; Diagnostic de sols pollues par des hydrocarbures aromatiques polycycliques (HAP) a l'aide de la spectrophotometrie UV

Energy Technology Data Exchange (ETDEWEB)

Crone, M

2000-01-28

Polycyclic aromatic hydrocarbons (PAHs) were produced by many pyrolytic or combustion processes. They were found in soils, often in high concentrations. Remediation of industrial sites contaminated by PAHs requires an initial diagnosis of the pollution. In this perspective, an analytical procedure based on UV spectrophotometry was developed and validated with about 80 soil samples. Different exploitation methods of the samples UV spectra enable to develop simple and rapid characterisation tools. A PAH UV index is proposed for the estimation of global PAH concentration. A more accurate exploitation of the spectra gives an indication on the presence or the absence of some individual PAH like benzo[a]pyrene. A maturity index based on a two wavelength approach constitutes an indicator of the potential evolution of soil contamination in natural conditions. Laboratory methodology was adapted to field analyses and a test kit was designed for this purpose. The test duration is 20 minutes. (author)

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

Science.gov (United States)

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. Copyright © 2016. Published by Elsevier B.V.

A new method of UA_CPE coupled with spectrophotometry for the faster and cost-effective detection of proline in fruit juice, honey, and wine.

Science.gov (United States)

Dağdeviren, Semahat; Altunay, Nail; Sayman, Yasin; Gürkan, Ramazan

2018-07-30

The study developed a new method for proline detection in honey, wine and fruit juice using ultrasound assisted-cloud point extraction (UA-CPE) and spectrophotometry. Initially, a quaternary complex was built, containing proline, histamine, Cu(II), and fluorescein at pH 5.5. Samples were treated with ethanol-water mixture before extraction and preconcentration, using an ultrasonic bath for 10 min at 40 °C (40 kHz, 300 W). After the optimization of variables affecting extraction efficiency, good linearity was obtained between 15 and 600 µg L -1 with sensitivity enhancement factor of 105. The limits of detection and quantification were 5.7 and 19.0 µg L -1 , respectively. The recovery percentage and relative standard deviations (RSD %) were between 95.3 and 103.3%, and 2.5 and 4.2%, respectively. The accuracy of the method was verified by the analysis of a standard reference material (SRM 2389a). Copyright © 2018 Elsevier Ltd. All rights reserved.

Redox equilibrium of U4+/U3+ in molten NaCl-2CsCl by UV-Vis spectrophotometry and cyclic voltammetry

International Nuclear Information System (INIS)

Nagai, Takayuki; Uehara, Akihiro; Fujii, Toshiyuki; Shirai, Osamu; Yamana, Hajimu; Sato, Nobuaki

2005-01-01

In order to investigate the redox equilibrium of uranium ions in molten NaCl-2CsCl, UV-Vis absorption spectro-photometry measurements were performed for U 4+ and U 3+ in molten NaCl-2CsCl at 923 K under simultaneous electrolytic control of their ratio. Prominent absorption bands at 480 and 570 nm were assigned to U 3+ , and their molar absorptivities were determined to be 1,260±42 and 963±32 mol -1 ·l·cm -1 respectively. From the dependence of the rest potential of the melt on the spectrophotometrically determined ratio of [U 4+ ]/[U 3+ ], the standard redox potential of the couple U 4+ /U 3+ at 923 K was determined to be -1.481±0.004 V vs. Cl 2 /Cl - . Cyclic voltammetry measurements were carried out for the couple U 4+ /U 3+ , and the results agreed well with this standard redox potential value. By the results of cyclic voltammetry, a temperature dependence of the standard redox potential was found to be -2.094+6.639 x 10 -4 T (T=823-923K). (author)

Determination of tin in biological reference materials by atomic absorption spectrophotometry and neutron activation analysis

International Nuclear Information System (INIS)

Chiba, M.; Iyengar, V.; Gills, T.

1991-01-01

Because of a lack of reliable analytical techniques for the determination of tin in biological materials, there have been no reference materials certified for this element. However, the authors' experience has shown that it is feasible to use both atomic absorption and nuclear activation techniques at least for selected matrices. Therefore, an investigation was undertaken to determine tin in several biological materials such as non-fat milk powder (NBS-SRM-1549), citrus leaves (NBS-SRM-1572), total diet (NIST-SRM-1548), mixed diet (NBS-RM-8431), and USDIET-I by atomic absorption spectrophotometry (AAS) and neutron activation analysis (NAA). AAS-ashed samples were extracted with MIBK and assayed using a Perkin Elmer model 5000 apparatus. NAA was carried out by irradiating the samples at the NIST reactor in the RT-4 facility and counting with the help of a Ge(Li) detector connected to a multichannel analyzer. The concentration of tin measured by both AAS and NAA agree well for USDIET-I, total diet, citrus leaves and non-fat milk powder (the concentration ranges for tin in these matrices were from 0.0025 to 3.8 micro g/g). However, in the case of mixed diet (RM-8431), the mean values found were 47 ± 5.6 (n = 19) by AAS and 55.5 ± 2.5 (n = 6) by INAA. Since RM-8431 is not certified it is difficult to draw conclusions. For apple and peach leaves, a distillation step was required. The results were apple leaves 0.085 ± 0.015 (n = 10) by AAS and < 0.2 (n = 3) by RNAA; for peach leaves 0.077 ± 0.02 (n = 9) by AAS and < 0.1 (n = 3) by RNAA. All concentrations are expressed in micro g/g dry weight

Comparison of Ho and Y complexation data obtained by electromigration methods, potentiometry and spectrophotometry

International Nuclear Information System (INIS)

Vinsova, H.; Koudelkova, M.; Ernestova, M.; Jedinakova-Krizova, V.

2003-01-01

Many of holmium and yttrium complex compounds of both organic and inorganic origin have been studied recently from the point of view of their radiopharmaceutical behavior. Complexes with Ho-166 and Y-90 can be either directly used as pharmaceutical preparations or they can be applied in a conjugate form with selected monoclonal antibody. Appropriate bifunctional chelation agents are necessary in the latter case for indirect binding of monoclonal antibody and selected radionuclide. Our present study has been focused on the characterization of radionuclide (metal) - ligand interaction using various analytical methods. Electromigration methods (capillary electrophoresis, capillary isotachophoresis), potentiometric titration and spectrophotometry have been tested from the point of view of their potential to determine conditional stability constants of holmium and yttrium complexes. A principle of an isotachophoretic determination of stability constants is based on the linear relation between logarithms of stability constant and a reduction of a zone of complex. For the calculation of thermodynamic constants using potentiometry it was necessary at first to determine the protonation constants of acid. Those were calculated using the computer program LETAGROP Etitr from data obtained by potentiometric acid-base titration. Consequently, the titration curves of holmium and yttrium with studied ligands and protonation constants of corresponding acid were applied for the calculation of metal-ligand stability constants. Spectrophotometric determination of stability constants of selected systems was based on the titration of holmium and yttrium nitrate solutions by Arsenazo III following by the titration of metal-Arsenazo III complex by selected ligand. Data obtained have been evaluated using the computation program OPIUM. Results obtained by all analytical methods tested in this study have been compared. It was found that direct potentiometric titration technique could not be

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

Energy Technology Data Exchange (ETDEWEB)

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

Spectrophotometry of peculiar B and A stars. XVII. 63 Andromedae, HD 34452, epsilon Ursae Majoris, CQ Ursae Majoris, CU Virginis, CS Virginis and Beta Coronae Borealis

International Nuclear Information System (INIS)

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

1985-01-01

Optical region spectrophotometry results are presented for seven Ap stars. Additional data for two silicon stars, HD 34452 and CU Vir, show that both have energy distributions that can be fit by a single global model atmosphere, except for the lambda 4200 and lambda 5200 broad absorption features. These features are strong in HD 34452 and show no evidence of variation, while they are weak in CU Vir but show clear evidence of variations. The energy distributions of the five cooler Ap stars cannot be fit by a single model atmosphere. CQ UMa, CS Vir and β CrB all show complicated variations with phase at different wavelengths. Their energy distributions show combined effects of flux redistribution and differential line blanketing. Except for epsilon UMa, none of these five stars show evidence of variations of the lambda 4200 or lambda 5200 broad absorption features

Diagnosis of soils polluted by aromatic hydrocarbons; Diagnostic de sols pollues par des hydrocarbures aromatiques polycycliques (HAP) a l'aide de la spectrophotometrie UV

Energy Technology Data Exchange (ETDEWEB)

Crone, M.

2000-01-28

Polycyclic aromatic hydrocarbons (PAHs) were produced by many pyrolytic or combustion processes. They were found in soils, often in high concentrations. Remediation of industrial sites contaminated by PAHs requires an initial diagnosis of the pollution. In this perspective, an analytical procedure based on UV spectrophotometry was developed and validated with about 80 soil samples. Different exploitation methods of the samples UV spectra enable to develop simple and rapid characterisation tools. A PAH UV index is proposed for the estimation of global PAH concentration. A more accurate exploitation of the spectra gives an indication on the presence or the absence of some individual PAH like benzo[a]pyrene. A maturity index based on a two wavelength approach constitutes an indicator of the potential evolution of soil contamination in natural conditions. Laboratory methodology was adapted to field analyses and a test kit was designed for this purpose. The test duration is 20 minutes. (author)

Determination of carcinogenic herbicides in milk samples using green non-ionic silicone surfactant of cloud point extraction and spectrophotometry.

Science.gov (United States)

Mohd, N I; Zain, N N M; Raoov, M; Mohamad, S

2018-04-01

A new cloud point methodology was successfully used for the extraction of carcinogenic pesticides in milk samples as a prior step to their determination by spectrophotometry. In this work, non-ionic silicone surfactant, also known as 3-(3-hydroxypropyl-heptatrimethylxyloxane), was chosen as a green extraction solvent because of its structure and properties. The effect of different parameters, such as the type of surfactant, concentration and volume of surfactant, pH, salt, temperature, incubation time and water content on the cloud point extraction of carcinogenic pesticides such as atrazine and propazine, was studied in detail and a set of optimum conditions was established. A good correlation coefficient ( R 2 ) in the range of 0.991-0.997 for all calibration curves was obtained. The limit of detection was 1.06 µg l -1 (atrazine) and 1.22 µg l -1 (propazine), and the limit of quantitation was 3.54 µg l -1 (atrazine) and 4.07 µg l -1 (propazine). Satisfactory recoveries in the range of 81-108% were determined in milk samples at 5 and 1000 µg l -1 , respectively, with low relative standard deviation, n  = 3 of 0.301-7.45% in milk matrices. The proposed method is very convenient, rapid, cost-effective and environmentally friendly for food analysis.

Conventional high-performance liquid chromatography versus derivative spectrophotometry for the determination of 1,3,6-pyrenetrisulfonic acid trisodium salt and 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt in the color additive D&C Green No. 8 (Pyranine).

Science.gov (United States)

Jitian, Simion; White, Samuel R; Yang, H-H Wendy; Weisz, Adrian

2014-01-10

Specifications in the U.S. Code of Federal Regulations for the color additive D&C Green No. 8 (Colour Index No. 59040) limit the levels of the subsidiary colors 1,3,6-pyrenetrisulfonic acid trisodium salt (P3S) and 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt (P4S). The present paper describes a comparative study of two possible methods to replace the currently used multi-step TLC/spectrophotometry method of separating and quantifying the minor components P3S and P4S in G8. One of the new approaches uses conventional high-performance liquid chromatography (HPLC) and the other, derivative spectrophotometry. While the derivative spectrophotometric method was shown to be inadequate for the analysis of minor components overwhelmed by components of much higher concentration, the HPLC method was proven highly effective. The closely related, very polar compounds P3S and P4S were separated by the new HPLC method in less than 4 min using a conventional HPLC instrument. P3S and P4S were quantified by using five-point calibration curves with data points that ranged from 0.45 to 7.63% and from 0.13 to 1.82%, by weight, for P3S and P4S, respectively. The HPLC method was applied to the analysis of test portions from 20 batches of D&C Green No. 8 submitted to the U.S. Food and Drug Administration for certification. Published by Elsevier B.V.

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

Science.gov (United States)

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

2014-04-05

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. Copyright © 2013 Elsevier B.V. All rights reserved.

The influence of a clear layer on near-infrared spectrophotometry measurements using a liquid neonatal head phantom

International Nuclear Information System (INIS)

Wolf, M.

1999-01-01

It is difficult to test near-infrared spectrophotometry instruments in vivo. Therefore we constructed a liquid phantom which mimics the neonatal head. It consists of a spherical 3.5 mm thick layer of silicone rubber simulating skin and bone and a 0.5 mm thick clear layer of polypropylene imitating cerebrospinal fluid. It acts as container for a liquid solution with Intralipid, 60 μmol l -1 haemoglobin and yeast. The solution was oxygenated using oxygen and then deoxygenated by the yeast. From the instrumental (Critikon 2020) algorithm, we found that with increasing scattering (0.5%, 1%, 1.5% and 2% Intralipid concentration) the reading was increasingly offset from the expected value of 0 μmol l -1 by 55.7, 68.6, 76.5 and 80.4 μmol l -1 (oxyhaemoglobin) and 16.0, 24.4, 29.6 and 31.7 μmol l -1 (deoxyhaemoglobin). This reduced the range of the oxygen saturation reading from the expected 100% to 31.5, 21.1, 14.3 and 11.5%. Haemoglobin concentration changes were increasingly underestimated by a factor of two to four. For a second algorithm based on the diffusion approximation the offsets were smaller: oxyhaemoglobin 11.4, 17.8, 22.5 and 25.1 μmol l -1 and deoxyhaemoglobin 1.3, 3.4, 5.2 and 6.0 μmol l -1 . The range of the oxygen saturation reading was higher: 41.3, 29.2, 23.4 and 16.6%. Concentration changes were underestimated by a factor of six to ten. This study demonstrates the need to develop algorithms which take into consideration anatomical structures. (author)

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

Science.gov (United States)

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.

Acquiring Sediment and Element Compositional Changes Based on a Diffuse Reflectance Spectrophotometry Technology from Cores Offshore Southwestern Taiwan

Science.gov (United States)

Pan, H. J.; Chen, M. T.

2014-12-01

Heavy summer monsoon rainfall along with typhoon-induced extreme precipitation cause frequent geological hazards that often threaten the human's safety and property in Taiwan. These geological hazards can be triggered by both natural factors, and/or have become deteriorated by perturbations from more and more human activities ever since few thousand years ago. However, due to the limit of instrumental records for observing long-term environmental changes in Taiwan, few evidence exist for distinguishing the human-induced impacts from natural climate change. Here we report a study on a high quality marine sediment core (MD103264) which were retrieved from the high sedimentation rate area from offshore southwestern Taiwan and present evidence for the long-term climate and possibly human-induced environmental changes since the last glacial. We are using the VIS-NIR Diffuse Reflectance Spectrophotometry (DRS) methods to study the cores. Interpreting the VIS-NIR reflectance spectra through the VARIMAX-rotation, principle component analysis (VPCA) helps conducting rapid and inexpensive measurements for acquiring high-resolution biogenic component, clay, and iron oxide mineral compositional data from the cores. We are also using X-Ray Fluorescence (XRF) analysis, which is also useful in determining the element compositional changes in the core. Our studies aim toward understanding the sediment and element compositional changes that reflect the patterns of changes in precipitation and soil erosion on land since the last glacial to the Holocene, during which the human activities (deforestation, agriculture, and land uses change) may have increased drastically. We will report and interpret the preliminary results of the optical analyses of the core.

Selective determination of thorium in water using dual-wavelength β-correction spectrophotometry and the reagent 4-(2-pyridylazo)-resorcinol

International Nuclear Information System (INIS)

Kadi, M.W.; El-Shahawi, M.S.

2011-01-01

A simple, fast, low cost, and precise direct β-correction spectrophotometric method was developed for thorium determination in water. The method is based on the reaction of Th(IV) with 4-(2-pyridylazo)-resorcinol (PAR) in aqueous solution of pH 5-6 and measuring the absorbance of the resulting red-colored complex at λ max 497 nm. The effective molar absorptivity of the Th(IV)-PAR complex was 2.52 x 10 4 L mol -1 cm -1 . Beer's law and Ringbom plots were obeyed in the concentration range 0.04-2.0 and 0.07-1.2 μg mL -1 of thorium ions using β-correction spectrophotometry, respectively. The limits of detection and quantification of Th(IV) were 0.02 and 0.066 μg mL -1 , respectively. The developed method was applied for the analysis of thorium in certified reference material (IAEA-soil-7), tap-, underground- and Red-sea water samples. The validation of the method was also tested by comparison with data obtained by ICP-MS. The method is convenient, less sensitive to common interfering species and less laborious than most of published methods. The statistical treatment of data in terms of Student t-tests and variance ratio f-tests has revealed no significance differences. The structure of the Th(IV)-PAR complex was determined with the aid of spectroscopic measurements (UV-Visible and Fourier Transform Infrared Spectroscopy). (author)

Determinação de fósforo biodisponível em rações de peixes utilizando extração assistida por ultra-som e espectrofotometria no visível Determination of bioavailable phosphorus in fish feeds by ultrasound extraction and visible spectrophotometry

OpenAIRE

Paula M. de Moraes; Vanessa R. Loureiro; Pedro M. Padilha; Renato de Cássio F. Neves; Mayra A. D. Saleh; Felipe A. dos Santos; Fábio A. Silva

2009-01-01

The aim of the present work was to develop and optimize a method for determination of bioavailable phosphorus in samples of feces and fish feed using ultrasound extraction and subsequent quantification by visible spectrophotometry. Using as extractor solution HNO3 0.50 mol L-1, the great conditions of extraction established were: sample mass - 100 mg, samples granulometry - < 60 µm, sonification time - five cycles of 40 s and ultrasound potency - 136 W. The proposed method was applied in stud...

Relative bioavailability studies on a locally manufactured aspirin tablets using UV spectrophotometry and HPLC

International Nuclear Information System (INIS)

Kwadzo, Ameko David

2005-11-01

Modern trends in drug analysis require use of less time consuming, efficient, cost effective, fast, reproducible, simple and convenient methods. Two analytical methods were employed for the determination, the UV spectrophotometry and the HPLC. Aspirin, which is rapidly deacetylated to salicylic acid after absorption into the plasma, is excreted in the urine. In determining the salicylic acid concentration in the urine, the absorbance was quantitated by a spectrometer at a wavelength of 540nm. Aspirin formed an amber coloured complex with ferric ions (Trinder’s reagent). The complex, which formed instantaneously at room temperature, was stable. The solution of the complex obeyed Beer’s law at 540nm, the wavelength of maximum absorption of radiation (λmax). Phenol—induced absorbance is quenched by acidifying the reaction mixture with phosphoric acid. An HPLC analytical method was used in determining the free salicylate excreted in the urine. The mobile phase employed is a validated method from the USP- XXII (1990) which consists of water, methanol and glacial acetic acid in the ratio 69: 28: 3 respectively. The chromatographic conditions involved a flow rate of 1.0ml/rnin, wavelength of maximum absorption of 236nrn, stationary phase Spherisorb S5 ODS 1 phase sep column with standard dimensions of 25.0 cm length and 4.6cm diameter and chart recorder speed of 5mm/min. The quality of the reference and the test tablets were assessed by a number of standard tests, which include uniformity of weight, friability, hardness and dissolution that fall within the BP 2000 specification. The observation from the study reveals that the relative bioavailability of aspirin (w.r.t. salicylic acid) were 103.39% and 94.93% for HPLC and UV respectively. The mean cumulative percentage of the drug excreted in both cases were ii .05% and 10.69% for test and reference respectively for HPLC and 76.45% and 80.53% for test and reference respectively for UV analysis. The cumulative amount

UV-Vis spectrophotometry of quinone flow battery electrolyte for in situ monitoring and improved electrochemical modeling of potential and quinhydrone formation.

Science.gov (United States)

Tong, Liuchuan; Chen, Qing; Wong, Andrew A; Gómez-Bombarelli, Rafael; Aspuru-Guzik, Alán; Gordon, Roy G; Aziz, Michael J

2017-12-06

Quinone-based aqueous flow batteries provide a potential opportunity for large-scale, low-cost energy storage due to their composition from earth abundant elements, high aqueous solubility, reversible redox kinetics and their chemical tunability such as reduction potential. In an operating flow battery utilizing 9,10-anthraquinone-2,7-disulfonic acid, the aggregation of an oxidized quinone and a reduced hydroquinone to form a quinhydrone dimer causes significant variations from ideal solution behavior and of optical absorption from the Beer-Lambert law. We utilize in situ UV-Vis spectrophotometry to establish (a), quinone, hydroquinone and quinhydrone molar attenuation profiles and (b), an equilibrium constant for formation of the quinhydrone dimer (K QHQ ) ∼ 80 M -1 . We use the molar optical attenuation profiles to identify the total molecular concentration and state of charge at arbitrary mixtures of quinone and hydroquinone. We report density functional theory calculations to support the quinhydrone UV-Vis measurements and to provide insight into the dimerization conformations. We instrument a quinone-bromine flow battery with a Pd-H reference electrode in order to demonstrate how complexation in both the negative (quinone) and positive (bromine) electrolytes directly impacts measured half-cell and full-cell voltages. This work shows how accounting for electrolyte complexation improves the accuracy of electrochemical modeling of flow battery electrolytes.

Use of micro-lightguide spectrophotometry for evaluation of microcirculation in the small and large intestines of horses without gastrointestinal disease.

Science.gov (United States)

Reichert, Christof; Kästner, Sabine B R; Hopster, Klaus; Rohn, Karl; Rötting, Anna K

2014-11-01

To evaluate the use of a micro-lightguide tissue spectrophotometer for measurement of tissue oxygenation and blood flow in the small and large intestines of horses under anesthesia. 13 adult horses without gastrointestinal disease. Horses were anesthetized and placed in dorsal recumbency. Ventral midline laparotomy was performed. Intestinal segments were exteriorized to obtain measurements. Spectrophotometric measurements of tissue oxygenation and regional blood flow of the jejunum and pelvic flexure were obtained under various conditions that were considered to have a potential effect on measurement accuracy. In addition, arterial oxygen saturation at the measuring sites was determined by use of pulse oximetry. 12,791 single measurements of oxygen saturation, relative amount of hemoglobin, and blood flow were obtained. Errors occurred in 381 of 12,791 (2.98%) measurements. Most measurement errors occurred when surgical lights were directed at the measuring site; covering the probe with the surgeon's hand did not eliminate this error source. No measurement errors were observed when the probe was positioned on the intestinal wall with room light, at the mesenteric side, or between the mesenteric and antimesenteric side. Values for blood flow had higher variability, and this was most likely caused by motion artifacts of the intestines. The micro-lightguide spectrophotometry system was easy to use on the small and large intestines of horses and provided rapid evaluation of the microcirculation. Results indicated that measurements should be performed with room light only and intestinal motion should be minimized.

Hydride generation coupled to microfunnel-assisted headspace liquid-phase microextraction for the determination of arsenic with UV-Vis spectrophotometry.

Science.gov (United States)

Hashemniaye-Torshizi, Reihaneh; Ashraf, Narges; Arbab-Zavar, Mohammad Hossein

2014-12-01

In this research, a microfunnel-assisted headspace liquid-phase microextraction technique has been used in combination with hydride generation to determine arsenic (As) by UV-Vis spectrophotometry. The method is based on the reduction of As to arsine (AsH3) in acidic media by sodium tetrahydroborate (NaBH4) followed by its subsequent reaction with silver diethyldithiocarbamate (AgDDC) to give an absorbing complex at 510 nm. The complexing reagent (AgDDC) has been dissolved in a 1:1 (by the volume ratio) mixture of chloroform/chlorobenzene microdroplet and exposed to the generated gaseous arsine via a reversed microfunnel in the headspace of the sample solution. Several operating parameters affecting the performance of the method have been examined and optimized. Acetonitrile solvent has been added to the working samples as a sensitivity enhancement agent. Under the optimized operating conditions, the detection limit has been measured to be 0.2 ng mL(-1) (based on 3sb/m criterion, n b = 8), and the calibration curve was linear in the range of 0.5-12 ng mL(-1). The relative standard deviation for eight replicate measurements was 1.9 %. Also, the effects of several potential interferences have been studied. The accuracy of the method was validated through the analysis of JR-1 geological standard reference material. The method has been successfully applied for the determination of arsenic in raw and spiked soft drink and water samples with the recoveries that ranged from 91 to 106 %.

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

Science.gov (United States)

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. Copyright © 2016

Colour analysis of the equine endometrium: comparison of spectrophotometry and computer-assisted analysis of photographs within the L*a*b* colour space system.

Science.gov (United States)

Neuhauser, S; Handler, J

2013-09-01

The aims of this study were to compare two different methods of quantifying the colour of the luminal surface of the equine endometrium and to relate the results to histopathological evidence of inflammation and fibrosis. The mucosal surfaces of 17 equine uteri obtained from an abattoir were assessed using a spectrophotometer and by computer-assisted analysis of photographs. Values were converted into L(*)a(*)b(*) colour space. Although there was significant correlation between the two methods of quantification, variations in 'brightness', 'red' and 'yellow' values were noted. Within a given uterus, measurements using the spectrophotometer did not differ significantly. Using photographic analysis, brightness differed between horns, although no differences in chromaticity were found. Histopathological classification of changes within endometria corresponded to measured differences in colour. Extensive fibrosis was associated with increased brightness and decreased chromaticity using both methods. Inflammation correlated with reduced chromaticity, when measured by spectrophotometry, and with reduced brightness and yellow values, when assessed photographically. For this technique to gain wider acceptance as a diagnostic tool, e.g. for the endoscopic evaluation of uterine mucosae in vivo, standardised illumination techniques will be required so that colours can be compared and interpreted accurately. Copyright © 2013 Elsevier Ltd. All rights reserved.

Polypyrrole-magnetite dispersive micro-solid-phase extraction combined with ultraviolet-visible spectrophotometry for the determination of rhodamine 6G and crystal violet in textile wastewater.

Science.gov (United States)

Kamaruddin, Amirah Farhan; Sanagi, Mohd Marsin; Wan Ibrahim, Wan Aini; Md Shukri, Dyia S; Abdul Keyon, Aemi S

2017-11-01

Polypyrrole-magnetite dispersive micro-solid-phase extraction method combined with ultraviolet-visible spectrophotometry was developed for the determination of selected cationic dyes in textile wastewater. Polypyrrole-magnetite was used as adsorbent due to its thermal stability, magnetic properties, and ability to adsorb Rhodamine 6G and crystal violet. Dispersive micro-solid-phase extraction parameters were optimized, including sample pH, adsorbent amount, extraction time, and desorption solvent. The optimum polypyrrole-magnetite dispersive micro-solid phase-extraction conditions were sample pH 8, 60 mg polypyrrole-magnetite adsorbent, 5 min of extraction time, and acetonitrile as the desorption solvent. Under the optimized conditions, the polypyrrole-magnetite dispersive micro-solid-phase extraction with ultraviolet-visible method showed good linearity in the range of 0.05-7 mg/L (R 2  > 0.9980). The method also showed a good limit of detection for the dyes (0.05 mg/L) and good analyte recoveries (97.4-111.3%) with relative standard deviations extraction and determination of dyes at trace concentration levels. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Elemental characterisation of strawberry grown in Islamabad by k0-instrumental neutron activation analysis and atomic absorption spectrophotometry and its dietary assessment

International Nuclear Information System (INIS)

Mohammad Wasim; Nasir Khalid; Mohammad Arif; Jamshed Hussain Zaidi

2012-01-01

Mineral contents of strawberry, collected from different farms of Islamabad were analysed by semi-absolute k 0-instrumental neutron activation analysis and atomic absorption spectrophotometry. The samples were irradiated at two research reactors located in Pakistan Institute of Nuclear Science and Technology (PINSTECH), Islamabad. The analytical methodologies were validated by analysing reference materials, IAEA-336 (lichen) and IAEA-V-10 (hay powder). In all the samples, a total of 26 elements were quantified, among them 16 elements (Ca, Cd, Cl, Co, Cr, Cs, Fe, K, Mg, Mn, Na, Pb, Ru, Sc, Sr and Zn) were found in all the samples. The determined elemental concentrations in strawberry were compared with the reported values from other countries. In comparison with the mineral contents of other fruits, strawberry stands best source of Mn and the second most important source of K after banana. Intake of trace metals through this source was calculated and it was found that strawberry provides Mn (1.95-3.68 mg/kg), Cr (19.2-46.3 x 10 -3 mg/kg), Fe (3.45-8.72 mg/kg), K (1,520-1,670 mg/kg) and Mg (100-220 mg/kg), which forms 26, 19, 14, 7 and 7% of the recommended dietary allowances for the respective metals. The daily intake of Cd and Pb were compared with the provisional tolerable weekly intake defined by FAO/WHO. (author)

Comparison of Spectrophotometry, Chromate Inhibition, and Cytofluorometry Versus Gene Sequencing for Detection of Heterozygously Glucose-6-Phosphate Dehydrogenase-Deficient Females.

Science.gov (United States)

Peters, Anna L; Veldthuis, Martijn; van Leeuwen, Karin; Bossuyt, Patrick M M; Vlaar, Alexander P J; van Bruggen, Robin; de Korte, Dirk; Van Noorden, Cornelis J F; van Zwieten, Rob

2017-11-01

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme deficiency worldwide. Detection of heterozygously deficient females can be difficult as residual activity in G6PD-sufficient red blood cells (RBCs) can mask deficiency. In this study, we compared accuracy of 4 methods for detection of G6PD deficiency in females. Blood samples from females more than 3 months of age were used for spectrophotometric measurement of G6PD activity and for determination of the percentage G6PD-negative RBCs by cytofluorometry. An additional sample from females suspected to have G6PD deficiency based on the spectrophotometric G6PD activity was used for measuring chromate inhibition and sequencing of the G6PD gene. Of 165 included females, 114 were suspected to have heterozygous deficiency. From 75 females, an extra sample was obtained. In this group, mutation analysis detected 27 heterozygously deficient females. The sensitivity of spectrophotometry, cytofluorometry, and chromate inhibition was calculated to be 0.52 (confidence interval [CI]: 0.32-0.71), 0.85 (CI: 0.66-0.96), and 0.96 (CI: 0.71-1.00, respectively, and the specificity was 1.00 (CI: 0.93-1.00), 0.88 (CI: 0.75-0.95), and 0.98 (CI: 0.89-1.00), respectively. Heterozygously G6PD-deficient females with a larger percentage of G6PD-sufficient RBCs are missed by routine methods measuring total G6PD activity. However, the majority of these females can be detected with both chromate inhibition and cytofluorometry.

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

Science.gov (United States)

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.

Estimation of perimortal percent carboxy-heme in nonstandard postmortem specimens using analysis of carbon monoxide by GC/MS and iron by flame atomic absorption spectrophotometry.

Science.gov (United States)

Middleberg, R A; Easterling, D E; Zelonis, S F; Rieders, F; Rieders, M F

1993-01-01

In decomposed, formalin-fixed, embalmed, exhumed, and some fire-dried cases in which normal blood is unavailable, the usual methods for determination of carboxyhemoglobin saturation frequently fail. To address these specimens, a method utilizing both gas chromatography/mass spectrometric (GC/MS) determination of carbon monoxide (CO) and flame atomic absorption spectrophotometry (FAAS) determination of iron (Fe), in the same specimen, was developed. The method is reported here, along with its application to seven pertinent forsensic death investigations. The CO analytical methodology involves acid liberation of the gas from the specimen aliquot in a headspace vial. After heating and equilibrating, a sample of the headspace vapor is injected into the GC/MS system with a gastight syringe. Quantitation is achieved by standard addition comparison utilizing the ideal gas law equation. Iron is quantified by FAAS analysis of the same aliquot used for the CO determination, following nitric acid digestion. The concentration is determined by comparison to a standard curve. A formula for determining the minimum percent carboxy-heme saturation was derived by using the ratio of the amount of CO to the amount of Fe in the aliquot analyzed. Tissue types analyzed include spleen, liver, muscle, dried blood, and unspecified decomposed tissue.

Ionic Liquid Dispersive Liquid-Liquid Microextraction Method for the Determination of Irinotecan, an Anticancer Drug, in Water and Urine Samples Using UV-Vis Spectrophotometry.

Science.gov (United States)

Uysal, Deniz; Karadaş, Cennet; Kara, Derya

2017-05-01

A new, simple, efficient, and environmentally friendly ionic liquid dispersive liquid-liquid microextraction method was developed for the determination of irinotecan, an anticancer drug, in water and urine samples using UV-Vis spectrophotometry. The ionic liquid 1-hexyl-3-methylimidazolium hexafluorophosphate was used as the extraction solvent, and ethanol was used as the disperser solvent. The main parameters affecting the extraction efficiency, including sample pH, volume of the ionic liquid, choice of the dispersive solvent and its volume, concentration of NaCl, and extraction and centrifugation times, were investigated and optimized. The effect of interfering species on the recovery of irinotecan was also examined. Under optimal conditions, the LOD (3σ) was 48.7 μg/L without any preconcentration. Because the urine sample was diluted 10-fold, the LOD for urine would be 487 μg/L. However, this could be improved 16-fold if preconcentration using a 40 mL aliquot of the sample is used. The proposed method was successfully applied to the determination of irinotecan in tap water, river water, and urine samples spiked with 10.20 mg/L for the water samples and 8.32 mg/L for the urine sample. The average recovery values of irinotecan determined were 99.1% for tap water, 109.4% for river water, and 96.1% for urine.

Instrumental analysis

Energy Technology Data Exchange (ETDEWEB)

Kim, Seung Jae; Seo, Seong Gyu

1995-03-15

This textbook deals with instrumental analysis, which consists of nine chapters. It has Introduction of analysis chemistry, the process of analysis and types and form of the analysis, Electrochemistry on basic theory, potentiometry and conductometry, electromagnetic radiant rays and optical components on introduction and application, Ultraviolet rays and Visible spectrophotometry, Atomic absorption spectrophotometry on introduction, flame emission spectrometry and plasma emission spectrometry. The others like infrared spectrophotometry, X-rays spectrophotometry and mass spectrometry, chromatography and the other instrumental analysis like radiochemistry.

Instrumental analysis

International Nuclear Information System (INIS)

Kim, Seung Jae; Seo, Seong Gyu

1995-03-01

This textbook deals with instrumental analysis, which consists of nine chapters. It has Introduction of analysis chemistry, the process of analysis and types and form of the analysis, Electrochemistry on basic theory, potentiometry and conductometry, electromagnetic radiant rays and optical components on introduction and application, Ultraviolet rays and Visible spectrophotometry, Atomic absorption spectrophotometry on introduction, flame emission spectrometry and plasma emission spectrometry. The others like infrared spectrophotometry, X-rays spectrophotometry and mass spectrometry, chromatography and the other instrumental analysis like radiochemistry.

Outcomes of CSF spectrophotometry in cases of suspected subarachnoid haemorrhage with negative CT: two years retrospective review in a Birmingham hospital.

Science.gov (United States)

Bakr, A; Silva, D; Cramb, R; Flint, G; Foroughi, M

2017-04-01

The aim of this study was to evaluate the adherence to current guidelines for the investigation of suspected subarachnoid haemorrhage and the prevalence and outcome of computed tomography (CT)-negative aneurysmal subarachnoid haemorrhage. A retrospective review in a single large tertiary referral centre. A total of 796 patients, aged 16-90 years, who underwent lumbar puncture (LP) for suspected subarachnoid haemorrhage (SAH) following a negative or equivocal CT scan between January 2012 and November 2013 (23 months). Xanthochromia reports were obtained using the hospital's department of biochemistry database and clinical data for these patients were reviewed using patient notes. Of 796 CSF reports reviewed, 728 (91%) were negative for xanthochromia, 31 (4%) were positive and 37 (5%) were equivocal. Only 2 out of the 31 patients with positive spectrophotometry results were subsequently found to have an underlying aneurysm on CT angiography. A further 9 out of these 31 patients underwent digital subtraction angiography, with no cerebral aneurysms being detected. Amongst the 37 patients with equivocal xanthochromia reports, 13 underwent CT angiography and only 1 cerebral aneurysm was detected. In patients with clinically suspected SAH but who have negative or questionable CT findings, CSF analysis is likely to be negative in the vast majority of cases, which was 91% in our series. In patients yielding positive or equivocal CSF results the likelihood of an aneurysm being detected is low, amounting to three out of 68 or approximately one in 23 (approximately 4%). Overall in suspected SAH cases where CT scan has been negative, the rate for the detection of cerebral aneurysm is three out of 796 cases (0.4%).

Spectrophotometry of four H II regions in the Perseus arm and a reassessment of galactic abundance gradients

International Nuclear Information System (INIS)

Talent, D.L.; Dufour, R.J.

1979-01-01

The results from deep spectrophotometry of four Perseus arm H II regions (NGC 1624, NGC 2359, NGC 7538, and NGC 7635) obtained with the KPNO IIDS are presented. The observed line strengths are used to derive electron temperatures, densities, and the relative concentrations of H, He, N, O, S, Cl, and Ar in the nebulae. These abundances are combined with similarly derived abundances for seven other well-observed galactic H II regions, and are used to estimate the magnitude of galactic abundance gradients over the 8--14 kpc region of the solar neighborhood.Significant radial gradients for oxygen and nitrogen are found: d log (O/H)/dR=-0.059 +- 0.017 kpc -1 and d log (N/H)/dR= -0.083 +- 0.018 kpc -1 , while only marginal evidence for a helium gradient is found: d log (He/H)/dR=-0.008 +- 0.008 kpc -1 . Little evidence for gradient in S/H is found. From the red [N II] and [S II] lines we found d log (N + /S + )/dR=-0.068 +- 0.024 kpc -1 , which suggests that a radial gradient in S/O exists in the Galaxy. The O/H gradient found in this study is similar to that found from planetary nebulae, while the N/H gradient is significantly smaller. These results suggest that most of the nitrogen in the interstellar medium of the Galaxy was produced by primary nucleosynthesis processes.We also find evidence that the radial O/H and N/H gradients for H II regions in a given spiral arm are 2 to 3 times steeper than the global gradients over the 8--14 kpc interval in galactocentric distance. For four H II regions in the Sagittarius arm we found d log (O/H)/dR=-0.24 kpc -1 and d log (N/H)/dR=-0.16 kpc -1 . For five H II regions in the Perseus arm we found d log (O/H)/dR=-0.18 kpc -1 and d log (N/H)/dR=-0.15 kpc -1 . The larger magnitudes of these gradients are greater than those of the global gradients by amounts which exceed reasonable errors in abundances and/or relative distances

Spectrophotometry of peculiar B and A stars. I. On the detection of the lambda4200 and lambda5200 broad, continuum features of peculiar A stars

International Nuclear Information System (INIS)

Adelman, S.J.

1979-01-01

Photometric indices are used to study the broad, continuum features that are present in the energy distributions of many peculiar A stars and that may be indicators of the atmospheric structure. Values of Maitzen's Δa index, which is a measure of the lambda5200 feature, are synthesized from spectrophotometric data to examine the properties of this photometric system as well as to establish a preliminary criterion of presence for the feature. Many Ap stars definitely exhibit this feature, which normal main sequence stars lack. Two indices Δiota and Δiota* are calculated from spectrophotometry to measure the strength of the lambda4200 feature. About 90% of the Ap stars are found to have definite positive results based on the preliminary criterion of presence of the latter index. For the Ap stars there is a general tendency for Δa to increase with Δiota and Δiota*. This most likely reflects the tendency for most abundances to increase together in the Ap stars. The HgMn stars have systematically larger Δiota* and Δa values than the normal stars. This does not necessarily mean that they have the lambda4200 and lambda5200 features of the peculiar A stars. To study this question requires careful comparison of the energy distributions of the HgMn stars with those of other stars and with the predictions of model atmospheres

Development and validation of alternative methods by non-aqueous acid-base titration and derivative ultraviolet spectrophotometry for quantification of sildenafil in raw material and tablets

Directory of Open Access Journals (Sweden)

Taízia Dutra Silva

2017-04-01

Full Text Available Sildenafil citrate (SILC is a potent phosphodiesterase-5 inhibitor used for erectile dysfunction and pulmonary hypertension. This study shows two simple, fast and alternative analytical methods for SILC determination by non-aqueous titration and by derivative ultraviolet spectrophotometry (DUS in active pharmaceutical ingredient and/or dosage forms. The quantitation method of SILC active pharmaceutical ingredient by non-aqueous acid-base titration was developed using methanol as solvent and 0.1 mol/L of perchloric acid in acetic acid as titrant. The endpoint was potentiometrically detected. The non-aqueous titration method shows satisfactory repeatability and intermediate precision (RSD 0.70-1.09%. The neutralization reaction occurred in the stoichiometric ratio 1:1 in methanol. The determination of SILC active pharmaceutical ingredient or dosage forms by DUS was developed in the linear range from 10 to 40 µg/mL, in 0.01 mol/L HCl, using the first order zero-peak method at λ 256 nm. The DUS method shows selectivity toward tablets excipients, appropriate linearity (R2 0.9996, trueness (recovery range 98.86-99.30%, repeatability and intermediate precision in three concentration levels (RSD 1.17-1.28%; 1.29-1.71%, respectively. Therefore, the methods developed are excellent alternatives to sophisticated instrumental methods and can be easily applied in any pharmaceutical laboratory routine due to simple and fast executions.

Un método de bajo costo para la determinación de cobre a nivel de vestigios en matrices de interés ambiental por espectrofotometría en fase sólida (EFS) A low-cost procedure for copper determination in natural waters and plant materials exploiting solid phase spectrophotometry

OpenAIRE

Roberto Gerardo Pellerano; Cesar Hamilton Romero; Hugo Arnoldo Acevedo; Francisco Antonio Vazquez

2007-01-01

A method for determining copper by solid phase spectrophotometry (SPS) was optimized using the Doehlert design. Copper(II) was sorbed on a styrene-divinylbenzene anion-exchange resin as a Cu(II)-1-(2-pyridylazo)-2-naphthol (PAN) complex, at pH 7.0. Resin phase absorbances at 560 and 800 nm were measured directly. The detection limit was found to be 2.5 µg L-1. The relative standard deviation on ten replicate determinations of 10 µg Cu(II) in 1000 mL samples was 1.1%. The linear range of the d...

Effect of electrostatic interaction between fluoxetine and lipid membranes on the partitioning of fluoxetine investigated using second derivative spectrophotometry and FTIR.

Science.gov (United States)

Do, Tien T T; Dao, Uyen P N; Bui, Huong T; Nguyen, Trang T

2017-10-01

The interaction between a drug molecule and lipid bilayers is highly important regarding the pharmaceutical activity of the drug. In this study, the interaction of fluoxetine, a well-known selective serotonin reuptake inhibitor antidepressant and lipid bilayers composed of 1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (DPPG) and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) was studied from the aspect of electrostatics using second derivative spectrophotometry and Fourier transform infrared spectroscopy (FTIR) in order to provide insights into the drug behavior. Changing pH from 7.4 to 9.5 to increases the neutral state of fluoxetine, the partitioning of fluoxetine into the zwitterionic DPPC large unilamellar vesicles (LUVs) was increased whereas it was reduced into the negatively charged DPPG LUVs. Fluoxetine was found to exhibit a disordering effect on the acyl chains of DPPC and DPPG bilayers upon its partitioning. In addition, increasing concentration of NaCl lessened the binding of fluoxetine into DPPG bilayers due to the reduction in electrostatic attraction between positively charged fluoxetine and negatively charged DPPG LUVs. In addition, the FTIR study revealed that increasing the NaCl concentration could trigger the shift to higher frequency of the CH 2 stretching as well as the notable blue shift in the PO 2 - regions of DPPG, indicating that fluoxetine had deeper penetration into DPPG LUVs. The differences in the NaCl concentration showed a negligible effect on the incorporation of fluoxetine into the zwitterionic DPPC LUVs. In summary, the electrostatic interaction plays an important role on the partitioning of a cationic amphiphilic SSIR drug into the lipid bilayers and the drug partitioning induces the lipids' conformational change. These imply a possible influence on the drug pharmacology. Copyright © 2017 Elsevier B.V. All rights reserved.

Study on interference of technetium in spectrophotometric estimation of uranium

International Nuclear Information System (INIS)

Revathi, P.; Saipriya, K.; Madhavan Kutty, V.K.; Srinivasa Rao, G.; Vijayakumar, N.; Kumar, T.

2015-01-01

Estimation of uranium is essential for process control purposes as well as to arrive optimum parameters for further waste management in reprocessing industry. Uranium estimation is done by spectrophotometry using ammonium thiocyanate, DBM, PAR and Br-PADAP as chromogenic reagents for colour development. Extractive spectrophotometry can also be used to eliminate some of the interfering ions. During inter method comparison, technetium was found to be interfering in the thiocyanate spectrophotometry. This study is an effort to find out the extent of technetium interference in the estimation of uranium by spectrophotometry using the above said chromogenic reagents. (author)

Enhanced Sensitivity to Detection Nanomolar Level of Cu2 + Compared to Spectrophotometry Method by Functionalized Gold Nanoparticles: Design of Sensor Assisted by Exploiting First-order Data with Chemometrics

Science.gov (United States)

Rasouli, Zolaikha; Ghavami, Raouf

2018-02-01

A simple, sensitive and efficient colorimetric assay platform for the determination of Cu2 + was proposed with the aim of developing sensitive detection based on the aggregation of AuNPs in presence of a histamine H2-receptor antagonist (famotidine, FAM) as recognition site. This study is the first to demonstrate that the molar extinction coefficients of the complexes formed by FAM and Cu2 + are very low (by analyzing the chemometrics methods on the first order data arising from different metal to ligand ratio method), leading to the undesirable sensitivity of FAM-based assays. To resolve the problem of low sensitivity, the colorimetry method based on the Cu2 +-induced aggregation of AuNPs functionalized with FAM was introduced. This procedure is accompanied by a color change from bright red to blue which can be observed with the naked eyes. Detection sensitivity obtained by the developed method increased about 100 fold compared with the spectrophotometry method. This sensor exhibited a good linear relation between the absorbance ratios at 670 to 520 nm (A670/520) and the concentration in the range 2-110 nM with LOD = 0.76 nM. The satisfactory analytical performance of the proposed sensor facilitates the development of simple and affordable UV-Vis chemosensors for environmental applications.

Determination of plutonium in highly radioactive liquid waste by spectrophotometry using neodymium as an internal standard for safeguards analysis. Japan support program for agency safeguards (JASPAS) JC-19

International Nuclear Information System (INIS)

Taguchi, Shigeo; Surugaya, Naoki; Sato, Soichi; Kurosawa, Akira; Watahiki, Masaru; Hiyama, Toshiaki

2006-06-01

A spectrophotometric determination using neodymium as an internal standard was developed for safeguards verification analysis of plutonium in highly radioactive liquid waste which is produced by the reprocessing of spent nuclear fuel. The internal standard is used as a means to analyze plutonium and also to authenticate the instrument conditions. The method offers reduced sample preparation and analysis time compared to isotope dilution mass spectrometry. The sample was mixed with a known amount of internal standard. Subsequently, plutonium was quantitatively oxidized to Pu(VI) by the addition of Ce(IV) for spectrophotometry. Plutonium concentration was calculated from a relation between Nd(III)/Pu(VI) molar extinction coefficient ratio and their absorbance ratio. The relative expanded uncertainty of the repeated analysis (n=5) was 8.9% (coverage factor k=2) for a highly radioactive liquid waste sample (173 mg L -1 ). The determination limit was 6 mg L -1 (ten fold's the standard deviation). This method was validated through comparison experiments with isotope dilution mass spectrometry. The analytical results of plutonium in highly radioactive liquid waste using this method were agree well with values obtained using isotope dilution mass spectrometry. The proposed method can be applied to independent on-site safeguards analysis at the Tokai Reprocessing Plant. (author)

High-Sensitivity Spectrophotometry.

Science.gov (United States)

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.…

Enamel Mineral Content Changes After Bleaching With High and Low Hydrogen Peroxide Concentrations: Colorimetric Spectrophotometry and Total Reflection X-ray Fluorescence Analyses.

Science.gov (United States)

Pinto, Avd; Bridi, E C; Amaral, Flb; França, Fmg; Turssi, C P; Pérez, C A; Martinez, E F; Flório, F M; Basting, R T

The purpose of this study was to evaluate the calcium (Ca) and phosphorous (P) content in enamel bleached with high and low concentrations of hydrogen peroxide (HP) using Total Reflection X-Ray Fluorescence (TXRF) and colorimetric spectrophotometry (SPEC). Forty-eight sound human third molars were used. Their roots were embedded in polystyrene resin and immersed for seven days in an artificial saliva solution. Then they were distributed into six groups to receive the bleaching treatments. The agents of high HP concentration (for in-office use) evaluated were Whiteness HP Maxx/FGM (35% HP), Whiteness HP Blue/FGM (35% HP, 2% calcium gluconate), Pola Office+/SDI (37.5% HP, 5% potassium nitrate), and Opalescence Boost/Ultradent (38% HP, 1.1% ion fluoride, 3% potassium nitrate); these agents were applied to enamel in three sessions. The agents of low HP concentration (for home use) evaluated were Pola Day/SDI (9.5% HP) and White Class 10%/FGM (10% HP, potassium nitrate, calcium, fluoride), and these agents were applied for 14 days. Enamel microbiopsies were evaluated by TXRF and SPEC analysis before the bleaching treatment (baseline), during the treatment, and 14 days after the end of the treatment. For TXRF, the Kruskal-Wallis test showed that Ca and P were not influenced by agent (p>0.05). For SPEC, Pola Office+, Opalescence Boost, Pola Day, and White Class 10% caused a decrease of Ca over time; there was a significant decrease of P over time to Pola Office+ and White Class 10%. The Spearman test showed no correlation between the Ca (p=0.987; r 2 =-0.020) and P (p=0.728, r 2 =0.038) obtained by SPEC and TXRF. For TXRF and SPEC, changes in Ca and P during bleaching occurred independently of the HP concentration used.

Determination of Lead and Cadmium in environment materials from the planned area for a nuclear power plant by atomic absorption spectrophotometry method

International Nuclear Information System (INIS)

Supriyanto, C; Djokowidodo; Isyuniarto; Heri-Wahyudi; Ashar-Andrianto

1996-01-01

The determination of Pb and Cd in environment materials (water, cassava leaves and soil) have been done by atomic absorption spectrophotometry method, The determination of Pb and Cd was done with graphite tube atomizer (GTA) method at optimum condition : wavelength for Pb and Cd 217.0 nm and 228.8 nm; temperature/time ashing 550 o C/37 sec and 350 o C/52 sec; temperature/time atomizing 2000 o C/5.1 sec and 2000 o C/5.2 sec. Modifier for Pb was 3 μL of Mg 1000 μg/ml and Cd was 2 μL of Pd 2000 μg/ml. The content Pb in Spalun river, Hulu Putih river and sea water Lemah Abang was 0.94 ± 0.03; 0.91± 0.02; 4.71 ± 0.26 ng/ml respectively; the Cd content was 1.23 ± 0.11; 0.48 ± 0.01; 0.55 ± 0.01 ng/ml respectively. The Pb dan Cd content in cassava leaves was 163.24 ± 3.72 and 18.45 ± 1.46 ng/g respectively, while the Pb content in soil at the depth variation 0 - 5, 5 - 10, 10 - 20 and 20 - 30 Cm was 2.35 ± 0.15; 2.86 ± 0.16; 1.97 ± 0.11 and 2.19 ± 0.06 μg/g respectively and the Cd content was 43.67 ± 1.52; 37.01 ± 1.01; 31.68 ± 0.17 and 36.97 ± 1.63 ng/g respectively. SRM Citrous leaves from NSB and SRM Soil 7 from the IAEA local used to control the quality of the analyzed method. The Pb, Cd content in SRM was in accordance with the value in the certified legend

Application of experimental design and derivative spectrophotometry methods in optimization and analysis of biosorption of binary mixtures of basic dyes from aqueous solutions.

Science.gov (United States)

Asfaram, Arash; Ghaedi, Mehrorang; Ghezelbash, Gholam Reza; Pepe, Francesco

2017-05-01

Simultaneous biosorption of malachite green (MG) and crystal violet (CV) on biosorbent Yarrowia lipolytica ISF7 was studied. An appropriate derivative spectrophotometry technique was used to evaluate the concentration of each dye in binary solutions, despite significant interferences in visible light absorbances. The effects of pH, temperature, growth time, initial MG and CV concentration in batch experiments were assessed using Design of Experiment (DOE) according to central composite second order response surface methodology (RSM). The analysis showed that the greatest biosorption efficiency (>99% for both dyes) can be obtained at pH 7.0, T=28°C, 24h mixing and 20mgL -1 initial concentrations for both MG and CV dyes. The quadratic constructed equation ability for fitting experimental data is judged based on criterions like R 2 values, significant p and lack-of-fit value strongly confirm its high adequacy and applicability for prediction of revel behavior of the system under study. The proposed model showed very high correlation coefficients (R 2 =0.9997 for CV and R 2 =0.9989 for MG), while supported by closeness of predicted and experimental value. A kinetic analysis was carried out, showing that for both dyes a pseudo-second order kinetic model adequately describes the available data. The Langmuir isotherm model in single and binary components has better performance for description of dyes biosorption with maximum monolayer biosorption capacity of 59.4 and 62.7mgg -1 in single component and 46.4 and 50.0mgg -1 for CV and MB in binary components, respectively. The surface structure of biosorbents and the possible biosorbents-dyes interactions between were also evaluated by Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM). The values of thermodynamic parameters including ΔG° and ΔH° strongly confirm which method is spontaneous and endothermic. Copyright © 2017. Published by Elsevier Inc.

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

Energy Technology Data Exchange (ETDEWEB)

Zheng, Jinjian, E-mail: jinjian.zheng@merck.com; Tan, Feng; Hartman, Robert

2015-09-03

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

Combination of sawdust from teak wood and rice husk activated carbon as adsorbent of Pb(II) ion and its analysis using solid-phase spectrophotometry (sps)

Science.gov (United States)

Saputro, S.; Mahardiani, L.; Wulandari, D. A.

2018-03-01

This research aimed to know the usage of sawdust of teak wood and rice husk waste as Pb (II) ion adsorbents in simulated liquid waste, the combined optimum mass required adsorbent to adsorb Pb(II) ion, the sensitivity of the solid-phase spectrophotometry (sps) method in determining the decrease of Pb (II) metal ion levels in the μg/L level. This research was conducted by experimental method in laboratory. Adsorbents used in this study were charcoal of sawdust sawdust activated using 15% ZnCl2 solution and activated rice husk using 2 N NaOH solution. The adsorption processes of sawdust and rice husk with Pb(II) solution was done by variation of mass combination with a ratio of 1: 0; 0: 1; 1: 1; 1: 2; and 2: 1. Analysis of Pb(II) ion concentration using SPS and characterization of sawdust and rice husk adsorbent ads using FTIR. The results showed that activated charcoal from sawdust of teak wood and rice husks can be used as Pb (II) metal ion adsorbents with adsorption capacity of 0.86 μg/L, charcoal from sawdust of teak wood and rice husk adsorbent with a combination of optimum mass contact of sawdust and rice husk is 2:1 as much as 3 grams can adsorb 42.80 μg/L. Solid-phase spectophotometry is a sensitive method for analysis of concentration decreasing levels of Pb(II) ion, after it was absorbed by sawdust of teak wood and rice husk with high sensitivity and has the limit of detection (LOD) of 0.06 μg/L.

Evaluation of phenolic content, total flavonoid and survey of antioxidant activity of leaves of Ficus carica and Pterocarya fraxinifolia trees using spectrophotometry and high performance liquid chromatograph methods

Directory of Open Access Journals (Sweden)

Naser Jafari

2015-09-01

Full Text Available In this research, to evaluate the antioxidant activity of leaf Pterocarya fraxinifolia (Juglandaceae and Ficus carica (Moraceae extract were carried out by spectrophotometry and high performance liquid chromatography methods. The leaves of P. fraxinifolia and F. carica were collected from Whitney and Shast Kalate (Golestan, Noor (Mazandaran and Asalem (Guilan forests in Iran. Methanolc extract was used in different experiments. The phenolic compounds (gallic acid, coumaric acid and quercetin were also measured by using high performance liquid chromatography (HPLC method.The maximum IC50 for DPPH radical-scavenging activity (595.12±21.4 μg ml-1 were observed in P. fraxinifolia leaves. According to the inhibition time, phenolic compound (gallic acid, coumaric acid and quercetin in F. carica leaves and gallic acid and coumaric acid were detected of Pterocarya leaves methanol extracts. The maximum amount of gallic acid (78.93 and coumaric acid (8.14 in extracts Pterocarya leaves Asalem and the lowest gallic acid (8.56 and coumaric acid (0.89 milligrams per gram was observed in Ficus leaf of Noor forest. Based on the standard chromatogram retention time of gallic acid (2.383, coumaric acid (3.817 and quercetin (7.217 mg/g was reported. This study showed that soil factors, such as potassium, sodium, phosphorus and nitrogen compounds with antioxidant phenolic extracts of the leaves of both plants there is a significant correlation.

Ionic liquid-based single-drop microextraction followed by liquid chromatography-ultraviolet spectrophotometry detection to determine typical UV filters in surface water samples.

Science.gov (United States)

Vidal, Lorena; Chisvert, Alberto; Canals, Antonio; Salvador, Amparo

2010-04-15

A user-friendly and inexpensive ionic liquid-based single-drop microextraction (IL-SDME) procedure has been developed to preconcentrate trace amounts of six typical UV filters extensively used in cosmetic products (i.e., 2-hydroxy-4-methoxybenzophenone, isoamyl 4-methoxycinnamate, 3-(4'-methylbenzylidene)camphor, 2-ethylhexyl 2-cyano-3,3-diphenylacrylate, 2-ethylhexyl 4-dimethylaminobenzoate and 2-ethylhexyl 4-methoxycinnamate) from surface water samples prior to analysis by liquid chromatography-ultraviolet spectrophotometry detection (LC-UV). A two-stage multivariate optimization approach was developed by means of a Plackett-Burman design for screening and selecting the significant variables involved in the SDME procedure, which were later optimized by means of a circumscribed central composite design. The studied variables were drop volume, sample volume, agitation speed, ionic strength, extraction time and ethanol quantity. Owing to particularities, ionic liquid type and pH of the sample were optimized separately. Under optimized experimental conditions (i.e., 10 microL of 1-hexyl-3-methylimidazolium hexafluorophosphate, 20 mL of sample containing 1% (v/v) ethanol and NaCl free adjusted to pH 2, 37 min extraction time and 1300 rpm agitation speed) enrichment factors up to ca. 100-fold were obtained depending on the target analyte. The method gave good levels of repeatability with relative standard deviations varying between 2.8 and 8.8% (n=6). Limits of detection were found in the low microg L(-1) range, varying between 0.06 and 3.0 microg L(-1) depending on the target analyte. Recovery studies from different types of surface water samples collected during the winter period, which were analysed and confirmed free of all target analytes, ranged between 92 and 115%, showing that the matrix had a negligible effect upon extraction. Finally, the proposed method was applied to the analysis of different water samples (taken from two beaches, two swimming pools and a

Functionalization of biosynthesized gold nanoparticle from aqueous ...

African Journals Online (AJOL)

The biosynthesized nanoparticles and formulated nanodrug were characterized using UV-Vis spectrophotometry, Zetasizer, Scanning and transmission Electron Microscopy (SEM; TEM), Energy Dispersive spectrophotometry (EDAX) and Fourier Transform Infra-red Spectroscopy. Polyethylene glycol and Lincomycin were ...

The synthesis of corncobs (zea mays) active charcoal and water hyacinth (eichornia crassipes) adsorbent to adsorb Pb(II) with it’s analysis using solid-phase spectrophotometry (sps)

Science.gov (United States)

Saputro, S.; Masykuri, M.; Mahardiani, L.; Kurniastuti, D.

2018-03-01

This research aim to examine the effect of the combination between corncobs and water hyacinth to adsorb lead (II), the most effective combination have determined by compared the ratio of corncobs adsorbent and water hyacinth to the increasing adsorption of the Pb(II), prove the effectiveness of the solid-phase spectrophotometry (sps) to determine the levels of Pb(II) as the result of the corncobs active charcoal adsorption and water hyacinth in the level of µg/L. The research method used is experimental method. The data collecting technique is carried out by several stages, which are carbonization using muffle furnace at a temperature of 350°C for 1.5 hours, activation of the corncobs charcoal and water hyacinth using HCl 1M and HCl 5M activator, contacting the adsorbent of corncobs active charcoal and water hyacinth with liquid waste simulation of Pb(II) using variation of corncobns and water hyacinth, 1:0; 0:1; 1:1; 2:1; 1:2, analysis of Pb(II) using an sps, characterization of corncobs active charcoal adsorbent and water hyacinth using FTIR. Research results show that the combined effect of activated charcoal corncobs and water hyacinth can increase the ability of the adsorbent to absorb Pb(II), the optimum adsorbent mass ratio of 1:1 with the absorption level of 90.33%, SPS is an effective method to analyze the decreasing level of Pb(II) as the adsorbtion result of the corncobs active charcoal and water hyacinth in the level of µg/L, with the limit of detection (LOD) of 0.06 µg/L.

Spectrophotometry of carbon stars

International Nuclear Information System (INIS)

Gow, C.E.

1975-01-01

Observations of over one hundred carbon stars have been made with the Indiana rapid spectral scanner in the red and, when possible, in the visual and blue regions of the spectrum. Five distinct subtypes of carbon stars (Barium, CH, R, N, and hydrogen deficient) are represented in the list of observed stars, although the emphasis was placed on the N stars when the observations were made. The rapid scanner was operated in the continuous sweep mode with the exit slit set at twenty angstroms, however, seeing fluctuations and guiding errors smear the spectrum to an effective resolution of approximately thirty angstroms. Nightly observations of Hayes standard stars yielded corrections for atmospheric extinction and instrumental response. The reduction scheme rests on two assumptions, that thin clouds are gray absorbers and the wavelength dependence of the sky transparency does not change during the course of the night. Several stars have been observed in the blue region of the spectrum with the Indiana SIT vidicon spectrometer at two angstroms resolution. It is possible to derive a color temperature for the yellow--red spectral region by fitting a black-body curve through two chosen continuum points. Photometric indices were calculated relative to the blackbody curve to measure the C 2 Swan band strength, the shape of the CN red (6,1) band to provide a measure of the 12 C/ 13 C isotope ratio, and in the hot carbon stars (Barium, CH, and R stars) the strength of an unidentified feature centered at 400 angstroms. An extensive abundance grid of model atmospheres was calculated using a modified version of the computer code ATLAS

Spectrophotometry of carbon stars

Energy Technology Data Exchange (ETDEWEB)

Oganesyan, R.K.; Karapetyan, M.S.; Nersisyan, S.E.

1986-01-01

The results are given of the spectrophotometric investigation of 56 carbon stars in the spectral range from 4000 to 6800 A with resolution 3 A. The observed energy distributions of these stars are determined relative to the flux at the wavelength /sub 0/ = 5556; they are presented in the form of graphs. The energy distributions have been obtained for the first time for 35 stars. Variation in the line Ba II 4554 A has been found in the spectra of St Cam, UU Aur, and RV Mon. Large changes have taken place in the spectra of RT UMa and SS Vir. It is noted that the spectra of carbon stars have a depression, this being situated in different spectral regions for individual groups of stars.

Combined Laser-Doppler Flowmetry and Spectrophotometry: Feasibility Study of a Novel Device for Monitoring Local Cortical Microcirculation during Aneurysm Surgery.

Science.gov (United States)

Sommer, Björn; Kreuzer, Maximilian; Bischoff, Barbara; Wolf, Dennis; Schmitt, Hubert; Eyupoglu, Ilker Y; Rössler, Karl; Buchfelder, Michael; Ganslandt, Oliver; Wiendieck, Kurt

2017-01-01

Background  Monitoring of cortical cerebral perfusion is essential, especially in neurovascular surgery. Study Aims  To test a novel noninvasive laser-Doppler flowmetry and spectrophotometry device for feasibility during elective cerebral aneurysm surgery. Material and Methods  In this prospective single-institution nonrandomized trial, we studied local cerebral microcirculation using the noninvasive laser-Doppler spectrophotometer "Oxygen-to-see" (O2C) in 20 consecutive patients (15 female, 5 male; median age: 60.5 ± 11.7 years) who were operated on for incidental cerebral aneurysms. Capillary-venous oxygenation (oxygen saturation ["SO 2 "]), postcapillary venous filling pressures (relative hemoglobin content ["rHb"]), blood cell velocity ("velo"), and blood flow ("flow") were measured in 7-mm tissue depth using a subdural fiberoptic probe. Results  Representative recordings were acquired immediately after dural opening over a median time span of 88 ± 21.8 seconds (range: 60-128 seconds) before surgical manipulation. Baseline values (median ± 2 standard deviations) of brain perfusion as measured with the O2C device were SO 2 , 39 ± 16.6%; rHb, 53 ± 18.6 arbitrary units (AU); velo, 60 ± 20.4 AU; and flow, 311 ± 72.8 AU. Placement of the self-retaining retractor led to a decrease in SO 2 of 17% ± 29% ( p  < .05) and flow of 10% ± 11% ( p  < .01); rHb increased by 18% ± 20% ( p  < .01), and velo remained unchanged. Retractor removal caused the opposite with an increased flow of 10% ± 7% ( p  < 0.001) and velo (3% ± 6%, p  = 0.11), but a decrease in SO 2 of 24% ± 33% ( p  = 0.09) and rHb of 12% ± 20% ( p =0.18). No neurologic or surgical complications occurred. Conclusion  Using this novel noninvasive system, we were able to measure local cerebral microcirculation during aneurysm surgery. Our data indicate that this device is able to detect changes during routine

Feasibility of Using Fluorescence Spectrophotometry to Develop a Sensitive Dye Immersion Method for Container Closure Integrity Testing of Prefilled Syringes.

Science.gov (United States)

Lu, Xujin; Lloyd, David K; Klohr, Steven E

2016-01-01

A feasibility study was conducted for a sensitive and robust dye immersion method for the measurement of container closure integrity of unopened prefilled syringes using fluorescence spectrophotometry as the detection method. A Varian Cary Eclipse spectrofluorometer was used with a custom-made sample holder to position the intact syringe in the sample compartment for fluorescence measurements. Methylene blue solution was initially evaluated as the fluorophore in a syringe with excitation at 607 nm and emission at 682 nm, which generated a limit of detection of 0.05 μg/mL. Further studies were conducted using rhodamine 123, a dye with stronger fluorescence. Using 480 nm excitation and 525 nm emission, the dye in the syringe could be easily detected at levels as low as 0.001 μg/mL. The relative standard deviation for 10 measurements of a sample of 0.005 μg/mL (with repositioning of the syringe after each measurement) was less than 1.1%. A number of operational parameters were optimized, including the photomultiplier tube voltage, excitation, and emission slit widths. The specificity of the testing was challenged by using marketed drug products and a protein sample, which showed no interference to the rhodamine detection. Results obtained from this study demonstrated that using rhodamine 123 for container closure integrity testing with in-situ (in-syringe) fluorescence measurements significantly enhanced the sensitivity and robustness of the testing and effectively overcame limitations of the traditional methylene blue method with visual or UV-visible absorption detection. Ensuring container closure integrity of injectable pharmaceutical products is necessary to maintain quality throughout the shelf life of a sterile drug product. Container closure integrity testing has routinely been used to evaluate closure integrity during product development and production line qualification of prefilled syringes, vials, and devices. However, container closure integrity testing

Analyses of polycyclic aromatic hydrocarbon (PAH) and chiral-PAH analogues-methyl-β-cyclodextrin guest-host inclusion complexes by fluorescence spectrophotometry and multivariate regression analysis.

Science.gov (United States)

Greene, LaVana; Elzey, Brianda; Franklin, Mariah; Fakayode, Sayo O

2017-03-05

The negative health impact of polycyclic aromatic hydrocarbons (PAHs) and differences in pharmacological activity of enantiomers of chiral molecules in humans highlights the need for analysis of PAHs and their chiral analogue molecules in humans. Herein, the first use of cyclodextrin guest-host inclusion complexation, fluorescence spectrophotometry, and chemometric approach to PAH (anthracene) and chiral-PAH analogue derivatives (1-(9-anthryl)-2,2,2-triflouroethanol (TFE)) analyses are reported. The binding constants (K b ), stoichiometry (n), and thermodynamic properties (Gibbs free energy (ΔG), enthalpy (ΔH), and entropy (ΔS)) of anthracene and enantiomers of TFE-methyl-β-cyclodextrin (Me-β-CD) guest-host complexes were also determined. Chemometric partial-least-square (PLS) regression analysis of emission spectra data of Me-β-CD-guest-host inclusion complexes was used for the determination of anthracene and TFE enantiomer concentrations in Me-β-CD-guest-host inclusion complex samples. The values of calculated K b and negative ΔG suggest the thermodynamic favorability of anthracene-Me-β-CD and enantiomeric of TFE-Me-β-CD inclusion complexation reactions. However, anthracene-Me-β-CD and enantiomer TFE-Me-β-CD inclusion complexations showed notable differences in the binding affinity behaviors and thermodynamic properties. The PLS regression analysis resulted in square-correlation-coefficients of 0.997530 or better and a low LOD of 3.81×10 -7 M for anthracene and 3.48×10 -8 M for TFE enantiomers at physiological conditions. Most importantly, PLS regression accurately determined the anthracene and TFE enantiomer concentrations with an average low error of 2.31% for anthracene, 4.44% for R-TFE and 3.60% for S-TFE. The results of the study are highly significant because of its high sensitivity and accuracy for analysis of PAH and chiral PAH analogue derivatives without the need of an expensive chiral column, enantiomeric resolution, or use of a polarized

Validation of quantitative analysis method for triamcinolone in ternary complexes by UV-Vis spectrophotometry

Directory of Open Access Journals (Sweden)

GEORGE DARLOS A. AQUINO

2011-06-01

Full Text Available Triamcinolone (TRI, a drug widely used in the treatment of ocular inflammatory diseases, is practically insoluble in water, which limits its use in eye drops. Cyclodextrins (CDs have been used to increase the solubility or dissolution rate of drugs. The purpose of the present study was to validate a UV-Vis spectrophotometric method for quantitative analysis of TRI in inclusion complexes with beta-cyclodextrin (B-CD associated with triethanolamine (TEA (ternary complex. The proposed analytical method was validated with respect to the parameters established by the Brazilian regulatory National Agency of Sanitary Monitoring (ANVISA. The analytical measurements of absorbance were made at 242nm, at room temperature, in a 1-cm path-length cuvette. The precision and accuracy studies were performed at five concentration levels (4, 8, 12, 18 and 20μg.mL-1. The B-CD associated with TEA did not provoke any alteration in the photochemical behavior of TRI. The results for the measured analytical parameters showed the success of the method. The standard curve was linear (r2 > 0.999 in the concentration range from 2 to 24 μg.mL-1. The method achieved good precision levels in the inter-day (relative standard deviation-RSD <3.4% and reproducibility (RSD <3.8% tests. The accuracy was about 80% and the pH changes introduced in the robustness study did not reveal any relevant interference at any of the studied concentrations. The experimental results demonstrate a simple, rapid and affordable UV-Vis spectrophotometric method that could be applied to the quantitation of TRI in this ternary complex. Keywords: Validation. Triamcinolone. Beta-cyclodextrin. UV- Vis spectrophotometry. Ternary complexes. RESUMO Validação de método de análise quantitativa para a triancinolona a partir de complexo ternário por espectrofotometria de UV-Vis A triancinolona (TRI é um fármaco amplamente utilizado no tratamento de doenças inflamatórias do globo ocular e �

Sugar dosimeters. Part 1. State of the art

International Nuclear Information System (INIS)

Peimel-Stuglik, Z.

2008-01-01

A review of the literature dealing with the possibility of using sugars, in particular sucrose, as dosimetric material is presented. All methods involved were divided according to analytical techniques used in dosimetric signal measurements (polarimetry, spectrophotometry and electron paramagnetic resonance - EPR). Double-signal sugar dosimeters (EPR + spectrophotometry) are also described. (author) [pl

Studies on the reaction of salicylidenebenzoic-hydrazide (SBH) with Ce3+, Th4+ and UO22+

International Nuclear Information System (INIS)

Issa, I.M.; Temerk, Y.M.; Abu Zhuri, A.Z.; El-Meligy, M.S.; Kamal, M.M.

1980-01-01

The stoichiometry and structure of salicylidenebenzoic-hydrazine (SBH) chelates with UO 2 (II), Ce(III) and Th(IV) in buffer-ethanol mixtures and in pure ethanol is studied applying conductometric titration, visible spectrophotometry and ir-spectrophotometry. The ir-spectra revealed that coordination takes place through the C=O and C=N groups. (auth.)

Spectrophotometric study of neptunium (VI) complexation by nitrate ions; Etude par spectrophotometrie de la complexation du neptunium au degre d'oxydation (VI) par les ions nitrates

Energy Technology Data Exchange (ETDEWEB)

Pochon, P. [CEA/VALRHO - site de Marcoule, Dept. de Recherche en Retraitement et en Vitrification (DRRV), 30 - Marcoule (France)]|[Conservatoire National des Arts et Metiers (CNAM), 75 - Paris (France)]|[Centre Regional Associe de Lyon, 69 (France)

2000-07-01

Neptunium(VI) complexation by nitrate ions was investigated by visible and near-infrared spectrophotometry, a technique suitable for observing the appearance and evolution of the species in solution. In the absence of reference spectra for Np(VI) nitrate- complexes, mathematical (factor analysis) tools were used to interpret the spectra. These chemo-metric techniques were first tested and validated on a simpler chemical system: Np(VI)complexation by the SiW{sub 11}O{sub 39}{sup 8-} anion. The test media used to investigate Np(VI) nitrate- complexes generally contain nitrate and perchlorate salts at high concentrations (high ionic strength). Media effects arising from the presence of cations, acidity or the perchlorate ion concentration are therefore significant, and no doubt account for the scattered values of the complexation constants published in the literature. The evolution of the neptunium spectra according to the parameters of the reaction medium illustrated these effects and allowed them to be quantified by a global 'perturbation constant'. In order to minimize the spectrum modifications due to media effects, the neptunium nitrate-complexes were studied at constant ionic strength in weak acidic media (2 mol.kg{sup -1}{sub H2O}) in the presence of sodium salts. The bulk formation constants and the spectrum of the NpO{sub 2}(NO{sub 3}){sup +} complex were determined for ionic strength values of 2.2, 4, 6 and 8 mol.kg{sup -1}{sub H2O}. The constants remained on the same order of magnitude regardless of the ionic strength; the thermodynamic constant {beta}{sub 1}{sup 0} determined from them according to specific interaction theory is thus probably of little significance. Conversely, the bulk constants can be corrected for the effects of the perchlorate ions by taking the global 'perturbation constant' into account. (author)

DARPA Antibody Technology Program Standardized Test Bed for Antibody Characterization: Characterization of an MS2 ScFv Antibody

Science.gov (United States)

2016-03-01

2 2.2 UV –Visible Spectrophotometry...3 M phosphoric acid or 3 M sodium hydroxide [Sigma-Aldrich] as necessary), and overhead pressure of 1 psi. When the OD inside the 100 L fermentor...chromatography media (GE Healthcare). 2.2 UV –Visible Spectrophotometry A NanoDrop ND-1000 spectrophotometer (Thermo Scientific; Waltham, MA

UV/VIS spektrofotometrie a možnosti jejího využití v rámci vzdělávání učitelů chemie

OpenAIRE

Hejsková, Veronika

2016-01-01

This master's thesis discusses the use of UV/VIS spectrophotometry in chemistry teacher education. Optical methods principles are described in theoretical part of the thesis, and. the main part is dedicated to UV-VIS spectrophotometry. Tasks for quantifying and qualifying substances determination are described in experimental part. Educational tasks are described in a way so that chemistry teachers could use for instructions.

Determination of thorium in the range of low concentrations

International Nuclear Information System (INIS)

Hill, R.; Lieser, K.H.

1992-01-01

Methods for the determination of Th in the range of low concentrations are compiled and discussed. Application of spectrophotometry and voltammetry is investigated. Spectrophotometry is applicable down to concentrations of the order of 0.1 μg/l as long as the ratio U:Th is low. Voltammetric determination of Th is not possible in the presence of Al. (orig.)

Determination of mixture valence plutonium and multicomponent by computer resolution analysis of absorption spectrum (UV/VIS/NIR) (CRAAS)

International Nuclear Information System (INIS)

Zhuang Weixin; Ye Guoan; Huang Lifeng; Sun Hongfang; Zhao Yanju

1996-09-01

A spectrophotometry has been developed which can directly determine a multi-component sample by spectrophotometry without any chemical separation. CRAAS (Computer Resolution Analysis of Absorption Spectrum) has been reported. It is different from the previous spectrophotometry depending on only one or several special absorption peak. The CRAAS deals with the whole region of absorption spectrum by mathematical statistics. So CRAAS has higher accuracy, stronger power and very high resolution. The trouble comes from overlap of different spectrum in each other has been solved because CRAAS depends on the whole spectrum. As long as two spectra have different shape, their concentrations can be determined even their special absorption peaks are seriously overlapped. The accuracy is about +-5%. (2 refs., 7 figs., 8 tabs.)

Speciation of inorganic antimony in polyethylene terephthalate (PET) bottled water using hydride generation atomic absorption spectrophotometry (HG-AAS)

International Nuclear Information System (INIS)

Markwo, Ali

2015-07-01

Antimony (Sb) is a regulated drinking water contaminant that has been found to leach from polyethylene terephthalate (PET) plastic containers into the waters stored in them. The common inorganic species of antimony in water are Sb(III) and Sb(V), with the former being more toxic and the latter being more soluble. In order to assess the extent to which waters stored in PET bottles are contaminated with inorganic Sb and to further examine the effect of typical storage conditions on migration rates, speciation analysis of inorganic Sb using hydride generation atomic absorption spectrophotometry (HG-AAS) was undertaken on selected PET plastic bottled waters marketed in the Greater Accra Region of Ghana. Six brands of PET plastic bottled waters were obtained at source on the day of packaging, and analyses undertaken on samples of the waters stored in the plastic containers at intervals of four weeks for twelve weeks, under three carefully chosen storage conditions distinctive of bottled water usage. Selected physicochemical properties of samples of the waters stored in the plastic containers and total Sb of samples of the plastic containers were also determined to discover the effect of some physical properties and certain major ions, and the influence of the different quality PET plastic types on Sb migration respectively. The study revealed amounts of total Sb in the PET plastic containers of the 6 brands ranging from 123.46 mg/kg to 146.45 mg/kg. The selected physicochemical properties of the waters stored in the PET plastic containers considered were pH (6.78 – 7.43), Ca2+ (1.61 – 12.39 mg/L), Mg2+ (1.00 – 4.96 mg/L), HCO3− (6.18 – 55.41 mg/L) and TDS (8.70 – 70.40 mg/L)). PET bottled waters of 5 out of the 6 brands contained Sb (initial total Sb ranging from 1.11 – 14.65 μg/L) before storage. Total Sb concentrations of the waters stored in the plastic containers were observed to increase with storage time under all the three storage conditions for

Non-Powered Spectrophotometry for Lighting

Data.gov (United States)

National Aeronautics and Space Administration — This process improvement innovation would like to suggest a non-powered method and tool set that can be developed to assist crewmembers and ground support teams with...

Far-ultraviolet spectrophotometry of Spica

Science.gov (United States)

Cook, Timothy A.; Cash, Webster; Snow, Theodore P.

1989-01-01

A spectrum of the star Spica (Alpha Virginis) from 960 to 1270 A was recorded by a rocket-borne spectrograph March 13, 1988. The spectrum, which has 3.4 A resolution, shows a much sharper drop-off in intensity near 1050 A than similar measurements made by the Voyager UVS, but is in good agreement with the spectrum obtained by Brune et al. in a 1977 sounding rocket. The disagreement with Voyager is a factor of 1.5 at 1100 A and grows to a factor of 5.7 at 960 A. This implies that the photometric standards between 912 and 1100 A may need some revision, and that the standard photospheric models for hot stars may err significantly near the Lyman limit.

A catalog of stellar spectrophotometry

Science.gov (United States)

Adelman, S. J.; Pyper, D. M.; Shore, S. N.; White, R. E.; Warren, W. H., Jr.

1989-01-01

A machine-readable catalog of stellar spectrophotometric measurements made with rotating grating scanner is introduced. Consideration is given to the processes by which the stellar data were collected and calibrated with the fluxes of Vega (Hayes and Latham, 1975). A sample page from the spectrophotometric catalog is presented.

Ultraviolet spectrophotometry of three LINERs

Science.gov (United States)

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.

UV spectrophotometry of the Metronidazole

Directory of Open Access Journals (Sweden)

O. I. Panasenko

2013-10-01

Full Text Available Objective. The purpose of this research was to study the UV spectrum of Metronidazole in different polarity solvents (water, 95 % ethanol, 0,1 M sodium hydroxide, 0,1 M hydrochloric acid and 5 M sulfuric acid solution, to establish the relationship between chemical structure of the analyzed compounds and the nature of their electronic spectrum. In addition, a detailed study of the ultraviolet spectra of Metronidazole in different solutions enables to select the optimal wavelength and a thinner design for Metronidazole in substance and dosage forms. Materials and methods. Spectrophotometer SPECORD 200-222U214 has been used for study of the UV spectra of Metronidazole, the quantitative methods were used. Measuring of the absorption of Metronidazole solutions has been carried out in quartz cuvettes with a layer thickness of 10 mm. Due to the fact that the test material shows selective absorption in the ultraviolet spectra, model compounds were studied at a concentration of 1 mg%. Study of electronic spectra was performed in the range of 200 to 400 nm, and the curve has been constructed in coordinates A = f (λ. It has been used water, 95% ethanol, 0,1 M NaOH, 0,1 M HCl and 5 M H2SO4 as solvents. The content of Metronidazole in substance and dosage forms calculated with the equations according to SPU. The results. Study of the UV spectra of Metronidazole and its model compounds showed that in short-wave part of spectrum due to absorption and excitation electrons of imidazole ring were transferred, and in long-wave – conjugation chromophore imidazole cycle and nitro group as electron acceptor occurred. Analysis of the UV spectra of Metronidazole enables to determine a maximum of the analytical quantification of the medicine. Conclusions. Metronidazole UV spectra in water, 95% ethanol, 0,1 M solution of NaOH, 0,1 M solution of HCl and 5 M solution of H2SO4 have been studied. Metronidazole UV spectra are characterized by two absorption bands in the range 228-230 nm and 276-332 nm in specifying solvents. Quantitative determination methods of Metronidazole in the substance (water and 95% ethanol at 230 nm, 0,5% solution for infusion (water at 230 nm and vaginal suppositories of 0,1 g (water at 230 nm have been developed and proposed. The error in the determination of metronidazole in the substance did not exceed ± 0,03, and in dosage forms - ± 0,05.

Spectrophotometry of the Ceres surface

Science.gov (United States)

Schröder, Stefan; Mottola, Stefano; Carsenty, Uri; Jaumann, Ralf; Keller, Uwe; Krohn, Katrin; Li, Jian-Yang; Matz, Klaus-Dieter; McFadden, Lucy; Otto, Katharina; Preusker, Frank; Roatsch, Thomas; Scholten, Frank; Stephan, Katrin; Wagner, Roland; Raymond, Carol; Russell, Chris

2015-11-01

The Dawn spacecraft is in orbit around dwarf planet Ceres. The onboard Framing Camera (FC) is mapping the surface through a clear filter and 7 narrow-band filters at various observational geometries and image resolutions. Generally, Ceres' appearance in these images is affected by shadows and shading, effects which obscure the intrinsic reflective properties of the surface. By means of photometric modeling we remove these effects and reconstruct the surface reflectance for each of the FC filters, creating albedo and color maps in the process. Considering these maps in unison provides clues to the physical nature and composition of the surface and the dominant geologic processes that shape the surface. We assess the nature of color variations in the visible wavelength range for Ceres globally. We identify which terrains express the dominant colors and investigate why some areas are exceptions to the rule. By correlating the color over the surface with geologic units we find an relatively strong enhancement of the reflectance towards the blue end of the visible spectrum for recent impacts and their ejecta.

[Recommended diet for reflux spectrophotometry].

Science.gov (United States)

Felix, Valter Nilton; Viebig, Ricardo Guilherme

2003-01-01

The spectrophotometric probe, which uses bilirubin as a marker for the detection of duodenoesophagic reflux is subject to interference from strongly colored foods, which can cause erroneously high bilirubin absorbance readings. To overcome this problem it is necessary to ingest a diet that is free from such substances. To test the absorbance of 48 different food substances in an in vitro environment. Dry foods were blended with water or milk and non-dry solid foods were blended undiluted. It was utilized the proper calibration recipient to test them. The absorbance of weakly colored foods was usually lesser than the commonly accepted threshold of 0.14, and the absorbance of strongly colored foods was usually above this. Thirty-two from the 48 substances tested are suitable when the absorbance threshold is set at 0.14, but scrambled eggs, lacteous flour mush, green beans, beetroot, carrot, chayote, squash, "baroa" potato, boiled corn, orange, cashew, purple grape, avocado, mango, papaya and peach can alter the results and must be avoided. From the foods evaluated, enough are suitable at the 0.14 threshold to enable a suitable diet to be constructed for most patients during Bilitec studies.

A simple and efficient ultrasonic-assisted extraction procedure combined with UV-Vis spectrophotometry for the pre-concentration and determination of folic acid (vitamin B9) in various sample matrices.

Science.gov (United States)

Gürkan, Ramazan; Altunay, Nail

2016-07-01

A simple and efficient ultrasonic-assisted extraction (UAE) procedure has been proposed for the pre-concentration of (2S)-2-[(4-{[(2-amino-4-hydroxypteridin-yl)methyl]amino}phenyl)formamido]pentanedioic acid (folic acid) in vegetables, pharmaceuticals and foods prior to determination at 540 nm using UV-Vis spectrophotometry. The method is based on hydrophobic ternary complex formation of folic acid with silver ions in the presence of cetyltrimethylammonium bromide (CTAB) as a sensitivity enhancer counter ion at pH 7.0, and then extraction into a micellar phase of polyethylene glycol monoalkyl ether (Genapol X-080). The impacts on the extraction efficiency and complex formation of analytical parameters such as sample pH, concentration of silver, concentration of surfactants and extraction time, ultrasonic time and sample volume, were investigated and optimised in detail. The matrix effect on the pre-concentration and determination of folic acid was investigated, and it was observed that the proposed method was highly selective against possible matrix co-extractives. Under optimised conditions, a good linear relationship between the analytical signal and folic acid concentration was obtained in the range of 0.6-180 μg l(-1) with a detection limit of 0.19 μg l(-1) and quantification limit of 0.63 μg l(-1). The applicability was evaluated using samples fortified at different concentration levels, and recoveries higher than 94.1% were obtained. The precision as the percent relative standard deviation (RSD%) was in range of 2.5-3.8% (10 and 40 μg l(-1), n = 5). The proposed method was validated by analysis of two standard reference materials (SRMs) and various real samples, and satisfactory results were obtained.

Application of carbon nanotubes modified with a Keggin polyoxometalate as a new sorbent for the hollow-fiber micro-solid-phase extraction of trace naproxen in hair samples with fluorescence spectrophotometry using factorial experimental design.

Science.gov (United States)

Naddaf, Ezzat; Ebrahimi, Mahmoud; Es'haghi, Zarrin; Bamoharram, Fatemeh Farrash

2015-07-01

A sensitive technique to determinate naproxen in hair samples was developed using hollow-fiber micro-solid-phase combined with fluorescence spectrophotometry. The incorporation of multi-walled carbon nanotubes modified with a Keggin polyoxometalate into a silica matrix prepared by the sol-gel method was reported. In this research, the Keggin carbon nanotubes /silica composite was used in the pores and lumen of a hollow fiber as the hollow-fiber micro-solid-phase extraction device. The device was used for the microextraction of the analyte from hair and water samples under the optimized conditions. An orthogonal array experimental design with an OA24 (4(6) ) matrix was employed to optimize the conditions. The effect of six factors influencing the extraction efficiency was investigated: pH, salt, volume of donor and desorption phase, extraction and desorption time. The effect of each factor was estimated using individual contributions as response functions in the screening process. Analysis of variance was employed for estimating the main significant factors and their contributions in the extraction. Calibration curve plot displayed linearity over a range of 0.2-10 ng/mL with detection limits of 0.072 and 0.08 ng/mL for hair and aqueous samples, respectively. The relative recoveries in the hair and aqueous matrices ranged from 103-95%. The relative standard deviation for fiber-to-fiber repeatability was 3.9%. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Novel Spectrophotometric Methods for Determination of Salicylamide and Ascorbic acid in their binary mixture

International Nuclear Information System (INIS)

Ali, N.W.; Zaazaa, H.E.S.; Abdelrahman, M.M.

2014-01-01

Simple, selective and precise four spectrophotometric methods were developed and validated for quantitative determination of Salicylamide (SAD) and Ascorbic acid (ASC, Vitamin C) in their binary mixture. Method A is Area under curve spectrophotometry, in which the area under curve in the wavelength ranges 225-245 nm and 265-285 nm were selected for determination of SAD and ASC. Method B is based on dual wavelength spectrophotometry, where ASC can be determined by difference in absorbance at 249.8 and 285.8 nm. On the same way; SAD is measured by difference in absorbance at 240.4 and 286.4 nm. Method C utilizes isoabsorptive point spectrophotometry where total concentration of SAD and ASC was calculated at their isoabsorptive points at 246.4 and 287 nm, while SAD concentration alone can be determined by first derivative spectrophotometry (1D) at 315.4 nm, then ASC concentration can be determined by subtraction. Method D is ratio subtraction spectrophotometry, where ASC can be determined by dividing the spectrum of the mixture by the spectrum of the SAD (as a divisor) followed by subtracting the constant absorbance value of the plateau region, then finally multiplying the obtained spectrum by the spectrum of the divisor. The developed methods have been successfully applied for determination of the studied drugs in different laboratory prepared mixtures and in their pharmaceutical formulation. Statistical comparison between the results obtained by applying the proposed methods and the reported HPLC method was done, and it was found that there was no significant difference between them regarding both accuracy and precision. (author)

Emodin (1,3,8-trihydroxy-6-methylanthraquinone): a spectrophotometric reagent for the determination of beryllium(II), magnesium(II) and calcium(II)

International Nuclear Information System (INIS)

Pal, T.; Jana, N.R.

1993-01-01

The individual determination of Be II , Mg II or Ca II by conventional spectrophotometry and simultaneous determination of Mg II and Ca II in mixtures by first-derivative spectrophotometry are possible at trace levels, using emodin (1,3,8-trihydroxy-6-methylanthraquinone) as spectrophotometric reagent. Interference from other metal species, application of these methods to rock samples and statistical analysis of the results are discussed. (author)

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

Energy Technology Data Exchange (ETDEWEB)

Kazemi, Elahe; Haji Shabani, Ali Mohammad [Department of Chemistry, Yazd University, Safaieh, 89195-741, Yazd (Iran, Islamic Republic of); Dadfarnia, Shayessteh, E-mail: sdadfarnia@yazd.ac.ir [Department of Chemistry, Yazd University, Safaieh, 89195-741, Yazd (Iran, Islamic Republic of); Abbasi, Amir [Department of Physics, Yazd University, Safaieh, 89195-741, Yazd (Iran, Islamic Republic of); Rashidian Vaziri, Mohammad Reza [Laser and Optics Research School, 14155-1339, Tehran (Iran, Islamic Republic of); Behjat, Abbas [Department of Physics, Yazd University, Safaieh, 89195-741, Yazd (Iran, Islamic Republic of)

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{sup −1}, a detection limit of 0.21 μg L{sup −1}, an enrichment factor of 167, and a relative standard deviation of 2.1% and 3.8% (n = 6) at 60 μg L{sup −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{sup −1}, a detection limit of 0.016 μg L{sup −1} and a relative standard deviation of 3.8% and 5.6% (n = 6) at 60 μg L{sup −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. - Graphical abstract: A novel, sensitive, fast, simple and convenient mixed hemimicelles

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

International Nuclear Information System (INIS)

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

2016-01-01

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. - Graphical abstract: A novel, sensitive, fast, simple and convenient mixed hemimicelles dispersive micro solid

Rapid chemical analysis of allanite

International Nuclear Information System (INIS)

Nishiyama, Goro; Hayashi, Hiroshi

1981-01-01

Rapid chemical analysis of allanite was studied by atomic absorption spectrophotometry. Powdered sample was fused with mixture of sodium carbonate anhydrous and borax (4 : 1 weight) in platinum crucible and sample solution was prepared. SiO 2 , Fe 2 O 3 , Al 2 O 3 , MnO and rare earth metals were determined by atomic absorption spectrophotometry, CaO, MgO and Ce 2 O 3 by titration, ThO 2 by colorimetry, and La 2 O 3 by flame photometry respectively. For sample solution treated with hydrofluoric acid and sulfuric acid. Na 2 O and K 2 O were determined by atomic absorption spectrophotometry, TiO 2 and P 2 O 5 by colorimetry. Chemical analyses for four samples were carried out and gave consistent results. (author)

The study of complex equilibria of uranium(VI) with selenate

International Nuclear Information System (INIS)

Lubal, P.; Havel, J.

1997-01-01

Uranyl (M)-selenate (L) complex equilibria in solution were investigated by spectrophotometry in visible range and potentiometry by means of uranyl ion selective electrode. The formation ML and ML 2 species was proved and the corresponding stability constants calculated were: log β 1 = 1.57 6 ± 0.01 6 , log β 2 = 2.42 3 ± 0.01 3 (I 3.0 mol 1 -1 Na(ClO 4 , SeO 4 ) (spectrophotometry) at 298.2 K. Using potentiometry the values for infinite dilution (I → 0 mol 1 -1 ) were: log β 1 = 2.64 ± 0.01, log β 2 ≤ 3.4 at 298.2 K. Absorption spectra of the complexes were calculated and analysed by deconvolution technique. Derivative spectrophotometry for the chemical model determination has also been successfully applied. (author)

Optical spectrophotometric atlas of Supernova 1987A in the LMC. I. The first 130 days

International Nuclear Information System (INIS)

Phillips, M.M.; Heathcote, S.R.; Hamuy, M.; Navarrete, M.

1988-01-01

Optical spectrophotometry of SN 1987A in the Large Magellanic Cloud (LMC) covering the first 5 months since outburst is presented. More than 80 spectra were obtained at Cerro Tololo over this period, mostly with the 2D-Frutti two-dimensional photon-counting detector on the 1-m telescope. The spectrophotometric calibration of the 2D-Frutti data is considered in detail. Through a comparison with broadband photometry, it is shown that the accuracy of the 2D-Frutti spectrophotometry is + or - 5 percent in absolute terms, and that the relative calibration for any single spectrum is accurate to + or - 3 percent. CCD spectrophotometry obtained on the first night of observation (Feb. 25, 1987) is also briefly discussed. Radial velocities for several prominent absorption and emission features are measured from these combined data. 13 references

Assessing radioactive concentrates and waste vapor condensate in solidifying radioactive wastes by bituminization

International Nuclear Information System (INIS)

Tibensky, L.; Krejci, F.; Breza, M.; Timulak, J.; Hladky, E.

1986-01-01

A brief overview is presented of chemical and radiochemical methods used in the world for the analysis of the concentrate of liquid radioactive wastes from nuclear power plants destined for bituminization. Most methods are also suitable for an analysis of the condensate of waste vapors produced in bituminization. The methods of analysis of the radioactive concentrate from the V-1 nuclear power plant in Jaslovske Bohunice and of the waste vapors condensate were developed and tested in practice. Gross gamma activity was measured using a well-type Na(Tl) scintillation detector, the content of radionuclides was determined using semiconductor Ge(Li) spectrometry. The concentration of boric acid in the concentrate was determined by titration with mannite; in the condensate, using spectrophotometry with curcumine. The content of nitrates in both the concentrate and the condensate was determined spectrophotometrically using salicylic acid, the content of nitrites was determined by spectrophotometry using sulfanilic acid and α-naphthylamine. Carbonates and chlorides were determined by titration, sodium and potassium by flame photometry. The content of organic acids was measured by gravimetry of extracted methyl esters, the content of surfactants by spectrophotometry. Infrared spectrophotometry was used in determining hydrocarbons in the waste vapor condensate. The measured value range and the measurement errors are shown for each method. (A.K.)

On-line measurement of crystalline color by color-image processing system; Gazo shori system wo mochiita kessho no online iro sokutei

Energy Technology Data Exchange (ETDEWEB)

Okayasu, S.; Katayama, M.; Shinohara, T. [Ajinomoto Co. Inc., Tokyo (Japan)

1996-01-20

Aiming for the stable operation and the rationalization of factory plant, the color-image processing has been tried to introduce into the on-line system to measure the crystalline color of L-Lysine in its refining process. Because the practical spectro-photometry was used to be employed by manual measurement. In this paper, the calculation formula of the transmittance by spectrophotometry is theoretically introduced by analyzing the relation of Lambert-Beer`s law of luminous transparency with the Kubelka-Munk`s function of the luminous dispersion using color image data. The parameters of the calculation formula were decided by actual measurement, so that the formula with accuracy value of {plus_minus}3% elucidated the possible estimation of transmittance by spectrophotometry. The system was tested on a commercial plant, and some issues are discussed. 8 refs., 8 figs., 3 tabs.

Flare activity on UV CETI: visible and IUE observations

International Nuclear Information System (INIS)

Phillips, K.J.H.; Bromage, G.E.; Dufton, P.L.; Keenan, F.P.; Kingston, A.E.

1988-06-01

Simultaneous far-ultraviolet (IUE) spectroscopy and optical photometry and spectrophotometry of a flare on UV Ceti are reported. The flare reached ΔU = 2sup(m) but showed only modest enhancements in the IUE spectra. The optical spectrophotometry indicated broadened Balmer line profiles during the flare, with Hβ and Hγ clearly showing red wings. The results are compared with other IUE and optical observations of UV Ceti, and their solar analogues. (author)

Flare activity on UV Ceti: visible and IUE observations

International Nuclear Information System (INIS)

Phillips, K.J.H.; Bromage, G.E.; Dufton, P.L.; Keenan, F.P.; Kingston, A.E.

1988-01-01

Simultaneous far-ultraviolet (IUE) spectroscopy and optical photometry and spectrophotometry of a flare on UV Ceti are reported. The flare reached ΔU=2 mag but showed only modest enhancements in the IUE spectra. The optical spectrophotometry indicated broadened Balmer line profiles during the flare, with Hβ and Hγ clearly showing red wings (∼ 100 km s -1 ). The results are compared with other IUE and optical observations of UV Ceti, and their solar analogues. (author)

Standard test methods for chemical, mass spectrometric, and spectrochemical analysis of nuclear-grade plutonium dioxide powders and pellets

CERN Document Server

American Society for Testing and Materials. Philadelphia

2010-01-01

1.1 These test methods cover procedures for the chemical, mass spectrometric, and spectrochemical analysis of nuclear-grade plutonium dioxide powders and pellets to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Sections Plutonium Sample Handling 8 to 10 Plutonium by Controlled-Potential Coulometry Plutonium by Ceric Sulfate Titration Plutonium by Amperometric Titration with Iron(II) Plutonium by Diode Array Spectrophotometry Nitrogen by Distillation Spectrophotometry Using Nessler Reagent 11 to 18 Carbon (Total) by Direct Combustion–Thermal Conductivity 19 to 30 Total Chlorine and Fluorine by Pyrohydrolysis 31 to 38 Sulfur by Distillation Spectrophotometry 39 to 47 Plutonium Isotopic Analysis by Mass Spectrometry Rare Earth Elements by Spectroscopy 48 to 55 Trace Elements by Carrier–Distillation Spectroscopy 56 to 63 Impurities by ICP-AES Impurity Elements by Spark-Source Mass Spectrography 64 to 70 Moisture by the Coulomet...

REVIEW ARTICLE: Spectrophotometric applications of digital signal processing

Science.gov (United States)

Morawski, Roman Z.

2006-09-01

Spectrophotometry is more and more often the method of choice not only in analysis of (bio)chemical substances, but also in the identification of physical properties of various objects and their classification. The applications of spectrophotometry include such diversified tasks as monitoring of optical telecommunications links, assessment of eating quality of food, forensic classification of papers, biometric identification of individuals, detection of insect infestation of seeds and classification of textiles. In all those applications, large numbers of data, generated by spectrophotometers, are processed by various digital means in order to extract measurement information. The main objective of this paper is to review the state-of-the-art methodology for digital signal processing (DSP) when applied to data provided by spectrophotometric transducers and spectrophotometers. First, a general methodology of DSP applications in spectrophotometry, based on DSP-oriented models of spectrophotometric data, is outlined. Then, the most important classes of DSP methods for processing spectrophotometric data—the methods for DSP-aided calibration of spectrophotometric instrumentation, the methods for the estimation of spectra on the basis of spectrophotometric data, the methods for the estimation of spectrum-related measurands on the basis of spectrophotometric data—are presented. Finally, the methods for preprocessing and postprocessing of spectrophotometric data are overviewed. Throughout the review, the applications of DSP are illustrated with numerous examples related to broadly understood spectrophotometry.

Interaction of the carbon monoxide-releasing molecule Ru(CO)3Cl(glycinate) (CORM-3) with Salmonella enterica serovar Typhimurium: in situ measurements of carbon monoxide binding by integrating cavity dual-beam spectrophotometry.

Science.gov (United States)

Rana, Namrata; McLean, Samantha; Mann, Brian E; Poole, Robert K

2014-12-01

Carbon monoxide (CO) is a toxic gas that binds to haems, but also plays critical signalling and cytoprotective roles in mammalian systems; despite problems associated with systemic delivery by inhalation of the gas, it may be employed therapeutically. CO delivered to cells and tissues by CO-releasing molecules (CO-RMs) has beneficial and toxic effects not mimicked by CO gas; CO-RMs are also attractive candidates as novel antimicrobial agents. Salmonella enterica serovar Typhimurium is an enteropathogen causing gastroenteritis in humans. Recent studies have implicated haem oxygenase-1 (HO-1), the protein that catalyses the degradation of haem into biliverdin, free iron and CO, in the host immune response to Salmonella infection. In several studies, CO administration via CO-RMs elicited many of the protective roles of HO-1 induction and so we investigated the effects of a well-characterized water-soluble CO-RM, Ru(CO)3Cl(glycinate) (CORM-3), on Salmonella. CORM-3 exhibits toxic effects at concentrations significantly lower than those reported to cause toxicity to RAW 264.7 macrophages. We demonstrated here, through oxyhaemoglobin assays, that CORM-3 did not release CO spontaneously in phosphate buffer, buffered minimal medium or very rich medium. CORM-3 was, however, accumulated to high levels intracellularly (as shown by inductively coupled plasma MS) and released CO inside cells. Using growing Salmonella cultures without prior concentration, we showed for the first time that sensitive dual-beam integrating cavity absorption spectrophotometry can detect directly the CO released from CORM-3 binding in real-time to haems of the bacterial electron transport chain. The toxic effects of CO-RMs suggested potential applications as adjuvants to antibiotics in antimicrobial therapy. © 2014 The Authors.

The spectroscopic analysis of {gamma}-irradiated glass by colorimetry, ESR and XPS

Energy Technology Data Exchange (ETDEWEB)

Hong, S.I. [College of Life Sciences and Biotechnology, Korea University, 5 ga Anam-dong, Seongbuk-Gu, Seoul 135-701 (Korea, Republic of); Lee, Y.N. [R and D Institute Biscuit Team, 131-1, Namyoung-dong, Youngsan-Gu, Seoul 140-708 (Korea, Republic of); Cho, S.Y. [College of Life Sciences and Biotechnology, Korea University, 5 ga Anam-dong, Seongbuk-Gu, Seoul 135-701 (Korea, Republic of); Whiteside, W.S. [Department of Packaging Science, 226 Poole Agricultural Center, Clemson University, Clemson, SC 29634-0320 (United States); Park, H.J. [College of Life Sciences and Biotechnology, Korea University, 5 ga Anam-dong, Seongbuk-Gu, Seoul 135-701 (Korea, Republic of)], E-mail: hjpark@korea.ac.kr

2008-09-15

The darkening of {gamma}-irradiated glass was related to the binding of Si-O and Sn-O, and the binding of Na-O. The dosimetric range of glass color change was evaluated by colorimetry, UV-Vis spectrophotometry and ESR. Colorimetry and UV-Vis spectrophotometry, revealed linear changes up to 9 kGy. For the calibration curve of {gamma}-irradiation, the signal of g=2.01 observed by ESR responded most sensitively with a linear increase with up to 12 kGy.

The spectroscopic analysis of γ-irradiated glass by colorimetry, ESR and XPS

International Nuclear Information System (INIS)

Hong, S.I.; Lee, Y.N.; Cho, S.Y.; Whiteside, W.S.; Park, H.J.

2008-01-01

The darkening of γ-irradiated glass was related to the binding of Si-O and Sn-O, and the binding of Na-O. The dosimetric range of glass color change was evaluated by colorimetry, UV-Vis spectrophotometry and ESR. Colorimetry and UV-Vis spectrophotometry, revealed linear changes up to 9 kGy. For the calibration curve of γ-irradiation, the signal of g=2.01 observed by ESR responded most sensitively with a linear increase with up to 12 kGy

Determination of trace impurities in materials

International Nuclear Information System (INIS)

Parashar, D.C.

1991-01-01

Research work done at the National Physical Laboratory to develop new methods which are more specific and/or more sensitive has been reviewed. These methods are based on the use of existing facilities viz. atomic absorption spectrophotometry, uv-visible spectrophotometry, gas chromatography and conventional chemical methods. It is possible to determine impurities like boron at 5ppb level, phosphorus at 100 ppb and oxygen non-stoichiometry in 1:2:3 compounds with higher accuracy. Boron is determined spectrophotometrically by forming a complex with curcumin and phosphorus is determined indirectly by atomic absorption spectrophotometry by forming phosphomolybdate complex with antimony or bismuth which have 1:1 ratio with phosphorus in the complex. Gas chromatographic technique has been used to evaluate the oxygen non-stoichiometry in high temperature superconductors (1:2:3 compound) where the HTc sample is dissolved in dilute nitric acid in helium environment and the oxygen released is determined using thermal conductivity detector. (author). 19 refs., 3 figs., 4 tabs

Determination of humic acid in alkali leaching solution of uranium by spectophotrometry-COD method

International Nuclear Information System (INIS)

Feng Yu; An Wei; Chen Shusen

2014-01-01

It is one of the main causes of extraction emulsification or resin toxicosis during alkali leaching process in uranium metallurgy which organic matters including humic acid exist in lixiviums. In order to study the effect of humic acid in uranium metallurgy, a method for determination of content of humic acid in aqueous solution need to be established. Spectrophotometry is a simple and convenient method in humic acid analysis. However, accuracy of spectrophotometry can be reduced greatly because of interference of uranium and other elements in the humic acid solutions. Although chemical oxygen demand (COD) method is a common analysis way of organic matters in aqueous solutions, the concentration of humic acid cannot be directly measured. In this paper, COD method is related with spectrophotometry to avoid the interference of uranium and ensure the accurate analysis of humic acid. The results showed that the detection limit of the method was 1.78 mg/L and the recovery rate was 101.2%. (authors)

Simple and rapid spectrophotometric determination of trace titanium (IV) enriched by nanometer size zirconium dioxide in natural water

International Nuclear Information System (INIS)

Zheng Fengying; Li Shunxing; Lin Luxiu; Cheng Liqing

2009-01-01

A novel method for preconcentration of Ti(IV) with nanometer size ZrO 2 and determination by spectrophotometry has been developed. Ti(IV) was selectively adsorbed on 300 mg ZrO 2 from 500 mL solution at pH 6.0, then eluted by 5 mL 11.3 mol L -1 HF. The eluent added was diantipyrylmethane (DAPM, as chromogenic reagent) and ascorbic acid (as masking agent), used for the analysis of Ti(IV) by measuring the absorbance at 390 nm with spectrophotometry, based on the chromogenic reaction between the Ti(IV) and DAPM. This method gave a concentration enhancement of 100 for 500 mL sample, eliminated the sizable interferences on direct determination with spectrophotometry. Detection limit (3σ, n = 11) of 0.1 μg L -1 was obtained. The method was applied to determine the concentration of Ti(IV) in river water and seawater and the analytical recoveries of Ti(IV) added to samples were 97.6-101.3%.

Contributions to the analysis of nuclear raw materials

International Nuclear Information System (INIS)

Korkisch, J.; Gross, H.

1975-01-01

A procedure is described for the separation of μg quantities of lead from large amounts of uranium and for making accessible an end-determination by means of atomic absorption spectrophotometry. The separation of the lead from the uranium and from other foreign ions present in the uranium matrix is accomplished by adsorption on a column of the strongly basic anion exchanger Dowex 1, X8 from 2M hydrobromic acid. Following elution of the adsorbed lead by means of 6M hydrochloric acid, the lead is determined either by means of atomic absorption spectrophotometry or by spectrophotometry with employment of the dithizone method. The procedure was employed for the determination of lead in standard specimens of U 3 0 8 (0.17 to 1.8 p.p.m. Pb) and of Yellow Cake (7.8 to 88 p.p.m. Pb). A good agreement of the results was attained in all cases. (author)

Spectrophotometry of Comet West 1976 VI

International Nuclear Information System (INIS)

Rozenbush, V.K.

1986-01-01

Spectra obtained for the coma, nuclear fragments A and D, and tail of Comet West 1976 VI on April 1, 2 and 7, 1976 are noted to encompass coma spectra which differed from those of the nuclear fragments, which exhibited a strong continuum with superimposed emissions that included a stronger CO(+)-band system than that of the coma. A detailed comparison between fragment spectra has revealed great differences in both quasi-simultaneously obtained and five-day-separated cases. The relative intensities of different CO(+) bands are compared to the theoretical ones, and the abundances of CO(+) ions corresponding to different vibrational transitions are determined relative to that of CN. 24 references

Multi-filter spectrophotometry of quasar environments

Science.gov (United States)

Craven, Sally E.; Hickson, Paul; Yee, Howard K. C.

1993-01-01

A many-filter photometric technique for determining redshifts and morphological types, by fitting spectral templates to spectral energy distributions, has good potential for application in surveys. Despite success in studies performed on simulated data, the results have not been fully reliable when applied to real, low signal-to-noise data. We are investigating techniques to improve the fitting process.

Ultraviolet and infrared spectrophotometry : some applications

NARCIS (Netherlands)

Koornneef, Jan

1976-01-01

De inhoud van dit proefschrift valt uiteen in twee delen doordat waarnerningen gepresenteerd en geinterpreteerd worden in twee ver uiteenliggende gedeelten van het electromagnetisch spectrum ... Zie: Samenvating

Optical spectrophotometry of Wolf-Rayet galaxies

Science.gov (United States)

Vacca, William D.; Conti, Peter S.

1992-01-01

We have obtained long-slit optical spectra of 10 Wolf-Rayet galaxies and four other starburst galaxies. Using the nebular emission lines we have determined the electron temperatures, electron densities, extinctions, oxygen abundances, mass of ionized hydrogen, and numbers of ionizing photons due to hot stars in these galaxies. The various forbidden line ratios clearly indicate a stellar origin for the emission-line spectrum. From the flux of the broad He II 4686 A emission feature we have estimated the number of Wolf-Rayet stars present. We have accounted for the contribution of these stars to the total ionizing flux and have calculated the ratio of the number of these stars to the number of O stars. Wolf-Rayet galaxies are among the youngest examples of the starburst phenomenon, which we observed at a propitious moment.

Coronagraph for astronomical imaging and spectrophotometry

Science.gov (United States)

Vilas, Faith; Smith, Bradford A.

1987-01-01

A coronagraph designed to minimize scattered light in astronomical observations caused by the structure of the primary mirror, secondary mirror, and secondary support structure of a Cassegrainian telescope is described. Direct (1:1) and reducing (2.7:1) imaging of astronomical fields are possible. High-quality images are produced. The coronagraph can be used with either a two-dimensional charge-coupled device or photographic film camera. The addition of transmission dispersing optics converts the coronagraph into a low-resolution spectrograph. The instrument is modular and portable for transport to different observatories.

Use of optical fibers in spectrophotometry

Science.gov (United States)

Ramsey, Lawrence W.

1988-01-01

The use of single or small numbers of fiber optic fibers in astronomical spectroscopy with the goal of greater spectrophotometric and radial velocity accuracy is discussed. The properties of multimode step index fibers which are most important for this application are outlined, as are laboratory tests of currently available fibers.

Direct Computation on the Kinetic Spectrophotometry

DEFF Research Database (Denmark)

Hansen, Jørgen-Walther; Broen Pedersen, P.

1974-01-01

This report describes an analog computer designed for calculations of transient absorption from photographed recordings of the oscilloscope trace of the transmitted light intensity. The computer calculates the optical density OD, the natural logarithm of OD, and the natural logarithm of the diffe...

Spectrophotometric determination of phenylpropanolamine in dosage forms using dimethylaminobenzaldehyde as a derivatizing reagent

International Nuclear Information System (INIS)

Rind, F.M.A.; Khushawar, M.Y.

2000-01-01

Phenylpropanolamine (PPA) was extracted from slightly alkaline medium in chloroform, derivatized with dimethylaminobenzaldehyde (DAB) and determined by spectrophotometry at 377 nm. Beer's law was obeyed for 4.5-13.5 mu g. After the extraction of PPA in organic phase, paracetamole remaining in the aqueous phase could also be determined by spectrophotometry at 291 nm. The method was applied for the determination of PPA and paracetamole in the pharmaceutical preparations. Tavagyl-D, sinulab and Panadol labels with RSD within 0.4-0.8%. (author)

The analysis of anode sludges, and their process solutions and beneficiation products

International Nuclear Information System (INIS)

Dixon, K.; Russell, G.M.; Wall, G.J.; Eddy, B.T.; Mallett, R.C.; Royal, S.J.

1979-01-01

As previous methods for the analysis of anode slimes have required lengthy separations, instrumental procedures were developed that require no preparation of the sample or only simple procedures such as acid digestion and fusion. Comparative values for various techniques are given. Methods for the analysis of process solutions and beneficiation products are examined and the procedures that have been adopted together with their relative merits and applicability are discussed. Methods of analysis include: atomic-absorption spectrophotometry, x-ray-fluorescence spectrophotometry, x-ray-fluorescence spectrometry, instrumental neutron-activation analysis and optical emission spectrometry

Geology and geochemistry of Massangana Granitoid Complex, Brazil, and its relation with tin mineralization

International Nuclear Information System (INIS)

Romanini, S.J.

1982-01-01

The geochemical and petroLogical characteristics of the Massangana Granitoid Complex, situated in the Rondonia Federal Territory, Brazil, aiming to discriminate the tin mineralized granitic rocks from the no mineralized ones. The collected samples consists of examples in tin mineralized and sterile phases. The elements traces were determined by x-ray fluorescence analysis, emission spectrography, molecular absorption spectrophotometry and atomic absorption spectrophotometry. The complex edifying evolved in four sucessive episodes called Massangana Phase, Bom Jardim Phase, Sao domingos Phase and Taboca Phase ordered stratigraphycally in this sequence. (author/M.C.K.) [pt

Indocyanine green plasma disappearance rate during the anhepatic phase of orthotopic liver transplantation.

Science.gov (United States)

Bruegger, Lukas; Studer, Peter; Schmid, Stefan W; Pestel, Gunther; Reichen, Juerg; Seiler, Christian; Candinas, Daniel; Inderbitzin, Daniel

2008-01-01

Non-invasive pulse spectrophotometry to measure indocyanine green (ICG) elimination correlates well with the conventional invasive ICG clearance test. Nevertheless, the precision of this method remains unclear for any application, including small-for-size liver remnants. We therefore measured ICG plasma disappearance rate (PDR) during the anhepatic phase of orthotopic liver transplantation using pulse spectrophotometry. Measurements were done in 24 patients. The median PDR after exclusion of two outliers and two patients with inconstant signal was 1.55%/min (95% confidence interval [CI]=0.8-2.2). No correlation with patient age, gender, body mass, blood loss, administration of fresh frozen plasma, norepinephrine dose, postoperative albumin (serum), or difference in pre and post transplant body weight was detected. In conclusion, we found an ICG-PDR different from zero in the anhepatic phase, an overestimation that may arise in particular from a redistribution into the interstitial space. If ICG pulse spectrophotometry is used to measure functional hepatic reserve, the verified average difference from zero (1.55%/min) determined in our study needs to be taken into account.

An appraisal of neutron activation analysis and other analytical techniques for the determination of arsenic, selenium and tin in environmental samples

International Nuclear Information System (INIS)

Peterson, P.J.; Girling, C.A.; Klumpp, D.W.; Minski, M.J.

1979-01-01

The paper presents an experimental comparison between neutron activation analysis, atomic absorption spectrophotometry and fluorescence spectrophotometry used for the determination of trace amounts of As, Se and Sn and the other two analytical techniques mentioned. Gamma-ray spectrometry has been used to determine 76 As (tsub(1/2)=26.3 h) after 1 day's irradiation at a thermal neutron flux of 1.6x10 12 n.cm -2 .s -1 . High sensitivity was also obtained using an atomic absorption spectrophotometer coupled with covalent hydride generation. Advantages of the latter technique include simplicity of operation, high speed of analysis and negligible background correction. When used in conjuction with selective reduction and a cold-trap this method quantitatively distinguishes between the valence states and some methylated derivatives. Selenium has been analysed by gamma-ray spectrometry using 77 Sesup(m) (tsub(1/2)=17.5 s) after cyclic activation at a thermal neutron flux of 2x10 12 n.cm -2 .s -1 . Atomic absorption spectrophotometry following hydride generation, or fluorescence spectrophotometry of the 2,3 diaminonaphthalene complex constitute additional sensitive analytical methods for the determination of Se. These have the added advantage that valence states can be selectively measured. Low concentrations of Sn have been determined by neutron activation analysis and by spectrophotometric techniques using phenylfluorone as the complexing reagent, but these methods depend on selective extraction of Sn(IV) iodide. Whilst maintaining high sensitivity, these problems were avoided by using the hydride generation technique with an atomic absorption spectrophotometer. Comparative analytical values for Bowen's kale and NBS orchard leaves are presented

Standardisation Study of Kwatha Curnas

Directory of Open Access Journals (Sweden)

M. K. Santosh

2004-01-01

Full Text Available The present paper deals with the standardization of kwatha curnas such as dhanyapanchak kwatha curna, guduchyadigana kwatha curna and stanyajanankashaya curna. These are the important Ayurvedic formulations used for peri-natal care of mother and child health. Standardization of kwatha curnas were achieved by physico-chemical analysis, qualitative inorganic and organic analysis, thin layer chromatography (TLC, UV- visible spectrophotometry and high performance liquid chromatographic (HPLC fingerprint studies. TLC study of kwatha curnas was carried out in Ethyl acetate: Methanol: Water solvent system. Ethanol extracts of kwatha curnas were used for UV- visible spectrophotometry and qualitative HPLC fingerprint study.

Determination of light rare earths and other elements in Cuban soils

International Nuclear Information System (INIS)

Lam Ramos, P.; Frias Fonseca, D.J.; Gonzalez Garcia, M.A.; Aguiar Lambert, D.E.; Estevez Alvarez, J.R.; Pupo Gonzalez, I.; Lopez Sanchez, D.R.

2001-01-01

The objective of the present study was the elaboration of a procedure for the determination of Y, La, Ce, Pr and Nd in soils by spectrophotometry with Arsenazo III preceded by a separation-concentration stage, which includes coprecipitation and ion exchange. Multielement analysis by energy dispersive X-ray fluorescence (including Y, La, Ce and Nd) and flame atomic absorption spectrophotometry was carried out simultaneously in order to obtain a general characterization of the soil samples. Certified reference materials and statistical intercomparison of the obtained results were used to evaluate the accuracy of the methods. The precision was examined by analyzing replicate samples. (author)

Spectral and spectral-frequency methods of investigating atmosphereless bodies of the Solar system

International Nuclear Information System (INIS)

Busarev, Vladimir V; Prokof'eva-Mikhailovskaya, Valentina V; Bochkov, Valerii V

2007-01-01

A method of reflectance spectrophotometry of atmosphereless bodies of the Solar system, its specificity, and the means of eliminating basic spectral noise are considered. As a development, joining the method of reflectance spectrophotometry with the frequency analysis of observational data series is proposed. The combined spectral-frequency method allows identification of formations with distinctive spectral features, and estimations of their sizes and distribution on the surface of atmospherelss celestial bodies. As applied to investigations of asteroids 21 Lutetia and 4 Vesta, the spectral frequency method has given us the possibility of obtaining fundamentally new information about minor planets. (instruments and methods of investigation)

Studies on antifungal activity and elemental composition of the medicinal plant trianthema pentendra linn

International Nuclear Information System (INIS)

Pirzada, A.J.; Shaikh, W.; Ghaffar, S.A.

2010-01-01

Antifungal activity of crude solvent and aqueous extracts of the medicinal plant, Trianthema pentendra Linn., against the dermatophytic fungi, Aspergillus niger, Aspergillus flavus, Paecilomyces varioti, Microsporum gypseum and Trichophyton rubrum revealed that ethanol and aqueous extracts were the most effective antifungal agents as compared to methanol, chloroform and ethyl acetate extracts. Some basic elements, Al, Ca, Cu, Fe, Mg, Mn, P, S and Zn were also determined in the medicinal plant, T. pentendra, using atomic absorption spectrophotometry and U.V spectrophotometry. T. pentendra contained considerable amount of elements which have therapeutic effects in skin diseases. (author)

High-pressure-high-temperature treatment of natural diamonds

CERN Document Server

Royen, J V

2002-01-01

The results are reported of high-pressure-high-temperature (HPHT) treatment experiments on natural diamonds of different origins and with different impurity contents. The diamonds are annealed in a temperature range up to 2000 sup o C at stabilizing pressures up to 7 GPa. The evolution is studied of different defects in the diamond crystal lattice. The influence of substitutional nitrogen atoms, plastic deformation and the combination of these is discussed. Diamonds are characterized at room and liquid nitrogen temperature using UV-visible spectrophotometry, Fourier transform infrared spectrophotometry and photoluminescence spectrometry. The economic implications of diamond HPHT treatments are discussed.

Fourier Transform Methods. Chapter 4

Science.gov (United States)

Kaplan, Simon G.; Quijada, Manuel A.

2015-01-01

This chapter describes the use of Fourier transform spectrometers (FTS) for accurate spectrophotometry over a wide spectral range. After a brief exposition of the basic concepts of FTS operation, we discuss instrument designs and their advantages and disadvantages relative to dispersive spectrometers. We then examine how common sources of error in spectrophotometry manifest themselves when using an FTS and ways to reduce the magnitude of these errors. Examples are given of applications to both basic and derived spectrophotometric quantities. Finally, we give recommendations for choosing the right instrument for a specific application, and how to ensure the accuracy of the measurement results..

Applied spectrophotometry: analysis of a biochemical mixture.

Science.gov (United States)

Trumbo, Toni A; Schultz, Emeric; Borland, Michael G; Pugh, Michael Eugene

2013-01-01

Spectrophotometric analysis is essential for determining biomolecule concentration of a solution and is employed ubiquitously in biochemistry and molecular biology. The application of the Beer-Lambert-Bouguer Lawis routinely used to determine the concentration of DNA, RNA or protein. There is however a significant difference in determining the concentration of a given species (RNA, DNA, protein) in isolation (a contrived circumstance) as opposed to determining that concentration in the presence of other species (a more realistic situation). To present the student with a more realistic laboratory experience and also to fill a hole that we believe exists in student experience prior to reaching a biochemistry course, we have devised a three week laboratory experience designed so that students learn to: connect laboratory practice with theory, apply the Beer-Lambert-Bougert Law to biochemical analyses, demonstrate the utility and limitations of example quantitative colorimetric assays, demonstrate the utility and limitations of UV analyses for biomolecules, develop strategies for analysis of a solution of unknown biomolecular composition, use digital micropipettors to make accurate and precise measurements, and apply graphing software. Copyright © 2013 Wiley Periodicals, Inc.

Moderate resolution spectrophotometry of high redshift quasars

Science.gov (United States)

Schneider, Donald P.; Schmidt, Maarten; Gunn, James E.

1991-01-01

A uniform set of photometry and high signal-to-noise moderate resolution spectroscopy of 33 quasars with redshifts larger than 3.1 is presented. The sample consists of 17 newly discovered quasars (two with redshifts in excess of 4.4) and 16 sources drawn from the literature. The objects in this sample have r magnitudes between 17.4 and 21.4; their luminosities range from -28.8 to -24.9. Three of the 33 objects are broad absorption line quasars. A number of possible high redshift damped Ly-alpha systems were found.

Spectrophotometry of six broad absorption line QSOs

Science.gov (United States)

Junkkarinen, Vesa T.; Burbidge, E. Margaret; Smith, Harding E.

1987-01-01

Spectrophotometric observations of six broad absorption-line QSOs (BALQSOs) are presented. The continua and emission lines are compared with those in the spectra of QSOs without BALs. A statistically significant difference is found in the emission-line intensity ratio for (N V 1240-A)/(C IV 1549-A). The median value of (N V)/(C IV) for the BALQSOs is two to three times the median for QSOs without BALs. The absorption features of the BALQSOs are described, and the column densities and limits on the ionization structure of the BAL region are discussed. If the dominant ionization mechanism is photoionization, then it is likely that either the ionizing spectrum is steep or the abundances are considerably different from solar. Collisional ionization may be a significant factor, but it cannot totally dominate the ionization rate.

Spectrophotometry of nearby field galaxies : The data

NARCIS (Netherlands)

Jansen, RA; Fabricant, D; Franx, M; Caldwell, N

We have obtained integrated and nuclear spectra as well as U, B, R surface photometry for a representative sample of 196 nearby galaxies. These galaxies span the entire Hubble sequence in morphological type, as well as a wide range of luminosities (M(B) = -14 to -22). Here we present the

Determining Iron Content in Foods by Spectrophotometry.

Science.gov (United States)

Adams, Paul E.

1995-01-01

Describes a laboratory experiment for secondary school chemistry students utilizing the classic reaction between the iron(III) ion and the thiocyanate ion. The experiment also works very well in other chemistry courses as an experience in spectrophotometric analysis. (PVD)

Spectrophotometry of seventeen comets. II - The continuum

Science.gov (United States)

Newburn, R. L., Jr.; Spinrad, H.

1985-01-01

One-hundred-twenty IDS scans of the continua in 17 comets are analyzed to determine dust production rates and color as a function of heliocentric distance. Improved theory indicates that the dust loading of gas typically varies between 0.05 and 0.3 by mass (assuming a geometric albedo of 0.05 and oxygen expansion at 1 km/s) except during outbursts, when it rises much higher. P/Encke near perihelion falls much lower yet, to 0.004 or less. Dust loading is not always constant as a function of time in a given comet. Dust color is typically reddish, as has often been noted before.

Far ultraviolet spectrophotometry of BD +28 4211

Science.gov (United States)

Cook, Timothy A.; Cash, Webster; Green, James C.

1991-01-01

The results are reported of a November 1989 rocket flight which recorded a flux-calibrated spectrum of BD +28 4211 from 912 to 1150 A with 1A resolution. BD +28 4211, an SdO-type star, is commonly used as an ultraviolet calibration source in the IUE wavelength band. The present work extends the useful range of this standard shortward of Lyman-alpha. Since previous experiments show marked disparity, this study can be useful in determining a standard in the 912 to 1216 A band.

Occultation Spectrophotometry of Extrasolar Planets with SOFIA

Science.gov (United States)

Angerhausen, Daniel; Huber, Klaus F.; Mandell, Avi M.; McElwain, Michael W.; Czesla, Stefan; Madhusudhan, Nikku

2012-01-01

The NASA/DLR Stratospheric Observatory for Infrared Astronomy (SOFIA), a 2.5- meter infrared telescope on board a Boeing 747-SP, will conduct 0.3 - 1,600 micrometer photometric, spectroscopic, and imaging observations from altitudes as high as 45,000 ft., where the average atmospheric transmission is greater than 80 percent. SOFIA's first light cameras and spectrometers, as well as future generations of instruments, will make important contributions to the characterization of the physical properties of exoplanets. Our analysis shows that optical and near-infrared photometric and spectrophotometric follow-up observations during planetary transits and eclipses will be feasible with SOFIA's instrumentation, in particular the HIPOFLITECAM optical/NIR instruments. The airborne-based platform has unique advantages in comparison to ground- and space-based observatories in this field of research which we will outline here. Furthermore we will present two exemplary science cases, that will be conducted in SOFIA's cycle 1.

Applied Spectrophotometry: Analysis of a Biochemical Mixture

Science.gov (United States)

Trumbo, Toni A.; Schultz, Emeric; Borland, Michael G.; Pugh, Michael Eugene

2013-01-01

Spectrophotometric analysis is essential for determining biomolecule concentration of a solution and is employed ubiquitously in biochemistry and molecular biology. The application of the Beer-Lambert-Bouguer Lawis routinely used to determine the concentration of DNA, RNA or protein. There is however a significant difference in determining the…

Differential NICMOS Spectrophotometry at High S/N

Science.gov (United States)

Gilliland, Ronald L.

2006-01-01

Transiting extrasolar planets present an opportunity for probing atmospheric conditions and constituents by taking advantage of different apparent radii, hence transit depth as a function of wavelength. Strong near-IR bands should support detection of water vapor via G141 spectroscopy of the bright star HD 209458 (H=6.13) by comparing in- and out-of-transit ratios of in- and out-of-band spectral intensity ratios. The reduction and analysis of science observations in which the goal is to support 1 part in 10,000, or better, development of spectral diagnostics using NICMOS grism-based spectroscopy is discussed.

Spectrophotometry of Epsilon Aur, 3295-8880 A

Science.gov (United States)

Lockwood, G. W.; Thompson, D. T.; Lutz, B. L.; Sowell, J.

1985-01-01

Spectrophotometric scans were obtained at 8 A resolution from 3295 to 8880 A on twenty nights before, during, and after the recent eclipse of epsilon Aurigae, beginning with a pre-eclipse observation on 5 March 1982 U.T. The observations were reduced to absolute flux using the standard stars 109 Vir or xi(2) Ceti. The data confirm that the eclipse is essentially gray over the entire visible spectrum, as others have noted from broadband photometry. High resolution echellograms (450 to 6700 A) made through mid-eclipse and the scans show changes in the equivalent widths of H alpha, Na D, and O I as large as a factor of two.

Spectrophotometry of Dust in Comet Hale-Bopp

Science.gov (United States)

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".

Near-Infrared Spectrophotometry of Phobos and Deimos

Science.gov (United States)

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

2002-01-01

We have observed the leading and trailing hemispheres of Phobos from 1.65 to 3.5 microns and Deimos from 1.65 to 3.12 microns near opposition. We find the trailing hemisphere of Phobos to be brighter than its leading hemisphere by 0.24 +/- 0.06 magnitude at 1.65 microns and brighter than Deimos by 0.98 +/- 0.07 magnitude at 1.65 microns. We see no difference larger than observational uncertainties in spectral slope between the leading and trailing hemispheres when the spectra are normalized to 1.65 microns. We find no 3-microns absorption feature due to hydrated minerals on either hemisphere to a level of approx. 5 - 10% on Phobos and approx. 20% on Deimos. When the infrared data are joined to visible and near-IR data obtained by previous workers, our data suggest the leading (Stickney-dominated) side of Phobos is best matched by T-class asteroids. The spectral slope of the trailing side of Phobos and leading side of Deimos are bracketed by the D-class asteroids. The best laboratory spectral matches to these parts of Phobos are mature lunar soils and heated carbonaceous chondrites. The lack of 3-microns absorption features on either side of Phobos argues against the presence of a large interior reservoir of water ice according to current models of Phobos' interior.

Determination of boron spectrophotometry in thorium sulfate

International Nuclear Information System (INIS)

Federgrun, L.; Abrao, A.

1976-01-01

A procedure for the determination of microquantities of boron in nuclear grade thorium sulfate is described. The method is based on the extraction of BF - 4 ion associated to monomethylthionine (MMT) in 1,2 - dichloroethane. The extraction of the colored BF - 4 -MMT complex does not allow the presence of sulfuric and phosphoric acids; other anions interfere seriously. This fact makes the dissolution of the thorium sulfate impracticable, since it is insoluble in both acids. On the other hand, the quantitative separation of thorium is mandatory, to avoid the precipitation of ThF 4 . To overcome this difficulty, the thorium sulfate is dissolved using a strong cationic ion exchanger, Th 4+ being totally retained into the resin. Boron is then analysed in the effluent. The procedure allows the determination of 0.2 to 10.0 microgramas of B, with a maximum error of 10%. Thorium sulfate samples with contents of 0.2 to 2.0μg B/gTh have being analysed [pt

Contribution to Casein Determination by UV Spectrophotometry

Directory of Open Access Journals (Sweden)

Stefanescu Raluca

2017-12-01

Full Text Available In the present paper, the interaction between copper ions and proteins is presented, in order to elaborate a simple and rapid spectrophotometric assay of casein in milk. Under alkaline conditions, copper ions form the biuret complex with the proteins, which can be used in protein determination. Although very specific, the biuret method is less sensitive. Using insoluble copper phosphate, casein is able to extract copper ions, with which it forms the biuret complex, while either the complex or copper ions could be determined in the ultraviolet range. Indeed, an increased absorbance of biuret complex at 215 nm was found. Nevertheless, copper ions can be determined in UV as well, their concentration being proportional to that of casein. When used tetraglycine instead casein, mass spectrometric measurements at pH higher than 11 revealed the formation of complexes with many copper ions bound to each peptide bond-containing molecule. Nevertheless, on diluting the biuret solution the complex may dissociate leading to very complex UV spectra that should be further studied.

Chemical, mass spectrometric, and spectrochemical analysis of nuclear-grade mixed oxides [(U,Pu)O2

International Nuclear Information System (INIS)

Anon.

1981-01-01

Mixed oxide, a mixture of uranium and plutonium oxides, is used as a nuclear-reactor fuel in the form of pellets. The plutonium content may be up to 10 wt %, and the diluent uranium may be of any U-235 enrichment. In order to be suitable for use as a nuclear fuel, the material must meet certain criteria for combined uranium and plutonium content, effective fissile content, and impurity content. Analytical procedures used to determine if mixed oxides comply with specifications are: uranium by controlled-potential coulometry; plutonium by controlled-potential coulometry; plutonium by amperometric titration with iron (II); nitrogen by distillation spectrophotometry using Nessler reagent; carbon (total) by direct combustion-thermal-conductivity; total chlorine and fluorine by pyrohydrolysis; sulfur by distillation-spectrophotometry; moisture by the coulometric, electrolytic moisture analyzer; isotopic composition by mass spectrometry; rare earths by copper spark spectroscopy; trace impurities by carrier distillation spectroscopy; impurities by spark-source mass spectrography; total gas in reactor-grade mixed dioxide pellets; tungsten by dithiol-spectrophotometry; rare earth elements by spectroscopy; plutonium-238 isotopic abundance by alpha spectrometry; uranium and plutonium isotopic analysis by mass spectrometry; oxygen-to-metal atom ratio by gravimetry

The use of xylenol orange (XO) reagent in molybdenum (MO) analysis

International Nuclear Information System (INIS)

Yusuf Nampira; Dian Anggraini

2012-01-01

The use of xylenol orange (XO) reagent in the analysis of Molybdenum (Mo) by spectrophotometry have been studied. The aim of this activity is to study the ability of xylenol orange to form a compound of molybdenum-xylenol orange complex to be analyzed by spectrophotometry. Some factors influencing the forming of the complex compound, for instance pH, time, comparison of XO/MO and the amount of Mo, are also studied. The materials used in this research includes ammonium molybdate (NH 4 ) 6 Mo 7 O 24 .4H 2 O), 0,5% xylenol orange and buffer solution (pH 1,5). Measurement result indicates that molybdenum content can be determined by spectrophotometry method at a wavelength of 563,6 nm. The maximum absorbance reached at a ratio of Molybdenum/Xylenol orange 1:2. The concentration of Mo was determined by using law of Lambert Beer, which stayed in the range of 2 ppm to 4 ppm. The stability of complex compound of molybdenum xylenol orange was shorter than 5 minutes. This measurement result can be used as a parameter in the determination of Mo element with UV-VIS spectrophotometer. (author)

Hydrolysis of Zr(4) with formation of mono- and polynuclear hydroxocomplexes in solutions

International Nuclear Information System (INIS)

Davydov, Yu.P.; Zabrodskij, V.N.

1987-01-01

The state of Zr(4) has been studied in the wide range of H + -ions concentrations (10 -3 -3.0 mol/l) and in the wide range of Zr(4) concentrations (10 -13 -10 -12 mol/l) in the solution using a set of such physical-chemical methods as spectrophotometry, ion exchange, dialysis, centrifugation. The conditions of formation of hydrated cations, monochange, dialysis, centrifugation. The conditions of formation of hydrated cations, mono- and polynuclear hydrocomplexes, colloidal-size particles have been determined. The thermodynamic stability of ZrOH 3+ and Zr(OH) 2 2+ complexes has been determined by the ion exchange and spectrophotometry methods

Development and validation of a dissolution test for diltiazem hydrochloride in immediate release capsules

Directory of Open Access Journals (Sweden)

Taciane Ferreira Mendonça

2011-01-01

Full Text Available This work describes the development and validation of a dissolution test for 60 mg of diltiazem hydrochloride in immediate release capsules. The best dissolution in vitro profile was achieved using potassium phosphate buffer at pH 6.8 as the dissolution medium and paddle as the apparatus at 50 rpm. The drug concentrations in the dissolution media were determined by UV spectrophotometry and HPLC and a statistical analysis revealed that there were significant differences between HPLC and spectrophotometry. This study illustrates the importance of an official method for the dissolution test, since there is no official monograph for diltiazem hydrochloride in capsules.

Chemical methods of rock analysis

National Research Council Canada - National Science Library

Jeffery, P. G; Hutchison, D

1981-01-01

.... Such methods include those based upon spectrophotometry, flame emission spectrometry and atomic absorption spectroscopy, as well as gravimetry, titrimetry and the use of ion-selective electrodes...

Determination of lithium, rubidium and strontium in foodstuffs

International Nuclear Information System (INIS)

Evans, W.H.; Read, J.I.

1985-01-01

For the determination of total lithium, rubidium and strontium in foodstuffs the organic matter is destroyed by a wet-oxidation procedure. Both lithium and rubidium are measured by flame atomic-emission spectrophotometry, rubidium with the addition of a radiation buffer and strontium is measured by flame atomic-absorption spectrophotometry using the same radiation buffer. The optimum conditions for measurement are described and interferences noted. The accuracy of the method was assessed by measuring the recovery of these metals from foodstuff homogenates and values for standard reference materials are listed, for comparison with certified levels where these exist. From the results obtained standard deviations were calculated and derived limits of detection and confidence intervals are given. (author)

Solid-phase extraction and high-performance liquid chromatographic separation of pigments of red wines.

Science.gov (United States)

Csiktusnádi Kiss, G A; Forgács, E; Cserháti, T; Candeias, M; Vilas-Boas, L; Bronze, R; Spranger, I

2000-08-11

The adsorption and desorption capacities of 11 different solid-phase extraction sorbents were tested for the preconcenration of pigments of various Hungarian red wines. The concentrates were evaluated by multiwavelengh spectrophotometry combined with a spectral mapping technique (SPM) and by reversed-phase high-performance liquid chromatography. The highest (10-fold) concentration of pigments was achieved on octadecylsilica sorbent. It can be used five times without losing adsorption and desorption characteristics. SPM indicated that multiwavelength spectrophotometry can be employed for the differentiation of red wines. Comparison of the chromatograms of pigments with and without preconcentration showed that preconcentration makes possible the separation and detection of pigments present in low concentration in red wines.

EPA Method 3135.2I: Cyanide, Total and Amenable in Aqueous and Solid Samples Automated Colorimetric With Manual Digestion

Science.gov (United States)

This method describes procedures for preparation and analysis of solid, water and wipe samples for detection and measurement of cyanide amendable to chlorination using acid digestion and spectrophotometry.

Diseño y validación de un método espectrofotométrico para el control de calidad del piroxicam jalea 0,5 % Design and validation of a spectrophotometry method used in quality control of a 0,5 % Piroxican jelly

Directory of Open Access Journals (Sweden)

Yania Suárez Pérez

2009-12-01

Full Text Available La jalea de piroxicam al 0,5 % es un nuevo producto en fase de desarrollo de la Empresa Laboratorio "Roberto Escudero Díaz". En el presente trabajo se diseñó un método por espectrofotometría UV, para lo cual se empleó ácido clorhídrico etanólico como disolvente y 328 nm como longitud de onda de máxima absorción. Se estableció un procedimiento simple y rápido para procesar la muestra previa al análisis. Posteriormente se aplicó la validación de este según exigencias regulatorias actuales. El método resultó suficientemente específico, lineal, preciso y exacto en el rango de 3,125 a 9,375 µg/mL. Se aplicó a la cuantificación del principio activo en 3 lotes de la formulación desarrollada, con resultados satisfactorios sin diferencias estadísticamente significativas según el procesamiento aplicado.The 0.5 % jelly Piroxican is a new product in developing phase from "Roberto Escudero Díaz" Laboratory Enterprise. In present paper a UV spectrophotometry method was designed using ethanol chloride acid as solvent and 328 nm as maximal absorption wave length. A simple and fast procedure was established to processing the sample previous to analysis. Subsequently, we applied the validation of it according current regulatory demands. Method was enough specific, linear, precise and exact at the 3.125 to 9.375 µg/mL. Active principle quantification was applied in three batches of developed formula achieving satisfactory results without statistically significant differences according the applied procedure.

Synthesis, characterization and pharmacological evaluation of ...

African Journals Online (AJOL)

microscope (SEM), mass spectrometry (EI-MS), ultraviolet-visible (UV-Vis) spectrophotometry, ... The new compounds were also investigated for their alkaline phosphatase (ALPs) inhibition, .... The antimicrobial properties of OMZ, HQL and.

Spectrophotometric Determination of Cilostazol in Tablet Dosage Form

African Journals Online (AJOL)

Erah

Purpose: To develop simple, rapid and selective spectrophotometric methods for ... Conclusion: These validated methods may be useful for routine analysis of cilostazol ... Keywords: Cilostazol tablets, UV spectrophotometry, Linear regression ...

First studies of lead pollution in Guanabara

International Nuclear Information System (INIS)

Silveira Branquinho, C.L. da.

1973-01-01

The main sources of direct lead intake are studied, and metal concentrations in several medium are examined. Lead was extracted by dithizone in C Cl 4 , being determined by optical spectrophotometry. 2 1 2 Pb was used as a radioactive tracer in low concentration measurements of the metal, and analysis of its 239 KeV peak was done by a Ge-Li detector. In blood samples, the metal was complexed and extracted with APDC in MIBK, being measured by flame less atomic absorption spectrophotometry. Air samples were also collected for periods of 24 hours and 90 minutes. Representative street dust samples were examined, showing a strict correlation with lead in air. It was also estimated the amount of lead in some human blood samples. (author)

Contribution to the study of uranium migration and some trace elements in solution from Pocos de Caldas uranium mining

International Nuclear Information System (INIS)

Zenaro, R.

1989-01-01

It was studied the chemical composition of ground water from four boreholes as a contribution to the hydrogeochemical studies in the Pocos de Caldas uranium mining. Methods for water analyses were selected and optimized in order to determine the main anions, specially the ones which form stable complexes with uranium ions. Fluoride and chloride were determined by potentiometry; phosphate, nitrate and silicate by spectrophotometry. Cations were determined by atomic absorption spectrophotometry flame emission and argon plasma emission excited by continuous current arch (DCP). Uranium was determined by fluorimetry with a concentration range from 3 to 7 ppb and its distribution calculated among the different species into solution through the measures of pH, Eh, anion amounts and stability of their respective complexes. (author) [pt

Fundamental studies to develop certified reference material to calibrate spectrophotometer in the ultraviolet region

International Nuclear Information System (INIS)

Da Conceição, F C; Borges, P P; Gomes, J F S

2016-01-01

Spectrophotometry is the technique used in a great number of laboratories around the world. Quantitative determination of a high number of inorganic, organic and biological species can be made by spectrophotometry using calibrated spectrophotometers. International standards require the use of optical filters to perform the calibration of spectrophotometers. One of the recommended materials is the crystalline potassium dichromate (K_2Cr_2O_7), which is used to prepare solutions in specific concentrations for calibration or verification of spectrophotometers in the ultraviolet (UV) spectral regions. This paper presents the results concerning the fundamental studies for developing a certified reference material (CRM) of crystalline potassium dichromate to be used as standard of spectrophotometers in order to contribute to reliable quantitative analyses. (paper)

ECO-FRIENDLY SYNTHESIS OF SILVER NANOPARTICLES ...

African Journals Online (AJOL)

userpc

Keywords: Silver nanoparticles; UV-Visible Spectrophotometry; Dynamic Light Scattering;. Transmission ... The eco- friendly protocol developed led to the synthesis ... lamp for. 5 minutes. (Omidiet al.,. 2014).Authentication of the formation of.

Facile growth of Ag@Pt bimetallic nanorods on electrochemically ...

Indian Academy of Sciences (India)

ppm in industrial and in agricultural effluents.6 Due to its toxicity and industrial significance, the accu- ... spectrophotometry, ion chromatography, chemilumi- nescence and titrimetry ... solutions were prepared using deionized (DI) water.

The use of spectrophotometry in FBR reprocessing analysis

International Nuclear Information System (INIS)

Brown, M.L.; Mills, C.L.; Kyffin, T.W.

1986-09-01

The spectrophotometric methods of analysis currently in use at DNPDE are described. It considers the ways in which the problems of containment and physical handling of active solutions have been overcome, and summarises performance of the methods during several PFR fuel reprocessing campaigns. The introduction of a new micro-computer controlled fibre-optic spectrophotometer is considered in terms of its advantages over the existing systems, both in safe sample handling and computational abilities. Its performance is compared with existing methods. Finally, a novel system for measurement of plutonium valency, and americium in plutonium using a ''spectral stripping'' technique, is discussed. The results of this method are compared with those obtained using conventional techniques. (author)

Spectrophotometry of RS Oph during the nebular phase

International Nuclear Information System (INIS)

Bohigas, J.; Echevarria, J.; Diego, F.; Sarmiento, J.A.

1989-01-01

Blue-wavelength spectroscopic observations of RS Oph, 201 day after the 1985 outburst are presented. An analysis of the TiO bands indicates a spectral type M4III for the secondary and a distance of 2 kpc to the system. The system of forbidden lines is excited by a shock wave, whereas Balmer emission is mainly produced by photoionization. The source of photons is probably residual thermonuclear burning occurring at the surface of the white dwarf. (author)

Application of atomic absorption in molecular analysis (spectrophotometry)

International Nuclear Information System (INIS)

Baliza, S.V.; Soledade, L.E.B.

1981-01-01

The apparatus of atomic absorption has been considered by all the experts in chemical analysis as one of the most important equipments in actual utilization in such field. Among its several applications one should emphasize direct and indirect metals analyses using flame, graphite furnace, cold vapor generator,... Besides such known applications, the authors have developed at the R and D Center of CSN a patent pendent method for the utilization of such equipment for molecular analysis, in substitution of a sophisticated and specific apparatus. (Author) [pt

Broad-band spectrophotometry of HAT-P-32 b

DEFF Research Database (Denmark)

Mallonn, M.; Bernt, I.; Herrero, E.

2016-01-01

Multicolour broad-band transit observations offer the opportunity to characterize the atmosphere of an extrasolar planet with small- to medium-sized telescopes. One of the most favourable targets is the hot Jupiter HAT-P-32 b. We combined 21 new transit observations of this planet with 36 previou...... makes a recent tentative detection of a scattering feature less likely. Instead, the available spectral measurements of HAT-P-32 b favour a completely flat spectrum from the near-UV to the near-IR. A plausible interpretation is a thick cloud cover at high altitudes....

Spectrophotometry of ring nebulae around Wolf-Rayet stars

International Nuclear Information System (INIS)

Kwitter, K.B.

1979-01-01

Spectrophotometric observations of four ring nebulae surrounding population I Wolf-Rayet (WN) stars have been obtained, and four additional filamentary nebulae in order to determine the physical conditions and chemical abundances in these objects. It was concluded that the ring nebulae are enriched in nitrogen and helium as a result of contamination of the ambient interstellar medium by the helium- and nitrogen-rich wind from the central Wolf-Rayet star. Of the additional nebulae studied, two were found to be Peimbert Type I planetary nebulae, overabundant in nitrogen and helium due to mixing of CNO processed material into the parent envelope prior to ejection. One of the remaining objects, a shell around an Oef star, is found to have normal abundances; the other, a small H II region around an early Be star, also exhibits normal abundances. It was attempted to interpret the ring nebulae and the Oef shell as interstellar bubbles, according to recent theory; it met with varying degrees of success. For two of the ring nebulae, the fraction of nebular mass contributed by the central star can be estimated from published stellar abundances. It was found that in these two cases, the stellar wind has provided less than 10% of the observed nebular mass

Spatially resolved spectrophotometry of Comet P/Stephan-Oterma

Science.gov (United States)

Cochran, A. L.; Barker, E. S.

1985-01-01

Observations of Comet P/Stephan-Oterma were made with an Intensified Dissector Scanner spectrograph on the McDonald Observatory 2.7-m telescope during the period from July 1980 to February 1981. These spectra cover a range of heliocentric distances from 2.3 AU preperihelion to 1.8 AU postperihelion. A small aperture was used to map the spatial distributions of the gases in the coma. Column densities of the observed cometary emissions (CN, C3, CH, and C2) were calculated, and it is shown that Stephan-Oterma appeared nearly spherically symmetric. These date are used by Cochran (1985) to constrain chemical models of Stephan-Oterma.

Spectrophotometry at 10 microns of T Tauri stars

Science.gov (United States)

Cohen, M.; Witteborn, F. C.

1985-01-01

New 8-13 micron spectra of 32 T Tau, or related young, stars are presented. Silicate emission features are commonly seen. Absorptions occur less frequently but also match the properties of silicate materials. The shape of the emission feature suggests that a more crystalline grain is responsible in the T Tau stars than those of the Trapezium region. The evolution of the silicate component of the circumstellar shell around T Tau stars, and its dependence upon stellar wind activity, visual linear polarization, and extinction are investigated. Several correlations suggest that the shells are likely to be flattened, disklike structures rather than spherical.

Applications of FT-IR spectrophotometry in cancer diagnostics.

Science.gov (United States)

Bunaciu, Andrei A; Hoang, Vu Dang; Aboul-Enein, Hassan Y

2015-01-01

This review provides a brief background to the application of infrared spectroscopy, including Fourier transform-infrared spectroscopy, in biological fluids. It is not meant to be complete or exhaustive but to provide the reader with sufficient background for selected applications in cancer diagnostics. Fourier transform-infrared spectroscopy (FT-IR) is a fast and nondestructive analytical method. The infrared spectrum of a mixture serves as the basis to quantitate its constituents, and a number of common clinical chemistry tests have proven to be feasible using this approach. This review focuses on biomedical FT-IR applications, published in the period 2009-2013, used for early detection of cancer through qualitative and quantitative analysis.

Spectrophotometry of Pluto from 3500 to 7350 A

International Nuclear Information System (INIS)

Barker, E.S.; Cochran, W.D.; Cochran, A.L.; Texas, University, Austin, Tex.)

1980-01-01

Spectra of Pluto have been obtained on six nights during February 1979 by the use of the Cassegrain Digicon spectrograph on the 2.1-m Struve reflector and the IDS spectrograph on the 2.7-m reflector of McDonald Observatory. These spectra, with nominal resolution of 6-7 A, have been reduced to relative fluxes. Relative albedos were then calculated using the solar irradiances of Arvesen et al. (1969). The spectra taken in the blue show no indication of the upturn in albedo at wavelengths less than 3800 A previously reported by Fix, et al. (1970). The lack of a UV upturn cannot be interpreted in terms of a Rayleigh scattering atmosphere unless the albedo of the underlying surface is known. From the lack of methane absorption at the wavelength of the 6190- or 7270-A methane bands, an upper limit of 1-3 m-am of gaseous CH4 is derived. The albedo curve has a constant slope between 3500 and 7300 A. The only other solar system body which has this feature is an S-type asteroid

Symbiotic binaries. Part 1. Spectrophotometry of AX Persei

International Nuclear Information System (INIS)

Mikolajewska, J.; Iijima, T.

1987-01-01

Secular and eclipse variations of optical emission lines during almost three orbital cycles of the symbiotic star AX Per are presented. The permitted lines show pronounced but nontotal eclipse effects while forbidden lines (i.e. [O3], [Ne3], [Fe7]) do not show such effects. The data are discussed in terms of physical conditions and geometry of the line formation region. The possible presence of the reflection of a hot star light from a red-giant companion is considered. 37 refs., 2 figs., 1 tab. (author)

Absolute spectrophotometry in M31 and M32

International Nuclear Information System (INIS)

Oke, J.B.; Schwarzschild, M.

1975-01-01

For a number of places in the bulge of M31, and for two places in M32, photometric scans from lambda=3300 A to lambda=10,600 A have been obtained with the multichannel spectrometer on the 5-m Hale telescope. The scans show that in both objects the color temperature (particulary shortward of 5000 A) decreases toward the center, and that the strength of the CN bands increases toward the center in both objects, in agreement with other, earlier observations. The new data can all be interpreted in terms of an increase of heavy-element abundance toward the center in both objects by a factor probably less than 2, and by an excess of heavy elements in M31 compard with M32 by a factor probably greater than 2, in qualitative agreement with earlier conclusions of other observers

Abstracts of the 3. Brazilian Meeting on Analytical Chemistry

International Nuclear Information System (INIS)

1985-01-01

Abstracts from experimental research works on analytical chemistry are presented. The following techniques were mainly used: differential pulse polarography, atomic absorption spectrophotometry, ion exchange chromatography and gamma spectroscopy. (C.L.B.) [pt

Determination of Heavy Metals in Leaves of Mangifera Indica ...

African Journals Online (AJOL)

Mango), Psidium guajava L. (Guava) and Anacardium occidentale L. (Cashew) grown in Trikania around the industrial area, were determined by atomic absorption spectrophotometry. The differences in the bioaccumulation of the metals varied.

2774-IJBCS-Article-Oluwafunmilola Elizabeth A

African Journals Online (AJOL)

hp

Keywords: Hydrodistillation, gas chromatography-mass spectrophotometry, terpenoids, esters. ... 'peraroja' in Mexico, 'bien me sube' or 'pan quesito' in ... Ackee seed is a moderate oil seed that could ... Data analysis was done using.

Validated Spectrophotometric Methods for Simultaneous Determination of Food Colorants and Sweeteners

Directory of Open Access Journals (Sweden)

Fatma Turak

2013-01-01

Full Text Available Two simple spectrophotometric methods have been proposed for simultaneous determination of two colorants (Indigotin and Brilliant Blue and two sweeteners (Acesulfame-K and Aspartame in synthetic mixtures and chewing gums without any prior separation or purification. The first method, derivative spectrophotometry (ZCDS, is based on recording the first derivative curves (for Indigotin, Brillant Blue, and Acesulfame-K and third-derivative curve (for Aspartame and determining each component using the zero-crossing technique. The other method, ratio derivative spectrophotometry (RDS, depends on application ratio spectra of first- and third-derivative spectrophotometry to resolve the interference due to spectral overlapping. Both colorants and sweeteners showed good linearity, with regression coefficients of 0.9992–0.9999. The LOD and LOQ values ranged from 0.05 to 0.33 μgmL−1 and from 0.06 to 0.47 μgmL−1, respectively. The intraday and interday precision tests produced good RSD% values (<0.81%; recoveries ranged from 99.78% to 100.67% for all two methods. The accuracy and precision of the methods have been determined, and the methods have been validated by analyzing synthetic mixtures containing colorants and sweeteners. Two methods were applied for the above combination, and satisfactory results were obtained. The results obtained by applying the ZCDS method were statistically compared with those obtained by the RDS method.

Influence of Salicylic Acid on the Antimicrobial Potential of Stevia ...

African Journals Online (AJOL)

extracts determined by gas chromatography-mass spectrophotometry (GC-MS). ... Conclusion: Stevia leaf extract has antimicrobial effect against soybean .... Table 1: Effect of salicylic acid on the oil composition of various Stevia leaf extracts.

In vitro Evaluation of Trimethoprim and Sulfamethoxazole from Fixed ...

African Journals Online (AJOL)

spectrophotometry, Fixed-dose combination generic drugs. Tropical Journal ... without testing their in-vivo performance [4]. In ..... pharmacokinetic parameter such as AUC, Cmax or Tmax. .... granules: factors affecting drug release in vitro. Int J.

Asphalt chemical fractionation

International Nuclear Information System (INIS)

Obando P, Klever N.

1998-01-01

Asphalt fractionation were carried out in the Esmeraldas Oil Refinery using n-pentane, SiO 2 and different mixture of benzene- methane. The fractions obtained were analyzed by Fourier's Transformed Infrared Spectrophotometry (FTIR)

Spectrophotometric studies on the behaviour of plutonium in basic media (Preprint No. CT-36)

International Nuclear Information System (INIS)

Ray, M.; Pius, I.C.; Charyulu, M.M.; Sivaramakrishnan, C.K.

1988-02-01

Behaviour of plutonium in different basic media has been studied using spectrophotometry. Stability of various oxidation states, their interconvertibility and their estimation in basic media have been investigated and results are reported. (author)

A Spectrophotometric Method for the Determination of Ramipril in ...

African Journals Online (AJOL)

HP

Purpose: To develop a simple and cost effective spectrophotometer method for the determination of. ACE inhibitor ramipril in dosage forms. Methods: UV spectrophotometry was used to develop and validate a simple method .... 2003 software.

Experimental Sensing and Density Functional Theory Study of an ...

African Journals Online (AJOL)

NICOLAAS

Moreover, the sensor also demonstrated good stability and acceptable reproducibility for the ... as chromatography,3–6 spectrophotometry,7–9 fluorescence10 in addition ...... for the determination of paracetamol at carbon nanotube modified.

U-Th-Geochemistry of Permian and Triassic sediments of the Drauzug, Carinthia, Austria

International Nuclear Information System (INIS)

Kurat, G.; Korkisch, J.; Niedermayr, G.; Seemann, R.

1976-05-01

Chemical analysis of samples of Triassic and Permian rocks from the Drauzug, Carinthia and Austria was carried out. U concentration was measured by flurimetry, Th and Cu by spectrophotometry using Thoronol method or Arsenazo III method for Th, Fe by titrimetry and V, Ba, Sr by atomic absorption spectrophotometry. The average U concentration ranged from 0.8 to 4.6 ppm and the Th concentration from 3.2 to 15.6 ppm depending upon the mineral material. The quartzporphyries contained the highest concentration of both. It was concluded that the Permian-Triassic series are very similar to the equivalent deposits in Northern Italy. Assuming a lateral displacement, the former represent the Northern marginal part of the latter and therefore are inferior in thickness and thus not favourable for larger U mineralization

FORMULA ESTABLISHMENT OF COLORLESS Pb(II COMPLEX WITH N-BENZOYL-N-PHENYL HYDROXYLAMINE (BPA USING ATOMIC ABSORPTION SPECTROSCOPY

Directory of Open Access Journals (Sweden)

Dhananjay B Sarode

2012-02-01

Full Text Available A new method for determination of stoichiometry of colorless complexes by using atomic absorption spectrophotometric technique in continuous variation method and slope ratio method was described here. This method can be used in same manner as that of mole ratio method and slope ratio method. In this method atomic absorption spectroscopy was used instead of UV-Vis spectrophotometry. Atomic absorption spectrophotometric technique is superior to UV-Vis spectrophotometry as it can be applied to colorless soluble complexes. Pb(II and n-benzoyl-n-phenyl hydroxylamine react to form colorless complex at pH 6.5, which can be easily determined by this method. It was found that Pb(II forms 1:2 complex with n-benzoyl-n-phenyl hydroxylamine and is quantitatively extracted back to aqueous solution for AAS analysis.

Kinetics and mechanism of azo dye destruction in advanced oxidation processes

International Nuclear Information System (INIS)

Wojnarovits, L.; Palfi, T.; Takacs, E.

2007-01-01

The kinetics and mechanism of dye destruction in advanced oxidation processes is discussed on the example of Apollofix Red (Ar-28) radiolysis in aqueous solution. When the reactive intermediate reacts with the color bearing part of the molecule causing with nearly 100% efficiency destruction of the conjugation, the dose dependence, or time dependence of color disappearance is linear. In this case, spectrophotometry can be used to follow-up dye decomposition. Linear dependence was observed when hydrated electrons or hydrogen atoms reacted with the dye. In hydroxyl radical reactions some colored products form with spectra similar to those of the starting dye molecules. For that reason, spectrophotometry gives false result about the intact dye molecule concentration. Analysis by the HPLC reveals logarithmic time dependence in agreement with a theoretical model developed

Manual of analytical methods for the Environmental Health Laboratory

International Nuclear Information System (INIS)

Gray, C.E.

1975-06-01

The manual contains four sections: absorption spectrophotometry; general radiochemical procedures; instrumental analysis; and calibration of field instruments. Included in the individual analyses using absorption spectrophotometry is one for total iodine in oil. Radiochemical procedures are given for: actinides in urine and water; 137 Cs in soil and vegetation; 137 Cs in soil, urine, vegetation, and water; enriched uranium in urine; gross beta activity in soil, urine, vegetation, and water; plutonium in urine and soil; 210 Po in urine and water; 24 Na in air, blood, urine, and water; 90 Sr in soil, vegetation, and water; tritium in urine, water, and on swipes; and total uranium on fallout trays and in soil, urine, and water. Among the individual instrumental analyses is a spectrographic method for determining beryllium in air samples and swipes. (U.S.)

Preparing photochromic nanofibers and animal cells using a photochromic compound of 1′,3′,3′-trimethyl-6-nitrospiro (2H-1-benzopyran-2,2′-indoline)

DEFF Research Database (Denmark)

Li, Xiaoqiang; Lin, Lin; Kanjwal, Muzafar Ahmed

2012-01-01

In this work, the photochromic compound 1′,3′,3′-trimethyl-6-nitrospiro (2H-1-benzopyran-2,2′-indoline) (NOSP) was synthesized by a two step process. The photochromic properties of NOSP were investigated by ultraviolet–visible (UV–Vis) spectrophotometry. The results showed that NOSP was very...... electrospinning were characterized by water contact angle measurements, ultraviolet–visible (UV–Vis) spectrophotometry and fluorescence microscopy. Morphology of photochromic PIEC was observed by fluorescence microscopy after being irradiated. It was shown that nanofibers from electrospun polymers and NOSP...... sensitive to UV irradiation with absorption peaks at about 336nm and 567nm. Our hypothesis was that both photochromic nanofibers and photochromic living animal cells could be obtained by combining them with NOSP. To test the hypothesis, photochromic nanofibers were fabricated by electrospinning from various...

Investigation of Argania spinosa L. (Skeels) polyphenols growing in ...

African Journals Online (AJOL)

micro

2016-12-07

Dec 7, 2016 ... The determination of flavonoids by spectrophotometry revealed the richness of Tindouf argan in ... Morocco is employed in numerous cosmetic patents in fields in USA and ..... Optimization of lead and cadmium binding by.

Journal of Chemical Sciences | Indian Academy of Sciences

Indian Academy of Sciences (India)

, they were monitored by UV spectrophotometry. The second order fits were automatically drawn, and the value of the second order rate constants (2) were automatically calculated using standard equations. At the temperature range studied, ...

Journal of Chemical Sciences | Indian Academy of Sciences

Indian Academy of Sciences (India)

MPTQ) with DNA was studied by UV-Vis and fluorescenc'e spectrophotometry as well as by hydrodynamic methods. On binding to DNA, the absorption spectrum underwent bathochromic and hypochromic shifts and the fluorescence was ...

Microprocessors in automatic chemical analysis

International Nuclear Information System (INIS)

Goujon de Beauvivier, M.; Perez, J.-J.

1979-01-01

Application of microprocessors to programming and computing of solutions chemical analysis by a sequential technique is examined. Safety, performances reliability are compared to other methods. An example is given on uranium titration by spectrophotometry [fr

Analytical chemistry of lanthanides

International Nuclear Information System (INIS)

Al-Sowdani, K.H.

1986-12-01

Candoluminescence of the lanthanides and the development of instruments for monitoring the phenomenon are described. The use of fluorescence spectroscopy, spectrofluorometry and spectrophotometry for the quantitative chemical analysis of the lanthanides is described. (U.K.)

Species-specific relationships between water transparency and male coloration within and between two closely related Lake Victoria cichlid species

NARCIS (Netherlands)

Castillo Cajas, Ruth F; Selz, Oliver M; Ripmeester, Erwin A P; Seehausen, Ole; Maan, Martine E

2012-01-01

Environmental variation in signalling conditions affects animal communication traits, with possible consequences for sexual selection and reproductive isolation. Using spectrophotometry, we studied how male coloration within and between populations of two closely related Lake Victoria cichlid

Journal of Pharmaceutical and Allied Sciences - Vol 9, No 1 (2012)

African Journals Online (AJOL)

Comparative Analysis of Imipramine Hydrochloride by UV-Spectrophotometry and Charge-Transfer Complexation · EMAIL FULL TEXT EMAIL FULL TEXT DOWNLOAD FULL TEXT DOWNLOAD FULL TEXT. KC Ofokansi, KC Nwosu, PF Uzor, AB Isah, 1429-1438 ...

Physico-Chemical and Microbiological Characterization of Soils ...

African Journals Online (AJOL)

acer

It also revealed high counts of bacteria and fungi in all the sampling sites. The viable ... greenhouse effect and global warming (Faruk et al., 2005). .... Flame emission spectrophotometry ..... Agiricultural University, Combatore, India,. 31st Jan ...

A study on the grafting reaction of isocyanates with hydroxyapatite particles

NARCIS (Netherlands)

Liu, Q.; de Wijn, J.R.; van Blitterswijk, Clemens

1998-01-01

The surface grafting reactions of a series of isocyanates with hydroxyapatite particles at different temperatures were studied by Infrared spectrophotometry (IR) and thermal gravimetric analysis (TGA). The study results show that both hexamethylene diisocyanate (HMDI) and isocyanatoethyl

Využití UV/VIS spektrofotometrie pro stanovení diklofenaku

Czech Academy of Sciences Publication Activity Database

Čapka, Lukáš; Zlámalová Gargošová, H.; Vávrová, M.; Urbánková, L.

2013-01-01

Roč. 107, č. 7 (2013), s. 550-554 ISSN 0009-2770 Institutional support: RVO:68081715 Keywords : diclofenac * UV-VIS spectrophotometry * environment * fate * pharmaceutical residues Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 0.196, year: 2013

UV, VISIBLE AND NIR SPECTRAL ANALYSIS OF EGGSHELLS IN THE CHARADRIIDAE FAMILY OF BIRDS

Science.gov (United States)

We employed reflectance spectrophotometry to quantify color and mineral composition of eggshells from several species of the bird family Charadriidae to characterize species physiology and to distinguish nesting habitat preferences. We used a Shimadzu spectrophotometer to measur...

An investigation of new commercial samples of methyl green and pyronin Y

DEFF Research Database (Denmark)

Lyon, H; Jakobsen, P; Høyer, P

1987-01-01

New commercial samples of Methyl Green (Gurr Certistain), Pyronine G (Gurr Certistain) and Pyronin Y (Polysciences) have been investigated using spectrophotometry, thin layer chromatography and nuclear magnetic resonance, in addition to standardized simultaneous and sequential staining methods...

Detection of p-coumaric acid from cell supernatant using surface enhanced Raman scattering

DEFF Research Database (Denmark)

Morelli, Lidia; Jendresen, Christian Bille; Zor, Kinga

2017-01-01

A standard protocol for analysis of microbial factories requires the screening of several populations in order to find the bestperforming ones. Standard analytical methods usually include high performance liquid chromatography (HPLC), thin layerchromatography (TLC) or spectrophotometry, which...

A further insight into the mechanism of Ag + biosorption by Lactobacillus sp. strain A09

Science.gov (United States)

Lin, Zhongyu; Zhou, Chaohui; Wu, Jianming; Zhou, Jianzhang; Wang, Lin

2005-04-01

The mechanism of Ag + biosorption by resting cell of Lactobacillus sp. strain A09 has been further investigated at the molecular level using spectroscopic techniques. The values of estimated equilibrium constants, rate constants, half-life periods and apparent enthalpies of the binding reaction were calculated via the determination of Ag + adsorbed by the biomass using atomic absorption spectrophotometry (AAS). The reductive ratio of the Ag + to Ag 0 by the A09 biomass was examined by X-ray photoelectron spectroscopy (XPS). Analysis for sulfur and nitrogen atomic contents in dry powder of the biomass with EA-1110 elemental analysis (EA) showed that amino acid residues retaining the reductive property of Ag + to Ag 0 are very small quantity, whereas glucose content in the hydrolysates of the biomass analyzed by ultraviolet-visible spectrophotometry (UV-vis) indicated that the amount of reducing sugars in the biomass is much larger than 2.71%. The fourier transform infrared (FTIR) spectrophotometry on blank and silver-loaded biomass demonstrated that the chemical functional group such as the free aldehyde group of the hemiacetalic hydroxyl group from reducing sugars, i.e. the hydrolysates of the polysaccharides from the cell wall plays a leading role in serving as the electron donor for reducing the Ag + to Ag 0. This result was further supported by characterizations on the interaction of the Ag + with glucose using X-ray powder diffractometry (XRD) and FTIR spectroscopy.

Effect of sowing date on grain quality of sorghum ( Sorghum bicolor ...

African Journals Online (AJOL)

IVHAA) while minerals; iron and zinc were determined using Atomic Absorption Spectrophotometry. Significant site by variety by sowing date interactions at P < 0.05 level of probability were obtained for protein, iron and zinc content of sorghum ...

Evaluation of radio stability of cimetidine in perfused rat stomach

International Nuclear Information System (INIS)

EL-Sayed, M.E.; Roushdy, H.M.; mohamed, S.H.; ElSayeh, H.B.M. EL-Sayeh.

1988-01-01

The stability of cimetidine towards gamma irradiation has been investigated. The pharmacological activity of cimetidine was screened by studying the effect of non-irradiated as well as irradiated drug on basal and histamine-stimulated gastric acid secretion in lumen-perfused rat preparation. This study revealed that gamma irradiated cimetidine was highly active inhibitor of basal and histamine-stimulated gastric acid secretion. Assessment of the chemical constitution of the drug before and after irradiation, using infrared (IR) spectrophotometry, ultraviolet (UV) spectrophotometry and nuclear magnetic resonance (NMR) spectroscopy were carried out. The physicochemical study revealed that irradiation of the drug at a dose level of 25 kGy has no remarkable effect on the chemical constitution of cimetidine. Results of the present study showed that cimetidine is chemically and pharmacologically stable when exposed to gamma-irradiation at a dose level of 25 kGy

Extraction of phenolic compounds from extra virgin olive oil by a natural deep eutectic solvent: Data on UV absorption of the extracts

Directory of Open Access Journals (Sweden)

Vito Michele Paradiso

2016-09-01

Full Text Available This data article refers to the paper “Towards green analysis of virgin olive oil phenolic compounds: extraction by a natural deep eutectic solvent and direct spectrophotometric detection” [1]. A deep eutectic solvent (DES based on lactic acid and glucose was used as green solvent for phenolic compounds. Eight standard phenolic compounds were solubilized in the DES. Then, a set of extra virgin olive oil (EVOO samples (n=65 were submitted to liquid–liquid extraction by the DES. The standard solutions and the extracts were analyzed by UV spectrophotometry. This article reports the spectral data of both the standard solutions and the 65 extracts, as well as the total phenolic content of the corresponding oils, assessed by the Folin–Ciocalteu assay. Keywords: Natural deep eutectic solvents, Extra virgin olive oil, Phenolic compounds, UV spectrophotometry

Biosythesis of Silver Nanoparticles using Putri Malu (Mimosa pudica Leaves Extract and Microwave Irradiation Method

Directory of Open Access Journals (Sweden)

Is Fatimah

2016-11-01

Full Text Available In this paper, the biosynthesis of silver nanoparticles (AgNPs using Mimosa pudica extract is discussed. Mimosa pudica leaves extract using water as solvent was used as bio-reductor to an aqueous solution of silver nitrate (AgNO3 and in order to accelerate the reduction, microwave irradiation method was applied. The AgNPs obtained were characterized using UV-Vis spectrophotometry, FTIR spectrophotometry, XRD, SEM-EDX, and particle size analysis based on dynamic scattering method. Effect of preparation method to the formation of AgNPs is also evaluated in antibacterial activity towards E.coli and P. aeruginosa. Rapid and ecofriendly biosynthesis of stable silver nanoparticles was observed in this study. The characterization results and antibacterial assay indicated the uniform and smaller particle size of AgNPs obtained by using microwave method and positively enhance the antibacterial activity against tested bacteria.

Atmospheric ammonia mixing ratios at an open-air cattle feeding facility.

Science.gov (United States)

Hiranuma, Naruki; Brooks, Sarah D; Thornton, Daniel C O; Auvermann, Brent W

2010-02-01

Mixing ratios of total and gaseous ammonia were measured at an open-air cattle feeding facility in the Texas Panhandle in the summers of 2007 and 2008. Samples were collected at the nominally upwind and downwind edges of the facility. In 2008, a series of far-field samples was also collected 3.5 km north of the facility. Ammonium concentrations were determined by two complementary laboratory methods, a novel application of visible spectrophotometry and standard ion chromatography (IC). Results of the two techniques agreed very well, and spectrophotometry is faster, easier, and cheaper than chromatography. Ammonia mixing ratios measured at the immediate downwind site were drastically higher (approximately 2900 parts per billion by volume [ppbv]) than thos measured at the upwind site (open-air animal feeding operations, especially under the hot and dry conditions present during these measurements.

Oxygenation and hemodynamics in left and right cerebral hemispheres during induction of veno-arterial extracorporeal membrane oxygenation.

NARCIS (Netherlands)

Heyst, A.F.J. van; Liem, D.; Hopman, J.C.W.; Staak, F.H.J.M. van der; Sengers, R.C.A.

2004-01-01

OBJECTIVE: Oxygenation and hemodynamics in the left and right cerebral hemispheres were measured during induction of veno-arterial extracorporeal membrane oxygenation (VA-ECMO). STUDY DESIGN: Using near infrared spectrophotometry, effects of right common carotid artery (RCCA) and right internal

Effects of solar radiation on glass

Science.gov (United States)

Tucker, Dennis S.; Kinser, Donald L.

1991-01-01

The effects of solar radiation of selected glasses are reported. Optical property degradation is studied using UV-Vis spectrophotometry. Strength changes are measured using a concentric ring bend test. Direct fracture toughness measurements using an indentation test are planned.

Perspective of spectrometry in determination of the compatibility and effectiveness of analgesia components in patients with radiologically profile

International Nuclear Information System (INIS)

Krasnosel'skij, M.V.; Kostya, P.Yu.; Khizhnyak, A.A.; Dikij, M.P.; Mjedvjedjeva, O.P.

2014-01-01

Spectrophotometry method was used to determine the stability of bupivacaine hydrochloride in the original condition and with different lipid environments on the basis of available medicines. The optical spectrum of the lipid fractions of bupivacaine was determined in dynamics

Micronuclei in red blood cells of armored catfish Hypostomus ...

African Journals Online (AJOL)

SERVER

2008-04-03

Apr 3, 2008 ... with micronuclei and 17 ± 0.005 mg/kg of total chrome in tissues, detected through atomic absorption spectrophotometry. .... and human cell lines, DNA damage induction by potas- .... Effects of metallic ion toxicity on human ...

Estimating rapidly and precisely the concentration of beta carotene in mango homogenates by measuring the amplitude of optothermal signals, values of chromaticity indices and the intensities of Raman peaks

NARCIS (Netherlands)

Bicanic, D.D.; Dimitrovski, D.; Luterotti, S.; Tiwisk, van C.; Buijnsters, J.G.; Doka, O.

2010-01-01

Rapid, quantitative information about the micronutrients (including beta carotene) in mango fruit is often desired. High performance liquid chromatography (HPLC) and spectrophotometry (SP), the two widely used methods in practice to quantify carotenoids, both require a time consuming and expensive

Rhipicephulus sanguineus (Brown Dog Tick)

African Journals Online (AJOL)

Department of Veterinary Microbiology and Parasitology, Faculty of Veterinaiy Medicine. ... bariierii, Ehrlichia coats, Rickerrsia conorii, .... (TAG) by an enzymatic method coupled with spectrophotometry using assay kit (Randox. Lab. Ltd., Co. Antrim, UK). Statistical analysis. Statistical analysis was performed with the use.

Exploiting direct and indirect methods for the detection of the total carotenoid content in dried pasta

NARCIS (Netherlands)

Doka, O.; Bicanic, D.D.; Végvári, G.; Buijnsters, J.G.; Spruijt, R.B.; Luterotti, S.

2010-01-01

The total carotenoid concentration (TCC) of several commercially available dried pastas prepared with or without eggs was assessed by means of the two well-established destructive approaches [spectrophotometry (SP) and high-performance liquid chromatography (HPLC)] and three non-destructive, direct

Application of laser-based photoacoustic spectroscopy and colorimetry for quantification of anthocyanin in hard boiled candy

NARCIS (Netherlands)

Kovács, Mihály; Dóka, Ottó; Bicanic, Dane; Ajtony, Zsolt

2017-01-01

The analytical performance of the newly proposed laser-based photoacoustic spectroscopy (LPAS) and colorimetric method for quantification of anthocyanin (E163) in commercially available hard boiled candies are compared to that of the spectrophotometry (SP). Both LPAS and colorimetry are direct

Simple and rapid quantification of total carotenoids in lyophilized apricots (prunus armeniaca L.) by means of reflectance colorimetry and photoacoustic spectrometry spectroscopy

NARCIS (Netherlands)

Doka, O.; Ficzek, G.; Luterotti, S.; Bicanic, D.D.; Spruijt, R.B.; Buijnsters, J.; Vegvari, G.

2013-01-01

Photoacoustic spectroscopy (PAS) and reflectance colorimetry are suggested as new tools for the analysis of total carotenoids in lyophilized apricot powders. The data obtained by these two techniques from seven apricot cultivars were compared to those acquired by spectrophotometry and

Functional optics of glossy buttercup flowers

NARCIS (Netherlands)

van der Kooi, Casper J; Elzenga, J Theo M; Dijksterhuis, Jan; Stavenga, Doekele G

2017-01-01

Buttercup (Ranunculus spp.) flowers are exceptional because they feature a distinct gloss (mirror-like reflection) in addition to their matte-yellow coloration. We investigated the optical properties of yellow petals of several Ranunculus and related species using (micro)spectrophotometry and

Development and Validation of Analytical Method for Losartan ...

African Journals Online (AJOL)

Development and Validation of Analytical Method for Losartan-Copper Complex Using UV-Vis Spectrophotometry. ... Tropical Journal of Pharmaceutical Research ... Purpose: To develop a new spectrophotometric method for the analysis of losartan potassium in pharmaceutical formulations by making its complex with ...

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

The exclusion of the aforementioned side products during the synthesis of monosubstituted porphyrins greatly reduced the complexity during purification of the product. Absorption spectrophotometry was performed on silica gel immobilizing porphyrin (CPTTP), free base tetraphenylporphyrin (H2TPP) and heteroaldehydes ...

Direct photothermal techniques for quantification of anthocyanins in sour cherry cultivars

NARCIS (Netherlands)

Doka, O.; Ficzek, G.; Bicanic, D.D.; Spruijt, R.B.; Luterotti, S.; Toth, M.; Buijnsters, J.G.; György Végvári, G.

2011-01-01

The analytical performance of the newly proposed laser-based photoacoustic spectroscopy (PAS) and of optothermal window (OW) method for quantification of total anthocyanin concentration (TAC) in five sour cherry varieties is compared to that of the spectrophotometry (SP). High performance liquid

Environmental controls on the seasonal carbon dioxide fluxes in the northeastern Indian Ocean

Digital Repository Service at National Institute of Oceanography (India)

Sardessai, S.; Maya, M.V.; Shetye, S.; PrasannaKumar, S.; Fernandes, V.; Paul, J.; Ramaiah, N.

the JGOFS protocol. Total carbon dioxide was determined by Coulometry using UIC Inc. instruments coulometer. pH on free ion (pHf) and total scale (pHT) was estimated by cresol red spectrophotometry12. Precision of analyses for carbon dioxide...

Trace Elements in Sediments of Selected Gutters and Bar – Beach ...

African Journals Online (AJOL)

Sediment samples were collected from selected gutters and Lagos bar beach for the investigation of trace element concentrations. The metals investigated were chromium, lead, arsenic, selenium, cadmium and barium using the atomic absorption spectrophotometry. The results obtained further revealed elevated ...

Application of UV-Vis spectrophotometric and chemiluminescent methods for the evaluation of the antioxidant action of curcumin

Czech Academy of Sciences Publication Activity Database

Stanchev, Stancho; Pencheva, I.; Konstantinov, S.; Obreshkova, D.; Hadjimitova, V.

2012-01-01

Roč. 77, č. 8 (2012), s. 1063-1069 ISSN 0352-5139 Institutional research plan: CEZ:AV0Z40550506 Keywords : curcumin * antioxidant * UV-Vis spectrophotometry * DNA complexation * chemiluminescence Subject RIV: CC - Organic Chemistry Impact factor: 0.912, year: 2012

Time-resolved spectrophotometry of HZ Herculis and DQ Herculis

International Nuclear Information System (INIS)

Chanan, G.A.

1978-01-01

The image-tube scanner at the 3 m telescope at Lick Observatory was employed to study the spectral changes which occur during the pulse period in the optical pulsars HZ Herculis (1.2 s period) and DQ Herculis (71 s period). The data acquisition is described and the tools needed for the data analysis developed. Then the results of the observations are presented. In the case of HZ Herculis (Hercules X-1), observations cover the binary phase interval 0.18 to 0.26 and are concerned only with those pulsations that have been shown (Middleditch and Nelson, 1976) to originate at the x-ray heated surface of the Roche lobe filling companion of the neutron star. It is found that these pulsations are distributed throughout the optical continuum. Observations appear to agree at least qualitatively with the numerical results of other investigators. The observations of DQ Herculis cover one full binary cycle, excluding eclipse. Again pulsations are found distributed throughout the continuum with generally weak wavelength dependence. However, in this case the emission line lambda 4686 (He II) is more strongly modulated than the underlying continuum and exhibits an unexpected effect: The pulse phase increases rapidly with increasing wavelength across the line. This effect can be understood in terms of a simple model in which the pulsations arise at the inner edge of the accretion disk, excited by radiation which originates at hot spots on the white dwarf and which sweeps around the disk as the degenerate star rotates. A similar model in which the pulsations arise predominantly from the back half of the surface of the disk appears in several respects to be more promising. The evident relation between the phase shift across the emission line and the so-called 360 0 phase shift through eclipse, discovered by Warner et al. (1972) is also discussed

Analysis of special recovery samples by Pu(III) spectrophotometry

International Nuclear Information System (INIS)

Van Hare, D.R.

1985-11-01

A simple spectrophotometric method has been developed to determine the plutonium concentration of FB-Line Special Recovery samples. The method is applicable over the 1 to 150 g/L range, with an accuracy and precision of better than 1%. 9 refs., 3 figs., 3 tabs

Spectrophotometry and organic matter on Iapetus. 1: Composition models

Science.gov (United States)

Wilson, Peter D.; Sagan, Carl

1995-01-01

Iapetus shows a greater hemispheric albedo asymmetry than any other body in the solar system. Hapke scattering theory and optical constants measured in the laboratory are used to identify possible compositions for the dark material on the leading hemisphere of Iapetus. The materials considered are poly-HCN, kerogen, Murchison organic residue, Titan tholin, ice tholin, and water ice. Three-component mixtures of these materials are modeled in intraparticle mixture of 25% poly-HCN, 10% Murchison residue, and 65% water ice is found to best fit the spectrum, albedo, and phase behavior of the dark material. The Murchison residue and/or water ice can be replaced by kerogen and ice tholin, respectively, and still produce very good fits. Areal and particle mixtures of poly-HCN, Titan tholin, and either ice tholin or Murchison residue are also possible models. Poly-HCN is a necessary component in almost all good models. The presence of poly-HCN can be further tested by high-resolution observations near 4.5 micrometers.

Morphology of bipolar planetary nebulae. I. Two-dimensional spectrophotometry

International Nuclear Information System (INIS)

Pascoli, G.

1990-01-01

Two-dimensional spectrophotometric observations of bipolar planetary nebulae were performed by using a CCD detector mounted at the Cassegrain focus of either 1.54 m Danish Telescope or 2.2 m German Telescope at La Silla (ESO) in Chile. Emission lines have been selected with the help of narrow band-pass interference filters (Δλ∼ 10 - 20 A). Isophotal maps in various lines Hα, [NII] λ 6584, [OIII] λ 5007 and [SII] λλ 6717-6731 are presented. Particular attention has been given to scrutinize the symmetries inside a few bipolar planetary nebulae, in order to subsequently investigate their space structure

Spectrophotometry of barium, CH, and R-type carbon stars

International Nuclear Information System (INIS)

Gow, C.E.

1976-01-01

Observations of 35 barium, CH, R, and hydrogen-deficient carbon stars, along with ten comparison K giants, have been made with the Indiana rapid spectrum scanner and the Indiana SIT vidicon spectrometer. The scanner observations cover a wavelength range of 3300--7000 A at 30-A resolution, while the SIT vidicon observations cover a wavelength range of 3800--5000 A at 2.5-A resolution. The data have been used to form molecular indices for a quantitative measurement of the strength of molecular features appearing in this region of the spectrum, and to compare the spectral energy distribution of carbon and oxygen stars over the entire observed wavelength range. We find the C 2 Swan index correlated strongly with both the strength of an unidentified feature centered near 4000 A, and the barium-to-hydrogen ratio. A detailed comparison of the spectral energy distribution of the barium stars with normal K giants shows that this unidentified absorption feature consists of two shallows depressions, one at 4000 A and another at 4325 A

Spectrophotometry in the far infrared. Optical and Hertzian processes

International Nuclear Information System (INIS)

Coste, Andre

1968-01-01

After a general study of problems related to instrumental spectroscopy in the far infrared, this research thesis examines the theory and technique of construction of slit spectrometers. The author then studied the possibilities to increase brightness and resolution using Fabry-Perot interferometers, and the Fourier transform interferential spectrometry, and finally addressed methods used with micro-waves

Time-resolved spectrophotometry of HZ Herculis and DQ Herculis

Energy Technology Data Exchange (ETDEWEB)

Chanan, G.A.

1978-01-01

The image-tube scanner at the 3 m telescope at Lick Observatory was employed to study the spectral changes which occur during the pulse period in the optical pulsars HZ Herculis (1.2 s period) and DQ Herculis (71 s period). The data acquisition is described and the tools needed for the data analysis developed. Then the results of the observations are presented. In the case of HZ Herculis (Hercules X-1), observations cover the binary phase interval 0.18 to 0.26 and are concerned only with those pulsations that have been shown (Middleditch and Nelson, 1976) to originate at the x-ray heated surface of the Roche lobe filling companion of the neutron star. It is found that these pulsations are distributed throughout the optical continuum. Observations appear to agree at least qualitatively with the numerical results of other investigators. The observations of DQ Herculis cover one full binary cycle, excluding eclipse. Again pulsations are found distributed throughout the continuum with generally weak wavelength dependence. However, in this case the emission line lambda 4686 (He II) is more strongly modulated than the underlying continuum and exhibits an unexpected effect: The pulse phase increases rapidly with increasing wavelength across the line. This effect can be understood in terms of a simple model in which the pulsations arise at the inner edge of the accretion disk, excited by radiation which originates at hot spots on the white dwarf and which sweeps around the disk as the degenerate star rotates. A similar model in which the pulsations arise predominantly from the back half of the surface of the disk appears in several respects to be more promising. The evident relation between the phase shift across the emission line and the so-called 360/sup 0/ phase shift through eclipse, discovered by Warner et al. (1972) is also discussed.

Spectrophotometry of emission-line stars in the magellanic clouds

Science.gov (United States)

Bohannan, Bruce

1990-01-01

The strong emission lines in the most luminous stars in the Magellanic Clouds indicate that these stars have such strong stellar winds that their photospheres are so masked that optical absorption lines do not provide an accurate measure of photospheric conditions. In the research funded by this grant, temperatures and gravities of emission-line stars both in the Large (LMC) and Small Magellanic Clouds (SMC) have been measured by fitting of continuum ultraviolet-optical fluxes observed with IUE with theoretical model atmospheres. Preliminary results from this work formed a major part of an invited review 'The Distribution of Types of Luminous Blue Variables'. Interpretation of the IUE observations obtained in this grant and archive data were also included in a talk at the First Boulder-Munich Hot Stars Workshop. Final results of these studies are now being completed for publication in refereed journals.

Imaging spectrophotometry of the nuclear outflow of NGC 1068

Science.gov (United States)

Cecil, Gerald

1990-01-01

This observational program (in conjunction with R. B. Tully (IfA, Honolulu), and J. Bland (Rice U., Houston)) aims to constrain the kinematic organization and dominant excitation mechanisms of ionized gas in active galaxies. More generally, researchers are interested in the dynamics of radiative, supersonic flows in the Interstellar Medium (ISM). Imaging Fabry-Perot interferometers and low-noise Charge Coupled Devices (CCDs) are used for complete spatial coverage of the complex gas distribution in circumnuclear narrow-line regions (NLRs). Extranuclear emission line widths in NLRs can exceed 3000 km s(-1), so to avoid inter-order confusion researchers use an etalon of 4000 km s(-1) free spectral range to map (N II) lambda lambda 6548, 6583 and H alpha. To maximize spatial resolution, researchers select nearby active systems independent of luminosity but known to possess interesting morphologies and/or high-velocity extranuclear ionized gas. Monochromatic images Full Width Half Maximum (FWHM) approx. 65 km s(-1) have thus far been obtained in 1 second or better seeing at the U. Hawaii 2.2m, CFH 3.6m, and CTIO 4.0m telescopes. These are stacked into grids of line profiles, of spectrophotometric quality, at sub-arcsecond increments across a 3 second field. To handle the approx. 20,000 to 300,000 useful spectra that arise from a typical night's work, researchers have developed a complete analysis and reduction package for VAX and Sun image workstations. Reduction involves parametrization of approx. 10 to the 8th raw data points to a few maps (e.g., velocities of each kinematic subsystem, continuum-free line fluxes) containing approx. 10 to the 5th pixels. Researchers identify kinematic and structural symmetries by examining these maps and the point to point variations of the synthesized line profiles. The combination of monochromatic images and full spatial sampling of line profiles has allowed them to isolate such symmetries and has led to reliable kinematic deprojections.

Characterization of tannin-metal complexes by UV-visible spectrophotometry

Science.gov (United States)

Tannins enter soils by plant decay and rain throughfall, but little is known of their effects on soils. Tannins may influence bioavailability and toxicity of metals by forming complexes and by mediating redox reactions. We evaluated the affinity and stoichiometry of Al(III) for a gallotannin, pent...

Improved optical spectrophotometry of supernova remnants in M33

Science.gov (United States)

Blair, W. P.; Kirshner, R. P.

1985-01-01

Optical spectra of SNRs in M33 have been used to investigate abundance gradients and SNR evolution in this galaxy. Abundances of O, N, and S are derived from the spectra using new shock models by Dopita et al. (1984). The results for N and S show abundance gradients similar to those in NGC 300 and the Galaxy. The O abundances may be affected by possible contamination from H II regions and low-velocity shocks. Electron densities derived from the forbidden S II 6717 A/6731 A line ratio are used with a pressure equilibrium argument to estimate the initial explosion energy for each SNR. Evolutionary models for the remnants are investigated, and the distribution of the number of remnants with diameter is found to be consistent with free expansion of the SNRs to diameters of about 26 pc. The results may also be consistent with Sedov evolution if the ranges of initial supernova energies and surrounding interstellar medium densities are large enough.

International Halley Watch: Discipline specialists for spectroscopy and spectrophotometry

Science.gov (United States)

Wyckoff, S.; Feston, M. C.; Wehinger, P.

1986-01-01

Spectroscopic observations of Comets P/Crommelin, P/Giacobini-Zinner and P/Halley are coordinated, preliminary results are delivered to the astronomical community and the data collected from observers throughout the world are archived. The ASU IHW Center has the additional responsibility of maintaining the IHW Electronic Bulletin Board which reports real-time information on the status of Comet P/Halley. Access to this electronic bulletin board via telephone modem connection is available to any astronomer upon request.

Optical spectrophotometry of oscillations and flickering in AE Aquarii

Science.gov (United States)

Welsh, William F.; Horne, Keith; Oke, J. B.

1993-01-01

We observed rapid variations in the nova-like cataclysmic variable AE Aquarii for 1.7 hr with 4.3 s time resolution using the 30-channel (3227-10494 A) spectrophotometer on the Hale 5 m telescope. The 16.5 and 33.0 s oscillations show a featureless blue spectrum that can be represented by a blackbody with temperature and area much smaller than the accretion disk. Models consisting of the sum of a K star spectrum and a hydrogen slab in LTE at T = 6000-10,000 K can fit the spectrum of AE Aquarii reasonably well. The spectrum of a flare indicates optically thin gas with T = 8000-12,000 K. The energy released by the flare is large compared to typical stellar flares.

Spectrophotometry of Wolf-Rayet stars. I - Continuum energy distributions

Science.gov (United States)

Morris, Patrick W.; Brownsberger, Kenneth R.; Conti, Peter S.; Massey, Philip; Vacca, William D.

1993-01-01

All available low-resolution IUE spectra are assembled for Galactic, LMC, and SMC W-R stars and are merged with ground-based optical and NIR spectra in order to collate in a systematic fashion the shapes of these energy distributions over the wavelength range 0.1-1 micron. They can be consistently fitted by a power law of the form F(lambda) is approximately equal to lambda exp -alpha over the range 1500-9000 A to derive color excesses E(B-V) and spectral indices by removing the 2175-A interstellar absorption feature. The WN star color excesses derived are found to be in good agreement with those of Schmutz and Vacca (1991) and Koesterke et al. (1991). Significant heterogeneity in spectral index values was generally seen with any given subtype, but the groups consisting of the combined set of Galactic and LMC W-R stars, the separate WN and WC sequences, and the Galactic and LMC W-R stars all showed a striking and consistent Gaussian-like frequency distribution of values.

Noise analysis for CCD-based ultraviolet and visible spectrophotometry.

Science.gov (United States)

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.