z-logo
Premium
Catalytic decomposition of propellant N 2 O Over Ir/Al 2 O 3 catalyst
Author(s) -
Lin Jian,
Li Lin,
Pan Xiaoli,
Wang Xiaodong,
Cong Yu,
Zhang Tao,
Zhu Shaomin
Publication year - 2016
Publication title -
aiche journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.958
H-Index - 167
eISSN - 1547-5905
pISSN - 0001-1541
DOI - 10.1002/aic.15324
Subject(s) - catalysis , decomposition , adsorption , chemistry , desorption , propellant , chemical decomposition , organic chemistry
N 2 O, as a green propellant alternative to N 2 H 4 , shows potential application in satellite propulsion system. The state of Ir species and the reaction behaviors on Ir/Al 2 O 3 in the oxidative environment during N 2 O decomposition were identified here. Two types of Ir sites existed in this catalyst and affected the process of N 2 O decomposition. The strong Ir sites facilitated the dissociative adsorption of N 2 O to form N 2 and adsorbed O atoms with adsorption heat of as high as 281 kJ/mol, which promoted the desorption of adsorbed O atoms and favored the self‐sustaining decomposition of N 2 O by raising the catalyst bed temperature. The other Ir sites interacted weakly with O atoms but facilitated their combination to form O 2 . The Ir/Al 2 O 3 catalyst then exhibited an excellent performance in initiating the decomposition of N 2 O at low temperature of 200°C and good stability in 0.1 N microthruster for orbit adjustment and attitude control of satellite. © 2016 American Institute of Chemical Engineers AIChE J , 62: 3973–3981, 2016

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom