Effects of Heterogenization Treatment on the Hot-Working Temperature and Mechanical Properties of Al-Cu-Mg-Mn-(Zr) Alloys.

This study investigated the effects of a minor Zr addition (0.15 wt%) and heterogenization treatment (one-stage/two-stage) on the hot-working temperature and mechanical properties in Al-4.9Cu-1.2Mg-0.9Mn alloy. The results indicated that the eutectic phases (α-Al + θ-Al2Cu + S-Al2CuMg) dissolved after heterogenization, retaining θ-Al2Cu and τ1-Al29Cu4Mn6 phases, while the onset melting temperature increased to approximately 17 °C. A change in the onset melting temperature and evolution of the microstructure is used to assess an improvement in hot-working behavior. With the minor Zr addition, the alloy exhibited enhanced mechanical properties due to grain growth inhibition. Zr-added alloys show 490 ± 3 MPa ultimate tensile strength and 77.5 ± 0.7 HRB hardness after T4 tempering, compared to 460 ± 2.2 MPa and 73.7 ± 0.4 HRB for un-added alloys. Additionally, combining minor Zr addition and two-stage heterogenization resulted in finer Al3Zr dispersoids. Two-stage heterogenized alloys had an average Al3Zr size of 15 ± 5 nm, while one-stage heterogenized alloys had an average size of 25 ± 8 nm. A partial decrease in the mechanical properties of the Zr-free alloy was observed after two-stage heterogenization. The one-stage heterogenized alloy had 75.4 ± 0.4 HRB hardness after being T4-tempered, whereas the two-stage heterogenized alloy had 73.7 ± 0.4 HRB hardness after being T4-tempered.

Effect of Natural Aging on the Stress Corrosion Cracking Behavior of A201-T7 Aluminum Alloy.

The effect of natural aging on the stress corrosion cracking (SCC) of A201-T7 alloy was investigated by the slow strain rate testing (SSRT), transmission electron microscopy (TEM), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), conductivity, and polarization testing. The results indicated that natural aging could significantly improve the resistance of the alloys to SCC. The ductility loss rate of the unaged alloy was 28%, while the rates for the 24 h and 96 h aged alloys were both 5%. The conductivity of the as-quenched alloy was 30.54 (%IACS), and the conductivity of the 24 h and 96 h aged alloys were decreased to 28.85 and 28.65. After T7 tempering, the conductivity of the unaged, 24 h, and 96 h aged alloys were increased to 32.54 (%IACS), 32.52 and 32.45. Besides, the enthalpy change of the 24 h and 96 h aged alloys increased by 36% and 37% compared to the unaged alloy. The clustering of the solute atoms would evidently be enhanced with the increasing time of natural aging. Natural aging after quenching is essential to improve the alloy's resistance to SCC. It might be due to the prevention of the formation of the precipitation free zone (PFZ) after T7 tempering.

Effects of Mn, Zn Additions and Cooling Rate on Mechanical and Corrosion Properties of Al-4.6Mg Casting Alloys.

The mechanical properties of the Al-Mg alloy can be enhanced by adding metallic elements, but a continuous distribution of precipitates at grain boundaries leads to intergranular corrosion during sensitization treatment. In the present work, Mn, Zn additions, water cooling and furnace cooling were executed to investigate their effects on the mechanical and corrosion properties of the Al-4.6Mg alloy. Our results show that adding Mn to Al-4.6Mg alloys may produce grain refinement and dispersion strengthening, increasing tensile strength and hardness. The presence of Mn did not affect the corrosion resistance of Al-Mg alloys. Adding Zn to the Al-4.6Mg alloy increased tensile strength and hardness, but decreased corrosion resistance. Combined, the addition of Mn and Zn to the Al-4.6Mg alloy exhibited the highest tensile strength and hardness, but seriously reduced corrosion resistance. Furnace cooling substituted for water quenching could avoid intergranular corrosion, but slightly decreased the tensile strength and hardness by 7.0% and 6.8%, respectively.

The Effects of a Trace Amount of Manganese and the Homogenization on the Recrystallization of Al-7Mg-0.15Ti Alloys.

The aim of this study is to explore the effects of Manganese addition and homogenization treatment on the microstructures and mechanical properties of the Al-7Mg-0.15Ti (B535.0) alloy. The optical microscopy, electrical conductivity measurements, transmission electron microscopy, scanning electron microscopy (SEM + EBSD), as well as Rockwell hardness and tensile tests, were exploited for this purpose. The main objectives are to refine the grain size, inhibit grain growth in the annealed state, and enhance the mechanical strength of the alloy. The results show that the addition of manganese to the Al-7Mg-0.15Ti alloys refined the as-cast and recrystallized grains of the alloys. During the homogenization process, Al4Mn high-temperature stable dispersoids were precipitated in the aluminum matrix. After annealing, the Al4Mn particles blocked the movement of grain boundaries during the growth of the recrystallized grains and inhibited grain growth. Consequently, the annealed alloys showed grain refinement and dispersion strengthening. The Al4Mn dispersoids of the alloys with manganese added were smaller and denser after a two-stage homogenization process compared to those that underwent a one-stage homogenization process. By contrast, for the alloys without the addition of manganese, the recrystallized grains showed normal growth after annealing, and different homogenization processes had no significantly different effects.

Rare metal-ion metathesis of a tetrahedral Zn(ii) core of a noncentrosymmetric (3,4)-connected 3D MOF.

An SHG-active noncentrosymmetric (3,4)-connected Zn(ii)-organic framework, {[Zn2(4-abpt)(3,4-pydc)2]·2DMAc·3MeOH·H2O}n (1-Zn), was synthesized using a mixed-ligand system. The 1-Zn framework undergoes metal metathesis, with the complete exchange of the tetrahedrally coordinated ZnII ions with CuII ions while retaining the integrity of the network.

Cost-Effective Hierarchical Catalysts for Promoting Hydrogen Release from Complex Hydrides.

Fe nanoparticles (∼10 nm), used to grow carbon nanotubes (CNTs), have an outstanding ability to catalyze the dehydrogenation of LiAlH4 . The CNTs help connect Fe and LiAlH4 and create microchannels among the composite, thus promoting the release of hydrogen. Inspired by these results, a supercritical-CO2 -fluid-assisted deposition technique is employed to decorate the Fe/CNTs with highly dispersed nanosized Ni (∼2 nm in diameter) for better performance. With the incorporation of 10 wt % of this hierarchical catalyst (Ni/Fe/CNTs), the initial dehydrogenation temperature of LiAlH4 is decreased from ∼135 to ∼40 °C. At 100 °C, this catalyzed LiAlH4 takes only ∼0.1 h to release 4.5 wt % hydrogen, which is more than 100 times faster than the time needed with pristine LiAlH4 . The dehydrogenation mechanism of the complex hydride is examined using in situ synchrotron X-ray diffraction.

Metal/graphene nanocomposites synthesized with the aid of supercritical fluid for promoting hydrogen release from complex hydrides.

With the aid of supercritical CO2, Fe-, Ni-, Pd-, and Au-nanoparticle-decorated nanostructured carbon materials (graphene, activated carbon, carbon black, and carbon nanotubes) are synthesized for catalyzing the dehydrogenation of LiAlH4. The effects of the metal nanoparticle size and distribution, and the type of carbon structure on the hydrogen release properties are investigated. The Fe/graphene nanocomposite, which consists of ∼2 nm Fe particles highly dispersed on graphene nanosheets, exhibits the highest catalytic performance. With this nanocomposite, the initial dehydrogenation temperature can be lowered (from ∼135 °C for pristine LiAlH4) to ∼40 °C without altering the reaction route (confirmed by in situ X-ray diffraction), and 4.5 wt% H2 can be released at 100 °C within 6 min, which is faster by more than 135-fold than the time required to release the same amount of H2 from pristine LiAlH4.

Buckyball-, carbon nanotube-, graphite-, and graphene-enhanced dehydrogenation of lithium aluminum hydride.

Compared to C60, carbon nanotubes, and graphite, graphene more effectively lowers the dehydrogenation temperature and improves the dehydrogenation kinetics of LiAlH4. With 15 wt% graphene incorporation, the initial hydrogen release temperature is ~80 °C (60 °C lower than that of pristine LiAlH4).