Seldom could metals and alloys maintain excellent properties in cryogenic condition, such as the ductility, owing to the restrained dislocation motion.However, a face-centered-cubic(FCC) CoCrFeNi highentropy alloy(HEA...Seldom could metals and alloys maintain excellent properties in cryogenic condition, such as the ductility, owing to the restrained dislocation motion.However, a face-centered-cubic(FCC) CoCrFeNi highentropy alloy(HEA) with great ductility is investigated under the cryogenic environment. The tensile strength of this alloy can reach a maximum at 1,251±10 MPa, and the strain to failure can stay at as large as 62% at the liquid helium temperature. We ascribe the high strength and ductility to the low stacking fault energy at extremely low temperatures,which facilitates the activation of deformation twinning.Moreover, the FCC→HCP(hexagonal close-packed) transition and serration lead to the sudden decline of ductility below 77 K. The dynamical modeling and analysis of serrations at 4.2 and 20 K verify the unstable state due to the FCC→HCP transition. The deformation twinning together with phase transformation at liquid helium temperature produces an adequate strain-hardening rate that sustains the stable plastic flow at high stresses, resulting in the serration feature.展开更多
In the present work, 3-methacryloxypropyltrimethoxy-silane silanized silica （SiO2-WD70） and 9,10-dihydro-9-oxa-10-phospha- phenanthrene-10-oxide immobilized silica （SiO2-WD70-DOPO） nanoparticles were prepared. Sil...In the present work, 3-methacryloxypropyltrimethoxy-silane silanized silica （SiO2-WD70） and 9,10-dihydro-9-oxa-10-phospha- phenanthrene-10-oxide immobilized silica （SiO2-WD70-DOPO） nanoparticles were prepared. Silica, SiO2-WD70 and SiO2- WD70-DOPO were incorporated into polypropylene （PP） by melt compounding. Differential scanning calorimetry （DSC）, X-ray diffraction （XRD） and polarized optical microscopy （POM） were employed to investigate the isothermal crystallization behavior of PP and PP/silica composites. The kinetic constant （kn）, and half crystallization time （t1/2） were calculated by Avrami equation, while the surface free energy of folding was calculated by Lauritzen-Hoffman theory. The increased k,, decreased t1/2 and the surface free energy （ere） in the order ofPP, PP/SiO2, PP/SiO2-WD70 and PP/SiO2-WD70-DOPO nanocomposites were attributed to the surface modification of silica. XRD indicated that SiO2-WD70-DOPO addition had no effect on PP crystal structure but accelerated the crystallization rate. POM determined that SiO2-WD70-DOPO addition promoted the nucleation of PP by inducing a higher nucleation density during isothermal conditions. The surface modified nanoparticle SiO2-WD70-DOPO might find possible application as a new type of inorganic nano-sized nucleation agent for PP.展开更多
基金supported in part by the Nationa Natural Science Foundation of China (51471025, 51671020, 51471024 and 11771407)the Department of Energy (DOE), Office of Fossil Energy, National Energy Technology Laboratory (DE-FE-0011194)+1 种基金the support from the US Army Research Office project (W911NF-13-1-0438)the support from the National Science Foundation (DMR-1611180 and 1809640)
文摘Seldom could metals and alloys maintain excellent properties in cryogenic condition, such as the ductility, owing to the restrained dislocation motion.However, a face-centered-cubic(FCC) CoCrFeNi highentropy alloy(HEA) with great ductility is investigated under the cryogenic environment. The tensile strength of this alloy can reach a maximum at 1,251±10 MPa, and the strain to failure can stay at as large as 62% at the liquid helium temperature. We ascribe the high strength and ductility to the low stacking fault energy at extremely low temperatures,which facilitates the activation of deformation twinning.Moreover, the FCC→HCP(hexagonal close-packed) transition and serration lead to the sudden decline of ductility below 77 K. The dynamical modeling and analysis of serrations at 4.2 and 20 K verify the unstable state due to the FCC→HCP transition. The deformation twinning together with phase transformation at liquid helium temperature produces an adequate strain-hardening rate that sustains the stable plastic flow at high stresses, resulting in the serration feature.
基金supported by the National Natural Science Foundation of China(51133009)the National Basic Research Program of China(2012CB720304)the“Strategic Priority Research Program”of the Chinese Academy of Sciences(XDA09030200)
文摘In the present work, 3-methacryloxypropyltrimethoxy-silane silanized silica （SiO2-WD70） and 9,10-dihydro-9-oxa-10-phospha- phenanthrene-10-oxide immobilized silica （SiO2-WD70-DOPO） nanoparticles were prepared. Silica, SiO2-WD70 and SiO2- WD70-DOPO were incorporated into polypropylene （PP） by melt compounding. Differential scanning calorimetry （DSC）, X-ray diffraction （XRD） and polarized optical microscopy （POM） were employed to investigate the isothermal crystallization behavior of PP and PP/silica composites. The kinetic constant （kn）, and half crystallization time （t1/2） were calculated by Avrami equation, while the surface free energy of folding was calculated by Lauritzen-Hoffman theory. The increased k,, decreased t1/2 and the surface free energy （ere） in the order ofPP, PP/SiO2, PP/SiO2-WD70 and PP/SiO2-WD70-DOPO nanocomposites were attributed to the surface modification of silica. XRD indicated that SiO2-WD70-DOPO addition had no effect on PP crystal structure but accelerated the crystallization rate. POM determined that SiO2-WD70-DOPO addition promoted the nucleation of PP by inducing a higher nucleation density during isothermal conditions. The surface modified nanoparticle SiO2-WD70-DOPO might find possible application as a new type of inorganic nano-sized nucleation agent for PP.
