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串联质谱法阐明硝基增塑剂的后期降解机制

Tandem MS Elucidation of the Late-Stage Degradation Mechanism of Nitroplasticizer.

作者信息

Chen Kitmin, Yang Dali

机构信息

MST-7: Engineered Materials, Material Sciences and Technology Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.

出版信息

ACS Omega. 2024 Aug 15;9(34):36600-36608. doi: 10.1021/acsomega.4c04923. eCollection 2024 Aug 27.

DOI:10.1021/acsomega.4c04923
PMID:39220529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11359627/
Abstract

Understanding the degradation behavior of nitroplasticizer (NP) and the subsequent production of nitro-organics is crucial for both environmental monitoring and material development. A nontargeted approach via LC-QTOF-MS was employed to thoroughly study the degradation mechanism of NP in its late aging stage. Both positive and negative modes of ESI were performed to increase the compound coverage. To shed light on the fragmentation behavior of NP degradants (e.g., compounds containing a high density of NO moieties and oxygen sites) in the positive mode, which is rarely reported, the high-resolution tandem MS information on precursor ions at / 251(+), 254(+), 266(+), and 270(+) and a pair of isomeric ions at / 284(+) was investigated to extract their common diagnostic ions and dissociation channels, including the neutral loss of 2,2-dinitropropanol, nitro-nitrite rearrangement, homolytic cleavage of NO, and simple inductive cleavage. Additionally, leveraging the sensitivity for nitroaromatics in the negative polarity, negative ions / 182(-) and 233(-) are identified as dinitroaniline and dinitronaphthol, respectively, which confirm the secondary hydrolysis pathway of the antioxidant (e.g., -phenyl-2-naphthylamine) postulated in our previous work. In addition to earlier findings, the detection of these eight degradants further supports the evidence of increased acid concentration and aging temperatures in the late-stage NP environment, which contribute to intricate degradation behaviors in different aging environments.

摘要

了解硝基增塑剂(NP)的降解行为以及随后硝基有机物的产生对于环境监测和材料开发都至关重要。采用基于液相色谱-四极杆飞行时间质谱(LC-QTOF-MS)的非靶向方法深入研究NP在老化后期的降解机制。进行了电喷雾电离(ESI)的正、负离子模式以增加化合物覆盖范围。为了阐明正离子模式下NP降解产物(例如含有高密度NO基团和氧位点的化合物)的碎裂行为(这方面报道很少),研究了质荷比为/ 251(+)、254(+)、266(+)、270(+)的前体离子以及一对质荷比为/ 284(+)的同分异构离子的高分辨率串联质谱信息,以提取它们共同的诊断离子和解离通道,包括2,2 - 二硝基丙醇的中性丢失、硝基 - 亚硝酸盐重排、NO的均裂裂解以及简单的诱导裂解。此外,利用负极性下对硝基芳烃的灵敏度,负离子/ 182(-)和233(-)分别被鉴定为二硝基苯胺和二硝基萘酚,这证实了我们之前工作中推测的抗氧化剂(例如 - 苯基 - 2 - 萘胺)的二次水解途径。除了早期的发现外,这八种降解产物的检测进一步支持了NP后期环境中酸浓度增加和老化温度升高的证据,这导致了不同老化环境中复杂的降解行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a8/11359627/dc0933ff5aa7/ao4c04923_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a8/11359627/473100c77d04/ao4c04923_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a8/11359627/1607f920fba1/ao4c04923_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a8/11359627/dc0933ff5aa7/ao4c04923_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a8/11359627/473100c77d04/ao4c04923_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a8/11359627/1607f920fba1/ao4c04923_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a8/11359627/dc0933ff5aa7/ao4c04923_0002.jpg

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本文引用的文献

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