Materials for the Simultaneous Entrapment and Catalytic Aerobic Oxidative Removal of Sulfur Mustard Simulants
Source abstract
Abstract
Materials that both sequester chemical warfare agents (CWAs) and then catalytically decontaminate the entrapped CWAs are highly sought. This article reports such a system for air-based catalytic removal of the sulfur mustard (HD) simulant, 2-chloroethyl ethyl sulfide (CEES). Hypercrosslinked polymers (HCPs) sequester CEES, and an HCP-embedded oxidation system comprising tribromide, nitrate, and acid (NOxBrxH+) simultaneously catalyzes the aerobic and selective, oxidative conversion of the entrapped CEES to the desired far less-toxic sulfoxide under ambient conditions (air and temperature). (NOxBrxH+) has been incorporated into three HCPs, a fluorobenzene HCP (HCP-F), a methylated HCP (HCP-M), and an HCP with acidic moieties (HCP-A). HCP-A acts as both an absorbing material and a catalytic component due to its acidic side chains. All three HCP/NOxBrxH+ systems work rapidly under these optimally mild conditions. No light or added oxidants are required. The HCP/NOxBrxH+ systems are recyclable.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Pesticide Exposure and Toxicity · Flame retardant materials and properties · Dendrimers and Hyperbranched Polymers
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States
Funding
Defense Threat Reduction Agency
References (28)
Show source-provided references
1. 10.1021/cr00016a00310.1021/cr00016a003 ↗
2. OPCW Fact-Finding Mission Confirms Likely Use of Chlorine in Saraqib, Syria, 2018. https://www.opcw.org/media-centre/news/2018/05/opcw-fact-finding-mission-confirms-likely-use-chlorine-saraqib-syria.
3. 10.1039/C7CC05657E10.1039/C7CC05657E ↗
4. 10.1016/j.molcata.2005.10.00610.1016/j.molcata.2005.10.006 ↗
5. 10.1038/nmat423810.1038/nmat4238 ↗
6. 10.1021/es502981y10.1021/es502981y ↗
7. 10.1021/ie801150y10.1021/ie801150y ↗
8. 10.1021/ie501055g10.1021/ie501055g ↗
9. 10.1021/acsami.7b0920910.1021/acsami.7b09209 ↗
10. 10.1039/B705025A10.1039/B705025A ↗
11. 10.1039/C6RA28131A10.1039/C6RA28131A ↗
12. Lodewyckx P. · 2006 · 7 · 475
13. 10.1039/C7PY00040E10.1039/C7PY00040E ↗
14. 10.1039/C8SC02640H10.1039/C8SC02640H ↗
15. 10.1016/0923-1137(90)90038-610.1016/0923-1137(90)90038-6 ↗
16. 10.1038/s42004-021-00465-710.1038/s42004-021-00465-7 ↗
17. 10.1021/cs200364310.1021/cs2003643 ↗
18. 10.1016/j.jhazmat.2018.11.04510.1016/j.jhazmat.2018.11.045 ↗
19. 10.1016/j.jhazmat.2019.12083010.1016/j.jhazmat.2019.120830 ↗
20. 10.1039/j2970000080210.1039/j29700000802 ↗
21. Kajigaeshi S. · 1995 · 7 · 29
22. 10.1016/j.tet.2004.11.04110.1016/j.tet.2004.11.041 ↗
23. 10.1021/jo001717810.1021/jo0017178 ↗
24. 10.1016/0013-4686(69)85038-310.1016/0013-4686(69)85038-3 ↗
25. 10.1016/j.jelechem.2004.09.02310.1016/j.jelechem.2004.09.023 ↗
26. 10.1016/j.seppur.2017.01.02610.1016/j.seppur.2017.01.026 ↗
27. 10.1016/j.jhazmat.2005.02.01810.1016/j.jhazmat.2005.02.018 ↗
28. 10.1007/s10973-017-6131-910.1007/s10973-017-6131-9 ↗