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dc.contributor.authorSu, Rui
dc.contributor.authorYu, Wenjing
dc.contributor.authorSun, Kaiju
dc.contributor.authorYang, Jie
dc.contributor.authorChen, Changbao
dc.contributor.authorLian, Wenhui
dc.contributor.authorLiu, Shuying
dc.contributor.authorYang, Hongmei
dc.date.accessioned2021-09-20T17:30:50Z
dc.date.available2021-09-20T17:30:50Z
dc.date.issued2019-02-19
dc.identifier.urihttps://hdl.handle.net/1721.1/131896
dc.description.abstractAbstract An innovative strategy for sustainably active oxygen capture using nitrogen (N2) instead of helium (He) as direct analysis in real-time (DART) gas is demonstrated in this work. DART MS was carried out to analyze different polarity compounds including organophosphorus pesticides, amino acids, hormones, and poly brominated diphenyl ethers by using He and N2 as DART gas, respectively. The unexpectedly characteristic ionization reactions, including replacement reaction where the sulfur atom of P=S group, were replaced by oxygen atom, oxidation ([M + nO + H]+ or [M + nO-H]− (n = 1, 2, 3, 4, 5)), and hydrogen loss (loss of two hydrogens) rapidly occurred in situ in the presence of N2 under ambient conditions without any additives. The reaction mechanisms were proposed and further confirmed by high-resolution tandem mass spectrometry. Our study under high temperature and high voltage provides a powerful tool for generating unique ionic species that may be difficult to form by other means, which also creates favorable conditions for the future study of the mechanism of DART MS. Graphical Abstracten_US
dc.publisherSpringer USen_US
dc.relation.isversionofhttps://doi.org/10.1007/s13361-019-02132-7en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSpringer USen_US
dc.titleThe Ion Source of Nitrogen Direct Analysis in Real-Time Mass Spectrometry as a Highly Efficient Reactor: Generation of Reactive Oxygen Speciesen_US
dc.typeArticleen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-09-24T21:48:11Z
dc.language.rfc3066en
dc.rights.holderAmerican Society for Mass Spectrometry
dspace.embargo.termsY
dspace.date.submission2020-09-24T21:48:11Z
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


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