Determination Systems of Nb and Ta in Geochemical Samples and Rare Earth ores by ICP-MS and ICP-AES

A method to deal with the conditions of incomplete digestion of geological samples, and the complexity of the analysis for present technologies, along with the routine methods of wet digestion on constant temperature electric heating plate with mixed acids and Na2O2 fusion pre-treatment method and t...

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Main Author: GAO Hui-yan
Format: Article
Language:English
Published: Science Press, PR China 2014-05-01
Series:Yankuang ceshi
Subjects:
Online Access:http://www.ykcs.ac.cn/cn/article/id/ba9800ad-b710-4e6e-889a-ca64ab436357
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author GAO Hui-yan
author_facet GAO Hui-yan
author_sort GAO Hui-yan
collection DOAJ
description A method to deal with the conditions of incomplete digestion of geological samples, and the complexity of the analysis for present technologies, along with the routine methods of wet digestion on constant temperature electric heating plate with mixed acids and Na2O2 fusion pre-treatment method and to ease the hydrolysis of Nb and Ta are describe in this paper. Both Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) and Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) were applied to establish two sets of analysis methods which can be used to detect the contents of Nb and Ta in geochemical exploration samples and rare earth ores. Wet digestion on constant temperature electric heating plate is suitable for low content and easy decomposition of samples with nitric acid-hydrofluoric acid-sulfuric acid by ICP-MS. Na2O2 fusion pre-treatment method is suitable for high content and insoluble samples by using ICP-AES. Through the analysis of a series of national certified reference samples of soil, stream sediments, rocks and rare earth ores, the results show that mixed acid pre-treatment coupled with ICP-MS had a linear range of 0-200 ng/mL and detection limits of Nb and Ta were 0.01 μg/g and 0.05 μg/g, respectively. The relative error was less than 10%, and the relative standard deviation (RSD) was less than 6%. The Na2O2 fusion pre-treatment coupled with ICP-AES had a linear range of 0-30 μg/mL, detection limits of Nb and Ta were 0.2 μg/g and 2.5 μg/g, respectively. The relative error was less than 10%, and the precision (RSD) was less than 7%. The two sets of analysis method satisfy the demand of analysis of Nb and Ta in samples with a complex matrix, a large range of content and large quantities of samples.
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spelling doaj.art-44862a30aa0449419015d21ea9cd5c172023-02-09T07:01:16ZengScience Press, PR ChinaYankuang ceshi0254-53572014-05-01333312320ykcs-33-3-312Determination Systems of Nb and Ta in Geochemical Samples and Rare Earth ores by ICP-MS and ICP-AESGAO Hui-yan0China Railway Resources Central Laboratory, Langfang 065000, ChinaA method to deal with the conditions of incomplete digestion of geological samples, and the complexity of the analysis for present technologies, along with the routine methods of wet digestion on constant temperature electric heating plate with mixed acids and Na2O2 fusion pre-treatment method and to ease the hydrolysis of Nb and Ta are describe in this paper. Both Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) and Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) were applied to establish two sets of analysis methods which can be used to detect the contents of Nb and Ta in geochemical exploration samples and rare earth ores. Wet digestion on constant temperature electric heating plate is suitable for low content and easy decomposition of samples with nitric acid-hydrofluoric acid-sulfuric acid by ICP-MS. Na2O2 fusion pre-treatment method is suitable for high content and insoluble samples by using ICP-AES. Through the analysis of a series of national certified reference samples of soil, stream sediments, rocks and rare earth ores, the results show that mixed acid pre-treatment coupled with ICP-MS had a linear range of 0-200 ng/mL and detection limits of Nb and Ta were 0.01 μg/g and 0.05 μg/g, respectively. The relative error was less than 10%, and the relative standard deviation (RSD) was less than 6%. The Na2O2 fusion pre-treatment coupled with ICP-AES had a linear range of 0-30 μg/mL, detection limits of Nb and Ta were 0.2 μg/g and 2.5 μg/g, respectively. The relative error was less than 10%, and the precision (RSD) was less than 7%. The two sets of analysis method satisfy the demand of analysis of Nb and Ta in samples with a complex matrix, a large range of content and large quantities of samples.http://www.ykcs.ac.cn/cn/article/id/ba9800ad-b710-4e6e-889a-ca64ab436357geochemical exploration samplesrare earth oresnbtaconstant temperature-electric heating plate digestionna2o2 fusioninductively coupled plasma-mass spectrometryinductively coupled plasma-atomic emission spectrometry
spellingShingle GAO Hui-yan
Determination Systems of Nb and Ta in Geochemical Samples and Rare Earth ores by ICP-MS and ICP-AES
Yankuang ceshi
geochemical exploration samples
rare earth ores
nb
ta
constant temperature-electric heating plate digestion
na2o2 fusion
inductively coupled plasma-mass spectrometry
inductively coupled plasma-atomic emission spectrometry
title Determination Systems of Nb and Ta in Geochemical Samples and Rare Earth ores by ICP-MS and ICP-AES
title_full Determination Systems of Nb and Ta in Geochemical Samples and Rare Earth ores by ICP-MS and ICP-AES
title_fullStr Determination Systems of Nb and Ta in Geochemical Samples and Rare Earth ores by ICP-MS and ICP-AES
title_full_unstemmed Determination Systems of Nb and Ta in Geochemical Samples and Rare Earth ores by ICP-MS and ICP-AES
title_short Determination Systems of Nb and Ta in Geochemical Samples and Rare Earth ores by ICP-MS and ICP-AES
title_sort determination systems of nb and ta in geochemical samples and rare earth ores by icp ms and icp aes
topic geochemical exploration samples
rare earth ores
nb
ta
constant temperature-electric heating plate digestion
na2o2 fusion
inductively coupled plasma-mass spectrometry
inductively coupled plasma-atomic emission spectrometry
url http://www.ykcs.ac.cn/cn/article/id/ba9800ad-b710-4e6e-889a-ca64ab436357
work_keys_str_mv AT gaohuiyan determinationsystemsofnbandtaingeochemicalsamplesandrareearthoresbyicpmsandicpaes