TY - JOUR
T1 - Compatibility and thermokinetics studies of octahydro- 1,3,5,7-tetranitro-1,3,5,7-tetrazocine with polyether-based polyurethane containing different curatives
AU - Singh, Arjun
AU - Kumar, Rajesh
AU - Soni, Pramod Kumar
AU - Singh, Vasundhara
N1 - Publisher Copyright:
© 2018, © 2018 Taylor & Francis Group, LLC.
PY - 2019/4/3
Y1 - 2019/4/3
N2 - A compatibility of energetic compound with polymeric matrices is of prime importance in the pre-formulation stage for developing of new energetic composite formulations. In the present work, the compatibility of octahydro-l,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) with polyether (PET) polyol (trade name SP-755)-based polyurethanes (PUs) containing different curatives such as 4,4ʹmethylene diphenyl diisocyanate (MDI), isophorone diisocyanate (IPDI), 2,2,4-trimethylhexamethylene diisocyanate (TMDI), and toluene diisocyanate (TDI) has been studied by using a differential scanning calorimetry method. The PET-based PUs were prepared by polymerization between PET polyol and different curatives, then these PUs were further mixed with HMX to study the compatibility and kinetic parameters. Results show that the compatibility and thermal stability are significantly influenced by the different curatives, and suggested thermals stability by thermal data follow the order for a mixture of HMX/SP-755/MDI > HMX/SP-755/TDI > HMX/SP-755/IPDI > HMX/SP-755/TMDI. The thermal degradation kinetics has also been investigated through non-isothermal conditions using the Kissinger and the isoconversional ASTM E689 kinetic methods. The finding shows that there was a significant variation in the apparent activation energy for a mixture of HMX/SP-755/MDI, HMX/SP-755/IPDI, HMX/SP-755/TMDI, and HMX/SP-755/TDI, which were 365.8, 257.7, 134.9, and 241.1 kJ mol −1 , respectively. The apparent activation energies obtained from the Kissinger method at maximum peak temperature are in reasonable agreement and consistent with isoconversional ASTM E689 kinetic method.
AB - A compatibility of energetic compound with polymeric matrices is of prime importance in the pre-formulation stage for developing of new energetic composite formulations. In the present work, the compatibility of octahydro-l,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) with polyether (PET) polyol (trade name SP-755)-based polyurethanes (PUs) containing different curatives such as 4,4ʹmethylene diphenyl diisocyanate (MDI), isophorone diisocyanate (IPDI), 2,2,4-trimethylhexamethylene diisocyanate (TMDI), and toluene diisocyanate (TDI) has been studied by using a differential scanning calorimetry method. The PET-based PUs were prepared by polymerization between PET polyol and different curatives, then these PUs were further mixed with HMX to study the compatibility and kinetic parameters. Results show that the compatibility and thermal stability are significantly influenced by the different curatives, and suggested thermals stability by thermal data follow the order for a mixture of HMX/SP-755/MDI > HMX/SP-755/TDI > HMX/SP-755/IPDI > HMX/SP-755/TMDI. The thermal degradation kinetics has also been investigated through non-isothermal conditions using the Kissinger and the isoconversional ASTM E689 kinetic methods. The finding shows that there was a significant variation in the apparent activation energy for a mixture of HMX/SP-755/MDI, HMX/SP-755/IPDI, HMX/SP-755/TMDI, and HMX/SP-755/TDI, which were 365.8, 257.7, 134.9, and 241.1 kJ mol −1 , respectively. The apparent activation energies obtained from the Kissinger method at maximum peak temperature are in reasonable agreement and consistent with isoconversional ASTM E689 kinetic method.
KW - Octahydro-l-tetranitro-1-tetrazocine
KW - compatibility
KW - kinetics
KW - polyether polyol
KW - thermal degradation
UR - http://www.scopus.com/inward/record.url?scp=85057595039&partnerID=8YFLogxK
U2 - 10.1080/07370652.2018.1552337
DO - 10.1080/07370652.2018.1552337
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AN - SCOPUS:85057595039
SN - 0737-0652
VL - 37
SP - 141
EP - 153
JO - Journal of Energetic Materials
JF - Journal of Energetic Materials
IS - 2
ER -