Growth and characterization of c-plane AlGaN on γ-LiAlO2

This study demonstrates a pure c-plane AlGaN epilayer grown on a γ-LiAlO₂ (1 0 0) (LAO) substrate with an AlN nucleation layer grown at a relatively low temperature (LT-AlN) by metal-organic chemical vapor deposition (MOCVD). The AlGaN film forms polycrystalline film with m- and c-plane when the nucleation layer grows at a temperature ranging from 660 to 680 °C. However, a pure c-plane AlGaN film with an Al content of approximately 20% can be obtained by increasing the LT-AlN nucleation layer growth temperature to 700 °C. This is because the nuclei density of AlN increases as the growth temperature increases, and a higher nuclei density of AlN deposited on LAO substrate helps prevent the deposition of m-plane AlGaN. Therefore, high-quality and crack-free AlGaN films can be obtained with a (0 0 0 2) ω-rocking curve FWHM of 547 arcsec and surface roughness of 0.79 nm (root-mean-square) using a 700-°C-grown LT-AlN nucleation layer.     

More spherical large fullerenes and multi-layer fullerene cages

According to the experimental investigation, the carbon nano-particles have spherical multi-layer structure (also called onion-like carbon structure). Theoretically, the optimum structures of these large fullerenes contain highly faceted shapes with icosahedral symmetry. This discrepancy in structure may be attributed to the formation mechanism. Thus, a method is devised to construct spherical large fullerenes (C₂₄₀, C₅₄₀, C₉₆₀, C₂₁₆₀, C₂₉₄₀, C₃₈₄₀, C₄₈₆₀) by using the triangular motif. The 5–7–5–7 shape defect is applied in this method for assembling the large spherical fullerenes which could transform the graphene sheet to a spherical motif via SW rearrangement. The geometry-optimized structures of large spherical fullerenes have been generated by molecular mechanics calculation. Then, the average radius and standard deviation of these large fullerenes were obtained to verify the spherical shape. The multi-layer fullerene with spherical shape was confirmed by the TEM observation. According to the structure analysis, the distance between two neighboring encapsulating carbons is about 3.5 Å, which approximately coincides with the distance between two layers of graphite. The van der Waals force per carbon atom and of multi-layer fullerene with the spherical shape generated by force field calculation, predict their relative stability.     

A theory for grain-size reduction in granular flows of spheres

Summary We derive a kinetic theory for homogeneous granular shear flows of identical spheres in which collisions between particles result in small fractures on their peripheries and, over time, effectively reduce their average diameter. In obtaining statistically averaged constitutive relations for the rates of energy dissipation and mass loss, we employ the integral expression derived by Jenkins and Savage [1983] for the collisional source of a particle property. However, in calculating the stress, we modify their expression for the collisional flux in order to ensure that the stress is symmetric when the particles interact through central forces. The constitutive relations are employed in the balance equations for mass, momentum, and energy in order to predict, for a fixed shear rate and particle number density, the manner in which the solid fraction, granular temperature, and induced stresses vary with time.

---

Zusammenfassung Wir entwickeln eine kinetische Theorie für die homogene Scherströmung von identischen Kugeln, in welcher die Zusammenstösse der Teilchen kleine Risse in ihrer Oberfläche verursachen und sich dadurch ihr mittlerer Durchmesser mit der Zeit verringert. Um die statistisch gemittelten konstitutiven Beziehungen für die Energiedissipations- und Massenverlustraten zu erhalten, verwenden wir den von Jenkins und Savage [1983] hergeleiteten Integralausdruck für die von den Kollisionen verursachte Quellenstärke einer Teilchenzustandsgrösse. Bei der Berechnung der Spannung verwenden wir jedoch einen abgeänderten Ausdruck für den Fluss durch Kollision; dadurch wird sichergestellt, dass der Spannungstensor symmetrisch ist, wenn die Kontaktkraft zwischen den Teilchen normal zur Kontaktebene wirkt. Die konstitutiven Beziehungen werden in die Gleichungen für die Erhaltung von Masse, Impuls und Energie eingesetzt, um zu berechnen, wie sich der Festkörperanteil, die Granulartemperatur und die induzierten Spannungen als Funktion der Zeit verändern; der Geschwindigkeitsgradient und die Anzahl Teilchen pro Volumen sind dabei konstant.

     

Induction of differentiation of human leukemia cells by various combinations of cytokines and low-molecular-weight inducers

To explore agents for differentiation therapy of leukemias, various combinations of cytokines and low-molecular-weight inducers were examined for differentiation-inducing activity toward three kinds of human leukemia-derived cell lines. The strongest differentiation inducing activity on promyelocytic HL60 cells and histiocytic U937 cells was obtained by combining recombinant tumor necrosis factor (rTNF), interferon-gamma (IFN-gamma), retinoic acid (RA), and 1 alpha,25-dihydroxyvitamin D3 (1 alpha,25(OH)2D3). For myeloblastic ML1 cells, the combination of rTNF, IFN-gamma, and RA had the strongest differentiation-inducing activity.     

A lab-scale digital acoustic emission system for source location

Experimental Techniques - A PC-based, fully digital and lab-scale acoustic emission system for 3-D source location was set up. To get good results, a sampling rate higher than the Nyquist frequency...     

A fuzzy simple additive weighting system under group decision-making for facility location selection with objective/subjective attributes

This work presents a new fuzzy multiple attributes decision-making (FMADM) approach, i.e., fuzzy simple additive weighting system (FSAWS), for solving facility location selection problems by using objective/subjective attributes under group decision-making (GDM) conditions. The proposed system integrates fuzzy set theory (FST), the factor rating system (FRS) and simple additive weighting (SAW) to evaluate facility locations alternatives. The FSAWS is applied to deal with both qualitative and quantitative dimensions. The FSAWS process considers the importance of each decision-maker, and the total scores for alternative locations are then derived by homo/heterogeneous group of decision-makers. Finally, a numerical example illustrates the procedure of the proposed FSAWS.     

Synthesis of PMMA‐b‐PBA block copolymer in homogeneous and miniemulsion systems by DPE controlled radical polymerization

In this research, poly(methyl methacrylate)‐b‐poly(butyl acrylate) (PMMA‐b‐PBA) block copolymers were prepared by 1,1‐diphenylethene (DPE) controlled radical polymerization in homogeneous and miniemulsion systems. First, monomer methyl methacrylate (MMA), initiator 2,2′‐azobisisobutyronitrile (AIBN) and a control agent DPE were bulk polymerized to form the DPE‐containing PMMA macroinitiator. Then the DPE‐containing PMMA was heated in the presence of a second monomer BA, the block copolymer was synthesized successfully. The effects of solvent and polymerization methods (homogeneous polymerization or miniemulsion polymerization) on the reaction rate, controlled living character, molecular weight (M_n) and molecular weight distribution (PDI) of polymers throughout the polymerization were studied and discussed. The results showed that, increasing the amounts of solvent reduced the reaction rate and viscosity of the polymerization system. It allowed more activation–deactivation cycles to occur at a given conversion thus better controlled living character and narrower molecular weight distribution of polymers were demonstrated throughout the polymerization. Furthermore, the polymerization carried out in miniemulsion system exhibited higher reaction rate and better controlled living character than those in homogeneous system. It was attributed to the compartmentalization of growing radicals and the enhanced deactivation reaction of DPE controlled radical polymerization in miniemulsified droplets. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4435–4445, 2009