Synthesis, characterization and thermal studies on furazan- and tetrazine-based high energy materials

被引:119
作者
Talawar, MB [1 ]
Sivabalan, R
Senthilkumar, N
Prabhu, G
Asthana, SN
机构
[1] High Energy Mat Res Lab, Pune 411021, Maharashtra, India
[2] Alagappa Univ, Dept Ind Chem, Karaikkudi 630003, Tamil Nadu, India
关键词
insensitive high energy materials; diaminofurazan (DAF); 3,3 '-diamino-4,4 '-azoxyfurazan (DAAF); 3,3 '-azobis(6-amino-1,2,4,5-tetrazine) (DAAT); 1,4-dihydrazino tetrazine (DHTz); thermolysis; cyclic voltammetry;
D O I
10.1016/j.jhazmat.2004.05.016
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This paper reports the synthesis of high energy materials (HEMs) viz. 3,3'-diamino-4,4'-azoxyfurazan (DAAF), 3,3(x')-azobis(6-amino-1,2,4,5-tetrazine) [DAAT] and 1,4-dihydrazino tetrazine (DHTz). The products obtained were characterized by IR, H-1 NMR, C-13 NMR and mass spectra. Thermolysis of these compounds carried out by applying TG-DTA and DSC techniques indicated that the thermal stability of DAAF and DAAT was in the temperature range of 230-250 degreesC, whereas that of DHTz was up to similar to140 degreesC. TG-FTIR of gaseous products of these compounds suggests the evolution of NH2CN/NH3 and HCN as major decomposition products. The impact and friction sensitivity data revealed that DAAF is insensitive to mechanical stimuli whereas DAAT and DHTz are vulnerable to impact stimuli. The cyclic voltammetric studies brought out that, DAAF, DAAT and DHTz are electroactive compounds and thereby can be detected at even low concentration at pH7 and 13. The theoretical predictions of explosive power of DAAF, DAAT and DHTz alone and their combinations with well-known insensitive high explosives using Becker-Kistiakowsky Wilson (BKW) code as well as that of propellants based on them by NASA-CEC-71 suggest their potential in specific systems. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 25
页数:15
相关论文
共 25 条
[1]  
ARVANI L, 1977, SENSITIVITY IMPACT F, V2, P111
[2]  
Chavez D. E., 2000, ANGEW CHEM, V112, P1861, DOI DOI 10.1002/(SICI)1521-3757(20000515)112:10<1861::AID-ANGE1861>3.0.CO
[3]  
2-B
[4]  
Chavez D.E., 1999, J. Energ. Mater, V17, P357, DOI DOI 10.1080/07370659908201796
[5]  
Chavez David., 2000, Journal of Energetic Materials, V18, P219, DOI [DOI 10.1080/07370650008216121, 10.1080/07370650008216121]
[6]  
Chavez DE, 2000, ANGEW CHEM INT EDIT, V39, P1791, DOI 10.1002/(SICI)1521-3773(20000515)39:10<1791::AID-ANIE1791>3.0.CO
[7]  
2-9
[8]  
CHAVEZ DE, 1998, J PYROTECHNICS, V7, P11
[9]   AN IMPROVED SYNTHESIS OF 3,6-DIAMINO-1,2,4,5-TETRAZINE .2. FROM TRIAMINOGUANIDINE AND 2,4-PENTANEDIONE [J].
COBURN, MD ;
BUNTAIN, GA ;
HARRIS, BW ;
HISKEY, MA ;
LEE, KY ;
OTT, DG .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1991, 28 (08) :2049-2050
[10]  
DOBRATZ BM, 1978, UCID1708 LAWR LIV NA