Effect of Ce and La on microstructure and properties of a 6xxx series type aluminum alloy

The increase in iron content in secondary sources of aluminum has led to an increase in the amount of Fe-bearing intermetallic phases in Al alloys. One of these intermetallics, β-AlFeSi, which is seen as the dominant phase in 6xxx series alloys, reduces bendability of wrought alloys, which in turn, limits their usage in the automotive industry. It is known that small additions of Sr prevent the formation of the β phase and facilitate the precipitation of a less detrimental intermetallic, α-AlFeSi, in as-cast alloys. It is worth investigating whether other elements cause a similar effect. Cerium and lanthanum as the least expensive representatives of rare-earth metals are tried as such elements. It is found that in alloys containing 0.1–0.2 wt.% of lanthanum, the fraction of β particles is pronouncedly less than that in the reference alloy. In addition to this advantage, much smaller grains are seen in the alloy with 0.2 wt.% La. Despite similarities between La and Ce, the latter metal neither modifies the microstructure nor noticeably affects the grain size. Moderate thermo-mechanical processing nullifies the beneficial effect of small La additions resulting in no improvement in the bendability of the alloy.

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Reducing thermal conductivity of crystalline solids at high temperature using embedded nanostructures

Thermal conductivity of a crystalline solid at high temperature is dominated by the Umklapp process because the number of high frequency phonons increases with temperature. It is challenging to reduce the thermal conductivity of crystalline solids at high temperature although it is widely known that, by increasing the atomic defect concentration, thermal conductivity of crystalline solids can be reduced at low temperature. By increasing the concentration of ErAs nanoparticles in In 0.53Ga 0.47As up to 6 atom %, we demonstrate a thermal conductivity reduction by almost a factor of 3 below that of In 0.53Ga 0.47As at high temperature. A theoretical model suggests that the mean free path of the low frequency phonons is suppressed by increasing the ErAs nanoparticle concentration.     

Experimental performance evaluation of an ammonia-fuelled microchannel reformer for hydrogen generation

Microchannel reactors appear attractive as integral parts of fuel processors to generate hydrogen (H₂) for portable and distributed fuel cell applications. The work described in this paper evaluates, characterizes, and demonstrates miniaturized H₂ production in a stand-alone ammonia-fuelled microchannel reformer. The performance of the microchannel reformer is investigated as a function of reaction temperature (450–700 °C) and gas-hourly-space-velocity (6520–32,600 Nml g_cat⁻¹ h⁻¹). The reformer operated in a daily start-up and shut-down (DSS)-like mode for a total 750 h comprising of 125 cycles, all to mimic frequent intermittent operation envisaged for fuel cell systems. The reformer exhibited remarkable operation demonstrating 98.7% NH₃ conversion at 32,600 Nml g_cat⁻¹ h⁻¹ and 700 °C to generate an estimated fuel cell power output of 5.7 W_e and power density of 16 kW_e L⁻¹ (based on effective reactor volume). At the same time, reformer operation yielded low pressure drop (<10 Pa mm⁻¹) for all conditions considered. Overall, the microchannel reformer performed sufficiently exceptional to warrant serious consideration in supplying H₂ to fuel cell systems.     

Water exchange-minimizing DCE-MRI protocol to detect changes in tumor vascular parameters: effect of bevacizumab/paclitaxel combination therapy

Objective

The purpose of this study was to assess changes in the tumor microvasculature induced by combination antiangiogenic therapy in MCF-7 breast tumor mouse models, using a noninvasive DCE-MRI method that minimizes the effect of water exchange.

Materials and methods

3D quantitative DCE-MRI images were acquired with a heavily T ₁-weighted saturation recovery gradient echo sequence with a recovery delay of 20 ms. Tumor vascular volume (VV) and vascular permeability-surface area product (PS) were obtained through a linear regression of the albumin-Gd-DTPA-enhanced dynamic image intensity on MCF-7 breast tumor mouse models treated with combination bevacizumab/paclitaxel therapy.

Results

Measured tumor VV values were significantly higher than the values that have been reported previously using quantitative T ₁ mapping, and are in good agreement with micro-CT (computed tomography) results reported earlier from other tumor models. A trend of decreasing tumor PS was detected in the group of MCF-7 tumor bearing mice treated with the bevacizumab/paclitaxel combination regimen.

Conclusion

VV and PS maps obtained by a heavily T ₁-weighted acquisition protocol revealed the large peripheral blood vessels as well as the permeable areas within the tumor. A 12-day/three-dose combination treatment of bevacizumab and paclitaxel resulted in delayed tumor growth and a trend of decreasing tumor vascular permeability surface area product.     

Electrical control of Förster energy transfer

Bringing together compounds of intrinsically different functionality, such as inorganic nanostructures and organic molecules, constitutes a particularly powerful route to creating novel functional devices with synergetic properties found in neither of the constituents. We introduce nanophotonic functional elements combining two classes of materials, semiconductor nanocrystals and dyes, whose physical nature arises as a superposition of the properties of the individual components. The strongly absorbing rod-like nanocrystals focus the incident radiation by photopumping the weakly absorbing dye via energy transfer. The CdSe/CdS nanorods exhibit a large quantum-confined Stark effect on the single-particle level, which enables direct control of the spectral resonance between donor and acceptor required for nanoscopic F?rster-type energy transfer in single nanorod-dye couples. With this far-field manipulation of a near-field phenomenon, the emission from single dye molecules can be controlled electrically. We propose that this effect could lead to the design of single-molecule optoelectronic switches providing building blocks for more complex nanophotonic circuitry.     

Growth of semiconducting GaN hollow spheres and nanotubes with very thin shells via a controllable liquid gallium-gas interface chemical reaction

An in situ liquid gallium-gas interface chemical reaction route has been developed to synthesize semiconducting hollow GaN nanospheres with very small shell size by carefully controlling the synthesis temperature and the ammonia reaction gas partial pressure. In this process the gallium droplet does not act as a catalyst but rather as a reactant and a template for the formation of hollow GaN structures. The diameter of the synthesized hollow GaN spheres is typically 20-25 nm and the shell thickness is 3.5-4.5 nm. The GaN nanotubes obtained at higher synthesis temperatures have a length of several hundreds of nanometers and a wall thickness of 3.5-5.0 nm. Both the hollow GaN spheres and nanotubes are polycrystalline and are composed of very fine GaN nanocrystalline particles with a diameter of 3.0-3.5 nm. The room-temperature photoluminescence (PL) spectra for the synthesized hollow GaN spheres and nanotubes, which have a narrow size distribution, display a sharp, blue-shifted band-edge emission peak at 3.52 eV (352 nm) due to quantum size effects.     

The Importance of Charge Transfer and Solvent Screening in the Interactions of Backbones and Functional Groups in Amino Acid Residues and Nucleotides

Quantum mechanical (QM) calculations at the level of density-functional tight-binding are applied to a protein–DNA complex (PDB: 2o8b) consisting of 3763 atoms, averaging 100 snapshots from molecular dynamics simulations. A detailed comparison of QM and force field (Amber) results is presented. It is shown that, when solvent screening is taken into account, the contributions of the backbones are small, and the binding of nucleotides in the double helix is governed by the base–base interactions. On the other hand, the backbones can make a substantial contribution to the binding of amino acid residues to nucleotides and other residues. The effect of charge transfer on the interactions is also analyzed, revealing that the actual charge of nucleotides and amino acid residues can differ by as much as 6 and 8% from the formal integer charge, respectively. The effect of interactions on topological models (protein -residue networks) is elucidated.     

Spin-Flip Raman Scattering on Electrons and Holes in Two-Dimensional (PEA)2PbI4 Perovskites

The class of Ruddlesden–Popper type (PEA)₂PbI₄ perovskites comprises 2D structures whose optical properties are determined by excitons with a large binding energy of about 260 meV. It complements the family of other 2D semiconductor materials by having the band structure typical for lead halide perovskites, that can be considered as inverted compared to conventional III–V and II–VI semiconductors. Accordingly, novel spin phenomena can be expected for them. Spin-flip Raman scattering is used here to measure the Zeeman splitting of electrons and holes in a magnetic field up to 10 T. From the recorded data, the electron and hole Landé factors (g-factors) are evaluated, their signs are determined, and their anisotropies are measured. The electron g-factor value changes from +2.11 out-of-plane to +2.50 in-plane, while the hole g-factor ranges between -0.13 and -0.51. The spin flips of the resident carriers are arranged via their interaction with photogenerated excitons. Also the double spin-flip process, where a resident electron and a resident hole interact with the same exciton, is observed showing a cumulative Raman shift. Dynamic nuclear spin polarization induced by spin-polarized holes is detected in corresponding changes of the hole Zeeman splitting. An Overhauser field of the polarized nuclei acting on the holes as large as 0.6 T can be achieved.