scholarly journals Chemical Warfare Agent Simulants in Gamble’s Fluid: Is the Fluid Toxic? Can It Be Made Safer by Inclusion of Solid Nanocrystalline Metal Oxides?

2013 ◽  
Vol 2013 ◽  
pp. 1-14 ◽  
Author(s):  
Dennis Karote ◽  
Brandon Walker ◽  
Huaien Dai ◽  
Ramaswamy Krishnamoorthi ◽  
Janis Voo ◽  
...  

The reactions of chemical warfare agent simulants, 2-chloroethyl ethyl sulfide (2-CEES) and di-i-propyl fluoro phosphate (DFP), in fluids have been investigated. Data analyses confirm the major degradation pathway to be hydrolysis of 2-CEES to 2-hydroxyethyl ethyl sulfide, along with minor self-condensation products. Among the three fluids examined, 2-CEES degradation was the fastest in Gamble’s fluid during a 96 h period. Upon addition of Exceptional Hazard Attenuation Materials (EHAMs) to 2-CEES containing Gamble’s fluid, degradation was generally improved during the first 24 h period. The 96 h outcome was similar for fluid samples with or without EHAM 2 and EHAM 4. EHAM 1-added fluid contained only one degradation product, 2-nitroethyl ethyl sulfide. DFP degradation was the slowest in Gamble’s fluid, but was enhanced by the addition of EHAMs. FTIR and solid state31P NMR confirm the destructive adsorption of 2-CEES and DFP by the EHAMs. The results collectively demonstrate that 2-CEES and DFP decompose to various extents in Gamble’s fluid over a 96 h period but the fluid still contains a considerable amount of intact simulant. EHAM 1 appears to be promising for 2-CEES and DFP mitigation while EHAM 2 and EHAM 4 work well for early on concentration reduction of 2-CEES and DFP.

2015 ◽  
Vol 54 (22) ◽  
pp. 10829-10833 ◽  
Author(s):  
Su-Young Moon ◽  
George W. Wagner ◽  
Joseph E. Mondloch ◽  
Gregory W. Peterson ◽  
Jared B. DeCoste ◽  
...  

2020 ◽  
Vol 18 (27) ◽  
pp. 5218-5227
Author(s):  
Beatrice Andrae ◽  
Daniel Bauer ◽  
Patrick Gaß ◽  
Marianne Koller ◽  
Franz Worek ◽  
...  

Cucurbit[7]uril and an acyclic cucurbituril cause the chemical warfare agent VX to preferentially decompose in basic aqueous solution under C–S bond cleavage rather than by the normally preferred hydrolysis of the P–O and P–S bonds.


2019 ◽  
Vol 55 (49) ◽  
pp. 7005-7008 ◽  
Author(s):  
Sergio J. Garibay ◽  
Omar K. Farha ◽  
Jared B. DeCoste

Amine linkers incorporated in Zr-MOFs aid in organophosphorous chemical warfare agent hydrolysis under solely aqueous conditions


1997 ◽  
Vol 15 (4) ◽  
pp. 297-312 ◽  
Author(s):  
Jan E. Kolakowski ◽  
Joseph J. Defrank ◽  
S. P. Harvey ◽  
Linda L. Szafraniec ◽  
William T. Beaudry ◽  
...  

Author(s):  
Bradley Gibbons ◽  
Eamon C. Bartlett ◽  
Meng Cai ◽  
Xiaozhou Yang ◽  
Eric M. Johnson ◽  
...  

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