Interpretation of α-Pinene Mass Spectra in APCI-Like Ambient Mass Spectrometry Using GC-Coupled Atmospheric Pressure Corona Discharge Ionization.

Q3 Physics and Astronomy
Mass spectrometry Pub Date : 2026-01-01 Epub Date: 2026-02-19 DOI:10.5702/massspectrometry.A0190
Ren Ishihara, Daisuke Fukuyama, Kanako Sekimoto
{"title":"Interpretation of α-Pinene Mass Spectra in APCI-Like Ambient Mass Spectrometry Using GC-Coupled Atmospheric Pressure Corona Discharge Ionization.","authors":"Ren Ishihara, Daisuke Fukuyama, Kanako Sekimoto","doi":"10.5702/massspectrometry.A0190","DOIUrl":null,"url":null,"abstract":"<p><p>Ambient mass spectrometry (AMS) enables real-time analysis without sample preparation, yet atmospheric pressure corona discharge ionization (APCI)-like ion sources can oxidize analytes in-source, obscuring spectral interpretation. We investigated α-pinene using atmospheric pressure corona discharge ionization mass spectrometry (APCDI-MS; one of APCI-like AMS) and, when needed, coupled gas chromatography (GC) to separate pre-existing oxidation products from species formed inside the ion source. By comparing adduct formation and product-ion patterns, we show that oxygenated ions from primary (pre-source) and secondary (in-source) oxidation display similar ion formation behavior, notably ready NH<sub>4</sub> <sup>+</sup>-adduct formation, whereas fragment ions rarely form NH<sub>4</sub> <sup>+</sup> adducts. GC-based characterization of in-source oxidation provides features that assist interpretation of APCI-like AMS spectra acquired without chromatography.</p>","PeriodicalId":18243,"journal":{"name":"Mass spectrometry","volume":"15 1","pages":"A0190"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12930354/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mass spectrometry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5702/massspectrometry.A0190","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/19 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Physics and Astronomy","Score":null,"Total":0}
引用次数: 0

Abstract

Ambient mass spectrometry (AMS) enables real-time analysis without sample preparation, yet atmospheric pressure corona discharge ionization (APCI)-like ion sources can oxidize analytes in-source, obscuring spectral interpretation. We investigated α-pinene using atmospheric pressure corona discharge ionization mass spectrometry (APCDI-MS; one of APCI-like AMS) and, when needed, coupled gas chromatography (GC) to separate pre-existing oxidation products from species formed inside the ion source. By comparing adduct formation and product-ion patterns, we show that oxygenated ions from primary (pre-source) and secondary (in-source) oxidation display similar ion formation behavior, notably ready NH4 +-adduct formation, whereas fragment ions rarely form NH4 + adducts. GC-based characterization of in-source oxidation provides features that assist interpretation of APCI-like AMS spectra acquired without chromatography.

用气相色谱耦合大气压电晕放电电离解释apci类环境质谱中α-蒎烯的质谱。
环境质谱法(AMS)无需样品制备即可实现实时分析,但类似大气压电晕放电电离(APCI)的离子源会在源内氧化分析物,从而模糊光谱解释。我们使用常压电晕放电电离质谱法(APCDI-MS,一种类似apci的AMS)研究α-蒎烯,必要时还使用耦合气相色谱法(GC)从离子源内形成的物质中分离出预先存在的氧化产物。通过比较加合物的形成和产物离子的模式,我们发现来自初级(前源)和次级(源内)氧化的氧化离子表现出相似的离子形成行为,特别是ready NH4 +加合物的形成,而片段离子很少形成NH4 +加合物。基于气相色谱的源内氧化表征提供了辅助解释apci样AMS光谱的特征,而无需色谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Mass spectrometry
Mass spectrometry Physics and Astronomy-Instrumentation
CiteScore
1.90
自引率
0.00%
发文量
3
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书