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Hydrogen Sorption Performance of Mg-Ni-C-TiO_(2) Mixtures

机译:Mg-Ni-C-TiO_(2)混合物的氢吸附性能

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Mg-Ni-C-TiO_(2) mixtures with fixed Mg: Ni: C ratio (80.75 wt(percent): 14.25 wt(percent): 5 wt(percent)) and TiO_(2) content increasing from 0.5 wt(percent) to 2.0 wt(percent) were prepared by high energy ball milling (BM) under Ar for 2 different times (45 min and 90 min) and characterized with respect to their kinetic and thermodynamic hydrogen sorption properties. The aim of the work was to study the influence of the TiO_(2) presence on the activation behavior and the sorption properties of the Mg: Ni: C ternary system, studied in detail in a previous paper. When TiO_(2) is added to the mixtures, the hydrogen active phases remain "free Mg" and Mg_(2)Ni, that fully hydrogenate during the charging runs, with formation of beta-MgH_(2) and Mg_(2)NiH_(4), but the number of charging/discharging cycles needed for the sorption activation (performed at 623 K and 35 bar/0.9 bar hydrogen pressure) is reduced from 10 to 7. Moreover, the addition of TiO_(2): (a) does not lead to a decrease in the gravimetric capacity with respect to the ternary system (6.4 wt(percent) H_(2)), suggesting that the oxide increases the sorption efficiency of the active phases; (b) does not affect the equilibrium pressures of the Mg/MgH_(2) and Mg_(2)Ni/Mg_(2)NiH_(4) systems; (c) leads to a small decrease in the hydrides starting dehydrogenation temperatures (5 K and 4 K respectively at H_(2) pressure velence 0.9 bar) and to a very small increase (1 kJ/mol H_(2)) in the desorption enthalpy; (d) is responsible of an appreciable increase in the sorption rates (up to 10 times for absorption and to 2.7 times for desorption).
机译:Mg-Ni-C-TiO_(2)混合物具有固定的Mg:Ni:C比(80.75 wt(%):14.25 wt(%):5 wt(%)),并且TiO_(2)的含量从0.5 wt(%)增加通过高能球磨(BM)在氩气下2次不同的时间(45分钟和90分钟)制得1到2.0重量%的硼,并对其动力学和热力学氢吸附特性进行了表征。这项工作的目的是研究TiO_(2)的存在对Mg:Ni:C三元体系的活化行为和吸附性能的影响,这在先前的论文中已有详细研究。当将TiO_(2)添加到混合物中时,氢活性相保持为“游离Mg”和Mg_(2)Ni,它们在充电过程中完全氢化,形成β-MgH_(2)和Mg_(2)NiH_ (4),但吸附活化所需的充电/放电循环数(在623 K和35 bar / 0.9 bar氢气压力下执行)从10减少到7。此外,TiO_(2)的添加:(a )不会导致相对于三元体系(6.4 wt(%)H_(2))的重量降低,表明氧化物增加了活性相的吸附效率; (b)不影响Mg / MgH_(2)和Mg_(2)Ni / Mg_(2)NiH_(4)系统的平衡压力; (c)导致氢化物起始脱氢温度的小幅下降(在H_(2)压力变化率0.9 bar时分别为5 K和4 K),并且解吸的增幅很小(1 kJ / mol H_(2))焓(d)引起吸附速率的显着提高(吸附速率最高可达10倍,解吸速率最高可达2.7倍)。

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