scholarly journals Effect of Different Amounts of TiF3 on the Reversible Hydrogen Storage Properties of 2LiBH4–Li3AlH6 Composite

2021 ◽  
Vol 9 ◽  
Author(s):  
Yun Li ◽  
Yuxian Zhang ◽  
Lixin Chen

Hydrogen is a potential green alternative to conventional energy carriers such as oil and coal. Compared with the storage of hydrogen in gaseous or liquid phases, the chemical storage of hydrogen in solid complex hydrides is safer and more effective. In this study, the complex hydride composite 2LiBH4–Li3AlH6 with different amounts of TiF3 was prepared by simple ball-milling and its hydrogen storage properties were investigated. Temperature programmed desorption and differential scanning calorimetry were used to characterize the de/rehydrogenation performance, and X-ray diffraction and scanning electron microscopy (SEM) were used to explore the phase structure and surface topography of the materials. The dehydrogenation temperature decreased by 48°C in 2LiBH4–Li3AlH6 with 15 wt% TiF3 composites compared to the composite without additives while the reaction kinetics was accelerated by 20%. In addition, the influence of hydrogen back pressure on the 2LiBH4–Li3AlH6 with 5 wt% TiF3 composite was also investigated. The results show that hydrogen back pressure between 2.5 and 3.5 bar can improve the reversible performance of the composite to some extent. With a back pressure of 3.5 bar, the second dehydrogenation capacity increased to 4.6 wt% from the 3.3 wt% in the 2LiBH4–Li3AlH6 composite without hydrogen back pressure. However, the dehydrogenation kinetics was hindered. About 150 h, which is 100 times the time required without back pressure, was needed to release 8.7 wt% of hydrogen at 3.5 bar hydrogen back pressure. The SEM results show that aluminum was aggregated after the second cycle of dehydrogenation at the hydrogen back pressure of 3 bar, resulting in the partial reversibility of the 5 wt% TiF3-added 2LiBH4–Li3AlH6 composite.

RSC Advances ◽  
2015 ◽  
Vol 5 (12) ◽  
pp. 9255-9260 ◽  
Author(s):  
F. A. Halim Yap ◽  
N. S. Mustafa ◽  
M. Ismail

It was found that the MgH2 + 10 wt% K2ZrF6 sample started to decompose at around 250 °C, which was 100 °C and lower than in as-milled MgH2. The re/dehydrogenation kinetics had also improved significantly compared to the undoped MgH2.


2009 ◽  
Vol 24 (4) ◽  
pp. 813-816 ◽  
Author(s):  
Yi-Xin LIU ◽  
Shu-Quan YANG ◽  
Dan-Dan ZHANG ◽  
Guang-Xu LI ◽  
Wen-Lou WEI ◽  
...  

2007 ◽  
Vol 446-447 ◽  
pp. 228-231 ◽  
Author(s):  
Xia Tang ◽  
Susanne M. Opalka ◽  
Bruce L. Laube ◽  
Feng-Jung Wu ◽  
Jamie R. Strickler ◽  
...  

2008 ◽  
Vol 1098 ◽  
Author(s):  
Young Joon Choi ◽  
Jun Lu ◽  
Hong Yong Sohn ◽  
Zak Fang

AbstractLithium based complex hydrides, including lithium aluminum hydrides and lithium borohydride (LiAlH4, Li3AlH6 and LiBH4), are among the most promising materials due to their high hydrogen contents. In the present work, we investigated the hydrogen storage properties of a new combined system of Li3AlH6-LiBH4. The samples were made with small amounts of catalyst under low energy milling conditions. Thermogravimetric analysis (TGA) of a Ti-doped Li3AlH6/2LiBH4 indicated that the degree of hydrogen release reached 7.3 wt. % by the time the sample reached 450iÆc under a heating rate of 2iÆC/min. This increased to 8.8 wt. % when the sample was held at 450iÆCfor additional 8 hours minutes under this condition. The dehydrogenation product was a mixture of LiH and AlB2. This product could be rehydrogenated up to 3.8 wt. % under 24.1 MPa hydrogen pressure and 450iÆC.


2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Jianxin Zou ◽  
Haiquan Sun ◽  
Xiaoqin Zeng ◽  
Gang Ji ◽  
Wenjiang Ding

In the present work, Mg-rich Mg-Ni ultrafine powders were prepared through an arc plasma method. The phase components, microstructure, and hydrogen storage properties of the powders were carefully investigated. It is found that Mg2Ni and MgNi2could be obtained directly from the vapor state reactions between Mg and Ni, depending on the local vapor content in the reaction chamber. A nanostructured MgH2 + Mg2NiH4hydrogen storage composite could be generated after hydrogenation of the Mg-Ni ultrafine powders. After dehydrogenation, MgH2and Mg2NiH4decomposed into nanograined Mg and Mg2Ni, respectively. Thermogravimetry/differential scanning calorimetry (TG/DSC) analyses showed that Mg2NiH4phase may play a catalytic role in the dehydriding process of the hydrogenated Mg ultrafine particles.


Energies ◽  
2021 ◽  
Vol 14 (23) ◽  
pp. 7853
Author(s):  
Thi-Thu Le ◽  
Claudio Pistidda ◽  
Julián Puszkiel ◽  
María Victoria Castro Riglos ◽  
David Michael Dreistadt ◽  
...  

In recent years, the use of selected additives for improving the kinetic behavior of the system 2LiH + MgB2 (Li-RHC) has been investigated. As a result, it has been reported that some additives (e.g., 3TiCl3·AlCl3), by reacting with the Li-RHC components, form nanostructured phases (e.g., AlTi3) possessing peculiar microstructural properties capable of enhancing the system’s kinetic behavior. The effect of in-house-produced AlTi3 nanoparticles on the hydrogenation/dehydrogenation kinetics of the 2LiH + MgB2 (Li-RHC) system is explored in this work, with the aim of reaching high hydrogen storage performance. Experimental results show that the AlTi3 nanoparticles significantly improve the reaction rate of the Li-RHC system, mainly for the dehydrogenation process. The observed improvement is most likely due to the similar structural properties between AlTi3 and MgB2 phases which provide an energetically favored path for the nucleation of MgB2. In comparison with the pristine material, the Li-RHC doped with AlTi3 nanoparticles has about a nine times faster dehydrogenation rate. The results obtained from the kinetic modeling indicate a change in the Li-RHC hydrogenation reaction mechanism in the presence of AlTi3 nanoparticles.


RSC Advances ◽  
2018 ◽  
Vol 8 (35) ◽  
pp. 19353-19361 ◽  
Author(s):  
Guang Xu ◽  
Wei Zhang ◽  
Ying Zhang ◽  
Xiaoxia Zhao ◽  
Ping Wen ◽  
...  

Fe3O4 nanoclusters highly dispersed on a porous graphene support were fabricated and significantly improved the dehydrogenation kinetics and rehydrogenation reversibility of LiBH4.


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