Method for measuring contents of chromium, nickel, arsenic, selenium, cadmium, mercury and lead in urine
A determination method and technology of lead content, applied in the field of urine collection, analysis and detection, and determination of trace elements in urine
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example 1
[0058] 1. Instruments and reagents: Inductively coupled plasma: Agilent, 7500A inductively coupled plasma mass spectrometer; Mars 5 microwave digestion instrument (CEM, USA), equipped with PTFE high-pressure closed digestion tank; electronic balance, CP225D, with a sensitivity of 0.0001g (Sartorius AG company); argon: 99.99% pure;
[0059] Ultra-pure water. Concentrated nitric acid with a mass percentage of 65% and hydrogen peroxide with a mass percentage of 30% are chromatographically pure; mixed standard and mercury standard (10.0 mg / L, Agilent, USA).
[0060] 2. Sample treatment: Take 10 mL of urine in a polypropylene bucket, put it into a microwave digestion tank, and then put it into a microwave digestion apparatus for microwave digestion. (The maximum liquid in the digestion tank is ?) Put 1 mL of 30% (v / v) hydrogen peroxide and 2.5 mL of 65% concentrated nitric acid into the digestion tank in turn, and then put it into the microwave digestion instrument, using the se...
example 2
[0065] As described in Example 1, the smoking volunteer urine sample numbered B was selected, and the total amount of heavy metals in the 24-hour urine sample was measured as follows:
[0066] chromium nickel arsenic selenium cadmium HG lead µg µg µg µg µg µg µg 21.1443 8.8386 29.9560 21.9138 0.4376 0.2620 3.2630
example 3
[0068] As described in Example 1, the smoking volunteer urine sample numbered C was selected, and the total level of heavy metals in the 24-hour urine sample was measured as follows:
[0069] chromium nickel arsenic selenium cadmium HG lead µg µg µg µg µg µg µg 38.0987 2.4883 12.2719 15.0335 0.7927 0.7445 2.3468
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