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 at pH 12 to 1.3 × 10 at pH 2. Bimolecular reaction rate constants for NTO with singlet oxygen and hydroxyl radical were measured to be (1.95 ± 0.15) × 10 and (3.28 ± 0.23) × 10 M s, 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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http://dx.doi.org/10.1021/acsestwater.2c00567 | DOI Listing |
Sci Total Environ
December 2024
Department of Environmental Science, The University of Arizona, 1177 E. 4th Street, Tucson, AZ 85721, USA.
The explosive formulations IMX-101 and IMX-104 are replacing conventional explosives in munitions, making them safer to transport and handle. However, munitions manufacturing and military training can lead to the environmental release of constituent insensitive munitions compounds (IMCs) such as 2,4-dinitroanisole (DNAN), 3-nitro-1,2,4-triazol-5-one (NTO), and nitroguanidine (NQ). These IMCs absorb ultraviolet light and transform photochemically into products with potentially greater toxicity.
View Article and Find Full Text PDFJ Phys Chem A
August 2024
Department of Chemistry, Physics & Atmospheric Sciences, Jackson State University, Jackson, Mississippi 39217, United States.
ACS ES T Water
March 2023
Civil & Environmental Engineering, The University of Iowa, Iowa City, Iowa52242, United States.
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.
View Article and Find Full Text PDFJ Colloid Interface Sci
May 2022
Institute of Petrochemical Technology, Jilin Institute of Chemical Technology, Jilin 132022, PR China. Electronic address:
The design and development of efficient and durable catalysts with visible-light response for photocatalytic hydrogen production and pollutants degradation is considered as one of the most challenging tasks. In present work, a novel CuWS/NiTiO (abbreviated as × CWS/NTO; x = 0.25, 0.
View Article and Find Full Text PDFChemosphere
October 2021
Biosphere 2, University of Arizona, Oracle, AZ, 85721-0158, United States; Department of Environmental Science, University of Arizona, Tucson, AZ, 85721-0038, United States. Electronic address:
New munition compounds have been developed to replace traditional explosives to prevent unintended detonations. However, insensitive munitions (IM) can leave large proportion of unexploded charge in the field, where it is subjected to photodegradation and dissolution in precipitation. The photolytic reactions occurring on the surfaces of IMX-101 and IMX-104 formulations and the subsequent fate of photolytic products in the environment were thoroughly investigated.
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