Self-Decontaminating Fibrous Materials Reactive toward Chemical Threats
Source abstract
Abstract
Polymers that possess highly nucleophilic pyrrolidinopyridine (Pyr) and primary amino (vinylamine, VAm) groups were prepared by free-radical copolymerization of N,N-diallylpyridin-4-amine (DAAP) and N-vinylformamide (NVF) followed by acidic hydrolysis of NVF into VAm. The resulting poly(DAAP-co-VAm-co-NVF) copolymers were water-soluble and reacted with water-dispersible polyurethane possessing a high content of unreacted isocyanate groups. Spray-coating of the nylon-cotton (NYCO), rayon, and poly(p-phenylene terephthalamide) (Kevlar 119) fibers pretreated with phosphoric acid resulted in covalent bonding of the polyurethane with the hydroxyl groups on the fiber surface. A second spray-coating of aqueous solutions of poly(DAAP-co-VAm-co-NVF) on the polyurethane-coated fiber enabled formation of urea linkages between unreacted isocyanate groups of the polyurethane layer and the amino groups of poly(DAAP-co-VAm-co-NVF). Fibers with poly(DAAP-co-VAm-co-NVF) attached were compared with fibers modified by adsorption of water-insoluble poly(butadiene-co-pyrrolidinopyridine) (polyBPP) in terms of the stability against polymer leaching in aqueous washing applications. While the fibers modified by attachment of poly(DAAP-co-VAm-co-NVF) exhibited negligible polymer leaching, over 65% of adsorbed polyBPP detached and leached from the fibers within 7 days. Rayon fibers modified by poly(DAAP-co-VAm-co-NVF) were tested for sorption of dimethyl methylphosphonate (DMMP) in the presence of moisture using dynamic vapor sorption technique. Capability of the fibers modified with poly(DAAP-co-VAm-co-NVF) to facilitate hydrolysis of the sorbed DMMP in the presence of moisture was uncovered. The self-decontaminating property of the modified fibers against chemical threats was tested using a CWA simulant diisopropylfluorophosphate (DFP) in aqueous media at pH 8.7. Fibers modified with poly(DAAP-co-VAm-co-NVF) facilitated hydrolysis of DFP with the half-lives up to an order of magnitude shorter than that of the unmodified fibers. The presented polymers and method of multilayer coating can lead to a development of self-decontaminating textiles and other materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Pesticide Exposure and Toxicity · Antimicrobial agents and applications · Flame retardant materials and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States
Surface Measurement Systems, Ltd., Unit 5, Wharfside, Rosemont Road, Alperton, London HA0 4PE, United Kingdom
Funding
Defense Threat Reduction Agency
References (50)
Show source-provided references
1. 10.1021/am200250d10.1021/am200250d ↗
2. Obendorf S. K. · AATCC Review · 2010 · 10 · 44
3. Dolez P. I. · 2013 · 14810.1533/9780857097620.1.148 ↗
4. 10.1039/c2jm16605d10.1039/c2jm16605d ↗
5. 10.1021/ie010034v10.1021/ie010034v ↗
6. 10.1002/1521-3765(20020603)8:11<2602::AID-CHEM2602>3.0.CO;2-310.1002/1521-3765(20020603)8:11<2602::AID-CHEM2602>3.0.CO;2-3 ↗
7. 10.1021/ie010732f10.1021/ie010732f ↗
8. 10.1002/adma.20040066010.1002/adma.200400660 ↗
9. 10.1021/ie801223b10.1021/ie801223b ↗
10. 10.1007/s10853-008-3114-z10.1007/s10853-008-3114-z ↗
11. 10.1021/bk-2011-1062.ch01210.1021/bk-2011-1062.ch012 ↗
12. 10.1021/cr100193y10.1021/cr100193y ↗
13. Nurfaizey A. H. · 2012 · 23610.1533/9780857095640.2.236 ↗
14. 10.1021/am504487j10.1021/am504487j ↗
15. 10.1021/es506045a10.1021/es506045a ↗
16. 10.1021/am506510q10.1021/am506510q ↗
17. 10.1021/ie501055g10.1021/ie501055g ↗
18. 10.1021/acsami.5b0690510.1021/acsami.5b06905 ↗
19. 10.1021/acs.iecr.5b0008910.1021/acs.iecr.5b00089 ↗
20. 10.1155/2013/21629310.1155/2013/216293 ↗
21. 10.1021/ie050692610.1021/ie0506926 ↗
22. 10.1021/ie061351a10.1021/ie061351a ↗
23. 10.1021/am302359b10.1021/am302359b ↗
24. 10.1021/ie801150y10.1021/ie801150y ↗
25. 10.5923/j.ajps.20120203.0410.5923/j.ajps.20120203.04 ↗
26. Yokley, E. M.; Nielsen, R. B.Hypernucleophilic Catalysts for Detoxification of Chemical Threat Agents. U.S. Patent 8252969 B2, August 28, 2012.
27. 10.1021/jo048252w10.1021/jo048252w ↗
28. 10.1021/jp953385u10.1021/jp953385u ↗
29. 10.1002/pol.1985.13023030510.1002/pol.1985.130230305 ↗
30. 10.1021/bk-1988-0364.ch00610.1021/bk-1988-0364.ch006 ↗
31. Narang, S.; Ventura, S.Immobilized 4-Dialkylaminopyridines: Supernucleophilic Chemical Decontaminating Agents; Technical Report 23208.1-CH prepared forU.S. Army Research Office:Research Triangle Park, NC, 1987; http://handle.dtic.mil/100.2/ADA190999.10.21236/ADA190999 ↗
32. 10.1021/ja00278a02410.1021/ja00278a024 ↗
33. 10.1021/ma00220a01610.1021/ma00220a016 ↗
34. 10.1016/0032-3861(96)87262-410.1016/0032-3861(96)87262-4 ↗
35. 10.1007/BF0094864910.1007/BF00948649 ↗
36. Desmodur Product Datasheet, ed.2013–03–18;Bayer MaterialScience:AG, Leverkusen, Germany, 2013.
37. 10.1016/j.polymer.2007.10.04010.1016/j.polymer.2007.10.040 ↗
38. 10.1006/jcis.2002.847910.1006/jcis.2002.8479 ↗
39. 10.1016/j.compscitech.2008.08.00610.1016/j.compscitech.2008.08.006 ↗
40. 10.1007/s12221-013-0059-x10.1007/s12221-013-0059-x ↗
41. 10.1016/S0266-3538(00)00074-910.1016/S0266-3538(00)00074-9 ↗
42. 10.1021/acsami.5b0079010.1021/acsami.5b00790 ↗
43. 10.1021/am200748y10.1021/am200748y ↗
44. 10.1021/acsami.5b0244610.1021/acsami.5b02446 ↗
45. 10.6028/jres.039.03210.6028/jres.039.032 ↗
46. 10.1021/la061341e10.1021/la061341e ↗
47. 10.1039/b913035g10.1039/b913035g ↗
48. 10.1002/mrc.241510.1002/mrc.2415 ↗
49. 10.1039/b818639a10.1039/b818639a ↗
50. 10.1021/cm902834a10.1021/cm902834a ↗