Nanoglass–Nanocrystal Composite—a Novel Material Class for Enhanced Strength–Plasticity Synergy

The properties of a material can be engineered by manipulating its atomic and chemical architecture. Nanoglasses which have been recently invented and comprise nanosized glassy particles separated by amorphous interfaces, have shown promising properties. A potential way to exploit the structural benefits of nanoglasses and of nanocrystalline materials is to optimize the composition to obtain crystals forming within the glassy particles. Here, a metastable Fe‐10 at% Sc nanoglass is synthesized. A complex hierarchical microstructure is evidenced experimentally at the atomic scale. This bulk material comprises grains of a Fe₉₀Sc₁₀ amorphous matrix separated by an amorphous interfacial network enriched and likely stabilized by hydrogen, and property‐enhancing pure‐Fe nanocrystals self‐assembled within the matrix. This composite structure leads a yield strength above 2.5 GPa with an exceptional quasi‐homogeneous plastic flow of more than 60% in compression. This work opens new pathways to design materials with even superior properties.     

Role of plunge depth on the joint formation and mechanical behavior of Al6063-AZ91 dissimilar lap joint produced by friction stir welding

Dissimilar lap joint of Al6063 aluminium and AZ91 magnesium alloys was successfully produced by friction stir welding. Three different plunge depths (3.2 mm, 3.25 mm, and 3.3 mm) were adopted during welding. Similar Al6063–Al6063 lap joints were also produced along with the dissimilar Al6063–AZ91 joints for the purpose of comparing the joint formation. With the increased plunge depth, the width of the similar Al6063 - Al6063 lap joint was increased. On the contrary, joint width was decreased for the dissimilar joint with increased plunge depths. The dissimilar joint was formed with a strong metallurgical bonding between the Al6063 and AZ91 alloys, which is attributed to the mechanical mixing of these alloys in the nugget zone. Additionally, the formation of intermetallics was also observed from the x-ray diffraction analysis. The variations within the measured hardness values were higher at the joint interface due to the mixing of aluminium and magnesium alloys in the nugget zone. From the tensile shear tests, increased strength and decreased elongation were measured with the increased plunge depth. The results demonstrate the importance of the plunge depth on the lap joint formation between dissimilar Al6063–AZ91 alloys during friction stir welding.     

Reactive acrylic liquid rubber with terminal and pendant carboxyl groups as a modifier for epoxy resin

Reactive acrylate rubbers with the terminal and pendent carboxyl groups have been investigated as a modifier for a room temperature curing epoxy resin. The liquid rubbers with varying molecular weights and carboxyl-functionality were synthesized by bulk polymerization of 2-ethyl hexyl acrylate using acrylic acid as a comonomer. The liquid rubbers were characterized by FTIR, ¹³C NMR spectroscopic analysis, nonaqueous titration, vapor pressure osmometry, and solubility characteristics. The liquid rubbers were incorporated into the epoxy resin by the prereact method and the effect of functionality on impact properties of the modified networks were investigated. The results were explained in terms of dynamic mechanical properties and morphology analyzed by scanning electron microscope (SEM). Polym. Eng. Sci. 47:26–33, 2007. © 2006 Society of Plastics Engineers.     

Enhancement in electrical and magnetodielectric properties of Ca‐ and Ba‐doped BiFeO3 polycrystalline ceramics

We carried out a comparative study on the electrical and magnetodielectric properties of polycrystalline BiFeO₃, Bi_0.9Ca_0.1FeO_2.95, Bi_0.9Ba_0.05Ca_0.05FeO_2.95, and Bi_0.9Ba_0.1FeO_2.95 ceramics. The two dielectric anomalies, near 25 K and 281 K, are observed for BiFeO₃. Interestingly, the anomaly near 25 K shifts towards a higher temperature above 60 K with Ca and/or Ba doping, attributed to the doping induced chemical pressure. In addition, the room temperature switchable magnetodielectric effect is witnessed for the doped BiFeO₃ compounds, due to the quadratic magnetoelectric coupling. This indicates the improved magnetoelectric coupling in BiFeO₃ with the Ca and Ba doping. This is essentially due to the enhanced magnetic ordering and reduced leakage current in BiFeO₃ after the doping.     

Non-oxidative thermal degradation of amines: GCMS/FTIR spectra analysis and molecular modeling

Aqueous amino solvents, such as monoethanolamine (ETA/MEA), methyl diethanolamine (MDEA) or amine blends, are the most widely used solvents in commercial CO₂ or acid gas separation applications. These commercial solvents have various disadvantages, such as the possibilities of the solvent to be degraded. This research examines the impact of non-oxidative thermal degradations on the performance of the CO₂ absorption and the degradation mechanism of amine solvents. The impact of degradation was conducted by measuring the CO₂ solubility of solvent that had been heated to 120°C for 2 h. Although the performance of CO₂ absorption was not significantly reduced, the degradation of amines was found. Supported by Fourier Transform Infrared (FTIR) and Gas Chromatography/Mass Spectrometer result, the suspected products of non-oxidative thermal degradation of MDEA were MEA and acetone.     

The Impact of Sequential Fluorination of π‐Conjugated Polymers on Charge Generation in All‐Polymer Solar Cells

The performance of all‐polymer solar cells (all‐PSCs) is often limited by the poor exciton dissociation process. Here, the design of a series of polymer donors ( P1 – P3 ) with different numbers of fluorine atoms on their backbone is presented and the influence of fluorination on charge generation in all‐PSCs is investigated. Sequential fluorination of the polymer backbones increases the dipole moment difference between the ground and excited states (Δµ_ge) from P1 (18.40 D) to P2 (25.11 D) and to P3 (28.47 D). The large Δµ_ge of P3 leads to efficient exciton dissociation with greatly suppressed charge recombination in P3 ‐based all‐PSCs. Additionally, the fluorination lowers the highest occupied molecular orbital energy level of P3 and P2 , leading to higher open‐circuit voltage (V_OC). The power conversion efficiency of the P3 ‐based all‐PSCs (6.42%) outperforms those of the P2 and P1 (5.00% and 2.65%)‐based devices. The reduced charge recombination and the enhanced polymer exciton lifetime in P3 ‐based all‐PSCs are confirmed by the measurements of light‐intensity dependent short‐circuit current density (J_SC) and V_OC, and time‐resolved photoluminescence. The results provide reciprocal understanding of the charge generation process associated with Δµ_ge in all‐PSCs and suggest an effective strategy for designing π‐conjugated polymers for high performance all‐PSCs.     

Soft Magnetic Properties of Fe-5wt%Al Alloy

In this investigation, a new soft magnetic material (iron with 5 wt% aluminum) has been developed using powder metallurgy processing. The microstructure and the magnetic properties of this new P/M alloy have been characterized at both room and elevated temperatures (up to 500°C). The influence of post-sintering (after initial processing) on the porosity and magnetic properties of this material has also been examined.

Test results show that the room temperature soft magnetic properties of this alloy are comparable to other commercially available soft magnetic materials such as P/M pure Fe, Fe-Si, Fe-P, etc. Post-sintering at 1316°C resulted in significant grain growth and lower porosity with more rounded pore morphology and improved the magnetic properties. While the magnetic induction of the alloy was essentially constant from room temperature to 500°C, the coercivity of the material decreased significantly at elevated temperature. This new P/M alloy may be a suitable soft magnetic material for high temperature (up to 500°C) applications.     

Mechanical characterization of new glass fiber reinforced epoxy composites

Glass fiber reinforced plastic (GFRP) composites were made using CTPEGA [carboxyl terminated poly(ethylene glycol) adipate] modified epoxy as a matrix and characterized for their flexural properties, impact strength and interlaminar shear stress (ILSS). The volume fraction of glass was about 0.45 for all the composites. The concentration of CTPEGA in the matrix was varied gradually from 0 to 40 phr (parts per hundred parts of resin), to investigate the effect of CTPEGA concentration on the mechanical properties of the composites. It was found that the flexural strength and ILSS gradually decreases with increase in CTPEGA concentration. However, the impact strength of the composites increases up to 20 phr of CTPEGA concentration and decreases thereafter. Scanning electron microscope (SEM) analysis of the fracture surface indicates massive plastic deformation in modified epoxy based composites. Polym. Compos. 25:165–171, 2004. © 2004 Society of Plastics Engineers.     

Toughening of epoxy resin by modification with 2‐ethylhexyl acrylate–acrylic acid copolymers

2‐Ethylhexyl acrylate–acrylic acid copolymers, ie carboxyl randomized poly(2‐ethylhexyl acrylate) (CRPEHA) (LR‐1 to LR‐6), with different molecular weights and functionality were synthesized. The liquid rubbers were characterized by FTIR spectroscopic analysis, non‐aqueous titration, vapour pressure osmometry (VPO) and viscosity measurements. All the liquid rubbers were reacted with the epoxy resin in 10:100 weight ratio using triphenyl phosphine as a catalyst. The modified epoxy networks were made by reacting the homogeneous prereacted resin with an ambient temperature hardener, triethylene tetramine (HY 951). The effect of the molecular weight and functionality of the liquid rubbers on the thermal and impact properties of the modified networks was investigated. © 2000 Society of Chemical Industry     

Toughening of epoxy resin using acrylate‐based liquid rubbers

Carboxyl‐terminated poly(2‐ethylhexyl acrylate) (CTPEHA) liquid rubbers of different molecular weights and functionalities (LR‐1 to LR‐6) were synthesized by bulk and solution polymerization techniques. The liquid rubbers were characterized by nonaqueous titration, vapor pressure osmometry, and gel permeation chromatography. The CTPEHA oligomers were prereacted with the epoxy resin, and the modified epoxy networks were made by curing with an ambient‐temperature curing agent. The impact properties of the modified epoxy networks were evaluated, and the effects of molecular weight, functionality of the liquid rubber, and ductility of the matrix on the impact strength of the modified networks were investigated. The morphology of the toughening behavior was analyzed using a scanning electron microscope. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 716–723, 2000