Freye Chris E, Snyder Christopher J
Los Alamos National Laboratory, Q-5, High Explosives Science and Technology, Los Alamos, New Mexico 87545, United States.
ACS Omega. 2022 Aug 18;7(34):30275-30280. doi: 10.1021/acsomega.2c03494. eCollection 2022 Aug 30.
Until now, it has been assumed that the primary decomposition pathway for the liquid plasticizer bis(2,2-dinitropropyl)acetal and bis(2,2-dinitropropyl)formal (BDNPA/F) was nitrous acid elimination (NAE). An ultrahigh-performance liquid chromatography (UHPLC) coupled to quadrupole time-of-flight mass spectrometry (QTOF) methodology was developed to discover and identify the degradation products of BDNPA/F. No evidence of NAE was found. However, two other degradation pathways were found: (1) hydrolysis of the acetal/formal functional group and (2) radical-based homolysis of the C-N bond, followed by hydrogen atom abstraction. Hydrolysis of BDNPA/F proceeds by the formation of 2,2-dinitropropanol (DNPOH) and 2,2-dinitropropyl hemiacetal/hemiformal, which further decompose into DNPOH and ethanal/methanal, respectively. Hydrolysis is the dominant decomposition pathway in all samples; however, at higher temperatures, C-N homolysis becomes more significant. Also, the solid PBX 9501 has different ratios of decomposition products than the liquid BDNPA/F due to the slower rate of diffusion through solids than liquids.
到目前为止,人们一直认为液体增塑剂双(2,2 - 二硝基丙基)乙缩醛和双(2,2 - 二硝基丙基)甲醛(BDNPA/F)的主要分解途径是亚硝酸消除(NAE)。开发了一种超高效液相色谱(UHPLC)与四极杆飞行时间质谱(QTOF)联用的方法来发现和鉴定BDNPA/F的降解产物。未发现NAE的证据。然而,发现了另外两条降解途径:(1)乙缩醛/甲醛官能团的水解和(2)基于自由基的C - N键均裂,随后发生氢原子夺取。BDNPA/F的水解通过形成2,2 - 二硝基丙醇(DNPOH)和2,2 - 二硝基丙基半缩醛/半缩甲醛进行,它们分别进一步分解为DNPOH和乙醛/甲醛。水解是所有样品中的主要分解途径;然而,在较高温度下,C - N均裂变得更加显著。此外,由于通过固体的扩散速率比液体慢,固体PBX 9501的分解产物比例与液体BDNPA/F不同。