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Photolysis of 3-Nitro-1,2,4-triazol-5-one: Mechanisms and Products
[Image: see text] Insensitive munitions formulations that include 3-nitro-1,2,4-triazol-5-one (NTO) are replacing traditional explosive compounds. While these new formulations have superior safety characteristics, the compounds have greater environmental mobility, raising concern over potential cont...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012174/ https://www.ncbi.nlm.nih.gov/pubmed/36936519 http://dx.doi.org/10.1021/acsestwater.2c00567 |
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author | Schroer, Hunter W. Londono, Esteban Li, Xueshu Lehmler, Hans-Joachim Arnold, William Just, Craig L. |
author_facet | Schroer, Hunter W. Londono, Esteban Li, Xueshu Lehmler, Hans-Joachim Arnold, William Just, Craig L. |
author_sort | Schroer, Hunter W. |
collection | PubMed |
description | [Image: see text] Insensitive munitions formulations that include 3-nitro-1,2,4-triazol-5-one (NTO) are replacing traditional explosive compounds. While these new formulations have superior safety characteristics, the compounds have greater environmental mobility, raising concern over potential contamination and cleanup of training and manufacturing facilities. Here, we examine the mechanisms and products of NTO photolysis in simulated sunlight to further inform NTO degradation in sunlit surface waters. We demonstrate that NTO produces singlet oxygen and that dissolved oxygen increases the NTO photolysis rate in deionized water. The rate of NTO photolysis is independent of concentration and decreases slightly in the presence of Suwannee River Natural Organic Matter. The apparent quantum yield of NTO generally decreases as pH increases, ranging from 2.0 × 10(–5) at pH 12 to 1.3 × 10(–3) at pH 2. Bimolecular reaction rate constants for NTO with singlet oxygen and hydroxyl radical were measured to be (1.95 ± 0.15) × 10(6) and (3.28 ± 0.23) × 10(10) M(–1) s(–1), respectively. Major photolysis reaction products were ammonium, nitrite, and nitrate, with nitrite produced in nearly stoichiometric yield upon the reaction of NTO with singlet oxygen. Environmental half-lives are predicted to span from 1.1 to 5.7 days. Taken together, these data enhance our understanding of NTO photolysis under environmentally relevant conditions. |
format | Online Article Text |
id | pubmed-10012174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100121742023-03-15 Photolysis of 3-Nitro-1,2,4-triazol-5-one: Mechanisms and Products Schroer, Hunter W. Londono, Esteban Li, Xueshu Lehmler, Hans-Joachim Arnold, William Just, Craig L. ACS ES T Water [Image: see text] Insensitive munitions formulations that include 3-nitro-1,2,4-triazol-5-one (NTO) are replacing traditional explosive compounds. While these new formulations have superior safety characteristics, the compounds have greater environmental mobility, raising concern over potential contamination and cleanup of training and manufacturing facilities. Here, we examine the mechanisms and products of NTO photolysis in simulated sunlight to further inform NTO degradation in sunlit surface waters. We demonstrate that NTO produces singlet oxygen and that dissolved oxygen increases the NTO photolysis rate in deionized water. The rate of NTO photolysis is independent of concentration and decreases slightly in the presence of Suwannee River Natural Organic Matter. The apparent quantum yield of NTO generally decreases as pH increases, ranging from 2.0 × 10(–5) at pH 12 to 1.3 × 10(–3) at pH 2. Bimolecular reaction rate constants for NTO with singlet oxygen and hydroxyl radical were measured to be (1.95 ± 0.15) × 10(6) and (3.28 ± 0.23) × 10(10) M(–1) s(–1), respectively. Major photolysis reaction products were ammonium, nitrite, and nitrate, with nitrite produced in nearly stoichiometric yield upon the reaction of NTO with singlet oxygen. Environmental half-lives are predicted to span from 1.1 to 5.7 days. Taken together, these data enhance our understanding of NTO photolysis under environmentally relevant conditions. American Chemical Society 2023-02-02 /pmc/articles/PMC10012174/ /pubmed/36936519 http://dx.doi.org/10.1021/acsestwater.2c00567 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Schroer, Hunter W. Londono, Esteban Li, Xueshu Lehmler, Hans-Joachim Arnold, William Just, Craig L. Photolysis of 3-Nitro-1,2,4-triazol-5-one: Mechanisms and Products |
title | Photolysis of
3-Nitro-1,2,4-triazol-5-one:
Mechanisms and Products |
title_full | Photolysis of
3-Nitro-1,2,4-triazol-5-one:
Mechanisms and Products |
title_fullStr | Photolysis of
3-Nitro-1,2,4-triazol-5-one:
Mechanisms and Products |
title_full_unstemmed | Photolysis of
3-Nitro-1,2,4-triazol-5-one:
Mechanisms and Products |
title_short | Photolysis of
3-Nitro-1,2,4-triazol-5-one:
Mechanisms and Products |
title_sort | photolysis of
3-nitro-1,2,4-triazol-5-one:
mechanisms and products |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012174/ https://www.ncbi.nlm.nih.gov/pubmed/36936519 http://dx.doi.org/10.1021/acsestwater.2c00567 |
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