HUANG Hai-bo,SHEN Jia-lin,CHEN Yu,LIU Jian-kun.Simultaneous Determination of Silver, Boron, Tin, Molybdenum and Lead in Geological Samples by Atomic Emission Spectrometer with Full Spectrum[J].Rock and Mineral Analysis,2020,39(4):555-565 |
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Simultaneous Determination of Silver, Boron, Tin, Molybdenum and Lead in Geological Samples by Atomic Emission Spectrometer with Full Spectrum |
Received:September 23, 2019 Revised:January 18, 2020 |
DOI:10.15898/j.cnki.11-2131/td.201909230137 |
Key words: geological sample metal and non-metal elements full spectrum atomic emission spectrometry second fitting analytical line conversion values |
Author Name | Affiliation | E-mail | HUANG Hai-bo | Nanjing Center of Geological Survey, China Geological Survey, Nanjing 210016, China | | SHEN Jia-lin | Nanjing Center of Geological Survey, China Geological Survey, Nanjing 210016, China | sjlilu@163.com | CHEN Yu | Nanjing Center of Geological Survey, China Geological Survey, Nanjing 210016, China | | LIU Jian-kun | Nanjing Center of Geological Survey, China Geological Survey, Nanjing 210016, China | |
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Abstract: |
BACKGROUND: The contents of silver, tin, boron, molybdenum, and lead in geological samples are extremely important for studying the metallogenic regularity and for geochemical prospecting. Current analytical methods rarely determine silver, tin, boron, molybdenum, and lead simultaneously. OBJECTIVES: To establish a method to simultaneously determine silver, tin, boron, molybdenum and lead in geological samples. METHODS: To eliminate the matrix interference, first-class standard materials (rock, soil and water sediments) were used for linear fitting of the synthetic silicate standard materials curve. By setting analytical line conversion values, different analytical line can be used for samples with different contents. RESULTS: The detection limits of silver, tin, boron, molybdenum, and lead were 0.0077μg/g, 0.19μg/g, 0.68μg/g, 0.058μg/g, 0.49μg/g, respectively. The precisions of the method were 3.23%-9.39%. The measured value of national first class standard materials including soil, water sediments and rock by this method was in accordance with standard values, with an absolute value of △logC<0.10. The qualified rates of actual sample were 92%-98%, and the qualified rate of the inspection sample was 100%. CONCLUSIONS: This method is easy to apply and can be used to analyze samples rapidly. It can also be used to avoid contamination during sample dilution. Compared with traditional atomic emission spectrometry that uses a single analytical spectrum line, this method can be used to obtain a value which is closer to the standard value of national standard materials. The detection limit of this method is much lower than the standard value of the specification of testing quality management for geological laboratories. |
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