journal article·2020-12-30Open access

Capture and Decomposition of the Nerve Agent Simulant, DMCP, Using the Zeolitic Imidazolate Framework (ZIF-8)

Amani M. Ebrahim, Anna M. Plonka, Ning Rui, Sooyeon Hwang, Wesley O. Gordon, Alex Balboa, Sanjaya D. Senanayake, Anatoly I. Frenkel

ACS Applied Materials & Interfaces· Volume 12· Issue 52

Abstract

Understanding mechanisms of decontamination of chemical warfare agents (CWA) is an area of intense research aimed at developing new filtration materials to protect soldiers and civilians in case of state-sponsored or terrorist attack. In this study, we employed complementary structural, chemical, and dynamic probes and in situ data collection, to elucidate the complex chemistry, capture, and decomposition of the CWA simulant, dimethyl chlorophosphonate (DMCP). Our work reveals key details of the reactive adsorption of DMCP and demonstrates the versatility of zeolitic imidazolate framework (ZIF-8) as a plausible material for CWA capture and decomposition. The in situ synchrotron-based powder X-ray diffraction (PXRD) and pair distribution function (PDF) studies, combined with Fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS), zinc K-edge X-ray absorption near edge structure (XANES), and Raman spectroscopies, showed that the unique structure, chemical state, and topology of ZIF-8 enable accessibility, adsorption, and hydrolysis of DMCP into the pores and revealed the importance of linker chemistry and Zn2+ sites for nerve agent decomposition. DMCP decontamination and decomposition product(s) formation were observed by thermogravimetric analysis, FT-IR spectroscopy, and phosphorus (P) K-edge XANES studies. Differential PDF analysis indicated that the average structure of ZIF-8 (at the 30 Å scale) remains unchanged after DMCP dosing and provided information on the dynamics of interactions of DMCP with the ZIF-8 framework. Using in situ PXRD and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), we showed that nearly 90% regeneration of the ZIF-8 structure and complete liberation of DMCP and decomposition products occur upon heating.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Energetic Materials and Combustion · Thermal and Kinetic Analysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York 11794, United States

Chemistry Division, Brookhaven National Laboratory, Upton, New York 11973, United States

Center for Functional Nanomaterials, Electron Microscopy Group, Brookhaven National Laboratory, Upton, New York 11973, United States

U.S. Army Combat Capabilities Development Command Chemical Biological Center, Aberdeen Proving Ground, Maryland 21010, United States

Funding

Army Research Office · Defense Threat Reduction Agency · Army Research Laboratory

References (70)

Show source-provided references
2. 10.1093/bjaceaccp/mkl05210.1093/bjaceaccp/mkl052 ↗
3. 10.1016/j.cbi.2008.05.01510.1016/j.cbi.2008.05.015 ↗
4. 10.4103/0975-7406.6849810.4103/0975-7406.68498 ↗
5. 10.1021/es049144u10.1021/es049144u ↗
6. Lagasse, B. A. Decomposition of Chemical Warfare Agent Simulants Utilizing Pyrolyzed Cotton Balls as Wicks. Master Thesis, Clemson University: South Carolina, 2020.10.1021/acsomega.0c01619 ↗
7. 10.1016/j.susc.2020.12163910.1016/j.susc.2020.121639 ↗
8. 10.1021/acsami.7b0918810.1021/acsami.7b09188 ↗
9. 10.1021/acsami.9b0235410.1021/acsami.9b02354 ↗
10. 10.1080/00032719.2020.176839910.1080/00032719.2020.1768399 ↗
11. 10.1021/jacs.9b0730110.1021/jacs.9b07301 ↗
12. 10.1021/acs.jpcc.7b0007010.1021/acs.jpcc.7b00070 ↗
13. 10.1038/s41598-017-00772-x10.1038/s41598-017-00772-x ↗
14. 10.1016/j.chemphys.2018.11.01310.1016/j.chemphys.2018.11.013 ↗
15. 10.1021/acsami.5b0690510.1021/acsami.5b06905 ↗
16. 10.1021/acsami.9b2083310.1021/acsami.9b20833 ↗
17. 10.1021/acs.chemrev.9b0082810.1021/acs.chemrev.9b00828 ↗
18. 10.1021/acsami.9b1948410.1021/acsami.9b19484 ↗
19. 10.1021/acsami.9b2169310.1021/acsami.9b21693 ↗
20. 10.1021/acsami.9b2015410.1021/acsami.9b20154 ↗
21. 10.1021/acs.jpcc.9b0557410.1021/acs.jpcc.9b05574 ↗
22. 10.1039/C7CS00108H10.1039/C7CS00108H ↗
23. 10.1038/nmat423810.1038/nmat4238 ↗
24. 10.1021/acs.jpclett.9b0311910.1021/acs.jpclett.9b03119 ↗
25. 10.1021/acsami.9b1847810.1021/acsami.9b18478 ↗
26. 10.1021/acsami.9b2224210.1021/acsami.9b22242 ↗
27. 10.1021/ar900116g10.1021/ar900116g ↗
28. 10.1073/pnas.060243910310.1073/pnas.0602439103 ↗
29. 10.1002/chem.20090214410.1002/chem.200902144 ↗
30. 10.1002/anie.20090264310.1002/anie.200902643 ↗
31. 10.1039/c2dt30774j10.1039/c2dt30774j ↗
32. 10.1021/ja403635b10.1021/ja403635b ↗
33. 10.1038/s41467-018-03878-610.1038/s41467-018-03878-6 ↗
34. 10.1021/jz300292y10.1021/jz300292y ↗
35. 10.1039/C5CC10222G10.1039/C5CC10222G ↗
36. 10.1021/acs.jpcc.6b0377210.1021/acs.jpcc.6b03772 ↗
37. 10.1021/acs.chemmater.9b0456510.1021/acs.chemmater.9b04565 ↗
38. 10.1021/cr60290a00310.1021/cr60290a003 ↗
39. 10.3389/fchem.2019.0019510.3389/fchem.2019.00195 ↗
40. 10.1093/nar/26.14.339210.1093/nar/26.14.3392 ↗
41. 10.1021/ja01257a04710.1021/ja01257a047 ↗
42. 10.1038/s41467-019-10357-z10.1038/s41467-019-10357-z ↗
43. 10.1021/ic049868710.1021/ic0498687 ↗
44. 10.1002/jhet.557039020610.1002/jhet.5570390206 ↗
45. 10.1039/dt993000155910.1039/dt9930001559 ↗
46. 10.1016/j.micromeso.2019.10981910.1016/j.micromeso.2019.109819 ↗
47. 10.1039/C6RA07582G10.1039/C6RA07582G ↗
48. 10.1021/ja204757x10.1021/ja204757x ↗
49. 10.1021/ja406081r10.1021/ja406081r ↗
50. 10.1039/C6MH00047A10.1039/C6MH00047A ↗
51. 10.1016/j.mcat.2020.11096510.1016/j.mcat.2020.110965 ↗
52. 10.1021/acsami.9b1949410.1021/acsami.9b19494 ↗
53. 10.1021/acs.jpclett.9b0100210.1021/acs.jpclett.9b01002 ↗
54. 10.1107/S090904950501271910.1107/S0909049505012719 ↗
55. 10.1107/S160057671600045510.1107/S1600576716000455 ↗
56. 10.1107/S002188981300353110.1107/S0021889813003531 ↗
57. 10.1088/0953-8984/19/33/33521910.1088/0953-8984/19/33/335219 ↗
58. 10.1021/acs.jpcc.6b0633710.1021/acs.jpcc.6b06337 ↗
59. 10.1039/C7NR07949D10.1039/C7NR07949D ↗
60. 10.1039/C8SC04044C10.1039/C8SC04044C ↗
61. 10.1039/c2cc33773h10.1039/c2cc33773h ↗
62. 10.1021/jp407792a10.1021/jp407792a ↗
63. 10.1021/jacs.5b0080310.1021/jacs.5b00803 ↗
64. 10.1002/chem.20190259910.1002/chem.201902599 ↗
65. 10.1021/acsami.7b1068210.1021/acsami.7b10682 ↗
66. 10.1021/acsami.7b1090210.1021/acsami.7b10902 ↗
67. 10.1039/C9CE00757A10.1039/C9CE00757A ↗
68. 10.1039/C9CC08724A10.1039/C9CC08724A ↗
69. 10.1021/jp404265s10.1021/jp404265s ↗
70. 10.1021/la301938f10.1021/la301938f ↗