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1

Slavin, Walter, Glen R. Carnrick, and S. Roy Koirtyohann. "Background Correction in Atomic Absorption Spectroscopy (AAS)." Critical Reviews in Analytical Chemistry 19, no. 2 (1988): 95–134. http://dx.doi.org/10.1080/10408348808085619.

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2

Slavin, Walter, Glen R. Carnrick, and S. Roy Koirtyohann. "Background Correction in Atomic Absorption Spectroscopy (AAS)." C R C Critical Reviews in Analytical Chemistry 19, no. 2 (1988): 95–134. http://dx.doi.org/10.1080/10408348808542809.

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3

Duan, Yixiang, Mingyi Hou, Zhaohui Du, and Qinhan Jin. "Evaluation of the Performance of Microwave-Induced Plasma Atomic Absorption Spectrometry (MIP-AAS)." Applied Spectroscopy 47, no. 11 (1993): 1871–79. http://dx.doi.org/10.1366/0003702934066037.

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An innovative method of MIP-AAS has been developed. The sample solution was introduced by using an ultrasonic nebulizer. The desolvation was accomplished by a heating tube and a combination of a water-cooled condenser and a concentrated sulfuric acid desiccator. Both an L-shaped and a T-shaped plasma discharge tube were used as the absorption cell in the experiment. The experimental parameters were carefully examined and optimized for the elements studied. Some comparison of properties for these two different absorption tubes was made, and the analytical performance of MIP-AAS was evaluated. T
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4

B, Magaji. "Heavy Metal Analysis on Some Water Samples Using Atomic Absorption Spectroscopy." Food Science & Nutrition Technology 8, no. 4 (2023): 1–6. http://dx.doi.org/10.23880/fsnt-16000315.

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Drinking water is vital for life existence worldwide which is used on a daily basis. The quality of this drinking water however varies from one product to another. In this study, analysis of four heavy metals: Zn, Cu, Cd, and Pb were done by AAS technique in four water samples; Tap water, Well water, Faro bottle water and KSUSTA table water. The results of the study showed that Pb was not detected in the Tap, Well, and Faro Bottle water samples but was however detected in the KSUSTA Table water sample (0.954 mg/L) well above the limits of USEPA (0.015 mg/L), WHO (0.01 mg/L), and SON (0.01 mg/L
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5

Dawson, J. B., R. J. Duffield, P. R. King, M. Hajizadeh-Saffar, and G. W. Fisher. "Signal processing in electrothermal atomization atomic absorption spectroscopy (ETA-AAS)." Spectrochimica Acta Part B: Atomic Spectroscopy 43, no. 9-11 (1988): 1133–40. http://dx.doi.org/10.1016/0584-8547(88)80157-5.

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6

Grzybek, Jan, and Bogusław Janczy. "Quantitative estimatation of lead, cadmium. and nickel contents by means of Atomic Absorption Spectroscopy in fruitbodies of some macromycetes in Poland." Acta Mycologica 26, no. 2 (2014): 17–23. http://dx.doi.org/10.5586/am.1990.008.

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Grzybek, Jan. "Estimation of lead, cadmium and nickel content by means of Atomic Absorption Spectroscopy in dry fruit bodies of some macromycetes growing in Poland. II." Acta Mycologica 27, no. 2 (2014): 213–20. http://dx.doi.org/10.5586/am.1992.019.

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8

Offem, J. O., and O. S. O. Edet. "Spectrophotometric determination of manganese based on thermally produced manganese (VI) compounds in plant ash." Journal of Agricultural Science 112, no. 3 (1989): 427–31. http://dx.doi.org/10.1017/s0021859600085890.

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Atomic Absorption Spectroscopy (AAS) is the usual method for the direct determination of small amounts of manganese in plant materials (Christian & Feldman 1970; Heanes, 1981) and other substances (Carnrick, Slavin & Manning, 1981). However, it uses the highly sophisticated and expensive Atomic Absorption Spectrometer, which requires a reasonable degree of technician expertise, and is therefore not suitable for routine chemical analyses in Third World countries.
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9

RIES, M. A. EL. "Spectrophotometric and Indirect Determination of Lincomycin by Atomic Absorption Spectroscopy (AAS)." Analytical Letters 27, no. 8 (1994): 1517–31. http://dx.doi.org/10.1080/00032719408006386.

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10

Rodlotu Yula, Hesty, Syaiful Bahri, Yuli Ambarwati, Iswadi Idris, and Ganjar Andhulang. "ANALISIS KANDUNGAN LOGAM BERAT MERKURI (Hg) PADA CUMICUMI (Loligo sp.) DENGAN MENGGUNAKAN METODE ATOMIC ABSORPTION SPECTROSCOPY (AAS)." ANALIT:ANALYTICAL AND ENVIRONMENTAL CHEMISTRY 6, no. 01 (2021): 83–91. http://dx.doi.org/10.23960/aec.v6.i1.2021.p83-91.

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Tingkat bahaya dari logam berat merkuri (Hg) yang ter-bioakumulasi pada cumi-cumi (Loligo sp.) tidak hanya memberikan implikasi bagi lingkungan, namun juga terhadap kesehatan manusia. Hal inilah yang menjadi dasar penelitian dikarenakan cumi-cumi memiliki kemampuan mengabsorpsi logam melalui jaringan otot dan didukung dengan tingginya produksi cumi-cumi di Indonesia yang mencapai 216 ribu ton per tahun 2018 berdasarkan data KKP RI yang sejalan dengan tingkat konsumsi. Selain itu, relevansi kebijakan Pemerintah Republik Indonesia dengan penandatanganan Konvensi Minamata tentang bahaya merkuri y
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11

Suvardhan, K., K. Suresh Kumar, K. M. Reddy, M. V. Jyothi, and P. Chiranjeevi. "Determination of Trace Metals with Newly Synthesized Coniine Dithiocarbamate by Atomic Absorption Spectroscopy." E-Journal of Chemistry 1, no. 2 (2004): 99–104. http://dx.doi.org/10.1155/2004/271531.

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A procedure is developed for the determination of Cd, Cu, Mo, Pb, Te and Ni in natural and spiked water by Atomic Absorption Spectroscopy (AAS) after preconcentration on a coniine dithiocarbamate supported by polyurethane. The sorbed elements are subsequently eluted with 5 mol L-1HNO3and the acid eluates are analysed by AAS. A 20 mL syringe served as a chromatographic preconcentration column. The sorption recoveries of elements were higher in the order of 99%. The method is also applied successfully for the determination of Cu, Cd, Mo, Pb, Te and Ni in natural and spiked water samples.
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12

Johnson, Nelson A. "Determination of Maduramicin by Liquid Chromatography with Atomic Absorption Spectrometric Detection." Journal of AOAC INTERNATIONAL 72, no. 2 (1989): 235–37. http://dx.doi.org/10.1093/jaoac/72.2.235.

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Abstract A liquid chromatograph was interfaced to an atomic absorption spectrometer for the detection and quantitation of maduramicin in feed matrixes at the 1-8 ppm level. Ionophores in general form strong 1:1 products with various metal cations, yielding complexes that are insoluble in water but very soluble in organic solvents. Maduramicin, a carboxylic, polyalcohol, polyether antibiotic, is labeled with the sodium cation and analyzed by atomic absorption spectroscopy (AAS). The lower limit of detection is approximately 100-200 ng maduramicin sodium salt. Feeds containing 1-8 ppm maduramici
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13

Bojago, Tsegaye, Adisu Dola, and Dr Getachew Worku. "Determination and comparisons of Heavy Metals in Moringa Stenopetala Leaf, Seed and Root: using Atomic Absorption Spectroscopy." International Journal of Scientific & Engineering Research 11, no. 8 (2020): 1–10. http://dx.doi.org/10.14299/ijser.2020.08.16.

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This study is aimed to determine and compare the concentration level of heavy metals (Cu, Fe, Pb and Cr) using Atomic Absorption Spectroscopy (AAS) of samples of fresh leaf, seed and root of Moringa stenopetala from Arbaminch area and Konso districts .
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14

Abad, Carlos, Stefan Florek, Helmut Becker-Ross, et al. "Zirconium permanent modifiers for graphite furnaces used in absorption spectrometry: understanding their structure and mechanism of action." Journal of Analytical Atomic Spectrometry 33, no. 12 (2018): 2034–42. http://dx.doi.org/10.1039/c8ja00190a.

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The mechanism of action of zirconium permanent modifiers on graphite surfaces was investigated in order to understand its influence on the analytical signal in atomic and molecular absorption spectrometry (AAS/MAS).
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15

Rehman, Ejaz UR, Shakeel UR Rehman, and Shafaat Ahmed. "6Li Atom Percentage Determination by Atomic Absorption–Emission Spectrometry Using a Natural Lithium Hollow Cathode Lamp." Applied Spectroscopy 63, no. 8 (2009): 971–73. http://dx.doi.org/10.1366/000370209788964566.

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A simple method has been developed for the determination of 6Li atom % using combined atomic emission–absorption spectrometry employing a commonly available natural lithium hollow cathode lamp. Unlike in previous practice, there is no need for specially fabricated and high cost 6Li and 7Li monoisotopic lamps in this method. The method requires adjustment of total lithium contents of the sample, i.e., 6Li + 7Li, to 2 μg-mL−1 based upon atomic emission spectroscopy (AES) ( Caes) against a 2 μg-mL−1 natural lithium standard. The concentration of the sample was then analyzed by atomic absorption s
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16

Shveta, Raje, T. Sane R., Mangaonkar Kiran та ін. "Determination of heavy metals from Cressα creticα using atomic absorption spectroscopic technique". Journal of Indian Chemical Society Vol. 83, Jun 2006 (2006): 611–12. https://doi.org/10.5281/zenodo.5820056.

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Herbal Research Laboratory, Ramnarain Ruia College, Matunga, Mumbai-400 019, India <em>E-mail </em>: shveta_raje@yahoo.co.in <em>Manuscript received 13 June 2005, revised 7 February 2006, accepted 3 March 2006</em> Most of the herbal medicines analysed for heavy metals, are found to be having higher concentration of one or more elements. Therefore, limit tests of heavy metals are essential for herbal medicines. There is also a need for heavy metal analysis to be an integral part of the standardization of herbal medicines. \(Cressa\) \(cretica\) is a common plant growing in sand) regions. It ha
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17

Santos, Jefferson Luiz Antunes, Jader Galba Busato, Rodrigo de Almeida Heringer, Juscimar da Silva, and Leonardo Barros Dobbss. "Arsenic quantification techniques and ISO/IEC 17025 accreditation in Brazil." Revista Brasileira de Gestão Ambiental e Sustentabilidade 6, no. 14 (2019): 803–17. http://dx.doi.org/10.21438/rbgas.061413.

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The importance of arsenic (As) quantification in environmental compartments is due to its risks to ecosystems and public health. There are reports of high concentrations of this metalloid in Brazil and technological differences between states are observed. The objective of this work was to present and discuss current scenarios of accreditation and compare the limit of quantification (LOQ) of As by analytical technique in Brazil. Data from accredited laboratories were collected on Inmetro website and in state metrological networks and then grouped and analyzed by state, matrix and analytical te
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18

Hepp, Nancy M. "X-Ray Fluorescence Determination of Manganese in FD&C Blue No. 1." Journal of AOAC INTERNATIONAL 81, no. 1 (1998): 89–92. http://dx.doi.org/10.1093/jaoac/81.1.89.

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Abstract An X-ray fluorescence (XRF) method was developed for determining manganese in FD&amp;C Blue No. 1 from simply prepared pressed pellets. Results were compared with those of atomic absorption spectroscopy (AAS) of acid-digested or ashed samples. Levels of manganese determined by XRF and AAS were equivalent. The limit of detection (3σ) for the XRF method was 3µg manganese/g dye. The 95% confidence interval at the specification level was 100 ± 10 μg manganese/g dye
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19

Purnomo, Frida Octavia, Dyah Ayuwati Waluyo, Dewi Adelia Larasati, Yolanda Rahmah Habibillah, Dwi Widiyawati, and Puspa Ayuningdyah Lestari. "ANALISIS KADAR MERKURI PADA KRIM PENCERAH WAJAH MENGGUNAKAN ATOMIC ABSORPTION SPECTROSCOPY (AAS)." Jurnal Kesehatan Tambusai 5, no. 4 (2024): 11076–84. https://doi.org/10.31004/jkt.v5i4.35758.

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Standar kecantikan setiap zaman semakin bertransformasi dan meningkat, pada zaman sekarang kerap menekankan pada tampilan fisik yang sempurna, bayak masyarakat yang menginginkan memiliki kulit yang putih namun dengan cara yang instan, karena tuntutan tersebut banyak orang mencari alternatif yang mudah dengan cara membuat krim pencerah dengan bahan yang berbahaya. Salah satu bahan berbahaya yang digunakan pada krim pencerah adalah merkuri yang dapat menghambat pembentukan melanosit (melanogenesis) jika digunakan dalam jangka waktu yang panjang. Tujuan penelitian ini untuk menganalisis dan mengi
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20

Koleleni, Yusuf Ismail. "Assessment of Mineral Compositions in Ginger Roots Using Atomic Absorption Spectroscopy (AAS)." Asian Journal of Food Research and Nutrition 4, no. 1 (2025): 86–100. https://doi.org/10.9734/ajfrn/2025/v4i1229.

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21

Prem, Lata Meena, Sandilya Avinash, and Sharma Sachin. "A review of Singular and Hyphenated Analytical techniques in Trace Element analysis." Chemistry Research Journal 4, no. 1 (2019): 117–24. https://doi.org/10.5281/zenodo.13752764.

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At micro trace levels there is a critical need for preconcentration, selective separation, and determine the various metal ions from complex matrices. Trace analysis and various&nbsp;analytical techniques which are used to determine the&nbsp;concentration&nbsp;of a&nbsp;chemical element is described. It can be broadly classified in to singular and hyphenated techniques. For analysis there are different types of singular techniques like Flame Atomic absorption spectroscopy (AAS),Neutron activation analysis (NAA),Graphite furnace atomic absorption spectrometry (GFAAS),&nbsp;inductively coupled p
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22

Pavski, Victor, and Chuni L. Chakrabarti. "Atomic Line Profiles in Hollow Cathode Lamps and a Glow Discharge Atomizer Determined by Fourier Transform Spectroscopy." Applied Spectroscopy 49, no. 7 (1995): 927–38. http://dx.doi.org/10.1366/0003702953964822.

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In an attempt to understand the implications of using glow discharge atomizers in atomic absorption spectrometry (AAS), line profiles and kinetic (Doppler) temperatures were measured in commercial hollow cathode lamps and a laboratory-constructed, jet-assisted dc glow discharge atomizer using a high-resolution Bomem Fourier transform spectrometer. Line profiles were measured in the hollow cathode lamps as current was increased from 1 to 30 mA for three resonance atomic lines (Mg 285.21 nm, Al 308.22 nm, and Pb 283.31 nm) having distinctly different hyperfine structure. Although the Al 308.22-n
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23

Mangay, John Carlo A., Eric T. Miranda, John Mark S. Anicas, Angel S. Recto, and Jan-Michael C. Cayme. "Characterization of Mortar from Church Ruins in Barangay Budiao, Daraga, Albay." MATEC Web of Conferences 213 (2018): 02001. http://dx.doi.org/10.1051/matecconf/201821302001.

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The lack of information about the correct ways of restoring historical masonry materials from cultural heritage structures tends to create more damage to the said structures. According to Cesare Brandi’s theory of restoration, existing historical materials must be replaced with their equivalent. This paper presents the chemical composition of historical mortars acquired from church ruins of barangay Budiao, Daraga, Albay, Philippines. The historical mortar sample was characterized using petrographic analysis, sieve analysis, atomic absorption spectroscopy (AAS), thermogravimetric analysis (TGA
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24

Pathiratne, K. A. S., and R. J. Lovett. "Isotopes and Atomic Absorption Spectrometry. Computer Simulations, Part I: Evaluation of the Simulation Model Using the Flame Atomic Absorption Determination of Lithium Isotope Abundances." Applied Spectroscopy 41, no. 2 (1987): 208–18. http://dx.doi.org/10.1366/000370287774987010.

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An evaluation of a computer model developed to calculate absorbances involving multi-isotopic elements is presented. With the use of the model, an independently performed flame atomic absorption experiment to determine isotope abundances of lithium is simulated. The necessity of having accurate values of the critical model parameters (damping constant, isotope shift, fine structure separation, and collisional shift) is demonstrated. The ability of the model to reveal experimental relationships which would be difficult to observe unless the experiments were performed with extreme care is shown.
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Anas, Ajwar, Sukainil Ahzan, and Dwi Sabda Budi Prasetya. "Pembuatan Filter Penangkap Emas (Au) Menggunakan Kitin dan Kitosan dari Cangkang Kepiting." Lensa : Jurnal Kependidikan Fisika 5, no. 2 (2017): 23. http://dx.doi.org/10.33394/j-lkf.v5i2.133.

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[Title: Manufacture of Gold (Au) Capture Filters Using Chitin and Chitosan from Crab Shells]. This study aims to analyze the ratio of absorption capacity between chitin, chitosan and chitin-chitosan mixture from crab shells as a Gold catcher filter (Au). The preparation of chitin and chitosan from crab shells begins with demineralization using 1.5 M HCl, deproteination using 3.5% NaOH and deacetylation using 60% HCl. Chitosan that formed characterized and analyz ed its ability to absorb gold using AAS (Atomic Absorbsion Spectroscopy). The result of analysis using AAS showed that chitin was abl
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26

Schur, Julia, Cesar M. Manna, Edit Y. Tshuva, and Ingo Ott. "Quantification of the titanium content in metallodrug-exposed tumor cells using HR-CS AAS." Metallodrugs 1, no. 1 (2014): 1–9. http://dx.doi.org/10.2478/medr-2014-0001.

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AbstractHigh-resolution continuum source atomic absorption spectroscopy (HR-CS AAS) is a valuable analytical technique for metal quantification because of its high sensitivity and selectivity for metal atoms as well as its improved background correction mode. However, the quantification of metals in biological materials, e.g. cell lysates, is still challenging because of matrix effects and other experimental complications. A method to quantify the titanium content of tumor cells exposed to titanium-based drugs was developed using HR-CS AAS. This method allows the quantification of titanium in
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27

Hepp, Nancy M. "Spectrometric Determination of Chromium in FD&C Blue No. 1 by X-Ray Fluorescence." Journal of AOAC INTERNATIONAL 79, no. 5 (1996): 1189–90. http://dx.doi.org/10.1093/jaoac/79.5.1189.

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Abstract An X-ray fluorescence spectrometry (XRF) method was developed and validated for determination of chromium in FD&amp;C Blue No. 1. Results of this analysis were compared with those obtained with an atomic absorption spectroscopy (AAS) method currently used by the U.S. Food and Drug Administration. Levels of Cr, as determined by the XRF and AAS methods, were comparable. The limit of quantitation for the XRF method is 4 μg Cr/g. The predicted 95% confidence interval at the specification level is 50 ± 5 μg/g.
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28

Sarode, Dhananjay B., Sopan T. Ingle, and Sanjay B. Attarde. "FORMULA ESTABLISHMENT OF COLORLESS Pb(II) COMPLEX WITH N-BENZOYL-N-PHENYL HYDROXYLAMINE (BPA) USING ATOMIC ABSORPTION SPECTROSCOPY." Indonesian Journal of Chemistry 12, no. 1 (2012): 12–19. http://dx.doi.org/10.22146/ijc.21366.

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A new method for determination of stoichiometry of colorless complexes by using atomic absorption spectrophotometric technique in continuous variation method and slope ratio method was described here. This method can be used in same manner as that of mole ratio method and slope ratio method. In this method atomic absorption spectroscopy was used instead of UV-Vis spectrophotometry. Atomic absorption spectrophotometric technique is superior to UV-Vis spectrophotometry as it can be applied to colorless soluble complexes. Pb(II) and n-benzoyl-n-phenyl hydroxylamine react to form colorless complex
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29

Jamali, Saifullah, M. Aslam Khoso, M. Haider Zaman, et al. "Elemental Analysis of Kohl Using Laser Ablation and Atomic Absorption Spectroscopy (AAS) techniques." Physica B: Condensed Matter 620 (November 2021): 413278. http://dx.doi.org/10.1016/j.physb.2021.413278.

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30

Rajeshwari, B. M., and S. J. Patil. "Heavy Metals Status in Soils of Ballari District using Atomic Absorption Spectroscopy (AAS)." Asian Journal of Research in Chemistry 11, no. 4 (2018): 701. http://dx.doi.org/10.5958/0974-4150.2018.00123.2.

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31

Panda, Swetapadma, and Pradip Sarkar. "Leaching behavior of copper slag aggregate cement-mortar by atomic absorption spectroscopy (AAS)." Materials Today: Proceedings 33 (2020): 5123–29. http://dx.doi.org/10.1016/j.matpr.2020.02.856.

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32

Benwal, Kirtika Sanjay, and Spriha Sharma. "Determination of Lead from Non-Branded Lipstick Samples Using Atomic Absorption Spectroscopy (AAS)." Journal of Punjab Academy of Forensic Medicine & Toxicology 22, no. 2 (2022): 100–106. http://dx.doi.org/10.5958/0974-083x.2022.00051.6.

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33

Llana, Marlon J., Kyrien Jewel Janeena L. Tabucan, John Alec Mari C. Cosico, Paul Eric C. Maglalang, and Jeremiah C. Millare. "Effects of Halloysite Nanotube (HNT) on the Cd<sup>2+</sup> Adsorption Capacity of Cellulose Acetate (CA) Thin Film Membranes." Key Engineering Materials 974 (February 16, 2024): 69–75. http://dx.doi.org/10.4028/p-wb3xfa.

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This paper aims to investigate the effects of adding and increasing the concentration of halloysite nanotube (HNT) to a cellulose acetate (CA) membrane which is produced through non-solvent-induced phase separation via hand casting. Different characterization tests are performed on the nanocomposite samples: Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), Fourier Transform Infrared Spectroscopy (FTIR), and Atomic Absorption Spectroscopy (AAS). The addition of the filler itself increases the presence of peaks and valleys on the surface of the nanocomposite membrane. The 5% HN
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34

Puchyr, Richard F., and Rubin Shapiro. "Determination of Trace Elements in Foods by HCl-HNO3 Leaching and Flame Atomic Absorption Spectroscopy." Journal of AOAC INTERNATIONAL 69, no. 5 (1986): 868–70. http://dx.doi.org/10.1093/jaoac/69.5.868.

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Abstract Aluminum, iron, tin, zinc, calcium, magnesium, nickel, copper, chromium, cadmium, and potassium in foods can be extracted by HC1- HN03 leaching and determined quantitatively using flame atomic absorption spectroscopy (AAS), with recoveries ranging from 90 to 110%. Thirty to 40 samples of almost any type of food sample can be analyzed routinely for 2 elements in 4-5 h. In contrast, one or 2 days are required when a wet-ash or dry-ash technique is used. Extraction consists of weighing 2-10 g samples into 125 mL Erlenmeyer flasks, adding 20 mL concentrated HCI-HNO3 (9 + 1), then heating
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35

Ruíz-Baltazar, A., R. Esparza, R. Pérez, and G. Rosas. "Spectroscopy Study of Silver Nanoparticles Produced by Chemical Reduction." Materials Science Forum 755 (April 2013): 15–20. http://dx.doi.org/10.4028/www.scientific.net/msf.755.15.

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In this study, Ag nanoparticles were synthesized using two chemical reduction agents; ethylene glycol and sodium borohydride. Different particle size distributions were obtained and characterized by transmission electron microscopy. Ag nanoparticles concentrations of 1, 2 and 4 parts per million (gmL-1) were prepared and studied by ultraviolet-visible spectroscopy (UV-Vis) and atomic absorption spectrophotometry (AAS). In the UV-Vis results a characteristic band at 420 nm were observed. However, when the concentration of silver decreased, a change in band intensity was detected. Atomic absorpt
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36

Wang, Pingxin, and James A. Holcombe. "Electrothermal Atomization with Atomic Absorption at Reduced Pressures for Studies of Analyte Distribution in Solids." Applied Spectroscopy 48, no. 6 (1994): 713–19. http://dx.doi.org/10.1366/000370294774369045.

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The spatial distribution of Pb in a NIST Standard Reference Material (SRM) C1253a copper alloy is determined by using an electrothermal atomizer atomic absorption spectrometry (ETA-AAS) system operated at reduced pressure. Three Pb absorbance peaks have been consistently observed at 0.1 Torr. It is proposed that the first peak belongs to the release process of Pb from the surface, the second peak may originate from grains until the Cu-Pb binary phase transformation to a homogeneous solution occurs, and the third peak arises from Pb in the bulk of the sample. The areas of the first two peaks ma
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37

Zhong, Liang Yan, and Ni Zhe-ming. "General computer program (AAS-TOOLS) for theoretical studies in electrothermal atomic absorption spectrometry." Journal of Analytical Atomic Spectrometry 9, no. 6 (1994): 669. http://dx.doi.org/10.1039/ja9940900669.

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38

Miksa, Irina Rudik, Carol L. Buckley, Nancy P. Carpenter, and Robert H. Poppenga. "Comparison of Selenium Determination in Liver Samples by Atomic Absorption Spectroscopy and Inductively Coupled Plasma–Mass Spectrometry." Journal of Veterinary Diagnostic Investigation 17, no. 4 (2005): 331–40. http://dx.doi.org/10.1177/104063870501700405.

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Selenium (Se) is an essential trace element that is often deficient in the natural diets of domestic animal species. The measurement of Se in whole blood or liver is the most accurate way to assess Se status for diagnostic purposes. This study was conducted to compare hydride generation atomic absorption spectroscopy (HG-AAS) with inductively coupled plasma–mass spectrometry (ICP-MS) for the detection and quantification of Se in liver samples. Sample digestion was accomplished with magnesium nitrate and nitric acid for HG-AAS and ICP-MS, respectively. The ICP-MS detection was optimized for 82S
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39

Parker, Mark, and R. Kenneth Marcus. "Investigation of Sample Atomization Using a Power-Modulated Radio-Frequency Glow Discharge Source." Applied Spectroscopy 50, no. 3 (1996): 366–76. http://dx.doi.org/10.1366/0003702963906276.

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A power-modulated (pulsed), radio-frequency glow discharge source by atomic absorption spectrophotometry (rf-GD-AAS) atomizer was used to evaluate the roles of applied power, pressure, orifice diameter, duty cycle, and power-on time in the production of gas-phase sample atoms. As expected, the response of the modulated rf-GD-AAS source generally followed the same trends as those exhibited by the more common continuous-powering scheme. The effects of discharge power and pressure on the observed plasma emission and absorbance transients are presented. Use of small duty cycles and higher instanta
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Kirchler, Christian, Raphael Henn, Julia Modl, et al. "Direct Determination of Ni2+-Capacity of IMAC Materials Using Near-Infrared Spectroscopy." Molecules 23, no. 12 (2018): 3072. http://dx.doi.org/10.3390/molecules23123072.

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The present paper reports a new method for the quantification of the Ni2+-capacity of an immobilized metal affinity chromatography (IMAC) material using near-infrared spectroscopy (NIRS). Conventional analyses using UV absorption spectroscopy or atomic absorption spectrometry (AAS) need to dissolve the silica-based metal chelate sorbent as sample pretreatment. In the first step, those methods were validated on the basis of an ideal homogenous NiSO4-solution and unveiled that UV with an intermediate precision of 2.6% relative standard deviation (RSD) had an advantage over AAS with an intermedia
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Maddox, William E., and Warren G. Kelliher. "X-Ray Fluorescence Analysis of Wear Metals in Used Lubricating Oils*." Advances in X-ray Analysis 29 (1985): 497–502. http://dx.doi.org/10.1154/s0376030800010636.

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Analyses of lubricating oils from aircraft engines, gear boxes and other lubricated mechanisms have been routinely performed by the military since the 1960's. The monitoring of the wear metal concentrations in the oil can lead to an early detection of abnormal wear and, consequently, the prevention of a malfunction or a complete failure of the aircraft. At the present time, almost all the analysis programs use atomic emission (AES) and/or atomic absorption (AAS) spectroscopy to determine elemental concentrations in the oils (1). These types of analysis require the close support of a laboratory
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Pan, Changkang, and Fred L. King. "Direct Determination of Trace Elements in Graphite Matrices Using Modulated Glow Discharge Atomic Absorption Spectrometry." Applied Spectroscopy 47, no. 3 (1993): 300–304. http://dx.doi.org/10.1366/0003702934066730.

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The trace element concentrations in high-purity graphites were determined by atomic absorption spectrometry (AAS) with the use of a modulated glow discharge atomizer. Glow discharge power was modulated at SO Hz to enhance sensitivity and to permit time-resolved atomic absorption measurements. The influence of discharge operating parameters including current, pressure, and plasma sampling on the analytical performance of this technique was investigated. This analytical technique was evaluated in terms of stability, sensitivity, reproducibility, and accuracy. The method of standard additions was
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Mohammed, Abdelhafeez M. A., Amna M. Ibrahim, Ayat A. Omran, Moawia E. Mohamed, and Sumaya E. M. Elsheikh. "Minerals Content, Essential Oils Composition and Physicochemical Properties of Citrus jambhiri Lush. (Rough Lemon) from the Sudan." International Letters of Chemistry, Physics and Astronomy 14 (September 2013): 25–30. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.14.25.

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Minerals content of Citrus jambhiri (rough lemon) fruit was qualitatively and quantitatively analyzed using atomic absorption spectroscopy (AAS) and flame atomic emission spectrometry (FAES). The peel, moisture and ash contents of rough lemon were found to be 18.35%, 23.75% and 2.04% respectively. Vitamin C (ascorbic acid) of rough lemon juice was found to be 70.0 mg/100 g. The chemical composition of essential oil of rough lemon peel was determined. The major compound was found to be limonene (84.5%) followed by sabinene, β-myrcene, α-terpineol, 1,3-tetradecadiene and linalool.
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Mohammed, Abdelhafeez M. A., Amna M. Ibrahim, Ayat A. Omran, Moawia E. Mohamed, and Sumaya E. M. Elsheikh. "Minerals Content, Essential Oils Composition and Physicochemical Properties of <i>Citrus jambhiri</i> Lush. (Rough Lemon) from the Sudan." International Letters of Chemistry, Physics and Astronomy 14 (May 19, 2013): 25–30. http://dx.doi.org/10.56431/p-g7aa90.

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Minerals content of Citrus jambhiri (rough lemon) fruit was qualitatively and quantitatively analyzed using atomic absorption spectroscopy (AAS) and flame atomic emission spectrometry (FAES). The peel, moisture and ash contents of rough lemon were found to be 18.35%, 23.75% and 2.04% respectively. Vitamin C (ascorbic acid) of rough lemon juice was found to be 70.0 mg/100 g. The chemical composition of essential oil of rough lemon peel was determined. The major compound was found to be limonene (84.5%) followed by sabinene, β-myrcene, α-terpineol, 1,3-tetradecadiene and linalool.
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Bartůněk, Vilém, David Sedmidubský, Štěpán Huber, Marie Švecová, Pavel Ulbrich, and Ondřej Jankovský. "Synthesis and Properties of Nanosized Stoichiometric Cobalt Ferrite Spinel." Materials 11, no. 7 (2018): 1241. http://dx.doi.org/10.3390/ma11071241.

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Nanoparticles with controllable sizes of ferrite spinel CoFe2O4 were formed by thermal treatment of cobalt-iron glycerolate. Thermal behavior during the heating was studied by differential thermal analysis combined with thermogravimetry. The precursor, as well as the prepared nanoparticles, were analyzed by a broad spectrum of analytic techniques (X-Ray photoelectron spectroscopy (XPS), X-Ray diffraction (XRD), Energy dispersive spectroscopy (EDS), Atomic absorption spectroscopy (AAS), Scanning electron microscopy (SEM), and Raman spectroscopy). The particle size of nanoparticles was obtained
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Porento, Mika, Veijo Sutinen, Timo Julku, and Risto Oikari. "Detection of Copper in Water Using On-Line Plasma-Excited Atomic Absorption Spectroscopy (AAS)." Applied Spectroscopy 65, no. 6 (2011): 678–83. http://dx.doi.org/10.1366/10-06051.

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Sofikitis, A. M., J. L. Colin, K. V. Desboeufs, and R. Losno. "Iron analysis in atmospheric water samples by atomic absorption spectroscopy (AAS) in water?methanol." Analytical and Bioanalytical Chemistry 378, no. 2 (2004): 460–64. http://dx.doi.org/10.1007/s00216-003-2282-6.

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Gagliano-Candela, Roberto, Anna P. Colucci, and Salvatore Napoli. "Determination of Firing Distance. Lead Analysis on the Target by Atomic Absorption Spectroscopy (AAS)." Journal of Forensic Sciences 53, no. 2 (2008): 321–24. http://dx.doi.org/10.1111/j.1556-4029.2008.00668.x.

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Vaessen, H. A. M. G., and C. G. van de Kamp. "Sodium and potassium assay of foods and biological substrates by atomic absorption spectroscopy (AAS)." Pure and Applied Chemistry 61, no. 1 (1989): 113–20. http://dx.doi.org/10.1351/pac198961010113.

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Pookmanee, Pusit, P. Thippraphan, P. Jansanthea, and Sukon Phanichphant. "Characterization and Adsorption Efficiency of the Natural and the Modified Diatomite via the Low Temperature Hydrothermal Route." Advanced Materials Research 506 (April 2012): 425–28. http://dx.doi.org/10.4028/www.scientific.net/amr.506.425.

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Natural diatomite was modified by manganese chloride via the low temperature hydrothermal route. The chemical properties and adsorption efficiency of the natural and the modified diatomite were characterized. The chemical compositions of the natural and the modified diatomite were determined by X-ray fluorescence spectroscopy (XRF) and energy dispersive X-ray spectrometry (EDXS). Morphology of the natural and the modified diatomite was investigated by scanning electron microscopy (SEM). The adsorptions of Cd (II) and Pb (II) ions onto the natural and the modified diatomite were determined by a
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