Promising Energetic Melt-Castable Material with Balanced Properties
Source abstract
Abstract
As one of the most widely used energetic materials to date, trinitrotoluene (TNT) suffers from several generally known drawbacks such as high toxicity, oil permeability, and poor mechanical properties, which are driving researchers to explore new high-performance energetic melt-castable materials for replacing TNT. However, it still remains a great challenge to discover a promising TNT alternative due to the multidimensional requirements for practical applications. Herein, we reported a new promising energetic melt-castable molecule, 4-methoxy-1-methyl-3,5-dinitro-1 H -pyrazole (named as DMDNP). Besides a reasonable melting point ( T m: 94.8 °C), good thermostability ( T d: 293.2 °C), and excellent chemical compatibility, DMDNP exhibits some obvious advantages over TNT including more environmentally friendly synthesis, high yield, low toxicity, low volume shrinkage, low mechanical and electrostatic sensitivities, etc., demonstrating well-balanced properties and great promise as a TNT replacement.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Energetic Materials and Combustion · Fullerene Chemistry and Applications · Rocket and propulsion systems research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Chemical Materials, China Academy of Engineering Physics, Mianyang 621900, China
State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University, Xi’an 710072, China
Funding
National Natural Science Foundation of China
References (36)
Show source-provided references
1. 10.1016/j.enmf.2021.01.00610.1016/j.enmf.2021.01.006 ↗
2. 10.1002/cplu.20160047010.1002/cplu.201600470 ↗
3. 10.1016/j.cej.2022.13505310.1016/j.cej.2022.135053 ↗
4. 10.1080/07370652.2019.166973510.1080/07370652.2019.1669735 ↗
5. 10.1002/prep.20110004710.1002/prep.201100047 ↗
6. 10.1021/acsomega.1c0111510.1021/acsomega.1c01115 ↗
7. 10.1002/anie.20110416410.1002/anie.201104164 ↗
8. Ek S. · J. Chem. Chem. Eng. · 2011 · 5 · 929
9. 10.1021/acs.jpcc.7b0758410.1021/acs.jpcc.7b07584 ↗
10. 10.1002/jhet.557039012110.1002/jhet.5570390121 ↗
11. 10.1002/prep.20160006510.1002/prep.201600065 ↗
12. 10.1134/S107042801608017010.1134/S1070428016080170 ↗
13. 10.1021/acs.oprd.8b0007610.1021/acs.oprd.8b00076 ↗
14. 10.1039/C9NJ01227C10.1039/C9NJ01227C ↗
15. 10.1080/07370652.2020.185964510.1080/07370652.2020.1859645 ↗
16. 10.1126/sciadv.abn317610.1126/sciadv.abn3176 ↗
17. 10.1016/j.enmf.2020.12.00210.1016/j.enmf.2020.12.002 ↗
18. 10.1088/1742-6596/2305/1/01201810.1088/1742-6596/2305/1/012018 ↗
19. 10.1002/jhet.102610.1002/jhet.1026 ↗
20. 10.1016/j.eng.2022.01.00810.1016/j.eng.2022.01.008 ↗
21. 10.1039/D1TA04441A10.1039/D1TA04441A ↗
22. 10.1016/j.chemosphere.2010.05.00410.1016/j.chemosphere.2010.05.004 ↗
23. 10.1039/B704980C10.1039/B704980C ↗
24. 10.1039/B715227B10.1039/B715227B ↗
25. 10.1021/ac60131a04510.1021/ac60131a045 ↗
26. 10.1246/bcsj.38.188110.1246/bcsj.38.1881 ↗
27. 10.14077/j.issn.1007-7812.2016.03.001110.14077/j.issn.1007-7812.2016.03.0011 ↗
28. 10.1007/s10973-017-6481-310.1007/s10973-017-6481-3 ↗
29. Frisch M. J. · 2013
30. Suceska M. · 2013
31. 10.1080/1040778060111507910.1080/10407780601115079 ↗
32. 10.1111/j.1600-0420.2005.00361.x10.1111/j.1600-0420.2005.00361.x ↗
33. 10.1021/jacs.9b1358610.1021/jacs.9b13586 ↗
34. 10.1016/j.nantod.2020.10087810.1016/j.nantod.2020.100878 ↗
35. 10.1021/acsnano.0c0554110.1021/acsnano.0c05541 ↗
36. 10.1021/jacs.1c0330310.1021/jacs.1c03303 ↗