• Korean Journal of Metals and Materials
• /
• v.50 no.11
• /
• pp.855-859
• /
• 2012

Samples with compositions of 80 wt% Mg-14 wt% Ni-6 wt% $Fe_2O_3$ and 80 wt% Mg-14 wt% Ni-6 wt% Ti were prepared by mechanical grinding under hydrogen (reactive mechanical grinding). Their hydrogen absorptions during reactive mechanical grinding were examined. TGA and BET analysis were employed to investigate the hydrogen storage properties of the prepared alloys. TGA analysis of the $Mg-14Ni-6Fe_2O_3$ showed an absorbed hydrogen quantity of 6.91 wt% while that of Mg-14Ni-6Ti was 2.59 wt%. BET analysis showed that the specific surface areas of $Mg-14Ni-6Fe_2O_3$ and Mg-14Ni-6Ti after reactive mechanical grinding were $264m^2/g$ and $64m^2/g$, respectively. The larger absorbed hydrogen quantity and the larger specific surface area of $Mg-14Ni-6Fe_2O_3$ after RMG than those of Mg-14Ni-6Ti after RMG showed that the effects of $Fe_2O_3$ addition are much stronger than those of Ti addition during reactive mechanical grinding.

• Korean Journal of Materials Research
• /
• v.24 no.3
• /
• pp.129-134
• /
• 2014

Pure $MgH_2$ was milled under a hydrogen atmosphere (reactive mechanical grinding, RMG). The hydrogen storage properties of the prepared samples were studied at a relatively low temperature of 423 K and were compared with those of pure Mg. The hydriding rate of the Mg was extremely low (0.0008 wt% H/min at n = 4), and the $MgH_2$ after RMG had higher hydriding rates than that of Mg at 423 K under 12 bar $H_2$. The initial hydriding rate of $MgH_2$ after RMG at 423 K under 12 bar $H_2$ was the highest (0.08 wt% H/min) at n = 2. At n = 2, the $MgH_2$ after RMG absorbed 0.39 wt% H for 5 min, and 1.21 wt% H for 60 min at 423K under 12 bar $H_2$. At 573 K under 12 bar $H_2$, the $MgH_2$ after RMG absorbed 4.86 wt% H for 5 min, and 5.52 wt% H for 60 min at n = 2. At 573 K and 423 K under 1.0 bar $H_2$, the $MgH_2$ after RMG and the Mg did not release hydrogen. The decrease in particle size and creation of defects by reactive mechanical grinding are believed to have led to the increase in the hydriding rate of the $MgH_2$ after RMG at a relatively low temperature of 423 K.

• Journal of Hydrogen and New Energy
• /
• v.14 no.4
• /
• pp.313-320
• /
• 2003

볼밀링법을 이용하여 타이타늄 스펀지와 칩 또는 스크랩으로부터 상온애서 직접 타이타늄 수소와 분말을 재조하는 실험을 행하였다. 실험결과 진공중에서 볼링을 행한 타이타늄 스펀지와 칩의 경우 24시간외 후 합금분말의 크기는 약 20 um 정도의 크기를 갖는 것을 확인하였다. 그러나 수소화 분위기에서 볼밀링을 행한 경우에 12시간 후 수소화분말의 입도는 0.1-0.2 um로 극히 미세한 합금 분말이 제조되었다. 수소분위기에서의 볼밀링에 의한 타이타늄 분말제조는 기존의 방법에 비해 열을 가하지 않고 타이타늄 수소화분말을 얻을 수 있다는 장점과 나노크기의 미세한 수소화 분말을 얻을 수 있음을 알 수 있었다.

• Journal of Hydrogen and New Energy
• /
• v.22 no.6
• /
• pp.787-793
• /
• 2011

A 76.5wt%Mg - 23.5wt%Ni (Mg-23.5Ni) sample was prepared by reactive mechanical grinding (RMG) and its hydriding and dehydriding properties were then investigated. Activation of the Mg-23.5Ni sample was completed only after two hydriding (under 12 bar $H_2$) - dehydriding (under 1.0 bar $H_2$) cycles at 593K. The reactive mechanical grinding of Mg with Ni is considered to facilitate nucleation and shorten diffusion distances of hydrogen atoms. After hydriding - dehydriding cycling, the Mg-23.5Ni sample contained Mg2Ni phase.