At present, immediate monitoring urinary arsenic is still a challenge for treating arsenic poisoning patients. Thus, a fast, reliable and accurate analytical approach is indispensable to monitor ultratrace arsenic in… Click to show full abstract
At present, immediate monitoring urinary arsenic is still a challenge for treating arsenic poisoning patients. Thus, a fast, reliable and accurate analytical approach is indispensable to monitor ultratrace arsenic in urine sample for health warning. In this work, a silicon nitride (SN) rod was first integrally utilized as a sample carrier for ≤50 μL urinary aliquot, an electric heater for removing water and ashing sample as well as a high voltage electrode for dielectric barrier discharge vaporization (DBDV). The direct analytical method of arsenic in urine without sample digestion was thus developed using atomic fluorescence spectrometer (AFS) as a model detector. After 4 V electrically heating the SN rod for 60 s, urine sample was dehydrated and ashed outside; then, DBD was exerted under 0.8 A with 0.8 L/min H2 + Ar (1:9, v:v) for 20 s to vaporize arsenic analyte from the SN rod. After optimization, 0.014 μg/L arsenic detection limit (LOD) was reached with favorable analytical precision (RSD <5%) and accuracy (91-110% recoveries) for real sample analysis. As a result, the whole analysis process only consumes <3 min to exclude complicated sample preparation; furthermore, the designed DBDV system only occupies 25 W and <2 kg, which renders a miniature sampling component to hyphenate with a miniature detector to detect arsenic. Thus, this direct sampling DBDV method extremely fulfills the fast, sensitive and precise detection of ultratrace arsenic in urine sample.
               
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