Diluted solution for measuring lead in whole blood by graphite furnace atomic absorption spectrometry
A technology of graphite furnace atom and diluent, which is applied in the field of diluent, can solve the problems of cumbersome operation, excessive blood, and increase the difficulty of clinical examination, etc., and achieve the effect of accurate and reliable measurement method, satisfactory measurement precision and accuracy
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Embodiment 1
[0022] The present invention provides a kind of dilution solution that is used for measuring lead in whole blood by graphite furnace atomic absorption method, and the dilution solution comprises 0.5% HNO3, 0.3% Triton-100, 1.2% NH by volume percentage 4 h 2 PO 4 , and the remainder of the secondary deionized water. The diluent can be obtained by purification or other means to meet higher purity.
[0023] When measuring lead in whole blood, acidify with nitric acid, dilute blood sample with Triton-100 solution as diluent, NH 4 h 2 PO 4 As a matrix modifier, it was determined by graphite furnace atomic absorption spectrophotometry. NH 4 h 2 PO 4 The role of: by optimizing the matrix modifier NH 4 h 2 PO 4 (0.2% ~ 2%), the ashing temperature of lead can be increased to 800 ℃ without loss of lead, which effectively eliminates the background interference in the atomization stage caused by the incomplete ashing of organic matter in the blood sample, reduces the background...
Embodiment 2
[0030] Present embodiment only will illustrate with the different part in embodiment 1, and described diluent comprises HNO3, 0.2% Triton-100, 1.6%NH by volume percentage 4 h 2 PO 4 , and the remainder of the secondary deionized water. Using this diluent to absorb the whole blood sample to test the lead content, the determination error is within 5.5%.
Embodiment 3
[0032] Present embodiment only will illustrate with the different part in embodiment 1, and described diluent comprises HNO3, 0.5% Triton-100, 0.8%NH by volume percentage 4 h 2 PO 4 , and the remainder of the secondary deionized water. Using this diluent to absorb the whole blood sample to test the lead content, the determination error is within 5.5%.
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