铂族金属铑的合金化活化溶解规律及其机理

对铂族金属铑添加金属铝粉进行合金化活化溶解规律及机理进行研究。采用XRD和SEM等技术对铝铑合金经稀酸溶出铝后所得的粉末状铑物料的微观结构物及相组成进行表征。研究结果表明:在铝粉与铑质量比为10、合金化活化温度为1 200℃、活化时间为120 min的条件下所得铝铑合金经稀酸溶出铝,所得铑物料采用王水溶解,铑的溶解率达到99%以上;该过程的机理主要在于铝铑合金经稀酸溶出铝后,所得铑物料粒度变细,处于高度分散状态,晶体结晶程度较差,晶格存在缺陷,具备较高的反应活性;该铑物料通过王水溶解,实现了铑的高效溶解。

Influence of thermomechanical treatment on recrystallization and softening resistance of Cu-6.5Fe-0.3Mg alloy

The recrystallization and softening resistance of a Cu-6.5Fe-0.3Mg(mass fraction,%)alloy prepared by Process 1(cold rolling heat treatment)and Process 2(hot/cold rolling heat treatment)were studied using Vickers hardness tests,tensile tests,scanning electron microscopy and transmission electron microscopy.The softening temperature,hardness and tensile strength of the alloy prepared by Process 2 were 110°C,HV 15 and 114 MPa higher,respectively,than those of the alloy prepared by Process 1 after aging at 300°C.The recrystallization activation energy of the alloys prepared by Process 1 and Process 2 were 72.83 and 98.11 kJ/mol,respectively.The pinning effects of the precipitates of the two alloys on grain boundaries and dislocations were basically the same.The softening mechanism was mainly attributed to the loss of dislocation strengthening.The higher Fe fiber density inhibited the average free migration path of dislocations and grain boundary migration in the alloy,which was the main reason for higher softening temperature of the alloy prepared by Process 2.

Fretting wear and friction oxidation behavior of 0Cr20Ni32AlTi alloy at high temperature

The fretting wear behavior of 0Cr20Ni32AlTi alloy was investigated with crossed cylinder contact under 80 N at 300 and 400 °C.Wear scar and debris were analyzed systematically by scanning electron microscopy and X-ray photoelectron spectroscopy.The results show that the friction logs are mixed fretting regime and gross slip regime with the magnitudes of displacement of 10 and 20 μm,respectively.Severe wear and friction oxidation occur on the material surface.A large number of granular debris produced in the fretting process can be easily congregated and adhered at the contact zone after repeated crushes.The resultant of friction oxidation is mainly composed of Fe3O4,Fe2O3,Cr2O3 and NiO.Temperature and friction are the major factors affecting the oxidation reaction rate.The fretting friction effect can enhance the oxidation reaction activity of surface atoms of 0Cr20Ni32AlTi alloy and reduce the oxidation activation energy.As result,the oxidation reaction rate is accelerated.

Microstructure and mechanical properties of Fe_3Al alloys prepared by MA-PAS and MA-HP

Fe3Al alloys with nearly full density were fabricated by plasma activated sintering（PAS） and hot pressing（HP） from mechanical alloyed Fe-28%Al（mole fraction） powders,respectively.It is found that A2-type Fe3Al alloys were obtained by PAS,and they had a heterogeneous grain size distribution,most areas had a grain size smaller than 500 nm,and other areas had a grain size of about 1 μm.Different to PAS,D03-type Fe3Al alloys with a grain size of of 1-2 μm were obtained by HP.The compression testing results show that yield strength values of Fe3Al alloys fabricated by PAS and HP are almost equal at an elevated temperature,and the compression yield strength was about 100 MPa for all at 800 ℃.The room temperature compression ductility of Fe3Al alloys by PAS was about 20%,which was superior to that of Fe3Al alloys prepared by HP and casting.

Microstructure and properties of ultra-fine tungsten heavy alloys prepared by mechanical alloying and electric current activated sintering

The microstructure and properties of the 93W-4Ni-2Co-1Fe(mass fraction,%) tungsten heavy alloys prepared by mechanical alloying and electric current activated sintering from mixed elemental powders were investigated.After 15 h milling,the average W grain size in the powders is decreased to 120 nm.For the powders milled for 15 h,the density,hardness and transverse rupture strength of the alloys sintered only by an intensive pulse electric current are the maximum.When the total sintering time keeps constant,the properties of the sintered alloys can be obviously improved by optimizing the sintering time of pulse-and constant-currents.A bulk ultrafine alloy with an average W grain size of about 340 nm can be obtained by sintering 15 h-milled powders in a total sintering time of 6 min.The corresponding sintered density,hardness and transverse rupture strength reach 16.78 g /cm3,HRA84.3 and 968 MPa,respectively.

Preparation and electro-catalytic activity of nanoporous palladium by dealloying rapidly-quenched Al_(70)Pd_(17)Fe_(13) quasicrystalline alloy

The formation of nanoporous Pd was studied by electro-chemical dealloying a rapidly-quenched Al70Pd17Fe13 quasicrystal alloy in dilute NaCl aqueous solution,and the electro-catalytic activity of the nanoporous Pd towards methanol electro-oxidation was evaluated by cyclic voltammetry in 1 mol/L KOH solution.XRD and TEM analyses revealed that nano-decomposition of quasicrystal grains occurred in the initial stage of dealloying,and the fully dealloyed sample was composed of FCC-Pd phase.Scanning electron microscopy observation indicated that a maze-like nanoporous pattern was formed in the dealloyed sample,consisting of percolated pores of 5.20 nm in diameter in a skeleton of randomly-orientated Pd nano-ligaments with a uniform thickness of^5 nm.A retention of^12 at.%Al in the Pd nano-ligments was determined by energy dispersive X-ray spectroscopy(EDS).The nanoporous Pd demonstrated obvious electro-catalytic activity towards methanol electro-oxidation in alkaline environment.

Effect of indium addition on corrosion of AP65 magnesium alloy

The effect of indium addition on the corrosion behavior of AP65 Mg alloy was examined. The indium modified AP65 exhibits accelerated pitting corrosion and overall corrosion, but there is almost no incubation period at the onset of corrosion. Polarization curve measurements indicate that the indium modified AP65 has more negative corrosion potential, which is an improvement aspect of the electrochemical activation. The corrosion current density increases from 0.126 to 0.868 mA/cm2 with and without 2.0% (mass fraction) indium addition. The mean potentials of AP65 negatively shift from -1.491 V to -1.584 V by adding 2.0% indium. The effect of indium addition on the corrosion performance of AP65 seems to be associated with the decrease of cathode-to-anode area ratio of the alloy, which may change the electrochemical anode and cathode polarization behavior of the alloy.

Formation mechanism of electroless plating nickel-based composite coating on highly active rare earth magnesium alloys and its corrosion resistance and adhesion performance

The process of preparing anodic oxide film containing active sites and electroless nickel plating on highly active rare earth magnesium alloy was developed.The formation mechanism of electroless nickel plating on active anodic oxide film and the structure and properties of the composite coating were studied by several surface and electrochemical techniques.The results showed that Ag nanograins with an average size of 10 nm were embedded into the anodic oxide film with pores of 0.1−2μm.Ag nanoparticles provided a catalytic site for the deposition of Ni-B alloy,and the Ni crystal nucleus was first grown in horizontal mode and then in cylindrical mode.The corrosion potential of the composite coating increased by 1.37 V and the corrosion current reduced two orders of magnitude due to the subsequent deposition of Ni-P alloy.The high corrosion resistance was attributed to the misaligning of these micro defects in the three different layers and the amorphous structure of the Ni-P alloy in the outer layer.These findings provide a new idea for electroless nickel plating on anodic oxide film.

Effective enhancement of electrochemical energy storage of cobalt-based nanocrystals by hybridization with nitrogen-doped carbon nanocages

Cobalt-based oxygenic compounds Co(OH)2,CoO and Co3 O4 are attractive for electrochemical energy storage owing to their high theoretical capacities and pseudocapacitive properties.Despite the great efforts to their compositional and morphological regulations,the performances to date are still quite limited owing to the low active surface area and sluggish charge transfer kinetics.Herein,different Co-based nanocrystals(Co-NCs)were conveniently anchored on the hierarchical nitrogen-doped carbon nanocages(hNCNCs)with high specific surface area and coexisting micro-meso-macropores to decrease the size and facilitate the charge transfer.Accordingly,a high specific capacity of1170 Fg^-1 is achieved at 2 Ag^-1 for the Co(OH)2/hNCNCs hybrid,in which the capacitance of Co(OH)2(2214 F gco(OH)2)is approaching to its theoretical maximum(2595 Fg^-1),demonstrating the high utilization of active materials by the hybridization with N-doped nanocarbons.This study also reveals that these Co-NCs store/release electrical energy via the same reversible redox reaction despite their different pristine compositions.This insight on the energy storage of Co-based nanomaterials suggests that the commonly-employed transformation of the Co-NCs from Co(OH)2 to CoO and Co3 O4 on carbon supports is unnecessary and even could be harmful to the energy storage performance.The result is instructive to develop high-energy-density electrodes from transition metal compounds.