共查询到20条相似文献,搜索用时 38 毫秒
1.
《International Journal of Hydrogen Energy》1999,24(2-3):141-143
Hydrogen interaction with Ce2Ni0.8Si1.2,Ce2NiSi, Ce2Ni1.2Si0.8 and Ce6Ni2Si3 compounds were studied. The new hydride phases containing 3.7, 4.4, 4.9,and 10.9 hydrogen atoms per formula unit correspondingly, have been synthesized andcharacterized by X-ray diffraction and thermodesorption methods. All hydrides preservedstructure type of the starting compounds with pronounced anisotropic distortion of crystal lattice.Some suggestions on hydrogen localization in interstitial sites have been proposed. 相似文献
2.
3.
通过对 1Cr17Ni2不锈钢相区变化的分析 ,从理论上阐述了 1Cr17Ni2钢的热处理的机理 ,并通过实例给出了能够同时使 1Cr17Ni2钢获得高强度和高韧性的热处理方法 相似文献
4.
通过试验研究摸索了1Cr12Ni2WMoVNbN材料的机械性能和微观金相组织特性,确定了最佳热处理工艺。 相似文献
5.
6.
《International Journal of Hydrogen Energy》2020,45(58):33478-33490
The Z-Scheme CdS quantum dots/Ni2P/Black Ti3+–TiO2 nanotubes with dual-functional Ni2P nanosheets are fabricated by a continuously electrospinning-annealing/reduction-chemical deposition method, there, the TiO2 nanotubes are fabricated via electrospinning, subsequently, the 2D Ni2P lamellas grow on the surface of nanotubes and the Ti3+/Ov ions are introduced by reduction, then CdS QDs are deposited on the surface of Ni2P lamellas. Evaluated by the photocatalytic hydrogen production, the photocatalytic performance of Z-Scheme CdS QDs/Ni2P/B–TiO2(~3303.85 μmol/g h) exhibits an obvious enhancement of about ~70 folds than unmodified TiO2. The main reasons for the HER enhancement are ascribed to that the Pt-like behavior 2D Ni2P and Ti3+ ions can accelerate the photo-generated electrons diffusing into water and reduce H2 activation barrier, the Z-Scheme heterojunction can accelerate the separating and transferring of photo-generated charge carriers, the Ov ions and hollow nanotubes can increase solar utilization, which can be supported by the electrochemical measurements. 相似文献
7.
《International Journal of Hydrogen Energy》2020,45(33):16528-16539
The decomposition of NH3 for hydrogen production was studied using Ni/La2O3 catalysts at varying compositions and temperatures prepared via surfactant-templated synthesis to elucidate the influence of catalyst active metal content, support composition and calcination temperature on the catalytic activity. The catalytic performance of all samples was studied between 300 and 600 °C under atmospheric pressure. The catalytic activity of the sample were as follows: 10Ni/La2O3-450 > 10Ni/La2O3-550 > 10Ni/La2O3-650 ≈ 10Ni/La2O3-750 ≈ 10Ni/La2O3-850. The excellent activity (100%) of 10Ni/La2O3-450 could be due to the high surface area, basicity strength and concentration of surface oxygen species of the catalyst as evidenced by BET, CO2-TPD and XPS. In addition, to adjust the activity of the catalyst support, the molar ratios of Mg and La were varied (1:1, 3:1, 5:1, 7:1 and 9:1). The 5Ni/5MgLa (5:1 M ratio) was found to be the most active (100%) relative to other Ni/MgLa formulations. Furthermore, the Ni content in the Ni/5MgLa sample was adjusted between 10 and 40 wt%. Increasing the Ni content of the catalysts increased NH3 conversion with the 40 wt% Ni formulation demonstrating complete NH3 conversion at 600 °C and a high gas hourly space velocities (GHSV) (30,000 mL∙h−1∙gcat−1). 相似文献
8.
《International Journal of Hydrogen Energy》2004,29(7):749-757
In the past years, the nickel–metal hydride rechargeable battery is already been widely used in many application fields, and is now replacing the nickel–cadmium battery. Electrochemical impedance spectroscopy technique is extensively used to reveal the electrode process kinetics, for example, Pb–H2SO4 battery, Ni–Cd battery. There are few reports on the EIS of Ni–MH battery. In this paper, an extensive study is focused on the electrochemical impedance spectroscopy of metal hydride electrode, β–Ni(OH)2 electrode and Ni–MH battery with different states of charge. 相似文献
9.
10.
《International Journal of Hydrogen Energy》1988,13(11):685-690
Measurements of the equilibrium isotopic effects in the Mg2Ni-hydrogen (deuterium) system are reported. The values of the enthalpies of transformation for the absorption and desorption reactions are critically compared to literature data. The dehydriding kinetics are studied, concluding that the reaction progresses by a nucleation and growth mechanism, with the hydrogen (deuterium) diffusion in the α-phase as a rate limiting process at high thermodynamic driving forces. The role of the hydride-solid solution (β/α) interface increases as the pressure approaches a value Po, lower than the equilibrium dissociation pressure. At pressure above this Po, the process becomes interface-controlled and an incubation time is observed in the dehydriding reactions. The activation energy for the hydrogen diffusion in α-phase has been tentatively evaluated from the kinetic data and compared to that reported in literature. 相似文献
11.
12.
13.
通过对1Cr17Ni2不锈钢相区变化的分析,从理论上阐述了1Cr17Ni2钢的热处理的机理,并通过实例给出了能够同时使1Cr17Ni2钢获和高韧性的热处理方法。 相似文献
14.
《Journal of power sources》2003,115(1):161-166
Mechanically alloyed Mg2Ni and a single air (oxygen) electrode are used as the anode and cathode, respectively, in a Mg2Ni|6 M KOH|O2 rechargeable metal-hydride–air (MH–air) battery. The battery is tested for self-discharge by measuring the open-circuit voltage (OCV) and cycling characteristics. Battery degradation after charge–discharge cycling is characterized by means of X-ray diffraction (XRD) and scanning electron microscopic (SEM) analyses. 相似文献
15.
《Journal of power sources》1999,79(2):256-261
Synthesis of LiNiO2 by heat-treatment of Li(OH)·H2O and Ni(OH)2 is reported. The influence of synthesis conditions on the electrochemical performance of the resulting LiNiO2 is investigated. Thermal analysis of the synthesis process shows that LiNiO2 formation proceeds through the transformation of Ni(OH)2 to a layered compound Ni1−x(OH)2−x, followed by solid reaction with LiOH. The most favorable condition is heating a mixture of Li(OH)·H2O and Ni(OH)2 at 650°C, and then at 720°C in oxygen. The resulting LiNiO2 exhibits a considerably high discharge capacity of 145 mA h g−1 and a sufficiently long cycle-life when cycled over a lithium composition range of 0.2≤x≤0.65. 相似文献
16.
17.
Active and stable Ni–Fe–SiO2 catalysts prepared by sol–gel method were employed for direct decomposition of undiluted methane to produce hydrogen and carbon filaments at 823 K and 923 K. The results indicated that the lifetime of Ni–Fe–SiO2 catalysts was much longer than Ni–SiO2 catalyst at a higher reaction temperature such as 923 K, however, a reverse trend was shown when methane decomposition took place at a lower reaction temperature such as 823 K. XRD studies suggested that iron atoms had entered into the Ni lattice and Ni–Fe alloy was formed in Ni–Fe–SiO2 catalysts. The structure of the carbon filaments generated over Ni–SiO2 and Ni–Fe–SiO2 was quite different. TEM studies showed that “multi-walled” carbon filaments were formed over 75%Ni–25%SiO2 catalyst, while “bamboo-shaped” carbon filaments generated over 35%Ni–40%Fe–25%SiO2 catalysts at 923 K. Raman spectra of the generated carbons demonstrated that the graphitic order of the “multi-walled” carbon filaments was lower than that of the “bamboo-shaped” carbon filaments. 相似文献
18.
1Cr 17Ni2不锈钢属于火电大机组零部件所采用的材料之一,因其组织中易产生铁素体而使钢的热加工工艺性能和热处理工艺性能下降。采用Thermo Calc软件对不同条件下1Cr 17Ni2不锈钢的平衡组织进行了定量计算,分析了温度和化学成分两因素对钢的平衡组织的影响规律,在此基础上提出了1Cr 17Ni2 不锈钢化学成分的控制范围和热加工及热处理的温度规范。结果表明,Thermo Calc预测结果与现有试验数据基本上吻合,可以用于指导1Cr 17Ni2 不锈钢的生产和使用。表1参9 相似文献
19.
使用2kw连续波CO2激光器在45^#钢表面进行激光熔敷Ni合金中添加50wt%Ni Cr包敷的Cr3C2复合粉的复合少层,并对激光熔敷层的晶体生长形态、物相和硬度进行了分析。结果表明:熔敷层由下至上可分为平面前沿生长区,胸状晶区及枝晶:熔敷区的近表层由高度细小的奥氏体枝晶和C7C3、Cr3C2等物组成,熔敷层的硬度平均高达HV0.2950-1200。添加Cr3C2粒子的激光熔敷层的显微硬度比镍基合金的显微硬度平均提高了HV0.2300。 相似文献
20.
La2O3改进Ni/γ-Al2O3催化剂上沼气重整制氢 总被引:1,自引:0,他引:1
为了寻求制备氢气的可再生资源及减少沼气的排放量,用浸渍法制备了不同La2O3含量的Ni/La2O3/γ Al2O3催化剂,用CH4/CO2体积比为1的混合气体模拟沼气,考察了还原温度、反应温度、空速等操作条件对该催化剂上沼气重整制氢性能的影响.并运用H2-TPR、TEM、TG-DSC等对催化剂进行了表征.结果表明:La2O3含量为6%的催化剂具有较好的综合性能;载体中掺杂适量La2O3能增加金属Ni的分散性,提高催化剂的可还原性及载体对CO2的吸附能力,从而改善了催化剂的活性及抗积炭性,使催化剂具有较好的稳定性.在100h的稳定性实验中,CH4及CO2转化率、H2及CO的选择性、H2/CO比平均值分别约为87.4%、88.8%、87.3%、93.8%及0.92.催化剂表面积炭速率非常低,仅为0.7279mg/(gcat·h). 相似文献