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Multiple probe concentrating of Au and Pd in geological samples for atomic absorption determination with two-stage probe atomization. / Volzhenin, Artem V.; Petrova, Natalya I.; Medvedev, Nickolay S. и др.

в: Microchemical Journal, Том 138, 01.05.2018, стр. 390-394.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Volzhenin AV, Petrova NI, Medvedev NS, Saprykin AI. Multiple probe concentrating of Au and Pd in geological samples for atomic absorption determination with two-stage probe atomization. Microchemical Journal. 2018 май 1;138:390-394. doi: 10.1016/j.microc.2018.01.037

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Volzhenin, Artem V. ; Petrova, Natalya I. ; Medvedev, Nickolay S. и др. / Multiple probe concentrating of Au and Pd in geological samples for atomic absorption determination with two-stage probe atomization. в: Microchemical Journal. 2018 ; Том 138. стр. 390-394.

BibTeX

@article{c885a837c2f549b0a5ce99fcb582825c,
title = "Multiple probe concentrating of Au and Pd in geological samples for atomic absorption determination with two-stage probe atomization",
abstract = "The two-stage probe atomization (TPA) technique for Au and Pd determination in geological samples by graphite furnace atomic absorption spectrometry (GFAAS) has been developed. Making use of TPA permitted Au and Pd determination in rocks and ores in the form of suspensions obtained by partial sample digestion in aqua regia. Concentrating of analytes on tungsten probe decreases matrix effects and relieves from the necessity of full sample digestion or preparatory matrix removing like extraction or sorption, reducing an analysis time from a few days to an hour and a half. The analytical signal dependence on number of concentrating cycles has been studied. Multiple concentrating of analytes on tungsten probe surface decreased limits of detection by 5 times compared with earlier results in TPA-GFAAS and expanded the range of Au and Pd concentrations which can be determined in rocks and ores by this technique. The achievable detection limits were found to be 3 × 10−3 and 7 × 10−3 μg/g for Au and Pd, respectively. The accuracy of method was confirmed by analyses of certified reference materials (CRMs) using the standard addition method. The relative standard deviation for 0.64 μg/g Au concentration was 6.0% and 6.5% for 0.30 μg/g Pd concentration (n = 5). The rapidness of the technique makes it rather important for industrial interest.",
keywords = "PLATINUM-GROUP METALS, GOLD, SPECTROMETRY, EXTRACTION, SEPARATION, ROCKS, ORES, AAS",
author = "Volzhenin, {Artem V.} and Petrova, {Natalya I.} and Medvedev, {Nickolay S.} and Saprykin, {Anatoly I.}",
year = "2018",
month = may,
day = "1",
doi = "10.1016/j.microc.2018.01.037",
language = "English",
volume = "138",
pages = "390--394",
journal = "Microchemical Journal",
issn = "0026-265X",
publisher = "Elsevier Science Inc.",

}

RIS

TY - JOUR

T1 - Multiple probe concentrating of Au and Pd in geological samples for atomic absorption determination with two-stage probe atomization

AU - Volzhenin, Artem V.

AU - Petrova, Natalya I.

AU - Medvedev, Nickolay S.

AU - Saprykin, Anatoly I.

PY - 2018/5/1

Y1 - 2018/5/1

N2 - The two-stage probe atomization (TPA) technique for Au and Pd determination in geological samples by graphite furnace atomic absorption spectrometry (GFAAS) has been developed. Making use of TPA permitted Au and Pd determination in rocks and ores in the form of suspensions obtained by partial sample digestion in aqua regia. Concentrating of analytes on tungsten probe decreases matrix effects and relieves from the necessity of full sample digestion or preparatory matrix removing like extraction or sorption, reducing an analysis time from a few days to an hour and a half. The analytical signal dependence on number of concentrating cycles has been studied. Multiple concentrating of analytes on tungsten probe surface decreased limits of detection by 5 times compared with earlier results in TPA-GFAAS and expanded the range of Au and Pd concentrations which can be determined in rocks and ores by this technique. The achievable detection limits were found to be 3 × 10−3 and 7 × 10−3 μg/g for Au and Pd, respectively. The accuracy of method was confirmed by analyses of certified reference materials (CRMs) using the standard addition method. The relative standard deviation for 0.64 μg/g Au concentration was 6.0% and 6.5% for 0.30 μg/g Pd concentration (n = 5). The rapidness of the technique makes it rather important for industrial interest.

AB - The two-stage probe atomization (TPA) technique for Au and Pd determination in geological samples by graphite furnace atomic absorption spectrometry (GFAAS) has been developed. Making use of TPA permitted Au and Pd determination in rocks and ores in the form of suspensions obtained by partial sample digestion in aqua regia. Concentrating of analytes on tungsten probe decreases matrix effects and relieves from the necessity of full sample digestion or preparatory matrix removing like extraction or sorption, reducing an analysis time from a few days to an hour and a half. The analytical signal dependence on number of concentrating cycles has been studied. Multiple concentrating of analytes on tungsten probe surface decreased limits of detection by 5 times compared with earlier results in TPA-GFAAS and expanded the range of Au and Pd concentrations which can be determined in rocks and ores by this technique. The achievable detection limits were found to be 3 × 10−3 and 7 × 10−3 μg/g for Au and Pd, respectively. The accuracy of method was confirmed by analyses of certified reference materials (CRMs) using the standard addition method. The relative standard deviation for 0.64 μg/g Au concentration was 6.0% and 6.5% for 0.30 μg/g Pd concentration (n = 5). The rapidness of the technique makes it rather important for industrial interest.

KW - PLATINUM-GROUP METALS

KW - GOLD

KW - SPECTROMETRY

KW - EXTRACTION

KW - SEPARATION

KW - ROCKS

KW - ORES

KW - AAS

UR - http://www.scopus.com/inward/record.url?scp=85047238143&partnerID=8YFLogxK

U2 - 10.1016/j.microc.2018.01.037

DO - 10.1016/j.microc.2018.01.037

M3 - Article

AN - SCOPUS:85047238143

VL - 138

SP - 390

EP - 394

JO - Microchemical Journal

JF - Microchemical Journal

SN - 0026-265X

ER -

ID: 17410419