Muravyev Nikita V, Monogarov Konstantin A, Asachenko Andrey F, Nechaev Mikhail S, Ananyev Ivan V, Fomenkov Igor V, Kiselev Vitaly G, Pivkina Alla N
Semenov Institute of Chemical Physics RAS, 4, Kosygina Str., 119991 Moscow, Russia.
Zelinsky Institute of Organic Chemistry RAS, 47, Leninsky Ave., 119991 Moscow, Russia and Topchiev Institute of Petrochemical Synthesis RAS, 29, Leninsky Ave., 119991 Moscow, Russia.
Phys Chem Chem Phys. 2016 Dec 21;19(1):436-449. doi: 10.1039/c6cp06498a.
Thermal decomposition of a novel promising high-performance explosive dihydroxylammonium 5,5'-bistetrazole-1,1'-diolate (TKX-50) was studied using a number of thermal analysis techniques (thermogravimetry, differential scanning calorimetry, and accelerating rate calorimetry, ARC). To obtain more comprehensive insight into the kinetics and mechanism of TKX-50 decomposition, a variety of complementary thermoanalytical experiments were performed under various conditions. Non-isothermal and isothermal kinetics were obtained at both atmospheric and low (up to 0.3 Torr) pressures. The gas products of thermolysis were detected in situ using IR spectroscopy, and the structure of solid-state decomposition products was determined by X-ray diffraction and scanning electron microscopy. Diammonium 5,5'-bistetrazole-1,1'-diolate (ABTOX) was directly identified to be the most important intermediate of the decomposition process. The important role of bistetrazole diol (BTO) in the mechanism of TKX-50 decomposition was also rationalized by thermolysis experiments with mixtures of TKX-50 and BTO. Several widely used thermoanalytical data processing techniques (Kissinger, isoconversional, formal kinetic approaches, etc.) were independently benchmarked against the ARC data, which are more germane to the real storage and application conditions of energetic materials. Our study revealed that none of the Arrhenius parameters reported before can properly describe the complex two-stage decomposition process of TKX-50. In contrast, we showed the superior performance of the isoconversional methods combined with isothermal measurements, which yielded the most reliable kinetic parameters of TKX-50 thermolysis. In contrast with the existing reports, the thermal stability of TKX-50 was determined in the ARC experiments to be lower than that of hexogen, but close to that of hexanitrohexaazaisowurtzitane (CL-20).
使用多种热分析技术(热重分析法、差示扫描量热法和加速量热法,ARC)对一种新型的、有前景的高性能炸药5,5'-双四唑-1,1'-二醇二羟铵盐(TKX-50)的热分解进行了研究。为了更全面地了解TKX-50分解的动力学和机理,在各种条件下进行了一系列互补的热分析实验。在常压和低(高达0.3托)压下获得了非等温及等温动力学数据。热解气体产物通过红外光谱原位检测,固态分解产物的结构通过X射线衍射和扫描电子显微镜确定。直接鉴定出5,5'-双四唑-1,1'-二醇二铵盐(ABTOX)是分解过程中最重要的中间体。通过TKX-50与双四唑二醇(BTO)混合物的热解实验,也阐明了BTO在TKX-50分解机理中的重要作用。几种广泛使用的热分析数据处理技术(基辛格法、等转化率法、形式动力学方法等)分别与ARC数据进行了对比,ARC数据与含能材料的实际储存和应用条件更为相关。我们的研究表明,之前报道的阿伦尼乌斯参数均无法恰当描述TKX-50复杂的两步分解过程。相比之下,我们展示了等转化率方法结合等温测量的卓越性能,该方法得出了TKX-50热解最可靠的动力学参数。与现有报道不同,在ARC实验中确定TKX-50的热稳定性低于黑索今,但接近六硝基六氮杂异伍兹烷(CL-20)。