1999
DOI: 10.1080/10426509908031618
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Thermal Degradation of Bis (2-Chloroethyl) Sulfide (Mustard Gas)

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Cited by 17 publications
(13 citation statements)
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“…While the exact mechanism varies based on the simulant, both CEES and TEP are primarily decomposed by a pericyclic reaction, which results in the expulsion of ethylene. 38 40 It is posited that the combustion of the ethylene formed allows the reaction to progress by continually adding energy to the system, until the simulant is fully consumed.…”
Section: Resultsmentioning
confidence: 99%
“…While the exact mechanism varies based on the simulant, both CEES and TEP are primarily decomposed by a pericyclic reaction, which results in the expulsion of ethylene. 38 40 It is posited that the combustion of the ethylene formed allows the reaction to progress by continually adding energy to the system, until the simulant is fully consumed.…”
Section: Resultsmentioning
confidence: 99%
“…The characteristic resonances at the 23 and 37 ppm chemical shifts were not seen, which suggested that any 1-(2-hydroxyethyl)-1,4-dithianium formed and reacted quickly. An additional mechanism for the formation of 1,4-dithiane from sulfur mustard is via the intermediates H-H (45, 44, 43, 38, 35, 28 ppm), Q (43, 34, 32 ppm), and S(CH 2 CH 2 ) 2 S + CH 2 CH 2 Cl, 1-(2-chloroethyl)-1,4-dithianium (38, 37, 43, 23 ppm) (Scheme 6) [28]. The characteristic resonances for the S(CH 2 CH 2 ) 2 S + CH 2 CH 2 Cl at the 23 and 38 ppm chemical shifts were not seen, thus any formed would have reacted quickly.…”
Section: Sulfonium Ion Formation and Decompositionmentioning
confidence: 98%
“…Wagner et al [28] studied the thermal degradation of sulfur mustard with and without water, finding that the "dry degradation" products were 1,2-dichloroethane, polysulfides Q (ClCH 2 CH 2 SCH 2 CH 2 SCH 2 CH 2 Cl), and 1,4-dithiane, whereas the "moist degradation" products were 1,4-oxathiane, 2-chloroethanol, and numerous sulfonium ions, including the major product S(CH 2 CH 2 ) 2 S + CH 2 CH 2 Cl and the minor product O(CH 2 CH 2 ) 2 S + CH 2 CH 2 OH.…”
Section: Introductionmentioning
confidence: 97%
“…Under these operating conditions, other unidentified reaction products were also observed in addition to mentioned light organic products. The available tests show that other decomposition products may also be obtained during the pyrolysis of sulfur mustard, which may include carbon disulfide, 1,2-dichloroethane, thiophene and methylthiophene (Faragher et al 1928;Wagner et al 1999;Battin-Leclerc et al 2000).…”
Section: Pyrolysismentioning
confidence: 99%