The role of conductive pathways in the conductivity and rheological behavior of poly(methyl methacrylate)–graphite composites

Up to now, research on the dynamic process of conductive network formation has tended to focus on composite particles with one‐dimensional geometry, such as carbon black and carbon nanotubes. However, studies on this subject based on fillers with two‐dimensional structure, such as graphite, are rare in the literature. In this work, the dynamic percolation and rheological properties of poly(methyl methacrylate) (PMMA)–graphite composites under an electric field were investigated. The activation energies of conductive network formation and polymer matrix mobility were calculated from the temperature dependence of the percolation time and the zero‐shear viscosity. It was found that the activation energy calculated from the zero‐shear viscosity was not influenced by the electric field in the concentration range investigated, but the electric field had an effect on the activation energy calculated from the percolation time. This finding emphasizes that the electrical and rheological properties have different physical origins. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43810.     

Temperature Dependence of Efficiency in GaInN/GaN Light‐Emitting Diodes with a GaInN Underlayer

The temperature dependence of the efficiency (i.e., temperature‐mediated efficiency droop) in blue light‐emitting diodes (LEDs) is investigated. A GaInN/GaN LED with a GaInN underlayer having an indium mole fraction of 8% shows less temperature dependence of efficiency, compared to the LED without an underlayer. Better carrier confinement in the active region of the LED with a GaInN underlayer is proposed to reduce carrier leakage from the active region at high temperature. The results indicate that the insertion of an underlayer leads to an improvement of the LED's radiative efficiency and its high‐temperature‐tolerant performance.     

Regime transition in viscous and pseudo viscous systems: A comparative study

A comprehensive quantitative study on the effect of liquid viscosity (1 ≤ µ_L ≤ 1149 mPa‐s) on the local flow phenomena of the gas phase in a small diameter bubble column is performed using ultrafast electron beam X‐ray tomography. The internal dynamic flow structure and the bubble size distribution shows a dual role of the liquid viscosity on the hydrodynamics. Further, the effect of solid concentration (C_s = 0.05, 0.20) on the local flow behavior of the gas phase is studied for the pseudo slurry viscosities similar to the liquid viscosities of the gas–liquid systems. The effects of liquid and pseudo slurry viscosities on flow structure, bubble size distribution, and gas phase distribution are compared. The bubble coalescence is significantly enhanced with the addition of particles as compared to the system without particles for apparently same viscosity. The superficial gas velocity at which transition from homogeneous bubbly to slug flow regime occurs is initiated by the addition of particles as compared to the particle free system for apparently same viscosity. © 2014 American Institute of Chemical Engineers AIChE J, 60: 3079–3090, 2014     

Thin-film solar cells

The R&D status of cells and modules based on hydrogenated amorphous silicon (a-Si:H) and those based on CdTe and CuInSe₂ is reviewed. The stability of a-Si:H solar cells is still a major concern. Improvements have been achieved on an empirical basis by application of multijunction structures, optimization of interfaces, etc. Stabilized efficiencies of close to 10% have been reported. In parallel, the introduction of the ‘defect-pool model’ led to remarkable progress in understanding; it follows that a-SiGe:H instead of a-Si:H should be used for the i-layer (absorber). Improved cell engineering concepts, however, such as enhancement of the built-in electric field via reduction of the i-layer thickness and/or folded structures, are believed to be more promising. Polycrystalline thin-film cells based on CdTe and CuInSe₂ are not affected by inherent degradation mechanisms. the specific properties of these materials demand heterojunctions, and particular problems arise due to the polycrystallinity of the films and to the lattice mismatch and mismatch of the electronic band structures of the materials involved. These are discussed in conjunction with measures currently applied for optimizing solar cell performance. Both cell types exhibit eficiencies in the range 16-17%. Estimations of production costs and energy payback times of thin-film photovoltaic modules are reviewed (even below 1 US$ W_p⁻¹ and as low as 4 months, respectively) and environmental concerns, especially for Cd-containing cells, are summarized.     

Microstructure-Mechanical Property Relationships in Hot Isostatically Pressed Alumina and Zirconia-Toughened Alumina

The rates of densification and the mechanical properties of pure Al₂O₃ and ZrO₂-toughened Al₂O₃ (ZTA) have been investigated as a function of the temperatures and time schedules used for hot isostatic pressing (HIP) as a postsintering heat treatment for samples which had already been pressureless sintered in air at 1460°C for 45 min. ZTA hot isostatically presed at 1400°C had a finer grain size and a narrower grain size distribution than ZTA hot isostatically pressed at 1600°C. At both HIP conditions, the density which could be obtained was almost the maximum theoretical density. The amount of grinding-induced and fracture-induced monoclinic ZrO₂ formed as a result of the tetragonal → monoclinic martensitic transformation in ZTA was higher in the samples hot isostatically pressed at 1400°C. ZTA hot isostatically pressed at 1600°C and 100 MPa had fewer flaws and higher strengths than ZTA hot isostatically pressed at 1400°C for the same time, with a gradual improvement in mechanical properties with increasing HIP time at each of these two temperatures. The best mechanical properties were obtained from ZTA hot isostatically pressed at 100 MPa and 1600°C for 1 h: these specimens had a four-point bend strength of 940 ± 15 MPa at room temperature and 540 ± 15 MPa at 1000°C and an indentation fracture toughness at room temperature of 9.4 ± 0.2 MPa·m^1/2.     

Influence of Molybdenum Silicide Additions on High-Temperature Oxidation Resistance of Silicon Nitride Materials

The influence of additions of molybdenum disilicide (MoSi₂) on the microstructure and the mechanical properties of a silicon nitride (Si₃N₄) material, with neodymium oxide (Nd₂O₃) and aluminum nitride (AIN) as sintering aids, was studied. The composites, containing 5, 10, and 17.6 wt% MoSi₂, were fabricated by hot pressing. All materials exhibited a similar phase composition, detected by X-ray diffractometry. Up to MoSi₂ additions of 10 wt%, mechanical properties such as strength, fracture toughness, or creep at 1400°C were not affected significantly, in comparison to that of monolithic Si₃N₄. The oxidation resistance of the composites, in terms of weight gain, degraded. After 1000 h of oxidation at 1400° and 1450°C in air, a greater weight gain (by a factor of approximately three) was obtained, in comparison to that of the material without MoSi₂. Nevertheless, after 1000 h of oxidation, the degradation in strength of the composites was considerably less severe than that of the material without MoSi₂. An additional layer was formed, caused by processes at the surface of the Si₃N₄ material, preventing the formation of pores, cracks, or glassy-phase-rich areas, which are common features of oxidation damage in Si₃N₄ materials. This surface layer, containing Mo₅Si₃ and silicon oxynitride (Si₂ON₂), was the result of reactions between MoSi₂, Si₃N₄, and the oxygen penetrating by diffusion into the material during the hightemperature treatment.     

Silicon Nitride/Molybdenum Disilicide Composite with Superior Long-Term Oxidation Resistance at 1500°C

The long-term high-temperature cyclic oxidation (100 cycles, 10⁴ h, 1500°C) of a Si₃N₄ material and a Si₃N₄/MoSi₂ composite, both fabricated with Y₂O₃ as a sintering additive, was studied. Both materials exhibited similar oxidation rates because of surface SiO₂ formation described by an almost parabolic law and a total weight gain of 3–4 mg/cm² after 10⁴ h. As a consequence of oxidation processes in the bulk, microstructural damage was found in the Si₃N₄ material. These effects were not observed in the composite. The remarkable microstructural stability observed offers the high potential of Si₃N₄/MoSi₂ composites for long-term structural applications at elevated temperatures up to 1500°C.     

Untersuchung fester Komplexe von Triphenylmethylsalzen mit Donatoren

Investigation of Solid Complexes of Triphenylmethyl Salts with Donors Triphenylmethyl salts form crystalline complexes, which can be characterized by UV-VIS reflexion spectroscopy as well as by thermal methods. The stability of the solid complexes is essentially determined by the size of the substituents in the cation (p-R-C₆H₄)₃C⁺ with R = CH₃, H, Br and by that of the aromate (benzene, toluene, p-xylene, mesitylene). In constrat to the behaviour in solution a change of the anion (SbCl₆⁻, FeCl₄⁻) has a strong influence on the stability. Because of the appearance of a charge-transfer absorption the complexes are described as EDA complexes.     

Ion beam analysis of a structural phase transition in porous TiO2/V2O5 ceramics with rough surfaces

TiO₂/V₂O₅ based ceramic materials applied in catalysis were investigated. Structural properties like the grain diameter of these pressed ceramic powders were analysed by means of Rutherford backscattering (RBS) making use of an analytic model to describe the energy spectra of porous rough samples. Grain diameters of these samples were deduced as function of process temperature and chemical composition and related to a phase transition from the TiO₂-Anatase/V₂O₅-Shcherbinaite to Rutile solid solution (Rutile-ss) structure. RBS data were compared to results of scanning electron microscopy (SEM). The activation energy for the sintering at the phase transition was estimated to 5.4 eV.