Desorption kinetics

Author(s):  
H.J. Kreuzer
Keyword(s):  
2002 ◽  
Vol 66 (3) ◽  
pp. 797 ◽  
Author(s):  
Leslie J. Glover ◽  
Matthew J. Eick ◽  
Patrick V. Brady

2021 ◽  
Vol 235-236 ◽  
pp. 106646
Author(s):  
P. Ciffroy ◽  
L. Carasco ◽  
D. Orjollet ◽  
C. Simonucci ◽  
L. Février

2014 ◽  
Vol 783-786 ◽  
pp. 264-269 ◽  
Author(s):  
Iya I. Tashlykova-Bushkevich ◽  
Keitaro Horikawa ◽  
Goroh Itoh

Hydrogen desorption kinetics for rapidly solidified high purity Al and Al-Cr alloy foils containing 1.0, 1.5 and 3.0 at % Cr were investigated by means of thermal desorption analysis (TDA) at a heating rate of 3.3°C/min. For the first time, it was found that oxide inclusions of Al2O3 are dominant high-temperature hydrogen traps compared with pores and secondary phase precipitates resulted in rapid solidification of Al and its alloys. The correspondent high-temperature evolution rate peak was identified to be positioned at 600°C for high purity Al and shifted to 630°C for Al-Cr alloys. Amount of hydrogen trapped by dislocations increases in the alloys depending on Cr content. Microstructural hydrogen trapping behaviour in low-and intermediate temperature regions observed here was in coincidence with previous data obtained for RS materials using thermal desorption spectroscopy (TDS). The present results on hydrogen thermal desorption evolution indicate that the effect of oxide surface layers becomes remarkable in TDA measurements and show advantages in combinations of both desorption analysis methods to investigate hydrogen desorption kinetics in materials.


2001 ◽  
Vol 676 ◽  
Author(s):  
W. Oelerich ◽  
T. Klassen ◽  
R. Bormann

ABSTRACTHydrogen is the ideal means of energy storage for transportation and conversion of energy in a comprehensive clean-energy concept. However, appropriate storage facilities, both for stationary and for mobile applications, are complicated, because of the very low boiling point of hydrogen (20.4 K at 1 atm) and its low density in the gaseous state (90 g/m3). Furthermore, the storage of hydrogen in liquid or gaseous form imposes safety problems, in particular for mobile applications, e.g. the future zero-emission vehicle. Metal hydrides are a safe alternative for H-storage and, in addition, have a high volumetric energy density that is about 60% higher than that of liquid hydrogen. Mg hydride has a high storage capacity by weight and is therefore favoured for automotive applications. However, so far light metal hydrides have not been considered competitive because of their rather sluggish sorption kinetics. Filling a tank could take several hours. Moreover, the hydrogen desorption temperature of about 300 °C is rather high for most applications. A breakthrough in hydrogen storage technology was achieved by preparing nanocrystalline hydrides using high-energy ball milling. These new materials show very fast aband desorption kinetics within few minutes, thus qualifying lightweight Mg-based hydrides for storage application. In this paper recent detailed results on the sorption behaviour of nanocrystalline Mg and Mg-based alloys are presented. In a following research effort the sorption kinetics of nanocrystalline Mg has been further enhanced by catalyst additions. Furthermore, different transition metals have been added to Mg to achieve a thermodynamic destabilisation of the hydride, thus lowering the desorption temperatures to about 230 °C. The newly developed materials are currently being tested in prototype storage tanks.


2011 ◽  
Vol 399-401 ◽  
pp. 1419-1424
Author(s):  
Yang Huan Zhang ◽  
Guo Fang Zhang ◽  
Xia Li ◽  
Zhong Hui Hou ◽  
Yin Zhang ◽  
...  

The nanocrystalline and amorphous Mg2Ni1-xCox (x=0, 0.1, 0.2, 0.3, 0.4) alloys were prepared by melt-spinning technique. The structures of the alloys were studied by XRD, SEM and HRTEM. The hydrogen absorption and desorption kinetics and the high rate discharge ability (HRD) of the alloys were measured. The results show that the as-spun Co-free alloy holds a typical nanocrystalline structure, whereas the as-spun alloys containing Co display a nanocrystalline and amorphous structure, confirming that the substitution of Co for Ni facilitates the glass formation in the Mg2Ni-type alloy. The substitution of Co for Ni evidently improves the hydriding and dehydriding kinetics and the HRD of the alloys. With an increase in the amount of Co substitution from 0 to 0.4, the HRD value rises from 52.9% to 60.3% for the as-cast alloy, and from 65.9% to 76.0% for the as-spun (30 m/s) alloy.


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