A Composite Formation Route to Well‐Crystalline Manganese Oxide Nanocrystals: High Catalytic Activity of Manganate–Alumina Nanocomposites

Manganese oxide nanocrystals are combined with aluminum oxide nanocrystals to improve their crystallinity via calcination without a significant increase of crystal size. A nanocomposite, consisting of two metal oxides, can be synthesized by the reaction between permanganate anions and aluminum oxyhydroxide keggin cations. The as‐prepared manganese oxide–aluminum oxide nanocomposite is X‐ray amorphous whereas heat‐treatment gives rise to the crystallization of an α‐MnO₂ phase at 600 °C and Mn₃O₄/Mn₂O₃ and γ‐Al₂O₃ phases at 800 °C. Electron microscopy and N₂ adsorption‐desorption‐isotherm analysis clearly demonstrate that the as‐prepared nanocomposite is composed of a porous assembly of monodisperse primary particles with a size of ～20 nm and a surface area of >410 m² g^?1. Of particular interest is that the small particle size of the as‐prepared nanocomposite is well‐maintained up to 600 °C, a result of the prevention of the growth of manganate grains through nanoscale mixing with alumina grains. The calcined nanocomposite shows very‐high catalytic activity for the oxidation of cyclohexene with an extremely high conversion efficiency of >95% within 15 min. The present results show that the improvement of the crystallinity without significant crystal growth is very crucial for optimizing the catalytic activity of manganese oxide nanocrystals.     

Three-scale analysis of BaTiO<Subscript>3</Subscript> piezoelectric thin films fabrication process and its experimental validation

A three-scale analysis of crystal growth process is newly proposed based on the first-principles calculation and on the finite element analysis in order to generate a new biocompatible piezoelectric thin film. Crystal growth process of lead-free BaTiO₃ thin films was designed and experimentally generated on SrTiO₃(100), (110), (111), and MgO(100) substrates using the radio-frequency magnetron sputtering method. Crystal structures of BaTiO₃ were measured by X-ray diffraction (XRD) θ/2θ scan. We used Pt for the electrode and measured piezoelectric strain constants d ₃₃ using the ferroelectric measurement system. As a result, analytical crystal orientation fractions on SrTiO₃(110) and (111) substrates had good quantitative agreement with experimental ones, and ones on SrTiO₃(100) and MgO(100) substrates corresponded with these experimental crystal structures. Furthermore, analytically determined piezoelectric strain constants d ₃₃ qualitatively showed a good agreement with experimental ones. Especially, for SrTiO₃(100) and MgO(100) substrates, the differences of d ₃₃ depending on orientation fractions were analyzed by the three-scale simulation accurately. Consequently, it is confirmed that the three-scale analysis is a useful simulation tool to design new biocompatible piezoelectric thin films.     

Design of high efficiency mixed refrigerant Joule–Thomson refrigerator for cooling HTS cable

The substitution of high temperature superconducting (HTS) cables for existing subterranean electric transmission lines is arising as a solution to continuously increasing electricity demand in urban areas. A cryogenic refrigeration system having the characteristics of high reliability, high efficiency, large cooling capacity, and low capital cost is essential to enable such a substitution. These requirements can be satisfied with a mixed refrigerant Joule–Thomson (MR JT) refrigerator. Unfortunately, usual MR JT refrigerators exhibit good performance at refrigeration temperatures above 80 K. A precooled neon–nitrogen MR JT refrigerator is proposed in this paper that can cool HTS cables at 70 K. The coefficient of performance (COP) of the proposed MR JT refrigerator is predicted to be 0.058 at 70 K (19.2% for exergy efficiency) with the optimized design variables. The COP can be improved further to 0.064 by enhancing the efficiency of the precooling cycle. The maximum achievable COP demonstrates the feasibility of MR JT refrigerator for cooling HTS cable.     

Molecular dynamics study on nanotube-resonators with mass migration applicable to both frequency-tuner and data-storage-media

We investigated the cantilevered carbon-nanotube-resonator including electromigratively movable nanoparticle via classical molecular dynamics simulations and continuum model. The change of the effective mass value, which was closely correlated with the position change of the encapsulated nanoparticle, could be regressed by a power function, the resonance frequency of the carbon-nanotube-resonator could be tuned by controlling the nanoparticle’s position, and the possible frequency-shift-ranges then reached 18–85%. The suggested device could be served as a data-storage-media for electromechanical nonvolatile-memory as well as a frequency-tuner.     

Study of Intrusion Detection Systems

Modern network systems have much trouble in security vulnerabilities such as buffer overflow, bugs in Microsoft Internet, sensor network routing protocol too simple, security flaws of applications, and operating systems. Moreover, wireless devices such as smart phones, personal digital assistants （PDAs）, and sensors have become economically feasible because of technological advances in wireless communication and manufacturing of small and low-cost sensors. There are typologies of vulnerabilities to be exploited in these devices. In order to improve securities, many mechanisms are adopted, including authentication, cryptography, access control, and intrusion detection systems （IDS）. In general, intrusion detection techniques can be categorized into two groups： misuse detection and anomaly detection. The misuse detection systems use patterns of weB-known attacks or weak spots of the systems to identify intrusions. The weakness of misuse detection systems is unable to detect any future （unknown） intrusion until corresponding attack signatures are intruded into the signature database. Anomaly detection methods try to determine whether the deviation is from the established normal usage patterns or not. The critical success of anomaly detection relies on the model of normal behaviors.     

Fabrication of Al matrix composite reinforced with submicrometer-sized Al<Subscript>2</Subscript>O<Subscript>3</Subscript> particles formed by combustion reaction between HEMM Al and V<Subscript>2</Subscript>O<Subscript>5</Subscript> composite particles during sintering

To fabricate an Al-V matrix composite reinforced with submicron-sized Al₂O₃ and Al_xV_y (Al₃V, Al₁₀V) phases, high energy mechanical milling (HEMM) and sintering were employed. By increasing the milling time, the size of mechanically milled powder was significantly reduced. In this study, the average powder size of 59 μm for Al, and 178 μm for V₂O₅ decreased with the formation of a new product, Al-Al₂O₃-Al_xV_y, with a size range from 1.3 μm to 2.6 μm formed by the in-situ combustion reaction during sintering of HEM milled Al and V₂O₅ composite powders. The in-situ reaction between Al and V₂O₅ during the HEMM and sintering transformed the Al₂O₃ and Al_xV_y (Al₃V, Al₁₀V) phases. Most of the reduced V reacted with excess the Al to form Al_xV_y (Al₃V, Al₁₀V) with very little V dissolved into Al matrix. By increasing the milling time and weight percentage of V₂O₅, the hardness of the Al-Al₂O₃-Al_xV_y composite sintered at 1173 K increased. The composite fabricated with the HEMM Al-20wt.%V₂O₅ composite powder and sintering at 1173 K for 2 h had the highest hardness.     

Preparation and characterization of carbon-encapsulated iron nanoparticles and their catalytic activity in the hydrogenation of levulinic acid

This study describes the synthesis of carbon-encapsulated iron nanoparticles using an ultrasonic method and also investigates their catalytic activity. These nanoparticles have been prepared using ultrasonic irradiation followed by annealing at various temperatures. As the annealing temperature of as-prepared α-Fe₂O₃ nanoparticles increased, the sample transformed into γ-Fe₂O₃, Fe₃O₄, and Fe nanoparticles via the reduction process without requiring any additional reducing agents such as H₂ gas, thus, creating a carbon shell surrounding the nanoparticles. By controlling the experimental conditions, Fe nanoparticles of various sizes can be formed with diameters in the range 100–800 nm; these nanoparticles are tightly encapsulated by 20-nm-thick carbon shells. Because of their high saturation magnetization 212 emu g^?1, the carbon-encapsulated Fe nanoparticles can be used for magnetic resonance imaging with a dramatically enhanced efficiency compared to commercially available T ₂ contrast agents. Moreover, the carbon-encapsulated Fe nanoparticles showed its superior catalytic activity and reusability for the hydrogenation of biomass-derived levulinic acid to GVL (99.6 %) in liquid phase.     

Semi-transparent thin film solar cells by a solution process

Easily processed, low cost, and highly efficient solar cells are desirable for photovoltaic conversion of solar energy to electricity. We present the fabrication of precursor solution processed CuInGaS2 (CIGS) thin film solar cells on transparent indium tin oxide (ITO) substrates. The CIGS absorber film was prepared by a spin-coating method, followed by two successive heat treatment processes. The first annealing process was on a hot plate at 300 °C for 30 min in air to remove carbon impurities in the film; this was followed by a sulfurization process at 500 °C in an H₂S(1%)/Ar environment to form a polycrystalline CIGS film. The absorber film with an optical band-gap of 1.52 eV and a thickness of about 1.1 µm was successfully synthesized. Because of the usage of a transparent glass substrate, a bifacial CIGS thin film device could be achieved; its power conversion efficiency was measured to be 6.64% and 0.96% for front and rear illumination, respectively, under standard irradiation conditions.     

Synthesis and properties of novel naphthalene-containing bismaleimides

New aromatic bismaleimides containing bis(phenoxy) naphthalene unit, were synthesized. They were prepared by reacting a diamine-containing naphthalene and maleic anhydride by the usual two-step procedure that included ring-opening addition to give bismaleamic acid, followed by cyclodehydration to bismaleimide. The monomers were characterized by infrared (IR), proton nuclear magnetic resonance (H-NMR), elemental analyses (EA), and mass spectra (MS). Their thermal polymerization was investigated by differential scanning calorimetry (DSC). The presence of a naphthalene group in the backbone of the bismaleimide had increased the curing temperature and reduced the reactivity of the maleimide bond. The glass transition temperatures of the polymers were in the range of 291–334°C. Thermogravimetric analyses of the cured resins showed higher thermal stability and char yield for naphthalene-containing bismaleimides than for the corresponding benzene analog. The observed char yield of the bismaleimide resins are in accordance with the calculated C/H ratios. © 1996 John Wiley & Sons, Inc.