Z.H.Li
,
X.P.Liu
,
Y.Gao and Z.Xu Research Institute of Surface Engineering
,
Taiyuan University of Technology
,
Taiyuan 030024
,
China
金属学报(英文版)
It, ageing high speed steel (AHSS) with high cobalt, has a strong ability of age hardening. However, it has two disadvantages, One is short of toughness, the other is its high price because of its too much alloy content especially cobalt. All of these effect on its widespread using. Now there is a new method without the two flows to form this steel in the surface of ingot iron by use of double glow plasma surface alloying technique.In this paper, the following three parts are introduced: the metallurgical process of this surface ageing high speed steel (SAHSS), the micro structure of the alloying layer, the alloy distribution in the layer. By using the designed source pole, the special alloying process, the required surface alloying content, just like the AHSS—Co23W11Mo7 can be achieved in the surface layer. This new method has wide prospect in the fields of tools, moulds and other wear resisting fields.
关键词:
SAHSS
,
null
,
null
张立春
,
何安强
,
叶恒强
,
张永昌
材料研究学报
用HRTEM、TEM及EDAX分析研究了Al─Li—Cu—Mg—Zr合金中的一种新相(暂名H相)和六角Z相的结构,确定H相具有四方点阵,点阵参数为α=2.8nm,c=2.4nm,EDAX分析表明H相和Z相均含Al、Mg、Cu发现H相与Z相的共存取向关系为[100]‖[1120]Z,[1010]H‖[0001]Z。还观察到Z相中一种特有的旋转畴结构
关键词:
Al─Li─Cu─Mg─Zr合金.四方H相
,
tetragonal H phase
,
hexagonal Z phase
张立春
,
何安强
,
吴玉琨
,
叶恒强
,
张永昌
金属学报
利用高分辨电镜(HRTEM)和常规电子显微术研究了快速凝固Al-Li-Cu—Mg—Zr合金中Z相和T相的结构关系,发现两相间两种确定的晶体学取向关系,并以此为依据解释了Z相和T相的某些结构缺陷两相的结构有密切关联,其中一相中缺陷的扩展会导致另一相的形成
关键词:
Al-Li-Cu-Mg-Zr合金
,
Z hexagonal phase
,
T f.c.c. phase
,
shear structure
李虎
,
王作成
,
薛长深
,
庄栋栋
,
王晓
,
张思勋
材料热处理学报
为了研究钢中合金元素Nb、B、Ni对低合金高强度H型钢抗层状撕裂能力(Z向性能)的影响,设计了对照试验,通过常温下拉力试验,对其力学性能尤其是断面收缩率进行了测试,使用XRD、SEM、TEM以及EDS对其组织和成分进行了分析.结果表明:微合金元素Nb、B和微量元素Ni对钢材的Z向性能产生了明显的不良影响,含有Nb、B和Ni,经过钢包精炼的Q345E钢的Z向性能显著低于不含Nb、B和Ni,未经钢包精炼且含有较多夹杂物的Q345B钢.其原因主要在于Nb、B、Ni的存在阻碍了钢材变形过程中位错在晶界和晶内的移动.
关键词:
低合金高强度钢
,
Z向性能
,
合金元素
,
夹杂物
,
阻碍位错
Journal of Materials Research
The effect of Li(3)N additive on the Li-Mg-N-H system was examined with respect to the reversible dehydrogenation performance. Screening Study with varying Li(3)N additions (5, 10, 20, and 30 mol%) demonstrates that all are effective for improving the hydrogen desorption capacity. Optimally, incorporation of 10 mol% Li(3)N improves the practical capacity from 3.9 wt% to approximately 4.7 wt% hydrogen at 200 degrees C, which drives the dehydrogenation reaction toward completion. Moreover, the capacity enhancement persists well over 10 de-/rehydrogenation cycles. Systematic x-ray diffraction examinations indicate that Li(3)N additive transforms into LiNH(2) and LiH phases and remains during hydrogen cycling. Combined structure/property investigations suggest that the LiNH(2) "seeding" should be responsible for the capacity enhancement, which reduces the kinetic barrier associated with the nucleation of intermediate LiNH(2). In addition, the concurrent incorporation of LiH is effective for mitigating the ammonia release.
关键词:
complex hydrides;improvement;mixtures;imides;amide;h-2
Journal of Physical Chemistry C
The Li-Mg-N-H system was prepared by reacting magnesium amide [Mg(NH(2))(2)] with lithium nitride (Li(3)N) and investigated with regard to the hydrogen storage properties. Our study shows that the present method is superior to the conventional route in enhancing the reversible dehydrogenation properties. Through optimizing the Li(3)N:Mg(NH(2))(2) ratio in the starting materials, the reversible capacity of U-Mg-N-H system increases to 4.9 wt %, 18% higher than that typically obtained from the Mg(NH(2))(2) + 2LiH mixture at 200 degrees C. Furthermore, increasing the Li(3)N:Mg(NH(2))(2) ratio is effective for mitigating the ammonia release from thus-prepared samples. Combined property/structure investigations indicate that the obtained enhancements should be ascribed to the effects of LiNH(2) and LiH that were in situ generated from the excess Li(3)N. LiNH(2) may promote the dehydrogenation reaction via seeding the reaction intermediate. The concurrently generated LiH acts as an effective ammonia trapping agent. These findings highlight the potential of "intermediate seeding" as a strategy to enhance the reversible hydrogen storage properties of metal-N-H systems.
关键词:
complex hydrides;ultrafast reaction;amide;improvement;desorption;linh2;destabilization;mechanism;mixtures;imides
裴增文
,
刘晓鹏
,
黄倬
,
李志念
,
王树茂
,
蒋利军
稀有金属
doi:10.3969/j.issn.0258-7076.2010.04.013
采用等容法研究了机械球磨工艺制备的Li-Mg-N-H材料储氧性能,结果发现,在室温下采用氦气对样品室体积进行标定时,由于Li-Mg-N-H材料对氦气有一定量的物理吸附,造成准确Li-Mg-N-H材料样品体积标定误差,进而造成Li-Mg-N-H储氢材料在503 K下放氢容量随压力的降低而增加异常变化.为准确标定样品体积,通过对Li-Mg-N-H材料室温氮气吸附容量测定,并采用迭代计算方法获得准确的储氢材料样品体积,进而测定Li-Mg-N-H储氢材料503 K下放氢PCT曲线,其表现为放氢容量随压力降低而减小的正常变化规律.Li-Mg-N-H储氢材料503 K,9.6 MPa氢压下的最大储氢容量为4.81%(质量分数),放氢过程表现为单一放氢平台特性.
关键词:
轻质储氢材料
,
Li-Mg-N-H
,
储氢性能
,
等容测试方法
Journal of Alloys and Compounds
Motivated by the ion migration mechanism proposed by David et al. [J. Am. Chem. Soc. 129 (2007) 1594-1601], we mechanically mill the Li3N/Co powder mixture to obtain defective Li3N-type structure with enhanced Li+ mobility. Compared with Li3N the hydrogen storage property of such defective phase is markedly improved, presumably due to the ion-migration-enhancing effect from the incorporation of Co and Fe (from milling utensils). During subsequent cycling, however, this effect cannot persist due to the precipitation of Co-Fe alloy upon hydrogenation. The close correlation between Co-Fe incorporation/precipitation and property variation of Li3N hydrogen storage material provides a preliminary evidence to support the ion migration mechanism. (C) 2007 Elsevier B.V. All rights reserved.
关键词:
Hydrogen absorbing materials;Nitride materials;hydrogen-storage;lithium amide;mechanism;nitride;batteries;mixtures;hydride;imides;linh2;anode
Energy & Environmental Science
The Li-Mg-B-H system that is prepared from 2LiH + MgB(2) or 2LiBH(4) + MgH(2) possesses high hydrogen capacity and relatively favorable thermodynamics, but it is greatly restricted in practical hydrogen storage applications by problematic H-exchange kinetics. In the present study, TiF(3) was mechanically milled with a 2LiH + MgB(2) mixture and examined with respect to its effect on reversible dehydrogenation of the Li-Mg-B-H system. Experimental study showed that TiF(3) is highly effective for promoting the two-step dehydrogenation reaction in the Li-Mg-B-H system. Compared to the neat 2LiH + MgB(2) sample, the 2LiH + MgB(2) + 0.01TiF(3) sample exhibits significantly reduced dehydrogenation temperature and markedly enhanced dehydriding rate at both steps. Furthermore, the catalytic enhancement arising upon adding TiF(3) additive was observed to persist well in the hydrogenation/dehydrogenation cycles. Based on the results of phase analysis and a series of designed experiments, the mechanism underlying the observed property improvement is discussed.
关键词:
complex hydrides;libh4;tif3;kinetics;naalh4
米菁
,
郝雷
,
刘晓鹏
,
杜淼
,
蒋利军
,
王树茂
金属功能材料
doi:10.13228/j.boyuan.issn1005-8192.2015053
基于对Li-Mg N-H体系放氢动力学机理的研究发现,其放氢过程的速率控制步骤是Li+、H+或H-的扩散.在实验中,原位析出的Li3Bi相增加了Li-Mg-N-H体系放氢过程中Li+离子的扩散速率,进而使得该体系在200℃下放氢量(质量分数)从4.37％增加到4.55％,达到90％放氢量的放氢时间从298 min缩短到11 min.
关键词:
储氢材料
,
Li-Mg-N-H Li3Bi
,
放氢
