CHINESE JOURNAL OF ENERGETIC MATERIALS
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BuNENA和PBT及其复合体系的热安全性研究
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南京理工大学

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航天化学能源全国重点实验室基金(NKLACP420251B33)


Thermal Safety of BuNENA, PBT, and the BuNENA/PBT Composite System
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School of Chemistry and Chemical Engineering,Nanjing University of Science and Technology

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    摘要:

    为综合评价含能增塑剂/黏结剂复合体系的热安全性,采用差示扫描量热(DSC)技术,结合慢速烤燃、5 s爆发点实验及自加速分解温度(SADT)计算,系统研究了N-丁基硝氧乙基硝胺(BuNENA)、3,3-二叠氮甲基氧丁环与四氢呋喃共聚物(PBT)及BuNENA/PBT(1∶1)体系的热分解行为、动力学特征与热安全特性。结果表明,BuNENA主要在180~240 ℃集中放热分解,PBT放热区间为220~300 ℃;复合后低温放热强度降低,主放热区向高温迁移,说明PBT可抑制BuNENA低温集中释能。动力学分析显示,BuNENA/PBT在较宽转化率范围内具有较高且稳定的表观活化能,热分解能垒提高。慢速烤燃实验中,复合体系起始反应温度相对于BuNENA由151.6 ℃升至162.5 ℃;5 s爆发点中结果由261.5 ℃ 升至290.2 ℃;以25 kg单包装规格作为热安全性评价条件时,BuNENA/PBT复合体系的不可逆自热温度TNR和自加速分解温度TSADT分别为134.7 ℃和128.1 ℃,较BuNENA分别提高11.2 ℃和22.6 ℃。PBT与BuNENA复合后可有效降低较低温阶段集中放热倾向,提高体系在慢速升温、短时热刺激及储存热环境下的安全裕度。

    Abstract:

    To comprehensively evaluate the thermal safety of energetic plasticizer/binder composite systems, a multiscale thermal analysis strategy was applied to N-butyl-N-(2-nitroxyethyl)nitramine (BuNENA), poly(3,3-bis(azidomethyl)oxetane-co-tetrahydrofuran) (PBT), and a BuNENA/PBT composite system with a mass ratio of 1∶1. Differential scanning calorimetry (DSC), non-isothermal kinetic analysis, slow cook-off tests, 5 s explosion point tests, and self-accelerating decomposition temperature (TSADT) calculations based on the Semenov model were used to investigate their thermal decomposition behavior and thermal safety characteristics. The DSC results showed that BuNENA mainly underwent exothermic decomposition at 180-240 ℃, whereas PBT decomposed in a higher temperature range of 220-300 ℃. The BuNENA/PBT composite exhibited two exothermic peaks, and the first exothermic peak shifted to a higher temperature with a reduced low-temperature exothermic intensity, indicating that PBT could suppress the concentrated heat release of BuNENA at relatively low temperatures. Kinetic analysis further showed that the apparent activation energy of the first decomposition stage of BuNENA/PBT increased compared with that of pure BuNENA, suggesting an enhanced thermal decomposition barrier. In the slow cook-off test, the initial reaction temperature increased from 151.6 ℃ for BuNENA to 162.5 ℃ for BuNENA/PBT. The 5 s explosion point increased from 261.5 ℃ to 290.2 ℃. For a 25 kg package, the no-return temperature (TNR) and SADT of BuNENA/PBT were 134.7 ℃ and 128.1 ℃, respectively, which were higher than those of BuNENA. These results indicate that compounding BuNENA with PBT can reduce low-temperature concentrated exothermicity and improve the thermal safety margin of BuNENA-based energetic composite systems under slow heating, transient thermal stimulation, and storage-related thermal conditions.

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李文龙,程志鹏,吕佳璐,等. BuNENA和PBT及其复合体系的热安全性研究[J]. 含能材料,DOI:10.11943/CJEM2026121.

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  • 收稿日期: 2026-05-20
  • 最后修改日期: 2026-06-29
  • 录用日期: 2026-06-23
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