Thermal Behavior and Decomposition Mechanism of Ammonium Perchlorate and Ammonium Nitrate in the Presence of Nanometer Triaminoguanidine Nitrate

Термическое поведение и механизм разложения перхлората аммония и нитрата аммония в присутствии наноразмерного нитрата триаминогуанидина
Yi Wang, Xiaolan Song, Fengsheng Li
2019-01-04

DSC-IR analysisammonium nitrateammonium perchloratethermal decomposition kineticstriaminoguanidine nitrate
High Resolution Image Download MS PowerPoint Slide Nanometer triaminoguanidine nitrate (TAGN) with mean size of 218.7 nm was fabricated, and its structures were characterized by scanning electron microscopy, X-ray diffraction, IR, and X-ray photoelectron spectroscopy analyses. As an energetic accelerator for thermal decomposition of ammonium perchlorate (AP) and ammonium nitrate (AN), 10% nano TAGN blended with AP and AN, and samples “[90% AP + 10% (nano TAGN)]” and “[90% AN + 10% (nano TAGN)]” were obtained, respectively. Differential scanning calorimetry (DSC) analyses were employed to investigate the decomposition kinetics and thermodynamics of the samples. The results indicated that [90% AP + 10% (nano TAGN)] presented a higher activation energy (152.34 kJ mol –1 ) than pure AP (117.21 kJ mol –1 ) and [90% AN + 10% (nano TAGN)] possessed a lower activation energy (147.51 kJ mol –1 ) than pure AN (161.40 kJ mol –1 ). All activation free energies (Δ G ≠ ) were positive values. This means that activation of the molecules was not a spontaneous process. The decomposition peak temperature of AP decreased from 478.5 °C (for pure AP) to 287.2 °C (for [90% AP + 10% (nano TAGN)]). The decomposition peak of AN also advanced via doping with nano TAGN. Using DSC-IR analysis, the decomposition products of nano TAGN, pure AP, [90% AP + 10% (nano TAGN)], pure AN, and [90% AN + 10% (nano TAGN)] were investigated, and their decomposition mechanisms were proposed. The key factors, i.e., the formation of hydrazine in the decomposition of nano TAGN, were speculated, which substantially promoted the consumption of HNO 3, HClO 4, and their decomposition products in kinetics. Additionally, the energy performances of AP- and AN-based propellants doping with TAGN were evaluated. It is disclosed that the introduction of TAGN would not result in improvement in the energy performance of propellants, but due to its energetic property and high hydrogen content, proper introduction of TAGN will not reduce the energy performance of propellants in a large degree compared with the introduction of inert catalysts.
1
Adding 10% nano-TAGN increased AP’s activation energy from 117.21 to 152.34 kJ mol−1, while decreasing AN’s activation energy from 161.40 to 147.51 kJ mol−1.
2
DSC-IR analyses supported mechanisms in which hydrazine formed during TAGN decomposition and promoted consumption of HNO3, HClO4, and their decomposition products.
3
Nano-TAGN dramatically lowered ammonium perchlorate’s decomposition peak temperature from 478.5 °C to 287.2 °C and advanced ammonium nitrate decomposition.
4
Nanometer triaminoguanidine nitrate (TAGN) was fabricated with a mean particle size of 218.7 nm and structurally characterized using microscopy and spectroscopic techniques.
5
TAGN addition did not improve propellant energy performance, although its energetic character and high hydrogen content may support appropriate formulation use.

Ammonium perchlorate and ammonium nitrate blended with 10% nanometer triaminoguanidine nitrate

Thermal decomposition behavior, kinetics, thermodynamics, products, and mechanisms of the AP/AN–nano-TAGN mixtures

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2019-01-04
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Yi Wang
Xiaolan Song
Fengsheng Li
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