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Enhanced Catalytic Effect of Ti(2)CT(x)-MXene on Thermal Decomposition Behavior of Ammonium Perchlorate

Transition metal carbonitrides (MXenes) are promising catalysts due to their special structures. Recently, many studies have shown that MXenes have a catalytic effect on the thermal decomposition of ammonium perchlorate (AP). However, the catalytic effects have not been extensively investigated. The...

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Detalles Bibliográficos
Autores principales: Li, Jingxiao, Du, Yulei, Wang, Xiaoyong, Zhi, Xuge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821882/
https://www.ncbi.nlm.nih.gov/pubmed/36614683
http://dx.doi.org/10.3390/ma16010344
Descripción
Sumario:Transition metal carbonitrides (MXenes) are promising catalysts due to their special structures. Recently, many studies have shown that MXenes have a catalytic effect on the thermal decomposition of ammonium perchlorate (AP). However, the catalytic effects have not been extensively investigated. Therefore, it is important to illustrate the catalytic mechanisms of pure MXene in AP thermal decomposition. Herein, the catalytic properties of Ti(2)CT(x) for ammonium perchlorate (AP) thermal decomposition were investigated by numerous catalytic experiments. The results showed that the high-temperature decomposition (HTD) decreased by 83 °C, and the decomposition heat of AP mixed with Ti(2)CT(x) increased by 1897.3 J/g. Moreover, the mass spectrum (MS) data showed that the NH(3), H(2)O, O(2), N(2)O, NO, HCl, and NO(2) were formed. In addition, according to the X-ray diffraction (XRD), Raman spectrum, high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), and X-ray photoelectron spectra (XPS) results, the Ti(2)CT(x) nanosheets can adsorb the gaseous products and react with them in-situ, generating anatase-TiO(2) and carbon layers. The Ti(2)CT(x), as-resulted anatase-TiO(2), and carbon can synergize and further catalyze the thermal decomposition of AP when both electron and proton transfers are accelerated during AP decomposition.