Copper nanoparticles were successfully prepared in large scale by means of anodic arc discharging plasma method in inert atmosphere. The particle size, specific surface area, crystal structure, and morphology of the s...Copper nanoparticles were successfully prepared in large scale by means of anodic arc discharging plasma method in inert atmosphere. The particle size, specific surface area, crystal structure, and morphology of the samples were characterized by X-ray diffraction （XRD）, BET equation, transmission electron microscopy （TEM）, and the corresponding selected area electron diffraction （SAED）. The experimental results indicate that the crystal structure of the samples is fcc structure the same as that of the bulk materials. The specific surface area is 11 m^2/g, the particle size distribution is 30 to 90 nm, and the average particle size is about 67 nm obtained from TEM and confirmed from XRD and BET results. The nanoparticles with uniform size, high purity, narrow size distribution and spherical shape can be prepared by this convenient and effective method.展开更多
TIG welding was used to deposit Co-8.8 Al-9.8 W-0.2 B superalloy on 304 austenite stainless steel. The form factor of weld, dilution ratio, microhardness, microstructure and distribution of alloying elements were inve...TIG welding was used to deposit Co-8.8 Al-9.8 W-0.2 B superalloy on 304 austenite stainless steel. The form factor of weld, dilution ratio, microhardness, microstructure and distribution of alloying elements were investigated. The microstructure of cladding layer was mainly hypoeutectic. The primary phases were cobalt-rich solid solution. The eutectic phase was composed of cobalt-rich solid solution,Co6W6C and Co Cx. When the boron content increased from 0.2% to 0.5%,the dilution ratio decreased,the primary phase became coarse and the microhardness decreased. When the boron content was from 0.5% to 2%,the dilution ratio and microhardness increased obviously,but the primary phase was refined.The hard phase of Co-8.8 Al-9.8 W became refined and the amount was raised,and the performance of cladding layer was improved with appropriate boron increase.展开更多
基金This work was financially supported by the Natural Science Foundation of Gansu Province, China (No. 3ZS042-B25-017)
文摘Copper nanoparticles were successfully prepared in large scale by means of anodic arc discharging plasma method in inert atmosphere. The particle size, specific surface area, crystal structure, and morphology of the samples were characterized by X-ray diffraction （XRD）, BET equation, transmission electron microscopy （TEM）, and the corresponding selected area electron diffraction （SAED）. The experimental results indicate that the crystal structure of the samples is fcc structure the same as that of the bulk materials. The specific surface area is 11 m^2/g, the particle size distribution is 30 to 90 nm, and the average particle size is about 67 nm obtained from TEM and confirmed from XRD and BET results. The nanoparticles with uniform size, high purity, narrow size distribution and spherical shape can be prepared by this convenient and effective method.
基金supported by the National Natural Science Foundation of China(Grant No.51561019)
文摘TIG welding was used to deposit Co-8.8 Al-9.8 W-0.2 B superalloy on 304 austenite stainless steel. The form factor of weld, dilution ratio, microhardness, microstructure and distribution of alloying elements were investigated. The microstructure of cladding layer was mainly hypoeutectic. The primary phases were cobalt-rich solid solution. The eutectic phase was composed of cobalt-rich solid solution,Co6W6C and Co Cx. When the boron content increased from 0.2% to 0.5%,the dilution ratio decreased,the primary phase became coarse and the microhardness decreased. When the boron content was from 0.5% to 2%,the dilution ratio and microhardness increased obviously,but the primary phase was refined.The hard phase of Co-8.8 Al-9.8 W became refined and the amount was raised,and the performance of cladding layer was improved with appropriate boron increase.
