The so-called 'negative difference effect'(NDE) was often defined by the increasing rate of hydrogen evolution from magnesium(Mg) surface under anodic polarization.In this work,a series of electrochemical test...The so-called 'negative difference effect'(NDE) was often defined by the increasing rate of hydrogen evolution from magnesium(Mg) surface under anodic polarization.In this work,a series of electrochemical tests and microstructure observations were performed to provide an evidence that the NDE of Mg-Li alloys can be retarded by increasing lithium content.Potentiostatic,galvanostatic and potentiodynamic polarization experiments using Mg-xLi(x=4,7.5 and 14 wt%) alloys electrodes indicated that Mg-4 Li alloy maintained the enhancing NDE prior to anodic dissolution as that of conventional Mg alloys.However,the emergence of β-Li phase weakened the NDE of duplex Mg-7.5 Li alloy at a low anodic current density,but it was still enhanced apparently after a high applied anodic value(more than 2 mA/cm^2).The surface observations,including the plane and cross-sectional morphologies,confirmed that the cracked surface film derived from the anodic dissolution resulted in the catalytic activity of NDE for Mg-4 Li and Mg-7.5 Li alloys.Furthermore,the NDE of Mg-14 Li alloy was suppressed obviously after a prior applied anodic polarization,which was attributed to the persistent and integrated surface film which endured a higher level of applied anodic potential and current.展开更多
Inferior absolute strength and dissolution properties are the main bottlenecks for the widespread application of dissolvable magnesium alloys in complex working environments for unconventional oil and gas resources.He...Inferior absolute strength and dissolution properties are the main bottlenecks for the widespread application of dissolvable magnesium alloys in complex working environments for unconventional oil and gas resources.Here,a novel functional peak-aged Mg-9.5Gd-2.7Y-0.9Zn-0.8Cu-0.4Ni(wt.%) alloy for fracturing tools is reported,and it possesses an ultimate tensile strength of 457.6 MPa,ultimate compressive strength of 620.7 MPa and dissolution rate of ~43.7 mg·cm^(-2)·h^(-1) in 3 wt.% KCl solutions at 93℃.The excellent strength of the agedalloy is primarily attributed to the combination of grain refinement,long-period stacking ordered(LPSO) strengthening,and precipitation strengthening induced by stacking fault and β’ phase,among which the precipitation strengthening is dominant.Further investigations confirm that the corrosion is triggered from the micro-galvanic coupling between the Mg matrix and the cathodic lamellar and block LPSO phases.Strip-shaped corrosion pits along with LPSO phases are subsequently formed,significantly accelerating corrosion.The β’ precipitates can effectively improve the strength without compromising the dissolution rate because of their nanoscale size.This study provides an excellent material selection for dissolvable fracturing tools and presents a strategy by which a synergistic combination of strength and dissolution rate is achieved via peak-aging treatment.展开更多
The eutectic Ag-Cu alloys exhibiting fine Ag-Cu lamellar eutectic structure formed upon rapid solidification have great potentials being used in various engineering fields.However,the desired fine primary lamellar eut...The eutectic Ag-Cu alloys exhibiting fine Ag-Cu lamellar eutectic structure formed upon rapid solidification have great potentials being used in various engineering fields.However,the desired fine primary lamellar eutectic structure(PLES)is usually replaced by a coarse anomalous eutectic structure(AES)when the undercooling prior to solidification exceeds a certain value.The forming mechanism of AES in the undercooled eutectic Ag-Cu alloy has been a controversial issue.In this work,the undercooled Ag-39.9 at.% Cu eutectic alloy is solidified under different cooling conditions by using techniques of melt fluxing and copper mold casting.The results show that the coupled eutectic growth of this alloy undergoes a transition from a slow eutectic-cellular growth(ECG)to a rapid eutectic-dendritic growth(EDG)above a undercooling of 72 K,accompanying with an abrupt change of the distribution and amount of AES in as-solidified microstructures.Two kinds of primary lamellar eutectic structures are formed by ECG and EDG during recalescence,respectively.The destabilization of PLES that causes the formation of AES is ascribed to two different mechanisms based on the microstructural examination and theoretical calculations.Below 72 K,the destabilization of PLES formed by slow ECG is caused by the mechanism of"termination migration"driven by interfacial energy.While above 72 K,the destabilization of PLES formed by rapid EDG is attributed to the unstable perturbation of interface driven by interfacial energy and solute supersaturation.展开更多
In this work, a direct green solid-phase reduction method for the fabrication of large yield of ordered phase Fe-Pt alloy nanoparticles was reported, in which inorganic salts were used as metal precursors and H_2-cont...In this work, a direct green solid-phase reduction method for the fabrication of large yield of ordered phase Fe-Pt alloy nanoparticles was reported, in which inorganic salts were used as metal precursors and H_2-containing atmosphere was used as reducer. Utilizing this method, the composition and chemical ordered phase, such as L1_2-Fe_3 Pt, L1_2-FePt_3, and L1_0-FePt phases can be easily achieved by one step reaction. The synthesized nanoparticles have clean surface because no organic precursors, no organic solutions or organic surfactants/ligands were used. Their magnetic performance and the formation mechanism of Fe-Pt alloy nanoparticles were also investigated. This strategy can be applied to synthesize many other types of alloy nanoparticles with desired composition and necessary crystal structure, which can be used for a variety of practical applications, such as in magnetism and catalyst research fields.展开更多
基金supported financially by the National Key Research and Development Program of China (Nos. 2017YFB0702001 and 2016YFB0301105)the National Natural Science Foundation of China Projects (Nos. 51901047,51871211 and51701129)+5 种基金the Doctor Startup Fund of Natural Science Foundation Program of Liaoning Province (No. 2019-BS-200)the Strategic New Industry Development Special Foundation of Shenzhen (No. JCYJ20170306141749970)the Funds of International Joint Laboratory for Light Alloys, the Liaoning Bai Qian Wan Talents Programthe Domain Foundation of Equipment Advance Research of 13th Five-year Plan (No. 61409220118)the Innovation Fund of Institute of Metal Research (IMR), Chinese Academy of Sciences (CAS)the National Basic Research Program of China (No. 2013CB632205)。
文摘The so-called 'negative difference effect'(NDE) was often defined by the increasing rate of hydrogen evolution from magnesium(Mg) surface under anodic polarization.In this work,a series of electrochemical tests and microstructure observations were performed to provide an evidence that the NDE of Mg-Li alloys can be retarded by increasing lithium content.Potentiostatic,galvanostatic and potentiodynamic polarization experiments using Mg-xLi(x=4,7.5 and 14 wt%) alloys electrodes indicated that Mg-4 Li alloy maintained the enhancing NDE prior to anodic dissolution as that of conventional Mg alloys.However,the emergence of β-Li phase weakened the NDE of duplex Mg-7.5 Li alloy at a low anodic current density,but it was still enhanced apparently after a high applied anodic value(more than 2 mA/cm^2).The surface observations,including the plane and cross-sectional morphologies,confirmed that the cracked surface film derived from the anodic dissolution resulted in the catalytic activity of NDE for Mg-4 Li and Mg-7.5 Li alloys.Furthermore,the NDE of Mg-14 Li alloy was suppressed obviously after a prior applied anodic polarization,which was attributed to the persistent and integrated surface film which endured a higher level of applied anodic potential and current.
基金The Major State Research and Development Program of China (No. 2021YFB3701100, No. SQ2020YFF0405156)the National Natural Science Foundation of China (No.52171097, No. 51971020)+2 种基金Beijing Laboratory of Metallic Materials and Processing for Modern Transportationthe Fundamental Research Funds for the Central Universities(No. FRF-IC-20–08)“Dingxinbeike” Project(G20200001105) for the international communication。
文摘Inferior absolute strength and dissolution properties are the main bottlenecks for the widespread application of dissolvable magnesium alloys in complex working environments for unconventional oil and gas resources.Here,a novel functional peak-aged Mg-9.5Gd-2.7Y-0.9Zn-0.8Cu-0.4Ni(wt.%) alloy for fracturing tools is reported,and it possesses an ultimate tensile strength of 457.6 MPa,ultimate compressive strength of 620.7 MPa and dissolution rate of ~43.7 mg·cm^(-2)·h^(-1) in 3 wt.% KCl solutions at 93℃.The excellent strength of the agedalloy is primarily attributed to the combination of grain refinement,long-period stacking ordered(LPSO) strengthening,and precipitation strengthening induced by stacking fault and β’ phase,among which the precipitation strengthening is dominant.Further investigations confirm that the corrosion is triggered from the micro-galvanic coupling between the Mg matrix and the cathodic lamellar and block LPSO phases.Strip-shaped corrosion pits along with LPSO phases are subsequently formed,significantly accelerating corrosion.The β’ precipitates can effectively improve the strength without compromising the dissolution rate because of their nanoscale size.This study provides an excellent material selection for dissolvable fracturing tools and presents a strategy by which a synergistic combination of strength and dissolution rate is achieved via peak-aging treatment.
基金the National Natural Science Foundation of China(Nos.51771153,51371147,51790481 and 51431008)the Innovation Guidance Support Project for Taicang Top Research Institutes(No.TC2018DYDS20)the Innovation Foundation for Doctor Dissertation of Northwestern Polytechnical University(CX201825)。
文摘The eutectic Ag-Cu alloys exhibiting fine Ag-Cu lamellar eutectic structure formed upon rapid solidification have great potentials being used in various engineering fields.However,the desired fine primary lamellar eutectic structure(PLES)is usually replaced by a coarse anomalous eutectic structure(AES)when the undercooling prior to solidification exceeds a certain value.The forming mechanism of AES in the undercooled eutectic Ag-Cu alloy has been a controversial issue.In this work,the undercooled Ag-39.9 at.% Cu eutectic alloy is solidified under different cooling conditions by using techniques of melt fluxing and copper mold casting.The results show that the coupled eutectic growth of this alloy undergoes a transition from a slow eutectic-cellular growth(ECG)to a rapid eutectic-dendritic growth(EDG)above a undercooling of 72 K,accompanying with an abrupt change of the distribution and amount of AES in as-solidified microstructures.Two kinds of primary lamellar eutectic structures are formed by ECG and EDG during recalescence,respectively.The destabilization of PLES that causes the formation of AES is ascribed to two different mechanisms based on the microstructural examination and theoretical calculations.Below 72 K,the destabilization of PLES formed by slow ECG is caused by the mechanism of"termination migration"driven by interfacial energy.While above 72 K,the destabilization of PLES formed by rapid EDG is attributed to the unstable perturbation of interface driven by interfacial energy and solute supersaturation.
基金financially supported by the National Natural Science Foundation of China (Grant Nos.51772220,51772219,51771095,51422106)Zhejiang Provincial Natural Science Foundation of China (No.D19E010001)the National Basic Research Program of China (Grant No.2014CB643702)
文摘In this work, a direct green solid-phase reduction method for the fabrication of large yield of ordered phase Fe-Pt alloy nanoparticles was reported, in which inorganic salts were used as metal precursors and H_2-containing atmosphere was used as reducer. Utilizing this method, the composition and chemical ordered phase, such as L1_2-Fe_3 Pt, L1_2-FePt_3, and L1_0-FePt phases can be easily achieved by one step reaction. The synthesized nanoparticles have clean surface because no organic precursors, no organic solutions or organic surfactants/ligands were used. Their magnetic performance and the formation mechanism of Fe-Pt alloy nanoparticles were also investigated. This strategy can be applied to synthesize many other types of alloy nanoparticles with desired composition and necessary crystal structure, which can be used for a variety of practical applications, such as in magnetism and catalyst research fields.
