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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...

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Autores principales: Schroer, Hunter W., Londono, Esteban, Li, Xueshu, Lehmler, Hans-Joachim, Arnold, William, Just, Craig L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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