Hydrolysis of Levinstein Mustard (H)

Abstract

Samples of Levinstein mustard (H) were removed from leaking munitions. These samples were labeled "liquid" and "solid," although both samples contained materials of both phases. The samples were analyzed by gas chromatography/mass spectrometry (GC/MS) and were found to contain HD as a minor component in both cases; The liquid sample was analyzed by 13C nuclear magnetic resonance (NMR) and was found to contain thiodiglycol as the single most abundant compound. Liquid and solid samples were hydrolyzed at a concentration of 15% H in water, with subsequent addition of an excess of NaOH. The hydrolysates were extracted with either chloroform, hexane, or cyclohexane and analyzed by GC/MS and in all cases were found to contain no HD at or above the drinking water level of 200 ppb. The GC/MS analysis of the solid sample showed a number of cyclic compounds not found in the liquid hydrolysate. In general, cyclohexane was found to be the preferred solvent for extraction because it provided a better NMR matrix than either hexane or chloroform and cleanly separated the extract from the large mass of high density solids on the bottom of the extract.

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Document Details

Document Type
Technical Report
Publication Date
Aug 01, 2003
Accession Number
ADA418867

Entities

People

  • Dennis K. Rohrbaugh
  • George Wayne Wagner
  • Kenneth B. Sumpter
  • Steven P. Harvey

Organizations

  • Edgewood Chemical Biological Center

Tags

Communities of Interest

  • Counter WMD
  • Ground and Sea Platforms
  • Weapons Technologies

DTIC Thesaurus Topics

  • Alkanes
  • Chemical Synthesis
  • Chemical Warfare Agents
  • Chemical Weapons
  • Chemistry
  • Chlorides
  • Drinking Water
  • Gas Chromatography
  • Hydrolysis
  • Magnetic Resonance
  • Mass Spectra
  • Mass Spectrometry
  • Materials
  • Nuclear Magnetic Resonance
  • Organic Chemistry
  • Spectra
  • Test Methods

Readers

  • Analytical Chemistry
  • Organic Chemistry