Bulk anisotropic Nd-Fe-B magnets were prepared from hydrogen-disproportionation-desorption-recombination（HDDR） powders via spark plasma sintering（SPS） and subsequent hot deformation. The influence of sintering tem...Bulk anisotropic Nd-Fe-B magnets were prepared from hydrogen-disproportionation-desorption-recombination（HDDR） powders via spark plasma sintering（SPS） and subsequent hot deformation. The influence of sintering temperature on the structure and magnetic properties of the spark plasma sintered Nd-Fe-B magnets were studied. The remanence Br, intrinsic coercivity Hcj, and the maximum energy product（BH）max, of sintered Nd-Fe-B magnets first increase and then decrease with the increase of sintering temperature, TSPS, from 650 °C to 900 °C. The optimal magnetic properties can be obtained when TSPS is 800 °C. The Nd-Fe-B magnet sinter treated at 800 °C was subjected to further hot deformation. Compared with the starting HDDR powders or the SPS treated magnets, the hot-deformed magnets present more obvious anisotropy and possess much better magnetic properties due to the good c-axis texture formed in the deformation process. The anisotropic magnet deformed at 800 °C with 50% compression ratio has a microstructure consisting of well aligned and platelet-shaped Nd2Fe14 B grains without abnormal grain growth and exhibits excellent magnetic properties parallel to the pressing axis.展开更多
Mg17Al12-hydride （abbreviated as MAH） was selected as a destabilization agent to improve de/rehydrogenation properties of LiBH4. 58LiBH4＋Mg17Al12-hydride composite was prepared by ball-milling. It is found that the...Mg17Al12-hydride （abbreviated as MAH） was selected as a destabilization agent to improve de/rehydrogenation properties of LiBH4. 58LiBH4＋Mg17Al12-hydride composite was prepared by ball-milling. It is found that the dehydrogenation of ball-milled LiBH4/MAH composite presents a two-step reaction for hydrogen release. The composite starts desorbing hydrogen at about 300 ℃ and yields 9.8%of hydrogen （mass fraction） below 500 ℃. By adding MAH, the dehydrogenation kinetics of LiBH4 is improved and the dehydrogenation temperature of LiBH4 is also lowered by 20 ℃. High rehydriding capacity of 8.3% was obtained for the dehydrogenated composite in the first cycle at 450 ℃. The XRD analysis shows the formation of MgB2 and AlB2 in the dehydrogenation process, which reduces the thermodynamics stability of LiBH4 system and is beneficial to the reversible hydrogen storage behaviors of LiBH4/MAH composite.展开更多
The release of hydroxyl ions from two variable charge soils associated with the adsorption of chloride in NaClO4 solutions was examined. The complete release required about 10 minutes. The release decreased with the i...The release of hydroxyl ions from two variable charge soils associated with the adsorption of chloride in NaClO4 solutions was examined. The complete release required about 10 minutes. The release decreased with the increase in the NaClO4 concentration at first and eventually was little affected by the latter. The adsorption of Cl- was almost linearly related with the quantity of NaCl added to the system, while the OHrelease-NaCl curve varied with the soil type and the concentration of NaClO4. The logarithm of the quantity of released OH- was linearly related with the pH. The ratio of released OH- to adsorbed Cl- was larger in dilute NaClO4 solutions than in concentrated solutions and decreased with increasing NaCl.展开更多
基金Project(NCET-10-0364)supported by the Program for New Century Excellent Talents in University,ChinaProject(2012ZG0006)supported by the Fundamental Research Funds for the Central Universities,ChinaProject(51174095)supported the National Natural Science Foundation of China
文摘Bulk anisotropic Nd-Fe-B magnets were prepared from hydrogen-disproportionation-desorption-recombination（HDDR） powders via spark plasma sintering（SPS） and subsequent hot deformation. The influence of sintering temperature on the structure and magnetic properties of the spark plasma sintered Nd-Fe-B magnets were studied. The remanence Br, intrinsic coercivity Hcj, and the maximum energy product（BH）max, of sintered Nd-Fe-B magnets first increase and then decrease with the increase of sintering temperature, TSPS, from 650 °C to 900 °C. The optimal magnetic properties can be obtained when TSPS is 800 °C. The Nd-Fe-B magnet sinter treated at 800 °C was subjected to further hot deformation. Compared with the starting HDDR powders or the SPS treated magnets, the hot-deformed magnets present more obvious anisotropy and possess much better magnetic properties due to the good c-axis texture formed in the deformation process. The anisotropic magnet deformed at 800 °C with 50% compression ratio has a microstructure consisting of well aligned and platelet-shaped Nd2Fe14 B grains without abnormal grain growth and exhibits excellent magnetic properties parallel to the pressing axis.
基金Project(2010CB631304)supported by the National Basic Research Program of ChinaProjects(51001090,51171173)supported by the National Natural Science Foundation of ChinaProject(20090101110050)supported by the University Doctoral Foundation of the Ministry of Education,China
文摘Mg17Al12-hydride （abbreviated as MAH） was selected as a destabilization agent to improve de/rehydrogenation properties of LiBH4. 58LiBH4＋Mg17Al12-hydride composite was prepared by ball-milling. It is found that the dehydrogenation of ball-milled LiBH4/MAH composite presents a two-step reaction for hydrogen release. The composite starts desorbing hydrogen at about 300 ℃ and yields 9.8%of hydrogen （mass fraction） below 500 ℃. By adding MAH, the dehydrogenation kinetics of LiBH4 is improved and the dehydrogenation temperature of LiBH4 is also lowered by 20 ℃. High rehydriding capacity of 8.3% was obtained for the dehydrogenated composite in the first cycle at 450 ℃. The XRD analysis shows the formation of MgB2 and AlB2 in the dehydrogenation process, which reduces the thermodynamics stability of LiBH4 system and is beneficial to the reversible hydrogen storage behaviors of LiBH4/MAH composite.
文摘The release of hydroxyl ions from two variable charge soils associated with the adsorption of chloride in NaClO4 solutions was examined. The complete release required about 10 minutes. The release decreased with the increase in the NaClO4 concentration at first and eventually was little affected by the latter. The adsorption of Cl- was almost linearly related with the quantity of NaCl added to the system, while the OHrelease-NaCl curve varied with the soil type and the concentration of NaClO4. The logarithm of the quantity of released OH- was linearly related with the pH. The ratio of released OH- to adsorbed Cl- was larger in dilute NaClO4 solutions than in concentrated solutions and decreased with increasing NaCl.
