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Journal articles on the topic 'Atomic absorption spectroscopy'

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Published: 4 June 2021
Last updated: 1 August 2024

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1

Boumans, Paul. "Atomic absorption spectroscopy." Spectrochimica Acta Part B: Atomic Spectroscopy 46, no. 3 (January 1991): 455–56. http://dx.doi.org/10.1016/0584-8547(91)80043-3.

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2

Broekaert, J. A. C. "Atomic absorption spectroscopy instrumentation." Spectrochimica Acta Part B: Atomic Spectroscopy 45, no. 8 (January 1990): 845–56. http://dx.doi.org/10.1016/0584-8547(90)80141-5.

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3

B, Magaji. "Heavy Metal Analysis on Some Water Samples Using Atomic Absorption Spectroscopy." Food Science & Nutrition Technology 8, no. 4 (October 5, 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) respectively. Also, the Well Water sample did not contain Cd, but was detected in the other three samples well above the standard limits. Cu was detected in all the samples below the limits by the regulatory bodies. The KSUSTA Table Water did not contain Zn while the other three water samples had Zn levels below the max limits. Hence, the Well water sample was shown to be the best or safer for consumption as it did not contain any Pb or Cd concentration and had Cu and Zn levels below the permissible limits by these agencies. Therefore, those consuming KSUSTA Table water, Faro Bottle water and Tap water in Aliero town should be cautious of the potential danger from the short or long term effect of Pb and Cd toxicity to the human body
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4

Macdonald, Lindesay R., Thomas C. O'Haver, Barbara J. Ottaway, and John M. Ottaway. "Communication. Background atomic absorption in graphite furnace atomic absorption spectrometry." Journal of Analytical Atomic Spectrometry 1, no. 6 (1986): 485. http://dx.doi.org/10.1039/ja9860100485.

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5

Mohammed, Abdul Moiz. "Elemental Analysis Using Atomic Absorption Spectroscopy." European Journal of Engineering and Technology Research 6, no. 7 (November 18, 2021): 48–51. http://dx.doi.org/10.24018/ej-eng.2021.6.7.2639.

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The resonance radiation study is a powerful means in obtaining valuable information concerning the behavior of individual atoms and molecules. Various quantitative techniques are available in order to determine the amount of analyte and analysis of trace elements in the sample. Some technique uses the principle, when the number of atoms in the path of light increases, the amount of light absorption increases. While other techniques use dissociation of chemical compound free atoms by supplying enough thermal energy. In this paper, an attempt is made to compare various analytical methods with their merits and demerits and the reasons for popularity of atomic absorption spectroscopy among researchers. Elemental analysis using atomic absorption spectroscopy of various elements that are found in nature particularly in foods and environment is also presented.
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6

Mohammed, Abdul Moiz. "Elemental Analysis Using Atomic Absorption Spectroscopy." European Journal of Engineering and Technology Research 6, no. 7 (November 18, 2021): 48–51. http://dx.doi.org/10.24018/ejeng.2021.6.7.2639.

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The resonance radiation study is a powerful means in obtaining valuable information concerning the behavior of individual atoms and molecules. Various quantitative techniques are available in order to determine the amount of analyte and analysis of trace elements in the sample. Some technique uses the principle, when the number of atoms in the path of light increases, the amount of light absorption increases. While other techniques use dissociation of chemical compound free atoms by supplying enough thermal energy. In this paper, an attempt is made to compare various analytical methods with their merits and demerits and the reasons for popularity of atomic absorption spectroscopy among researchers. Elemental analysis using atomic absorption spectroscopy of various elements that are found in nature particularly in foods and environment is also presented.
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7

Slavin, W. "Accuracy in furnace atomic-absorption spectroscopy." Journal of Research of the National Bureau of Standards 93, no. 3 (May 1988): 445. http://dx.doi.org/10.6028/jres.093.113.

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8

Delves, H. T. "Atomic Absorption Spectroscopy in Clinical Analysis." Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 24, no. 6 (November 1987): 529–51. http://dx.doi.org/10.1177/000456328702400601.

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9

LAGALANTE, ANTHONY F. "Atomic Absorption Spectroscopy: A Tutorial Review*." Applied Spectroscopy Reviews 34, no. 3 (September 27, 2004): 173–89. http://dx.doi.org/10.1081/asr-100100844.

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10

Zehr, Bradley D., and Judith P. Vankuren. "Characterizing flame atomic absorption spectroscopy parameters." Spectrochimica Acta Part B: Atomic Spectroscopy 49, no. 6 (June 1994): 627–32. http://dx.doi.org/10.1016/0584-8547(94)80055-3.

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11

Journal, Baghdad Science. "Determination and evaluation of principal minerals in Negella sativa by atomic absorption technical methods." Baghdad Science Journal 8, no. 1 (March 13, 2011): 263–67. http://dx.doi.org/10.21123/bsj.8.1.263-267.

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Determination and evaluation of principal minerals in Negella sativa by atomic absorption technical methods were showed, using wet ashing method. This work was done on Negella sativa because of wide using of this plant in many formulations ( in food or medicine ).two types of atomic absorptions were used : first, flame atomic absorption spectroscopy, for minerals of high concentrations such as, Na, Mg, K, Fe, Ca, Li, Ni, Zn, Mn, Cu. Second, flameless atomic absorption spectroscopy, for minerals of low concentrations such as, Al, Si, V, B, Pb, Co, Cd, Cr ,Si, Hg, Sn .The results showed the existence of many minerals in Negella sativa useful to human sanity with acceptable dietary allowance. On other side, the presence of harmful minerals to human sanity(Pb, Cd, Hg ) were negligible.
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12

Mahmood, Samia kahlil. "Determination and evaluation of principal minerals in Negella sativa by atomic absorption technical methods." Baghdad Science Journal 8, no. 1 (March 13, 2011): 263–67. http://dx.doi.org/10.21123/bsj.2011.8.1.263-267.

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Determination and evaluation of principal minerals in Negella sativa by atomic absorption technical methods were showed, using wet ashing method. This work was done on Negella sativa because of wide using of this plant in many formulations ( in food or medicine ).two types of atomic absorptions were used : first, flame atomic absorption spectroscopy, for minerals of high concentrations such as, Na, Mg, K, Fe, Ca, Li, Ni, Zn, Mn, Cu. Second, flameless atomic absorption spectroscopy, for minerals of low concentrations such as, Al, Si, V, B, Pb, Co, Cd, Cr ,Si, Hg, Sn .The results showed the existence of many minerals in Negella sativa useful to human sanity with acceptable dietary allowance. On other side, the presence of harmful minerals to human sanity(Pb, Cd, Hg ) were negligible.
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13

Sturgeon, Ralph E. "Atomic absorption spectroscopy—present and future aspects." J. Anal. At. Spectrom. 7, no. 2 (1992): 13N—16N. http://dx.doi.org/10.1039/ja992070013n.

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14

Stankovich, Larisa, David Wicks, Sasko Despotovski, and Dong Liang. "Atomic Absorption Spectroscopy in Ion Channel Screening." ASSAY and Drug Development Technologies 2, no. 5 (October 2004): 569–74. http://dx.doi.org/10.1089/adt.2004.2.569.

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15

Sturgeon, Ralph E. "Atomic absorption spectroscopy—present and future aspects." Analyst 117, no. 3 (1992): 233–36. http://dx.doi.org/10.1039/an9921700233.

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16

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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17

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 (January 1988): 95–134. http://dx.doi.org/10.1080/10408348808542809.

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18

Hannaford, P. "The oscillator strength in atomic absorption spectroscopy." Spectrochimica Acta Part B: Atomic Spectroscopy 49, no. 12-14 (October 1994): 1581–93. http://dx.doi.org/10.1016/0584-8547(94)80132-0.

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19

El-Brashy, Amina M., and Sheikha M. Al-Ghannam. "Determination of Histidine by Atomic Absorption Spectroscopy." Journal of AOAC INTERNATIONAL 80, no. 4 (July 1, 1997): 741–45. http://dx.doi.org/10.1093/jaoac/80.4.741.

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Abstract Two atomic absorption spectrophotometric methods are described for determination of histidine. The first is based on reaction of histidine with mercury(II) ions in phosphate buffer (pH 9). The second is based on reaction of histidine with iron(III) ions in neutral medium. The precipitate formed in both methods is separated by centrifugation, and the equivalent Hg(II) or Fe(III) ions as well as surplus ions in the filtrate are determined by atomic absorption at 253.6 and 248.3 nm for Hg and Fe, respectively. Amounts of histidine are calculated from calibration graphs prepared by standard addition methods or by regression equations. The procedures were successfully applied to assay of histidine in dosage forms after thin-layer chromatographic separation. Results compared favorably with those of the official method.
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20

Ham, Norman S., and J. B. Willis. "Atomization problems in atomic absorption spectroscopy—IV." Spectrochimica Acta Part B: Atomic Spectroscopy 40, no. 10-12 (January 1985): 1607–29. http://dx.doi.org/10.1016/0584-8547(85)80182-8.

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21

Hannaford, P. "The Oscillator Strength in Atomic Absorption Spectroscopy." Microchemical Journal 63, no. 1 (September 1999): 43–52. http://dx.doi.org/10.1006/mchj.1999.1766.

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22

Sneddon, Joseph. "Electrostatic Precipitation Atomic Absorption Spectrometry." Applied Spectroscopy 44, no. 9 (November 1990): 1562–65. http://dx.doi.org/10.1366/0003702904417931.

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23

Wang, Weizhi, R. H. Hammond, M. M. Fejer, and M. R. Beasley. "Atomic flux measurement by diode-laser-based atomic absorption spectroscopy." Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films 17, no. 5 (September 1999): 2676–84. http://dx.doi.org/10.1116/1.581929.

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24

O'Grady, Clare E., Iain L. Marr, and Malcolm S. Cresser. "Observations on impactors in flame atomic-absorption spectroscopy." Analyst 110, no. 5 (1985): 435. http://dx.doi.org/10.1039/an9851000435.

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25

Slavin, Walter. "ATOMIC ABSORPTION SPECTROSCOPY: WHY HAS IT BECOME SUCCESSFUL?" Analytical Chemistry 63, no. 21 (November 1991): 1033A—1038A. http://dx.doi.org/10.1021/ac00021a723.

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26

Gough, David S., Peter Hannaford, and R. Martin Lowe. "Studies of sputtering atomizers for atomic absorption spectroscopy." Analytical Chemistry 61, no. 15 (August 1989): 1652–55. http://dx.doi.org/10.1021/ac00190a013.

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27

Hergenröder, R., and K. Niemax. "Atomic absorption spectroscopy with tunable semiconductor diode lasers." TrAC Trends in Analytical Chemistry 8, no. 9 (October 1989): 333–35. http://dx.doi.org/10.1016/0165-9936(89)87040-2.

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28

Shelton, J. P. "Atomic absorption spectroscopy — a personal recollection, 1947–1958." Spectrochimica Acta Part B: Atomic Spectroscopy 54, no. 14 (December 1999): 1961–66. http://dx.doi.org/10.1016/s0584-8547(99)00139-1.

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29

Ayad, Magda M., S. E. Khayyal, and N. M. Farrag. "Microdetermination of cinchona alkaloids by atomic absorption spectroscopy." Spectrochimica Acta Part B: Atomic Spectroscopy 40, no. 9 (January 1985): 1205–9. http://dx.doi.org/10.1016/0584-8547(85)80147-6.

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30

Hergenröder, R., and K. Niemax. "Laser atomic absorption spectroscopy applying semiconductor diode lasers." Spectrochimica Acta Part B: Atomic Spectroscopy 43, no. 12 (January 1988): 1443–49. http://dx.doi.org/10.1016/0584-8547(88)80183-6.

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31

Butcher, David J. "ADVANCES IN ELECTROTHERMAL ATOMIZATION FOR ATOMIC ABSORPTION AND ATOMIC FLUORESCENCE." Applied Spectroscopy Reviews 37, no. 3 (January 10, 2002): 305–19. http://dx.doi.org/10.1081/asr-120014278.

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32

Aver'yanov, I. S., L. S. Zakharov, A. S. Makarov, A. F. Belozerov, E. A. Vandyukov, A. I. Safin, G. Z. Badrutdinova, I. G. Izotova, and A. A. Ostanin. "Using atomic-emission and atomic-absorption spectroscopy to analyze semiconductor materials." Journal of Optical Technology 67, no. 12 (December 1, 2000): 1078. http://dx.doi.org/10.1364/jot.67.001078.

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33

Natelson, Samuel. "Organic analysis using atomic absorption spectrometry." Microchemical Journal 31, no. 1 (February 1985): 132. http://dx.doi.org/10.1016/0026-265x(85)90021-9.

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34

Milov, Yu M. "Resonance monochromator in atomic-absorption and atomic-fluorescence spectrometry." Journal of Applied Spectroscopy 44, no. 5 (May 1986): 444–47. http://dx.doi.org/10.1007/bf00667064.

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35

Kuchma, Elena, Stanislav Kubrin, and Alexander Soldatov. "The Local Atomic Structure of Colloidal Superparamagnetic Iron Oxide Nanoparticles for Theranostics in Oncology." Biomedicines 6, no. 3 (July 18, 2018): 78. http://dx.doi.org/10.3390/biomedicines6030078.

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The paper contains an overview of modern spectroscopic methods for studying the local atomic structure of superparamagnetic nanoparticles based on iron oxide (SPIONs), which are an important class of materials promising for theranostics in oncology. Practically important properties of small and ultra small nanoparticles are determined primarily by their shape, size, and features of the local atomic, electronic, and magnetic structures, for the study of which the standard characterization methods developed for macroscopic materials are not optimal. The paper analyzes results of the studies of SPIONs local atomic structure carried out by X-ray absorption spectroscopy at synchrotron radiation sources and Mössbauer spectroscopy during the last decade.
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36

Wu, Peng, Shaopan He, Bin Luo, and Xiandeng Hou. "Flame Furnace Atomic Absorption Spectrometry: A Review." Applied Spectroscopy Reviews 44, no. 5 (July 23, 2009): 411–37. http://dx.doi.org/10.1080/05704920903018585.

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37

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 (April 30, 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 yang telah ditetapkan sebagai permasalahan global, peraturan BPOM No.5/2018, dan SNI 7387-2009 tentang batasan maksimum cemaran logam berat dalam pangan olahan menjadi acuan pendukung. Tujuan penelitian ini yaitu untuk mengetahui kadar logam berat merkuri (Hg) yang terakumulasi dalam daging cumi-cumi. Kadar logam berat Hg pada cumi-cumi dianalisis menggunakan metode Atomic Absorption Spectroscopy (AAS) melalui sampel jaringan otot daging. Secara keseluruhan, data analisis menunjukkan bahwa kandungan logam berat merkuri (Hg) pada daging cumi-cumi adalah 0,038 μg/g (uji#1) dan 0,035 μg/g (uji#2) dimana lebih rendah dari standar baku mutu PerBPOM dan SNI 7387-2009 tersebut yaitu 0,5 mg/kg dan 1,0 mg/kg, masing-masing. Oleh karena itu, hasil tersebut mengindikasikan bahwa cumi-cumi tersebut aman untuk dikonsumsi.
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38

Langley, J., R. A. Beaman, J. Baran, A. N. Davies, and W. Jeremy Jones. "Concentration-modulated absorption spectroscopy." Optics Letters 10, no. 7 (July 1, 1985): 327. http://dx.doi.org/10.1364/ol.10.000327.

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39

Chao Shen, Chao Shen, Yujun Zhang Yujun Zhang, and Jiazheng Ni Jiazheng Ni. "Compact cylindrical multipass cell for laser absorption spectroscopy." Chinese Optics Letters 11, no. 9 (2013): 091201–91205. http://dx.doi.org/10.3788/col201311.091201.

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40

Greenway, G. M. "Flow injection atomic absorption spectrometry." Analytica Chimica Acta 343, no. 3 (May 1997): 295–96. http://dx.doi.org/10.1016/s0003-2670(97)89599-2.

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41

Yan, Xiu-Ping, and Zhe-Ming Ni. "Vapour generation atomic absorption spectrometry." Analytica Chimica Acta 291, no. 1-2 (June 1994): 89–105. http://dx.doi.org/10.1016/0003-2670(94)85130-1.

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42

HASHIMOTO, Masao S., Hideo YAMADA, Kohnosuke OHISHI, and Kazuo YASUDA. "Dynamic range enhancement for flameless Zeeman atomic absorption spectroscopy." Analytical Sciences 2, no. 2 (1986): 109–12. http://dx.doi.org/10.2116/analsci.2.109.

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43

Smeyers-Verbeke, J., and D. Verbeelen. "Determination of aluminum in bone by atomic absorption spectroscopy." Clinical Chemistry 31, no. 7 (July 1, 1985): 1172–74. http://dx.doi.org/10.1093/clinchem/31.7.1172.

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Abstract In developing this method for determination of Al in bone we paid special attention to the homogenization of bone samples, which presents great difficulties for trace-element analysis. To minimize the risk of contamination, we preferred low-temperature ashing over classical wet-digestion techniques for destruction of the organic material. Graphite-furnace atomic absorption spectroscopy is used for measurement of Al. For Al concentrations exceeding 15 micrograms/g, direct standardization against a calibration line can be used (between-run CV, 5.9%). For Al concentrations within the normal range (less than 15 micrograms/g) the standard-addition technique should be applied. Comparison of results by the method with those by a procedure based on extraction of Al with a saturated solution of EDTA revealed that, although the latter method gave considerably lower results for three of 13 samples, there was no statistical difference between results by the two methods.
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44

Merten, Jonathan, and Bruce Johnson. "Massing a laser-induced plasma with atomic absorption spectroscopy." Spectrochimica Acta Part B: Atomic Spectroscopy 149 (November 2018): 124–31. http://dx.doi.org/10.1016/j.sab.2018.07.023.

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45

Song, Ningfang, Xiangxiang Lu, Xiaobin Xu, Xiong Pan, Wei Li, Di Hu, and Jixun Liu. "Measurement of frequency sweep nonlinearity using atomic absorption spectroscopy." Optics Communications 407 (January 2018): 165–68. http://dx.doi.org/10.1016/j.optcom.2017.09.043.

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46

Cheskis, S., and S. A. Kovalenko. "Detection of atomic oxygen in flames by absorption spectroscopy." Applied Physics B Lasers and Optics 59, no. 5 (November 1994): 543–46. http://dx.doi.org/10.1007/bf01082398.

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47

Opwis, Klaus, Dierk Knittel, and Eckhard Schollmeyer. "Quantitative analysis of immobilized metalloenzymes by atomic absorption spectroscopy." Analytical and Bioanalytical Chemistry 380, no. 7-8 (November 5, 2004): 937–41. http://dx.doi.org/10.1007/s00216-004-2875-8.

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48

Roberts, W. L., and P. M. Rainey. "Antimony Quantification in Leishmania by Electrothermal Atomic Absorption Spectroscopy." Analytical Biochemistry 211, no. 1 (May 1993): 1–6. http://dx.doi.org/10.1006/abio.1993.1223.

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49

Lebedev, Vyacheslav, Joshua H. Bartlett, and Alonso Castro. "Isotope-resolved atomic beam laser spectroscopy of natural uranium." Journal of Analytical Atomic Spectrometry 33, no. 11 (2018): 1862–66. http://dx.doi.org/10.1039/c8ja00242h.

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50

Kureichik, K. P., S. L. Pisarev, N. V. Kozlovskii, V. I. Kharitonchik, and A. Z. Ibragim. "Compact Atomic-Absorption Graphite-Atomizer Spectrometer." Journal of Applied Spectroscopy 70, no. 5 (September 2003): 814–16. http://dx.doi.org/10.1023/b:japs.0000008885.13596.8f.

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