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Matrix Volatilization ICP-OES And ICP-MS For Trace Elements Analysis In High-Purity Tellurium Materials Научная публикация

Журнал Atomic Spectroscopy
ISSN: 0195-5373
Вых. Данные Год: 2022, Том: 44, Номер: 1, Страницы: 430-436 Страниц : 7 DOI: 10.46770/as.2022.248
Ключевые слова Trace elements analysis, ICP-MS, ICP-AES, high-purity tellurium, preliminary concetration, limits of detection
Авторы Medvedev Nickolay S. 1 , Orlov Nikita A. 1,2 , Saprykin Anatoly I. 1,2
Организации
1 Nikolaev Institute of Inorganic Chemistry, Siberian Branch of Russian Academy of Sciences (NIIC SB RAS)
2 Novosibirsk National Research State University

Реферат: A method for the analysis of high-purity tellurium employing inductively coupled plasma optical emission spectroscopy (ICP-OES) and ICP mass spectrometry (ICP-MS) is proposed, entailing the preliminary concentration of trace elements by matrix volatilization. Vacuum distillation under heating was used for sample matrix volatilization (Te). The effects of temperature and duration of matrix volatilization on analyte loss were carefully studied. The tellurium analysis method involving preliminary concentration of traces by matrix volatilization provides analyte limits of detection (LODs) of up to several tenths of 1 ng g-1 for ICP-OES and up to hundredths of ng g-1 for ICP-MS. It was demonstrated that matrix volatilization improved the analyte LODs by an average of 20–30-fold compared to that attained using conventional ICP-OES and ICP-MS analyses. The accuracy of the proposed method was confirmed by conducting a «spike» experiment that entailed all of the preliminary concentration stages and analysis of a real high-purity tellurium sample.
Библиографическая ссылка: Medvedev N.S. , Orlov N.A. , Saprykin A.I.
Matrix Volatilization ICP-OES And ICP-MS For Trace Elements Analysis In High-Purity Tellurium Materials
Atomic Spectroscopy. 2022. V.44. N1. P.430-436. DOI: 10.46770/as.2022.248 WOS Scopus OpenAlex
Даты:
Поступила в редакцию: 12 дек. 2022 г.
Принята к публикации: 22 дек. 2022 г.
Опубликована online: 23 дек. 2022 г.
Идентификаторы БД:
Web of science: WOS:000905271400002
Scopus: 2-s2.0-85145483469
OpenAlex: W4323287976
Цитирование в БД:
БД Цитирований
OpenAlex 5
Web of science 8
Scopus 7
Альметрики: