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Direct bonding of AZ31B and ZrO_(2) induced by interfacial sono-oxidation reaction at a low temperature
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作者 z.l.li J.Wang +4 位作者 S.L.Yi X.G.Song J.H.Fu Y.Shi J.C.Feng 《Journal of Magnesium and Alloys》 2025年第9期4316-4326,共11页
Recently,the presentation of the metal-ceramic composite structure design provides an alternative idea for the improvement of components service performance,while conventional methods for joining metals and ceramics h... Recently,the presentation of the metal-ceramic composite structure design provides an alternative idea for the improvement of components service performance,while conventional methods for joining metals and ceramics have to involve a high heat input.However,due to the low melting point of magnesium alloys,the magnesium alloys-ceramics joining system necessitates a low joining temperature.Ultrasonic vibrations can induce numerous defects in the solid matrix,which can effectively promote atomic diffusion and metallurgical bonding between solid-phase interfaces at low temperatures.Thus,ultrasonic-assisted bonding is a highly promising method for achieving rapid and reliable joining between metals and ceramics without the use of interlayers.In this study,the direct bonding of AZ31B alloy with ZrO_(2) ceramic was successfully achieved at 200℃.A polycrystal spinel MgAl_(2)O_(4) with an average thickness of 55 nm was identified at the AZ31B/ZrO_(2) interface.The average shear strength of joints reached 30.47 MPa.Furthermore,the dynamic recrystallization of AZ31B and the oxygendepletion behavior of ZrO_(2) during the bonding process were characterized to illustrate the contribution of ultrasonic vibration to joint bonding.Consequently,the solid interfacial sono-oxidation reaction is proposed to discuss the bonding mechanism of the joint in detail. 展开更多
关键词 AZ31b-ZrO_(2)joints Direct bonding Ultrasonic waves Sono-oxidation reaction Nano-scale MgAl_(2)O_(4)
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Reactive destabilization and bidirectional catalyzation for reversible hydrogen storage of LiBH_(4) by novel waxberry-like nano-additive assembled from ultrafine Fe_(3)O_(4) particles 被引量:2
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作者 S.Wang M.H.Wu +5 位作者 Y.Y.Zhu z.l.li Y.X.Yang Y.Z.Li H.F.Liu M.X.Gao 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2024年第6期63-71,共9页
LiBH_(4) containing 18.5 wt.%H_(2) is an attractive high-capacity hydrogen storage material,however,it suffers from high operation temperature and poor reversibility.Herein,a novel and low-cost bifunctional additive,w... LiBH_(4) containing 18.5 wt.%H_(2) is an attractive high-capacity hydrogen storage material,however,it suffers from high operation temperature and poor reversibility.Herein,a novel and low-cost bifunctional additive,waxberry-like Fe_(3)O_(4) secondary nanospheres assembled from ultrafine primary Fe_(3)O_(4) nanoparticles,is synthesized,which exhibits significant destabilization and bidirectional catalyzation towards(de)hydrogenation of LiBH_(4).With an optimized addition of 30 wt.% waxberry-like Fe_(3)O_(4),the system initiated dehydrogenation below 100℃ and released a total of 8.1 wt.%H_(2) to 400℃.After 10 cycles,a capacity retention of 70% was achieved,greatly superior to previously reported oxides-modified systems.The destabilizing and catalyzing mechanisms of waxberry-like Fe_(3)O_(4) on LiBH_(4) were systematically analyzed by phase and microstructural evolutions during dehydrogenation and hydrogenation cycling as well as density functional theory(DFT)calculations.The present work provides new insights in developing advanced nano-additives with unique structural and multifunctional designs towards LiBH4 hydrogen storage. 展开更多
关键词 LiBH_(4) Hydrogen storage Waxberry-like Fe_(3)O_(4) DESTABILIZATION Catalysis
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