2020
DOI: 10.1016/j.forsciint.2019.110102
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Chemical attribution of the home-made explosive ETN – Part I: Liquid chromatography-mass spectrometry analysis of partially nitrated erythritol impurities

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Cited by 18 publications
(10 citation statements)
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References 29 publications
(44 reference statements)
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“…This method was used by our lab to prepare SHN, but the recovered product SHN often melted between 44–55 °C, rather than the expected 55 °C. Initially, this was thought to be the result of impurities in the product such as the penta‐ or lower nitrated species, which has been reported with other nitrate esters [11]. Varying synthesis conditions to include different nitration times (4 to 18 hours), reaction temperatures, and recrystallization procedures did not improve the melting point.…”
Section: Resultsmentioning
confidence: 93%
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“…This method was used by our lab to prepare SHN, but the recovered product SHN often melted between 44–55 °C, rather than the expected 55 °C. Initially, this was thought to be the result of impurities in the product such as the penta‐ or lower nitrated species, which has been reported with other nitrate esters [11]. Varying synthesis conditions to include different nitration times (4 to 18 hours), reaction temperatures, and recrystallization procedures did not improve the melting point.…”
Section: Resultsmentioning
confidence: 93%
“…PETN has two known polymorphs that depend on the crystallization technique [28]. Researchers have examined the crystallization of ETN, but to date, no other phases have been observed [9, 11].…”
Section: Resultsmentioning
confidence: 99%
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“…Similar work was performed by Bezemer et al . using HPLC‐MS to investigate the relationship of partially nitrated erythritol impurities to precursors used in the synthesis of ETN [14]. An outcome of our work and Bezemer et al .…”
Section: Introductionmentioning
confidence: 75%
“…High‐pressure liquid chromatography mass spectrometry (HPLC‐MS) is an analytical technique commonly employed for untargeted identification of impurities (i. e. any compounds not specifically screened for) and targeted quantification of impurities (i. e. compounds with known identities that are specifically screened for, often with standards) within substances of interest [3–5]. HPLC‐MS analyses involve the injection of a liquid solution into a separation column.…”
Section: Introductionmentioning
confidence: 99%