Method development for forensic oil identification by direct analysis in real time time-of-flight mass spectrometry
文献情報
Krishnaja Tikkisetty, Taylor Filewood, Jeffrey Yan, Honoria Kwok, Pamela Brunswick, Robert Cody, Dayue Shang
The current well-established chromatography and mass spectrometry based oil spill identification procedures, such as those outlined by the European Committee for Standardization, are highly reliable as methods, highly defensible in the court of law, and widely applicable to the majority of oil spill situations. Nevertheless, the methodology is time consuming and labour intensive, which may not be ideal when dealing with an emergency oil spill situation. In this study, direct analysis in real time time-of-flight mass spectrometry (DART/TOFMS) was used to successfully develop an efficient oil identification method. To confirm the accuracy of this method spilled oil samples were tested from five previous years of blind round robin testing organized by the oil spill identification network of experts (OSINET) under the Bonn Agreement. Heatmap inspection, principal component analysis and finally discriminant analysis of principal components were used to arrive at final predictions regarding the identities of the spilled oil samples. The results were compared with the results of previous gas chromatography flame ionization detection (GC/FID) and gas chromatography triple quadrupole mass spectrometry (GC/MS/MS) analyses of the same oils. While taking only about a tenth of the time, the DART/TOFMS analysis produced results similar to those of classical GC/FID and GC/MS/MS (EI+) procedures. The ability of DART/TOFMS to display this level of validity exemplifies its potential to be a new tool for supplementing classical analyses for oil spill forensics.
おすすめジャーナル

Drug Discovery Today

Journal of Natural Medicines

Journal of Peptide Science

Russian Journal of General Chemistry

Crystallography Reports

New Journal of Chemistry

Chemical Communications

Current Opinion in Colloid & Interface Science

Organic Process Research & Development

Russian Journal of Bioorganic Chemistry
関連文献
Core cross-linked star (CCS) polymers with temperature and salt dual responsiveness: synthesis, formation of high internal phase emulsions (HIPEs) and triggered demulsification
Qijing Chen, Yuanyuan Xu, Xueteng Cao, Lianjie Qin, Zesheng An
DOI: 10.1039/C3PY00942D
Facile synthesis of chain end functionalized polyethylenes via epoxide ring-opening and thiol–ene addition click chemistry
Huayi Li, Jin-Yong Dong, Youliang Hu
DOI: 10.1039/C3PY00727H
Porphyrin-containing hyperbranched supramolecular polymers: enhancing 1O2-generation efficiency by supramolecular polymerization
Yiliu Liu, Zehuan Huang, Kai Liu, Hans Kelgtermans, Wim Dehaen, Zhiqiang Wang, Xi Zhang
DOI: 10.1039/C3PY01036H
Introduction of self-healing properties into covalent polymer networks via the photodissociation of alkoxyamine junctions
Siham Telitel, Yoshifumi Amamoto, Julien Poly, Fabrice Morlet-Savary, Olivier Soppera, Jacques Lalevée, Krzysztof Matyjaszewski
DOI: 10.1039/C3PY01162C
The synthesis and characterization of supramolecular elastomers based on linear carboxyl-terminated polydimethylsiloxane oligomers
Lin Yang, Yaling Lin, Lianshi Wang, Anqiang Zhang
DOI: 10.1039/C3PY01005H
RAFT/MADIX (co)polymerization of vinyl trifluoroacetate: a means to many ends
Jean-Daniel Marty, Mathias Destarac
DOI: 10.1039/C3PY01109G
Synthesis of high molar mass poly(n-butyl acrylate) and poly(2-ethylhexyl acrylate) by SET-LRP in mixtures of fluorinated alcohols with DMSO
Shampa R. Samanta, Virgil Percec
DOI: 10.1039/C3PY01008B
Combining oxyanionic polymerization and click-chemistry: a general strategy for the synthesis of polyether polyol macromonomers
Anja Thomas, Kerstin Niederer, Frederik Wurm, Holger Frey
DOI: 10.1039/C3PY01078C
A comparative study of polymers containing naphthodifuranone and benzodifuranone units in the main chain
Haichang Zhang, Jun Zhang, Bernd Tieke
DOI: 10.1039/C3PY01101A
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...
掲載誌
Analytical Methods

Analytical Methods welcomes early applications of new analytical and bioanalytical methods and technology demonstrating the potential for societal impact. We require that methods and technology reported in the journal are sufficiently innovative, robust, accurate, and compared to other available methods for the intended application. Developments with interdisciplinary approaches are particularly welcome. Systems should be proven with suitably complex and analytically challenging samples. We encourage developments within, but not limited to, the following technologies and applications: global health, point-of-care and molecular diagnostics biosensors and bioengineering drug development and pharmaceutical analysis applied microfluidics and nanotechnology omics studies, such as proteomics, metabolomics or glycomics environmental, agricultural and food science neuroscience biochemical and clinical analysis forensic analysis industrial process and method development

![[(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure](https://static.chemtradehub.com/structs/100/100431-55-8-7104.webp)
![N-[2-(4-Hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide structure N-[2-(4-Hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide structure](https://static.chemtradehub.com/structs/109/109032-22-6-7c88.webp)

