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

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<sub>2</sub> moieties and oxygen sites) in the positive mode, which is rarely reported, the high-resolution tandem MS information on precursor ions at <i>m</i>/<i>z</i> 251(+), 254(+), 266(+), and 270(+) and a pair of isomeric ions at <i>m</i>/<i>z</i> 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<sub>2</sub>, and simple inductive cleavage. Additionally, leveraging the sensitivity for nitroaromatics in the negative polarity, negative ions <i>m</i>/<i>z</i> 182(-) and 233(-) are identified as dinitroaniline and dinitronaphthol, respectively, which confirm the secondary hydrolysis pathway of the antioxidant (e.g., <i>N</i>-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.

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Publication Details

Journal
ACS Omega
Published
2024-08-15
DOI
https://doi.org/10.1021/acsomega.4c04923
Primary Topic
Analytical chemistry methods development
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Kitmin Chen, Dali Yang
ACS Omega
Analytical chemistry methods development
article

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

Kitmin Chen, Dali Yang
article en

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<sub>2</sub> moieties and oxygen sites) in the positive mode, which is rarely reported, the high-resolution tandem MS information on precursor ions at <i>m</i>/<i>z</i> 251(+), 254(+), 266(+), and 270(+) and a pair of isomeric ions at <i>m</i>/<i>z</i> 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<sub>2</sub>, and simple inductive cleavage. Additionally, leveraging the sensitivity for nitroaromatics in the negative polarity, negative ions <i>m</i>/<i>z</i> 182(-) and 233(-) are identified as dinitroaniline and dinitronaphthol, respectively, which confirm the secondary hydrolysis pathway of the antioxidant (e.g., <i>N</i>-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.

ACS OmegaVol. 9(34)
Los Alamos National Laboratory (US), Material Sciences (United States) (US)
U.S. Department of Energy, National Nuclear Security Administration, Los Alamos National Laboratory
Clean water and sanitation
Openalex Percentile: Top 88%
Analytical chemistry methods development
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