TY - JOUR
T1 - In situ synthesis NiO@TiO2/MXene as a promoter for ammonium perchlorate based solid propellants
AU - Bai, Chaofei
AU - Yang, De Sheng
AU - Liu, Chang
AU - Zhu, Feng Dan
AU - Tu, Cheng Zhao
AU - Li, Guoping
AU - Luo, Yunjun
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2024/4/15
Y1 - 2024/4/15
N2 - The carrier can widely affect or even dominate the catalytic activity and selectivity of nanoparticles for ammonium perchlorate (AP). In this work, a novel catalyst NiO@TiO2/MXene (TN) nanocomposite was prepared by a simple hydrothermal method using two-dimensional MXene as the catalyst carrier. System characterization reveals that the utilization of MXene supports facilitates effective dispersion of NiO nanoparticles. TiO2/MXene itself exhibits commendable catalytic activity and possesses a substantial specific surface area, thereby enabling regulation of the catalytic performance of NiO. TN surpasses both NiO and TiO2/MXene in promoting the high temperature decomposition (HTD) of AP. By increasing the concentration of Ni2+ in the precursor, the loading capacity of NiO on the carrier is enhanced, consequently improving its catalytic capability towards AP. As the load of NiO increases, there is a decrease in high decomposition temperature (THTD) from 437.3 ℃ to 313.3 ℃, a reduction in activation energy (Ea) from 216.1kJ/mol to 114.6 kJ/mol, and an increase in heat release by 118 %. NH3-TPD and O2-TPD studies have shown that catalysts with strong surface adsorption capacity for NH3 and O2 exhibit excellent catalytic performance, leading to differences in their catalytic behavior. TG/FT-IR analysis further confirms that TN nanocomposites accelerate N2O conversion to NO, which contributes to rapid AP decomposition.
AB - The carrier can widely affect or even dominate the catalytic activity and selectivity of nanoparticles for ammonium perchlorate (AP). In this work, a novel catalyst NiO@TiO2/MXene (TN) nanocomposite was prepared by a simple hydrothermal method using two-dimensional MXene as the catalyst carrier. System characterization reveals that the utilization of MXene supports facilitates effective dispersion of NiO nanoparticles. TiO2/MXene itself exhibits commendable catalytic activity and possesses a substantial specific surface area, thereby enabling regulation of the catalytic performance of NiO. TN surpasses both NiO and TiO2/MXene in promoting the high temperature decomposition (HTD) of AP. By increasing the concentration of Ni2+ in the precursor, the loading capacity of NiO on the carrier is enhanced, consequently improving its catalytic capability towards AP. As the load of NiO increases, there is a decrease in high decomposition temperature (THTD) from 437.3 ℃ to 313.3 ℃, a reduction in activation energy (Ea) from 216.1kJ/mol to 114.6 kJ/mol, and an increase in heat release by 118 %. NH3-TPD and O2-TPD studies have shown that catalysts with strong surface adsorption capacity for NH3 and O2 exhibit excellent catalytic performance, leading to differences in their catalytic behavior. TG/FT-IR analysis further confirms that TN nanocomposites accelerate N2O conversion to NO, which contributes to rapid AP decomposition.
KW - Ammonium perchlorate
KW - Catalytic performance
KW - NiO@TiO/MXene
UR - http://www.scopus.com/inward/record.url?scp=85182438716&partnerID=8YFLogxK
U2 - 10.1016/j.apsusc.2023.159228
DO - 10.1016/j.apsusc.2023.159228
M3 - Article
AN - SCOPUS:85182438716
SN - 0169-4332
VL - 652
JO - Applied Surface Science
JF - Applied Surface Science
M1 - 159228
ER -