高氯酸铵
催化作用
双金属片
差示扫描量热法
热分解
二茂铁
分解
无机化学
纳米颗粒
化学
氧化物
活化能
化学工程
材料科学
固体燃料火箭
热解
化学分解
反应机理
氧化铁
量热法
油胺
烷基
粒径
热分析
苯
离子键合
协同催化
氧化还原
作者
Cristián Valdebenito,José Gaete,Claudio Osorio,Yuvaraja Dibdalli,Ángel Norambuena,Nathalie Lecaros,Cristián Carrasco,Héctor Reyes,Gabriel Abarca,César Morales-Verdejo
出处
期刊:ACS omega
[American Chemical Society]
日期:2023-09-14
卷期号:8 (38): 35242-35255
被引量:13
标识
DOI:10.1021/acsomega.3c04996
摘要
We reported mono and bimetallic ferrocene-based 1,2,3-triazolyl compounds as potential burning rate catalysts in their neutral and ionic forms. All complexes reported here were characterized using 1H and 13C NMR, elemental analysis, and Mössbauer spectroscopy, which was performed for neutral and oxide compounds. The complexes present quasireversible redox potentials with higher oxidative ability than ferrocene and catocene under the same conditions. The complexes were tested as catalysts on the thermal decomposition of ammonium perchlorate (AP) and examined by a differential scanning calorimetry technique to gain further knowledge about their catalytic behavior. Compound 1 causes a decrease of the high-temperature decomposition (HTD) of AP positively, decreasing the decomposition temperature of AP to 345 °C and consequently increasing the energy release to 1939 J·g-1. We took the residues from the pans after testing from the DSC to elucidate the underlying reaction pathways. We obtained the size of the nanostructures formed after thermal decomposition of AP determined by the TEM technique. The diameter and size distribution of iron oxide nanoparticles formed depend on the alkyl sidechain of the triazolium ring, which induces the formation of nanoparticles with a double diameter and size distribution compared to their neutral analogues, suggesting that the possible intermediate for the mechanism degradation of AP by ferrocene derivatives is nanoscale Fe2O3 or similar oxides.
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