Fast Determination of Rare Earth Elements in Tea Samples by ICP-MS with Modified Oxygen Flask Combustion
被引:2
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作者:
Zhou Zhou
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机构:
Wuhan Inst Technol, Wuhan 430074, Peoples R China
Chinese Acad Sci, Changchun Inst Appl Chem, Changchun 130022, Peoples R ChinaWuhan Inst Technol, Wuhan 430074, Peoples R China
Zhou Zhou
[1
,2
]
Guo Jun-Fang
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机构:
Wuhan Inst Technol, Wuhan 430074, Peoples R ChinaWuhan Inst Technol, Wuhan 430074, Peoples R China
Guo Jun-Fang
[1
]
Duan Tai-Cheng
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机构:
Chinese Acad Sci, Changchun Inst Appl Chem, Changchun 130022, Peoples R ChinaWuhan Inst Technol, Wuhan 430074, Peoples R China
Duan Tai-Cheng
[2
]
Huang Kai-Lun
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机构:
Northeast Normal Univ, Sch Phys, Changchun 130022, Peoples R ChinaWuhan Inst Technol, Wuhan 430074, Peoples R China
Huang Kai-Lun
[3
]
Ning Jia-Gui
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机构:Wuhan Inst Technol, Wuhan 430074, Peoples R China
Ning Jia-Gui
机构:
[1] Wuhan Inst Technol, Wuhan 430074, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Changchun 130022, Peoples R China
[3] Northeast Normal Univ, Sch Phys, Changchun 130022, Peoples R China
A new method for accurate determination of 15 rare earth elements including Y-Lu in tea samples by inductively coupled plasma. mass spectrometry(ICP-MS) was proposed. Sample preparation was based on the modified oxygen flask combustion technique. By using quartz cloth coated with glycerol instead of filter paper as the ignition agent, a total amount of 0. 1 g sample could be completely burned in a 500-mL flask. Key factors affecting the sample preparation effect were systematically investigated, and it was found that the extraction efficiencies of over 90% for all the analytes could be realized with 5 mL of 4% HNO3 + 1% HF (V/V) as the extractant for the combustion residue and the total extraction process could be finished in one minute under sonication, which resulted in a very fast sample preparation procedure that could be completed in less than 3 minutes. The relative standard deviations (RSD) of six parallel determination values were between 2. 7% and 5. 5%, and the detection limits ranged from 0. 001 mg/kg to 0. 006 mg/kg. Three tea standard reference materials were analyzed with the method and the detection results agreed well with the standard values. The method was successfully applied to three real samples analysis.