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Sample records for absorption spectrophotometry gfaas

  1. Computer programs for absorption spectrophotometry.

    PubMed

    Jones, R N

    1969-03-01

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

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

    SciTech Connect

    Bass, D A; TenKate, L B

    1993-11-01

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

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

    ERIC Educational Resources Information Center

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

    2004-01-01

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

  4. Development of mixed-waste analysis capability for graphite furnace atomic absorption spectrophotometry

    SciTech Connect

    Bass, D.A.; TenKate, L.B.; Wroblewski, A.

    1995-03-01

    Graphite furnace atomic absorption spectrophotometer (GFAAS) are typically configured with ventilation to capture potentially toxic and corrosive gases emitted from the vaporization of sample aliquots. When radioactive elements are present, additional concerns (such as meeting safety guidelines and ALARA principles) must be addressed. This report describes a modification to a GFAAS that provides additional containment of vaporized sample aliquots. The modification was found to increase containment by a factor of 80, given expected operating conditions. The use of the modification allows more mixed-waste samples to be analyzed, permits higher levels of radioactive samples to be analyzed, or exposes the analyst to less airborne radioactivity. The containment apparatus was attached to a Perkin-Elmer Zeeman 5000 spectrophotometer for analysis of mixed-waste samples; however, it could also be used on other systems and in other applications where greater containment of vaporized material is desired.

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

    PubMed

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

    1985-01-01

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

  6. Electrothermal atomic absorption spectrophotometry of nickel in tissue homogenates

    SciTech Connect

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

    1985-01-01

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

  7. Solidified floating organic drop microextraction (SFODME) for simultaneous separation/preconcentration and determination of cobalt and nickel by graphite furnace atomic absorption spectrometry (GFAAS).

    PubMed

    Bidabadi, Mahboubeh Shirani; Dadfarnia, Shayessteh; Shabani, Ali Mohammad Haji

    2009-07-15

    Solidified floating organic drop microextraction (SFODME), combined with graphite furnace atomic absorption spectrometry (GFAAS) was proposed for simultaneous separation/enrichment and determination of trace amounts of nickel and cobalt in surface waters and sea water. 1-(2-Pyridylazo)-2-naphthol (PAN) was used as chelating agent. The main parameters affecting the performance of SFODME, such as pH, concentration of PAN, extraction time, stirring rate, extraction temperature, sample volume and nature of the solvent were optimized. Under the optimum experimental conditions, a good relative standard deviation for six determination of 20 ng l(-1) of Co(II) and Ni(II) were 4.6 and 3.6%, respectively. An enrichment factor of 502 and 497 and detection limits of 0.4 and 0.3 ng l(-1) for cobalt and nickel were obtained, respectively. The procedure was applied to tap water, well water, river water and sea water, and accuracy was assessed through the analysis of certified reference water or recovery experiments. PMID:19117672

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

    PubMed

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

    1985-01-01

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

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

    ERIC Educational Resources Information Center

    Kuntzleman, Thomas S.; Jacobson, Erik C.

    2016-01-01

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

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

    NASA Technical Reports Server (NTRS)

    Lee, G. H.

    1967-01-01

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

  11. Cinchocaine hydrochloride determination by atomic absorption spectrometry and spectrophotometry.

    PubMed

    Abdel-Ghani, Nour T; Youssef, Ahmed F A; Awady, Mohamed A

    2005-05-01

    Two sensitive spectrophotometric and atomic absorption spectrometric procedures have been developed for determination of cinchocaine hydrochloride (Cin.Cl) in pure form and in pharmaceutical formulation. The spectrophotometric method was based on formation of an insoluble colored ion-associate between the cited drug and tetrathiocyanatocobaltate (CoTC) or hexathiocyanatochromate (CrTC) which dissolved and extracted in an organic solvent. The optimal experimental conditions for quantitative extraction such as pH, concentration of the reagents and solvent were studied. Toluene and iso-butyl alcohol proved to be the most suitable solvents for quantitative extraction of Cin-CoTC and Cin-CrTC ion-associates with maximum absorbance at 620 and 555 nm, respectively. The optimum concentration ranges, molar absorptivities, Ringbom ranges and Sandell sensitivities were also evaluated. The atomic absorption spectrometric method is based on measuring of the excess cobalt or chromium in the aqueous solution, after precipitation of the drug, at 240.7 and 357.9 nm, respectively. Linear application ranges, characteristic masses and detection limits were 57.99-361.9, 50.40 and 4.22 microg ml(-1) of Cin.Cl, in case of CoTC, while 37.99-379.9, 18.94 and 0.81 microg ml(-1) in case of CrTC. PMID:15910814

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

    USGS Publications Warehouse

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

    1969-01-01

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

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

    SciTech Connect

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

    1986-05-01

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

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

    USGS Publications Warehouse

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

    1985-01-01

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

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

    PubMed

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

    1985-03-01

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

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

    PubMed

    Uneo, S; Susa, N; Furukawa, Y

    1995-08-01

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

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

    PubMed

    Phifer, E C

    1995-01-01

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

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

    PubMed

    Liu, Jin; Zhang, Huai-Gang

    2010-04-01

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

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

    PubMed

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

    2008-12-01

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

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

    PubMed

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

    1980-01-01

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

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

    USGS Publications Warehouse

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

    1971-01-01

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

  2. NHEXAS PHASE I MARYLAND STUDY--STANDARD OPERATING PROCEDURE FOR ANALYSIS OF METALS BY GF-AAS (L07)

    EPA Science Inventory

    This SOP describes the preparation, operation, calibration, and maintenance of the graphite furnace-atomic absorption spectrometry (GFAAS) instrument for the analysis of metals in environmental samples: namely air filters, dermal wipes, soil, and dust by vacuum. The analysis was...

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

    SciTech Connect

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

    1988-01-01

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

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

    EPA Science Inventory

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

  5. GFAAS determination of mercury in muscle samples of fish from Amazon, Brazil.

    PubMed

    Moraes, Paula M; Santos, Felipe A; Cavecci, Bruna; Padilha, Cilene C F; Vieira, José C S; Roldan, Paulo S; Padilha, Pedro de M

    2013-12-01

    In the present study, a simple, rapid and sensitive method was developed for the determination of mercury concentrations in the muscle tissue of fish from the Brazilian Amazon using graphite furnace atomic absorption spectrometry (GFAAS) following acid mineralization of the samples in an ultrasonic cold water bath. Using copper nitrate as a chemical modifier in solution and sodium tungstate as permanent modifier, we were able to attain thermal stabilization of the mercury up to the atomisation temperature of 1600 °C in the GFAAS assay. The calculated limits of detection (LOD) and quantification (LOQ) were 0.014 and 0.047 mg kg(-1), respectively. PMID:23871002

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

    PubMed

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

    2015-08-01

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

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

    USGS Publications Warehouse

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

    1994-01-01

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

  8. A simple instrument for ultraviolet-visible absorption spectrophotometry in high temperature molten salt media

    NASA Astrophysics Data System (ADS)

    Li, Jianzhong; Dasgupta, Purnendu K.

    2000-06-01

    An inexpensive (absorption spectroscopic studies in molten chloride salts. The spectrometer consists of a replaceable fused silica cell of 9×9 mm square exterior cross-section housed in a temperature-controlled ceramic tubular furnace of 13 mm inner diameter. Light communication to and from the cell occurs via a pair of 1 mm core silica-on-silica optical fibers from diametrically opposite sides. The light source is a pulsed xenon flash lamp and detection is accomplished by a photodiode array spectrometer card housed in a personal computer. The system has been operated up to temperatures of 950 °C. The effective spectral range is 280-650 nm at 900 °C; higher wavelengths can be accessed at lower operating temperatures. A spectral snapshot can be acquired in as little as 1 ms. With 1 s integration time, the intrinsic system noise level is ˜2×10-4 absorbance units. The system is compact and energy efficient. Applications of the system are demonstrated with spectral studies of some metal chloride systems in an equimolar sodium and potassium chloride eutectic.

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

    SciTech Connect

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

    1986-07-01

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

  10. GFAAS determination of selenium in infant formulas using a microwave digestion method.

    PubMed

    Alegria, A; Barbera, R; Farré, R; Moreno, A

    1994-01-01

    A method for determining the selenium content of infant formulas is proposed. It includes wet digestion with nitric acid and hydrogen peroxide in medium pressure teflon bombs in a microwave oven and determination by graphite furnace atomic absorption spectrometry (GFAAS). The absence of interferences is checked. Values obtained for the limit of detection (19.4 ng/g), precision (RSD = 2.2%) and accuracy by analysis of a reference material show that the method is reliable. PMID:7935739

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

    USGS Publications Warehouse

    McLain, B.J.

    1993-01-01

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

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

    PubMed

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

    2014-05-01

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

  13. Optimization of Ultrasound-Assisted Extraction of Cr, Cu, Zn, Cd, and Pb from Sediment, Followed by FAAS and GFAAS Analysis.

    PubMed

    Mimura, Aparecida M S; Oliveira, Marcone A L; Ciminelli, Virginia S T; Silva, Julio C J

    2016-01-01

    An ultrasound method for simultaneous extraction of Cr, Cu, Zn, Cd, and Pb from sediment, and determination by flame atomic absorption spectrometry (FAAS) and graphite furnace atomic absorption spectrometry (GFAAS) was proposed. The experimental results obtained using analytical curves and the method of standard additions agreed at a confidence level of 95% for all the analytes, as determined by FAAS and GFAAS, indicating no significant matrix effects. Recoveries ranged from 80.1 to 93.7% (certified reference material) and from 89 to 107% (spike tests). The LOD and LOQ results from the method were consistent with the techniques used (FAAS and GFAAS), with high analytical throughput. The proposed method was then used to determine Cr, Cu, Zn, Cd, and Pb in river sediment samples from Rio Doce, Minas Gerais, Brazil. The results indicated levels below those permitted by Brazilian legislation for all the analytes, with the exception of Cr. PMID:26851077

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

    ERIC Educational Resources Information Center

    Williamson, Mark A.

    1989-01-01

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

  15. Matrix effects on the determination of manganese in geological materials by atomic-absorption spectrophotometry under different flame conditions

    USGS Publications Warehouse

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

    1978-01-01

    Suppression caused by five of the seven matrix elements studied (Si, Al, Fe, Ca and Mg) was observed in the atomic-absorption determination of manganese in geological materials, when synthetic solutions and the recommended oxidizing air-acetylene flame were used. The magnitude of the suppression effects depends on (1) the kind and concentration of the interfering elements, (2) the type of acid medium, and (3) the concentration of manganese to be determined. All interferences noted are removed or alleviated by using a reducing nitrous oxide-acetylene flame. The atomic-absorption method using this flame can be applied to the determination of total and extractable manganese in a wide range of geological materials without interferences. Analyses of six U.S. Geological Survey rock standards for manganese gave results in agreement with the reported values. ?? 1978.

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

    PubMed

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

    2014-09-01

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

  17. Preconcentration and determination of cadmium by GFAAS after solid-phase extraction with synthetic zeolite.

    PubMed

    Minamisawa, Hiroaki; Okunugi, Ryoko; Minamisawa, Mayumi; Tanaka, Satoshi; Saitoh, Kazunori; Arai, Nobumasa; Shibukawa, Masami

    2006-05-01

    The solid-phase extraction (SPE) method for the preconcentration of trace amounts of cadmium using synthetic zeolite A-4 and its determination by graphite furnace atomic absorption spectrometry (GFAAS) was investigated. The preconcentration conditions, such as the optimum pH range of the sample solution for the adsorption of cadmium and the kind of acid solution for dissolving the cadmium-adsorbed synthetic zeolite A-4, as well as the measurement conditions for the determination of cadmium by GFAAS, e.g., the ashing and atomizing temperature, were investigated. Quantitative recovery of cadmium onto zeolite A-4 from the sample solution over the pH range 2.0 - 9.0 was achieved by the batch method. After the solid-phase (cadmium-adsorbed zeolite A-4) was separated from the sample solution by a membrane filter, it was dissolved in 2.0 cm(3) of 2.0 mol dm(-3) nitric acid. An aliquot of the resulting solution was injected into the graphite furnace. In GFAAS measurements an alternate gas (Ar, 90%; O(2), 10%) was used as a sheath gas, and the ashing temperature and atomizing temperature were 400 degrees C and 1600 degrees C, respectively. The detection limit (3 sigma) for cadmium was 0.002 microg dm(-3). The relative standard deviation at 0.010 microg dm(-3) was 3.5 - 4.5% (n = 5). The proposed method has been successfully applied to the analysis of trace cadmium in environmental water samples. PMID:16770049

  18. Comparison of Adsorbed Mercury Screening Method With Cold-Vapor Atomic Absorption Spectrophotometry for Determination of Mercury in Soil

    NASA Technical Reports Server (NTRS)

    Easterling, Donald F.; Hovanitz, Edward S.; Street, Kenneth W.

    2000-01-01

    A field screening method for the determination of elemental mercury in environmental soil samples involves the thermal desorption of the mercury from the sample onto gold and then the thermal desorption from the gold to a gold-film mercury vapor analyzer. This field screening method contains a large number of conditions that could be optimized for the various types of soils encountered. In this study, the conditions were optimized for the determination of mercury in silty clay materials, and the results were comparable to the cold-vapor atomic absorption spectrophotometric method of determination. This paper discusses the benefits and disadvantages of employing the field screening method and provides the sequence of conditions that must be optimized to employ this method of determination on other soil types.

  19. Low-volume, high-sensitivity assay for cadmium in blood and urine using conventional atomic absorption spectrophotometry.

    SciTech Connect

    Cerny, E. A.; Bhattacharyya, M. H.; Biosciences Division

    2003-03-15

    An assay for cadmium in whole blood and urine using deuterium background-correction electrothermal atomic absorption spectroscopy (D2-ETAAS) was developed. Cadmium (in a 1- to 2-ml sample) was bound to 15 mg anion-exchange resin, interfering ions were removed in a 2-ml Bio-Spin column, and cadmium was extracted into 100 {mu}l 1 M nitric acid for analysis. Cadmium in the sample extract was concentrated 7-fold for blood and 10-fold for urine over the starting material. These steps produced cadmium atomic absorption traces with high signal to background ratios and allowed analysis against aqueous standards. At {approx}0.1 ng Cd/ml, mean intra- and interassay coefficients of variation were 11-12%. Cadmium recovery for 0.1 to 0.6 ng added cadmium was 107{+-}4% for blood and 94{+-}4% for urine (mean{+-}SE, n=3). The mean detection limit (mean + 3x SD of blank) was 0.008 ng/ml for blood and 0.003 ng/ml for urine. Samples from 'unexposed' animals including humans ranged from 0.051{+-}0.000 to 0.229{+-}0.035 ng/ml. Values were approximately 10-fold lower than those obtained by the method of Stoeppler and Brandt using Zeeman background-correction ETAAS. This new high-sensitivity, low-volume assay will be useful for epidemiological studies, even those involving children, and will provide a means to help determine the contribution of cadmium to disease incidence in the general population.

  20. Determination of total tin in geological materials by electrothermal atomic-absorption spectrophotometry using a tungsten-impregnated graphite furnace

    USGS Publications Warehouse

    Zhou, L.; Chao, T.T.; Meier, A.L.

    1984-01-01

    An electrothermal atomic-absorption spectrophotometric method is described for the determination of total tin in geological materials, with use of a tungsten-impregnated graphite furnace. The sample is decomposed by fusion with lithium metaborate and the melt is dissolved in 10% hydrochloric acid. Tin is then extracted into trioctylphosphine oxide-methyl isobutyl ketone prior to atomization. Impregnation of the furnace with a sodium tungstate solution increases the sensitivity of the determination and improves the precision of the results. The limits of determination are 0.5-20 ppm of tin in the sample. Higher tin values can be determined by dilution of the extract. Replicate analyses of eighteen geological reference samples with diverse matrices gave relative standard deviations ranging from 2.0 to 10.8% with an average of 4.6%. Average tin values for reference samples were in general agreement with, but more precise than, those reported by others. Apparent recoveries of tin added to various samples ranged from 95 to 111% with an average of 102%. ?? 1984.

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

    USGS Publications Warehouse

    Damrau, D.L.

    1993-01-01

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

  2. Direct determination of metallic elements in crude oils and petroleum products by GF-AAS using a two solvent mixture

    SciTech Connect

    Platteau, O.

    1994-12-31

    The very low detection limits attainable for element determinations by graphite furnace atomic absorption spectrometry (GF-AAS) is of particular interest to directly analyze metallic elements in materials difficult to handle, for which sample preparation procedures are troublesome and time-consuming. Crude oils and their by-products known as {open_quote}black products{close_quote} are this type of materials. Both the wet and dry ashing procedures, currently applied to obtain an aqueous solution containing the elements of interest, are lengthy and have a high probability for sample contamination by the addition of reagents and sample handling. The simple dilution with an adequate solvent is by far a better alternative but, the results obtained by some authors show a significant dependence on the matrix. Also, in these determinations organometallic compounds soluble in the selected solvent must be used as standards, these materials are expensive, many are unstable and their similarity to a typical organic matrix is highly questionable. As an alternative to these procedures, a two solvent mixture have been tested which allows the use of aqueous inorganic solutions of standards to perform the elements determinations by GF-AAS. The mixture is composed of 2,6-dimethyl-4-heptanone (DEBK) and isopropanol (ISOPOH). It has been established that a mixture of DIBK/lSOPOH (1+4) can tolerate up to 30% of water by volume. Determinations of V and Ni by GF-AAS in samples of crude oil dissolved in the mentioned solvents mixture and those prepared by dry ashing as well as by X-ray fluorescence analysis, show good recoveries for the proposed method. The results for Ni were acceptable only after the addition of a solution of 1500 ppm Pd 10% (m/V) or dodecylbenzene sulfonic acid (DRSA) as matrix modifiers to the sample (1+4, V/V) in the graphite furnace.

  3. Identification of metal-binding to proteins in seed samples using RF-HPLC-UV, GFAAS and MALDI-TOF-MS.

    PubMed

    Rigueira, Leila M B; Lana, Diogo A P D; Dos Santos, Daniel M; Pimenta, Adriano M; Augusti, Rodinei; Costa, Leticia M

    2016-11-15

    An extraction procedure using Tris-HCl buffer solution was employed in order to extract water-soluble proteins from seed samples of oat, wheat and soybean. Initially, the total protein concentration was determined by the Bradford method in each solution, after the extraction procedure. The soybean sample showed a higher concentration of total protein compared to the others. The protein extracts obtained were separated by reverse-phase chromatography (RP-HPLC-UV). The protein fractions were collected and analyzed by graphite furnace atomic absorption spectrometry (GFAAS) and matrix-assisted laser desorption/ionization (MALDI-TOF-MS) for determination of Cu, Fe, Mn and Zn and identification of proteins, respectively. The combination of techniques such as RP-HPLC-UV, GFAAS and MALDI-TOF-MS allowed the identification of several proteins bound to metals present in the seed samples. PMID:27283712

  4. [Determination of lead in microemulsified rapeseed oil and bio-diesel oil by GFAAS].

    PubMed

    Li, Sheng-qing; He, Xiao-min; Du, Ping; Wang, Min; Chen, Hao; Wu, Mou-cheng

    2008-10-01

    Bio-diesel oil has attracted much attention as a substitutable energy sources for its renewable and eco-friendly property. However, problems of lead contamination in fuel are also emphasized increasingly at present. So it was of quite significance to determine the contents of lead in bio-diesel oil and its raw material rapeseed oil. An effective method was developed for the rapid determination of lead in rapeseed oil and bio-diesel oil by graphite furnace atomic absorption spectrometry (GFAAS) after their stabilization as microemulsions. In this research work, polyethyleneglycol octyl phenyl ether and n-butanol were used for emulsifier and auxiliary emulsifying agent, respectively. For Pb, efficient thermal stabilization was obtained using NH4H2PO4 as matrix modifier. Sample stabilization was necessary because of evident analyte losses that occurred immediately after sampling. Excellent long-term sample stabilization and the influence of the microemulsion composition on the GFAAS response were observed by mixing different organic solvents. The ashing and atomization temperature and ramp rate influenced the sensitivity obtained for Ph. Take this into account, the optimum conditions of the graphite furnace atomic absorption spectrometric determination of Pb in rapeseed oil and bio-diesel oil samples were investigated. The results showed that the microemulsion was quite stable when the value of V(20% polyethyleneglycol octyl phenyl ether), V(n-butanol), V(oil) and V(water) was 0.1: 8.9: 0.5: 0.5, without matrix interference effect. The determination limit of the proposed method was 126.2 microg x L(-1) for Pb, comfortably below the values found in the analyzed samples. The recoveries were from 81.8% to 109.0%, which performed using the addition of different concentrations of lead to bio-diesel oil, rapeseed oil and petrochemical diesel samples. The relative standard deviation of determination was 5.84%. This work showed the great efficiency of the microemulsion

  5. Liquid-phase microextraction combined with graphite furnace atomic absorption spectrometry: A review.

    PubMed

    de la Calle, Inmaculada; Pena-Pereira, Francisco; Lavilla, Isela; Bendicho, Carlos

    2016-09-14

    An overview of the combination of liquid-phase microextraction (LPME) techniques with graphite furnace atomic absorption spectrometry (GFAAS) is reported herein. The high sensitivity of GFAAS is significantly enhanced by its association with a variety of miniaturized solvent extraction approaches. LPME-GFAAS thus represents a powerful combination for determination of metals, metalloids and organometallic compounds at (ultra)trace level. Different LPME modes used with GFAAS are briefly described, and the experimental parameters that show an impact in those microextraction processes are discussed. Special attention is paid to those parameters affecting GFAAS analysis. Main issues found when coupling LPME and GFAAS, as well as those strategies reported in the literature to solve them, are summarized. Relevant applications published on the topic so far are included. PMID:27566338

  6. [Determination of trace extractable lead in artificial acid sweat from ecological textiles by GFAAS].

    PubMed

    Liu, Chong-Hua; Fang, Han; Lin, Xiao-Yang; Zhang, Xiao-Li; Deng, Zhi-Guang; Li, Yun-Song

    2009-11-01

    Extractable trace level lead in artificial sweat solution from ecological textiles is a key item limited by eco-textile standard. But the content of this extractable Pb is not so easy to determine for the strict limit of eco-textile standard, the complicatedness of extractable solution matrix and the strong background interference of NaCl. In the present paper a method for the determination of trace extractable lead in artificial acid sweat from ecological textiles by graphite furnace atomic absorption spectrometry (GFAAS) is described. Based on a number of experiments by using different single and mixed matrix modifiers including (NH4)2 H2PO4, NH4 NO3, Pd(NO3)2, Ni(NO3)2 and ascorbic acid, an effective modifier and its quantity were selected and the graphite furnace operating parameters were optimized. Experimental test results revealed that adding 5 mL (1 : 1) mixed solution of 50 g x L(-1) ammonium nitrate and 100 mg x L(-1) palladium regent was an effective way to inhibit volatile lead and reduce background signals. The detection limit could reach a low level of 0.7 microg x L(-1). The relative standard deviation was 3.2%. Under the optimum experimental conditions, the recoveries ranged between 95.5% and 105%. PMID:20102007

  7. [Determination of total mercury in water samples, sediments and solids in suspension in aquatic systems by cold-vapor atomic absorption spectrophotometry].

    PubMed

    Vieira, J L; Passarelli, M M

    1996-06-01

    The use of metallic mercury in the extraction and concentration of gold causes the discarding of tons of this metal in the environment, leading to a considerable increase in the natural levels of the same and the contamination of the surrounding areas. Thus it is extremely important to monitor the presence of this metal in various sectors of the environment with a view aiming to preventing human exposure to excessive concentrations which can result in serious episodes of mercury poisoning. It is also important to estimate the possibility of river sediments becoming potential sources of contamination of human beings. The determination of total mercury was undertaken by using cold vapor atomic absorption spectrometry. River waters, as well as sediments and suspended solids were used as samples for the standardization of the analytical procedure. Later on, this method was tested on samples originating in gold mining areas for the purpose of assessing its validity. PMID:9110471

  8. Determination of sub-microgram amounts of selenium in geological materials by atomic-absorption spectrophotometry with electrothermal atomisation after solvent extraction

    USGS Publications Warehouse

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

    1981-01-01

    An atomic-absorption spectrophotometric method with electrothermal atomisation has been developed for the determination of selenium in geological materials. The sample is decomposed with a mixture of nitric, perchloric and hydrofluoric acids and heated with hydrochloric acid to reduce selenium to selenium (IV). Selenium is then extracted into toluene from a hydrochloric acid - hydrobromic acid medium containing iron. A few microlitres of the toluene extract are injected into a carbon rod atomiser, using a nickel solution as a matrix modifier. The limits of determination are 0.2-200 p.p.m. of selenium in a geological sample. For concentrations between 0.05 and 0.2 p.p.m., back-extraction of the selenium into dilute hydrochloric acid is employed before atomisation. Selenium values for reference samples obtained by replicate analysis are in general agreement with those reported by other workers, with relative standard deviations ranging from 4.1 to 8.8%. Recoveries of selenium spiked at two levels were 98-108%. Major and trace elements commonly encountered in geological materials do not interfere. Arsenic has a suppressing effect on the selenium signals, but only when its concentration is greater than 1000 p.p.m. Nitric acid interferes seriously with the extraction of selenium and must be removed by evaporation in the sample-digestion step.

  9. Direct determination of particulate elements in edible oils and fats using an ultrasonic slurry sampler with graphite furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    van Dalen, Gerard; de Galan, Leo

    1994-12-01

    Through the use of an ultrasonic slurry mixer, graphite furnace atomic absorption spectrometry (GFAAS) can be applied for the fully automated determination of particulate iron and nickel in edible oils and fats. The unsupervised ultrasonic slurry autosampler yields the same accuracy and somewhat better precision than the much more laborious manual GFAAS method.

  10. Preparation and characterization of magnetic nanoparticles for the on-line determination of gold, palladium, and platinum in mine samples based on flow injection micro-column preconcentration coupled with graphite furnace atomic absorption spectrometry.

    PubMed

    Ye, Juanjuan; Liu, Shuxia; Tian, Miaomiao; Li, Wanjun; Hu, Bin; Zhou, Weihong; Jia, Qiong

    2014-01-01

    A simple and highly selective procedure for on-line determination of trace levels of Au, Pd, and Pt in mine samples has been developed using flow injection-column adsorption preconcentration coupled with graphite furnace atomic absorption spectrophotometry (FI-column-GFAAS). The precious metals were adsorbed on the as-synthesized magnetic nanoparticles functionalized with 4'-aminobenzo-15-crown-5-ether packed into a micro-column and then eluted with 2% thiourea + 0.1 mol L(-1) HCl solution prior to the determination by GFAAS. The properties of the magnetic adsorbents were investigated by scanning electron microscope (SEM), X-ray diffraction (XRD), and vibrating sample magnetometer (VSM). Various experimental parameters affecting the preconcentration of Au, Pd, and Pt were investigated and optimized. Under the optimal experimental conditions, the detection limits of the developed technique were 0.16 ng mL(-1) for Au, 0.28 ng mL(-1) for Pd, and 1.01 ng mL(-1) for Pt, with enrichment factors of 24.3, 13.9, and 17.8, respectively. Precisions, evaluated as repeatability of results, were 1.1%, 3.9%, and 4.4% respectively for Au, Pd, and Pt. The developed method was validated by the analysis of Au, Pd, and Pt in certified reference materials and mine samples with satisfactory results. PMID:24274293

  11. Spectrophotometry: Past and Present

    NASA Astrophysics Data System (ADS)

    Adelman, Saul J.

    2009-01-01

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

  12. Method 200.12 - Determination of Trace Elements in Marine Waters by StabilizedTemperature Graphite Furnace Atomic Absorption

    EPA Science Inventory

    This method provides procedures for the determination of total recoverable elements by graphite furnace atomic absorption (GFAA) in marine waters, including estuarine, ocean and brines with salinities of up to 35 ppt.

  13. Determination of selenium by GFAAS in slurries of fish feces to estimate the bioavailability of this micronutrient in feed used in pisciculture.

    PubMed

    Silva, Fábio A; Neves, Renato C F; Quintero-Pinto, Luis G; Padilha, Cilene C F; Jorge, Sônia M A; Barros, Margarida M; Pezzato, Luiz E; Padilha, Pedro M

    2007-07-01

    This paper presents a simple, fast and sensitive method to determine selenium in samples of feces and of fish feed by graphite furnace atomic absorption spectrometry (GFAAS) through the direct introduction of slurries of the samples into the spectrometer's graphite tube. The limits of detection (LOD) and quantification (LOQ) calculated for 20 readings of the blank of the standard slurries (0.50% m/v of feces or feed devoid of selenium) were 0.31 microg l(-1) and 1.03 microg l(-1), respectively, for the standard feces slurries and 0.35 microg l(-1) and 1.16 microg l(-1), respectively, for the standard feed slurries. The proposed method was applied in studies of bioavailability of selenium in different fish feeds and the results proved consistent with that obtained from samples mineralized by acid digestion using the microwave oven. PMID:17448523

  14. High-Sensitivity Spectrophotometry.

    ERIC Educational Resources Information Center

    Harris, T. D.

    1982-01-01

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

  15. Spectrophotometry of comets at optical wavelengths

    NASA Technical Reports Server (NTRS)

    Ahearn, M. F.

    1982-01-01

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

  16. Infrared Spectrophotometry of PHOBOS

    NASA Astrophysics Data System (ADS)

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

    1999-09-01

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

  17. Multi-filter spectrophotometry simulations

    NASA Technical Reports Server (NTRS)

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

    1993-01-01

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

  18. Absolute spectrophotometry of Neptune - 3390 to 7800 A

    NASA Astrophysics Data System (ADS)

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

    1983-07-01

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

  19. Ultraviolet spectrophotometry of degenerate stars

    NASA Technical Reports Server (NTRS)

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

    1979-01-01

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

  20. Evaluation of alcohol content and metal impurities in liquid dietary supplements by sHSS-GC-FID and GFAAS techniques.

    PubMed

    Mornar, Ana; Sertić, Miranda; Amidžić Klarić, Daniela; Klarić, Ilija; Stipanović, Ksenija; Nigović, Biljana

    2016-11-15

    Despite efforts by many dietary supplements' manufactures to reduce or replace ethanol, many products containing ethanol in concentrations up to 70% are available on market. Furthermore, botanical dietary supplements can vary in metal content as a function of the environment, processing equipment and product containers. Therefore, the aim of study was to develop a new rapid and highly sensitive method for simultaneous determination of ethanol and its impurities in dietary supplements by sHSS-GC-FID technique. In addition, contamination with metals by GFAAS technique was evaluated. The proposed sHSS-GC-FID method was successfully applied for analysis of 93 samples containing various amounts of ethanol. It should be highlighted that the dramatic variation from manufacture's claims was found in even one third of products. Furthermore, high amounts of ethanol were found in several products especially designed for children and in one product labeled as "alcohol-free". Metal impurities were below the limits established by USP. PMID:27283634

  1. Absolute Spectrophotometry of 237 Open Cluster Stars

    NASA Astrophysics Data System (ADS)

    Clampitt, L.; Burstein, D.

    1994-12-01

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

  2. U.S.-MEXICO BORDER PROGRAM ARIZONA BORDER STUDY--STANDARD OPERATING PROCEDURE FOR OPERATION, CALIBRATION, AND MAINTENANCE OF THE PERKIN-ELMER ZEEMAN/5000 SYSTEM ATOMIC ABSORPTION SPECTROPHOTOMETER (BCO-L-6.0)

    EPA Science Inventory

    The purpose of this SOP is to outline the start-up, calibration, operation, and maintenance procedures for the Perkin-Elmer 5000 atomic absorption spectrophotometer (PE 5000 AA), and the Perkin Elmer 5000 Zeeman graphite furnace atomic absorption spectrophotometer (PE 5000Z GFAA)...

  3. NHEXAS PHASE I ARIZONA STUDY--STANDARD OPERATING PROCEDURE FOR OPERATION, CALIBRATION AND MAINTENANCE OF THE PERKIN-ELMER ZEEMAN/5000 SYSTEM ATOMIC ABSORPTION SPECTROMETER (BCO-L-6.0)

    EPA Science Inventory

    The purpose of this SOP is to outline the start-up, calibration, operation, and maintenance procedures for the Perkin-Elmer 5000 atomic absorption spectrophotometer (PE 5000 AA), and the Perkin Elmer 5000 Zeeman graphite furnace atomic absorption spectrophotometer (PE 5000Z GFAA)...

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

    NASA Astrophysics Data System (ADS)

    Zhao, Guangyuan; Li, Bo

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

  5. Ultraviolet spectrophotometry of three LINERs

    NASA Technical Reports Server (NTRS)

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

    1986-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    1983-03-01

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

  7. Determination of total selenium in pharmaceutical and herbal supplements by hydride generation and graphite furnace atomic absorption spectrometry.

    PubMed

    Kazi, Tasneem G; Kolachi, Nida F; Afridi, Hassan I; Brahman, Kapil Dev; Shah, Faheem

    2014-01-01

    The total selenium (Se) was determined in herbal and pharmaceutical supplements used for liver diseases. The total Se contents were determined in different pharmaceutical and herbal supplements by hydride generation atomic absorption spectrometry (HGAAS) and graphite furnace atomic absorption spectrometry (GFAAS) after microwave-assisted acid digestion. The accuracy of the techniques was evaluated by using certified reference material and the standard addition method. The recoveries of total Se were 99.4 and 99.0% for HGAAS and GFAAS, respectively. The precision of the techniques expressed as RSD were 2.34 and 4.54% for HGAAS and GFAAS measurements, respectively. The LOD values for HGAAS and GFAAS were 0.025 and 0.052 pglg, respectively. The concentrations of Se in pharmaceutical and herbal supplements were found in the range of 19.2-53.8 and 25.0-42.5 pg/g, respectively, corresponding to 35-76% and 45-76% of the total recommended dose of Se for adults. PMID:25632445

  8. [Determination of trace lead in Chinese medicinal materials by GFAAS with PdCl2 as a matrix modifier].

    PubMed

    Qin, Fan-xin; Zhang, Ming-shi; Hu, Ji-wei; Huang, Xian-fei; Zhang, Dan

    2007-10-01

    A method for the determination of lead in Chinese medicinal materials by GFAAS with PdCl2 as a matrix modifier was established. By comparing PdCl2 with NH4H2PO4 in improving effect on the determination of Pb, the dosage of PdCl2, acidity of medium, interference of coexistent ion, recovery of the method, precision of the method, and the detection limit were checked. The programmed temperature of graphite furnace was optimized. The results show that the improving effect of PdCl2 on Pb determination is better than that of NH4H2PO4. The dosage of PdCl2 is 0.3 microg. The best medium should be 1.0% HCl. The three kinds of acids, 0.4% H2SO4, 1.0% HClO4 and 1.8% HCl, did not weaken the signal of lead. The recovery of the method is 90%-104% and the precision is < 5.0%. The characteristic mass is 8.5 pg. The detection limit is 0.066 mg x kg(-1). It is concluded that the method is simple, sensitive, accurate and credible, and can be used widely. PMID:18306811

  9. A Low-Cost Quantitative Absorption Spectrophotometer

    ERIC Educational Resources Information Center

    Albert, Daniel R.; Todt, Michael A.; Davis, H. Floyd

    2012-01-01

    In an effort to make absorption spectrophotometry available to high school chemistry and physics classes, we have designed an inexpensive visible light absorption spectrophotometer. The spectrophotometer was constructed using LEGO blocks, a light emitting diode, optical elements (including a lens), a slide-mounted diffraction grating, and a…

  10. NICKEL ABSORPTION AND KINETICS IN HUMAN VOLUNTEERS

    EPA Science Inventory

    Mathematical modelling was performed of the kinetics of nickel absorption, distribution and elimination in healthy human volunteers, who ingested NiS04 in drinking water or added food. ickel was analyzed by electrothermal atomic absorption spectrophotometry in serum, urine, and f...

  11. Spectrophotometry of Io - Preliminary Voyager 1 results

    NASA Technical Reports Server (NTRS)

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

    1980-01-01

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

  12. Analysis of gunshot residues as trace in nasal mucus by GFAAS.

    PubMed

    Aliste, Marina; Chávez, Luis Guillermo

    2016-04-01

    When a gun is fired, the majority of gunshot residues are deposited on the shooter's hands. But these residues disappear through contact with surfaces or washing. Therefore, the maximum time frame to find GSR on a suspect's hands is 8h. The mucus, inside of a nostril, forms a surface layer where they are trapped foreign particles. In this way, mucus inside of a gunshot suspect's nostrils could act like an adhesive medium to stick on it gaseous particles from a gunshot. In this study, the presence of GSR in nasal mucus and its residence time is examined. A new procedure for the sampling of possible gunshot residue accumulated in the nasal mucus is designed. Samples are taken with cotton swabs moistened with a solution of EDTA and, after an acid digestion, are analysed by graphite furnace atomic absorption spectrometry. In addition, samples of hands are taken for comparison purposes. GSR recovery has been successful. The concentration of GSR in nasal mucus is found to be lower than on the hands, but with a longer residence time. Thus, it is possible to expand the sampling time of a suspect also, as nasal mucus cannot be contaminated by handling weapons. PMID:26874050

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

    SciTech Connect

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

    1991-02-01

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

  14. Determination of ruthenium in pharmaceutical compounds by graphite furnace atomic absorption spectroscopy.

    PubMed

    Jia, Xiujuan; Wang, Tiebang; Bu, Xiaodong; Tu, Qiang; Spencer, Sandra

    2006-04-11

    A graphite furnace atomic absorption (GFAA) spectrometric method for the determination of ruthenium (Rh) in solid and liquid pharmaceutical compounds has been developed. Samples are dissolved or diluted in dimethyl sulfoxide (DMSO) without any other treatment before they were analyzed by GFAA with a carefully designed heating program to avoid pre-atomization signal loss and to achieve suitable sensitivity. Various inorganic and organic solvents were tested and compared and DMSO was found to be the most suitable. In addition, ruthenium was found to be stable in DMSO for at least 5 days. Spike recoveries ranged from 81 to 100% and the limit of quantitation (LOQ) was determined to be 0.5 microg g(-1) for solid samples or 0.005 microg ml(-1) for liquid samples based a 100-fold dilution. The same set of samples was also analyzed by ICP-MS with a different sample preparation method, and excellent agreement was achieved. PMID:16314066

  15. Optical Region Spectrophotometry: Past and Present

    NASA Astrophysics Data System (ADS)

    Adelman, Saul J.

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

  16. PMAS - Faint Object 3D Spectrophotometry

    NASA Astrophysics Data System (ADS)

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

    2002-01-01

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

  17. Hollow fiber liquid phase microextraction combined with graphite furnace atomic absorption spectrometry for the determination of methylmercury in human hair and sludge samples

    NASA Astrophysics Data System (ADS)

    Jiang, Hongmei; Hu, Bin; Chen, Beibei; Zu, Wanqing

    2008-07-01

    Two methods, based on hollow fiber liquid-liquid-liquid (three phase) microextraction (HF-LLLME) and hollow fiber liquid phase (two phase) microextraction (HF-LPME), have been developed and critically compared for the determination of methylmercury content in human hair and sludge by graphite furnace atomic absorption spectrometry (GFAAS). In HF-LPME, methylmercury was extracted into the organic phase (toluene) prior to its determination by GFAAS, while inorganic mercury remained as a free species in the sample solution. In HF-LLLME, methylmercury was first extracted into the organic phase (toluene) and then into the acceptor phase (4% thiourea in 1 mol L - 1 HCl) prior to its determination by GFAAS, while inorganic mercury remained in the sample solution. The total mercury was determined by inductively coupled plasma-mass spectrometry (ICP-MS), and the levels of inorganic mercury in both HF-LLLME and HF-LPME were obtained by subtracting methylmercury from total mercury. The factors affecting the microextraction of methylmercury, including organic solvent, extraction time, stirring rate and ionic strength, were investigated and the optimal extraction conditions were established for both HF-LLLPME and HF-LPME. With a consumption of 3.0 mL of the sample solution, the enrichment factors were 204 and 55 for HF-LLLPME and HF-LPME, respectively. The limits of detection (LODs) for methylmercury were 0.1 μg L - 1 and 0.4 μg L - 1 (as Hg) with precisions (RSDs (%), c = 5 μg L - 1 (as Hg), n = 5) of 13% and 11% for HF-LLLPME-GFAAS and HF-LPME-GFAAS, respectively. For ICP-MS determination of total mercury, a limit of detection of 39 ng L - 1 was obtained. Finally, HF-LLLME-GFAAS was applied to the determination of methylmercury content in human hair and sludge, and the recoveries for the spiked samples were in the range of 99-113%. In order to validate the method, HF-LLLME-GFAAS was also applied to the analysis of a certified reference material of NRCC DORM-2 dogfish

  18. Cell effects on high-resolution transmission spectrophotometry

    NASA Astrophysics Data System (ADS)

    Soares, Oliverio D.

    1998-12-01

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

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

    ERIC Educational Resources Information Center

    Altemose, Ines R.

    1986-01-01

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

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

    ERIC Educational Resources Information Center

    Foster, N.; And Others

    1985-01-01

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

  1. Wavelength Anomalies in UV-Vis Spectrophotometry

    NASA Astrophysics Data System (ADS)

    Tellinghuisen, J.

    2012-06-01

    Commercial spectrophotometers are great tools for recording absorption spectra of low-to-moderate resolution and high photometic quality. However, in the case of at least one such instrument, the Shimadzu UV-2101PC (and by assumption, similar Shimadzu models), the wavelength accuracy may not match the photometric accuracy. In fact the wavelength varies with slit width, spectral sampling interval, and even the specified range, with a smoothing algorithm invoked any time the spectrum includes more than 65 sampled wavelengths. This behavior appears not to be documented anywhere, but it has been present for at least 20 years and persists even in the latest software available to run the instrument. The wavelength shifts can be as large as 1 nm, so for applications where wavelength accuracy better than this is important, wavelength calibration must be done with care to ensure that the results are valid for the parameters used to record the target spectra.

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

    PubMed

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

    2013-09-12

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

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

    SciTech Connect

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

    1985-05-20

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

  4. Spectrophotometry of 237 Stars in 7 Open Clusters

    NASA Astrophysics Data System (ADS)

    Clampitt, Lori; Burstein, David

    1997-08-01

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

  5. Determination of chromium by GFAAS in slurries of fish feces to estimate the apparent digestibility of nutrients in feed used in pisciculture.

    PubMed

    Silva, Fabio Arlindo; Padilha, Cilene C Federici; Pezzato, Luis Edvaldo; Barros, Margarida Maria; Padilha, Pedro M

    2006-06-15

    This paper presents a simple, fast and sensitive method to determine chromic oxide (used as a biological marker of fish feed) in samples of fish feces by GFAAS through the direct introduction of slurries of the samples into the spectrometer's graphite tube. The standard samples of feces and of fish feed containing 0.10-1.00mgkg(-1) of Cr(2)O(3) were pre-frozen for 1min in liquid nitrogen and then ground a cryogenic mill for 2min, which reduced the samples' grain size to less than 60mum. The standard slurries were prepared by mixing 20mg of standard samples of fish feed or feces with 1mL of a solution containing 0.05% (v/v) of Triton X-100 and 0.50% (v/v) of suprapure HNO(3) directly in the spectrometer's automatic sampling glass. The final concentrations of Cr(2)O(3) present in the standard slurries were 2, 4, 8, 16 and 20mugL(-1). After sonicating the mixture for 20s, 10muL of standard slurries were injected into the graphite tube, whose internal wall was lined with a metallic palladium film that acted as a permanent chemical modifier. The limits of detection (LOD) and quantification (LOQ) calculated for 20 readings of the blank of the standard slurries (2%, m/v of feces or feed devoid of minerals) were 0.81 and 2.70mugL(-1) of Cr(2)O(3) for the standard feces slurries, 0.84 and 2.83mugL(-1) of Cr(2)O(3) for the standard feed slurries. The proposed method was applied in studies of nutrient digestibility of different fish feeds and its results proved compatible with the results obtained from samples pre-mineralized by acid digestion. PMID:18970675

  6. Study of the roles of chemical modifiers in determining boron using graphite furnace atomic absorption spectrometry and optimization of the temperature profile during atomization.

    PubMed

    Yamamoto, Yuhei; Shirasaki, Toshihiro; Yonetani, Akira; Imai, Shoji

    2015-01-01

    The measurement conditions for determining boron using graphite furnace-atomic absorption spectrometry (GF-AAS) were investigated. Differences in the boron absorbance profiles were found using three different commercially available GF-AAS instruments when the graphite atomizers in them were not tuned. The boron absorbances found with and without adjusting the graphite atomizers suggested that achieving an adequate absorbance for the determination of boron requires a sharp temperature profile that overshoots the target temperature during the atomization process. Chemical modifiers that could improve the boron absorbance without the need for using coating agents were tested. Calcium carbonate improved the boron absorbance but did not suppress variability in the peak height. Improvement of boron absorbance was comparatively less using iron nitrate or copper nitrate than using calcium carbonate, but variability in the peak height was clearly suppressed using iron nitrate or copper nitrate. The limit of detection was 0.0026 mg L(-1) when iron nitrate was used. It appears that iron nitrate is a useful new chemical modifier for the quick and simple determination of boron using GF-AAS. PMID:25958863

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

    SciTech Connect

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

    2008-05-01

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

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

    DOEpatents

    Chai, Xin-Sheng; Zhu, Jun Yong

    2002-01-01

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

  9. Redox speciation analysis of dissolved iron in estuarine and coastal waters with on-line solid phase extraction and graphite furnace atomic absorption spectrometry detection.

    PubMed

    Chen, Yaojin; Feng, Sichao; Huang, Yongming; Yuan, Dongxing

    2015-05-01

    An automatic on-line solid phase extraction (SPE) system employing the flow injection (FI) technique directly coupled to a graphite furnace atomic absorption spectrometer (GFAAS) was established for speciation and determination of dissolved iron in estuarine and coastal waters. Fe(II) was mixed with ferrozine solution in a sample stream to form the Fe(II)-ferrozine complex which was extracted onto a C18 SPE cartridge, eluted with eluent and detected with GFAAS. In a parallel flow channel, Fe(III) was reduced to Fe(II) with ascorbic acid and then detected in the same way as Fe(II). The home-made interface between FI-SPE and GFAAS efficiently realized the sample introduction to the furnace in a semi-automated way. Parameters of the FI-SPE system and graphite furnace program were optimized based on a univariate experimental design and an orthogonal array design. The salinity effect on the method sensitivity was investigated. The proposed method provided a detection limit of 1.38 nmol L(-1) for Fe(II) and 1.87 nmol L(-1) for Fe(II+III). With variation of the sample loading volume, a broadened determination range of 2.5-200 nmol L(-1) iron could be obtained. The proposed method was successfully applied to analyze iron species in samples collected from the Jiulongjiang Estuary, Fujian, China. With the 2-cartridge FI-SPE system developed, on-line simultaneous determination of Fe species with GFAAS was achieved for the first time. PMID:25770602

  10. Graphite furnace-atomic absorption spectrophotometric determination of palladium in soil.

    PubMed

    Patel, K S; Sharma, P C; Hoffmann, P

    2000-08-01

    A new and sensitive procedure for the graphite furnace-atomic absorption spectrophotometric (GF-AAS) determination of Pd in soil at nanogram level is described. The method is based on prior separation and enrichment of the metal as Pd(II)-SnCl3- -N-butylacetamide (BAA) complex into 1-pentanol (PN) by solvent extraction method. The value of the molar absorptivity of the complex in three solvents, i.e. ethyl acetate, 1-pentanol, chloroform, lie in the range of (0.70-2.75) x 10(4) L mol(-1) cm(-1) at lambda(max) 360-440 nm. The metal could be enriched into organic solvent, i.e. PN, up to 10-folds. The sensitivity (A = 0.0044) of the method in the term of the peak height was 0.5 ng Pd/mL of the aqueous solution at an enrichment factor (EF) of 5. Optimization of analytical variables during enrichment and GF-AAS determination of the metal are discussed. The method has been applied for the analysis of Pd to soil samples derived from roads and highways in Germany. PMID:11220609

  11. [Determination of nine trace elements in Dioscorea opposita thumb by flame atomic absorption spectrophotometry].

    PubMed

    Zhang, Wei; Zhang, Zhuo-Yong; Shi, Yan-Zhi; Fan, Guo-Qiang

    2006-05-01

    The contents of the potassium, calcium, sodium, magnesium, copper, zinc, iron, manganese, strontium and nickel in Dioscorea opposita thumb were determined. The relative standard deviation(RSD) of the first eight contents is 0.43%, 1.10%, 4.41%, 0.68%, 1.44%, 1.88%, 1.29% and 0.03% respectively, and the percentage recovery is 90.0%-111.0%. The method is convenient and accurate. It can be used to determine the trace elements simultaneousy in Dioscorea opposita thumb. PMID:16883880

  12. Separation and preconcentration of platinum-group metals from spent autocatalysts solutions using a hetero-polymeric S, N-containing sorbent and determination by high-resolution continuum source graphite furnace atomic absorption spectrometry.

    PubMed

    Eskina, Vasilina V; Dalnova, Olga A; Filatova, Daria G; Baranovskaya, Vasilisa B; Karpov, Yuri A

    2016-10-01

    This paper describes the potential of high-resolution continuum source graphite furnace atomic absorption spectrometry for determination of Pt, Pd and Rh after separation and concentration by original in-house developed heterochain polymer S, N-containing sorbent. The methods of sample preparation of spent ceramic-based autocatalysts were considered, two of which were used: autoclave decomposition in mixture of acids HCl:HNO3 (3:1) and high-temperature melting with K2S2O7. Both methods anyway limit the direct determination of analytes by HR CS GFAAS. Using the first method it is an incomplete digestion of spent autocatalysts samples, since the precipitate is Si, and the rhodium metal dissolves with difficulty and partially passes into solution. In contrast to the first method, the second method allow to completely transfer analytes into solution, however, the background signal produced by the chemical composition of the flux, overlaps the analytical zone. It was found, that Pt, Pd and Rh contained in the spent ceramic automotive catalysts could be effectively separated and concentrated by heterochain polymer S, N-containing sorbent, which has high sorption capacity, selectivity and resistant to dilute acids. The chosen HR CS GFAAS analysis conditions enable us to determine Pt, Pd and Rh with good metrological characteristics. The concentrations of Pt, Pd and Rh in two samples of automobile exhaust catalysts were found in range of 0.00015-0.00050; 0.170-0.189; 0.0180-0.0210wt%, respectively. The relative standard deviation obtained by HR CS GFAAS was not more than 5%. Limits of detection by HR CS GFAAS achieved were 6.2·10(-6)wt% for Pt, 1.8·10(-6)wt% for Pd, and 3.4·10(-6)wt% for Rh. Limits of determination achieved by HR CS GFAAS were 1.1·10(-5)wt% for Pt, 6.9·10(-5)wt% for Pd, and 8.3·10(-5)wt% for Rh. To control the accuracy of PGM in sorption concentrates by HR CS GFAAS method, it was appropriate to conduct an inter-method comparative experiment. The

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

    NASA Technical Reports Server (NTRS)

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

    1990-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2015-06-01

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

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

    PubMed

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

    1969-09-01

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

  16. Spectrophotometry of Planetary Nebulae in the Bulge of M31

    NASA Astrophysics Data System (ADS)

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

    2004-03-01

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

  17. Voyager absolute far-ultraviolet spectrophotometry of hot stars

    NASA Technical Reports Server (NTRS)

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

    1982-01-01

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

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

    PubMed

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

    2009-01-15

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

  19. HUBBLE SPACE TELESCOPE SPECTROPHOTOMETRY AND MODELS FOR SOLAR ANALOGS

    SciTech Connect

    Bohlin, R. C.

    2010-04-15

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

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

    NASA Astrophysics Data System (ADS)

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

    2006-02-01

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

  1. The role of spectrophotometry in the diagnosis of melanoma

    PubMed Central

    2010-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2001-05-01

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

  3. Characterising the atmospheres of transiting exoplanets using narrowband spectrophotometry

    NASA Astrophysics Data System (ADS)

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

    2015-08-01

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

  4. Studying the interaction between silica nanoparticles and metals by spectrophotometry

    NASA Astrophysics Data System (ADS)

    Revina, A. A.; Potapov, V. V.; Baranova, E. K.; Smirnov, Yu. V.

    2013-02-01

    The optical absorption spectra of water silica sols containing nanoparticles (NPs) of metals (Ag, Pd, Fe, and Pt) are investigated. Silica sols are obtained from natural hydrothermal solutions via membrane concentration (ultrafiltration). Water sols of silica with specific sizes, pH values, ζ potentials of SiO2 NP surfaces, and low concentrations of SiO2 NPs are used. Plasmon resonance in optical absorption spectra is used to study the interaction between silica and metal NPs. Parameters of plasmon resonance (position, height, and half-width of optical absorption bands), from which the degree of interaction is assessed, are determined. Relationships between the optical properties of the surfaces of nanoparticle-size silica particles, the method of their production, and the effect of adsorbed metal particles on these properties are established.

  5. Cholesterol absorption.

    PubMed

    Ostlund, Richard E

    2002-03-01

    Cholesterol absorption is a key regulatory point in human lipid metabolism because it determines the amount of endogenous biliary as well as dietary cholesterol that is retained, thereby influencing whole body cholesterol balance. Plant sterols (phytosterols) and the drug ezetimibe reduce cholesterol absorption and low-density lipoprotein cholesterol in clinical trials, complementing the statin drugs, which inhibit cholesterol biosynthesis. The mechanism of cholesterol absorption is not completely known but involves the genes ABC1, ABCG5, and ABCG8, which are members of the ATP-binding cassette protein family and appear to remove unwanted cholesterol and phytosterols from the enterocyte. ABC1 is upregulated by the liver X (LXR) and retinoid X (RXR) nuclear receptors. Acylcholesterol acytransferase-2 is an intestinal enzyme that esterifies absorbed cholesterol and increases cholesterol absorption when dietary intake is high. New clinical treatments based on better understanding of absorption physiology are likely to substantially improve clinical cholesterol management in the future. PMID:17033296

  6. Evaluation of four sample treatments for determination of platinum in automotive catalytic converters by graphite furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Puig, Ana I.; Alvarado, José I.

    2006-09-01

    Conventional and microwave assisted digestion, both using aqua regia, alkaline fusion with lithium metaborate and aqueous slurries were evaluated as sample treatments for determination of Pt in automotive catalytic converters by Graphite Furnace Atomic Absorption Spectrometry (GF-AAS). Determination of platinum by GF-AAS in samples of the catalytic converter's substrates, prepared by the four methods described, indicates that the highest platinum concentration i.e. maximum Pt extraction in the range of 748 ± 15-998 ± 10 μg mL - 1 , is obtained for samples dissolved by alkaline fusion, closely followed by analysis of aqueous plus Triton X-100 slurries 708 ± 14-958 ± 10 μg mL - 1 , while neither one of the acid digestion procedures achieved total dissolution of the samples. Slurry analysis is thus shown to be a viable alternative and is recommended, based on its speed and ease of implementation. Aqueous standards calibration curves and the standard addition methods were also compared. The results showed that no appreciable matrix effects are present, regardless of the sample preparation procedure used. Precision of the measurements, expressed as percentage relative standard deviation, ranged between 2.5 to 4.9%. Accuracy of the results was assessed by recovery tests which rendered values between 98.9 and 100.9%.

  7. Determination of vanadium in soils and sediments by the slurry sampling graphite furnace atomic absorption spectrometry using permanent modifiers.

    PubMed

    Dobrowolski, Ryszard; Adamczyk, Agnieszka; Otto, Magdalena

    2013-09-15

    A new analytical procedure for vanadium (V) determination in soils and sediments by the slurry sampling graphite furnace atomic absorption spectrometry (slurry sampling GFAAS) using the mixed permanent modifiers is described. Moreover, the comparison of action of the modifiers based on the iridium (Ir) and carbide-forming elements: tungsten (W) and niobium (Nb) deposited on the graphite tubes is studied, especially in terms of their analytical utility and determination sensitivity. The mechanism of their action was investigated using an X-ray diffraction technique (XRD) and scanning electron microscopy (SEM) equipped with an energy dispersive X-ray detector (EDX). Finally, the mixture of 0.3 μg of Ir and 0.04 μg of Nb was used for the graphite tube permanent modification. The analytical procedure was optimized on the basis of the data from pyrolysis and atomization temperature curves studies. The results obtained for the four certified reference materials (marine sediments: PACS-1 and MESS-1, lake sediment: SL-1, soil: San Joaquin Soil SRM 2709), using the slurry sampling GFAAS and the standard calibration method, were in good agreement with the certified values. The detection and quantification limits and characteristic mass calculated for the proposed procedure were 0.04 µg/g, 0.16 µg/g and 11.9 pg, respectively. The precision (RSD% less than 8%) and the accuracy of vanadium determination in the soil and sediment samples were acceptable. PMID:23708618

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

    PubMed

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

    2013-01-01

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

  9. 3 micron spectrophotometry of Comet Halley - Evidence for water ice

    NASA Technical Reports Server (NTRS)

    Bregman, Jesse D.; Tielens, A. G. G. M.; Witteborn, Fred C.; Rank, David M.; Wooden, Diane

    1988-01-01

    Structure has been observed in the 3-3.6 micron preperihelion spectrum of Comet Halley consistent with either an absorption band near 3.1 microns or emission near 3.3 microns. The results suggest that a large fraction of the water molecules lost by the comet are initially ejected in the form of small ice particles rather than in the gas phase.

  10. Magnetic solid-phase extraction combined with graphite furnace atomic absorption spectrometry for speciation of Cr(III) and Cr(VI) in environmental waters.

    PubMed

    Jiang, Hong-mei; Yang, Ting; Wang, Yan-hong; Lian, Hong-zhen; Hu, Xin

    2013-11-15

    A new approach of magnetic solid phase extraction (MSPE) coupled with graphite furnace atomic absorption spectrometry (GFAAS) has been developed for the speciation of Cr(III) and Cr(VI) using zincon-immobilized silica-coated magnetic Fe3O4 nanoparticles (Zincon-Si-MNPs) as the MSPE absorbent. Cr(III) was quantitatively reserved on the absorbent at pH 9.1 while total Cr was reserved at pH 6.5. The absorbed Cr species were eluted by using 2 mol/L HCl and detected by GFAAS. The concentration of Cr(VI) could be calculated by subtracting Cr(III) from total Cr. All the parameters affecting the separation and extraction efficiency of Cr species such as pH, extraction time, concentration and volume of eluent, sample volume and influence of co-existing ions were systematically examined and the optimized conditions were established accordingly. The detection limit (LOD) of the method was 0.016 and 0.011 ng mL(-1) for Cr(III) and Cr(VI), respectively, with the enrichment factor of 100 and 150. The precisions of this method (Relative standard deviation, RSD, n=7) for Cr(III) and Cr(VI) at 0.1 ng mL(-1) were 6.0% and 6.2%, respectively. In order to validate the proposed method, a certified reference material of environmental water was analyzed, and the result of Cr speciation was in good agreement with the certified value. This MSPE-GFAAS method has been successfully applied for the speciation of Cr(III) and Cr(VI) in lake and tap waters with the recoveries of 88-109% for the spiked samples. Moreover, the MSPE separation mechanism of Cr(III) and Cr(VI) based on their adsorption-desorption on Zincon-Si-MNPs has been explained through various spectroscopic characterization. PMID:24148416

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

    NASA Astrophysics Data System (ADS)

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

    2001-06-01

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

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

    PubMed

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

    2010-11-01

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

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

    PubMed

    Hazeki, O; Tamura, M

    1989-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2013-06-01

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

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

    PubMed

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

    2011-01-01

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

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

    ERIC Educational Resources Information Center

    Billmeyer, Fred W., Jr.; And Others

    1981-01-01

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

  17. A comparison of simultaneous plasma, atomic absorption, and iron colorimetric determinations of major and trace constituents in acid mine waters

    USGS Publications Warehouse

    Ball, J.W.; Nordstrom, D.K.

    1994-01-01

    Sixty-three water samples collected during June to October 1982 from the Leviathan/Bryant Creek drainage basin were originally analyzed by simultaneous multielement direct-current plasma (DCP) atomic-emission spectrometry, flame atomic-absorption spectrometry, graphite-furnace atomic-absorption spectrometry (GFAAS) (thallium only), ultraviolet-visible spectrometry, and hydride-generation atomic-absorption spectrometry.Determinations were made for the following metallic and semi-metallic constituents: AI, As, B, Ba, Be, Bi, Cd, Ca, Cr, Co, Cu, Fe(11), Fe(total), Li, Pb, Mg, Mn, Mo, Ni, K, Sb, Se, Si, Na, Sr, TI, V, and Zn. These samples were re-analyzed later by simultaneous multielement inductively coupled plasma (ICP) atomic-emission spectrometry and Zeeman-corrected GFAAS to determine the concentrations of many of the same constituents with improved accuracy, precision, and sensitivity. The result of this analysis has been the generation of comparative concentration values for a significant subset of the solute constituents. Many of the more recently determined values replace less-than-detection values for the trace metals; others constitute duplicate analyses for the major constituents. The multiple determinations have yielded a more complete, accurate, and precise set of analytical data. They also have resulted in an opportunity to compare the performance of the plasma-emission instruments operated in their respective simultaneous multielement modes. Flame atomic-absorption spectrometry was judged best for Na and K and hydride-generation atomic-absorption spectrometry was judged best for As because of their lower detection limit and relative freedom from interelement spectral effects. Colorimetric determination using ferrozine as the color agent was judged most accurate, precise, and sensitive for Fe. Cadmium, lead, and vanadium concentrations were too low in this set of samples to enable a determination of whether ICP or DCP is a more suitable technique. Of

  18. [Determination of trace manganese in coal gangue by catalytic spectrophotometry].

    PubMed

    Xia, C; He, X

    2001-02-01

    In HAc-NaAc solution trace Mn(II) catalyzes strongly decolorization reaction of bright green SF(BGSF) by oxidizing with potassium periodate and its catalytic extent is linear with the contents of Mn(II) in the certain range. Based on this study, a catalysis spectrophotometric method for determining trace Mn(II) was developed. The results show that the maximum absorption of the complex is at 651 nm and the detection limits of the method is 0.060 microgram.L-1 for Mn(II) and Beer's law is obeyed for Mn(II) in the range of 0.03-0.3 microgram.50 mL-1. The method has been applied to the determination of trace Mn in coal gangue with satisfactory results. PMID:12953587

  19. Vacuum ultraviolet spectrophotometry and effective temperatures of hot stars

    NASA Technical Reports Server (NTRS)

    Brune, W. H.; Mount, G. H.; Feldman, P. D.

    1979-01-01

    Absolutely calibrated ultraviolet stellar spectra from 3100 A to the hydrogen absorption edge at 912 A were obtained on 1977 February 17 by rocket observations above Woomera, Australia. Spectra taken at 15 A resolution have been compared with the observed fluxes from OAO 2 and with recent model-atmosphere fluxes of Kurucz for five hot stars: Gamma (2) Vel, Zeta Pup, Alpha Eri, Beta Cen, and Alpha Vir. The present data give fluxes which are generally lower than those obtained from OAO 2, with the largest deviations of about 20% between 1400 and 1700 A. Agreement with the models is good, although the model fluxes are substantially larger than the observed values below 1200 A. This discrepancy is greater for the higher-temperature stars. Effective temperatures are also determined and are in good agreement with previous results.

  20. Spectrophotometry of emission-line stars in the magellanic clouds

    NASA Technical Reports Server (NTRS)

    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.

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

    NASA Technical Reports Server (NTRS)

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

    1985-01-01

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

  2. Matrix elimination method for the determination of precious metals in ores using electrothermal atomic absorption spectrometry.

    PubMed

    Salih, Bekir; Celikbiçak, Omür; Döker, Serhat; Doğan, Mehmet

    2007-03-28

    Poly(N-(hydroxymethyl)methacrylamide)-1-allyl-2-thiourea) hydrogels, poly(NHMMA-ATU), were synthesized by gamma radiation using (60)Co gamma source in the ternary mixture of NHMMA-ATU-H(2)O. These hydrogels were used for the specific gold, silver, platinum and palladium recovery, pre-concentration and matrix elimination from the solutions containing trace amounts of precious metal ions. Elimination of inorganic matrices such as different transition and heavy metal ions, and anions was performed by adjusting the solution pH to 0.5 that was the selective adsorption pH of the precious metal ions. Desorption of the precious metal ions was performed by using 0.8 M thiourea in 3M HCl as the most efficient desorbing agent with recovery values more than 95%. In the desorption medium, thiourea effect on the atomic signal was eliminated by selecting proper pyrolysis and atomization temperatures for all precious metal ions. Precision and the accuracy of the results were improved in the graphite furnace-atomic absorption spectrometer (GFAAS) measurements by applying the developed matrix elimination method performing the adsorption at pH 0.5. Pre-concentration factors of the studied precious metal ions were found to be at least 1000-fold. Detection limits of the precious metal ions were found to be less than 10 ng L(-1) of the all studied precious metal ions by using the proposed pre-concentration method. Determination of trace levels of the precious metals in the sea-water, anode slime, geological samples and photographic fixer solutions were performed using GFAAS clearly after applying the adsorption-desorption cycle onto the poly(NHMMA-UTU) hydrogels. PMID:17386783

  3. Solid sampling determination of lithium and sodium additives in microsamples of yttrium oxyorthosilicate by high-resolution continuum source graphite furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Laczai, Nikoletta; Kovács, László; Péter, Ágnes; Bencs, László

    2016-03-01

    Solid sampling high resolution continuum source graphite furnace atomic absorption spectrometry (SS-HR-CS-GFAAS) methods were developed and studied for the fast and sensitive quantitation of Li and Na additives in microsamples of cerium-doped yttrium oxyorthosilicate (Y2SiO5:Ce) scintillator materials. The methods were optimized for solid samples by studying a set of GFAAS conditions (i.e., the sample mass, sensitivity of the analytical lines, and graphite furnace heating programs). Powdered samples in the mass range of 0.099-0.422 mg were dispensed onto graphite sample insertion boats, weighed and analyzed. Pyrolysis and atomization temperatures were optimized by the use of single-element standard solutions of Li and Na (acidified with 0.144 mol/L HNO3) at the Li I 610.353 nm and Na I 285.3013 nm analytical lines. For calibration purposes, the method of standard addition with Li and Na solutions was applied. The correlation coefficients (R values) of the calibration graphs were not worse than 0.9678. The limit of detection for oxyorthosilicate samples was 20 μg/g and 80 μg/g for Li and Na, respectively. The alkaline content of the solid samples were found to be in the range of 0.89 and 8.4 mg/g, respectively. The accuracy of the results was verified by means of analyzing certified reference samples, using methods of standard (solution) addition calibration.

  4. Solid phase chelating extraction and separation of inorganic antimony species in pharmaceutical and water samples for graphite furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Zih-Perényi, Katalin; Jankovics, Péter; Sugár, Éva; Lásztity, Alexandra

    2008-03-01

    A separation procedure for antimony(III) and antimony(V) was developed with the use of chelating celluloses. Sb(III) was separately pre-concentrated on imino diacetic acid-ethyl cellulose in the acidic pH range, in which the uptake of Sb(V) was negligible in the μg L - 1 concentration range. On the other hand, both Sb species Sb(V) and Sb(III) were pre-concentrated on a chloride form of 2,2'-diaminodiethylamine-cellulose. These solid phase extraction procedures were combined with graphite furnace atomic absorption spectrometry (SPE-GFAAS) for Sb detection. Pharmaceutical compounds of organic and inorganic types (ten compounds), as well as mineral water samples (twelve types) were analyzed. Detection limits of 0.18 µg L - 1 Sb(III) and 0.25 µg L - 1 Sb(V) were found in aqueous sample solutions and water samples, respectively, considering a 25-fold pre-concentration. The total Sb, mostly in the form of Sb(V), could be determined in phosphate-containing pharmaceuticals, while in phosphoric acid, Sb(III) was the dominant form. In all other types of samples the Sb content was below the detection threshold, and therefore, the potential suitability of the SPE-GFAAS method for the determination of Sb(III) species was proven by recovery tests of spiked samples. This method ensures the required detection power with regard to the allowable Sb limits established by international organizations.

  5. Spectrophotometry of Wolf-Rayet stars. I - Continuum energy distributions

    NASA Technical Reports Server (NTRS)

    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.

  6. Spectrophotometry of Pluto from 3500 to 7350 A

    SciTech Connect

    Barker, E.S.; Cochran, W.D.; Cochran, A.L.

    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.

  7. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; determination of arsenic and selenium in water and sediment by graphite furnace atomic absorption spectrometry

    USGS Publications Warehouse

    Jones, Sandra R.; Garbarino, John R.

    1999-01-01

    Graphite furnace-atomic absorption spectrometry (GF-AAS) is a sensitive, precise, and accurate technique that can be used to determine arsenic and selenium in samples of water and sediment. The GF-AAS method has been developed to replace the hydride generation-atomic absorption spectrometry (HG-AAS) methods because the method detection limits are similar, bias and variability are comparable, and interferences are minimal. Advantages of the GF-AAS method include shorter sample preparation time, increased sample throughput from simultaneous multielement analysis, reduced amount of chemical waste, reduced sample volume requirements, increased linear concentration range, and the use of a more accurate digestion procedure. The linear concentration range for arsenic and selenium is 1 to 50 micrograms per liter in solution; the current method detection limit for arsenic in solution is 0.9 microgram per liter; the method detection limit for selenium in solution is 1 microgram per liter. This report describes results that were obtained using stop-flow and low-flow conditions during atomization. The bias and variability of the simultaneous determination of arsenic and selenium by GF-AAS under both conditions are supported with results from standard reference materials--water and sediment, real water samples, and spike recovery measurements. Arsenic and selenium results for all Standard Reference Water Samples analyzed were within one standard deviation of the most probable values. Long-term spike recoveries at 6.25, 25.0, 37.5 micrograms per liter in reagent-, ground-, and surface-water samples for arsenic averaged 103 plus or minus 2 percent using low-flow conditions and 104 plus or minus 4 percent using stop-flow conditions. Corresponding recoveries for selenium were 98 plus or minus 13 percent using low-flow conditions and 87 plus or minus 24 percent using stop-flow conditions. Spike recoveries at 25 micrograms per liter in 120 water samples ranged from 97 to 99 percent

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

    SciTech Connect

    Wang Naixing; Si Zhikun; Jiang Wei

    1996-09-01

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

  9. The Uranian satellites and Hyperion - New spectrophotometry and compositional implications

    NASA Technical Reports Server (NTRS)

    Brown, R. H.

    1983-01-01

    New reflectance spectra at 3.5 percent resolution have been obtained for Ariel, Titania, Oberon, and Hyperion in the 0.8 to 1.6-micron spectrum region. The new spectra show no absorptions other than the 1.5 micron water-ice feature (within the precision of the data), and demonstrate extension into the 0.8- to 1.6 micron region of the 1.5- to 2.5 micron spectral similarity ofo Ariel to Hyperion (Brown and Cruikshank, 1983). The new data confirm the presence of a dark, spectrally bland component on/in the water-ice surfaces of the Uranian satellites, which, with some reservations, has spectral similarities to the dark substance on the leading side of lapetus and the dark material on/in the surface of Hyperion, as well as other dark, spectrally neutral substances such as charcoal. Attempts were made to match the spectra of Ariel, Titania, and Oberon with additive reflectance mixes (aeral coverage) of fine-grained water frost and various dark components such as charcoal, lampblack, and charcoal-water-ice mixtures. The results were broad limits on the amounts of possible areal coverage of a charcoal-like spectral component on the surfaces of the Uranian satellites, but the data are not of sufficient precision to conclusively determine whether the dominant mode of contaminant dispersal is areal or voluminal. The effect of highly variegated albedos on the diameters derived by Brown, Cruikshank, and Morrison (1982) is found to be small.

  10. Direct determination of Cu, Mn, Pb, and Zn in beer by thermospray flame furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Nascentes, Clésia C.; Kamogawa, Marcos Y.; Fernandes, Kelly G.; Arruda, Marco A. Z.; Nogueira, Ana Rita A.; Nóbrega, Joaquim A.

    2005-06-01

    In this work, thermospray flame furnace atomic absorption spectrometry (TS-FF-AAS) was employed for Cu, Mn, Pb, and Zn determination in beer without any sample digestion. The system was optimized and calibration was based on the analyte addition technique. A sample volume of 300 μl was introduced into the hot Ni tube at a flow-rate of 0.4 ml min -1 using 0.14 mol l -1 nitric acid solution or air as carrier. Different Brazilian beers were directly analyzed after ultrasonic degasification. Results were compared with those obtained by graphite furnace atomic absorption spectrometry (GFAAS). The detection limits obtained for Cu, Mn, Pb, and Zn in aqueous solution were 2.2, 18, 1.6, and 0.9 μg l -1, respectively. The relative standard deviations varied from 2.7% to 7.3% ( n=8) for solutions containing the analytes in the 25-50 μg l -1 range. The concentration ranges obtained for analytes in beer samples were: Cu: 38.0-155 μg l -1; Mn: 110-348 μg l -1, Pb: 13.0-32.9 μg l -1, and Zn: 52.7-226 μg l -1. Results obtained by TS-FF-AAS and GFAAS were in agreement at a 95% confidence level. The proposed method is fast and simple, since sample digestion is not required and sensitivity can be improved without using expensive devices. The TS-FF-AAS presented suitable sensitivity for determination of Cu, Mn, Pb, and Zn in the quality control of a brewery.

  11. Methane absorption variations in the spectrum of Pluto

    SciTech Connect

    Buie, M.W.; Fink, U.

    1987-06-01

    The lightcurve phases of 0.18, 0.35, 0.49, and 0.98 covered by 5600-10,500 A absolute spectrophotometry of Pluto during four nights include minimum (0.98) light and one near-maximum (0.49) light. The spectra are noted to exhibit significant methane band absorption depth variations at 6200, 7200, 7900, 8400, 8600, 8900, and 10,000 A, with the minimum absorption occurring at minimum light and thereby indicating a 30-percent change in the methane column abundance in the course of three days. An attempt is made to model this absorption strength variation with rotational phase terms of an isotropic surface distribution of methane frost and a clear layer of CH4 gas. 34 references.

  12. Red supergiants in the LMC - II. Spectrophotometry and model atmospheres

    NASA Astrophysics Data System (ADS)

    Oestreicher, M. O.; Schmidt-Kaler, Th.

    1998-09-01

    Spectrophotometric observations for 88 red supergiant candidates in the Large Magellanic Cloud are presented. The spectra range from 4800 to 7700Angstroms with a resolution of 10Angstroms. The error in the absolute fluxes is 0.04 to 0.05mag. The molecular bands of the member stars are often rather weak, i.e. many of these are not M- but K-type supergiants. The data are available on the Strasbourg stellar data base (CDS). Most of the red (super)giant model atmospheres available up to now do not reproduce the observations well. The models of Kurucz and Lejeune, Cuisinier & Buser - often applied especially to population synthesis - correctly describe the strengths of atomic lines and the overall increase of the flux towards the red, but strongly underestimate the strengths of molecular bands. The models presented by Plez, however, tend to reproduce the observed spectra well, except for the blue, as they include a more complete list of opacity sources. Concerning physical properties, only the Plez models give reliable results. Considering the relation between effective temperature and the strengths of molecular bands, both the Kurucz and Lejeune models predict much higher temperatures than derived from the interferometric radius measurements discussed by Schmidt-Kaler and Dyck et al. The temperatures given by the Plez models show a much better agreement with these observations. Furthermore, the relation between T_eff and molecular absorption is much more clearly defined. When considering metallicities, however, the Plez models also fail, as they predict a [Fe/H] distribution that is much too broad, and furthermore an increase of T_eff with increasing [Fe/H] which clearly contradicts models of stellar evolution. The effective temperatures based on the Plez models range mostly from 3500 to 4100K. The surface gravities derived on the basis of the Geneva evolutionary models range from logg=-0.3 to 0.3, while the bolometric luminosities based on BVRIJHK observations range

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

    ERIC Educational Resources Information Center

    Lehman, Thomas A.; Everett, Wayne W.

    1982-01-01

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

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

    PubMed

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

    2013-05-01

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

  15. ABSORPTION ANALYZER

    DOEpatents

    Brooksbank, W.A. Jr.; Leddicotte, G.W.; Strain, J.E.; Hendon, H.H. Jr.

    1961-11-14

    A means was developed for continuously computing and indicating the isotopic assay of a process solution and for automatically controlling the process output of isotope separation equipment to provide a continuous output of the desired isotopic ratio. A counter tube is surrounded with a sample to be analyzed so that the tube is exactly in the center of the sample. A source of fast neutrons is provided and is spaced from the sample. The neutrons from the source are thermalized by causing them to pass through a neutron moderator, and the neutrons are allowed to diffuse radially through the sample to actuate the counter. A reference counter in a known sample of pure solvent is also actuated by the thermal neutrons from the neutron source. The number of neutrons which actuate the detectors is a function of a concentration of the elements in solution and their neutron absorption cross sections. The pulses produced by the detectors responsive to each neu tron passing therethrough are amplified and counted. The respective times required to accumulate a selected number of counts are measured by associated timing devices. The concentration of a particular element in solution may be determined by utilizing the following relation: T2/Ti = BCR, where B is a constant proportional to the absorption cross sections, T2 is the time of count collection for the unknown solution, Ti is the time of count collection for the pure solvent, R is the isotopic ratlo, and C is the molar concentration of the element to be determined. Knowing the slope constant B for any element and when the chemical concentration is known, the isotopic concentration may be readily determined, and conversely when the isotopic ratio is known, the chemical concentrations may be determined. (AEC)

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

    PubMed

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

    2001-09-13

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

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

    NASA Astrophysics Data System (ADS)

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

    2011-09-01

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

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

    PubMed

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

    2011-09-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2012-01-01

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

  20. Model calculation of the characteristic mass for convective and diffusive vapor transport in graphite furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Bencs, László; Laczai, Nikoletta; Ajtony, Zsolt

    2015-07-01

    A combination of former convective-diffusive vapor-transport models is described to extend the calculation scheme for sensitivity (characteristic mass - m0) in graphite furnace atomic absorption spectrometry (GFAAS). This approach encompasses the influence of forced convection of the internal furnace gas (mini-flow) combined with concentration diffusion of the analyte atoms on the residence time in a spatially isothermal furnace, i.e., the standard design of the transversely heated graphite atomizer (THGA). A couple of relationships for the diffusional and convectional residence times were studied and compared, including in factors accounting for the effects of the sample/platform dimension and the dosing hole. These model approaches were subsequently applied for the particular cases of Ag, As, Cd, Co, Cr, Cu, Fe, Hg, Mg, Mn, Mo, Ni, Pb, Sb, Se, Sn, V and Zn analytes. For the verification of the accuracy of the calculations, the experimental m0 values were determined with the application of a standard THGA furnace, operating either under stopped, or mini-flow (50 cm3 min- 1) of the internal sheath gas during atomization. The theoretical and experimental ratios of m0(mini-flow)-to-m0(stop-flow) were closely similar for each study analyte. Likewise, the calculated m0 data gave a fairly good agreement with the corresponding experimental m0 values for stopped and mini-flow conditions, i.e., it ranged between 0.62 and 1.8 with an average of 1.05 ± 0.27. This indicates the usability of the current model calculations for checking the operation of a given GFAAS instrument and the applied methodology.

  1. Trace and Essential Elements Analysis in Cymbopogon citratus (DC.) Stapf Samples by Graphite Furnace-Atomic Absorption Spectroscopy and Its Health Concern.

    PubMed

    Anal, Jasha Momo H

    2014-01-01

    Cymbopogon citratus (DC.) Stapf commonly known as lemon grass is used extensively as green tea and even as herbal tea ingredient across the world. Plants have the ability to uptake metals as nutrient from the soil and its environment which are so essential for their physiological and biochemical growth. Concentrations of these twelve trace elements, namely, Mg, Ca, Cr, Mn, Fe, Ni, Cu, Zn, Mo, As, Cd, and Pb, are analysed by graphite furnace-atomic absorption spectroscopy (GF-AAS) and are compared with the permissible limits of FAO/WHO, ICMR, and NIH, USA, which are found to be within permissible limits. Toxic metals like As, Cd, and Pb, analysed are within the tolerable daily diet limit and at low concentration. PMID:25525430

  2. Trace and Essential Elements Analysis in Cymbopogon citratus (DC.) Stapf Samples by Graphite Furnace-Atomic Absorption Spectroscopy and Its Health Concern

    PubMed Central

    Anal, Jasha Momo H.

    2014-01-01

    Cymbopogon citratus (DC.) Stapf commonly known as lemon grass is used extensively as green tea and even as herbal tea ingredient across the world. Plants have the ability to uptake metals as nutrient from the soil and its environment which are so essential for their physiological and biochemical growth. Concentrations of these twelve trace elements, namely, Mg, Ca, Cr, Mn, Fe, Ni, Cu, Zn, Mo, As, Cd, and Pb, are analysed by graphite furnace-atomic absorption spectroscopy (GF-AAS) and are compared with the permissible limits of FAO/WHO, ICMR, and NIH, USA, which are found to be within permissible limits. Toxic metals like As, Cd, and Pb, analysed are within the tolerable daily diet limit and at low concentration. PMID:25525430

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

    PubMed

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

    1980-03-01

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

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

    NASA Astrophysics Data System (ADS)

    Sei, Norihiro; Takahashi, Toshiharu

    2014-01-01

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

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

    PubMed

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

    2011-08-15

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

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

    NASA Technical Reports Server (NTRS)

    Warren, W. H., Jr.

    1982-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1993-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1984-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1980-01-01

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

  10. A thin-walled metallic hollow cathode as an atomizer for Zeeman atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Ganeyev, A. A.; Sholupov, S. E.

    1998-03-01

    A new kind of glow discharge atomizer, a thin-walled metallic hollow cathode (TMHC) combined with Zeeman atomic absorption spectrometry using high frequency modulated light polarization (ZAAS-HFM), is studied. A theoretically suggested, and experimentally confirmed, model of the atom confinement in the TMHC yields the appearance of the diffusion traps for atoms at both ends of the cathode, which increases the residence time of the analyte atoms in the analysis volume. The high atomization efficiency in the glow discharge atomizer (caused by the ionic-thermal mechanism of sputtering) and the high selectivity of ZAAS-HFM are demonstrated in the analysis of complex matrix samples such as whole blood and urine. The analytical system TMHC + ZAAS-HFM is characterized by low detection limits, which are comparable to those of graphite furnace atomic absorption spectrometry (GFAAS). Owing to its rather low average power consumption (30-50 W) the TMHC can be used in a portable and mobile spectrometer, and is therefore suitable for the in situ analysis of various sample materials.

  11. Absorption spectra of irradiated XRCT radiochromic film

    NASA Astrophysics Data System (ADS)

    Butson, Martin J.; Cheung, Tsang; Yu, Peter K. N.

    2006-06-01

    Gafchromic XRCT radiochromic film is a self-developing high sensitivity radiochromic film product which can be used for assessment of delivered radiation doses which could match applications such as computed tomography (CT) dosimetry. The film automatically changes colour upon irradiation changing from a yellow to green/brown colour. The absorption spectra of Gafchromic XRCT radiochromic film as measured with reflectance spectrophotometry have been investigated to analyse the dosimetry characteristics of the film. Results show two main absorption peaks produced from irradiation located at 636 nm and 585 nm. This is similar to EBT Gafchromic film. A high level of sensitivity is found for this film with a 1 cGy applied dose producing an approximate net optical density change of 0.3 at 636 nm. This high sensitivity combined with its relatively energy independent nature around the 100 kVp to 150 kVp x-ray energy range provides a unique enhancement in dosimetric measurement capabilities over currently available dosimetry films for CT applications.

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

    PubMed

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

    1999-04-01

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

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

    NASA Technical Reports Server (NTRS)

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

    2000-01-01

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

  14. Light absorption by anthocyanins in juvenile, stressed, and senescing leaves

    PubMed Central

    Merzlyak, Mark N.; Chivkunova, Olga B.; Solovchenko, Alexei E.; Naqvi, K. Razi

    2008-01-01

    The optical properties of leaves from five species, Norway maple (Acer platanoides L.), cotoneaster (Cotoneaster alaunica Golite), hazel (Corylus avellana L.), Siberian dogwood (Cornus alba L.), and Virginia creeper (Parthenocissus quinquefolia (L.) Planch.), differing in pigment composition and at different stages of ontogenesis, were studied. Anthocyanin absorption maxima in vivo, as estimated with spectrophotometry of intact anthocyanic versus acyanic leaves and microspectrophotometry of vacuoles in the leaf cross-sections, were found between 537 nm and 542 nm, showing a red shift of 5–20 nm compared with the corresponding maxima in acidic water–methanol extracts. In non-senescent leaves, strong anthocyanin absorption was found between 500 nm and 600 nm (with a 70–80 nm apparent bandwidth). By and large, absorption by anthocyanin in leaves followed a modified form of the Lambert–Beer law, showing a linear trend up to a content of nearly 50 nmol cm−2, and permitting thereby a non-invasive determination of anthocyanin content. The apparent specific absorption coefficients of anthocyanins at 550 nm showed no substantial dependence on the species. Anthocyanin contribution to total light absorption at 550 nm was followed in maple leaves in the course of autumn senescence. Photoprotection by vacuolar anthocyanins is discussed with special regard to their distribution within a leaf; radiation screening by anthocyanins predominantly localized in the epidermal cells in A. platanoides and C. avellana leaves was also evaluated. PMID:18796701

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

    PubMed

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

    2015-01-01

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

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

    PubMed

    Amin, Alaa S

    2014-01-01

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

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

    PubMed

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

    2014-04-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1982-01-01

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

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

    PubMed Central

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

    2016-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    1999-05-01

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

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

    SciTech Connect

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

    1989-04-01

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

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

    PubMed

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

    2013-06-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2006-06-01

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

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

    PubMed

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

    2016-01-01

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

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

    NASA Technical Reports Server (NTRS)

    Torres-Dodgen, Ana V.; Massey, Philip

    1988-01-01

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

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

    SciTech Connect

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

    2008-10-08

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

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

    NASA Technical Reports Server (NTRS)

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

    1986-01-01

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

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

    PubMed

    Baranowska, I; Pieszko, C

    2000-12-01

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

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

    PubMed

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

    2010-08-01

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

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

    NASA Astrophysics Data System (ADS)

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

    1996-01-01

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

  11. Formation of a liquid organic ion associate in aqueous solution and its application to the GF-AAS determination of trace cadmium in environmental water as a complex with 2-(5-bromo-2-pyridylazo)-5-(N-propyl-N-sulfopropylamino)phenol.

    PubMed

    Hata, Noriko; Hieda, Shiho; Yamada, Mika; Yasui, Rie; Kuramitz, Hideki; Taguchi, Shigeru

    2008-07-01

    The formation of a liquid organic ion associate in an aqueous sample was applied to the concentration and determination of cadmium in environmental water samples. Cadmium was converted into a complex with 2-(5-bromo-2-pyridylazo)-5-(N-propyl-N-sulfopropylamino)phenol (5-Br-PAPS) in a 40-mL sample solution, and was extracted into a liquid ion associate of phenolsulfonate and benzethonium during phase formation. More than 400-fold enrichment was easily attained by this technique, because the volume of the liquid organic phase formed was very small, ca. 2 microL. After dilution of the organic phase with a small volume of 2-methoxyethanol, the cadmium in the solution was determined by GF-AAS. The detection limit was 0.09 ng/L (3sigma(b)). This method was applied to the determination of cadmium in river water and seawater. PMID:18614838

  12. Enhanced squeezing by absorption

    NASA Astrophysics Data System (ADS)

    Grünwald, P.; Vogel, W.

    2016-04-01

    Absorption is usually expected to be detrimental to quantum coherence effects. However, there have been few studies into the situation for complex absorption spectra. We consider the resonance fluorescence of excitons in a semiconductor quantum well. The creation of excitons requires absorption of the incoming pump-laser light. Thus, the absorption spectrum of the medium acts as a spectral filter for the emitted light. Surprisingly, absorption can even improve quantum effects, as is demonstrated for the squeezing of the resonance fluorescence of the quantum-well system. This effect can be explained by an improved phase matching due to absorption.

  13. Determination of cadmium in biodiesel using microemulsion and electrothermal atomization atomic absorption spectrometry.

    PubMed

    Lima, Adriana S; Silva, Deise G; Teixeira, Leonardo S G

    2015-01-01

    This work aimed to prepare biodiesel microemulsions for the subsequent quantification of cadmium via graphite furnace atomic absorption spectrometry (GFAAS). The biodiesel samples were prepared using n-propanol as an emulsifier, 10% (v/v) nitric acid as the aqueous phase, and biodiesel. Pseudoternary phase diagrams were constructed to determine the microemulsion region with the specified components. The optimized conditions for microemulsion formation were 57.6% (v/v) n-propanol, 21.2% (v/v) biodiesel, and 21.2% (v/v) nitric acid solution. The stability of the microemulsified system was investigated using aqueous and organic standards, and the system was found to be stable for at least 240 min. The applied pyrolysis and atomization temperatures were 800 and 2000 °C, respectively, and 5 μg of aluminum was used as the chemical modifier. The obtained limits of detection and quantification were 0.2 and 0.5 μg kg(-1), respectively, and the characteristic mass was 1.6 pg. The precision, expressed as the relative standard deviation (% R.S.D., n = 10), was 2.5% for a sample with a cadmium concentration of 6.5 μg kg(-1). The accuracy was determined from addition and recovery experiments, with results varying from 93 to 108% recovery. This study demonstrates that the proposed method based on the use of a microemulsion formation in sample preparation can be applied as an efficient alternative for the determination of cadmium in biodiesel by GFAAS. Cadmium determination in biodiesel samples of different origins (soybean, corn, cotton, and sunflower) was evaluated after acid digestion using the inductively coupled plasma-mass spectrometry (ICP-MS) technique, and the obtained results were compared to the results obtained using the proposed method. The paired t test (95% confidence level) did not show significant differences. The concentrations of cadmium found ranged from 5.3 to 8.0 μg kg(-1). PMID:25381584

  14. Sensitive magnetic nanoparticle-based immunoassay of phosphorylated acetylcholinesterase using protein cage templated lead phosphate for signal amplification with graphite furnace atomic absorption spectrometry detection

    PubMed Central

    Liang, Pei; Kang, Caiyan; Yang, Enjian; Ge, Xiaoxiao; Du, Dan; Lin, Yuehe

    2016-01-01

    We developed a new magnetic nanoparticles sandwich-like immunoassay using protein cage nanoparticles (PCN) for signal amplification together with graphite furnace atomic absorption spectrometry (GFAAS) for quantification of organophosphorylated acetylcholinesterase adduct (OP-AChE), the biomarker of exposure to organophosphate pesticides (OPs) and nerve agents. OP-AChE adducts were firstly captured by titanium dioxide coated magnetic nanoparticles (TiO2-MNPs) from the sample matrixes through metal chelation with phospho-moieties, and then selectively recognized by anti-AChE antibody labeled on PCN which was packed with lead phosphate in its cavity (PCN-anti-AChE). The sandwich-like immunoreaction was performed among TiO2-MNPs, OP-AChE and PCN-anti-AChE to form TiO2-MNPs/OP-AChE/PCN-anti-AChE immunocomplex. The complex could be easily isolated from the sample solution with the help of magnet, and the released lead ions from PCN were detected by GFAAS for the quantification of OP-AChE. Greatly enhanced sensitivity was achieved because PCN increased the amount of metal ions in the cavity of each apoferritin. The proposed immunoassay yielded a linear response over a broad OP-AChE concentrations from 0.01 nM to 2 nM, with a detection limit of 2 pM, which has enough sensitivity for monitoring of low-dose exposure to OPs. This new method showed an acceptable stability and reproducibility and was validated with OP-AChE spiked human plasma. PMID:26953358

  15. A sensitive magnetic nanoparticle-based immunoassay of phosphorylated acetylcholinesterase using protein cage templated lead phosphate for signal amplification with graphite furnace atomic absorption spectrometry detection.

    PubMed

    Liang, Pei; Kang, Caiyan; Yang, Enjian; Ge, Xiaoxiao; Du, Dan; Lin, Yuehe

    2016-04-01

    We developed a new magnetic nanoparticle sandwich-like immunoassay using protein cage nanoparticles (PCN) for signal amplification together with graphite furnace atomic absorption spectrometry (GFAAS) for the quantification of an organophosphorylated acetylcholinesterase adduct (OP-AChE), the biomarker of exposure to organophosphate pesticides (OPs) and nerve agents. OP-AChE adducts were firstly captured by titanium dioxide coated magnetic nanoparticles (TiO2-MNPs) from the sample matrixes through metal chelation with phospho-moieties, and then selectively recognized by anti-AChE antibody labeled on PCN which was packed with lead phosphate in its cavity (PCN-anti-AChE). The sandwich-like immunoreaction was performed among TiO2-MNPs, OP-AChE and PCN-anti-AChE to form a TiO2-MNP/OP-AChE/PCN-anti-AChE immunocomplex. The complex could be easily isolated from the sample solution with the help of magnet, and the released lead ions from PCN were detected by GFAAS for the quantification of OP-AChE. Greatly enhanced sensitivity was achieved because PCN increased the amount of metal ions in the cavity of each apoferritin. The proposed immunoassay yielded a linear response over a broad range of OP-AChE concentrations from 0.01 nM to 2 nM, with a detection limit of 2 pM, which has enough sensitivity for monitoring of low-dose exposure to OPs. This new method showed an acceptable stability and reproducibility and was validated with OP-AChE spiked human plasma. PMID:26953358

  16. Determination of gold in geological materials by carbon slurry sampling graphite furnace atomic absorption spectrometry.

    PubMed

    Dobrowolski, Ryszard; Kuryło, Michał; Otto, Magdalena; Mróz, Agnieszka

    2012-09-15

    A simple and cost effective preconcentration method on modified activated carbons is described for the determination of traces of gold (Au) in geological samples by carbon slurry sampling graphite furnace atomic absorption spectrometry (GFAAS). The basic parameters affecting the adsorption capacity of Au(III) ions on modified activated carbons were studied in detail and the effect of activated carbons modification has been determined by studying the initial runs of adsorption isotherms. The influence of chlorides and nitrates on adsorption ability of Au(III) ions onto the modified activated carbons for diluted aqueous solution was also studied in detail in respect to the determination of gold in solid materials after digestion steps in the analytical procedure, which usually involves the application of aqua regia. SEM-EDX and XPS studies confirmed that the surface reduction of Au(III) ions to Au(0) is the main gold adsorption mechanism on the activated carbon. Determination of gold after its preconcentration on the modified activated carbon was validated by applying certified reference materials. The experimental results are in good agreement with the certified values. The proposed method has been successfully applied for the determination of Au in real samples using aqueous standards. PMID:22967620

  17. D-xylose absorption

    MedlinePlus

    ... this page: //medlineplus.gov/ency/article/003606.htm D-xylose absorption To use the sharing features on this page, please enable JavaScript. D-xylose absorption is a laboratory test to determine ...

  18. Optical Absorption, Stability and Structure of NpO2+ Complexeswith Dicarboxylic Acids

    SciTech Connect

    Guoxin Tian; Linfeng Rao

    2006-01-04

    Complexation of NpO2+ with oxalic acid (OX),2,2'-oxydiacetic acid (ODA), 2,2'-iminodiacetic acid (IDA) and 2,2'-thiodiacetic acid (TDA), has been studied using spectrophotometry in1 M NaClO4. Both the position and the intensity of the absorption band of NpO2+ at 980 nm are affected by the formation of NpO2+/dicarboxylate complexes, providing useful information on the complexation strength, the coordination mode and the structure of the complexes.

  19. Spatial variability of absorption properties in Lake Balaton, Hungary

    NASA Astrophysics Data System (ADS)

    Riddick, C. A.; Hunter, P. D.; Tyler, A. N.; Vicente, V. M.; Groom, S.; Horváth, H.; Kovacs, A.; Preston, T.; Presing, M.

    2013-12-01

    In order to improve robustness of current remote sensing algorithms for lake monitoring, it is vital to understand the variability of inherent optical properties (IOPs) within a lake. In this study, absorption coefficients were measured in situ at 38 stations in Lake Balaton, Hungary, using a WET Labs AC-S and AC-9 and compared to concurrent absorption measurements by dual beam spectrophotometry in the laboratory. The spatial variability of bulk and chlorophyll-specific absorption coefficients was examined across 5 basins, demonstrating a gradient in total absorption corresponding to the trophic gradient. Our data suggests that sampling conditions had an impact on particulate absorption, affecting the proportion attributed to non-algal particles (aNAP), phytoplankton (aph) or color dissolved organic matter (aCDOM). The specific absorption of phytoplankton (a*ph) spectra showed a distinct peak in the UV portion of the spectra in Basins 3 and 4 (east), which may be due to the presence of phytoplankton photoprotective pigments to compensate for lower CDOM levels in these basins. In contrast to oceans, particulate attenuation (cp) had a weaker relationship to chlorophyll-a (R2=0.15) than to total suspended matter (R2=0.84), particularly the inorganic fraction. Additionally, the relative contribution of particulate scattering (bp) to attenuation was significantly higher in Lake Balaton (up to 85-99%) than that found in previous lacustrine studies. bp also demonstrated a gradient across the lake, where values increased as the water progressed from phytoplankton-dominated to mineral-dominated. These results provide knowledge of the heterogeneity of the IOPs within Lake Balaton, which is to be considered for the future improvement of bio-optical algorithms for constituent retrieval in inland waters.

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

    PubMed

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

    2004-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-06-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1978-01-01

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

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

    NASA Astrophysics Data System (ADS)

    Khodadoust, Saeid; Ghaedi, Mehrorang

    2014-12-01

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

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

    NASA Astrophysics Data System (ADS)

    Sarkar, Ritabrata; Chakrabarti, Sandip Kumar

    2010-08-01

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

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

    PubMed

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

    2005-03-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2013-01-01

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

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

    NASA Astrophysics Data System (ADS)

    Zheng, Qi; Liu, Zhihong; Cai, Ruxiu

    2005-04-01

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

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

    PubMed

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

    2016-03-01

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

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

    PubMed

    Zia, H; Price, J C

    1976-02-01

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

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

    PubMed

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

    2015-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    1999-05-01

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

  12. Solid methane on Triton and Pluto - 3- to 4-micron spectrophotometry

    SciTech Connect

    Spencer, J.R.; Buie, M.W.; Bjoraker, G.L. Space Telescope Science Institute, Baltimore, MD NASA, Goddard Space Flight Center, Greenbelt, MD )

    1990-12-01

    Methane has been identified in the Pluto/Charon system on the basis of absorption features in the reflectance spectrum at 1.5 and 2.3 microns; attention is presently given to observations of a 3.25 micron-centered deep absorption feature in Triton and Pluto/Charon system reflectance spectra. This absorption may indicate the presence of solid methane, constituting either the dominant surface species or a mixture with a highly transparent substance, such as N2 frost. 35 refs.

  13. Blood oxygen saturation determined by transmission spectrophotometry of hemolyzed blood samples

    NASA Technical Reports Server (NTRS)

    Malik, W. M.

    1967-01-01

    Use of the Lambert-Beer Transmission Law determines blood oxygen saturation of hemolyzed blood samples. This simplified method is based on the difference in optical absorption properties of hemoglobin and oxyhemoglobin.

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  15. Solar absorption surface panel

    DOEpatents

    Santala, Teuvo J.

    1978-01-01

    A composite metal of aluminum and nickel is used to form an economical solar absorption surface for a collector plate wherein an intermetallic compound of the aluminum and nickel provides a surface morphology with high absorptance and relatively low infrared emittance along with good durability.

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

    PubMed

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

    2015-11-15

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

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

    SciTech Connect

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

    1990-01-01

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

  18. Petawatt laser absorption bounded

    PubMed Central

    Levy, Matthew C.; Wilks, Scott C.; Tabak, Max; Libby, Stephen B.; Baring, Matthew G.

    2014-01-01

    The interaction of petawatt (1015 W) lasers with solid matter forms the basis for advanced scientific applications such as table-top particle accelerators, ultrafast imaging systems and laser fusion. Key metrics for these applications relate to absorption, yet conditions in this regime are so nonlinear that it is often impossible to know the fraction of absorbed light f, and even the range of f is unknown. Here using a relativistic Rankine-Hugoniot-like analysis, we show for the first time that f exhibits a theoretical maximum and minimum. These bounds constrain nonlinear absorption mechanisms across the petawatt regime, forbidding high absorption values at low laser power and low absorption values at high laser power. For applications needing to circumvent the absorption bounds, these results will accelerate a shift from solid targets, towards structured and multilayer targets, and lead the development of new materials. PMID:24938656

  19. Petawatt laser absorption bounded

    NASA Astrophysics Data System (ADS)

    Levy, Matthew C.; Wilks, Scott C.; Tabak, Max; Libby, Stephen B.; Baring, Matthew G.

    2014-06-01

    The interaction of petawatt (1015 W) lasers with solid matter forms the basis for advanced scientific applications such as table-top particle accelerators, ultrafast imaging systems and laser fusion. Key metrics for these applications relate to absorption, yet conditions in this regime are so nonlinear that it is often impossible to know the fraction of absorbed light f, and even the range of f is unknown. Here using a relativistic Rankine-Hugoniot-like analysis, we show for the first time that f exhibits a theoretical maximum and minimum. These bounds constrain nonlinear absorption mechanisms across the petawatt regime, forbidding high absorption values at low laser power and low absorption values at high laser power. For applications needing to circumvent the absorption bounds, these results will accelerate a shift from solid targets, towards structured and multilayer targets, and lead the development of new materials.

  20. Percutaneous absorption of drugs.

    PubMed

    Wester, R C; Maibach, H I

    1992-10-01

    The skin is an evolutionary masterpiece of living tissue which is the final control unit for determining the local and systemic availability of any drug which must pass into and through it. In vivo in humans, many factors will affect the absorption of drugs. These include individual biological variation and may be influenced by race. The skin site of the body will also influence percutaneous absorption. Generally, those body parts exposed to the open environment (and to cosmetics, drugs and hazardous toxic substances) are most affected. Treating patients may involve single daily drug treatment or multiple daily administration. Finally, the body will be washed (normal daily process or when there is concern about skin decontamination) and this will influence percutaneous absorption. The vehicle of a drug will affect release of drug to skin. On skin, the interrelationships of this form of administration involve drug concentration, surface area exposed, frequency and time of exposure. These interrelationships determine percutaneous absorption. Accounting for all the drug administered is desirable in controlled studies. The bioavailability of the drug then is assessed in relationship to its efficacy and toxicity in drug development. There are methods, both quantitative and qualitative, in vitro and in vivo, for studying percutaneous absorption of drugs. Animal models are substituted for humans to determine percutaneous absorption. Each of these methods thus becomes a factor in determining percutaneous absorption because they predict absorption in humans. The relevance of these predictions to humans in vivo is of intense research interest. The most relevant determination of percutaneous absorption of a drug in humans is when the drug in its approved formulation is applied in vivo to humans in the intended clinical situation. Deviation from this scenario involves the introduction of variables which may alter percutaneous absorption. PMID:1296607

  1. Study on the effects of nitrilotriproprionic acid and 4,5-dihydroxy-1,3-benzene disulphonate on the fractionation of beryllium in human serum using graphite furnace atomic absorption spectrometry

    PubMed Central

    Stephan, Chadi H; Fournier, Michel; Brousseau, Pauline; Sauvé, Sébastien

    2008-01-01

    Background Occupational exposure to beryllium may cause Chronic Beryllium Disease (CBD), a lung disorder initiated by an electrostatic interaction with the MHC class II human leukocyte antigen (HLA). Molecular studies have found a significant correlation between the electrostatic potential at the HLA-DP surface and disease susceptibility. CBD can therefore be treated by chelation therapy. In this work, we studied the effect of two complexing agents, nitrilotriproprionic acid (NTP) and 4,5-dihydroxy-1,3-benzene disulphonate (Tiron), on the fractionation of beryllium in human serum analysed by graphite furnace atomic absorption spectrometry (GFAAS). Results We found the average serum beryllium concentration of fourteen non-exposed individuals to be 0.53 (± 0.14) μg l-1, with 21 (± 3)% of the beryllium mass bound to the low molecular weight fraction (LMW), and 79 (± 3)% bound to the high molecular weight fraction (HMW). The addition of Tiron increased the beryllium mass in the HMW fraction, while NTP was not seen to have any influence on the fractionation of beryllium between the two fractions. NTP was, however, shown to complex 94.5% of the Be mass in the LMW fraction. The beryllium GFAAS detection limit, calculated as three times the standard deviation of 10 replicates of the lowest standard (0.05 μg L-1), was 6.0 (± 0.2) ng L-1. Conclusion The concentration of beryllium or its fractionation in human serum was not affected by sex or smoking habit. On average, three quarters of the beryllium in serum were found in the HMW fraction. Of the two ligands tested, only Tiron was effective in mobilising beryllium under physiological conditions, thus increasing the Be content in the HMW fraction. PMID:18479524

  2. Speciation of As(III) and As(V) in water samples by graphite furnace atomic absorption spectrometry after solid phase extraction combined with dispersive liquid-liquid microextraction based on the solidification of floating organic drop.

    PubMed

    Shamsipur, Mojtaba; Fattahi, Nazir; Assadi, Yaghoub; Sadeghi, Marzieh; Sharafi, Kiomars

    2014-12-01

    A solid phase extraction (SPE) coupled with dispersive liquid-liquid microextraction based on the solidification of floating organic drop (DLLME-SFO) method, using diethyldithiphosphate (DDTP) as a proper chelating agent, has been developed as an ultra preconcentration technique for the determination of inorganic arsenic in water samples prior to graphite furnace atomic absorption spectrometry (GFAAS). Variables affecting the performance of both steps were thoroughly investigated. Under optimized conditions, 100mL of As(ΙΙΙ) solution was first concentrated using a solid phase sorbent. The extract was collected in 2.0 mL of acetone and 60.0 µL of 1-undecanol was added into the collecting solvent. The mixture was then injected rapidly into 5.0 mL of pure water for further DLLME-SFO. Total inorganic As(III, V) was extracted similarly after reduction of As(V) to As(III) with potassium iodide and sodium thiosulfate and As(V) concentration was calculated by difference. A mixture of Pd(NO3)2 and Mg(NO3)2 was used as a chemical modifier in GFAAS. The analytical characteristics of the method were determined. The calibration graph was linear in the rage of 10-100 ng L(-1) with detection limit of 2.5 ng L(-1). Repeatability (intra-day) and reproducibility (inter-day) of method based on seven replicate measurements of 80 ng L(-1) of As(ΙΙΙ) were 6.8% and 7.5%, respectively. The method was successfully applied to speciation of As(III), As(V) and determination of the total amount of As in water samples and in a certified reference material (NIST RSM 1643e). PMID:25159375

  3. Spectrophotometry of Pluto-Charon mutual events - Individual spectra of Pluto and Charon

    NASA Technical Reports Server (NTRS)

    Sawyer, S. R.; Barker, E. S.; Cochran, A. L.; Cochran, W. D.

    1987-01-01

    Time-resolved spectra of the March 3 and April 4, 1987 mutual events of Pluto and Charon, obtained with spectral coverage from 5500 to 10,000 A with 25-A spectral resolution, are discussed. Charon has a featureless reflectance spectrum, with no evidence of methane absorption. Charon's reflectance appears neutral in color and corresponds to a geometric albedo of about 0.37 at 6000 A. The Pluto reflectance spectrum displays methane absorption bands at 7300, 7900, 8400, 8600, and 8900 A and is red in color, with a geometric albedo of about 0.56 at 6000 A.

  4. Determination of copper in tap water using solid-phase spectrophotometry

    NASA Technical Reports Server (NTRS)

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

    1994-01-01

    A new application of ion exchange films is presented. The films are used in a simple analytical method of directly determining low concentrations of Cu(2+) in aqueous solutions, in particular, drinking water. The basis for this new test method is the color and absorption intensity of the ion when adsorbed onto the film. The film takes on the characteristic color of the adsorbed cation, which is concentrated on the film by many orders of magnitude. The linear relationship between absorbance (corrected for variations in film thickness) and solution concentration makes the determinations possible. These determinations agree well with flame atomic absorption determinations.

  5. Quasar Absorption Studies

    NASA Technical Reports Server (NTRS)

    Mushotzky, Richard (Technical Monitor); Elvis, Martin

    2004-01-01

    The aim of the proposal is to investigate the absorption properties of a sample of inter-mediate redshift quasars. The main goals of the project are: Measure the redshift and the column density of the X-ray absorbers; test the correlation between absorption and redshift suggested by ROSAT and ASCA data; constrain the absorber ionization status and metallicity; constrain the absorber dust content and composition through the comparison between the amount of X-ray absorption and optical dust extinction. Unanticipated low energy cut-offs where discovered in ROSAT spectra of quasars and confirmed by ASCA, BeppoSAX and Chandra. In most cases it was not possible to constrain adequately the redshift of the absorber from the X-ray data alone. Two possibilities remain open: a) absorption at the quasar redshift; and b) intervening absorption. The evidences in favour of intrinsic absorption are all indirect. Sensitive XMM observations can discriminate between these different scenarios. If the absorption is at the quasar redshift we can study whether the quasar environment evolves with the Cosmic time.

  6. [Determination of aluminum in wheat flour food by microwave digestion-high resolution continuum source graphite furnace atomic absorption spectrometry].

    PubMed

    Ren, Ting; Zhao, Li-jiao; Zhong, Ru-gang

    2011-12-01

    The contents of aluminum (Al) in four kinds of wheat flour food (noodle, dumpling wrapper, twisted cruller and soda biscuit) were determined by high resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS GFAAS) combined with microwave digestion. The samples were completely digested by the mixture of HNO3 and H2O2 in closed polytetrafluoroethylene (PTFE) vessels. The conditions for microwave digestion, pyrolysis temperature and atomization temperature were optimized. The optimum experimental conditions were determined as follows. The microwave digestion was performed with HNO3/H2O2 7:1 (volume ratio), microwave power 1000 W and 190 degrees C for 40 minutes. The optimum pyrolysis temperature was 1350 degrees C and the optimum atomization temperature was 2400 degrees C. Magnesium nitrate solution with the concentration of 1 g x L(-1) was used as the matrix modifier. The correlation coefficient for the standard curve was 0.9999, the relative standard deviation (RSD) was from 1.7% to 2.4%, and the recovery for the samples was from 98.16% to 102.67%. The assay method for the determination of Al in wheat flour food established in this study has referential importance for the constituent of the correlated food standards. PMID:22295801

  7. Determination of Beryllium in Soil and Sediment by Graphite Furnace Atomic Absorption with a Microwave-Acid Digestion Method.

    PubMed

    Lin, Hai-lan; Gan, Jie; Yu, Lei; Zhu, Ri-long; Tian, Yun; Luo, Yue-ping

    2015-11-01

    A method for determination of beryllium in soils and sediments by microwave-acid digestion/graphite furnace atomic absorption (GFAA) is described. In this paper, the working conditions of the instrument are optimized, the drawing of calibration curve is expounded, the pretreatment process of soil and sediments (including microwave heating process and the selection of digestion system) is discussed, and the interference of coexisting elements is examined. The sample was pretreated by microwave digestion parameters using HNO₃/ HCl/HF mixed acid system. The method is fast and simple without matrix modifier, and has no interference by coexisting ions, and has high repeatability and reproducibility. Under the optimal experimental conditions, the limit of detection (LOD) is 0.004 9 mg · kg⁻¹ (sample quantity 0.200 0 g, sample volume 25 mL), and the limits of quantitation (LOQ) is 0.20 mg · kg⁻¹. This method is used to measure the standard samples and actual samples, whether in the laboratory, or between laboratories, has good accuracy and precision. PMID:26978948

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

    PubMed

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

    2013-01-01

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

  9. Sorption of trace metals on human hair and application for cadmium and lead pre-concentration with flame atomic absorption determination.

    PubMed

    Sweileh, Jamal A

    2003-02-01

    Human hair shavings were characterized as a sorbent for trace metals. At pH 7.0 metal sorption follows the order Pb(II)>Cd(II)>Cr(VI)>Fe(III)>Cu(II)>Ni(II)>Mn(VI). Metal recovery is quantitative for Pb and Cd after 30 min of equilibration. Recovery of other metals is less quantitative and varies with pH. For example, while Cu is best recovered at pH 5, Ni and Mn are sorbed optimally in the basic pH region. Sorbed metals can be washed off the sorbent with 0.5 mol L(-1) strong mineral acids or more completely with 0.1 mol L(-1) ethylenediaminetetraacetic acid (EDTA). Typical sorption isotherms were obtained for Cd and Pb with sorption capacities of 39 and 26 micromol g(-1), respectively. Hair sorbent was used for 40-fold pre-concentration of Cd and Pb from treated wastewater samples followed by flame atomic absorption spectroscopic (FAAS) determination. Comparison of the data obtained for lead and cadmium by the proposed pre-concentration method with that by graphite furnace atomic absorption spectroscopy (GFAAS) showed 79 to 86% recovery and comparable analytical precision. Common cations and anions at the levels normally present in natural water do not interfere in the proposed pre-concentration-FAAS method. PMID:12589512

  10. Compounds affecting cholesterol absorption

    NASA Technical Reports Server (NTRS)

    Hua, Duy H. (Inventor); Koo, Sung I. (Inventor); Noh, Sang K. (Inventor)

    2004-01-01

    A class of novel compounds is described for use in affecting lymphatic absorption of cholesterol. Compounds of particular interest are defined by Formula I: ##STR1## or a pharmaceutically acceptable salt thereof.

  11. Absorption heat pump system

    DOEpatents

    Grossman, Gershon

    1984-01-01

    The efficiency of an absorption heat pump system is improved by conducting liquid from a second stage evaporator thereof to an auxiliary heat exchanger positioned downstream of a primary heat exchanger in the desorber of the system.

  12. Absorption heat pump system

    DOEpatents

    Grossman, G.

    1982-06-16

    The efficiency of an absorption heat pump system is improved by conducting liquid from a second stage evaporator thereof to an auxiliary heat exchanger positioned downstream of a primary heat exchanger in the desorber of the system.

  13. Dipeptide absorption in man

    PubMed Central

    Hellier, M. D.; Holdsworth, C. D.; McColl, I.; Perrett, D.

    1972-01-01

    A quantitative perfusion method has been used to study intestinal absorption of two dipeptides—glycyl-glycine and glycyl-l-alanine—in normal subjects. In each case, the constituent amino acids were absorbed faster when presented as dipeptides than as free amino acids, suggesting intact dipeptide transport. During absorption constituent amino acids were measured within the lumen and it is suggested that these represent amino acids which have diffused back to the lumen after absorption as dipeptide. Portal blood analyses during absorption of a third dipeptide, glycyl-l-lysine, have shown that this dipeptide, known to be transported intact from the intestinal lumen, is hydrolysed to its constitutent amino acids before it reaches portal venous blood. PMID:4652039

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

    PubMed

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

    2016-06-01

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

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

    SciTech Connect

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

    2006-03-15

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

  16. Optical absorption measurement system

    DOEpatents

    Draggoo, Vaughn G.; Morton, Richard G.; Sawicki, Richard H.; Bissinger, Horst D.

    1989-01-01

    The system of the present invention contemplates a non-intrusive method for measuring the temperature rise of optical elements under high laser power optical loading to determine the absorption coefficient. The method comprises irradiating the optical element with a high average power laser beam, viewing the optical element with an infrared camera to determine the temperature across the optical element and calculating the absorption of the optical element from the temperature.

  17. Solar selective absorption coatings

    DOEpatents

    Mahoney, Alan R.; Reed, Scott T.; Ashley, Carol S.; Martinez, F. Edward

    2004-08-31

    A new class of solar selective absorption coatings are disclosed. These coatings comprise a structured metallic overlayer such that the overlayer has a sub-micron structure designed to efficiently absorb solar radiation, while retaining low thermal emissivity for infrared thermal radiation. A sol-gel layer protects the structured metallic overlayer from mechanical, thermal, and environmental degradation. Processes for producing such solar selective absorption coatings are also disclosed.

  18. Solar selective absorption coatings

    DOEpatents

    Mahoney, Alan R.; Reed, Scott T.; Ashley, Carol S.; Martinez, F. Edward

    2003-10-14

    A new class of solar selective absorption coatings are disclosed. These coatings comprise a structured metallic overlayer such that the overlayer has a sub-micron structure designed to efficiently absorb solar radiation, while retaining low thermal emissivity for infrared thermal radiation. A sol-gel layer protects the structured metallic overlayer from mechanical, thermal, and environmental degradation. Processes for producing such solar selective absorption coatings are also disclosed.

  19. Novel ratio difference at coabsorptive point spectrophotometric method for determination of components with wide variation in their absorptivities.

    PubMed

    Saad, Ahmed S; Abo-Talib, Nisreen F; El-Ghobashy, Mohamed R

    2016-01-01

    Different methods have been introduced to enhance selectivity of UV-spectrophotometry thus enabling accurate determination of co-formulated components, however mixtures whose components exhibit wide variation in absorptivities has been an obstacle against application of UV-spectrophotometry. The developed ratio difference at coabsorptive point method (RDC) represents a simple effective solution for the mentioned problem, where the additive property of light absorbance enabled the consideration of the two components as multiples of the lower absorptivity component at certain wavelength (coabsorptive point), at which their total concentration multiples could be determined, whereas the other component was selectively determined by applying the ratio difference method in a single step. Mixture of perindopril arginine (PA) and amlodipine besylate (AM) figures that problem, where the low absorptivity of PA relative to AM hinders selective spectrophotometric determination of PA. The developed method successfully determined both components in the overlapped region of their spectra with accuracy 99.39±1.60 and 100.51±1.21, for PA and AM, respectively. The method was validated as per the USP guidelines and showed no significant difference upon statistical comparison with reported chromatographic method. PMID:26253440

  20. Novel ratio difference at coabsorptive point spectrophotometric method for determination of components with wide variation in their absorptivities

    NASA Astrophysics Data System (ADS)

    Saad, Ahmed S.; Abo-Talib, Nisreen F.; El-Ghobashy, Mohamed R.

    2016-01-01

    Different methods have been introduced to enhance selectivity of UV-spectrophotometry thus enabling accurate determination of co-formulated components, however mixtures whose components exhibit wide variation in absorptivities has been an obstacle against application of UV-spectrophotometry. The developed ratio difference at coabsorptive point method (RDC) represents a simple effective solution for the mentioned problem, where the additive property of light absorbance enabled the consideration of the two components as multiples of the lower absorptivity component at certain wavelength (coabsorptive point), at which their total concentration multiples could be determined, whereas the other component was selectively determined by applying the ratio difference method in a single step. Mixture of perindopril arginine (PA) and amlodipine besylate (AM) figures that problem, where the low absorptivity of PA relative to AM hinders selective spectrophotometric determination of PA. The developed method successfully determined both components in the overlapped region of their spectra with accuracy 99.39 ± 1.60 and 100.51 ± 1.21, for PA and AM, respectively. The method was validated as per the USP guidelines and showed no significant difference upon statistical comparison with reported chromatographic method.

  1. Seven-effect absorption refrigeration

    DOEpatents

    DeVault, Robert C.; Biermann, Wendell J.

    1989-01-01

    A seven-effect absorption refrigeration cycle is disclosed utilizing three absorption circuits. In addition, a heat exchanger is used for heating the generator of the low absorption circuit with heat rejected from the condenser and absorber of the medium absorption circuit. A heat exchanger is also provided for heating the generator of the medium absorption circuit with heat rejected from the condenser and absorber of the high absorption circuit. If desired, another heat exchanger can also be provided for heating the evaporator of the high absorption circuit with rejected heat from either the condenser or absorber of the low absorption circuit.

  2. Seven-effect absorption refrigeration

    DOEpatents

    DeVault, R.C.; Biermann, W.J.

    1989-05-09

    A seven-effect absorption refrigeration cycle is disclosed utilizing three absorption circuits. In addition, a heat exchanger is used for heating the generator of the low absorption circuit with heat rejected from the condenser and absorber of the medium absorption circuit. A heat exchanger is also provided for heating the generator of the medium absorption circuit with heat rejected from the condenser and absorber of the high absorption circuit. If desired, another heat exchanger can also be provided for heating the evaporator of the high absorption circuit with rejected heat from either the condenser or absorber of the low absorption circuit. 1 fig.

  3. Ligandless, ion pair-based and ultrasound assisted emulsification solidified floating organic drop microextraction for simultaneous preconcentration of ultra-trace amounts of gold and thallium and determination by GFAAS.

    PubMed

    Fazelirad, Hamid; Taher, Mohammad Ali

    2013-01-15

    In the present work, a new, simple and efficient method for simultaneous preconcentration of ultra-trace amounts of gold and thallium is developed using an ion pair based-ultrasound assisted emulsification-solidified floating organic drop microextraction procedure before graphite furnace atomic absorption spectrometry determination. This methodology was used to preconcentrate the ion pairs formed between AuCl(4)(-) and TlCl(4)(-) and [C(23)H(42)]N(+) in a microliter-range volume of 1-undecanol. Several factors affecting the microextraction efficiency, such as HCl volume, type and volume of extraction solvent, sonication time, sample volume, temperature, ionic strength and [C(23)H(42)]NCl volume were investigated and optimized. Under the optimized conditions, the enrichment factor of 441 and 443 and calibration graphs of 2.2-89 and 22.2-667 ng L(-1) for gold and thallium were obtained, respectively. The intra- and inter-day precision of ± 4.4 and ± 4.9% for Au and ± 4.8 and ± 5.4% for Tl were obtained. The detection limit was 0.66 ng L(-1) for Au and 4.67 ng L(-1) for Tl. The results show that the liquid-liquid pretreatment using ion pair forming, is sensitive, rapid, simple and safe method for the simultaneous preconcentration of gold and thallium. The method was successfully applied for determination of gold and thallium in natural water and hair samples. PMID:23200402

  4. Simultaneous determination of mercury and organic carbon in sediment and soils using a direct mercury analyzer based on thermal decomposition-atomic absorption spectrophotometry.

    PubMed

    Chen, Jingjing; Chakravarty, Pragya; Davidson, Gregg R; Wren, Daniel G; Locke, Martin A; Zhou, Ying; Brown, Garry; Cizdziel, James V

    2015-04-29

    The purpose of this work was to study the feasibility of using a direct mercury analyzer (DMA) to simultaneously determine mercury (Hg) and organic matter content in sediment and soils. Organic carbon was estimated by re-weighing the sample boats post analysis to obtain loss-on-ignition (LOI) data. The DMA-LOI results were statistically similar (p<0.05) to the conventional muffle furnace approach. A regression equation was developed to convert DMA-LOI data to total organic carbon (TOC), which varied between 0.2% and 13.0%. Thus, mercury analyzers based on combustion can provide accurate estimates of organic carbon content in non-calcareous sediment and soils; however, weight gain from moisture (post-analysis), measurement uncertainty, and sample representativeness should all be taken into account. Sediment cores from seasonal wetland and open water areas from six oxbow lakes in the Mississippi River alluvial flood plain were analyzed. Wetland sediments generally had higher levels of Hg than open water areas owing to a greater fraction of fine particles and higher levels of organic matter. Annual loading of Hg in open water areas was estimated at 4.3, 13.4, 19.2, 20.7, 129, and 135 ng cm(-2) yr(-1) for Beasley, Roundaway, Hampton, Washington, Wolf and Sky Lakes, respectively. Generally, the interval with the highest Hg flux was dated to the 1960s and 1970s. PMID:25847156

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

    PubMed

    Cielecka-Piontek, Judyta

    2013-07-01

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

  6. Petawatt laser absorption bounded

    NASA Astrophysics Data System (ADS)

    Levy, Matthew; Wilks, Scott; Tabak, Max; Libby, Stephen; Baring, Matthew

    2014-10-01

    The interaction of petawatt (1015 W) lasers with solid matter forms the basis for advanced scientific applications such as table-top relativistic particle accelerators, ultrafast charged particle imaging systems and fast ignition inertial confinement fusion. Key metrics for these applications relate to absorption, yet conditions in this regime are so nonlinear that it is often impossible to know the fraction of absorbed light f, and even the range of f is unknown. In this presentation, using a relativistic Rankine-Hugoniot-like analysis, we show how to derive the theoretical maximum and minimum of f. These boundaries constrain nonlinear absorption mechanisms across the petawatt regime, forbidding high absorption values at low laser power and low absorption values at high laser power. Close agreement is shown with several dozens of published experimental data points and simulation results, helping to confirm the theory. For applications needing to circumvent the absorption bounds, these results will accelerate a shift from solid targets, towards structured and multilayer targets, and lead the development of new materials.

  7. Percutaneous absorption from soil.

    PubMed

    Andersen, Rosa Marie; Coman, Garrett; Blickenstaff, Nicholas R; Maibach, Howard I

    2014-01-01

    Abstract Some natural sites, as a result of contaminants emitted into the air and subsequently deposited in soil or accidental industrial release, have high levels of organic and non-organic chemicals in soil. In occupational and recreation settings, these could be potential sources of percutaneous exposure to humans. When investigating percutaneous absorption from soil - in vitro or vivo - soil load, particle size, layering, soil "age" time, along with the methods of performing the experiment and analyzing the results must be taken into consideration. Skin absorption from soil is generally reduced compared with uptake from water/acetone. However, the absorption of some compounds, e.g., pentachlorophenol, chlorodane and PCB 1254, are similar. Lipophilic compounds like dichlorodiphenyltrichloroethane, benzo[A]pyrene, and metals have the tendency to form reservoirs in skin. Thus, one should take caution in interpreting results directly from in vitro studies for risk assessment; in vivo validations are often required for the most relevant risk assessment. PMID:25205703

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

    PubMed

    Zheng, Jinjian; Tan, Feng; Hartman, Robert

    2015-09-01

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

  9. Multiplasmon Absorption in Graphene

    NASA Astrophysics Data System (ADS)

    Jablan, Marinko; Chang, Darrick E.

    2015-06-01

    We show that graphene possesses a strong nonlinear optical response in the form of multiplasmon absorption, with exciting implications in classical and quantum nonlinear optics. Specifically, we predict that graphene nanoribbons can be used as saturable absorbers with low saturation intensity in the far-infrared and terahertz spectrum. Moreover, we predict that two-plasmon absorption and extreme localization of plasmon fields in graphene nanodisks can lead to a plasmon blockade effect, in which a single quantized plasmon strongly suppresses the possibility of exciting a second plasmon.

  10. Chaotic Systems with Absorption

    NASA Astrophysics Data System (ADS)

    Altmann, Eduardo G.; Portela, Jefferson S. E.; Tél, Tamás

    2013-10-01

    Motivated by applications in optics and acoustics we develop a dynamical-system approach to describe absorption in chaotic systems. We introduce an operator formalism from which we obtain (i) a general formula for the escape rate κ in terms of the natural conditionally invariant measure of the system, (ii) an increased multifractality when compared to the spectrum of dimensions Dq obtained without taking absorption and return times into account, and (iii) a generalization of the Kantz-Grassberger formula that expresses D1 in terms of κ, the positive Lyapunov exponent, the average return time, and a new quantity, the reflection rate. Simulations in the cardioid billiard confirm these results.

  11. Absorption heat pump system

    DOEpatents

    Grossman, Gershon; Perez-Blanco, Horacio

    1984-01-01

    An improvement in an absorption heat pump cycle is obtained by adding adiabatic absorption and desorption steps to the absorber and desorber of the system. The adiabatic processes make it possible to obtain the highest temperature in the absorber before any heat is removed from it and the lowest temperature in the desorber before heat is added to it, allowing for efficient utilization of the thermodynamic availability of the heat supply stream. The improved system can operate with a larger difference between high and low working fluid concentrations, less circulation losses, and more efficient heat exchange than a conventional system.

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

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  13. Scanning spectrophotometry for the dynamic study of tissue respiration in intact organs.

    PubMed

    Jarry, G; Marzouki, L; Debray, S; Ghesquiere, S; Besson, B; Hung, B M; Laurent, D

    1986-04-01

    For use with intact perfused organs a spectrophotometer system has been developed, both for dual-wavelength absorption measurements and for spectral scanning. A monochromator is used for illumination and scanning in the visible and near infrared. Optic fibres conduct light to the specimen under examination and from the specimen to a detecting photomultiplier. System control is exercised by a microcomputer, which also processes the collected data. The performance of the system on isolated perfused rat heart is demonstrated, in the spectral scanning mode and in the dual-wavelength mode, by studying simultaneously the kinetics of cytochrome aa3, and myoglobin oxidation-reduction. PMID:3012201

  14. Two-Phonon Absorption

    ERIC Educational Resources Information Center

    Hamilton, M. W.

    2007-01-01

    A nonlinear aspect of the acousto-optic interaction that is analogous to multi-photon absorption is discussed. An experiment is described in which the second-order acousto-optically scattered intensity is measured and found to scale with the square of the acoustic intensity. This experiment using a commercially available acousto-optic modulator is…

  15. Total absorption Cherenkov spectrometers

    NASA Astrophysics Data System (ADS)

    Malinovski, E. I.

    2015-05-01

    A short review of 50 years of work done with Cherenkov detectors in laboratories at the Lebedev Physical Institute is presented. The report considers some issues concerning the use of Cherenkov total absorption counters based on lead glass and heavy crystals in accelerator experiments.

  16. Cholesterol Absorption and Metabolism.

    PubMed

    Howles, Philip N

    2016-01-01

    Inhibitors of cholesterol absorption have been sought for decades as a means to treat and prevent cardiovascular diseases (CVDs) associated with hypercholesterolemia. Ezetimibe is the one clear success story in this regard, and other compounds with similar efficacy continue to be sought. In the last decade, the laboratory mouse, with all its genetic power, has become the premier experimental model for discovering the mechanisms underlying cholesterol absorption and has become a critical tool for preclinical testing of potential pharmaceutical entities. This chapter briefly reviews the history of cholesterol absorption research and the various gene candidates that have come under consideration as drug targets. The most common and versatile method of measuring cholesterol absorption is described in detail along with important considerations when interpreting results, and an alternative method is also presented. In recent years, reverse cholesterol transport (RCT) has become an area of intense new interest for drug discovery since this process is now considered another key to reducing CVD risk. The ultimate measure of RCT is sterol excretion and a detailed description is given for measuring neutral and acidic fecal sterols and interpreting the results. PMID:27150091

  17. Lipids: Absorption and transport

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Due to the hydrophobic nature of lipids, dietary fat is handled differently than protein or carbohydrate with respect with digestion and absorption. Dietary fats are broken down throughout the gastrointestinal system. A unique group of enzymes and cofactors allows this process to proceed in an eff...

  18. ZINC ABSORPTION BY INFANTS

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Zinc is a vital mineral in human nutrition, and rare cases of overt zinc deficiency are well described in term and preterm infants. A variety of methods have been developed to assess zinc absorption, retention, and balance in humans, either using mass (metabolic) balance or stable isotope-based METH...

  19. Absorption driven focus shift

    NASA Astrophysics Data System (ADS)

    Harrop, N.; Wolf, S.; Maerten, O.; Dudek, K.; Ballach, S.; Kramer, R.

    2016-03-01

    Modern high brilliance near infrared lasers have seen a tremendous growth in applications throughout the world. Increased productivity has been achieved by higher laser power and increased brilliance of lasers. Positive impacts on the performance and costs of parts are opposed to threats on process stability and quality, namely shift of focus position over time. A high initial process quality will be reduced by contamination of optics, eventually leading to a focus shift or even destruction of the optics. Focus analysis at full power of multi-kilowatt high brilliance lasers is a very demanding task because of high power densities in the spot and the high power load on optical elements. With the newly developed high power projection optics, the High-Power Micro-Spot Monitor High Brilliance (HP-MSM-HB) is able to measure focus diameter as low as 20 μm at power levels up to 10 kW at very low internal focus shift. A main driving factor behind thermally induced focus shift is the absorption level of the optical element. A newly developed measuring system is designed to determine the relative absorption level in reference to a gold standard. Test results presented show a direct correlation between absorption levels and focus shift. The ability to determine the absorption level of optical elements as well as their performance at full processing power before they are put to use, enables a high level of quality assurance for optics manufacturers and processing head manufacturers alike.

  20. Ultrasensitive determination of cadmium in seawater by hollow fiber supported liquid membrane extraction coupled with graphite furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Peng, Jin-feng; Liu, Rui; Liu, Jing-fu; He, Bin; Hu, Xia-lin; Jiang, Gui-bin

    2007-05-01

    A new procedure, based on hollow fiber supported liquid membrane preconcentration coupled with graphite furnace atomic absorption spectrometry (GFAAS) detection, was developed for the determination of trace Cd in seawater samples. With 1-octanol that contained a mixture of dithizone (carrier) and oleic acid immobilized in the pores of the polypropylene hollow fiber as a liquid membrane, Cd was selectively extracted from water samples into 0.05 M HNO 3 that filled the lumen of the hollow fiber as a stripping solution. The main extraction related parameters were optimized, and the effects of salinity and some coexisting interferants were also evaluated. Under the optimum extraction conditions, an enrichment factor of 387 was obtained for a 100-mL sample solution. In combination with graphite furnace atomic absorption spectrometry, a very low detection limit (0.8 ng L - 1 ) and a relative standard deviation (2.5% at 50 ng L - 1 level) were achieved. Five seawater samples were analyzed by the proposed method without dilution, with detected Cd concentration in the range of 56.4-264.8 ng L - 1 and the relative spiked recoveries over 89%. For comparison, these samples were also analyzed by the Inductively Coupled Plasma Mass Spectrometry (ICP-MS) method after a 10-fold dilution for matrix effect elimination. Statistical analysis with a one-way ANOVA shows no significant differences (at 0.05 level) between the results obtained by the proposed and ICP-MS methods. Additionally, analysis of certified reference materials (GBW (E) 080040) shows good agreement with the certified value. These results indicate that this present method is very sensitive and reliable, and can effectively eliminate complex matrix interferences in seawater samples.

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

    PubMed

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

    2016-06-01

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

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

    PubMed

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

    2008-09-10

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

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

    PubMed

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

    2010-11-01

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

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

    SciTech Connect

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

    2002-11-30

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

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

    PubMed

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

    2016-04-01

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

  6. 69. INTERIOR VIEW OF THE ABSORPTION TOWER BUILDING, ABSORPTION TOWER ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    69. INTERIOR VIEW OF THE ABSORPTION TOWER BUILDING, ABSORPTION TOWER UNDER CONSTRUCTION. (DATE UNKNOWN). - United States Nitrate Plant No. 2, Reservation Road, Muscle Shoals, Muscle Shoals, Colbert County, AL

  7. Catalog of far-ultraviolet objective-prism spectrophotometry: Skylab experiment S-019, ultraviolet steller astronomy

    NASA Technical Reports Server (NTRS)

    Henize, K. G.; Wray, J. D.; Parsons, S. B.; Benedict, G. F.

    1979-01-01

    Ultraviolet stellar spectra in the wavelength region from 1300 to 5000 A (130 to 500) were photographed during the three manned Skylab missions using a 15 cm aperture objective-prism telescope. The prismatic dispersion varied from 58 A mm/1 at 1400 A to 1600 A mm/1 at 3000 A. Approximately 1000 spectra representing 500 stars were measured and reduced to observed fluxes. About 100 stars show absorption lines of Si IV, C IV, or C II. Numerous line features are also recorded in supergiant stars, shell stars, A and F stars, and Wolf-Rayet stars. Most of the stars in the catalog are of spectral class B, with a number of O and A type stars and a sampling of WC, WN, F and C type stars. Spectrophotometric results are tabulated for these 500 stars.

  8. Spectrophotometry /0.33 to 1.07 microns/ of 433 Eros and compositional implications

    NASA Technical Reports Server (NTRS)

    Pieters, C.; Gaffey, M. J.; Chapman, C. R.; Mccord, T. B.

    1976-01-01

    The spectral reflectance (0.33-1.07 micrometers) for the asteroid 433 Eros was determined as a function of rotational phase during January 28-30, and February 15, 1975. Interpretation of absorption features suggests Eros is composed of an undifferentiated assemblage of moderate to high temperature minerals (iron, pyroxene, and olivine, but no carbon). H-type ordinary chondrites are such assemblages, but it would be premature to conclude that Eros is like an H chondrite meteorite in composition until a better understanding is reached of possible physical differences between laboratory powders and asteroid regoliths for metal-bearing assemblages. There are no large-scale major compositional variations on the different sides of Eros.

  9. Double beam spectrophotometry in the far ultraviolet. 1: 1150 A to 3600 A.

    PubMed

    Schmitt, R G; Brehm, R K

    1966-07-01

    The instrument described is a double beam spectrophotometer with a wavelength range of 1150 A to 3600 A. Continua are supplied by three microwave-excited, rare-gas discharge lamps and a standard hydrogen lamp. A 1-m, normal-incidence, concave-grating monochromator is used. The beam splitting arrangement is an oscillating toroidal mirror, resonant at 11.3 c/s and arranged so that only a single reflection in each beam is required. The detectors are type EMI 6255S, each with a sodium salicylate phosphor. A ratio recording measuring system is used, with absorbance indicated on a 1.5-cycle logarithmic recorder. The performance data include vapor absorption spectra of several organic compounds and spectral reflectance measurements of magnesium-fluoride-coated aluminum surfaces. Stray light measurements are made by considering the constancy of absorbance vs pressure of water vapor at several wavelengths. PMID:20049029

  10. [Rate of controlled-release urea pervasion through membrane determined by ultraviolet spectrophotometry].

    PubMed

    Zuo, Xiu-jin; Wang, Zhen-xin; Dai, Xiao-min; Zhou, Yi; Ma, Xiao-jun

    2006-06-01

    Application of controlled-release nitrogenous fertilizers can improve the efficiency of fertilizers and reduce the environmental pollution. Controlled-release urea (coated urea) is one of the controlled-release nitrogenous fertilizers developed quickly in the recent years. The rate of controlled-release urea pervasion through membrane is the most important index of the capacity of controlled release. There is a maximum absorption at lambda=426 nm with complex in acidic solution, using p-dimethylaminozenzaldehyde as color reagent, and the absorbance exhibits a linear reponses to the urea concentration over the range of 7.5-210 microg x mL(-1). The method for determining the rate of controlled-release urea pervasion through membrane was realized through determining the content of urea in the liquor, the recovery efficiency of the method is 96.1%-103.9%. PMID:16961255

  11. Metallicity determinations for globular clusters through spectrophotometry of their integrated light

    NASA Astrophysics Data System (ADS)

    Brodie, J. P.; Hanes, D. A.

    1986-01-01

    Using an appropriately weighted combination of 16 indices of absorption line strength measured in low-dispersion spectra of the integrated light of globular clusters, metallicities Fe/H are determined for thirty-six clusters in the Galaxy. The results confirm the suggestion that Zinn's (1980) scale suffers a systematic error in the region of intermediate metallicity and support an explanation in which his metallicity-indicative Q39 index has been diluted by excess ultraviolet light in clusters with anomalously rich blue horizontal branches. The methods, which involve the measurement of spectral features arising from many species, produce estimates of metallicity which are insensitive to this problem. Good agreement is found with several recent studies, but a disagreement is noted for the most metal-rich clusters studied by Frogel, Cohen, and Persson (1983). Finally, a similar method with a modified calibration is used to determine metallicities for the nuclei of six galaxies.

  12. Seasonal skin colour changes in a sample teenage population measured by reflection spectrophotometry

    NASA Astrophysics Data System (ADS)

    Stringer, M. R.; Cruse-Sawyer, J. E.

    2007-11-01

    As part of a classroom-based research project, reflectance spectra from the skin of a group of teenage school students were recorded over a four-month period, from early spring to mid-summer. The relative changes in skin colour during the course of the study were quantified by integrating over the full wavelength range of the normalized reflectance spectra. Measurements made upon the inner forearm and the back of the hand produce results which indicate a decrease in total reflectance (increase in absorption) corresponding to different levels of tanning for limited and extended exposure to ambient sunlight, respectively. The rate of change of skin colour qualitatively matches that of the solar illuminance.

  13. Chaotic systems with absorption.

    PubMed

    Altmann, Eduardo G; Portela, Jefferson S E; Tél, Tamás

    2013-10-01

    Motivated by applications in optics and acoustics we develop a dynamical-system approach to describe absorption in chaotic systems. We introduce an operator formalism from which we obtain (i) a general formula for the escape rate κ in terms of the natural conditionally invariant measure of the system, (ii) an increased multifractality when compared to the spectrum of dimensions D(q) obtained without taking absorption and return times into account, and (iii) a generalization of the Kantz-Grassberger formula that expresses D(1) in terms of κ, the positive Lyapunov exponent, the average return time, and a new quantity, the reflection rate. Simulations in the cardioid billiard confirm these results. PMID:24138240

  14. Pathways of iron absorption.

    PubMed

    Conrad, Marcel E; Umbreit, Jay N

    2002-01-01

    Iron is vital for all living organisms but excess iron can be lethal because it facilitates free radical formation. Thus iron absorption is carefully regulated to maintain an equilibrium between absorption and body loss of iron. In countries where meat is a significant part of the diet, most body iron is derived from dietary heme because heme binds few of the dietary chelators that bind inorganic iron. Uptake of heme into enterocytes occurs as a metalloporphyrin in an endosomal process. Intracellular iron is released from heme by heme oxygenase to enter plasma as inorganic iron. Ferric iron is absorbed via a beta(3) integrin and mobilferrin pathway (IMP) which is unshared with other nutritional metals. Ferrous iron uptake is facilitated by a DMT-1 pathway which is shared with manganese. In the iron deficient gut, large quantities of both mobilferrin and DMT-1 are found in goblet cells and intraluminal mucins suggesting that they are secreted with mucin into the intestinal lumen to bind iron to facilitate uptake by the cells. In the cytoplasm, IMP and DMT associate in a large protein complex called paraferritin which serves as a ferrireductase. Paraferritin solublizes iron binding proteins and reduces iron to make iron available for production of iron containing proteins such as heme. Iron uptake by intestinal absorptive cells is regulated by the iron concentration within the cell. Except in hemochromatosis it remains in equilibrium with total body stores via transferrin receptors on the basolateral membrane of absorptive cells. Increased intracellular iron either up-regulates or satiates iron binding proteins on regulatory proteins to alter their location in the intestinal mucosa. PMID:12547224

  15. Relic Neutrino Absorption Spectroscopy

    SciTech Connect

    Eberle, b

    2004-01-28

    Resonant annihilation of extremely high-energy cosmic neutrinos on big-bang relic anti-neutrinos (and vice versa) into Z-bosons leads to sizable absorption dips in the neutrino flux to be observed at Earth. The high-energy edges of these dips are fixed, via the resonance energies, by the neutrino masses alone. Their depths are determined by the cosmic neutrino background density, by the cosmological parameters determining the expansion rate of the universe, and by the large redshift history of the cosmic neutrino sources. We investigate the possibility of determining the existence of the cosmic neutrino background within the next decade from a measurement of these absorption dips in the neutrino flux. As a by-product, we study the prospects to infer the absolute neutrino mass scale. We find that, with the presently planned neutrino detectors (ANITA, Auger, EUSO, OWL, RICE, and SalSA) operating in the relevant energy regime above 10{sup 21} eV, relic neutrino absorption spectroscopy becomes a realistic possibility. It requires, however, the existence of extremely powerful neutrino sources, which should be opaque to nucleons and high-energy photons to evade present constraints. Furthermore, the neutrino mass spectrum must be quasi-degenerate to optimize the dip, which implies m{sub {nu}} 0.1 eV for the lightest neutrino. With a second generation of neutrino detectors, these demanding requirements can be relaxed considerably.

  16. Novel ion imprinted magnetic mesoporous silica for selective magnetic solid phase extraction of trace Cd followed by graphite furnace atomic absorption spectrometry detection

    NASA Astrophysics Data System (ADS)

    Zhao, Bingshan; He, Man; Chen, Beibei; Hu, Bin

    2015-05-01

    Determination of trace Cd in environmental, biological and food samples is of great significance to toxicological research and environmental pollution monitoring. While the direct determination of Cd in real-world samples is difficult due to its low concentration and the complex matrix. Herein, a novel Cd(II)-ion imprinted magnetic mesoporous silica (Cd(II)-II-MMS) was prepared and was employed as a selective magnetic solid-phase extraction (MSPE) material for extraction of trace Cd in real-world samples followed by graphite furnace atomic absorption spectrometry (GFAAS) detection. Under the optimized conditions, the detection limit of the proposed method was 6.1 ng L- 1 for Cd with the relative standard deviation (RSD) of 4.0% (c = 50 ng L- 1, n = 7), and the enrichment factor was 50-fold. To validate the proposed method, Certified Reference Materials of GSBZ 50009-88 environmental water, ZK018-1 lyophilized human urine and NIES10-b rice flour were analyzed and the determined values were in a good agreement with the certified values. The proposed method exhibited a robust anti-interference ability due to the good selectivity of Cd(II)-II-MMS toward Cd(II). It was successfully employed for the determination of trace Cd(II) in environmental water, human urine and rice samples with recoveries of 89.3-116%, demonstrating that the proposed method has good application potential in real world samples with complex matrix.

  17. Determination of macro and trace elements in multivitamin dietary supplements by high-resolution continuum source graphite furnace atomic absorption spectrometry with slurry sampling.

    PubMed

    Krawczyk, Magdalena

    2014-01-01

    In this research, three different commercially available multivitamin dietary supplements were analyzed by high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS GFAAS) with slurry sampling. The concentrations of Cr, Cu, Fe, Mn, and Se were determined and compared to the amounts stated by producers. The safety of multivitamin dietary supplements depends on various factors including the manufacturing process and the purity and origins of the raw ingredients. For this reason, this research determined concentrations of several toxic elements (As, Cd, and Pb). Microwave-assisted high pressure Teflon bomb digestion was used to determine total amounts of elements in samples. Samples were prepared as slurries at a concentration of 0.1% (m/v) for macro elements (Cr, Cu, Fe, Mn, and Se) and at a concentration of % (m/v) for trace elements (As, Cd, and Pb) in acidic media (3M HNO3). The influence of acid concentration, Triton X-100 addition, sonication time, and sonication power on absorbance was investigated. The accuracy of this method was validated by analyses of NRCC LUTS-1 (Lobster hepatopancreas), NRCC DORM-1 (Dogfish Muscle), NRCC DOLT-2 (Dogfish Liver), NBS SRM 1570 (Spinach Leaves) and NBS SRM 1573 (Tomato Leaves) certified reference materials. The measured elements contents in these reference materials (except NRCC DOLT-2) were in satisfactory agreement with the certified values according to the t-test for a 95% confidence level. PMID:24176741

  18. Development of a simple method for the determination of lead in lipstick using alkaline solubilization and graphite furnace atomic absorption spectrometry.

    PubMed

    Soares, Aline Rodrigues; Nascentes, Clésia Cristina

    2013-02-15

    A simple method was developed for determining the total lead content in lipstick samples by graphite furnace atomic absorption spectrometry (GFAAS) after treatment with tetramethylammonium hydroxide (TMAH). Multivariate optimization was used to establish the optimal conditions of sample preparation. The graphite furnace heating program was optimized through pyrolysis and atomization curves. An aliquot containing approximately 50mg of the sample was mixed with TMAH and heated in a water bath at 60°C for 60 min. Using Nb as the permanent modifier and Pd as the chemical modifier, the optimal temperatures were 900°C and 1800°C for pyrolysis and atomization, respectively. Under optimum conditions, the working range was from 1.73 to 50.0 μg L(-1), with detection and quantification limits of 0.20 and 0.34 μg g(-1), respectively. The precision was evaluated under conditions of repeatability and intermediate precision and showed standard deviations of 2.37%-4.61% and 4.93%-9.75%, respectively. The % recovery ranged from 96.2% to 109%, and no significant differences were found between the results obtained using the proposed method and the microwave decomposition method for real samples. Lead was detected in 21 tested lipstick samples; the lead content in these samples ranged from 0.27 to 4.54 μg g(-1). PMID:23598019

  19. Separation and preconcentration of trace level of lead in one drop of blood sample by using graphite furnace atomic absorption spectrometry.

    PubMed

    Shrivas, Kamlesh; Patel, Devesh Kumar

    2010-04-15

    Drop-to-drop solvent microextraction (DDSME) assisted with ultrasonication is applied for the determination of lead in one drop (30 microL) of blood sample by using graphite furnace atomic absorption spectrometry (GF-AAS). The optimum extraction efficiency of lead was observed for 10 min extraction time at pH 5.0 with 2 microL of organic solvent that containing 0.5 M of Cyanex-302. The optimized methodology exhibited good linearity in the range of 0.3-30.0 ng mL(-1) lead with relative standard deviations (RSD) from 2.5 to 4.4%. The method is found to be simple and rapid for the analysis of lead in micro amount of blood sample with the limit of detection (LOD) of 0.08 ng mL(-1). The application of the proposed method has been successfully tested for the determination of lead in blood samples. The results showed that under the optimized experimental conditions, the method showed good sensitivity and recovery %, as well as advantages such as linearity, simplicity, low cost and high feasibility. PMID:20004520

  20. Electronic absorption spectra of U3+ and U4+ in molten LiCl-RbCl eutectic

    NASA Astrophysics Data System (ADS)

    Nagai, T.; Uehara, A.; Fujii, T.; Sato, N.; Yamana, H.

    2010-03-01

    In the non-aqueous reprocessing process of spent nuclear fuels by the pyro-electrochemical method, a spent fuel is dissolved into molten LiCl-KCl and NaCl-CsCl eutectics and dissolved uranium and plutonium are collected as either metal or oxide. However, the binary alkali chloride mixture with the lowest melting point is the LiCl-RbCl eutectic. In this study, electronic absorption spectra of U3+ and U4+ in molten LiCl-RbCl eutectic at various temperatures between 673 and 973 K were measured by the UV/Vis/NIR spectrophotometry. We confirmed that these spectra were similar to those in molten LiCl-KCl and NaCl-CsCl eutectics. The sensitive absorption bands of U4+ in LiCl-RbCl eutectic were found at 22000, 16500, 14900, 8600, and 4950 cm-1. The large absorption bands of U4+ over 25000 cm-1 increased with increasing melt temperature, while absorption peaks at 15500-4000 cm-1 decreased. The large absorption bands of U3+ in LiCl-RbCl eutectic were observed over 14000 cm-1. The sensitive absorption bands of U3+ at Vis/NIR region were found at 13300, 11500-11200, 9800-9400, and 8250 cm-1, and these peaks decreased with increasing temperature.

  1. Corrosion Problems in Absorption Chillers

    ERIC Educational Resources Information Center

    Stetson, Bruce

    1978-01-01

    Absorption chillers use a lithium bromide solution as the medium of absorption and water as the refrigerant. Discussed are corrosion and related problems, tests and remedies, and cleaning procedures. (Author/MLF)

  2. Acoustic Absorption Characteristics of People.

    ERIC Educational Resources Information Center

    Kingsbury, H. F.; Wallace, W. J.

    1968-01-01

    The acoustic absorption characteristics of informally dressed college students in typical classroom seating are shown to differ substantially from data for formally dressed audiences in upholstered seating. Absorption data, expressed as sabins per person or absorption coefficient per square foot, shows that there is considerable variation between…

  3. Determination of trace amount of oxalic acid with zirconium(IV)-(DBS-arsenazo) by spectrophotometry

    NASA Astrophysics Data System (ADS)

    Zhai, Qing-Zhou

    2008-11-01

    A novel method is proposed for the determination of trace amount of oxalic acid in the present article. In 1.0 M hydrochloric acid medium, oxalic acid can react with the zirconium(IV) in Zr(IV)-(DBS-arsenazo) complex and replaces the DBS-arsenazo to produce a hyperchromic effect at 520 nm. The hyperchromic degree is proportional to the concentration of the oxalic acid added over a defined range. Based on this property, a new method for the spectrophotometric determination of trace oxalic acid was developed. Beer's law is held over the concentration range of 9.0 × 10 -6 to 5.0 × 10 -4 M for oxalic acid with a correlation coefficient of 0.9995. The apparent molar absorptivity of the method is ɛ520 nm = 1.16 × 10 3 L mol -1 cm -1 and the detection limit for oxalic acid is 0.815 μg/mL. The developed method was directly applied to the determination of oxalic acid in tomato samples with satisfactory results.

  4. Spectrophotometry of zonal cloud structure variations on Jupiter, 1988-1993

    NASA Astrophysics Data System (ADS)

    Tejfel, V. G.; Vdovichenko, V. D.; Sinyaeva, N. V.; Mosina, S. A.; Gajsina, W. N.; Kharitonova, G. A.; Aksenov, A. N.

    1994-04-01

    Global changes of zonal cloud structure on Jupiter have been observed and analyzed from data obtained with a 1-m telescope and a low-dispersion spectrograph in the spectral range wavelengths 400-680 nm, and with a 70-cm telescope and planetary three-channel spectrometer in the spectral range wavelengths 320-1100 nm during each Jovian apparition from 1988 to 1992. Variations of the observed meridional intensity profiles and relative spectrophotometric gradients are described as well as the changes of absolute spectral reflectivity of five main belts on Jupiter (North and South Equatorial belts, North and South Tropical zones, and Equatorial region). Some peculiarities in the behavior of spectrophotometric gradients may be interpreted as a result of increased Rayleigh scattering in the gas layer over the deeper effective cloud boundary within main dark belts. The polar limb darkening varies only slightly with wavelength and it may be considered as evidence for dark aerosols in the stratosphere at high latitudes. The intensity of the methane absorption band centered at 8860 A shows an increase from the equator to temperate latitudes throughout the 1988-1992 period, despite the large variations in belt and zone reflectivities observed during this period in the southern hemisphere.

  5. Optical spectrum of HDE 226868 = Cygnus X-1. II. Spectrophotometry and mass estimates

    SciTech Connect

    Gies, D.R.; Bolton, C.T.

    1986-05-01

    In part I of this series, Gies and Bolton (1982) have presented the results of radial velocity measures of 78 high-dispersion spectrograms of HDE 226868 = Cyg X-1. For the present study, 55 of the best plates considered by Gies and Bolton were selected to form 10 average spectra. An overall mean spectrum with S/N ratio = 300 was formed by coadding the 10 averaged spectra. There is no evidence for statistically significant variations of the spectral type about the mean value of 09.7 Iab, and all the absorption line strengths are normal for the spectral type. Evidence is presented that the He II lambda 4846 emission line is formed in the stellar wind above the substellar point on the visible star. Probable values regarding the mass for the visible star and its companion are 33 and 16 solar masses, respectively. Theoretical He II lambda 4686 emission line profiles are computed for the focused stellar wind model for the Cyg X-1 system considered by Friend and Castor (1982). 105 references.

  6. Milli-tesla NMR and spectrophotometry of liquids hyperpolarized by dissolution dynamic nuclear polarization.

    PubMed

    Zhu, Yue; Chen, Chia-Hsiu; Wilson, Zechariah; Savukov, Igor; Hilty, Christian

    2016-09-01

    Hyperpolarization methods offer a unique means of improving low signal strength obtained in low-field NMR. Here, simultaneous measurements of NMR at a field of 0.7mT and laser optical absorption from samples hyperpolarized by dissolution dynamic nuclear polarization (D-DNP) are reported. The NMR measurement field closely corresponds to a typical field encountered during sample injection in a D-DNP experiment. The optical spectroscopy allows determination of the concentration of the free radical required for DNP. Correlation of radical concentration to NMR measurement of spin polarization and spin-lattice relaxation time allows determination of relaxivity and can be used for optimization of the D-DNP process. Further, the observation of the nuclear Overhauser effect originating from hyperpolarized spins is demonstrated. Signals from (1)H and (19)F in a mixture of trifluoroethanol and water are detected in a single spectrum, while different atoms of the same type are distinguished by J-coupling patterns. The resulting signal changes of individual peaks are indicative of molecular contact, suggesting a new application area of hyperpolarized low-field NMR for the determination of intermolecular interactions. PMID:27423094

  7. IUE and visual spectrophotometry of Markarian 9, Markarian 10, and 3C 390.3

    NASA Technical Reports Server (NTRS)

    Oke, J. B.; Goodrich, R. W.

    1981-01-01

    Ultraviolet spectra from IUE are combined with visual spectra for the three type I Seyfert galaxies Mrk 9, Mrk 10, and 3C 390.3. The 2175 A interstellar feature is measured well enough in Mrk 9 to indicate that the extinction corresponding to E(B-V) = 0.14 + or - 0.04 is in the galaxy. Mrk 10 displays evidence for 2175 A absorption and also yields E(B-V) = 0.14 + or - 0.07, while the continuum for 3C 390.3 is too weak to positively detect the feature. It is found, after correcting for reddening, that the line-intensity ratio L(alpha)/H(beta) ranges from 8 to 18, while that for H(alpha)/H(beta) goes from 2.1 to 5.4. It is noted that the He II 1640/4686 line ratio is uncertain but appears to be consistent with the recombination value of about 8. If photoionization is assumed, a comparison of the strengths of L(alpha) and H(beta) with the UV ionizing flux suggests that H(beta) is enhanced rather than L(alpha) depressed. When a comparison is made with similar ratios in quasars, L(alpha) is found to be much stronger and H(beta) slightly stronger in Seyferts than in quasars.

  8. Evidence for an elemental sulfur component of the clouds from Venus spectrophotometry

    NASA Technical Reports Server (NTRS)

    Hapke, B.; Nelson, R.

    1975-01-01

    The decrease in the reflectivity of Venus in the near-UV can be explained if the clouds contain particles of elemental sulfur in addition to sulfuric acid. The low-resolution McDonald-Pittsburgh spectrum can be fitted by two sulfur-containing, multiple-scattering cloud models: (1) a mixed cloud consisting of one particle of elemental sulfur of radius 10 microns for every 670 particles of sulfuric acid of radius 1 micron, and (2) a layered cloud of optical thickness tau = 1.0 consisting of one-micron particles of sulfuric acid overlying a thick cloud of elemental sulfur particles of radius 3.6 microns. Some of the sulfur is incompletely polymerized. The source of the sulfur is photo-dissociation of COS, although some may also be recycled from the lower atmosphere. The sulfur plays a crucial role in the planetary meteorology of Venus since it is responsible for the bulk of the absorption of solar energy.

  9. Imaging Spectrophotometry of the Jet/ISM Interaction in IC5063

    NASA Technical Reports Server (NTRS)

    Cecil, G.; Schuft, B.; Morse, J.; Bland-Hawthorn, J.

    2004-01-01

    IC5063 is a somewhat dusty z=0.0110 S0 galaxy with a Seyfert 2 nucleus. It has a triple radio source that spans 3 arcsec, mostly blueshifted H I absorption that spans 700 km/s, and ionization cones that extend for more than 2 arcmins. We obtained fully sampled [O III]\\lambda5007 grids at 0."9 and 70 km/s FWHM resolution using the Rutgers Fabry-Perot system on the Blanco 4m telescope. Complementary long-slit spectra using the RC spectrograph on the Blanco, and Taurus Tunable Filter spectral images in H\\alpha and [N II]\\lambda6583, were also obtained to assess gaseous ionization conditions. We present the results of our analysis, and correlate spectral structures to those visible in archival WFPC2 images. We find that, in the region near the radio triple, gaseous ionization and line velocity width is tightly correlated, in excellent quantitative agreement with the high-velocity shock regime in the diagnostic emission-line ratio diagrams of Dopita & Sutherland. We separate kinematically gas in normal disk rotation that is illuminated by the AGN in the ionization cones from that agitated mechanically by the jet, and assess the energy input from both processes.

  10. Milli-tesla NMR and spectrophotometry of liquids hyperpolarized by dissolution dynamic nuclear polarization

    NASA Astrophysics Data System (ADS)

    Zhu, Yue; Chen, Chia-Hsiu; Wilson, Zechariah; Savukov, Igor; Hilty, Christian

    2016-09-01

    Hyperpolarization methods offer a unique means of improving low signal strength obtained in low-field NMR. Here, simultaneous measurements of NMR at a field of 0.7 mT and laser optical absorption from samples hyperpolarized by dissolution dynamic nuclear polarization (D-DNP) are reported. The NMR measurement field closely corresponds to a typical field encountered during sample injection in a D-DNP experiment. The optical spectroscopy allows determination of the concentration of the free radical required for DNP. Correlation of radical concentration to NMR measurement of spin polarization and spin-lattice relaxation time allows determination of relaxivity and can be used for optimization of the D-DNP process. Further, the observation of the nuclear Overhauser effect originating from hyperpolarized spins is demonstrated. Signals from 1H and 19F in a mixture of trifluoroethanol and water are detected in a single spectrum, while different atoms of the same type are distinguished by J-coupling patterns. The resulting signal changes of individual peaks are indicative of molecular contact, suggesting a new application area of hyperpolarized low-field NMR for the determination of intermolecular interactions.

  11. Quantitation of Pyrantel Pamoate in Pharmaceuticals Using Permanganate by Visible Spectrophotometry

    NASA Astrophysics Data System (ADS)

    Rajendraprasad, N.; Basavaiah, K.

    2014-03-01

    Two simple, accurate and precise spectrophotometric methods are developed and validated for the assay of pyrantel pamoate (PP) in pharmaceuticals. The methods employ the oxidative property of potassium permanganate (KMnO4) in acidic and alkaline conditions. In the first method (method A), PP is converted into its free base, pyrantel (PR), and treated with known excess of KMnO4 in acidic condition followed by the measurement of unreacted KMnO4 at 550 nm. Method B is based on the registration of absorbance of green colored chromogen formed due to the reduction of KMnO4 by PP in alkaline condition. The methods obeyed Beer's law over a range of 1-20 μg/ml in inverse manner, and 0.75-15 μg/ml for method A and method B, respectively, with apparent molar absorptivity values of 1.05ṡ104 and 2.85ṡ104 lṡmol-1ṡcm-1. The optical parameters such as limits of detection (LOD), quantification (LOQ), and the Sandell sensitivity values are also reported. The accuracy and precision of the methods are assessed on intra- and inter-day basis. A recovery study by standard addition procedure is also carried out for further assurance of accuracy. The developed methods are successfully applied to determine PP in tablets. The results are more satisfactory as per current ICH guidelines.

  12. Absorption heat pumps

    NASA Astrophysics Data System (ADS)

    Huhtinen, M.; Heikkilae, M.; Andersson, R.

    1987-03-01

    The aim of the study was to analyze the technical and economic feasibility of absorption heat pumps in Finland. The work was done as a case study: the technical and economic analyses have been carried out for six different cases, where in each the suitable size and type of the heat pump plant and the auxiliary components and connections were specified. The study also detailed the costs concerning the procurement, installation and test runs of the machinery, as well as the savings in energy costs incurred by the introduction of the plant. Conclusions were drawn of the economic viability of the applications studied. The following cases were analyzed: heat recovery from flue gases and productin of district heat in plants using peat, natural gas, and municipal wastes as a fuel. Heat recovery in the pulp and paper industry for the upgrading of pressure of secondary steam and for the heating of white liquor and combustion and drying the air. Heat recovery in a peat-fulled heat and power plant from flue gases that have been used for the drying of peat. According to the study, the absorption heat pump suits best to the production of district heat, when the heat source is the primary energy is steam produced by the boiler. Included in the flue as condensing is the purification of flue gases. Accordingly, benefit is gained on two levels in thick applications. In heat and power plants the use of absorption heat pumps is less economical, due to the fact that the steam used by the pump reduces the production of electricity, which is rated clearly higher than heat.

  13. An atomic-absorption method for the determination of gold in large samples of geologic materials

    USGS Publications Warehouse

    VanSickle, Gordon H.; Lakin, Hubert William

    1968-01-01

    A laboratory method for the determination of gold in large (100-gram) samples has been developed for use in the study of the gold content of placer deposits and of trace amounts of gold in other geologic materials. In this method the sample is digested with bromine and ethyl ether, the gold is extracted into methyl isobutyl ketone, and the determination is made by atomicabsorption spectrophotometry. The lower limit of detection is 0.005 part per million in the sample. The few data obtained so far by this method agree favorably with those obtained by assay and by other atomic-absorption methods. About 25 determinations can be made per man-day.

  14. Scattering with absorptive interaction

    NASA Astrophysics Data System (ADS)

    Cassing, W.; Stingl, M.; Weiguny, A.

    1982-07-01

    The S matrix for a wide class of complex and nonlocal potentials is studied, with special attention given to the motion of singularities in the complex k plane as a function of the imaginary coupling strength. Modifications of Levinson's theorem are obtained and discussed. Analytic approximations to the S matrix in the vicinity of narrow resonances are exhibited and compared to numerical results of resonating-group calculations. The problem of defining resonances in the case of complex interactions is discussed, making contact with the usual analysis of scattering in terms of Argand diagrams. NUCLEAR REACTIONS Scattering theory, S matrix for absorptive potentials.

  15. Ultraviolet absorption hygrometer

    DOEpatents

    Gersh, M.E.; Bien, F.; Bernstein, L.S.

    1986-12-09

    An ultraviolet absorption hygrometer is provided including a source of pulsed ultraviolet radiation for providing radiation in a first wavelength region where water absorbs significantly and in a second proximate wavelength region where water absorbs weakly. Ultraviolet radiation in the first and second regions which has been transmitted through a sample path of atmosphere is detected. The intensity of the radiation transmitted in each of the first and second regions is compared and from this comparison the amount of water in the sample path is determined. 5 figs.

  16. Ultraviolet absorption hygrometer

    DOEpatents

    Gersh, Michael E.; Bien, Fritz; Bernstein, Lawrence S.

    1986-01-01

    An ultraviolet absorption hygrometer is provided including a source of pulsed ultraviolet radiation for providing radiation in a first wavelength region where water absorbs significantly and in a second proximate wavelength region where water absorbs weakly. Ultraviolet radiation in the first and second regions which has been transmitted through a sample path of atmosphere is detected. The intensity of the radiation transmitted in each of the first and second regions is compared and from this comparison the amount of water in the sample path is determined.

  17. [Simultaneous determination of platinum (IV) and palladium (II) using spectrophotometry method].

    PubMed

    Ma, Dong-Lan; Wang, Yun; Ma, Kuang-Biao; Wang, Jin-Ye

    2009-10-01

    The N-(m-methylphenyl)-N'-(sodium p-aminobenzenesulfonate)-thiourea (MMPT) was good reagent of water solubility. In the medium of an HAc-NaAc buffer solution and hexadecyltrimethylammonium bromide (CTMAB), MMPT can react with platinum (IV) and palladium (II) to form green and brown soluble complex. The maximum absorbance of the complex was at lambdaPt(max) = 754.4 nm and lambdaPD(max) = 304.6 nm. Beer's law was obeyed with the concentration in the range of 0-32.0 microg Pt(IV)/25 mL and 0-25.0 microg Pd(II)/25 mL for platinum (IV) and palladium(II) respectively. The correlated coefficient was r754.4 = 0.999 5 for platinum (IV); and r304.6 = 0.999 9 for palladium (II). Their molar absorption coefficients were epsilonPT(754.4 = 8.6 x 10(4) L x mol(-1) x cm(-1) and epsilonPd(304.6) = 7.4 x 10(4) L x mol(-1) x cm(-1) respectively. The contents of platinum (IV) and palladium (II) were converted by determination of the absorbency of mix solution of platinum (IV) and palladium (II) at 754.4 and 304.6 nm. Only Cu2+ and Co2+ interfered with the determination of palladium (II) among 50 coexistent ions, so the selectivity was good. It can be used for the determination of content of synthesis samples. The relative standard deviation (RSD) was less than 2.0%, and the recovery (%) was in the range of 96%-104%. The results are satisfactory. Because the reagent reacts with platinum (IV) and palladium (II) to form water soluble complex and does not require pre-separation for simultaneous determination of platinum (IV) and palladium (II), the method is easy to operate, rapid and environment-friendly. PMID:20038071

  18. The HI absorption "Zoo"

    NASA Astrophysics Data System (ADS)

    Geréb, K.; Maccagni, F. M.; Morganti, R.; Oosterloo, T. A.

    2015-03-01

    We present an analysis of the H I 21 cm absorption in a sample of 101 flux-selected radio AGN (S1.4 GHz> 50 mJy) observed with the Westerbork Synthesis Radio Telescope (WSRT). We detect H I absorption in 32 objects (30% of the sample). In a previous paper, we performed a spectral stacking analysis on the radio sources, while here we characterize the absorption spectra of the individual detections using the recently presented busy function. The H I absorption spectra show a broad variety of widths, shapes, and kinematical properties. The full width half maximum (FWHM) of the busy function fits of the detected H I lines lies in the range 32 km s-1absorption (FW20) lies in the range 63 km s-1 200 km s-1). We study the kinematical and radio source properties of each group, with the goal of identifying different morphological structures of H I. Narrow lines mostly lie at the systemic velocity and are likely produced by regularly rotating H I disks or gas clouds. More H I disks can be present among galaxies with lines of intermediate widths; however, the H I in these sources is more unsettled. We study the asymmetry parameter and blueshift/redshift distribution of the lines as a function of their width. We find a trend for which narrow profiles are also symmetric, while broad lines are the most asymmetric. Among the broadest lines, more lines appear blueshifted than redshifted, similarly to what was found by previous studies. Interestingly, symmetric broad lines are absent from the sample. We argue that if a profile is broad, it is also asymmetric and shifted relative to the systemic velocity because it is tracing unsettled H I gas. In particular, besides three of the broadest (up to FW20 = 825 km s-1

  19. Measuring absorption coefficient of scattering liquids using a tube inside an integrating sphere.

    PubMed

    Villanueva, Yolanda; Veenstra, Colin; Steenbergen, Wiendelt

    2016-04-10

    A method for measuring the absorption coefficient μa of absorbing and scattering liquid samples is presented. The sample is injected into a small transparent tube mounted through an integrating sphere. Two models for determining the absorption coefficient using the relative optical output signal are described and validated using aqueous ink absorbers of 0.5 vol.% (0.3  mm-1a<1.55  mm-1) and 1.0 vol.% (1.0  mm-1a<4.0  mm-1) concentrations with 1 vol.% (μs'≈1.4  mm-1) and 10 vol.% (μs'≈14  mm-1) Intralipid dilutions. The low concentrations give μa and μs values, which are comparable with those of biological tissues. One model assumes a uniform light distribution within the sample, which is valid for low absorption. Another model considers light attenuation that obeys Lambert-Beer's law, which may be used for relatively high absorption. Measurements with low and high scattering samples are done for the wavelength range of 400-900 nm. Measured spectra of purely absorbing samples are within 15% agreement with measurements using standard transmission spectrophotometry. For 0.5 vol.% ink absorbers and at wavelengths below 700 nm, measured μa values are higher for samples with low scattering and lower for those with high scattering. At wavelengths above 700 nm, measured μa values do not vary significantly with amount of scattering. For 1.0 vol.% ink absorbers, measured spectra do not change with low scattering. These results indicate that the method can be used for measuring absorption spectra of scattering liquid samples with optical properties similar to biological absorbers, particularly at wavelengths above 700 nm, which is difficult to accomplish with standard transmission spectrophotometry. PMID:27139871

  20. Determination of silicon and aluminum in silicon carbide nanocrystals by high-resolution continuum source graphite furnace atomic absorption spectrometry.

    PubMed

    Dravecz, Gabriella; Bencs, László; Beke, Dávid; Gali, Adam

    2016-01-15

    The determination of Al contaminant and the main component Si in silicon carbide (SiC) nanocrystals with the size-distribution of 1-8nm dispersed in an aqueous solution was developed using high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS-GFAAS). The vaporization/atomization processes were investigated in a transversally heated graphite atomizer by evaporating solution samples of Al and Si preserved in various media (HCl, HNO3). For Si, the best results were obtained by applying a mixture of 5µg Pd plus 5µg Mg, whereas for Al, 10µg Mg (each as nitrate solution) was dispensed with the samples, but the results obtained without modifier were found to be better. This way a maximum pyrolysis temperature of 1200°C for Si and 1300°C for Al could be used, and the optimum (compromise) atomization temperature was 2400°C for both analytes. The Si and Al contents of different sized SiC nanocrystals, dispersed in aqueous solutions, were determined against aqueous (external) calibration standards. The correlation coefficients (R values) of the calibrations were found to be 0.9963 for Si and 0.9991 for Al. The upper limit of the linear calibration range was 2mg/l Si and 0.25mg/l Al. The limit of detection was 3µg/l for Si and 0.5µg/l for Al. The characteristic mass (m0) was calculated to be 389pg Si and 6.4pg Al. The Si and Al content in the solution samples were found to be in the range of 1.0-1.7mg/l and 0.1-0.25mg/l, respectively. PMID:26592606

  1. Differential optoacoustic absorption detector

    NASA Technical Reports Server (NTRS)

    Shumate, M. S. (Inventor)

    1978-01-01

    A differential optoacoustic absorption detector employed two tapered cells in tandem or in parallel. When operated in tandem, two mirrors were used at one end remote from the source of the beam of light directed into one cell back through the other, and a lens to focus the light beam into the one cell at a principal focus half way between the reflecting mirror. Each cell was tapered to conform to the shape of the beam so that the volume of one was the same as for the other, and the volume of each received maximum illumination. The axes of the cells were placed as close to each other as possible in order to connect a differential pressure detector to the cells with connecting passages of minimum length. An alternative arrangement employed a beam splitter and two lenses to operate the cells in parallel.

  2. Cloud absorption radiometer

    NASA Technical Reports Server (NTRS)

    Strange, M. G.

    1988-01-01

    The Cloud Absorption Radiometer (CAR) was developed to measure spectrally how light is scattered by clouds and to determine the single scattering albedo, important to meteorology and climate studies, with unprecedented accuracy. This measurement is based on ratios of downwelling to upwelling radiation within clouds, and so is not strongly dependent upon absolute radiometric calibration of the instrument. The CAR has a 5-inch aperture and 1 degree IFOV, and spatially scans in a plane orthogonal to the flight vector from the zenith to nadir at 1.7 revolutions per second. Incoming light is measured in 13 spectral bands, using silicon, germanium, and indium-antimonide detectors. Data from each channel is digitally recorded in flight with 10-bit (0.1 percent) resolution. The instrument incorporates several novel features. These features are briefly detailed.

  3. Analyzing Water's Optical Absorption

    NASA Technical Reports Server (NTRS)

    2002-01-01

    A cooperative agreement between World Precision Instruments (WPI), Inc., and Stennis Space Center has led the UltraPath(TM) device, which provides a more efficient method for analyzing the optical absorption of water samples at sea. UltraPath is a unique, high-performance absorbance spectrophotometer with user-selectable light path lengths. It is an ideal tool for any study requiring precise and highly sensitive spectroscopic determination of analytes, either in the laboratory or the field. As a low-cost, rugged, and portable system capable of high- sensitivity measurements in widely divergent waters, UltraPath will help scientists examine the role that coastal ocean environments play in the global carbon cycle. UltraPath(TM) is a trademark of World Precision Instruments, Inc. LWCC(TM) is a trademark of World Precision Instruments, Inc.

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

    NASA Astrophysics Data System (ADS)

    Adelman, S. J.

    1981-02-01

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

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

    PubMed Central

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

    2011-01-01

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

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

    PubMed

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

    2010-04-01

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

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

    SciTech Connect

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

    2013-06-01

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

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

    NASA Astrophysics Data System (ADS)

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

    1998-12-01

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

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

    NASA Astrophysics Data System (ADS)

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

    1996-10-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

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

    PubMed

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

    2015-09-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2011-02-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2014-03-01

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

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

    PubMed

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

    2015-01-01

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

  15. Percutaneous absorption in preterm infants.

    PubMed

    West, D P; Halket, J M; Harvey, D R; Hadgraft, J; Solomon, L M; Harper, J I

    1987-11-01

    The skin of preterm infants varies considerably in its level of maturity. To understand skin absorption in premature infants better, we report a technique for the assessment of percutaneous absorption at various gestational and postnatal ages using stable, isotope-labeled (13C6) benzoic acid. Our results indicate that in the preterm infant, this method detects enhanced skin absorption in the first postnatal days, which declines over three weeks to that expected of a full-term infant. This approach also indicates an inverse relationship between gestational age and skin absorption, as well as postnatal age and skin absorption. The reported technique is a safe and noninvasive method using a model skin penetrant for the study of percutaneous absorption in preterm infants from which basic data may be derived to add to our understanding of skin barrier function. PMID:3422856

  16. Optical Absorption in Liquid Semiconductors

    NASA Astrophysics Data System (ADS)

    Bell, Florian Gene

    An infrared absorption cell has been developed which is suitable for high temperature liquids which have absorptions in the range .1-10('3) cm('-1). The cell is constructed by clamping a gasket between two flat optical windows. This unique design allows the use of any optical windows chemically compatible with the liquid. The long -wavelength limit of the measurements is therefore limited only by the choice of the optical windows. The thickness of the cell can easily be set during assembly, and can be varied from 50 (mu)m to .5 cm. Measurements of the optical absorption edge were performed on the liquid alloy Se(,1-x)Tl(,x) for x = 0, .001, .002, .003, .005, .007, and .009, from the melting point up to 475(DEGREES)C. The absorption was found to be exponential in the photon energy over the experimental range from 0.3 eV to 1.2 eV. The absorption increased linearly with concentration according to the empirical relation (alpha)(,T)(h(nu)) = (alpha)(,1) + (alpha)(,2)x, and the absorption (alpha)(,1) was interpreted as the absorption in the absence of T1. (alpha)(,1) also agreed with the measured absorption in 100% Se at corresponding temperatures and energies. The excess absorption defined by (DELTA)(alpha) = (alpha)(,T)(h(nu))-(alpha)(,1) was interpreted as the absorption associated with Tl and was found to be thermally activated with an activation energy E(,t) = 0.5 eV. The exponential edge is explained as absorption on atoms immersed in strong electric fields surrounding ions. The strong fields give rise to an absorption tail similar to the Franz-Keldysh effect. A simple calculation is performed which is based on the Dow-Redfield theory of absorption in an electric field with excitonic effects included. The excess absorption at low photon energies is proportional to the square of the concentration of ions, which are proposed to exist in the liquid according to the relation C(,i) (PROPORTIONAL) x(' 1/2)(.)e('-E)t('/kT), which is the origin of the thermal activation

  17. X-ray Absorption Spectroscopy

    SciTech Connect

    Yano, Junko; Yachandra, Vittal K.

    2009-07-09

    This review gives a brief description of the theory and application of X-ray absorption spectroscopy, both X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS), especially, pertaining to photosynthesis. The advantages and limitations of the methods are discussed. Recent advances in extended EXAFS and polarized EXAFS using oriented membranes and single crystals are explained. Developments in theory in understanding the XANES spectra are described. The application of X-ray absorption spectroscopy to the study of the Mn4Ca cluster in Photosystem II is presented.

  18. Measuring Binding Affinity of Protein-Ligand Interaction Using Spectrophotometry: Binding of Neutral Red to Riboflavin-Binding Protein

    ERIC Educational Resources Information Center

    Chenprakhon, Pirom; Sucharitakul, Jeerus; Panijpan, Bhinyo; Chaiyen, Pimchai

    2010-01-01

    The dissociation constant, K[subscript d], of the binding of riboflavin-binding protein (RP) with neutral red (NR) can be determined by titrating RP to a fixed concentration of NR. Upon adding RP to the NR solution, the maximum absorption peak of NR shifts to 545 nm from 450 nm for the free NR. The change of the absorption can be used to determine…

  19. Peat as a natural solid-phase for copper preconcentration and determination in a multicommuted flow system coupled to flame atomic absorption spectrometry.

    PubMed

    Gonzáles, A P S; Firmino, M A; Nomura, C S; Rocha, F R P; Oliveira, P V; Gaubeur, I

    2009-03-23

    The physical and chemical characteristics of peat were assessed through measurement of pH, percentage of organic matter, cationic exchange capacity (CEC), elemental analysis, infrared spectroscopy and quantitative analysis of metals by ICP OES. Despite the material showed to be very acid in view of the percentage of organic matter, its CEC was significant, showing potential for retention of metal ions. This characteristic was exploited by coupling a peat mini-column to a flow system based on the multicommutation approach for the in-line copper concentration prior to flame atomic absorption spectrometric determination. Cu(II) ions were adsorbed at pH 4.5 and eluted with 0.50 molL(-1) HNO(3). The influence of chemical and hydrodynamic parameters, such as sample pH, buffer concentration, eluent type and concentration, sample flow-rate and preconcentration time were investigated. Under the optimized conditions, a linear response was observed between 16 and 100 microgL(-1), with a detection limit estimated as 3 microgL(-1) at the 99.7% confidence level and an enrichment factor of 16. The relative standard deviation was estimated as 3.3% (n=20). The mini-column was used for at least 100 sampling cycles without significant variation in the analytical response. Recoveries from copper spiked to lake water or groundwater as well as concentrates used in hemodialysis were in the 97.3-111% range. The results obtained for copper determination in these samples agreed with those achieved by graphite furnace atomic absorption spectrometry (GFAAS) at the 95% confidence level. PMID:19264168

  20. 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.

    PubMed

    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. PMID:25085864

  1. Intestinal folate absorption

    PubMed Central

    Strum, Williamson; Nixon, Peter F.; Bertino, Joseph B.; Binder, Henry J.

    1971-01-01

    Intestinal absorption of the monoglutamate form of the principal dietary and circulating folate compound, 5-methyltetrahydrofolic acid (5-MTHF), was studied in the rat utilizing a synthetic highly purified radiolabeled diastereoisomer. Chromatography confirmed that the compound was not altered after transfer from the mucosa to the serosa. Accumulation against a concentration gradient was not observed in duodenal, jejunal, or ileal segments at 5-MTHF concentration from 0.5 to 500 nmoles/liter. Unidirectional transmural flux determination also did not indicate a significant net flux. Mucosal to serosal transfer of 5-MTHF was similar in all segments of the intestine and increased in a linear fashion with increased initial mucosal concentrations. Further, no alteration in 5-MTHF transfer was found when studied in the presence of metabolic inhibitors or folate compounds. These results indicate that 5-MTHF is not absorbed by the rat small intestine by a carrier-mediated system and suggest that 5-MTHF transfer most likely represents diffusion. Images PMID:5564397

  2. Solar Absorption in Cloudy Atmospheres

    NASA Technical Reports Server (NTRS)

    Harshvardhan; Ridgway, William; Ramaswamy, V.; Freidenreich, S. M.; Batey, Michael

    1996-01-01

    The theoretical computations used to compute spectral absorption of solar radiation are discussed. Radiative properties relevant to the cloud absorption problem are presented and placed in the context of radiative forcing. Implications for future measuring programs and the effect of horizontal inhomogeneities are discussed.

  3. Atlas of Infrared Absorption Lines

    NASA Technical Reports Server (NTRS)

    Park, J. H.

    1977-01-01

    This atlas of infrared absorption line contains absorption line parameters (line strength vs. wavenumber) from 500 to 7000 cm(exp-1) for 15 gases: H2O, CO2, O3, N2O, CO, CH4, O2, SO2, NO, NO2, NH3, HCl, HF, HNO3 and CH3Cl.

  4. Hot tube atomic absorption spectrochemistry.

    PubMed

    Woodriff, R; Stone, R W

    1968-07-01

    A small, commercially available atomic absorption instrument is used with a heated graphite tube for the atomic absorption analysis of liquid and solid silver samples. Operating conditions of the furnace are described and a sensitivity of about 5 ng of silver is reported. PMID:20068797

  5. Subgap Absorption in Conjugated Polymers

    DOE R&D Accomplishments Database

    Sinclair, M.; Seager, C. H.; McBranch, D.; Heeger, A. J; Baker, G. L.

    1991-01-01

    Along with X{sup (3)}, the magnitude of the optical absorption in the transparent window below the principal absorption edge is an important parameter which will ultimately determine the utility of conjugated polymers in active integrated optical devices. With an absorptance sensitivity of < 10{sup {minus}5}, Photothermal Deflection Spectroscopy (PDS) is ideal for determining the absorption coefficients of thin films of transparent'' materials. We have used PDS to measure the optical absorption spectra of the conjugated polymers poly(1,4-phenylene-vinylene) (and derivitives) and polydiacetylene-4BCMU in the spectral region from 0.55 eV to 3 eV. Our spectra show that the shape of the absorption edge varies considerably from polymer to polymer, with polydiacetylene-4BCMU having the steepest absorption edge. The minimum absorption coefficients measured varied somewhat with sample age and quality, but were typically in the range 1 cm{sup {minus}1} to 10 cm{sup {minus}1}. In the region below 1 eV, overtones of C-H stretching modes were observed, indicating that further improvements in transparency in this spectral region might be achieved via deuteration of fluorination.

  6. Atmospheric absorption of sound - Update

    NASA Technical Reports Server (NTRS)

    Bass, H. E.; Sutherland, L. C.; Zuckerwar, A. J.

    1990-01-01

    Best current expressions for the vibrational relaxation times of oxygen and nitrogen in the atmosphere are used to compute total absorption. The resulting graphs of total absorption as a function of frequency for different humidities should be used in lieu of the graph published earlier by Evans et al (1972).

  7. Optical absorption of silicon nanowires

    SciTech Connect

    Xu, T.; Lambert, Y.; Krzeminski, C.; Grandidier, B.; Stievenard, D.; Leveque, G.; Akjouj, A.; Pennec, Y.; Djafari-Rouhani, B.

    2012-08-01

    We report on simulations and measurements of the optical absorption of silicon nanowires (NWs) versus their diameter. We first address the simulation of the optical absorption based on two different theoretical methods: the first one, based on the Green function formalism, is useful to calculate the scattering and absorption properties of a single or a finite set of NWs. The second one, based on the finite difference time domain (FDTD) method, is well-adapted to deal with a periodic set of NWs. In both cases, an increase of the onset energy for the absorption is found with increasing diameter. Such effect is experimentally illustrated, when photoconductivity measurements are performed on single tapered Si nanowires connected between a set of several electrodes. An increase of the nanowire diameter reveals a spectral shift of the photocurrent intensity peak towards lower photon energies that allow to tune the absorption onset from the ultraviolet radiations to the visible light spectrum.

  8. Ultraviolet absorption spectrum of HOCl

    NASA Technical Reports Server (NTRS)

    Burkholder, James B.

    1993-01-01

    The room temperature UV absorption spectrum of HOCl was measured over the wavelength range 200 to 380 nm with a diode array spectrometer. The absorption spectrum was identified from UV absorption spectra recorded following UV photolysis of equilibrium mixtures of Cl2O/H2O/HOCl. The HOCl spectrum is continuous with a maximum at 242 nm and a secondary peak at 304 nm. The measured absorption cross section at 242 nm was (2.1 +/- 0.3) x 10 exp -19/sq cm (2 sigma error limits). These results are in excellent agreement with the work of Knauth et al. (1979) but in poor agreement with the more recent measurements of Mishalanie et al. (1986) and Permien et al. (1988). An HOCl nu2 infrared band intensity of 230 +/- 35/sq cm atm was determined based on this UV absorption cross section. The present results are compared with these previous measurements and the discrepancies are discussed.

  9. Gas-absorption process

    DOEpatents

    Stephenson, Michael J.; Eby, Robert S.

    1978-01-01

    This invention is an improved gas-absorption process for the recovery of a desired component from a feed-gas mixture containing the same. In the preferred form of the invention, the process operations are conducted in a closed-loop system including a gas-liquid contacting column having upper, intermediate, and lower contacting zones. A liquid absorbent for the desired component is circulated through the loop, being passed downwardly through the column, regenerated, withdrawn from a reboiler, and then recycled to the column. A novel technique is employed to concentrate the desired component in a narrow section of the intermediate zone. This technique comprises maintaining the temperature of the liquid-phase input to the intermediate zone at a sufficiently lower value than that of the gas-phase input to the zone to effect condensation of a major part of the absorbent-vapor upflow to the section. This establishes a steep temperature gradient in the section. The stripping factors below this section are selected to ensure that virtually all of the gases in the downflowing absorbent from the section are desorbed. The stripping factors above the section are selected to ensure re-dissolution of the desired component but not the less-soluble diluent gases. As a result, a peak concentration of the desired component is established in the section, and gas rich in that component can be withdrawn therefrom. The new process provides important advantages. The chief advantage is that the process operations can be conducted in a single column in which the contacting zones operate at essentially the same pressure.

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

    PubMed Central

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

    2015-01-01

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

  11. Gastrointestinal citrate absorption in nephrolithiasis

    NASA Technical Reports Server (NTRS)

    Fegan, J.; Khan, R.; Poindexter, J.; Pak, C. Y.

    1992-01-01

    Gastrointestinal absorption of citrate was measured in stone patients with idiopathic hypocitraturia to determine if citrate malabsorption could account for low urinary citrate. Citrate absorption was measured directly from recovery of orally administered potassium citrate (40 mEq.) in the intestinal lavage fluid, using an intestinal washout technique. In 7 stone patients citrate absorption, serum citrate levels, peak citrate concentration in serum and area under the curve were not significantly different from those of 7 normal subjects. Citrate absorption was rapid and efficient in both groups, with 96 to 98% absorbed within 3 hours. The absorption of citrate was less efficient from a tablet preparation of potassium citrate than from a liquid preparation, probably due to a delayed release of citrate from wax matrix. However, citrate absorption from solid potassium citrate was still high at 91%, compared to 98% for a liquid preparation. Thus, hypocitraturia is unlikely to be due to an impaired gastrointestinal absorption of citrate in stone patients without overt bowel disease.

  12. Preconcentration by coprecipitation of arsenic and tin in natural waters with a Ni-pyrrolidine dithiocarbamate complex and their direct determination by solid-sampling atomic-absorption spectrometry.

    PubMed

    Zhang, Q; Minami, H; Imoue, S; Atsuya, I

    2001-08-01

    A method for the determination of trace amounts of arsenic and tin in natural waters is described. Trace amounts of arsenic and tin were preconcentrated by coprecipitation with a Ni-ammonium pyrrolidine dithiocarbamate (APDC) complex. The coprecipitates obtained were directly analyzed by graphite-furnace atomic-absorption spectrometry (GFAAS) using the Ni-APDC complex solid-sampling technique. The coprecipitation conditions used for the trace amounts of arsenic and tin in natural water were investigated in detail. It was found that arsenic and tin at sub-ng mL(-1) levels were both coprecipitated quantitatively by Ni(PDC)2 in the pH range 2-3. The concentration factors by coprecipitation reached approximately 40,000 when 2 mg nickel was added as a carrier element to 500 mL of the water sample. The proposed method has been applied to the determination of trace amounts of arsenic and tin in river water and seawater reference materials, and the detection limits for arsenic and tin, which were calculated from three times of the standard deviation of the procedural blanks, are 0.02 ng mL(-1) and 0.04 ng mL(-1), respectively, for 500-mL volumes of water sample. PMID:11569865

  13. Cobalt internal standard for Ni to assist the simultaneous determination of Mo and Ni in plant materials by high-resolution continuum source graphite furnace atomic absorption spectrometry employing direct solid sample analysis.

    PubMed

    de Babos, Diego Victor; Bechlin, Marcos André; Barros, Ariane Isis; Ferreira, Edilene Cristina; Gomes Neto, José Anchieta; de Oliveira, Silvana Ruella

    2016-05-15

    A new method is proposed for the simultaneous determination of Mo and Ni in plant materials by high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS GFAAS), employing direct solid sample analysis (DSS) and internal standardization (IS). Cobalt was used as internal standard to minimize matrix effects during Ni determinations, enabling the use of aqueous standards for calibration. Correlation coefficients for the calibration curves were typically better than 0.9937. The performance of the method was checked by analysis of six plant certified reference materials, and the results for Mo and Ni were in agreement with the certified values (95% confidence level, t-test). Analysis was made of different types of plant materials used as renewable sources of energy, including sugarcane leaves, banana tree fiber, soybean straw, coffee pods, orange bagasse, peanut hulls, and sugarcane bagasse. The concentrations found for Mo and Ni ranged from 0.08 to 0.63 ng mg(-1) and from 0.41 to 6.92 ng mg(-1), respectively. Precision (RSD) varied from 2.1% to 11% for Mo and from 3.7% to 10% for Ni. Limits of quantification of 0.055 and 0.074 ng were obtained for Mo and Ni, respectively. PMID:26992542

  14. Percutaneous absorption of Octopirox.

    PubMed

    Black, J G; Kamat, V B

    1988-01-01

    containing 1% Octopirox is 29,400, so that the possibility of systemic effects due to absorption through the skin is remote. PMID:3345970

  15. Resonant Absorption of Bessel Beams

    NASA Astrophysics Data System (ADS)

    Fan, J.; Parra, E.; Milchberg, H. M.

    1999-11-01

    We report the first observation of enhanced laser-plasma optical absorption in a subcritical density plasma resulting from spatial resonances, here in the laser breakdown of a gas with a Bessel beam. The enhancement in absorption is directly correlated to enhancements both in confinement of laser radiation to the plasma and in its heating. Under certain conditions, azimuthal asymmetry in the laser beam is essential for efficient gas breakdown. Simulations of this absorption consistently explain the experimental observations. This work is supported by the National Science Foundation (PHY-9515509) and the US Department of Energy (DEF G0297 ER 41039).

  16. Complexation of Lactate with Nd(III) and Eu(III) at Variable Temperatures: Studies by Potentiometry, Microcalorimetry, Optical Absorption and Luminescence Spectroscopy

    SciTech Connect

    Tian, Guoxin; Martin, Leigh R.; Rao, Linfeng

    2010-10-01

    Complexation of neodymium(III) and europium(III) with lactate was studied at variable temperatures by potentiometry, absorption spectrophotometry, luminescence spectroscopy and microcalorimetry. Stability constants of three successive lactate complexes (ML{sup 2+}, ML{sup 2+} and ML{sub 3}(aq), where M stands for Nd and Eu, and L stands for lactate) at 10, 25, 40, 55 and 70 C were determined. The enthalpies of complexation at 25 C were determined by microcalorimetry. Thermodynamic data show that the complexation of trivalent lanthanides (Nd{sup 3+} and Eu{sup 3+}) with lactate is exothermic, and the complexation becomes weaker at higher temperatures. Results from optical absorption and luminescence spectroscopy suggest that the complexes are inner-sphere chelate complexes in which the protonated {alpha}-hydroxyl group of lactate participates in the complexation.

  17. Evaluation of intensity and energy interaction parameters for the complexation of Pr(III) with selected nucleoside and nucleotide through absorption spectral studies.

    PubMed

    Bendangsenla, N; Moaienla, T; David Singh, Th; Sumitra, Ch; Rajmuhon Singh, N; Indira Devi, M

    2013-02-15

    The interactions of Pr(III) with nucleosides and nucleotides have been studied in different organic solvents employing absorption difference and comparative absorption spectrophotometry. The magnitudes of the variations in both energy and intensity interaction parameters were used to explore the degree of outer and inner sphere co-ordination, incidence of covalency and the extent of metal 4f-orbital involvement in chemical bonding. Various electronic spectral parameters like Slater-Condon (F(k)), Racah (E(k)), Lande parameter (ξ(4f)), Nephelauxatic ratio (β), bonding (b(1/2)), percentage covalency (δ) and intensity parameters like oscillator strength (P) and Judd Ofelt electronic dipole intensity parameter (T(λ), λ=2,4,6) have been evaluated. The variation of these evaluated parameters were employed to interpret the nature of binding of Pr(III) with different ligands i.e. Adenosine/ATP in presence and absence of Ca(2+). PMID:23257345

  18. Selective determination of antimony(III) and antimony(V) with ammonium pyrrolidinedithiocarbamate, sodium diethyldithiocarbamate and dithizone by atomic-absorption spectrometry with a carbon-tube atomizer.

    PubMed

    Kamada, T; Yamamoto, Y

    1977-05-01

    The extraction behaviour of antimony(III) and antimony(V) with ammonium pyrrolidinedithiocarbamate, sodium diethyldithiocarbamate and dithizone in organic solvents has been investigated by means of frameless atomic-absorption spectrophotometry with a carbon-tube atomizer. The selective extraction of antimony(III) and differential determination of antimony(III) and antimony(V) have been developed. With ammonium pyrrolidinedithiocarbamate and methyl isobutyl ketone, when the aqueous phase/solvent volume ratio is 50 ml/10 ml and the injection volume in the carbon tube is 20 mul, the sensitivity for antimony is 0.2 ng/ml for 1% absorption. The relative standard deviations are ca. 2%. Interferences by many metal ions can be prevented by masking with EDTA. The proposed methods have been applied satisfactorily to determination of antimony(III) and antimony(V) in various types of water. PMID:18962096

  19. Determination of gold, indium, tellurium and thallium in the same sample digest of geological materials by atomic-absorption spectroscopy and two-step solvent extraction

    USGS Publications Warehouse

    Hubert, A.E.; Chao, T.T.

    1985-01-01

    A rock, soil, or stream-sediment sample is decomposed with hydrofluoric acid, aqua regia, and hydrobromic acid-bromine solution. Gold, thallium, indium and tellurium are separated and concentrated from the sample digest by a two-step MIBK extraction at two concentrations of hydrobromic add. Gold and thallium are first extracted from 0.1M hydrobromic acid medium, then indium and tellurium are extracted from 3M hydrobromic acid in the presence of ascorbic acid to eliminate iron interference. The elements are then determined by flame atomic-absorption spectrophotometry. The two-step solvent extraction can also be used in conjunction with electrothermal atomic-absorption methods to lower the detection limits for all four metals in geological materials. ?? 1985.

  20. The rediscovery of absorption chillers

    SciTech Connect

    Katzel, J.

    1992-04-23

    Absorption chillers are back - and for two very good reasons: they are environmentally sound and, in many cases, economically attractive. One factor fueling this resurgence is the outlook for natural gas, the energy source of most absorption systems. Deregulation has spurred exploration, and forecasts indicate an abundant supply and relatively low prices through 2050. Threats of global warming and depletion of the ozone layer also are forces driving the absorption chiller market. Being a good corporate citizen today means minimizing or eliminating the use of chlorofluorocarbons (CFCs), the basis of many refrigerants used in mechanical chillers. Even as chemical and chiller manufacturers alike work to develop substitute refrigerants, the perfect alternative has yet to be found. Absorption units are free of these problems, a benefit that appeals to many people.

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

    PubMed

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

    2014-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2012-04-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2006-03-01

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

  4. Ultraviolet cometary spectrophotometry

    NASA Technical Reports Server (NTRS)

    Ahearn, M. F.

    1983-01-01

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

  5. Aprotic solvents effect on the UV-visible absorption spectra of bixin.

    PubMed

    Rahmalia, Winda; Fabre, Jean-François; Usman, Thamrin; Mouloungui, Zéphirin

    2014-10-15

    We describe here the effects of aprotic solvents on the spectroscopic characteristics of bixin. Bixin was dissolved in dimethyl sulfoxide, acetone, dichloromethane, ethyl acetate, chloroform, dimethyl carbonate, cyclohexane and hexane, separately, and its spectra in the resulting solutions were determined by UV-visible spectrophotometry at normal pressure and room temperature. We analyzed the effect of aprotic solvents on λmax according to Onsager cavity model and Hansen theory, and determined the approximate absorption coefficient with the Beer-Lambert law. We found that the UV-visible absorption spectra of bixin were found to be solvent dependent. The S0→S2 transition energy of bixin in solution was dependent principally on the refractive index of the solvents and the bixin-solvent dispersion interaction. There was a small influence of the solvents dielectric constant, permanent dipole interaction and hydrogen bonding occurred between bixin and solvents. The absorbance of bixin in various solvents, with the exception of hexane, increased linearly with concentration. PMID:24840486

  6. Aprotic solvents effect on the UV-visible absorption spectra of bixin

    NASA Astrophysics Data System (ADS)

    Rahmalia, Winda; Fabre, Jean-François; Usman, Thamrin; Mouloungui, Zéphirin

    2014-10-01

    We describe here the effects of aprotic solvents on the spectroscopic characteristics of bixin. Bixin was dissolved in dimethyl sulfoxide, acetone, dichloromethane, ethyl acetate, chloroform, dimethyl carbonate, cyclohexane and hexane, separately, and its spectra in the resulting solutions were determined by UV-visible spectrophotometry at normal pressure and room temperature. We analyzed the effect of aprotic solvents on λmax according to Onsager cavity model and Hansen theory, and determined the approximate absorption coefficient with the Beer-Lambert law. We found that the UV-visible absorption spectra of bixin were found to be solvent dependent. The S0 → S2 transition energy of bixin in solution was dependent principally on the refractive index of the solvents and the bixin-solvent dispersion interaction. There was a small influence of the solvents dielectric constant, permanent dipole interaction and hydrogen bonding occurred between bixin and solvents. The absorbance of bixin in various solvents, with the exception of hexane, increased linearly with concentration.

  7. 10 CFR 26.161 - Cutoff levels for validity testing.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... the first aliquot and a different confirmatory test (e.g., multi-wavelength spectrophotometry, ion...., multi-wavelength spectrophotometry, ion chromatography, atomic absorption spectrophotometry, capillary...-wavelength spectrophotometry, ion chromatography, inductively coupled plasma-mass spectrometry) with...

  8. Application of derivative spectrophotometry under orthogonal polynomial at unequal intervals: Determination of metronidazole and nystatin in their pharmaceutical mixture

    NASA Astrophysics Data System (ADS)

    Korany, Mohamed A.; Abdine, Heba H.; Ragab, Marwa A. A.; Aboras, Sara I.

    2015-05-01

    This paper discusses a general method for the use of orthogonal polynomials for unequal intervals (OPUI) to eliminate interferences in two-component spectrophotometric analysis. In this paper, a new approach was developed by using first derivative D1 curve instead of absorbance curve to be convoluted using OPUI method for the determination of metronidazole (MTR) and nystatin (NYS) in their mixture. After applying derivative treatment of the absorption data many maxima and minima points appeared giving characteristic shape for each drug allowing the selection of different number of points for the OPUI method for each drug. This allows the specific and selective determination of each drug in presence of the other and in presence of any matrix interference. The method is particularly useful when the two absorption spectra have considerable overlap. The results obtained are encouraging and suggest that the method can be widely applied to similar problems.

  9. Absorption of different lead compounds

    PubMed Central

    Barltrop, D.; Meek, F.

    1975-01-01

    A rapid method for the determination of relative absorption of dietary lead by rats is described. The influence of age, weight and dose rate has been determined and using standard conditions the tissue lead content of blood, kidney and femur are significantly correlated with each other and are a function of ingested lead. Eight lead compounds were evaluated using this technique and the findings related to lead acetate as a reference compound. Of the inorganic preparations studied, lead carbonate (basic) and metallic lead showed a twelve-fold difference in absorption, with the remaining compounds giving intermediate values. The absorption of lead from four organic compounds was determined from diets containing 7·5% corn oil added to the standard diet. Lead tallate was absorbed to the same degree as lead acetate, but lesser absorptions resulted from lead octoate, naphthenate and alsynate. The addition of corn oil to a final concentration of 7·5% of the diet enhanced the absorption of lead acetate. PMID:1208290

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

    PubMed

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

    2015-09-01

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

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

    PubMed

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

    2009-12-01

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

  12. Simple, rapid spectrophotometry of urinary N-acetyl-beta-D-glucosaminidase, with use of a new chromogenic substrate.

    PubMed

    Noto, A; Ogawa, Y; Mori, S; Yoshioka, M; Kitakaze, T; Hori, T; Nakamura, M; Miyake, T

    1983-10-01

    We have developed a new spectrophotometric assay for urinary N-acetyl-beta-D-glucosaminidase (NAGase) with use of sodio m-cresolsulfonphthaleinyl N-acetyl-beta-D-glucosaminide (MCP-NAG). MCP-NAG was synthesized from acetochloro-glucosamine and m-cresolsulfonphthalein (MCP) in four steps. MCP-NAG reacts well with NAGase (Km = 0.41 mmol/L) and is highly water soluble. The absorption maximum and molar absorptivity of the aglycone MCP are 580 nm and 40 670, respectively. Spectral overlap of interfering substances at 580 nm is almost negligible, so that the urine blank can be omitted from the assay procedure. The high molar absorptivity of MCP gives sufficient analytical sensitivity at a reaction time of 15 min. The correlation between the MCP-NAG method (y) and the fluorimetric method (x) involving 4-methylumbelliferyl N-acetyl-beta-D-glucosaminide is represented by the equation y = 0.995x - 0.669 (r = 0.991). Thus, the present method provides practical advantages over conventional methods, for use in the routine laboratory. PMID:6616814

  13. Thermodynamic derivatives of infrared absorptance

    NASA Technical Reports Server (NTRS)

    Broersma, S.; Walls, W. L.

    1974-01-01

    Calculation of the concentration, pressure, and temperature dependence of the spectral absorptance of a vibrational absorption band. A smooth thermodynamic dependence was found for wavelength intervals where the average absorptance is less than 0.65. Individual rotational lines, whose parameters are often well known, were used as bases in the calculation of medium resolution spectra. Two modes of calculation were combined: well-separated rotational lines plus interaction terms, or strongly overlapping lines that were represented by a compound line of similar shape plus corrections. The 1.9- and 6.3-micron bands of H2O and the 4.3-micron band of CO2 were examined in detail and compared with experiment.

  14. Absorption properties of identical atoms

    SciTech Connect

    Sancho, Pedro

    2013-09-15

    Emission rates and other optical properties of multi-particle systems in collective and entangled states differ from those in product ones. We show the existence of similar effects in the absorption probabilities for (anti)symmetrized states of two identical atoms. The effects strongly depend on the overlapping between the atoms and differ for bosons and fermions. We propose a viable experimental verification of these ideas. -- Highlights: •The absorption rates of a pair of identical atoms in product and (anti)symmetrized states are different. •The modifications of the optical properties are essentially determined by the overlapping between the atoms. •The absorption properties differ, in some cases, for bosons and fermions.

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

    PubMed

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

    2015-06-01

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

  16. Enhanced absorption cycle computer model

    NASA Astrophysics Data System (ADS)

    Grossman, G.; Wilk, M.

    1993-09-01

    Absorption heat pumps have received renewed and increasing attention in the past two decades. The rising cost of electricity has made the particular features of this heat-powered cycle attractive for both residential and industrial applications. Solar-powered absorption chillers, gas-fired domestic heat pumps, and waste-heat-powered industrial temperature boosters are a few of the applications recently subjected to intensive research and development. The absorption heat pump research community has begun to search for both advanced cycles in various multistage configurations and new working fluid combinations with potential for enhanced performance and reliability. The development of working absorption systems has created a need for reliable and effective system simulations. A computer code has been developed for simulation of absorption systems at steady state in a flexible and modular form, making it possible to investigate various cycle configurations with different working fluids. The code is based on unit subroutines containing the governing equations for the system's components and property subroutines containing thermodynamic properties of the working fluids. The user conveys to the computer an image of his cycle by specifying the different subunits and their interconnections. Based on this information, the program calculates the temperature, flow rate, concentration, pressure, and vapor fraction at each state point in the system, and the heat duty at each unit, from which the coefficient of performance (COP) may be determined. This report describes the code and its operation, including improvements introduced into the present version. Simulation results are described for LiBr-H2O triple-effect cycles, LiCl-H2O solar-powered open absorption cycles, and NH3-H2O single-effect and generator-absorber heat exchange cycles. An appendix contains the user's manual.

  17. Solar powered absorption air conditioning

    NASA Astrophysics Data System (ADS)

    Vardon, J. M.

    1980-04-01

    Artificial means of providing or removing heat from the building are discussed along with the problem of the appropriate building design and construction for a suitable heat climate inside the building. The use of a lithium bromide-water absorption chiller, powered by a hot water store heated by an array of stationary flat collectors, is analyzed. An iterative method of predicting the cooling output from a LiBr-water absorption refrigeration plant having variable heat input is described and a model allowing investigation of the performance of a solar collector and thermal storage system is developed.

  18. Periodic microwave absorption in superconductors

    SciTech Connect

    Martinek, J.; Stankowski, J. )

    1994-08-01

    A model explaining the presence of a periodic train of microwave absorption lines in the magnetic modulated microwave absorption (MMMA) spectra of high- and low-temperature superconductors is proposed. The model assumes the occurrence of regular superconducting current loops, closed by Josephson junctions, in these materials. The system of such loops is considered within the basic model of the rf superconducting quantum interference device taking into account the effect of thermal fluctuations. The magnetic-field and temperature dependencies of the MMMA obtained on the basis of the proposed model are in qualitative agreement with experimental data.

  19. Absorption-heat-pump system

    DOEpatents

    Grossman, G.; Perez-Blanco, H.

    1983-06-16

    An improvement in an absorption heat pump cycle is obtained by adding adiabatic absorption and desorption steps to the absorber and desorber of the system. The adiabatic processes make it possible to obtain the highest temperature in the absorber before any heat is removed from it and the lowest temperature in the desorber before heat is added to it, allowing for efficient utilization of the thermodynamic availability of the heat supply stream. The improved system can operate with a larger difference between high and low working fluid concentrations, less circulation losses, and more efficient heat exchange than a conventional system.

  20. Catalysis of CO₂ absorption in aqueous solution by inorganic oxoanions and their application to post combustion capture.

    PubMed

    Phan, Duong T; Maeder, Marcel; Burns, Robert C; Puxty, Graeme

    2014-04-15

    To reduce CO2 emission into the atmosphere, particularly from coal-fired power stations, post combustion capture (PCC) using amine-based solvents to chemically absorb CO2 has been extensively developed. From an infrastructure viewpoint, the faster the absorption of CO2, the smaller the absorber required. The use of catalysts for this process has been broadly studied. In this manuscript, a study of the catalytic efficiencies of inorganic oxoanions such as arsenite, arsenate, phosphite, phosphate, and borate is described. The kinetics of the accelerated CO2 absorption at 25 °C was investigated using stopped-flow spectrophotometry. The catalytic rate constants of these anions for the reaction of CO2 with H2O were determined to be 137.7(3), 30.3(7), 69(2), 32.7(9), and 13.66(7) M(-1)s(-1), respectively. A new mechanism for the catalytic reaction of oxoanions with CO2 has also been proposed. The applicability of these catalysts to PCC was further studied by simulation of the absorption process under PCC conditions using their experimental catalytic rate constants. Arsenite and phosphite were confirmed to be the best catalysts for CO2 capture. However, considering the toxicological effect of arsenic and the oxidative instability of phosphite, phosphate would be the most promising inorganic catalyst for PCC process from the series of inorganic oxoanions studied. PMID:24660867

  1. Aerosol Absorption Measurements in MILAGRO.

    NASA Astrophysics Data System (ADS)

    Gaffney, J. S.; Marley, N. A.; Arnott, W. P.; Paredes-Miranda, L.; Barnard, J. C.

    2007-12-01

    During the month of March 2006, a number of instruments were used to determine the absorption characteristics of aerosols found in the Mexico City Megacity and nearby Valley of Mexico. These measurements were taken as part of the Department of Energy's Megacity Aerosol Experiment - Mexico City (MAX-Mex) that was carried out in collaboration with the Megacity Interactions: Local and Global Research Observations (MILAGRO) campaign. MILAGRO was a joint effort between the DOE, NSF, NASA, and Mexican agencies aimed at understanding the impacts of a megacity on the urban and regional scale. A super-site was operated at the Instituto Mexicano de Petroleo in Mexico City (designated T-0) and at the Universidad Technologica de Tecamac (designated T-1) that was located about 35 km to the north east of the T-0 site in the State of Mexico. A third site was located at a private rancho in the State of Hidalgo approximately another 35 km to the northeast (designated T-2). Aerosol absorption measurements were taken in real time using a number of instruments at the T-0 and T-1 sites. These included a seven wavelength aethalometer, a multi-angle absorption photometer (MAAP), and a photo-acoustic spectrometer. Aerosol absorption was also derived from spectral radiometers including a multi-filter rotating band spectral radiometer (MFRSR). The results clearly indicate that there is significant aerosol absorption by the aerosols in the Mexico City megacity region. The absorption can lead to single scattering albedo reduction leading to values below 0.5 under some circumstances. The absorption is also found to deviate from that expected for a "well-behaved" soot anticipated from diesel engine emissions, i.e. from a simple 1/lambda wavelength dependence for absorption. Indeed, enhanced absorption is seen in the region of 300-450 nm in many cases, particularly in the afternoon periods indicating that secondary organic aerosols are contributing to the aerosol absorption. This is likely due

  2. Ultraviolet and Light Absorption Spectrometry.

    ERIC Educational Resources Information Center

    Hargis, L. G.; Howell, J. A.

    1984-01-01

    Reviews developments in ultraviolet and light absorption spectrometry from December 1981 through November 1983, focusing on the chemistry involved in developing suitable reagents, absorbing systems, and methods of determination, and on physical aspects of the procedures. Includes lists of spectrophotometric methods for metals, non-metals, and…

  3. Slow light and saturable absorption

    NASA Astrophysics Data System (ADS)

    Selden, A. C.

    2009-06-01

    Quantitative analysis of slow light experiments utilising coherent population oscillation (CPO) in a range of saturably absorbing media, including ruby and alexandrite, Er3+:Y2SiO5, bacteriorhodopsin, semiconductor quantum devices and erbium-doped optical fibres, shows that the observations may be more simply interpreted as saturable absorption phenomena. A basic two-level model of a saturable absorber displays all the effects normally associated with slow light, namely phase shift and modulation gain of the transmitted signal, hole burning in the modulation frequency spectrum and power broadening of the spectral hole, each arising from the finite response time of the non-linear absorption. Only where hole-burning in the optical spectrum is observed (using independent pump and probe beams), or pulse delays exceeding the limits set by saturable absorption are obtained, can reasonable confidence be placed in the observation of slow light in such experiments. Superluminal (“fast light”) phenomena in media with reverse saturable absorption (RSA) may be similarly explained.

  4. Migrant labor absorption in Malaysia.

    PubMed

    Nayagam, J

    1992-01-01

    The use of migrant workers to ease labor shortages caused by rapid industrialization in Malaysia during the twentieth century is examined. "This paper will focus on: (1) the extent, composition and distribution of migrant workers; (2) the labor shortage and absorption of migrant workers; and (3) the role of migrant workers in the government's economic restructuring process." PMID:12285766

  5. Simultaneous determination of Fe(III) and Al(III) by first-derivative spectrophotometry and partial least-squares (PLS-2) method - application to post-haemodialysis fluids.

    PubMed

    Aguerssif, Nadia; Benamor, Mohamed; Kachbi, Malek; Draa, Mohamed Tahar

    2008-01-01

    Derivative spectrophotometry (graphical method) and partial least-squares regression (numerical method) methods were developed for the spectrophotometric multi-component analysis of post-haemodialysis fluids and synthetic mixtures containing Al(III) and Fe(III) without any chemical separation. The complexes of these metal ions with chrome azurol S were formed immediately at pH 5.5 and were stable for at least 3h. The graphical method is based on the use of first-derivative spectra for evaluation because working wavelength determination was more precise and spectral overlap was less than in the ordinary spectra. Two wavelengths at which the complexes exhibited maximum absorption values for Fe(III) and Al(III) were selected as analytical wavelengths, i.e., 675 and 623.5 nm, respectively. Lambert-Beer's law is obeyed between 0.0896-8.064 microg/mL Fe(III) and 0.054-0.486 microg/mL Al(III). Limits of detection for Fe(III) and Al(III) were 0.056 and 0.044 microg/mL, respectively. The reproducibility, expressed as variation coefficients, for two sets of 10 standard mixtures containing 3.584 microg/mL Fe(III) and 0.27 microg/mL Al(III) were 1.9% and 2% for iron and aluminium, respectively. In the numerical method, a training set was randomly prepared by using 14 samples. The concentration of each component has been varied in the linear range of the analytical signal. The spectral regions between 510 and 720 nm were selected for the analysis of the binary mixture of Fe(III)/Al(III). The proposed methods were validated by using synthetic binary mixtures and applied to the simultaneous determination of Fe(III) and Al(III) in post-haemodialysis samples. The obtained results were compared with each other; in general, both multi-component methods gave rise to similar recovery results for laboratory-prepared mixtures and real samples. PMID:18755392

  6. Aerosol Absorption and Radiative Forcing

    NASA Technical Reports Server (NTRS)

    Stier, Philip; Seinfeld, J. H.; Kinne, Stefan; Boucher, Olivier

    2007-01-01

    We present a comprehensive examination of aerosol absorption with a focus on evaluating the sensitivity of the global distribution of aerosol absorption to key uncertainties in the process representation. For this purpose we extended the comprehensive aerosol-climate model ECHAM5-HAM by effective medium approximations for the calculation of aerosol effective refractive indices, updated black carbon refractive indices, new cloud radiative properties considering the effect of aerosol inclusions, as well as by modules for the calculation of long-wave aerosol radiative properties and instantaneous aerosol forcing. The evaluation of the simulated aerosol absorption optical depth with the AERONET sun-photometer network shows a good agreement in the large scale global patterns. On a regional basis it becomes evident that the update of the BC refractive indices to Bond and Bergstrom (2006) significantly improves the previous underestimation of the aerosol absorption optical depth. In the global annual-mean, absorption acts to reduce the shortwave anthropogenic aerosol top-of-atmosphere (TOA) radiative forcing clear-sky from -0.79 to -0.53 W m(sup -2) (33%) and all-sky from -0.47 to -0.13W m(sup -2 (72%). Our results confirm that basic assumptions about the BC refractive index play a key role for aerosol absorption and radiative forcing. The effect of the usage of more accurate effective medium approximations is comparably small. We demonstrate that the diversity in the AeroCom land-surface albedo fields contributes to the uncertainty in the simulated anthropogenic aerosol radiative forcings: the usage of an upper versus lower bound of the AeroCom land albedos introduces a global annual-mean TOA forcing range of 0.19W m(sup -2) (36%) clear-sky and of 0.12W m(sup -2) (92%) all-sky. The consideration of black carbon inclusions on cloud radiative properties results in a small global annual-mean all-sky absorption of 0.05W m(sup -2) and a positive TOA forcing perturbation of 0

  7. Study on solid phase extraction and graphite furnace atomic absorption spectrometry for the determination of nickel, silver, cobalt, copper, cadmium and lead with MCI GEL CHP 20Y as sorbent.

    PubMed

    Yang, Guangyu; Fen, Weibo; Lei, Chun; Xiao, Weilie; Sun, Handong

    2009-02-15

    A solid phase extraction and graphite furnace atomic absorption spectrometry (GFAAS) for the determination of nickel, silver, cobalt, copper, cadmium and lead with MCI GEL CHP 20Y as sorbent was studied. Trace amounts of chromium, nickel, silver, cobalt, copper, cadmium and lead were reacted with 2-(2-quinolinil-azo)-4-methyl-1,3-dihydroxidobenzene (QAMDHB) followed by adsorption onto MCI GEL CHP 20Y solid phase extraction column, and 1.0molL(-1) HNO(3) was used as eluent. The metal ions in 300mL solution can be concentrated to 1.0mL, representing an enrichment factor of 300 was achieved. The recoveries of analytes at pH 8.0 with 1.0g of resin were greater than 95% without interference from alkaline, earth alkaline and some metal ions. When detected with graphite furnace atomic absorption spectrometry, the detection limits in the original samples were 1.4ngL(-1) for Cr(III), 1.0ngL(-1) for Ni(II), 0.85ngL(-1) for Ag(I), 1.2ngL(-1) for Co(II), 1.0ngL(-1) for Cu(II), 1.2ngL(-1) for Cd(II) and 1.3ngL(-1) for Pb(II). The validation of the procedure was performed by the analysis of the certified standard reference materials, and the presented procedure was applied to the determination of analytes in biological, water and soil samples with good results (recoveries range from 89 to 104%, and R.S.D.% lower than 3.2%. The results agreed with the standard value or reference method). PMID:18562094

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

    PubMed

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

    2011-09-15

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

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

    NASA Astrophysics Data System (ADS)

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

    2013-09-01

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

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

    PubMed

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

    2015-01-01

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

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

    PubMed

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

    2016-04-15

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

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

    PubMed

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

    2013-09-01

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

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

    PubMed

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

    2010-07-26

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

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

    NASA Astrophysics Data System (ADS)

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

    2000-12-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2002-11-01

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

  17. Direct sample introduction of wines in graphite furnace atomic absorption spectrometry for the simultaneous determination of arsenic, cadmium, copper and lead content.

    PubMed

    Ajtony, Zsolt; Szoboszlai, Norbert; Suskó, Emoke Klaudia; Mezei, Pál; György, Krisztina; Bencs, László

    2008-07-30

    A multi-element graphite furnace atomic absorption spectrometry (GFAAS) method was elaborated for the simultaneous determination of As, Cd, Cu, and Pb in wine samples of various sugar contents using the transversally heated graphite atomizer (THGA) with end-capped tubes and integrated graphite platforms (IGPs). For comparative GFAAS analyses, direct injection (i.e., dispensing the sample onto the IGP) and digestion-based (i.e., adding oxidizing agents, such as HNO(3) and/or H(2)O(2) to the sample solutions) methods were optimized with the application of chemical modifiers. The mixture of 5 microg Pd (applied as nitrate) plus 3 microg Mg(NO(3))(2) chemical modifier was proven to be optimal for the present set of analytes and matrix, it allowing the optimal 600 degrees C pyrolysis and 2200 degrees C atomization temperatures, respectively. The IGP of the THGA was pre-heated at 70 degrees C to prevent the sputtering and/or foaming of sample solutions with a high organic content, dispensed together with the modifier solution, which method also improved the reproducibility of the determinations. With the digestion-based method, the recovery ranged between 87 and 122%, while with the direct injection method it was between 96 and 102% for Cd, Cu, and Pb, whereas a lower, compromise recovery of 45-85% was realized for As. The detection limits (LODs) were found to be 5.0, 0.03, 1.2, and 0.8 microg l(-1) for As, Cd, Cu, and Pb, respectively. The characteristic mass (m(0)) data were 24 pg As, 1.3 pg Cd, 13 pg Cu, and 35 pg Pb. The upper limits of the linear calibration range were 100, 2, 100, and 200 microg l(-1) for As, Cd, Cu, and Pb, respectively. The precisions were not worse than 4.8, 3.1, 3.7, and 2.3% for As, Cd, Cu, and Pb, respectively. For arsenic, a higher amount of the modifier (e.g., 20 microg Pd plus 12 microg Mg(NO(3))(2)) could be recommended to overcome the interference from the presence of sulphate and phosphate in wines. Although this method increased the

  18. The Intestinal Absorption of Folates

    PubMed Central

    Visentin, Michele; Diop-Bove, Ndeye; Zhao, Rongbao; Goldman, I. David

    2014-01-01

    The properties of intestinal folate absorption were documented decades ago. However, it was only recently that the proton-coupled folate transporter (PCFT) was identified and its critical role in folate transport across the apical brush-border membrane of the proximal small intestine established by the loss-of-function mutations identified in the PCFT gene in subjects with hereditary folate malabsorption and, more recently, by the Pcft-null mouse. This article reviews the current understanding of the properties of PCFT-mediated transport and how they differ from those of the reduced folate carrier. Other processes that contribute to the transport of folates across the enterocyte, along with the contribution of the enterohepatic circulation, are considered. Important unresolved issues are addressed, including the mechanism of intestinal folate absorption in the absence of PCFT and regulation of PCFT gene expression. The impact of a variety of ions, organic molecules, and drugs on PCFT-mediated folate transport is described. PMID:24512081

  19. The intestinal absorption of folates.

    PubMed

    Visentin, Michele; Diop-Bove, Ndeye; Zhao, Rongbao; Goldman, I David

    2014-01-01

    The properties of intestinal folate absorption were documented decades ago. However, it was only recently that the proton-coupled folate transporter (PCFT) was identified and its critical role in folate transport across the apical brush-border membrane of the proximal small intestine established by the loss-of-function mutations identified in the PCFT gene in subjects with hereditary folate malabsorption and, more recently, by the Pcft-null mouse. This article reviews the current understanding of the properties of PCFT-mediated transport and how they differ from those of the reduced folate carrier. Other processes that contribute to the transport of folates across the enterocyte, along with the contribution of the enterohepatic circulation, are considered. Important unresolved issues are addressed, including the mechanism of intestinal folate absorption in the absence of PCFT and regulation of PCFT gene expression. The impact of a variety of ions, organic molecules, and drugs on PCFT-mediated folate transport is described. PMID:24512081

  20. Maximum entropy and drug absorption.

    PubMed

    Charter, M K; Gull, S F

    1991-10-01

    The application of maximum entropy to the calculation of drug absorption rates was introduced in an earlier paper. Here it is developed further, and the whole procedure is presented as a problem in scientific inference to be solved using Bayes' theorem. Blood samples do not need to be taken at equally spaced intervals, and no smoothing, interpolation, extrapolation, or other preprocessing of the data is necessary. The resulting input rate estimates are smooth and physiologically realistic, even with noisy data, and their accuracy is quantified. Derived quantities such as the proportion of the dose absorbed, and the mean and median absorption times, are also obtained, together with their error estimates. There are no arbitrarily valued parameters in the analysis, and no specific functional form, such as an exponential or polynomial, is assumed for the input rate functions. PMID:1783989

  1. Optical absorption in trilayer graphene

    NASA Astrophysics Data System (ADS)

    Li, Xiao; Zhang, Fan; Niu, Qian

    2013-03-01

    We use a low energy effective model to analyze the optical responses of trilayer graphene samples. We first show that optical absorption of the ABA-stacked trilayer has strong dependence on both the Fermi energy and optical frequency, which is in sharp contrast to that of ABC-stacked trilayer graphene. Secondly, we are able to determine the possible existence of trigonal warping effects in the bandstructure of ABC-stacked trilayer graphene by a divergence in the absorption spectra at around 10 meV. In addition, we can partially distinguish the vairious broken symmetry states driven by electron-electron interactions in ABC-stacked trilayer graphene. In particular, the quantum anomalous Hall (QAH) state is sensitive to the polarization of the incident light, giving a way to detect its possible existence.

  2. Photodetector with enhanced light absorption

    DOEpatents

    Kane, James

    1985-01-01

    A photodetector including a light transmissive electrically conducting layer having a textured surface with a semiconductor body thereon. This layer traps incident light thereby enhancing the absorption of light by the semiconductor body. A photodetector comprising a textured light transmissive electrically conducting layer of SnO.sub.2 and a body of hydrogenated amorphous silicon has a conversion efficiency about fifty percent greater than that of comparative cells. The invention also includes a method of fabricating the photodetector of the invention.

  3. Absorption properties of identical atoms

    NASA Astrophysics Data System (ADS)

    Sancho, Pedro

    2013-09-01

    Emission rates and other optical properties of multi-particle systems in collective and entangled states differ from those in product ones. We show the existence of similar effects in the absorption probabilities for (anti)symmetrized states of two identical atoms. The effects strongly depend on the overlapping between the atoms and differ for bosons and fermions. We propose a viable experimental verification of these ideas.

  4. Geometrical interpretation of optical absorption

    SciTech Connect

    Monzon, J. J.; Barriuso, A. G.; Sanchez-Soto, L. L.; Montesinos-Amilibia, J. M.

    2011-08-15

    We reinterpret the transfer matrix for an absorbing system in very simple geometrical terms. In appropriate variables, the system appears as performing a Lorentz transformation in a (1 + 3)-dimensional space. Using homogeneous coordinates, we map that action on the unit sphere, which is at the realm of the Klein model of hyperbolic geometry. The effects of absorption appear then as a loxodromic transformation, that is, a rhumb line crossing all the meridians at the same angle.

  5. Multiphonon infrared absorption in silicon

    NASA Astrophysics Data System (ADS)

    Pradhan, M. M.; Garg, R. K.; Arora, M.

    1987-01-01

    Investigations have been carried out on silicon crystals, grown by float zone (FZ) and Czochralski (CZ) methods, of infrared absorption bands using a Fourier transform infrared spectrophotometer. Multiphonon bands are identified in the light of recent theoretical calculations based on the total energy of silicon crystal lattice. Theoretical results of Ihm et al. (1) and Yin and Cohen (2,3) are found to be in good agreement with the experimental observations of multiphonon infrared bands.

  6. GAX absorption cycle design process

    SciTech Connect

    Priedeman, D.K.; Christensen, R.N.

    1999-07-01

    This paper presents an absorption system design process that relies on computer simulations that are validated by experimental findings. An ammonia-water absorption heat pump cycle at 3 refrigeration tons (RT) and chillers at 3.3 RT and 5 RT (10.5 kW, 11.6 kW, and 17.6 kW) were initially modeled and then built and tested. The experimental results were used to calibrate both the cycle simulation and the component simulations, yielding computer design routines that could accurately predict component and cycle performance. Each system was a generator-absorber heat exchange (GAX) cycle, and all were sized for residential and light commercial use, where very little absorption equipment is currently used. The specific findings of the 5 RT (17.6 kW) chiller are presented. Modeling incorporated a heat loss from the gas-fired generator and pressure drops in both the evaporator and absorber. Simulation results and experimental findings agreed closely and validated the modeling method and simulation software.

  7. Purge needs in absorption chillers

    SciTech Connect

    Murray, J.G. )

    1993-10-01

    Absorption chillers are regaining a significant share of large tonnage chiller sales, such as they had 20 years ago. Gas-fired chillers are now available that have a base energy (ultimate fuel usage) consumption rate per ton comparable to that in electric units. Effective purging in an absorption chiller is an absolute necessity to achieve the low chilled water temperature needed for dehumidification and to fully benefit from the energy savings offered by double-effect cycles. Although the purge system is usually not shown on the typical cycle schematic, its proper functioning is a key requirement for satisfactory machine operation. This article discusses the effect of noncondensible (N/C) gases on the absorption cooling process and the basics of purge systems. In addition, the article discusses the rationale for the important design step of selecting the location of the N/C probe, and discusses purge systems applicable to the direct-fired, double-effect machines now entering the marketplace.

  8. Formaldehyde absorption toward W51

    NASA Technical Reports Server (NTRS)

    Kogut, A.; Smoot, G. F.; Bennett, C. L.; Petuchowski, S. J.

    1989-01-01

    Formaldehyde (H2CO) absorption toward the H II region complex W51A (G49.5 - 0.4) in the 6 cm and 2 cm wavelength rotational transitions has been measured with angular resolution of about 0.15 pc. The continuum H II region shows a large, previously undetected shell structure 5.5 pc along the major axis. The absorption, converted to optical depth, shows a higher degree of clumping throughout the map than previous maps at lower resolution; in particular, two narrow regions of enhanced opacity are observed. The absorption in the velocity range 64-67 km/s LSR extends over most of the region, with an observed velocity gradient of 5.2 km/s pc. The opacity structure largely parallels the velocity structure, with a ridge of enhanced opacity to the north of the highest velocity feature. The S/N of the maps allows accurate modeling of the spectral profiles. Nine distinct clumps in the foreground clouds have been identified and parametrized, and column densities for the 1(11) and 2(12) rotational levels of orthoformaldehyde have been derived.

  9. Ultra-sensitive determination of cadmium in rice and water by UV-vis spectrophotometry after single drop microextraction.

    PubMed

    Wen, Xiaodong; Deng, Qingwen; Guo, Jie; Yang, Shengchun

    2011-08-01

    In this work, a new method based on single drop microextraction (SDME) preconcentration using tetrachloromethane (CCl(4)) as extraction solvent was proposed for the spectrophotometric determination of cadmium in rice and water samples. The influence factors relevant to SDME, such as type and volume of extractant, stirring rate and time, dithizone concentration, pH, drop volume and instrumental conditions were studied systematically. Under the optimal conditions, the limit of detection (LOD) was 0.5 ng L(-1), with sensitivity enhancement factor (EF) of 128. The different maximum absorption wavelength caused by the different extraction acidity compared with some conventional works and the enhancement effect of acetone (dilution solvent) for the spectrophotometric determination were the two key factors of the high EF and sensitivity. The proposed method was applied to the determination of rice and water samples with satisfactory analytical results. The proposed method was simple, rapid, cost-efficient and sensitive. PMID:21530375

  10. Ultra-sensitive determination of cadmium in rice and water by UV-vis spectrophotometry after single drop microextraction

    NASA Astrophysics Data System (ADS)

    Wen, Xiaodong; Deng, Qingwen; Guo, Jie; Yang, Shengchun

    2011-08-01

    In this work, a new method based on single drop microextraction (SDME) preconcentration using tetrachloromethane (CCl 4) as extraction solvent was proposed for the spectrophotometric determination of cadmium in rice and water samples. The influence factors relevant to SDME, such as type and volume of extractant, stirring rate and time, dithizone concentration, pH, drop volume and instrumental conditions were studied systematically. Under the optimal conditions, the limit of detection (LOD) was 0.5 ng L -1, with sensitivity enhancement factor (EF) of 128. The different maximum absorption wavelength caused by the different extraction acidity compared with some conventional works and the enhancement effect of acetone (dilution solvent) for the spectrophotometric determination were the two key factors of the high EF and sensitivity. The proposed method was applied to the determination of rice and water samples with satisfactory analytical results. The proposed method was simple, rapid, cost-efficient and sensitive.

  11. Airborne spectrophotometry of Eta Carinae from 4.5 to 7.5 microns and a model for source morphology

    NASA Technical Reports Server (NTRS)

    Russell, Ray W.; Lynch, David K.; Hackwell, John A.; Rudy, Richard J.; Rossano, George S.; Castelaz, M. W.

    1987-01-01

    Spectrophotometric observations of Eta Car between 4.5 and 7.5 microns show a featureless thermal-like spectrum with no fine-structure lines or broad emission or absorption features. The color temperature of the spectrum is approximately 375 K. High spatial resolution maps at 3.5, 4.8, and 10 microns obtained from the ground are used to discuss the dust distribution and temperature structure, and to present a model for general source morphology. The upper limit to the brightness of the forbidden Ar II fine-structure emission line at 6.98 microns is less than 7 x 10 to the -16th W/sq cm, which still allows for a significant overabundance of argon and is consistent with the evolved nature of the source.

  12. A search for methane in the atmosphere of GJ 1214b via GTC narrow-band transmission spectrophotometry

    NASA Astrophysics Data System (ADS)

    Wilson, P. A.; Colón, K. D.; Sing, D. K.; Ballester, G. E.; Désert, J.-M.; Ehrenreich, D.; Ford, E. B.; Fortney, J. J.; Lecavelier des Etangs, A.; López-Morales, M.; Morley, C. V.; Pettitt, A. R.; Pont, F.; Vidal-Madjar, A.

    2014-03-01

    We present narrow-band photometric measurements of the exoplanet GJ 1214b using the 10.4 m Gran Telescopio Canarias and the Optical System for Imaging and low Resolution Integrated Spectroscopy instrument. Using tuneable filters, we observed a total of five transits, three of which were observed at two wavelengths nearly simultaneously, producing a total of eight individual light curves, six of these probed the possible existence of a methane absorption feature in the 8770-8850 Å region at high resolution. We detect no increase in the planet-to-star radius ratio across the methane feature with a change in radius ratio of Δ overline{R} = -0.0007 ± 0.0017 corresponding to a scaleheight (H) change of -0.5 ± 1.2H across the methane feature, assuming a hydrogen-dominated atmosphere. We find that a variety of water and cloudy atmospheric models fit the data well, but find that cloud-free models provide poor fits. These observations support a flat transmission spectrum resulting from the presence of a high-altitude haze or a water-rich atmosphere, in agreement with previous studies. In this study, the observations are pre-dominantly limited by the photometric quality and the limited number of data points (resulting from a long observing cadence), which make the determination of the systematic noise challenging. With tuneable filters capable of high-resolution measurements (R ≈ 600-750) of narrow absorption features, the interpretation of our results are also limited by the absence of high-resolution methane models below 1 μm.

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

    PubMed

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

    2008-01-01

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

  14. Absorption Spectroscopy in Homogeneous and Micellar Solutions.

    ERIC Educational Resources Information Center

    Shah, S. Sadiq; Henscheid, Leonard G.

    1983-01-01

    Describes an experiment which has helped physical chemistry students learn principles of absorption spectroscopy, the effect of solvent polarity on absorption spectra, and some micellar chemistry. Background information and experimental procedures are provided. (JN)

  15. Absorption, Creativity, Peak Experiences, Empathy, and Psychoticism.

    ERIC Educational Resources Information Center

    Mathes, Eugene W.; And Others

    Tellegen and Atkinson suggested that the trait of absorption may play a part in meditative skill, creativity, capacity for peak experiences, and empathy. Although the absorption-meditative skill relationship has been confirmed, other predictions have not been tested. Tellegen and Atkinson's Absorption Scale was completed by undergraduates in four…

  16. ADAPTATION IN ZINC ABSORPTION FROM WHOLE DIETS

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Limited evidence suggests that humans increase zinc (Zn) absorption in response to low Zn intake. Aim: To assess human Zn absorption from whole diets varying in Zn content, and short-term adaptation to meet apparent Zn requirements. Method: Using 65Zn and whole body counting, Zn absorption by 83 hea...

  17. Computational and experimental study of a multi-layer absorptivity enhanced thin film silicon solar cell

    NASA Astrophysics Data System (ADS)

    Hajimirza, Shima; Howell, John R.

    2014-08-01

    We report on the computational design, fabrication and validation of a multi-layer silicon based thin film solar cell. The cell structure consists of a thin absorber layer of amorphous silicon deposited on a back-reflector aluminum layer and coated on top with ITO transparent conductive oxide. The structure is mounted on a glass substrate. We first use constrained optimization techniques along with numerical solvers of the electromagnetic equations (i.e. FDTD) to tune the geometry of the design. The resulting structure suggests that photon absorptivity in the thin film silicon can be enhanced by as much as 100% over the uncoated layer. The proposed design is then fabricated using thin film deposition techniques, along with a control sample of bare silicon absorber for comparison. AFM imaging and spectrophotometry experiments are applied to image and record the surface roughness and measure the reflectivity spectrum of the sample. Using the measured reflectivity spectrum, we then use inverse optimization to estimate the realized thin film dimensions, deposition error and unwanted oxidation volume. At the end, we use a statistical Monte Carlo analysis as a second method of verification to demonstrate that the measured spectra are in accordance with the expected curves from simulation, and to estimate the effects of fabrication error.

  18. Advanced regenerative absorption refrigeration cycles

    DOEpatents

    Dao, Kim

    1990-01-01

    Multi-effect regenerative absorption cycles which provide a high coefficient of performance (COP) at relatively high input temperatures. An absorber-coupled double-effect regenerative cycle (ADR cycle) (10) is provided having a single-effect absorption cycle (SEA cycle) (11) as a topping subcycle and a single-effect regenerative absorption cycle (1R cycle) (12) as a bottoming subcycle. The SEA cycle (11) includes a boiler (13), a condenser (21), an expansion device (28), an evaporator (31), and an absorber (40), all operatively connected together. The 1R cycle (12) includes a multistage boiler (48), a multi-stage resorber (51), a multisection regenerator (49) and also uses the condenser (21), expansion device (28) and evaporator (31) of the SEA topping subcycle (11), all operatively connected together. External heat is applied to the SEA boiler (13) for operation up to about 500 degrees F., with most of the high pressure vapor going to the condenser (21) and evaporator (31) being generated by the regenerator (49). The substantially adiabatic and isothermal functioning of the SER subcycle (12) provides a high COP. For higher input temperatures of up to 700 degrees F., another SEA cycle (111) is used as a topping subcycle, with the absorber (140) of the topping subcycle being heat coupled to the boiler (13) of an ADR cycle (10). The 1R cycle (12) itself is an improvement in that all resorber stages (50b-f) have a portion of their output pumped to boiling conduits (71a-f) through the regenerator (49), which conduits are connected to and at the same pressure as the highest pressure stage (48a) of the 1R multistage boiler (48).

  19. The effect of nanocrystallite size in monoclinic HfO{sub 2} films on lattice expansion and near-edge optical absorption

    SciTech Connect

    Cisneros-Morales, M. C.; Aita, C. R.

    2010-05-10

    Nanocrystalline monoclinic HfO{sub 2} films were sputter deposited on fused silica substrates, air annealed at 573 to 1273 K to affect crystallite growth, and analyzed by x-ray diffraction and spectrophotometry. Lattice expansion occurs with diminishing crystallite size. O 2p->Hf 5d interband absorption dominates the optical edge at energy E>=6.24 eV, with an optical band gap, E{sub o}=5.48+-0.023, which is independent of crystallite size. However, the strength of a localized resonant band, with onset at 5.65 eV and maximum at 5.94 eV, is affected by crystallite size. Its polaronic origin in a perfect HfO{sub 2} lattice is discussed.

  20. Carbon Dioxide Absorption Heat Pump

    NASA Technical Reports Server (NTRS)

    Jones, Jack A. (Inventor)

    2002-01-01

    A carbon dioxide absorption heat pump cycle is disclosed using a high pressure stage and a super-critical cooling stage to provide a non-toxic system. Using carbon dioxide gas as the working fluid in the system, the present invention desorbs the CO2 from an absorbent and cools the gas in the super-critical state to deliver heat thereby. The cooled CO2 gas is then expanded thereby providing cooling and is returned to an absorber for further cycling. Strategic use of heat exchangers can increase the efficiency and performance of the system.

  1. NEUTRON ABSORPTION AND SHIELDING DEVICE

    DOEpatents

    Axelrad, I.R.

    1960-06-21

    A neutron absorption and shielding device is described which is adapted for mounting in a radiation shielding wall surrounding a radioactive area through which instrumentation leads and the like may safely pass without permitting gamma or neutron radiation to pass to the exterior. The shielding device comprises a container having at least one nonrectilinear tube or passageway means extending therethrough, which is adapted to contain instrumentation leads or the like, a layer of a substance capable of absorbing gamma rays, and a solid resinous composition adapted to attenuate fast-moving neutrons and capture slow- moving or thermal neutrons.

  2. Save by absorption heat pumping

    SciTech Connect

    Davidson, W.F.; Campagne, W.V.L.

    1987-12-01

    The author compares absorption heat pumping (AHP) to mechanical vapor compressor (MVC) heat pumping. The moving part of the AHP is a pump easy to maintain and inexpensive to spare. The mechanical component of the MVC is a vapor compressor which requires more maintenance and is cost-prohibitive to spare. Also, in the MVC system, a purified product stream is heat pumped in an open compressor, thus risking product contamination. In the AHP system, the cold and hot utilities are heat pumped. Therefore, product integrity with an AHP system is well protected as in a conventional fractionation column.

  3. Visible absorption spectrum of liquid ethylene

    PubMed Central

    Nelson, Edward T.; Patel, C. Kumar N.

    1981-01-01

    The visible absorption spectrum of liquid ethylene at ≈ 108 K from 5500 Å to 7200 Å was measured by using a pulsed tunable dye laser, immersed-transducer, gated-detection opto-acoustic spectroscopy technique. The absorption features show the strongest band with an absorption coefficient of ≈2 × 10-2 cm-1 and the weakest band with an absorption coefficient of ≈1 × 10-4 cm-1. Proposed assignments of the observed absorption peaks involve combinations of overtones of local and normal modes of vibration of ethylene. PMID:16592978

  4. Simultaneous spectrophotometric determination of Celecoxib and Diacerein in bulk and capsule by absorption correction method and chemometric methods

    NASA Astrophysics Data System (ADS)

    Patel, N. S.; Nandurbarkar, V. P.; Patel, A. J.; Patel, S. G.

    Two methods, absorption correction and multivariate spectrophotometric methods were developed for simultaneous estimation of Celecoxib (CEL) and Diacerein (DIA) in combined dosage form. Absorption correction method involves direct estimation of DIA at wavelength 341 nm in which CEL has zero absorbance and shows no interference. For estimation of CEL, corrected absorbance was calculated at 253 nm due to the interference of DIA at this wavelength. Linearity was observed in the range of 6-22 μg mL-1 for CEL and 3-11 μg mL-1 for DIA. The method was validated as per ICH guidelines. Chemometric methods including classical least square (CLS), inverse least square (ILS), principal component regression (PCR) and partial least square (PLS) were studied for simultaneous determination of CEL and DIA in capsule using spectrophotometry. A set of 25 standard mixtures containing both drugs were prepared in range of 5-25 μg mL-1 for CEL and 3-15 μg mL-1 for DIA. Analytical figure of merit (FOM), such as sensitivity, selectivity, analytical sensitivity, limit of detection and limit of quantitation were determined for chemometric methods. The proposed methods were applied for determination of two components from combined dosage form.

  5. Application and validation of chemometrics-assisted spectrophotometry and liquid chromatography for the simultaneous determination of six-component pharmaceuticals.

    PubMed

    El-Gindy, Alaa; Emara, Samy; Mostafa, Ahmed

    2006-05-01

    Three methods are developed for the simultaneous determination of theophylline anhydrous (TH), guaiphenesin (GP), diphenhydramine hydrochloride (DP), methylparaben (MP), propylparaben (PP) and sodium benzoate (BZ) in pharmaceutical syrup. The chromatographic method depends on a high performance liquid chromatographic separation on a reversed-phase C(18) column at ambient temperature with mobile phase consisting of 25 mM KH2PO4, pH 3.2-acetonitrile (60:40, v/v). Quantitation was achieved with UV detection at 222 nm based on peak area. The other two chemometric methods applied were partial least squares (PLS-1) and principal component regression (PCR). These approaches were successfully applied to quantify the six components in the studied mixture using information included in the UV absorption spectra of appropriate solutions in the wavelength range of 220-270 nm with Deltalambda=0.4 nm. The calibration PLS-1 and PCR models were evaluated by internal validation (prediction of compounds in its own designed training set of calibration), by cross-validation (obtaining statistical parameters that show the efficiency for a calibration fit model) and by external validation over synthetic and pharmaceutical preparation. The results of PLS-1 and PCR methods were compared with the HPLC method and a good agreement was found. PMID:16414231

  6. Percutaneous absorption of selenium sulfide

    SciTech Connect

    Farley, J.; Skelly, E.M.; Weber, C.B.

    1986-01-01

    The purpose of this study was to determine selenium levels in the urine of Tinea patients before and after overnight application of a 2.5% selenium sulfide lotion. Selenium was measured by atomic absorption spectroscopy (AAS). Hydride generation and carbon rod atomization were studied. It was concluded from this study that selenium is absorbed through intact skin. Selenium is then excreted, at least partially, in urine, for at least a week following treatment. The data show that absorption and excretion of selenium vary on an individual basis. Selenium levels in urine following a single application of selenium sulfide lotion do not indicate that toxic amounts of selenium are being absorbed. Repeated treatments with SeS/sub 2/ result in selenium concentrations in urine which are significantly higher than normal. Significant matrix effects are observed in the carbon rod atomization of urine samples for selenium determinations, even in the presence of a matrix modifier such as nickel. The method of standard additions is required to obtain accurate results in the direct determination of selenium in urine by carbon rod AAS.

  7. Iron Absorption in Drosophila melanogaster

    PubMed Central

    Mandilaras, Konstantinos; Pathmanathan, Tharse; Missirlis, Fanis

    2013-01-01

    The way in which Drosophila melanogaster acquires iron from the diet remains poorly understood despite iron absorption being of vital significance for larval growth. To describe the process of organismal iron absorption, consideration needs to be given to cellular iron import, storage, export and how intestinal epithelial cells sense and respond to iron availability. Here we review studies on the Divalent Metal Transporter-1 homolog Malvolio (iron import), the recent discovery that Multicopper Oxidase-1 has ferroxidase activity (iron export) and the role of ferritin in the process of iron acquisition (iron storage). We also describe what is known about iron regulation in insect cells. We then draw upon knowledge from mammalian iron homeostasis to identify candidate genes in flies. Questions arise from the lack of conservation in Drosophila for key mammalian players, such as ferroportin, hepcidin and all the components of the hemochromatosis-related pathway. Drosophila and other insects also lack erythropoiesis. Thus, systemic iron regulation is likely to be conveyed by different signaling pathways and tissue requirements. The significance of regulating intestinal iron uptake is inferred from reports linking Drosophila developmental, immune, heat-shock and behavioral responses to iron sequestration. PMID:23686013

  8. Iron absorption in Drosophila melanogaster.

    PubMed

    Mandilaras, Konstantinos; Pathmanathan, Tharse; Missirlis, Fanis

    2013-05-01

    The way in which Drosophila melanogaster acquires iron from the diet remains poorly understood despite iron absorption being of vital significance for larval growth. To describe the process of organismal iron absorption, consideration needs to be given to cellular iron import, storage, export and how intestinal epithelial cells sense and respond to iron availability. Here we review studies on the Divalent Metal Transporter-1 homolog Malvolio (iron import), the recent discovery that Multicopper Oxidase-1 has ferroxidase activity (iron export) and the role of ferritin in the process of iron acquisition (iron storage). We also describe what is known about iron regulation in insect cells. We then draw upon knowledge from mammalian iron homeostasis to identify candidate genes in flies. Questions arise from the lack of conservation in Drosophila for key mammalian players, such as ferroportin, hepcidin and all the components of the hemochromatosis-related pathway. Drosophila and other insects also lack erythropoiesis. Thus, systemic iron regulation is likely to be conveyed by different signaling pathways and tissue requirements. The significance of regulating intestinal iron uptake is inferred from reports linking Drosophila developmental, immune, heat-shock and behavioral responses to iron sequestration. PMID:23686013

  9. Formaldehyde Absorption toward W51

    SciTech Connect

    Kogut, A.; Smoot, G.F.; Bennett, C.L.; Petuchowski, S.J.

    1988-04-01

    We have measured formaldehyde (H{sub 2}CO) absorption toward the HII region complex W51A (G49.5-0.4) in the 6 cm and 2 cm wavelength rotational transitions with angular resolution of approximately 4 inch. The continuum HII region shows a large, previously undetected shell structure 5.5 pc along the major axis. We observe no H{sub 2}CO emission in regions of low continuum intensity. The absorption, converted to optical depth, shows a higher degree of clumping than previous maps at lower resolution. The good S/N of the maps allows accurate estimation of the complicated line profiles, showing some of the absorbing clouds to be quite patchy. We list the properties of the opacity spectra for a number of positions both in the clumps and in the more diffuse regions of the absorbing clouds, and derive column densities for the 1{sub 11} and 2{sub 12} rotational levels of ortho-formaldehyde.

  10. The Star Formation History and Metal Content of the Green Peas. New Detailed GTC-OSIRIS Spectrophotometry of Three Galaxies

    NASA Astrophysics Data System (ADS)

    Amorín, R.; Pérez-Montero, E.; Vílchez, J. M.; Papaderos, P.

    2012-04-01

    We present deep broadband imaging and long-slit spectroscopy of three compact, low-mass starburst galaxies at redshift z ~ 0.2-0.3, also referred to as Green Peas (GP). We measure physical properties of the ionized gas and derive abundances for several species with high precision. We find that the three GPs display relatively low extinction, low oxygen abundances, and remarkably high nitrogen-to-oxygen ratios. We also report on the detection of clear signatures of Wolf-Rayet (W-R) stars in these galaxies. We carry out a pilot spectral synthesis study using a combination of both population and evolutionary synthesis models. Their outputs are in qualitative agreement, strongly suggesting a formation history dominated by starbursts. In agreement with the presence of W-R stars, these models show that these GPs currently undergo a major starburst producing between ~4% and ~20% of their stellar mass. However, as models imply, they are old galaxies that formed most of their stellar mass several Gyr ago. The presence of old stars has been spectroscopically verified in one of the galaxies by the detection of Mg I λλ5167, 5173 absorption lines. Additionally, we perform a surface photometry study based on Hubble Space Telescope data, which indicates that the three galaxies possess an exponential low surface brightness envelope. If due to stellar emission, the latter is structurally compatible with the evolved hosts of luminous blue compact dwarf (BCD)/H II galaxies, suggesting that GPs are identifiable with major episodes in the assembly history of local BCDs. These conclusions highlight the importance of these objects as laboratories for studying galaxy evolution at late cosmic epochs.

  11. THE STAR FORMATION HISTORY AND METAL CONTENT OF THE GREEN PEAS. NEW DETAILED GTC-OSIRIS SPECTROPHOTOMETRY OF THREE GALAXIES

    SciTech Connect

    Amorin, R.; Perez-Montero, E.; Vilchez, J. M.

    2012-04-20

    We present deep broadband imaging and long-slit spectroscopy of three compact, low-mass starburst galaxies at redshift z {approx} 0.2-0.3, also referred to as Green Peas (GP). We measure physical properties of the ionized gas and derive abundances for several species with high precision. We find that the three GPs display relatively low extinction, low oxygen abundances, and remarkably high nitrogen-to-oxygen ratios. We also report on the detection of clear signatures of Wolf-Rayet (W-R) stars in these galaxies. We carry out a pilot spectral synthesis study using a combination of both population and evolutionary synthesis models. Their outputs are in qualitative agreement, strongly suggesting a formation history dominated by starbursts. In agreement with the presence of W-R stars, these models show that these GPs currently undergo a major starburst producing between {approx}4% and {approx}20% of their stellar mass. However, as models imply, they are old galaxies that formed most of their stellar mass several Gyr ago. The presence of old stars has been spectroscopically verified in one of the galaxies by the detection of Mg I {lambda}{lambda}5167, 5173 absorption lines. Additionally, we perform a surface photometry study based on Hubble Space Telescope data, which indicates that the three galaxies possess an exponential low surface brightness envelope. If due to stellar emission, the latter is structurally compatible with the evolved hosts of luminous blue compact dwarf (BCD)/H II galaxies, suggesting that GPs are identifiable with major episodes in the assembly history of local BCDs. These conclusions highlight the importance of these objects as laboratories for studying galaxy evolution at late cosmic epochs.

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

    PubMed Central

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

    2013-01-01

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

  13. Determination of bromhexine in cough-cold syrups by absorption spectrophotometry and multivariate calibration using partial least-squares and hybrid linear analyses. Application of a novel method of wavelength selection.

    PubMed

    Goicoechea, H C; Olivieri, A C

    1999-07-12

    The mucolitic bromhexine [N-(2-amino-3,5-dibromobenzyl)-N-methylcyclohexylamine] has been determined in cough suppressant syrups by multivariate spectrophotometric calibration, together with partial least-squares (PLS-1) and hybrid linear analysis (HLA). Notwithstanding the spectral overlapping between bromhexine and syrup excipients, as well as the intrinsic variability of the latter in unknown samples, the recoveries are excellent. A novel method of wavelength selection was also applied, based on the concept of net analyte signal regression, as adapted to the HLA methodology. This method allows one to improve the performance of both PLS-1 and HLA in samples containing nonmodeled interferences. PMID:18967655

  14. A novel approach in dispersive liquid-liquid microextraction based on the use of an auxiliary solvent for adjustment of density UV-VIS spectrophotometric and graphite furnace atomic absorption spectrometric determination of gold based on ion pair formation.

    PubMed

    Kocúrová, Lívia; Balogh, Ioseph S; Skrlíková, Jana; Posta, József; Andruch, Vasil

    2010-10-15

    This paper presents a novel approach to dispersive liquid-liquid microextraction (DLLME), based on the use of an auxiliary solvent for the adjustment of density. The procedure utilises a solvent system consisting of a dispersive solvent, an extraction solvent and an auxiliary solvent, which allows for the use of solvents having a density lower than that of water as an extraction solvent while preserving simple phase separation by centrifugation. The suggested approach could be an alternative to procedures described in the literature in recent months and which have been devoted to solving the same problem. The efficiency of the suggested approach is demonstrated through the determination of gold based on the formation of the ion pair [Au(CN)(2)](-) anion with Astra Phloxine (R) reagent and its extraction using the DLLME procedure with subsequent UV-VIS spectrophotometric and graphite furnace atomic absorption spectrometric detection. The optimum conditions were found to be: pH 3; 0.8 mmol L(-1) K(4)[Fe(CN)(6)]; 0.12 mmol L(-1) R; dispersive solvent, methanol; extraction solvent, toluene; auxiliary solvent, tetrachloromethane. The calibration plots were linear in the ranges 0.39-4.7 mg L(-1) and 0.5-39.4 μg L(-1) for UV-VIS and GFAAS detection, respectively; thus enables the application of the developed method in two ranges differing from one from another by three orders of magnitude. The presented approach can be applied to the development of DLLME procedures for the determination of other compounds extractable by organic solvents with a density lower than that of water. PMID:20875602

  15. Multistage quantum absorption heat pumps

    NASA Astrophysics Data System (ADS)

    Correa, Luis A.

    2014-04-01

    It is well known that heat pumps, while being all limited by the same basic thermodynamic laws, may find realization on systems as "small" and "quantum" as a three-level maser. In order to quantitatively assess how the performance of these devices scales with their size, we design generalized N-dimensional ideal heat pumps by merging N -2 elementary three-level stages. We set them to operate in the absorption chiller mode between given hot and cold baths and study their maximum achievable cooling power and the corresponding efficiency as a function of N. While the efficiency at maximum power is roughly size-independent, the power itself slightly increases with the dimension, quickly saturating to a constant. Thus, interestingly, scaling up autonomous quantum heat pumps does not render a significant enhancement beyond the optimal double-stage configuration.

  16. Multistage quantum absorption heat pumps.

    PubMed

    Correa, Luis A

    2014-04-01

    It is well known that heat pumps, while being all limited by the same basic thermodynamic laws, may find realization on systems as "small" and "quantum" as a three-level maser. In order to quantitatively assess how the performance of these devices scales with their size, we design generalized N-dimensional ideal heat pumps by merging N-2 elementary three-level stages. We set them to operate in the absorption chiller mode between given hot and cold baths and study their maximum achievable cooling power and the corresponding efficiency as a function of N. While the efficiency at maximum power is roughly size-independent, the power itself slightly increases with the dimension, quickly saturating to a constant. Thus, interestingly, scaling up autonomous quantum heat pumps does not render a significant enhancement beyond the optimal double-stage configuration. PMID:24827213

  17. Quantum-enhanced absorption refrigerators

    PubMed Central

    Correa, Luis A.; Palao, José P.; Alonso, Daniel; Adesso, Gerardo

    2014-01-01

    Thermodynamics is a branch of science blessed by an unparalleled combination of generality of scope and formal simplicity. Based on few natural assumptions together with the four laws, it sets the boundaries between possible and impossible in macroscopic aggregates of matter. This triggered groundbreaking achievements in physics, chemistry and engineering over the last two centuries. Close analogues of those fundamental laws are now being established at the level of individual quantum systems, thus placing limits on the operation of quantum-mechanical devices. Here we study quantum absorption refrigerators, which are driven by heat rather than external work. We establish thermodynamic performance bounds for these machines and investigate their quantum origin. We also show how those bounds may be pushed beyond what is classically achievable, by suitably tailoring the environmental fluctuations via quantum reservoir engineering techniques. Such superefficient quantum-enhanced cooling realises a promising step towards the technological exploitation of autonomous quantum refrigerators. PMID:24492860

  18. Energy absorption by polymer crazing

    NASA Technical Reports Server (NTRS)

    Pang, S. S.; Zhang, Z. D.; Chern, S. S.; Hsiao, C. C.

    1983-01-01

    During the past thirty years, a tremendous amount of research was done on the development of crazing in polymers. The phenomenon of crazing was recognized as an unusual deformation behavior associated with a process of molecular orientation in a solid to resist failure. The craze absorbs a fairly large amount of energy during the crazing process. When a craze does occur the surrounding bulk material is usually stretched to several hundred percent of its original dimension and creates a new phase. The total energy absorbed by a craze during the crazing process in creep was calculated analytically with the help of some experimental measurements. A comparison of the energy absorption by the new phase and that by the original bulk uncrazed medium is made.

  19. Transient simulation of absorption machines

    NASA Astrophysics Data System (ADS)

    Anand, D. K.; Allen, R. W.; Kumar, B.

    A model for a water-cooled Lithium-Bromide/water absorption chiller is presented. Its transient response both during the start-up phase and during the shut-off period is predicted. The simulation model incorporates such influencing factors as the thermodynamic properties of the working fluid, the absorbent, the heat-transfer configuration of different components of the chiller and related physical data. The time constants of different components are controlled by a set of key parameters that have been identified. The results show a variable but at times significant amount of time delay before the chiller capacity gets close to its steady-state value. The model is intended to provide an insight into the mechanism of build-up to steady-state performance. By recognizing the significant factors contributing to transient degradation, steps can be taken to reduce such degradation.

  20. Acoustic Absorption in Porous Materials

    NASA Technical Reports Server (NTRS)

    Kuczmarski, Maria A.; Johnston, James C.

    2011-01-01

    An understanding of both the areas of materials science and acoustics is necessary to successfully develop materials for acoustic absorption applications. This paper presents the basic knowledge and approaches for determining the acoustic performance of porous materials in a manner that will help materials researchers new to this area gain the understanding and skills necessary to make meaningful contributions to this field of study. Beginning with the basics and making as few assumptions as possible, this paper reviews relevant topics in the acoustic performance of porous materials, which are often used to make acoustic bulk absorbers, moving from the physics of sound wave interactions with porous materials to measurement techniques for flow resistivity, characteristic impedance, and wavenumber.

  1. Graphene intracavity spaser absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Lozovik, Yu. E.; Nechepurenko, I. A.; Dorofeenko, A. V.

    2016-09-01

    We propose an intracavity plasmon absorption spectroscopy method based on graphene active plasmonics. It is shown that the plasmonic cavity contribution to the sensitivity is proportional to the quality factor Q of the graphene plasmonic cavity and reaches two orders of magnitude. The addition of gain medium into the cavity increases the sensitivity of method. Maximum sensitivity is reached in the vicinity of the plasmon generation threshold. The gain contribution to the sensitivity is proportional to Q1/2. The giant amplification of sensitivity in the graphene plasmon generator is associated with a huge path length, limited only by the decoherence processes. An analytical estimation of the sensitivity to loss caused by analyzed particles (molecules, nanoparticles, etc.) normalized by the single pass plasmon scheme is derived. Usage of graphene nanoflakes as plasmonic cavity allows a high spatial resolution to be reached, in addition to high sensitivity.

  2. Neutron scattering and absorption properties

    SciTech Connect

    Holden, N.E.

    1993-12-01

    The Table in this report presents an evaluated set of values for the experimental quantities, which characterize the properties for scattering and absorption of neutrons. The neutron cross section is given for room temperature neutrons, 20.43{degree}C, corresponds to a thermal neutron energy of 0.0253 electron volts (eV) or a neutron velocity of 2200 meters/second. The neutron resonance integral is defined over the energy range from 0.5 eV to 0.1 {times} 10{sup 6} eV, or 0.1 MeV. A list of the major references used is given below. The literature cutoff data is October 1993. Uncertainties are given in parentheses. Parentheses with two or more numbers indicate values to the excited states(s) and to the ground state of the product nucleus.

  3. Backscatter absorption gas imaging system

    DOEpatents

    McRae, Jr., Thomas G.

    1985-01-01

    A video imaging system for detecting hazardous gas leaks. Visual displays of invisible gas clouds are produced by radiation augmentation of the field of view of an imaging device by radiation corresponding to an absorption line of the gas to be detected. The field of view of an imager is irradiated by a laser. The imager receives both backscattered laser light and background radiation. When a detectable gas is present, the backscattered laser light is highly attenuated, producing a region of contrast or shadow on the image. A flying spot imaging system is utilized to synchronously irradiate and scan the area to lower laser power requirements. The imager signal is processed to produce a video display.

  4. Backscatter absorption gas imaging system

    DOEpatents

    McRae, T.G. Jr.

    A video imaging system for detecting hazardous gas leaks. Visual displays of invisible gas clouds are produced by radiation augmentation of the field of view of an imaging device by radiation corresponding to an absorption line of the gas to be detected. The field of view of an imager is irradiated by a laser. The imager receives both backscattered laser light and background radiation. When a detectable gas is present, the backscattered laser light is highly attenuated, producing a region of contrast or shadow on the image. A flying spot imaging system is utilized to synchronously irradiate and scan the area to lower laser power requirements. The imager signal is processed to produce a video display.

  5. HI Absorption in Merger Remnants

    NASA Technical Reports Server (NTRS)

    Teng, Stacy H.; Veileux, Sylvain; Baker, Andrew J.

    2012-01-01

    It has been proposed that ultraluminous infrared galaxies (ULIRGs) pass through a luminous starburst phase, followed by a dust-enshrouded AGN phase, and finally evolve into optically bright "naked" quasars once they shed their gas/dust reservoirs through powerful wind events. We present the results of our recent 21- cm HI survey of 21 merger remnants with the Green Bank Telescope. These remnants were selected from the QUEST (Quasar/ULIRG Evolution Study) sample of ULIRGs and PG quasars; our targets are all bolometrically dominated by AGN and sample all phases of the proposed ULIRG -> IR-excess quasar -> optical quasar sequence. We explore whether there is an evolutionary connection between ULIRGs and quasars by looking for the occurrence of HI absorption tracing neutral gas outflows; our results will allow us to identify where along the sequence the majority of a merger's gas reservoir is expelled.

  6. Quantum-enhanced absorption refrigerators

    NASA Astrophysics Data System (ADS)

    Correa, Luis A.; Palao, José P.; Alonso, Daniel; Adesso, Gerardo

    2014-02-01

    Thermodynamics is a branch of science blessed by an unparalleled combination of generality of scope and formal simplicity. Based on few natural assumptions together with the four laws, it sets the boundaries between possible and impossible in macroscopic aggregates of matter. This triggered groundbreaking achievements in physics, chemistry and engineering over the last two centuries. Close analogues of those fundamental laws are now being established at the level of individual quantum systems, thus placing limits on the operation of quantum-mechanical devices. Here we study quantum absorption refrigerators, which are driven by heat rather than external work. We establish thermodynamic performance bounds for these machines and investigate their quantum origin. We also show how those bounds may be pushed beyond what is classically achievable, by suitably tailoring the environmental fluctuations via quantum reservoir engineering techniques. Such superefficient quantum-enhanced cooling realises a promising step towards the technological exploitation of autonomous quantum refrigerators.

  7. Quantum-enhanced absorption refrigerators.

    PubMed

    Correa, Luis A; Palao, José P; Alonso, Daniel; Adesso, Gerardo

    2014-01-01

    Thermodynamics is a branch of science blessed by an unparalleled combination of generality of scope and formal simplicity. Based on few natural assumptions together with the four laws, it sets the boundaries between possible and impossible in macroscopic aggregates of matter. This triggered groundbreaking achievements in physics, chemistry and engineering over the last two centuries. Close analogues of those fundamental laws are now being established at the level of individual quantum systems, thus placing limits on the operation of quantum-mechanical devices. Here we study quantum absorption refrigerators, which are driven by heat rather than external work. We establish thermodynamic performance bounds for these machines and investigate their quantum origin. We also show how those bounds may be pushed beyond what is classically achievable, by suitably tailoring the environmental fluctuations via quantum reservoir engineering techniques. Such superefficient quantum-enhanced cooling realises a promising step towards the technological exploitation of autonomous quantum refrigerators. PMID:24492860

  8. Olefin recovery via chemical absorption

    SciTech Connect

    Barchas, R.

    1998-06-01

    The recovery of fight olefins in petrochemical plants has generally been accomplished through cryogenic distillation, a process which is very capital and energy intensive. In an effort to simplify the recovery process and reduce its cost, BP Chemicals has developed a chemical absorption technology based on an aqueous silver nitrate solution. Stone & Webster is now marketing, licensing, and engineering the technology. The process is commercially ready for recovering olefins from olefin derivative plant vent gases, such as vents from polyethylene, polypropylene, ethylene oxide, and synthetic ethanol units. The process can also be used to debottleneck C{sub 2} or C{sub 3} splinters, or to improve olefin product purity. This paper presents the olefin recovery imp technology, discusses its applications, and presents economics for the recovery of ethylene and propylene.

  9. In vivo measurements of the influence of the skin on cerebral oxygenation changes measured with near-infrared spectrophotometry (NIRS)

    NASA Astrophysics Data System (ADS)

    Klaessens, John H. G. M.; van Os, Sandra H. G.; Hopman, Jeroen C. W.; Liem, K. D.; van de Bor, Margot; Thijssen, Johan M.

    2004-07-01

    Goal: To investigate the influence of skin on the accuracy and precision of regional cerebral oxygenation measurements using CW-NIRS and to reduce the inter individual variability of NIRS measurements by normalization with data from an extra wavelength. Method: Three piglets (7.8-9.3 kg) were anesthetized, paralyzed and mechanically ventilated. Receiving optodes were placed over the left and right hemisphere (C3, C4 EEG placement code) and one emitting optode on Cz position (optode distance=1.8cm). Optical densities (OD) were measured for 3 wavelengths (767, 850, 905 nm) (OXYMON) during stable normoxic, mild and deep hypoxemic conditions (SaO2=100%, 80% and 60%) of one minute in each region. This was repeated 3 times: all optodes with skin (condition 1); one receiving optode directly on the skull (2); emitting and also receiving optode on the skull (3). The absolute cO2Hb, cHHb, ctHb concentrations (μmol/L) were calculated from the OD's and changes with respect to the SaO2=100% condition were estimated. Because ODs varied over a large range, the light intensity was externally attenuated to adapt to the range of the spectrophotometer. The data were then corrected for these attenuation effects and for pathlength changes caused by skin removal using the OD at the independent wavelength (λ=975nm). Results: Removal of the skin resulted in an increase of the absorption values (average 0.25 OD in condition 2 and 0.42 OD in condition 3 with respect to condition 1). The change from normoxic to medium, and to deep hypoxic conditions produced a decrease of cO2Hb (-15, and -29 μmol/L, respectively), an increase in cHHb (+16, and +35 μmol/L) and in ctHb (+1, and +5 μmol/L). Total skin removal yielded an extra change in cO2Hb (-5, -1 μmol/L), cHHb (+8, +9 μmol/L), and ctHb (+3, +8 μmol /L). The coefficient of variability of the absolute concentration changes was considerably decreased by the normalization of densities by the density obtained at 795 nm. Conclusion: Skin

  10. Infrared absorption modeling of VOx microbolometer

    NASA Astrophysics Data System (ADS)

    Aggoun, Mehdi; Jiang, Jianliang; Khan, M. K.

    2015-08-01

    The absorption model plays an important role in the design of the microbolometer structure regarding the determination of the optimum thickness of the structure layers. Moreover, the infrared absorption depends on the wavelength of the radiation and the material properties. In this paper, we presented an Infrared absorption model with absorption coefficient of 96% at maximum absorption wavelength of 9.89μm which is very close to the expected value 10μm. This model was established by using MATLAB so that the simulation of the infrared absorption of the VOx microbolometer could be accomplished. In order to confirm the role of this modeling in the design of the device structure, comparison with other structures is also studied in this paper.

  11. Analysis of frequency dependent pump light absorption

    NASA Astrophysics Data System (ADS)

    Wohlmuth, Matthias; Pflaum, Christoph

    2011-03-01

    Simulations have to accurately model thermal lensing in order to help improving resonator design of diode pumped solid state lasers. To this end, a precise description of the pump light absorption is an important prerequisite. In this paper, we discuss the frequency dependency of the pump light absorption in the laser crystal and its influence on the simulated laser performance. The results show that the pump light absorption has to include the spectral overlap of the emitting pump source and the absorbing laser material. This information can either be used for a fully frequency dependent absorption model or, at least in the shown examples, to compute an effective value for an exponential Beer-Lambert law of absorption. This is particularly significant at pump wavelengths coinciding with a peak of absorption. Consequences for laser stability and performance are analyzed for different pump wavelengths in a Nd:YAG laser.

  12. Adopting steam-driven absorption cooling

    SciTech Connect

    Rose, D.T.; Perez-Blanco, H.; Ryan, W.A.

    1995-10-01

    Proper installation, water quality, and maintenance are essential to operating a cost-effective absorption system. Concerns about energy efficiency and the use of chlorofluorocarbons have led to the greater use of absorption machines for cooling applications. These machines, which reclaim condenser or exhaust-gas heat, are used in the most advanced cogeneration systems. Although absorption technology has a long history--with mixed success--its versatility has only recently begun to payoff.

  13. Conditions and drugs interfering with thyroxine absorption.

    PubMed

    Liwanpo, Llanyee; Hershman, Jerome M

    2009-12-01

    Food, dietary fibre and espresso coffee interfere with the absorption of levothyroxine. Malabsorptive disorders reported to affect the absorption of levothyroxine include coeliac disease, inflammatory bowel disease, lactose intolerance as well as Helicobacter pylori (H. pylori) infection and atrophic gastritis. Many commonly used drugs, such as bile acid sequestrants, ferrous sulphate, sucralfate, calcium carbonate, aluminium-containing antacids, phosphate binders, raloxifene and proton-pump inhibitors, have also been shown to interfere with the absorption of levothyroxine. PMID:19942153

  14. The HST quasar absorption line key project. 4: HST faint-object spectrograph and ground-based observations of the unusual low-redshift broad absorption-line quasi-stellar object PG 0043+039

    NASA Technical Reports Server (NTRS)

    Turnshek, David A.; Espey, Brian R.; Kopko, Michael, Jr.; Rauch, Michael; Weymann, Ray J.; Jannuzi, Buell T.; Boksenberg, Alec; Bergeron, Jacqueline; Hartig, George F.; Sargent, W. L. W.

    1994-01-01

    Hubble Space Telescope Faint Object Spectrograph (HST FOS) observations have shown that the spectrum of the low-redshift (z(sub em) approximately equal to 0.384) QSO PG 0043+039 exhibits weak broad absorption lines (BALs). The BALs were discovered during the course of UV spectrophotometry made for the HST Quasar Absorption Line Key Project. The HST data are analyzed along with ground-based optical and IUE spectrophotometry. The object is found to have a number of atypical properties relative to normal non-BAL QSOs. The observed continuum is atypical in the sense that it is much weaker than that of a normal optically selected QSO at rest wavelengths approximately less than 2200 A. Intrinsic reddening of E(B-V) approximately equal to 0.11 mag by dust similar to that found in the SMC at the redshift of PG 0043+039 conservatively accounts for the observed continuum shape moderately well. These observed characteristics are typical of low-ionization BAL QSOs, but convincing evidence for BALs due to low-ionization transitions of Mg II, Al III, Al II, or C II does not exist. Therefore, this object may be a misaligned BAL QSO having many of the characteristics of low-ionization BAL QSOs with the sight line passing through a putative dusty region, but evidently missing clouds of high enough column density to produce observable low-ionization BALs. If the intrinsic dust-extinction model is correct, the observations suggest that the dust is not confined to the presumably higher density, low-ionization BAL clouds, but that it has drifted to nearby high-ionization BAL regions. We also consider other possible mechanisms for producing the shape of the continuous energy distribution which cannot be ruled out. We compare the Fe II emission in PG 0043+039 with that in another Key Project QSO, NGC 2841-UB 3, which has optical Fe II emission comparable in strength to that in PG 0043+039, but has anomalously weak UV Fe II emission. In addition, from an analysis of UV and optical

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

    NASA Astrophysics Data System (ADS)

    Eikje, Natalja Skrebova; Arase, Seiji

    2008-02-01

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

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

    PubMed

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

    2015-06-01

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

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

    PubMed

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

    2007-01-01

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

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

    PubMed

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

    2012-01-01

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

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

    PubMed

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

    2005-10-01

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

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

    PubMed

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

    2009-06-15

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

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

    NASA Astrophysics Data System (ADS)

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

    2007-01-01

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

  2. Nutrient absorption and intestinal adaptation with ageing.

    PubMed

    Woudstra, Trudy; Thomson, Alan B R

    2002-02-01

    Malabsorption of carbohydrates, lipids, amino acids, minerals and vitamins has been described in the elderly. The ability of the intestine to adapt may be impaired in the elderly and this may lead to further malnutrition. Dietary manipulation may prove to be useful to enhance the needed intestinal absorption with ageing. There is an age-associated increase in the prevalence of dyslipidaemia as well as diabetes. These conditions may benefit from nutritional intervention targeted at reducing the absorption of some nutrients. With the continued characterization of the proteins involved in sterol and fatty acid absorption, therapeutic interventions to modify absorption may become available in the future. PMID:11977925

  3. Absorption Optics of Aqueous Foams

    NASA Astrophysics Data System (ADS)

    Bandyopadhyay, Ranjini; Gittings, Alex; Durian, D. J.

    2002-11-01

    Aqueous foams are composed of gas bubbles packed together in a small volume of soapy water. The large number of gas-liquid interfaces in foams results in very strong scattering of light, which explains the opaque nature of conventional aqueous foams such as shaving foams and mousse. For dry foams, the interfaces can take the following three forms: the soap films where two bubbles meet, the triangular plateau borders where three soap films meet and the vertices where four plateau borders meet. Previous experiments have shown that most of the scattering occurs from the plateau borders 2,3 and the transport mean free path of light (l*), the bubble radius (R) and the liquid fraction of foam (epsilon) is related through the relation l*=R/(epsilon0.5). To understand the reflection and scattering of light at the gas-bubble interfaces, we study the absorption of photons in the liquid network as a function of the foam absorptivity. We do this to confirm if the time spent by the photons in the liquid phase is proportional to the liquid fraction of the foam. Our results indicate that for a specific range of liquid fractions (0.05 is less than e is less than 0.1), the photons seem to get trapped in the liquid network. This result is independent of the absorptivity of the foam and leads us to conclude that under appropriate conditions, an aqueous foam behaves very much like an optical fiber network. Aqueous foam is generated in the lab by the method of turbulent mixing of N2 gas with a jet of alpha-olefin-sulfonate (AOS) solution. The foam has been made absorbing by dissolving small quantities of rhodamine dye (R = 0.005 g/l, R = 0.01 g/l and R = 0.0124 g/l) in the AOS solution. The transmission of photons through the foams of liquid fractions 0.0297 is less than e is less than 0.35 has been studied using Diffuse Transmission Spectroscopy (DTS). For each liquid fraction, the transport mean free path l* (the length over which the photon travels before it gets completely

  4. Transient simulation of absorption machines

    SciTech Connect

    Anand, D.K.; Allen, R.W.; Kumar, B.

    1982-08-01

    This paper presents a model for a water-cooled Lithium-Bromide/water absorption chiller and predicts its transient response both during the start-up phase and during the shutoff period. The simulation model incorporates such influencing factors as the thermodynamic properties of the working fluid, the absorbent, the heat-transfer configuration of different components of the chiller and related physical data. The time constants of different components are controlled by a set of key parameters that have been identified in this study. The results show a variable but at times significant amount of time delay before the chiller capacity gets close to its steadystate value. The model is intended to provide an insight into the mechanism of build-up to steady-state performance. By recognizing the significant factors contributing to transient degradation, steps can be taken to reduce such degradation. The evaluation of the residual capacity in the shut-off period will yield more realistic estimates of chiller COP for a chiller satisfying dynamic space cooling load.

  5. Transient simulation of absorption machines

    NASA Astrophysics Data System (ADS)

    Anand, D. K.; Allen, R. W.; Kumar, B.

    1982-08-01

    This paper presents a model for a water-cooled Lithium-Bromide/water absorption chiller and predicts its transient response both during the start-up phase and during the shutoff period. The simulation model incorporates such influencing factors as the thermodynamic properties of the working fluid, the absorbent, the heat-transfer configuration of different components of the chiller and related physical data. The time constants of different components are controlled by a set of key parameters that have been identified in this study. The results show a variable but at times significant amount of time delay before the chiller capacity gets close to its steady-state value. The model is intended to provide an insight into the mechanism of build-up to steady-state performance. By recognizing the significant factors contributing to transient degradation, steps can be taken to reduce such degradation. The evaluation of the residual capacity in the shut-off period will yield more realistic estimates of chiller COP for a chiller satisfying dynamic space cooling load.

  6. Fluid absorption solar energy receiver

    NASA Technical Reports Server (NTRS)

    Bair, Edward J.

    1993-01-01

    A conventional solar dynamic system transmits solar energy to the flowing fluid of a thermodynamic cycle through structures which contain the gas and thermal energy storage material. Such a heat transfer mechanism dictates that the structure operate at a higher temperature than the fluid. This investigation reports on a fluid absorption receiver where only a part of the solar energy is transmitted to the structure. The other part is absorbed directly by the fluid. By proportioning these two heat transfer paths the energy to the structure can preheat the fluid, while the energy absorbed directly by the fluid raises the fluid to its final working temperature. The surface temperatures need not exceed the output temperature of the fluid. This makes the output temperature of the gas the maximum temperature in the system. The gas can have local maximum temperatures higher than the output working temperature. However local high temperatures are quickly equilibrated, and since the gas does not emit radiation, local high temperatures do not result in a radiative heat loss. Thermal radiation, thermal conductivity, and heat exchange with the gas all help equilibrate the surface temperature.

  7. The absorption of polymeric composites

    NASA Astrophysics Data System (ADS)

    Řídký, R.; Popovič, M.; Rolc, S.; Drdlová, M.; Krátký, J.

    2016-06-01

    An absorption capacity of soft, viscoelastic materials at high strain rates is important for wide range of practical applications. Nowadays there are many variants of numerical models suitable for this kind of analysis. The main difficulty is in selection of the most realistic numerical model and a correct setup of many unknown material constants. Cooperation between theoretical simulations and real testing is next crucial point in the investigation process. Standard open source material database offer material properties valid for strain rates less than 250 s-1. There are experiments suitable for analysis of material properties with strain rates close to 2000 s-1. The high strain-rate characteristics of a specific porous blast energy absorbing material measured by modified Split Hopkinson Pressure Bar apparatus is presented in this study. Testing these low impedance materials using a metallic split Hopkinson pressure bar setup results in poor signal to noise ratios due to impedance mismatching. These difficulties are overcome by using polymeric Hopkinson bars. Conventional Hopkinson bar analysis cannot be used on the polymeric bars due to the viscoelastic nature of the bar material. One of the possible solution leads to complex and frequency depended Young modulus of testing bars material. This testing technique was applied to materials composed of porous glass/ceramic filler and polymeric binder, with density of 125 - 300 kg/m3 and particle size in range of 50 µm - 2 mm. The achieved material model was verified in practical application of sandwich structure includes polymeric composites under a blast test.

  8. Gastrointestinal absorption of metallic mercury.

    PubMed

    Sandborgh-Englund, Gunilla; Einarsson, Curt; Sandström, Magnus; Ekstrand, Jan

    2004-09-01

    The absorption of mercury from the gastrointestinal systems of 7 subjects, of whom none had any amalgam fillings, was examined in this study. The authors obtained quantitative information about mercury concentration in plasma and duodenal fluid after the gastrointestinal systems of the subjects were exposed to liquid elemental mercury enclosed in rubber balloons (i.e., approximately 20 g of mercury), using a standard procedure followed for the sampling of bile. Plasma samples were collected prior to exposure, as well as up to 10 d following exposure, and duodenal fluid was collected 1 h, 2 h, 4 h, and 6 h during the intubation process. The authors studied the kinetics of dissolution in vitro by leaching elemental liquid mercury and mercuric chloride. The results of this study supported the hypothesis that metallic mercury is oxidized in the gastrointestinal tract. In addition, the authors determined that duodenal intubation, while using liquid metallic mercury in rubber bags, resulted in the diffusion of minor amounts of atomic elemental mercury through the rubber walls. The absorbed amount of mercury that reached the central circulation was comparable to a daily dose of mercury from dental amalgam in the amalgam-bearing population. PMID:16381485

  9. Light absorption in distorted graphene

    NASA Astrophysics Data System (ADS)

    Hernández-Ortiz, Saúl; Valenzuela, David; Raya, Alfredo; Sánchez-Madrigal, Saúl

    2016-04-01

    We model the low energy dynamics of graphene in the continuum in terms of a version of reduced quantum electrodynamics (QED) restricting fermions to a (2 + 1)-dimensional brane, while photons remain within the (3 + 1)-dimensional bulk. For charge carriers, besides the Dirac mass gap, we consider a Haldane mass term which is induced by parametrizing an effective parity 𝒫 and time-reversal 𝒯 symmetry breaking that occurs on the brane when distortions of the honeycomb array are such that the equivalence between sublattices is lost. We make use of the relativistic Kubo formula and carry out an explicit calculation of the transverse conductivity. As expected, the filling factor is a half (in natural units) for each fermion species. Furthermore, assuming that a sample of this material is radiated perpendicularly with polarized monochromatic light of frequency ω, from the modified Maxwell’s equations we address the problem of light absorption in graphene in terms of the said conductivity. We observe that light penetrating the sample changes its angle of polarization solely by effect of the induced mass, in analogy to the Faraday effect but in absence of magnetic fields. This effect might be relevant for the development of optic filters based on mechanical stretching of graphene flakes.

  10. Predicting Moisture Absorption in Composite Materials

    NASA Technical Reports Server (NTRS)

    Haines, J. R.

    1984-01-01

    Heat transport programs adaptable for absorption analysis. Lightweight sandwich panel specimen used for comparison of water absorption measurements with program predictions. In program model, moisture -- like heat in heat-transport problem moves through variety of materials and structures along complex paths.

  11. High-Absorptance Radiative Heat Sink

    NASA Technical Reports Server (NTRS)

    Cafferty, T.

    1983-01-01

    Absorptance of black-painted open-cell aluminum honeycomb improved by cutting honeycomb at angle or bias rather than straight across. This ensures honeycomb cavities escapes. At each reflection radiation attenuated by absorption. Applications include space-background simulators, space radiators, solar absorbers, and passive coolers for terrestrial use.

  12. Cosmic ray variations during PCA type absorption

    NASA Technical Reports Server (NTRS)

    Kozin, I. D.

    1972-01-01

    It is shown based on data on the cosmic-ray neutron component, ionospheric soundings, and measurements of cosmic radio-emission absorption at Vostok station (Antarctica) that the ionization of the lower ionosphere increases during low intensity of Forbush-type cosmic rays. This is manifested in increased absorption and the appearance of strong sporadic layers in the E-region.

  13. The electronic absorption edge of petroleum

    SciTech Connect

    Mullins, O.C.; Mitra-Kirtley, S.; Zhu, Yifu

    1992-09-01

    The electronic absorption spectra of more than 20 crude oils and asphaltenes are examined. The spectral location of the electronic absorption edge varies over a wide range, from the near-infrared for heavy oils and asphaltenes to the near-UV for gas condensates. The functional form of the electronic absorption edge for all crude oils (measured) is characteristic of the {open_quotes}Urbach tail,{close_quotes} a phenomenology which describes electronic absorption edges in wide-ranging materials. The crude oils all show similar Urbach widths, which are significantly larger than those generally found for various materials but are similar to those previously reported for asphaltenes. Monotonically increasing absorption at higher photon energy continues for all crude oils until the spectral region is reached where single-ring aromatics dominate absorption. However, the rate of increasing absorption at higher energies moderates, thereby deviating from the Urbach behavior. Fluorescence emission spectra exhibit small red shifts from the excitation wavelength and small fluorescence peak widths in the Urbach regions of different crude oils, but show large red shifts and large peak widths in spectral regions which deviate from the Urbach behavior. This observation implies that the Urbach spectral region is dominated by lowest-energy electronic absorption of corresponding chromophores. Thus, the Urbach tail gives a direct measure of the population distribution of chromophores in crude oils. Implied population distributions are consistent with thermally activated growth of large chromophores from small ones. 12 refs., 8 figs.

  14. Iron absorption from intrinsically-labeled lentils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Low iron (Fe) absorption from important staple foods may contribute to Fe deficiency in developing countries. To date, there are few studies examining the Fe bioavailability of pulse crops as commonly prepared and consumed by humans. The objectives of this study were to characterize the Fe absorpt...

  15. Photoelectric absorption cross sections with variable abundances

    NASA Technical Reports Server (NTRS)

    Balucinska-Church, Monika; Mccammon, Dan

    1992-01-01

    Polynomial fit coefficients have been obtained for the energy dependences of the photoelectric absorption cross sections of 17 astrophysically important elements. These results allow the calculation of X-ray absorption in the energy range 0.03-10 keV in material with noncosmic abundances.

  16. On the absorption of alendronate in rats.

    PubMed

    Lin, J H; Chen, I W; deLuna, F A

    1994-12-01

    Alendronate is an antiosteolytic agent under investigation for the treatment of a number of bone disorders. Since the compound is a zwitterion with five pKa values and is completely ionized in the intestine at the physiological pH, absorption is poor; less than 1% of an oral dose is available systemically in rats. In the present studies, absorption was found to be predominantly in the upper part of the small intestine. Administration of buffered solutions of alendronate (pH 2-11) did not improve absorption. Whereas food markedly impaired the absorption of alendronate, EDTA enhanced absorption in a dose-dependent manner. Pretreatment of rats with ulcerogenic agents, mepirizole, acetylsalicylic acid, or indomethacin, resulted in a 3-7-fold increase in the oral absorption of alendronate. The absorption of phenol red, added as an indicator of intestinal tissue damage, was also increased in rats with experimental peptic ulcers. The enhanced absorption of alendronate observed in rats with experimental peptic ulcers was attributed to the alteration of the integrity of the intestinal membrane. PMID:7891304

  17. Atmospheric Solar Heating in Minor Absorption Bands

    NASA Technical Reports Server (NTRS)

    Chou, Ming-Dah

    1998-01-01

    Solar radiation is the primary source of energy driving atmospheric and oceanic circulations. Concerned with the huge computing time required for computing radiative transfer in weather and climate models, solar heating in minor absorption bands has often been neglected. The individual contributions of these minor bands to the atmospheric heating is small, but collectively they are not negligible. The solar heating in minor bands includes the absorption due to water vapor in the photosynthetically active radiation (PAR) spectral region from 14284/cm to 25000/cm, the ozone absorption and Rayleigh scattering in the near infrared, as well as the O2 and CO2 absorption in a number of weak bands. Detailed high spectral- and angular-resolution calculations show that the total effect of these minor absorption is to enhance the atmospheric solar heating by approximately 10%. Depending upon the strength of the absorption and the overlapping among gaseous absorption, different approaches are applied to parameterize these minor absorption. The parameterizations are accurate and require little extra time for computing radiative fluxes. They have been efficiently implemented in the various atmospheric models at NASA/Goddard Space Flight Center, including cloud ensemble, mesoscale, and climate models.

  18. Do Atoms Really "Emit" Absorption Lines?

    ERIC Educational Resources Information Center

    Brecher, Kenneth

    1991-01-01

    Presents three absorption line sources that enhance student understanding of the phenomena associated with the interaction of light with matter and help dispel the misconception that atoms "emit" absorption lines. Sources include neodymium, food coloring and other common household liquids, and fluorescent materials. (MDH)

  19. VAPID: Voigt Absorption-Profile [Interstellar] Dabbler

    NASA Astrophysics Data System (ADS)

    Howarth, Ian D.

    2015-06-01

    VAPID (Voigt Absorption Profile [Interstellar] Dabbler) models interstellar absorption lines. It predicts profiles and optimizes model parameters by least-squares fitting to observed spectra. VAPID allows cloud parameters to be optimized with respect to several different data set simultaneously; those data sets may include observations of different transitions of a given species, and may have different S/N ratios and resolutions.

  20. Absorption of ozone by porous particles

    SciTech Connect

    Afanas'ev, V.P.; Dorofeev, S.B.; Sinitsyn, V.I.; Smirnov, B.M.

    1981-11-01

    The absorption of ozone by porous zeolite, silica gel, and activated carbon particles has been studied experimentally. It was shown that in addition to absorption, dissociation of ozone on the surface plays an important and sometimes decisive role. The results obtained were used to analyze the nature of ball lightning.

  1. Low absorptance porcelain-on-aluminum coating

    NASA Technical Reports Server (NTRS)

    Leggett, H.

    1979-01-01

    Porcelain thermal-control coating for aluminum sheet and foil has solar absorptance of 0.22. Specially formulated coating absorptance is highly stable, changing only 0.03 after 1,000 hours of exposure to simulated sunlight and can be applied by standard commercial methods.

  2. Creating semiconductor metafilms with designer absorption spectra

    PubMed Central

    Kim, Soo Jin; Fan, Pengyu; Kang, Ju-Hyung; Brongersma, Mark L.

    2015-01-01

    The optical properties of semiconductors are typically considered intrinsic and fixed. Here we leverage the rapid developments in the field of optical metamaterials to create ultrathin semiconductor metafilms with designer absorption spectra. We show how such metafilms can be constructed by placing one or more types of high-index semiconductor antennas into a dense array with subwavelength spacings. It is argued that the large absorption cross-section of semiconductor antennas and their weak near-field coupling open a unique opportunity to create strongly absorbing metafilms whose spectral absorption properties directly reflect those of the individual antennas. Using experiments and simulations, we demonstrate that near-unity absorption at one or more target wavelengths of interest can be achieved in a sub-50-nm-thick metafilm using judiciously sized and spaced Ge nanobeams. The ability to create semiconductor metafilms with custom absorption spectra opens up new design strategies for planar optoelectronic devices and solar cells. PMID:26184335

  3. Single-molecule imaging by optical absorption

    NASA Astrophysics Data System (ADS)

    Celebrano, Michele; Kukura, Philipp; Renn, Alois; Sandoghdar, Vahid

    2011-02-01

    To date, optical studies of single molecules at room temperature have relied on the use of materials with high fluorescence quantum yield combined with efficient spectral rejection of background light. To extend single-molecule studies to a much larger pallet of substances that absorb but do not fluoresce, scientists have explored the photothermal effect, interferometry, direct attenuation and stimulated emission. Indeed, very recently, three groups have succeeded in achieving single-molecule sensitivity in absorption. Here, we apply modulation-free transmission measurements known from absorption spectrometers to image single molecules under ambient conditions both in the emissive and strongly quenched states. We arrive at quantitative values for the absorption cross-section of single molecules at different wavelengths and thereby set the ground for single-molecule absorption spectroscopy. Our work has important implications for research ranging from absorption and infrared spectroscopy to sensing of unlabelled proteins at the single-molecule level.

  4. Absorption of carbonyl sulfide in aqueous methyldiethanolamine

    SciTech Connect

    Al-Ghawas, H.A.; Ruiz-Ibanez, G.; Sandall, O.C. )

    1988-01-01

    The absorption of carbonyl sulfide in aqueous methyldiethanolamine (MDEA) was studied over a range of temperatures and MDEA concentrations. MDEA is commonly used for selective absorption of hydrogen sulfide in the presence of carbon dioxide. However, sulfur in the form of COS may also be present and it is necessary that estimates of absorption rates of this compound be made. The objective of this study is to determine the physiochemical properties needed to predict COS absorption rates in aqueous MDEA. Free gas solubility and the diffusivity of COS in MDEA solutions were measured over the temperature range 15 to 40{sup 0}C for MDEA concentrations up to 30 weight per cent using the nitrous oxide analogy method. Solubilities were measured volumetrically in an equilibrium cell and diffusivities were measured using a laminar liquid jet absorber. The kinetics of the reaction between COS and MDEA were studied by measuring absorption rates in a single wetted-sphere absorber.

  5. Creating semiconductor metafilms with designer absorption spectra

    NASA Astrophysics Data System (ADS)

    Kim, Soo Jin; Fan, Pengyu; Kang, Ju-Hyung; Brongersma, Mark L.

    2015-07-01

    The optical properties of semiconductors are typically considered intrinsic and fixed. Here we leverage the rapid developments in the field of optical metamaterials to create ultrathin semiconductor metafilms with designer absorption spectra. We show how such metafilms can be constructed by placing one or more types of high-index semiconductor antennas into a dense array with subwavelength spacings. It is argued that the large absorption cross-section of semiconductor antennas and their weak near-field coupling open a unique opportunity to create strongly absorbing metafilms whose spectral absorption properties directly reflect those of the individual antennas. Using experiments and simulations, we demonstrate that near-unity absorption at one or more target wavelengths of interest can be achieved in a sub-50-nm-thick metafilm using judiciously sized and spaced Ge nanobeams. The ability to create semiconductor metafilms with custom absorption spectra opens up new design strategies for planar optoelectronic devices and solar cells.

  6. Creating semiconductor metafilms with designer absorption spectra.

    PubMed

    Kim, Soo Jin; Fan, Pengyu; Kang, Ju-Hyung; Brongersma, Mark L

    2015-01-01

    The optical properties of semiconductors are typically considered intrinsic and fixed. Here we leverage the rapid developments in the field of optical metamaterials to create ultrathin semiconductor metafilms with designer absorption spectra. We show how such metafilms can be constructed by placing one or more types of high-index semiconductor antennas into a dense array with subwavelength spacings. It is argued that the large absorption cross-section of semiconductor antennas and their weak near-field coupling open a unique opportunity to create strongly absorbing metafilms whose spectral absorption properties directly reflect those of the individual antennas. Using experiments and simulations, we demonstrate that near-unity absorption at one or more target wavelengths of interest can be achieved in a sub-50-nm-thick metafilm using judiciously sized and spaced Ge nanobeams. The ability to create semiconductor metafilms with custom absorption spectra opens up new design strategies for planar optoelectronic devices and solar cells. PMID:26184335

  7. Novel absorption detection techniques for capillary electrophoresis

    SciTech Connect

    Xue, Y.

    1994-07-27

    Capillary electrophoresis (CE) has emerged as one of the most versatile separation methods. However, efficient separation is not sufficient unless coupled to adequate detection. The narrow inner diameter (I.D.) of the capillary column raises a big challenge to detection methods. For UV-vis absorption detection, the concentration sensitivity is only at the {mu}M level. Most commercial CE instruments are equipped with incoherent UV-vis lamps. Low-brightness, instability and inefficient coupling of the light source with the capillary limit the further improvement of UV-vis absorption detection in CE. The goals of this research have been to show the utility of laser-based absorption detection. The approaches involve: on-column double-beam laser absorption detection and its application to the detection of small ions and proteins, and absorption detection with the bubble-shaped flow cell.

  8. Time-dependent oral absorption models

    NASA Technical Reports Server (NTRS)

    Higaki, K.; Yamashita, S.; Amidon, G. L.

    2001-01-01

    The plasma concentration-time profiles following oral administration of drugs are often irregular and cannot be interpreted easily with conventional models based on first- or zero-order absorption kinetics and lag time. Six new models were developed using a time-dependent absorption rate coefficient, ka(t), wherein the time dependency was varied to account for the dynamic processes such as changes in fluid absorption or secretion, in absorption surface area, and in motility with time, in the gastrointestinal tract. In the present study, the plasma concentration profiles of propranolol obtained in human subjects following oral dosing were analyzed using the newly derived models based on mass balance and compared with the conventional models. Nonlinear regression analysis indicated that the conventional compartment model including lag time (CLAG model) could not predict the rapid initial increase in plasma concentration after dosing and the predicted Cmax values were much lower than that observed. On the other hand, all models with the time-dependent absorption rate coefficient, ka(t), were superior to the CLAG model in predicting plasma concentration profiles. Based on Akaike's Information Criterion (AIC), the fluid absorption model without lag time (FA model) exhibited the best overall fit to the data. The two-phase model including lag time, TPLAG model was also found to be a good model judging from the values of sum of squares. This model also described the irregular profiles of plasma concentration with time and frequently predicted Cmax values satisfactorily. A comparison of the absorption rate profiles also suggested that the TPLAG model is better at prediction of irregular absorption kinetics than the FA model. In conclusion, the incorporation of a time-dependent absorption rate coefficient ka(t) allows the prediction of nonlinear absorption characteristics in a more reliable manner.

  9. Graphene oxide-TiO2 composite solid phase extraction combined with graphite furnace atomic absorption spectrometry for the speciation of inorganic selenium in water samples.

    PubMed

    Zhang, Yanan; Chen, Beibei; Wu, Shaowei; He, Man; Hu, Bin

    2016-07-01

    In this paper, a method of graphene oxide (GO)-TiO2 composite solid phase extraction followed by graphite furnace atomic absorption spectrometry (GFAAS) detection was proposed for the speciation of inorganic selenium in environmental waters. The adsorption behavior of inorganic Se(IV) and Se(VI) on the GO-TiO2(1:1) composite was investigated. It was found that Se(IV) was quantitatively retained on the GO-TiO2 composites within a wide pH range of 0.5-10, while Se(VI) was quantitatively adsorbed on GO-TiO2(1:1) composite at pH 0.5-2, and no obvious adsorption of Se(VI) within the pH range of 4-10 was found. By selecting pH 6.0, Se(IV) could be easily determined. After reduction of Se(VI), total Se was determined by the proposed method, and Se(VI) was calculated as the difference between the total Se and Se(IV). The factors affecting the separation/preconcentration of Se(IV) and Se(VI) were studied. Under the optimum conditions, the isothermal adsorption of Se(IV) on the GO-TiO2(1:1) composite fitted Langmuir model; a linear range over 0.1-12ngmL(-1) was obtained. The limit of detection (LOD) and precision of the method for Se(IV) was 0.04ngmL(-1) and 9.4% (cSe(IV)=0.5ngmL(-1), n=7), respectively. In order to verify the accuracy of the method, a standard water sample (GSBZ50031-94) was analyzed, and the determined value was in a good agreement to the certified value. The established method was applied to inorganic Se speciation in environmental water samples and the recovery of 87.4-102% was obtained for the spiked samples. PMID:27154702

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

    NASA Astrophysics Data System (ADS)

    Guinan, Edward

    2014-10-01

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

  11. Absorption chillers: Technology for the future

    SciTech Connect

    Garland, P.W.; Garland, R.W.

    1997-12-31

    In an era of heightened awareness of energy efficiency and the associated environmental impacts, many industries worldwide are exploring ``environmentally friendly`` technologies that provide equivalent or improved performance while reducing or eliminating harmful side-effects. The refrigeration and air-conditioning industry, due to its reliance on CFCs and HCFCs, has invested in research in alternatives to the industry standard vapor compression machines. One alternative technology with great promise is chemical absorption. Absorption chillers offer comparable refrigeration output with reduced SO{sub 2}, CO{sub 2}, and NO{sub x} emissions. Absorption chillers do not use CFCs or HCFCs, refrigerants that contribute to ozone depletion and global warming. Additionally, gas-fired absorption chillers can save significant amounts in energy costs when used in combination with a vapor compression chiller in a hybrid system. The hybrid system can take advantage of the comparatively low price of natural gas (per unit ton) and rely on the high performance of vapor compression when electricity prices are lower. The purpose of this article is to provide an introduction for those new to absorption technology as well as a discussion of selected high efficiency cycles, a discussion on the technology of coupling absorption with vapor compression systems to form a hybrid system, and the environmental impacts of absorption.

  12. On the statistics of quasar absorption lines

    NASA Astrophysics Data System (ADS)

    Zuiderwijk, E. J.

    1984-12-01

    The distribution of absorption lines in 13 quasar spectra is analyzed and shown to be fully consistent with the hypothesis of randomly, but not uniformly, distributed absorption features. The analysis by Libby et al. (1984), in which it is claimed that the number of wavelength coincidences among absorption lines in different quasar spectra (as measured in the rest frame of the quasars) is much larger than expected, implying absorbers in the quasars themselves, is totally invalid. Instead, the number of these coincidences is fully commensurate with the expected one on the assumption of randomness.

  13. Coherent Absorption of N00N States.

    PubMed

    Roger, Thomas; Restuccia, Sara; Lyons, Ashley; Giovannini, Daniel; Romero, Jacquiline; Jeffers, John; Padgett, Miles; Faccio, Daniele

    2016-07-01

    Recent results in deeply subwavelength thickness films demonstrate coherent control and logical gate operations with both classical and single-photon light sources. However, quantum processing and devices typically involve more than one photon and nontrivial input quantum states. Here we experimentally investigate two-photon N00N state coherent absorption in a multilayer graphene film. Depending on the N00N state input phase, it is possible to selectively choose between single- or two-photon absorption of the input state in the graphene film. These results demonstrate that coherent absorption in the quantum regime exhibits unique features, opening up applications in multiphoton spectroscopy and imaging. PMID:27447505

  14. Strong terahertz absorption using thin metamaterial structures

    SciTech Connect

    Alves, Fabio; Kearney, Brian; Grbovic, Dragoslav; Lavrik, Nickolay V; Karunasiri, Gamani

    2012-01-01

    Metamaterial absorbers with nearly 100% absorption in the terahertz (THz) spectral band have been designed and fabricated using a periodic array of aluminum (Al) squares and an Al ground plane separated by a thin silicon dioxide (SiO{sub 2}) dielectric film. The entire structure is less than 1.6 mm thick making it suitable for the fabrication of microbolometers or bi-material sensors for THz imaging. Films with different dielectric layer thicknesses exhibited resonant absorption at 4.1, 4.2, and 4.5 THz with strengths of 98%, 95%, and 88%, respectively. The measured absorption spectra are in good agreement with simulations using finite element modeling.

  15. Coherent perfect absorption in chiral metamaterials.

    PubMed

    Ye, Yuqian; Hay, Darrick; Shi, Zhimin

    2016-07-15

    We study the coherent perfect absorption (CPA) of a chiral structure and derive analytically the CPA condition for transversely isotropic chiral structures in circular polarization bases. The coherent absorption of such a chiral system is generally polarization dependent and can be tuned by the relative phase between the coherent input beams. To demonstrate our theoretical predictions, a chiral metamaterial absorber operating in the terahertz frequency range is optimized. We numerically demonstrate that a coherent absorption of 99.5% can be achieved. Moreover, we show that an optimized CPA chiral structure can be used as an interferometric control of polarization state of the output beams with constant output intensity. PMID:27420535

  16. Coherent Absorption of N00N States

    NASA Astrophysics Data System (ADS)

    Roger, Thomas; Restuccia, Sara; Lyons, Ashley; Giovannini, Daniel; Romero, Jacquiline; Jeffers, John; Padgett, Miles; Faccio, Daniele

    2016-07-01

    Recent results in deeply subwavelength thickness films demonstrate coherent control and logical gate operations with both classical and single-photon light sources. However, quantum processing and devices typically involve more than one photon and nontrivial input quantum states. Here we experimentally investigate two-photon N00N state coherent absorption in a multilayer graphene film. Depending on the N00N state input phase, it is possible to selectively choose between single- or two-photon absorption of the input state in the graphene film. These results demonstrate that coherent absorption in the quantum regime exhibits unique features, opening up applications in multiphoton spectroscopy and imaging.

  17. Total absorption by degenerate critical coupling

    SciTech Connect

    Piper, Jessica R. Liu, Victor; Fan, Shanhui

    2014-06-23

    We consider a mirror-symmetric resonator with two ports. We show that, when excited from a single port, complete absorption can be achieved through critical coupling to degenerate resonances with opposite symmetry. Moreover, any time two resonances with opposite symmetry are degenerate in frequency and absorption is always significantly enhanced. In contrast, when two resonances with the same symmetry are nearly degenerate, there is no absorption enhancement. We numerically demonstrate these effects using a graphene monolayer on top of a photonic crystal slab, illuminated from a single side in the near-infrared.

  18. Selective coherent perfect absorption in metamaterials

    SciTech Connect

    Nie, Guangyu; Shi, Quanchao; Zhu, Zheng; Shi, Jinhui

    2014-11-17

    We show multi-band coherent perfect absorption (CPA) in simple bilayered asymmetrically split ring metamaterials. The selectivity of absorption can be accomplished by separately excited electric and magnetic modes in a standing wave formed by two coherent counterpropagating beams. In particular, each CPA can be completely switched on/off by the phase of a second coherent wave. We propose a practical scheme for realizing multi-band coherent perfect absorption of 100% that is allowed to work from microwave to optical frequency.

  19. NHEXAS PHASE I REGION 5 STUDY--STANDARD OPERATING PROCEDURE--ANALYSIS OF TEFLON FILTERS USED IN PERSONAL AIR MONITORING SAMPLERS FOR LEAD, ARSENIC, CADMIUM, AND CHROMIUM (RTI/ACS-AP-209-111)

    EPA Science Inventory

    This protocol provides guidelines for the analysis of Teflon filter samples for toxic metals, either by graphite furnace atomic absorption spectrometry (GFAAS) or by hydride generation atomic fluorescence spectrometry (HGAFS). This method involves the extraction of analytes from ...

  20. Performance Analysis of Solution Transportation Absorption Chiller

    NASA Astrophysics Data System (ADS)

    Kiani, Behdad; Hamamoto, Yoshinori; Akisawa, Atsushi; Kashiwagi, Takao

    Thermally activated advanced absorption cycles are considered promising candidates to replace CFCs, HCFCs and HFCs for residential and commercial applications. In such absorption systems, it is desirable to utilize the waste heat from industries for heating and cooling applications in commercial and residential sectors. For this purpose, it is necessary to transport energy over some distance because the waste heat source and demand are generally located apart from each other. Transportation of steam, hot water or chilled water requires high construction costs for insulation. There is an efficient method of energy transportation using absorption system called “ Solution Transportation Absorption System (STA)”. The solution is transported at an ambient temperature so that tube-insulations not required. This paper shows the simulation of the abovementioned system and the optimal result, using mathematical optimization. The optimum system with industry‧s waste heat utilization is obtained. At the end, the effect on the pollution emission and energy conservation is obtained.

  1. Triple-effect absorption chiller cycles

    SciTech Connect

    DeVault, R.C.; Grossman, G.

    1992-06-01

    Gas-fired absorption chillers are widely used for air-conditioning buildings. Even the highest efficiency double-effect absorption chillers used more primary energy for air-conditioning buildings than the better electric chillers. Two different triple-effect absorption chiller cycles are capable of substantial performance improvement over equivalent double-effect cycles. One cycle uses two condensers and two absorbers to achieve the ``triple effect.`` A second cycle, the Double-Condenser Coupled Triple-Effect, uses three condensers as well as a third condenser subcooler (which exchanges heat with the lowest temperature first-effect generator). These triple-effect absorption cycles have the potential to be as energy efficient (on a primary fuel basis) as the best electric chillers. 19 refs.

  2. Triple-effect absorption chiller cycles

    SciTech Connect

    DeVault, R.C. ); Grossman, G. )

    1992-01-01

    Gas-fired absorption chillers are widely used for air-conditioning buildings. Even the highest efficiency double-effect absorption chillers used more primary energy for air-conditioning buildings than the better electric chillers. Two different triple-effect absorption chiller cycles are capable of substantial performance improvement over equivalent double-effect cycles. One cycle uses two condensers and two absorbers to achieve the triple effect.'' A second cycle, the Double-Condenser Coupled Triple-Effect, uses three condensers as well as a third condenser subcooler (which exchanges heat with the lowest temperature first-effect generator). These triple-effect absorption cycles have the potential to be as energy efficient (on a primary fuel basis) as the best electric chillers. 19 refs.

  3. Absorption chillers: Part of the solution

    SciTech Connect

    Occhionero, A.J. ); Hughes, P.J. ); Reid, E.A. )

    1991-01-01

    Acid rain, ozone depletion, global warming, and implementation economics are considered as they relate to the advisability of expanding the application of absorption chillers. Introductory and background information are provided to put the discussion in the proper context. Then all four issues are discussed separately as they relate to absorption chillers. Acid rain and ozone depletion concerns, and implementation economics, are found to support the expanded use of absorption chillers. The global warming concern is found to be more of a gray area, but the areas of benefit correspond well with the conditions of greatest economic advantage. All things considered, absorption chillers are believed to be part of the environmental and economic solution. It is further believed that integrated resource planning (IRP) processes that consider electric and gas technologies on an equal footing would come to the same conclusion for many regions of the United States. 9 refs., 3 tabs.

  4. Narrow Absorption Components in Be Star Winds

    NASA Technical Reports Server (NTRS)

    Grady, C. A.

    1985-01-01

    The stars omega Ori (B2 IIIe), 66 Oph (B2 IVe), and 59 Cyg (B1.5 IVe) are discussed. The extent to which the narrow absorption components in these Be stars differs from narrow components in the O stars and gamma Cas is explored. Any models or mechanisms for the formation of narrow absorption features in the UV resonance lines of Be star spectra must account for the presence of multiple narrow absorption features which are variable in number, radial velocity, and strength. Models predicting a high and low density structure to the stellar wind caused by instabilities in a flow driven by radiation pressure or by variable mass loss may be more successful in describing the behavior of winds in early Be stars. These models appear to be capable of producing single absorption components in the velocity range observed for O stars and very early Be stars.

  5. Electromagnetically induced absorption via incoherent collisions

    SciTech Connect

    Yang Xihua; Sheng Jiteng; Xiao Min

    2011-10-15

    We conduct theoretical studies on electromagnetically induced absorption via incoherent collisions in an inhomogeneously broadened ladder-type three-level system with the density-matrix approach. The effects of the collision-induced coherence decay rates as well as the probe laser field intensity on the probe field absorption are examined. It is shown that with the increase of the collisional decay rates in a moderate range, a narrow dip due to electromagnetically induced transparency superimposed on the Doppler-broadened absorption background can be turned into a narrow peak under the conditions that the probe field intensity is not very weak as compared to the pump field, which results from the enhancement of constructive interference and suppression of destructive interference between one-photon and multiphoton transition pathways. The physical origin of the collision-assisted electromagnetically induced absorption is analyzed with a power-series solution of the density-matrix equations.

  6. Induced Transparency and Absorption in Coupled Microresonators

    NASA Technical Reports Server (NTRS)

    Smith, David D.; Chang, Hongrok

    2004-01-01

    We review the conditions for the occurrence of coherence phenomena in passive coupled optical microresonators. We derive the effective steady-state response and determine conditions for induced transparency and absorption in these systems.

  7. Absorption enhancement in graphene photonic crystal structures.

    PubMed

    Khaleque, Abdul; Hattori, Haroldo T

    2016-04-10

    Graphene, a single layer of carbon atoms arranged in a honeycomb lattice, is attracting significant interest because of its potential applications in electronic and optoelectronic devices. Although graphene exhibits almost uniform absorption within a large wavelength range, its interaction with light is weak. In this paper, the enhancement of the optical absorption in graphene photonic crystal structures is studied: the structure is modified by introducing scatterers and mirrors. It is shown that the absorption of the graphene photonic crystal structure can be enhanced about four times (nearly 40%) with respect to initial reference absorption of 9.8%. The study can be a useful tool for investigating graphene physics in different optical settings. PMID:27139857

  8. Absorption cross section of canonical acoustic holes

    SciTech Connect

    Crispino, Luis C. B.; Oliveira, Ednilton S.; Matsas, George E. A.

    2007-11-15

    We compute numerically the absorption cross section of a canonical acoustic hole for sound waves with arbitrary frequencies. Our outputs are in full agreement with the expected low- and high-frequency limits.

  9. Impedance Characteristics of the Plasma Absorption Probe

    NASA Astrophysics Data System (ADS)

    Yamazawa, Yohei

    2009-10-01

    The plasma absorption probe (PAP) is a diagnostics for determination of spatially resolved electron density.footnotetextH. Kokura, et al., Jpn. J. Appl. Phys. 38 5262 (1999). PAP has attracted considerable interest because of its applicability in a reactive plasma. The simple structure of the probe allows us a robust measurement while the mechanism of the absorption is complicated and there are still some uncertainty.footnotetextM. Lapke, et al., Appl. Phys. Lett. 90, 121502 (2007) In this study, we focus on the frequency characteristics of the impedance instead of the absorption spectrum. An electromagnetic field simulation reveals that there is only one parallel resonance in the impedance characteristics even in a case there are many peaks in absorption spectrum. Thus, the impedance characteristics provide a clue to understanding the mechanism.

  10. Multiphoton absorption in amyloid protein fibres

    NASA Astrophysics Data System (ADS)

    Hanczyc, Piotr; Samoc, Marek; Norden, Bengt

    2013-12-01

    Fibrillization of peptides leads to the formation of amyloid fibres, which, when in large aggregates, are responsible for diseases such as Alzheimer's and Parkinson's. Here, we show that amyloids have strong nonlinear optical absorption, which is not present in native non-fibrillized protein. Z-scan and pump-probe experiments indicate that insulin and lysozyme β-amyloids, as well as α-synuclein fibres, exhibit either two-photon, three-photon or higher multiphoton absorption processes, depending on the wavelength of light. We propose that the enhanced multiphoton absorption is due to a cooperative mechanism involving through-space dipolar coupling between excited states of aromatic amino acids densely packed in the fibrous structures. This finding will provide the opportunity to develop nonlinear optical techniques to detect and study amyloid structures and also suggests that new protein-based materials with sizable multiphoton absorption could be designed for specific applications in nanotechnology, photonics and optoelectronics.

  11. Absorption refrigeration machine driven by solar heat

    NASA Astrophysics Data System (ADS)

    Keizer, C.; Liem, S. H.

    1980-04-01

    A mathematical model of a single and a two stage solar absorption refrigeration system is developed in which data of collectors and weather data can be implicated. The influence of the generator, the absorber efficiencies, and the cooling temperature on the coefficient of performance (COP) of a single and two stage absorption refrigeration process are investigated. For low generator temperatures the absorber efficiency has more influence on COP than the generator efficiency. Only spectral selective double window and high performance collectors can be used for air cooled solar absorption refrigeration systems at an evaporator temperature of -5 C. It is concluded that a water cooled solar absorption refrigeration system in combination with a solar tapwater installation for household use can be achieved with 6 to 8 square meters high performance collector area.

  12. Seasonal Solar Thermal Absorption Energy Storage Development.

    PubMed

    Daguenet-Frick, Xavier; Gantenbein, Paul; Rommel, Mathias; Fumey, Benjamin; Weber, Robert; Gooneseker, Kanishka; Williamson, Tommy

    2015-01-01

    This article describes a thermochemical seasonal storage with emphasis on the development of a reaction zone for an absorption/desorption unit. The heat and mass exchanges are modelled and the design of a suitable reaction zone is explained. A tube bundle concept is retained for the heat and mass exchangers and the units are manufactured and commissioned. Furthermore, experimental results of both absorption and desorption processes are presented and the exchanged power is compared to the results of the simulations. PMID:26842331

  13. Percutaneous absorption in diseased skin: an overview.

    PubMed

    Chiang, Audris; Tudela, Emilie; Maibach, Howard I

    2012-08-01

    The stratum corneum's (SC) functions include protection from external hazardous environments, prevention of water loss and regulation of body temperature. While intact skin absorption studies are abundant, studies on compromised skin permeability are less common, although products are often used to treat affected skin. We reviewed literature on percutaneous absorption through abnormal skin models. Tape stripping is used to disrupt water barrier function. Studies demonstrated that physicochemical properties influence the stripping effect: water-soluble drugs are more affected. Abrasion did not affect absorption as much. Freezing is commonly used to preserve skin. It does not seem to modify water absorption, but still increases the penetration of compounds. Comparatively, heating the skin consistently increased percutaneous absorption. Removing SC lipids may increase percutaneous absorption of drugs. Many organic solvents are employed to delipidize. Delipidization with chloroform-methanol increased hydrophilic compound permeability, but not lipophilic. Acetone pre-treatment enhanced hydrophilic compound penetration. More data is needed to determine influence on highly lipophilic compound penetration. Sodium lauryl sulfate (SLS) induces irritant dermatitis and is frequently used as a model. Studies revealed that SLS increases hydrophilic compound absorption, but not lipophilic. However, skin irritation with other chemicals increases lipophilic penetration as much as hydrophilic. Animal studies show that UV exposure increases percutaneous absorption whereas human studies do not. Human studies show increased penetration in psoriatic and atopic dermatitis skin. The data summarized here begin to characterize flux alteration associated with damaged skin. Understanding the degree of alteration requires interpretation of involved conditions and the enlarging of our database to a more complete physicochemical spectrum. PMID:22912973

  14. Ultraviolet absorption cross sections of hydrogen peroxide

    NASA Technical Reports Server (NTRS)

    Lin, C. L.; Rohatgi, N. K.; Demore, W. B.

    1978-01-01

    Absorption cross-sections of hydrogen peroxide vapor and of neutral aqueous solutions of hydrogen peroxide were measured in the wavelength range from 195 to 350 nm at 296 K. The spectrophotometric procedure is described, and the reported cross-sections are compared with values obtained by other researchers. Photodissociation coefficients of atmospheric H2O2 were calculated for direct absorption of unscattered solar radiation, and the vertical distributions of these coefficients are shown for various solar zenith angles.

  15. The economics of solar powered absorption cooling

    NASA Technical Reports Server (NTRS)

    Bartlett, J. C.

    1978-01-01

    Analytic procedure evaluates cost of combining absorption-cycle chiller with solar-energy system in residential or commercial application. Procedure assumes that solar-energy system already exists to heat building and that cooling system must be added. Decision is whether to cool building with conventional vapor-compression-cycle chiller or to use solar-energy system to provide heat input to absorption chiller.

  16. Geometric absorption of electromagnetic angular momentum

    NASA Astrophysics Data System (ADS)

    Konz, C.; Benford, Gregory

    2003-10-01

    Circularly polarized electromagnetic fields carry both energy and angular momentum. We investigate the conditions under which a circularly polarized wave field transfers angular momentum to a perfectly conducting macroscopic object, using exact electromagnetic wave theory in a steady-state calculation. We find that axisymmetric perfect conductors cannot absorb or radiate angular momentum when illuminated. However, any asymmetry allows absorption. A rigorous, steady-state solution of the boundary value problem for the reflection from a perfectly conducting infinite wedge shows that waves convey angular momentum at the edges of asymmetries. Conductors can also radiate angular momentum, so their geometric absorption coefficient for angular momentum can be negative. Such absorption or radiation depends solely on the specific geometry of the conductor. The geometric absorption coefficient can be as high as 0.8, and the coefficient for radiation can be -0.4, larger than typical material absorption coefficients. We apply the results to recent experiments which spun roof-shaped aluminum sheets with polarized microwave beams. Applications of geometric, instead of material, absorption can be quite varied. Though experiments testing these ideas will be simpler at microwavelengths, the ideas work for optical ones as well.

  17. High temperature measurement of water vapor absorption

    NASA Technical Reports Server (NTRS)

    Keefer, Dennis; Lewis, J. W. L.; Eskridge, Richard

    1985-01-01

    An investigation was undertaken to measure the absorption coefficient, at a wavelength of 10.6 microns, for mixtures of water vapor and a diluent gas at high temperature and pressure. The experimental concept was to create the desired conditions of temperature and pressure in a laser absorption wave, similar to that which would be created in a laser propulsion system. A simplified numerical model was developed to predict the characteristics of the absorption wave and to estimate the laser intensity threshold for initiation. A non-intrusive method for temperature measurement utilizing optical laser-beam deflection (OLD) and optical spark breakdown produced by an excimer laser, was thoroughly investigated and found suitable for the non-equilibrium conditions expected in the wave. Experiments were performed to verify the temperature measurement technique, to screen possible materials for surface initiation of the laser absorption wave and to attempt to initiate an absorption wave using the 1.5 kW carbon dioxide laser. The OLD technique was proven for air and for argon, but spark breakdown could not be produced in helium. It was not possible to initiate a laser absorption wave in mixtures of water and helium or water and argon using the 1.5 kW laser, a result which was consistent with the model prediction.

  18. Lyman-α Absorption from Heliotail ENAs

    NASA Astrophysics Data System (ADS)

    Wood, Brian E.; Izmodenov, Vladislav V.

    2010-12-01

    The energetic neutral atoms (ENAs) that the Interstellar Boundary Explorer (IBEX) is currently studying are messengers from the termination shock and beyond. Ultraviolet spectra from the Hubble Space Telescope (HST) provide another way to study these ENAs, which are capable of producing detectable absorption signatures in HST Lyman-α spectra of nearby stars. This broad, shallow absorption is only observed within 20° of the downwind direction. Only the lengthy downwind lines of sight through the long heliotail build up enough column density of ENAs to yield detectable absorption. The absorption therefore represents the first real observational detection of the heliotail. We try to connect ENA fluxes observed by IBEX with the Lyman-α absorption observed by HST. In the downwind direction, IBEX observes ENA fluxes that increase towards lower energies, at least to 0.2 keV, but consistency with the HST measurements seems to require that the ENA fluxes at least flatten if not decrease below 0.2 keV. The ``ribbon'' of ENAs detected by IBEX is not detected in Lyman-α absorption, which may be a problem for any explanation of the ribbon that proposes a source beyond our heliosphere.

  19. Spectral Absorption Properties of Atmospheric Aerosols

    NASA Technical Reports Server (NTRS)

    Bergstrom, R. W.; Pilewskie, P.; Russell, P. B.; Redemann, J.; Bond, T. C.; Quinn, P. K.; Sierau, B.

    2007-01-01

    We have determined the solar spectral absorption optical depth of atmospheric aerosols for specific case studies during several field programs (three cases have been reported previously; two are new results). We combined airborne measurements of the solar net radiant flux density and the aerosol optical depth with a detailed radiative transfer model for all but one of the cases. The field programs (SAFARI 2000, ACE Asia, PRIDE, TARFOX, INTEX-A) contained aerosols representing the major absorbing aerosol types: pollution, biomass burning, desert dust and mixtures. In all cases the spectral absorption optical depth decreases with wavelength and can be approximated with a power-law wavelength dependence (Absorption Angstrom Exponent or AAE). We compare our results with other recent spectral absorption measurements and attempt to briefly summarize the state of knowledge of aerosol absorption spectra in the atmosphere. We discuss the limitations in using the AAE for calculating the solar absorption. We also discuss the resulting spectral single scattering albedo for these cases.

  20. Co-precipitation of Ni, Cr, Mn, Pb and Zn in industrial wastewater and sediment samples with copper(II) cyclo-hexylmethyldithiocarbamate for their flame atomic absorption spectrometric determination.

    PubMed

    Ipeaiyeda, Ayodele Rotimi; Odola, Adekunle Johnson

    2012-01-01

    A co-precipitation technique for nickel(II), chromium(II), manganese(II), lead(II) and zinc(II) with the aid of copper(II) cyclo-hexylmethyldithiocarbamate was established. The influences of some analytical parameters such as pH, sample volume, amounts of cyclo-hexylmethyldithiocarbamate and copper(II) on the recovery of metal ions were investigated. The heavy metals in the precipitate were determined by flame atomic absorption spectrophotometry. The range of detection limits for the heavy metals was 0.003-0.005 mg/L. The atomic spectrometric technique with co-precipitation procedure was successfully applied for the determination of Ni, Cr, Mn, Pb and Zn in industrial wastewater and sediment samples from Ladipo stream in Lagos, Nigeria. The mean concentrations for these metals using co-precipitation procedure were not significantly different from corresponding concentrations obtained using spectrometric techniques without co-precipitation procedure. PMID:22678206

  1. Resonant absorption and not-so-resonant absorption in short, intense laser irradiated plasma

    SciTech Connect

    Ge, Z. Y.; Zhuo, H. B.; Ma, Y. Y.; Yang, X. H.; Yu, T. P.; Zou, D. B.; Yin, Y.; Shao, F. Q.; Yu, W.; Luan, S. X.; Zhou, C. T.; Institute of Applied Physics and Computational Mathematics, Beijing 100088 ; Peng, X. J.

    2013-07-15

    An analytical model for laser-plasma interaction during the oblique incidence by an ultrashort ultraintense p-polarized laser on a solid-density plasma is proposed. Both the resonant absorption and not-so-resonant absorption are self-consistently included. Different from the previous theoretical works, the physics of resonant absorption is found to be valid in more general conditions as the steepening of the electron density profile is considered. Even for a relativistic intensity laser, resonant absorption can still exist under certain plasma scale length. For shorter plasma scale length or higher laser intensity, the not-so-resonant absorption tends to be dominant, since the electron density is steepened to a critical level by the ponderomotive force. The laser energy absorption rates for both mechanisms are discussed in detail, and the difference and transition between these two mechanisms are presented.

  2. Kinetic study of the quenching reaction of singlet oxygen by seven rice bran extracts in ethanol solution. Development of a singlet oxygen absorption capacity (SOAC) assay method.

    PubMed

    Mukai, Kazuo; Ishikawa, Eri; Abe, Takumi; Ouchi, Aya; Nagaoka, Shin-Ichi; Murata, Kazumasa; Miyazawa, Teruo; Nakagawa, Kiyotaka

    2015-01-01

    Measurements of singlet oxygen ((1)O2) quenching rates (kQ (S)) and the relative singlet oxygen absorption capacity (SOAC) values were performed for seven rice bran extracts 1-7, which contained different concentrations of antioxidants (AOs) (such as α-, β-, γ-, and δ-tocopherols and -tocotrienols, three carotenoids (lutein, β-carotene, and zeaxanthin), and γ-oryzanol), in ethanol at 35 °C using UV-vis spectrophotometry. The concentrations of four tocopherols and four tocotrienols, three carotenoids, and γ-oryzanol contained in the extracts were determined using HPLC-MS/MS, UV-HPLC, and UV-vis absorption spectroscopy, respectively. Furthermore, comparisons of kQ (S) (Obsd.) values observed for the above extracts 1-7 with the sum of the product {[Formula: see text] [AO-i]} of the [Formula: see text] values obtained for each AO-i and the concentration ([AO-i]) of AO-i contained in extracts 1-7 were performed. From the results, it has been ascertained that the SOAC method is applicable to general food extracts to evaluate their (1)O2-quenching activity. PMID:26222314

  3. Further advancement of differential optical absorption spectroscopy: theory of orthogonal optical absorption spectroscopy.

    PubMed

    Liudchik, Alexander M

    2014-08-10

    A modified version of the differential optical absorption spectroscopy (DOAS) method is presented. The technique is called orthogonal optical absorption spectroscopy (OOAS). A widespread variant of DOAS with smoothing of the registered spectrum and absorption cross sections being made employing a polynomial regression is a particular case of OOAS. The concept of OOAS provides a variety of new possibilities for constructing computational schemes and analyzing the influence of different error sources on calculated concentrations. PMID:25320931

  4. Water-related absorption in fibrous diamonds

    NASA Astrophysics Data System (ADS)

    Zedgenizov, D. A.; Shiryaev, A. A.; Kagi, H.; Navon, O.

    2003-04-01

    Cubic and coated diamonds from several localities (Brasil, Canada, Yakutia) were investigated using spectroscopic techniques. Special emphasis was put on investigation of water-related features of transmission Infra-red and Raman spectra. Presence of molecular water is inferred from broad absorption bands in IR at 3420 and 1640 cm-1. These bands were observed in many of the investigated samples. It is likely that molecular water is present in microinclusions in liquid state, since no clear indications of solid H_2O (ice VI-VII, Kagi et al., 2000) were found. Comparison of absorption by HOH and OH vibrations shows that diamonds can be separated into two principal groups: those containing liquid water (direct proportionality of OH and HOH absorption) and those with stronger absorption by OH group. Fraction of diamonds in every group depends on their provenance. There might be positive correlation between internal pressure in microinclusions (determined using quartz barometer, Navon et al., 1988) and affiliation with diamonds containing liquid water. In many cases absorption by HOH vibration is considerably lower than absorption by hydroxyl (OH) group. This may be explained if OH groups are partially present in mineral and/or melt inclusions. This hypothesis is supported by following fact: in diamonds with strong absorption by silicates and other minerals shape and position of the OH band differs from that in diamonds with low absorption by minerals. Moreover, in Raman spectra of individual inclusions sometimes the broad band at 3100 cm-1 is observed. This band is OH-related. In some samples water distribution is not homogeneous. Central part of the diamond usually contains more water than outer parts, but this is not a general rule for all the samples. Water absorption usually correlated with absorption of other components (carbonates, silicates and others). At that fibrous diamonds with relatively high content of silicates are characterized by molecular water. OH

  5. Optical absorption components of light-modulated absorption spectrum of CdS

    NASA Technical Reports Server (NTRS)

    Conway, E. J.; Long, E. R.

    1975-01-01

    The amplitude and decay coefficient of light-induced modulation of absorption (LIMA) was measured as a function of wavelength from 535 to 850 nm for single-crystal CdS. The decay coefficient exhibited a discontinuous resonance at 710 nm which was due to the overlap and cancellation of two opposing absorption changes. A method was developed to separate these opposing absorption changes using the measured decay coefficients. The discrete-level-to-band energy for one absorption change was found to be 1.64 eV. An improved model was developed which contains two associated levels in the band gap separated by 0.32 eV.

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

    SciTech Connect

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

    2010-10-15

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

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

    NASA Astrophysics Data System (ADS)

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

    2010-10-01

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

  8. Synoptic Spectrophotometry Enabled by SMARTS

    NASA Astrophysics Data System (ADS)

    Walter, Frederick M.

    2011-05-01

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

  9. Multichannel spectrophotometry of stellar flares

    NASA Technical Reports Server (NTRS)

    Mochnacki, S. W.; Zirin, H.

    1980-01-01

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

  10. Fast spectrophotometry with compressive sensing

    NASA Astrophysics Data System (ADS)

    Starling, David; Storer, Ian

    2015-03-01

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

  11. Photoelectric spectrophotometry of radio galaxies

    NASA Technical Reports Server (NTRS)

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

    1978-01-01

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

  12. Submillimeter spectrophotometry in the Pamirs

    NASA Astrophysics Data System (ADS)

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

    1989-07-01

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

  13. Absorption and emission of silicon nanocrystals embedded in SiC: Eliminating Fabry-Pérot interference

    SciTech Connect

    Schnabel, M.; Summonte, C.; Canino, M.; Dyakov, S. A.; López-Conesa, L.; Löper, P.; Janz, S.; Wilshaw, P. R.

    2015-01-28

    Silicon nanocrystals embedded in SiC are studied by spectrophotometry and photoluminescence (PL) spectroscopy. Absorptivities are found to be affected by residual Fabry-Pérot interference arising from measurements of reflection and transmission at locations of different film thickness. Multiple computational and experimental methods to avoid these errors in thin film measurements, in general, are discussed. Corrected absorptivity depends on the quantity of Si embedded in the SiC but is independent of the Si crystallinity, indicating a relaxation of the k-conservation criterion for optical transitions in the nanocrystals. Tauc gaps of 1.8–2.0 and 2.12 eV are determined for Si nanoclusters and SiC, respectively. PL spectra exhibit a red-shift of ∼100 nm per nm nominal Si nanocluster diameter, which is in agreement with quantum confinement but revealed to be an artifact entirely due to Fabry-Pérot interference. Several simple experimental methods to diagnose or avoid interference in PL measurements are developed that are applicable to all thin films. Corrected PL is rather weak and invariant with passivation, indicating that non-paramagnetic defects are responsible for rapid non-radiative recombination. They are also responsible for the broad, sub-gap PL of the SiC, and can wholly account for the form of the PL of samples with Si nanoclusters. The PL intensity of samples with Si nanoclusters, however, can only be explained with an increased density of luminescent defects in the SiC due to Si nanoclusters, efficient tunneling of photogenerated carriers from Si nanoclusters to SiC defects, or with emission from a-Si nanoclusters. Films prepared on Si exhibit much weaker PL than the same films prepared on quartz substrates.

  14. The ALFALFA HI Absorption Pilot Project

    NASA Astrophysics Data System (ADS)

    Macdonald, Erin; Darling, J.; ALFALFA Team

    2009-01-01

    We present the results of a pilot project to search for HI 21 cm absorption in the Arecibo Legacy Fast Arecibo L-Band Feed Array (ALFALFA) Survey. This project is the first to conduct a "blind" wide-area search for HI absorption in the local universe. The search covered 517.0 deg2 spanning 10.9h < α < 14.95h and +7.7o < δ < +16.3o. The ALFALFA survey covers -650 km s-1 < cz < 17,500 km s-1, for a Δz = 0.054 along each line of sight (11% of the cz span is lost to radio frequency interference and Galactic HI emission). There are 243 sources toward which all damped Lyα systems (N(HI) > 2x1020 cm-2) could be detected, and 3282 sources toward which N(HI) > 2x1021 cm-2 columns could be detected (assuming 100 K spin temperature, 30 km s-1 line width, and unity filling factor). We performed Green Bank Telescope follow-up observations of 13 possible absorption lines and the 250 strong sources (> 220 mJy) in our survey region. One previously known intrinsic HI absorption line in UGC 6081 was re-detected, but no additional lines were identified in the survey region. Nevertheless, this pilot project demonstrates the value and feasibility of large-area absorption line searches commensal with emission line surveys. An absorption line search of the entire 7000 deg2 ALFALFA Survey is a worthwhile undertaking, not only to identify HI absorption systems in the local universe, but to measure the fraction of HI gas not accounted for by emission line surveys. ALFALFA is a legacy survey at the Arecibo Observatory supported by NAIC and NSF.

  15. Inversion of instantaneous equivalent absorption coefficient and its application

    SciTech Connect

    Weihua, W. )

    1992-01-01

    Absorption coefficient is an important parameter for reservoir description. The major troubles in extracting absorption coefficient from seismic data are amplitude and waveform distortions; they greatly restrict the inversion which is based on reflection amplitude variation or reflection frequency variation. This paper presents a new method which avoids amplitude and uses waveform variation gradient in wave propagation to make the inversion of absorption coefficient. Apparent absorption coefficient and pseudo absorption coefficient are adopted so as to remove the influence which the waveform distortion due to thin bed tuning brings to absorption coefficient extraction. The final instantaneous equivalent absorption coefficient, a true absorption coefficient which reflects real absorptive character of a seismic medium, can be obtained by subtracting the pseudo absorption coefficient (inversely calculated using maximum entropy) from the apparent absorption coefficient the authors have calculated.

  16. UV laser long-path absorption spectroscopy

    NASA Technical Reports Server (NTRS)

    Dorn, Hans-Peter; Brauers, Theo; Neuroth, Rudolf

    1994-01-01

    Long path Differential Optical Absorption Spectroscopy (DOAS) using a picosecond UV laser as a light source was developed in our institute. Tropospheric OH radicals are measured by their rotational absorption lines around 308 nm. The spectra are obtained using a high resolution spectrograph. The detection system has been improved over the formerly used optomechanical scanning device by application of a photodiode array which increased the observed spectral range by a factor of 6 and which utilizes the light much more effectively leading to a considerable reduction of the measurement time. This technique provides direct measurements of OH because the signal is given by the product of the absorption coefficient and the OH concentration along the light path according to Lambert-Beers law. No calibration is needed. Since the integrated absorption coefficient is well known the accuracy of the measurement essentially depends on the extent to which the OH absorption pattern can be detected in the spectra. No interference by self generated OH radicals in the detection lightpath has been observed. The large bandwidth (greater than 0.15 nm) and the high spectral resolution (1.5 pm) allows absolute determination of interferences by other trace gas absorptions. The measurement error is directly accessible from the absorption-signal to baseline-noise ratio in the spectra. The applicability of the method strongly depends on visibility. Elevated concentrations of aerosols lead to considerable attenuation of the laser light which reduces the S/N-ratio. In the moderately polluted air of Julich, where we performed a number of OH measurement spectra. In addition absorption features of unidentified species were frequently detected. A quantitative deconvolution even of the known species is not easy to achieve and can leave residual structures in the spectra. Thus interferences usually increase the noise and deteriorate the OH detection sensitivity. Using diode arrays for sensitive

  17. Simulating a 4-effect absorption chiller

    SciTech Connect

    Grossman, G.; Zaltash, A.; Adcock, P.W.; DeVault, R.C.

    1995-06-01

    Absorption chillers are heat-operated refrigeration machines that operate on one of the earliest known principles of refrigeration. Current absorption chillers typically use either steam or a gas-fired burner as the energy source. All current gas-fired absorption cooling systems are based on the well known single-effect or double-effect cycles. To further improve utilization of the high temperature heat available from natural gas, a variety of triple-effect cycles have been proposed and are being developed that are capable of substantial performance improvement over equivalent double-effect cycles. This article describes a study that investigated the possibility of even further improving utilization of the high temperature heat available from natural gas combustion. During the study, performance simulation was conducted for a 4-effect lithium bromide/water cycle. From an environmental perspective, absorption chillers provide several benefits. They use absorption pairs (such as lithium bromide/water) as the working fluids, rather than chlorofluorocarbons or hydrochlorofluorocarbons, which contribute to ozone depletion and global warming.

  18. Zinc absorption in inflammatory bowel disease

    SciTech Connect

    Valberg, L.S.; Flanagan, P.R.; Kertesz, A.; Bondy, D.C.

    1986-07-01

    Zinc absorption was measured in 29 patients with inflammatory bowel disease and a wide spectrum of disease activity to determine its relationship to disease activity, general nutritional state, and zinc status. Patients with severe disease requiring either supplementary oral or parenteral nutrition were excluded. The mean 65ZnCl2 absorption, in the patients, determined using a 65Zn and 51Cr stool-counting test, 45 +/- 17% (SD), was significantly lower than the values, 54 +/- 16%, in 30 healthy controls, P less than 0.05. Low 65ZnCl2 absorption was related to undernutrition, but not to disease activity in the absence of undernutrition or to zinc status estimated by leukocyte zinc measurements. Mean plasma zinc or leukocyte zinc concentrations in patients did not differ significantly from controls, and only two patients with moderate disease had leukocyte zinc values below the 5th percentile of normal. In another group of nine patients with inflammatory bowel disease of mild-to-moderate severity and minimal nutritional impairment, 65Zn absorption from an extrinsically labeled turkey test meal was 31 +/- 10% compared to 33 +/- 7% in 17 healthy controls, P greater than 0.1. Thus, impairment in 65ZnCl2 absorption in the patients selected for this study was only evident in undernourished persons with moderate or severe disease activity, but biochemical evidence of zinc deficiency was uncommon, and clinical features of zinc depletion were not encountered.

  19. Absorption effects in diffusing wave spectroscopy.

    PubMed

    Sarmiento-Gomez, Erick; Morales-Cruzado, Beatriz; Castillo, Rolando

    2014-07-20

    The effect of absorption in diffusing wave spectroscopy (DWS) was studied using an absorption-dependent diffusive equation for describing the light propagation within a turbid liquid where dielectric microspheres have been embedded. Here, we propose an expression for the time-averaged light intensity autocorrelation function that correctly describes the time fluctuations for the scattered light, in the regime where the diffusion approximation accurately describes the light propagation. This correction was suspected previously, but it was not formally derived from a light diffusive equation. As in the case of no absorption, we obtained that time fluctuations of the scattered light can be related to the mean square displacement of the embedded particles. However, if a correction for absorption is not taken into account, the colloidal dynamics can be misinterpreted. Experimental results show that this new formulation correctly describes the time fluctuations of scattered light. This new procedure extends the applicability of DWS, and it opens the possibility of doing microrheology with this optical method in systems where absorption cannot be avoided. PMID:25090203

  20. Methane overtone absorption by intracavity laser spectroscopy

    NASA Technical Reports Server (NTRS)

    Obrien, James J.

    1990-01-01

    Interpretation of planetary methane (CH4) visible-near IR spectra, used to develop models of planetary atmospheres, has been hampered by a lack of suitable laboratory spectroscopic data. The particular CH4 spectral bands are due to intrinsically weak, high overtone-combination transitions too complex for classical spectroscopic analysis. The traditional multipass cell approach to measuring spectra of weakly absorbing species is insufficiently sensitive to yield reliable results for some of the weakest CH4 absorption features and is difficult to apply at the temperatures of the planetary environments. A time modulated form of intracavity laser spectroscopy (ILS), has been shown to provide effective absorption pathlengths of 100 to 200 km with sample cells less than 1 m long. The optical physics governing this technique and the experimental parameters important for obtaining reliable, quantitative results are now well understood. Quantitative data for CH4 absorption obtained by ILS have been reported recently. Illustrative ILS data for CH4 absorption in the 619.7 nm and 681.9 nm bands are presented. New ILS facilities at UM-St. Louis will be used to measure CH4 absorption in the 700 to 1000 nm region under conditions appropriate to the planetary atmospheres.