Search / Korean Journal of Chemical Engineering
Korean Chemical Engineering Research,
Vol.45, No.3, 291-297, 2007
Sulfur Mustard(HD)의 가수분해
Hydrolysis of Sulfur Mustard(HD) in Water
수포작용제의 일종인 sulfur mustard(HD, bis 2-chloroethylsulfide)를 무해한 물질로 전환하기 위한 공정 운영조건을 찾기 위하여 물에 의한 HD 가수분해 반응을 연구하고 분석절차를 수립하였다. 반응은 2단계로 진행하였다. 먼저, HD 10~20 wt%를 90 ℃ 물에서 2시간 동안 가수분해 한 후 상온에서 가성소다 수용액(2.1 당량)을 주입하면서 반응시간에 따른 HD의 농도변화를 측정하였다. 이 실험조건에서 HD의 분해효율은 99.99% 이상 이었으며 가수분해 후의 최종 분해물질은 thiodiglycol 68 wt%, 1,2-bis(2-hydroxyethylthio)ethane 8 wt% 및 bis(2-hydroxyethylthioethyl)ether 24 wt% 이었다.
The hydrolysis reaction of sulfur mustard(HD, bis 2-chloroethylsulfide), one type of the blister agents was studied in water to find the operation conditions which can convert HD into less toxic compounds. The reaction was proceeded into two steps. First, 10~20 wt% of HD was hydrolyzed in water at 90 ℃ for 2 hr and aqueous sodium hydroxide solution(2.1 eq) was subsequently added to the reaction mixture at room temperature. The efficiency of HD hydrolysis at this experimental conditions was greater than 99.99% and the final degradation products of HD were 68 wt% of thiodiglycol, 8 wt% of 1,2-bis(2-hydroxyethylthio)ethane and 24 wt% of bis(2-hydroxyethylthioethyl)ether.
[References]
  1. Somani SM, Chemical Warfare Agents, CRC Press, Boca Raton, 2001
  2. Fact Sheets, The U.S. Army Chemical Materials Agency(CMA), http://www.cma,army.mil
  3. U. S. National Research Council, “Review and Evaluation of Alternative Technologies for Demilitarization of Assembled Chemical Weapons, Appendix D,” National Academic Press, Washington D.C., USA, 1999
  4. National Research Council, “Interim Design Assessment for the Blue Grass Chemical Agent Destruction Pilot Plant,” National Academic Press, Washington D.C., 2005
  5. Chemical Weapons Convention, Organization for the Prohibition of Chemical Weapons. http://www.opcw.nl
  6. NATO Advanced Research Workshop, Destruction of Chemical Weapons: Report of the NATO Advanced Research Workshop on Destruction of Military Toxic Waste, Naaldwijik, Netherlands, May(1994). http://www.opcw.nl/chemhaz/arwnaal1.htm
  7. Workshop on Advances in the Alternative Demilitarization Technologies, Reston, Virginia, U.S.A., 1995
  8. Lee JC, J. Kor. Soc. Wast. Man., 16(3), 217, 1999
  9. Yang YC, Baker JA, Ward JR, Chem. Rev., 92, 1729, 1992
  10. Yang YC, Szafraniec LL, Beaudry WT, Ward JR, J. Org. Chem., 53, 3293, 1988
  11. Harvey SP, Beaudry WT, Bossell PC, Kolakowski JE, Procell LR, Rohrbaugh DL, Sorrick DC, Stroup AN, Szafraniec LL, Yang YC, Wagner GW, ERDEC-TR-385, Chemical Research, Development and Engineering Center, APG, U.S.A., 1997
  12. Harvey SP, Kolakowski JE, Sumpter KB, Szafraniec LL, Harley MV, Rohrbaugh DK, ECBC-TR-121, Chemical Biologcal Center, APG, U.S.A., 2000
  13. Gupta AK, Dubey DL, Kaushik MP, J. Hazard. Mater., B139, 154, 2007
  14. Lee JC, Lee YH, Park H, Choi SJ, HWAHAK KONGHAK, 41(4), 464, 2003
  15. Yoon Y, Choi HH, Chung ST, Choe S, J. Korean Ind. Eng. Chem., 14(8), 1051, 2003
  16. Lee YH, Lee JC, Hong D, Korean Chem. Eng. Res., 45(2), 172, 2007
  17. Irvine DA, Early JP, Cassidy DP, Harvey SP, Water Sci. Technol., 35(1), 67, 1997
  18. Creasy WR, Stuff JR, Williams B, Morrissey K, Mays J, Duevel R, Durst HD, J. Chromatogr. A, 774, 253, 1997
  19. D’Agostino PA, Hancock JR, Chenier CL, J. Chromatogr. A, 1058, 97, 2004
  20. Hanaoka S, Nomura K, Wada T, J. Chromatogr. A, 1101, 268, 2006