K. Zhang
,
YQ. Wang
,
B.L. Zhou
,
YH. Zhou and H.L. Li (Institute of Metal Research
,
Chinese Academy of Scie11ces
,
Shenyang 110015
,
China International Center of Materials Physics
,
Chinese Academy of Sciences
,
Shenyang 110015
,
China Dept. of Materials Science and Engineering
,
Northwestern Polytechnical University
,
Xi'an 710072
,
China)
金属学报(英文版)
The mechanical properties and deformation mechanisms of unidirectional carbon fiber reiopreed magnesium composites under tensile loading are studied. Two different materials are used as fiber coatings: a single silica and a gradient C/SiC/SiO2. The results show that, under the same preparation conditions, composite with the former coating is broken in a non-cumulative mode and its failure stress is rather low. Conversely, the latter coating demonstrates much better efficiency and the cormsponding composite is broken in a cumttlative mode.
关键词:
tensile properties
,
null
,
null
材料科学技术（英文）
A large quantity of laminated fine grain zones were observed in the Al-Mg-Li alloy weld metal by manual TIG, which was not found in ordinary Al alloy welds. The fine grain zone is formed because of the Al-3(Zr,Ti) particles in the filler metal and the manual filling of filler metal in welding process.
关键词:
MA Zongyi YAO Zhongkai Harbin Institute of Technology
,
Harbin
,
China
金属学报(英文版)
The SiC_w/Al composite prepared by squeeze casting has a combination of superior room temperature specific strength and modulus together with excellent thermal properties.The extrusion can make an improvement on the strength and ductility of the composite from 582 MPa as squeeze casted up to 639 MPa,and on the transformation from isotropic to the anisotropic structure.This seems to be explained by the orientation of whiskers and the densification of dislocations in matrix.TEM observation indicates that the stacking fault is the usual planar defect on the SiC_w surface. composite;;SiC whisker;;Al alloy;;microstructure
关键词:
composite
,
null
,
null
,
null
Nabil S. Youssef
,
K.H.Hegab
材料科学技术（英文）
Some transition metal chelates of two ligands L1 and L2 were prepared and characterized by elemental analysis. The IR and 1H NMR spectra of several chelates of two ligands L1 and L2 showed the involvement of the azo group in chelation with the transition metal ions, in most of the studied chelates, and that the two ligands L1 and L2 showed the involvement of the azo group in chelation with the transition metal ions, in most of the studied chelates, and that the two ligands L1 and L2 were coordinated either in the enol or the keto form. IR spetra also showed that Fe(III)-, Ni(II)-, Mn(II)-, VO(II)-L1 and Cu(II)-L2 chelates behaved in a bidentate manner, in contrast with the two (1:1) M:L cobalt chelates with the two ligands are tridentate. TG analysis indicated the presence of three to twelve water molecules of hydration eliminated on heating up to 150°C and one or two coordinated water molecules removed at 150-180°C. The octahedral structure is proposed for all the chelates, except Cu(II)-L2 and Ni(II)-L1 chelates which have square planar geometry, based on their electronic spectra.
关键词:
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
Corrosion
This paper introduces the design of a localized corrosion rate monitoring instrument that can monitor and evaluate the maximum and stable localized corrosion rate of a nonpassivable metal in a corrosive environment by measuring the current density in a corrosion sensor with an occluded anode.
关键词:
instrument;localized corrosion rate;monitor
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
