| Literature DB >> 27098411 |
Akihiko Okumura1, Yasuaki Takada2, Susumu Watanabe3, Hiroaki Hashimoto3, Naoya Ezawa4, Yasuo Seto5, Yasuo Takayama6,7, Ryoji Sekioka6,7, Shintaro Yamaguchi6,7, Shintaro Kishi6,7, Takafumi Satoh6,7, Tomohide Kondo6,7, Hisayuki Nagashima6,7, Tomoki Nagoya6.
Abstract
We propose detecting a fragment ion (Ph2As(+)) using counter-flow introduction atmospheric pressure chemical ionization ion trap mass spectrometry for sensitive air monitoring of chemical warfare vomiting agents diphenylchloroarsine (DA) and diphenylcyanoarsine (DC). The liquid sample containing of DA, DC, and bis(diphenylarsine)oxide (BDPAO) was heated in a dry air line, and the generated vapor was mixed into the humidified air flowing through the sampling line of a mass spectrometer. Humidity effect on the air monitoring was investigated by varying the humidity of the analyzed air sample. Evidence of the in-line conversion of DA and DC to diphenylarsine hydroxide (DPAH) and then BDPAO was obtained by comparing the chronograms of various ions from the beginning of heating. Multiple-stage mass spectrometry revealed that the protonated molecule (MH(+)) of DA, DC, DPAH, and BDPAO could produce Ph2As(+) through their in-source fragmentation. Among the signals of the ions that were investigated, the Ph2As(+) signal was the most intense and increased to reach a plateau with the increased air humidity, whereas the MH(+) signal of DA decreased. It was suggested that DA and DC were converted in-line into BDPAO, which was a major source of Ph2As(+). Graphical Abstract ᅟ.Entities:
Keywords: Air monitoring; Atmospheric pressure chemical ionization; Chemical warfare agent; Diphenylchloroarsine; Diphenylcyanoarsine; Hydrolysis; In-source fragmentation; Multiple-stage mass spectrometry; Protonation
Year: 2016 PMID: 27098411 DOI: 10.1007/s13361-016-1394-0
Source DB: PubMed Journal: J Am Soc Mass Spectrom ISSN: 1044-0305 Impact factor: 3.109