New Preparation Method of CdS Clusters Encapsulated in Y-Type Zeolites

CdS clusters encapsulated in Y-type zeolite were prepared by a novel technique with non-aqueous systems. The mechanical mixture of CdCl₂· 2.5H₂O crystal with Y-type zeolite was heated at 773 K, followed by the H₂S treatment at 373 K, resulting in the formation of CdS clusters with the size <2.3 nm.     

Sensorless Position Control Using Feedforward Internal Force for Completely Restrained Parallel-Wire-Driven Systems

Generally, point-to-point control for a completely restrained (CR) parallel-wire-driven system requires a balancing internal force to prevent slackening of wires, along with a feedback term based on some displacement sensor. This paper specifically describes CR systems' internal force properties, then presents the possibility of motion convergence at a desired position when the internal force balancing at a position is given as sensorless feedforward input. Subsequently, we use the property of internal force positively for sensorless position control. This positioning method is applicable for low-cost manipulation, which does not require high accuracy, and for emergency positioning of systems when sensors malfunction.     

Formation of high-purity organic thin films by gas flow deposition and the effect of impurities on device characteristics

A gas flow deposition (GFD) system was developed to manufacture large-scale organic light-emitting diodes (OLEDs). A N,N′-di(1-naphthyl)-N,N′-diphenylbenzidine (α-NPD) thin film with a high purity of 99.97% was obtained using the GFD system. The film properties such as morphology, and electrical and optical characteristics were almost the same as those of films made by conventional vacuum thermal evaporation.     

Electrical properties and microstructure in the system ceria-alkaline earth oxide

The ionic conduction of oxygen in the ceria-alkaline earth oxide system was investigated as a function of temperature, partial pressure of oxygen and oxide composition, together with its crystal structure, density, and microstructure. Undoped ceria and its solid solution with alkaline earth oxides have a cubic fluorite structure. The ionic conductivity of ceria is greatly enhanced by additions of calcia and strontia, even when they are added in excess of the solubility limit. The conductivities of ceria-calcia and ceria-strontia were much higher than those of calcia-and yttria-stabilized zirconia. Up to the limit of calcia and strontia, the ionic transference number was nearly unity in the temperature range between 600 and 900°C. With an increase in calcia and strontia content, the ionic conductivity was little affected by the presence of a second phase of CaO and SrCeO₃.     

ESR studies of the effect of zeolite structures on motional dynamics of NO2

Electron spin resonance (ESR) spectroscopy was used to study the effect of zeolite structure on the motional dynamics of NO₂ adsorbed on the zeolites. The temperature-dependent ESR spectral line shapes were quantitatively analyzed using the slow-motion ESR theory. It was observed that the motional dynamics of NO₂ is strongly dependent on the structure of the zeolite (Beta-type, ZSM-5, mordenite, L-type and ferrierite zeolites). The following important observations were made. (1) In zeolites with similar channel structures, the diffusion rate of NO₂ is proportional to the channel size, and the order of the diffusion rates is Beta-type>ZSM-5>ferrierite and L-type>mordenite. (2) The diffusion of NO₂ is faster in the zeolites with multi-dimensional channels (Beta-type, ZSM-5 and ferrierite) than that in those with uni-dimensional channels (L-type and mordenite).     

Radiation‐initiated graft polymerization of methylmethacrylate onto poly(tetrafluoroethylene): Characterization by 1H‐NMR

A broad‐line ¹H‐NMR study was carried out to examine the local structure of poly(methylmethacrylate) (PMMA) grafted onto Poly(tetrafluoroethylene) (PTFE). The NMR spectra were observed for three different samples with 1.0, 5.4, and 7.0 wt % PMMA over the temperature range from 150 to 380 K. With the help of selectively deuterated PMMA (PMMA‐d₅ and PMMA‐d₈)‐grafted samples, the NMR spectra were analyzed in terms of two components—a Gaussian (G) component, and a Lorentzian (L) component. Based on the second moments (〈ΔH²〉) analysis, the L and G components were attributed to the ¹H–¹H dipolar interactions within one CH₃ group and the interactions of CH₃ groups that are closely located in aggregated PMMA chains. Combining the results with the temperature dependence of 〈ΔH²〉 and the angular resolved XPS, the location and rotational motion of PMMA grafted onto PTFE are discussed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 1386–1394, 1999     

Promotion Effect of FeOx Addition on the Catalytic Activity of Supported Cu Catalysts for the Water–gas Shift Reaction

Among the supported Cu–FeO_x catalysts, Al₂O₃-supported Cu–FeO_x catalyst exhibited the highest activity for WGS reaction. The enhancement of the catalytic activity by adding FeO_x to Cu/Al₂O₃ could be interpreted by the two possibilities; one is the formation of highly dispersed Cu⁰ and the other is the participation of reduced FeO_x in WGS reaction in the presence of Cu⁰.     

Electrochemical insertion and extraction of lithium-ion at nano-sized LiMn2O4 particles prepared by a spray pyrolysis method

Nano-sized LiMn₂O₄ particles were prepared at 1023 K by electrospray pyrolysis in which they were directly deposited on a Pt substrate in gas phase. Cyclic voltammetry gave very sharp and symmetrical redox peaks at ca. 4.0 and 4.1 V vs. Li/Li⁺ owing to the insertion and extraction of lithium-ion at LiMn₂O₄. However, the redox peaks broadened and their peak separation in an electrode potential increased when aggregated nano-sized LiMn₂O₄ particles were used. In Nyquist plots, a semi-circle due to lithium-ion transfer resistance appeared at potentials above 3.90 V. The values of the lithium-ion transfer resistances were small for dispersed nano-sized LiMn₂O₄ particles. On the other hand, the lithium-ion transfer resistances increased and the Warburg impedance became obvious as the nano-sized LiMn₂O₄ particles aggregated. These results clearly indicate that the apparent rapid diffusion of lithium-ion can be attained using well-dispersed nano-sized particles of electroactive materials.