Kinetics of thermal decomposition of aluminium hydride: I-non-isothermal decomposition under vacuum and in inert atmosphere (argon)

被引:65
作者
Ismail, IMK [1 ]
Hawkins, T [1 ]
机构
[1] USAF, Res Lab, PRSP, ERC Inc, Edwards AFB, CA 93523 USA
关键词
aluminium hydride; decomposition; shelf-life prediction; model free kinetics; thermal stability;
D O I
10.1016/j.tca.2005.08.029
中图分类号
O414.1 [热力学];
学科分类号
摘要
Recently, interest in aluminium hydride (alane) as a rocket propulsion ingredient has been renewed due to improvements in its manufacturing process and an increase in thermal stability. When alane is added to solid propellant formulations, rocket performance is enhanced and the specific impulse increases. Preliminary work was performed at AFRL on the characterization and evaluation of two alane samples. Decomposition kinetics were determined from gravimetric TGA data and volumetric vacuum thermal stability (VTS) results. Chemical analysis showed the samples had 88.30% (by weight) aluminium and 9.96% hydrogen. The average density, as measured by helium pycnometery, was 1.486 g/cc. Scanning electron microscopy showed that the particles were mostly composed of sharp edged crystallographic polyhedral such as simple cubes, cubic octahedrons and hexagonal prisms. Thermogravimetric analysis was utilized to investigate the decomposition kinetics of alane in argon atmosphere and to shed light on the mechanism of alane decomposition. Two kinetic models were successfully developed and used to propose a mechanism for the complete decomposition of alane and to predict its shelf-life during storage. Alane decomposes in two steps. The slowest (rate-determining) step is solely controlled by solid state nucleation of aluminium crystals; the fastest step is due to growth of the crystals. Thus, during decomposition, hydrogen gas is liberated and the initial polyhedral AlH3 crystals yield a final mix of amorphous aluminium and aluminium crystals. After establishing the kinetic model, prediction calculations indicated that alane can be stored in inert atmosphere at temperatures below 10 degrees C for long. periods of time (e.g., 15 years) without significant decomposition. After 15 years of storage, the kinetic model predicts similar to 0.1% decomposition, but storage at higher temperatures in (e.g. 30 degrees C) is not recommended. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 43
页数:12
相关论文
共 31 条
[1]   Granulation, Phase Change, and Microstructure - Kinetics of Phase Change. III [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1941, 9 (02) :177-184
[2]   Kinetics of phase change I - General theory [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1939, 7 (12) :1103-1112
[3]  
Avrami M., 1940, J CHEM PHYS, V8, P212, DOI [10.1063/1.1750631, DOI 10.1063/1.1750631]
[4]   PREPARATION AND PROPERTIES OF ALUMINUM-HYDRIDE [J].
BROWER, FM ;
MATZEK, NE ;
REIGLER, PF ;
RINN, HW ;
ROBERTS, CB ;
SCHMIDT, DL ;
SNOVER, JA ;
TERADA, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (09) :2450-2453
[5]   The dimerization of cyclopentadiene - a test reaction for the kinetic analysis of DSC measurements and the performance of a kinetic evaluation program [J].
Flammersheim, HJ ;
Opfermann, J .
THERMOCHIMICA ACTA, 1999, 337 (1-2) :149-153
[6]  
Flynn J.H., 1969, POLYM LETT, V4, P323, DOI DOI 10.1002/POL.1966.110040504
[7]   A QUICK DIRECT METHOD FOR DETERMINATION OF ACTIVATION ENERGY FROM THERMOGRAVIMETRIC DATA [J].
FLYNN, JH ;
WALL, LA .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER LETTERS, 1966, 4 (5PB) :323-&
[8]   CROSS-SECTIONAL AREAS OF ADSORBED N2, AR, KR, AND O2 ON CARBONS AND FUMED SILICAS AT LIQUID-NITROGEN TEMPERATURE [J].
ISMAIL, IMK .
LANGMUIR, 1992, 8 (02) :360-365
[9]  
Johnson WA, 1939, T AM I MIN MET ENG, V135, P416
[10]   VARIATION OF PEAK TEMPERATURE WITH HEATING RATE IN DIFFERENTIAL THERMAL ANALYSIS [J].
KISSINGER, HE .
JOURNAL OF RESEARCH OF THE NATIONAL BUREAU OF STANDARDS, 1956, 57 (04) :217-221