Table 1.
France | Germany | Japan | |
---|---|---|---|
Sample preparation | Samples (300 μl) were transferred into a 13-ml polypropylene tube and mixed with 2,700 μl dilution solution. Dilution solution was made by adding 10 ml 25% NH4OH, 250 mg EDTA dipotassium salt and 250 μl Triton X-100 into a volumetric flask and filled up to 500 ml with double distilled water. |
Samples (300 μl) were transferred into a 13-ml polypropylene tube and mixed with 2,700 μl dilution solution. Dilution solution was made by adding 10 ml 25% NH4OH, 250 mg EDTA dipotassium salt and 250 μl Triton X-100 into a volumetric flask and filled up to 500 ml with double distilled water. |
Samples (200 μl) were diluted (1:19) with the dilution solution and vortex mixed. Dilution solution consisted of 2% v/v butan-1-ol, 0.1% TMAH, 0.5 g l−1 POE and 0.5 g l−1 H4EDTA |
Instrumental analysis | ICP-MS (Agilent 7500) with ASX 500 auto-sampler | ICP-DRC-MS (Agilent 7500cx) with ASX 500 auto-sampler | ICP-MS (Agilent 7700 ICP-MS) with auto-sampler |
Calibration and calculation | External calibration was used. The limit of quantitation was 0.15 μg l−1. | External calibration was used. The limit of quantitation was 0.15 μg l−1. | External calibration was used. The limit of quantitation was 0.14 μg l−1. |