A new LCL-lens array with electrodes of interlaced structure to be applied for auto-stereoscopic 3D displays

A new design of the liquid crystal lenticular (LCL) lens array with interlaced electrodes is proposed to realize an auto-stereoscopic 3D display. The structure of interlaced electrodes aims to generate a desired non-uniform electric filed to improve the focusing ability of the LCL-lens array with lower voltage drives. This paper is organized as first to describe the design criteria of a lenticular lens sheet for wide extended graphics array LCD panel. Based on the designed lenticular lens array, an LCL-lens array with proposed interlaced electrodes is next designed. The fabrication and the detailed structure are given. A series of experiments are then conducted and successfully verify the focusing capability and desired 3D display functions, that is, to separate two images to right and left eyes. Also, the developed auto-stereoscopic 3D display is able to adapt to varied viewer locations with favorable imaging quality.     

Mesoporous silica with short-range MFI structure

A new type of mesoporous silica has been prepared which showed 780 m²/g of BET surface area and 0.6 ml/g of primary mesopores narrowly distributed around 4.2 nm. More importantly however, is that it showed short-range zeolite crystallinity as demonstrated by FTIR and XRD analysis, and hydrophobicity as demonstrated by water and n-hexane adsorption.

This material was synthesized via a dual-template, three-step hydrothermal–flocculation–steaming synthesis procedure developed by us recently. Briefly, MFI nanoprecursors (NPs) were first prepared by a low-temperature hydrothermal step using TPAOH as template for zeolite structure, and then flocculated using a surfactant that served as the template for the mesopores. The collected NPs are mesoporous silica exhibiting short-range MFI domains when directly calcined. However, the steaming step promoted the crystallization of the NPs and created uniform mesopores. It was found that almost every detail in these procedures affected the properties of the final product. The most important variables, however, were identified as the duration the flocculants were kept in contact with the liquid phase, and the humidity under which the steaming was conducted. By properly adjusting the procedures, the said mesoporous silica, as well as nanocrystals having high external surface area, could be produced at will.     

Solid-state NMR studies on phase behavior and motional mobility in binary blends of polystyrene and poly(cyclohexyl methacrylate)

The phase behavior and motional mobility in binary blends of polystyrene (PS) and poly(cyclohexyl methacrylate) (PCHMA) have been investigated by solid state ¹³C NMR techniques. The blend miscibility has been studied by examining the ¹H spin-relaxation times in the laboratory frame (T₁^H) and in the rotating frame (T_1ρ^H) for the PCHMA/PS blends with various compositions and pure components. The T_1ρ^H results show that PCHMA and PS are intimately mixed at the molecular level within the blends at all compositions. In addition, according to the results of carbon T_1ρ relaxation time measurements, we conclude that mixing is intimate enough to cause a reduction in local chain mobility for PS, but an increase in side chain mobility for PCHMA.     

Equilibrium and kinetic studies of the extraction of chelated copper(II) anions with Aliquat 336

The equilibrium and kinetics of solvent extraction of Cu²⁺ from aqueous solutions containing equimolar EDTA with Aliquat 336 in n‐decanol and kerosene at 298 K were investigated. The concentrations of Cu²⁺ (8–50 mol m^?3), Cl^? (5–60 mol m^?3), and Aliquat 336 (20–100 mol m^?3) were varied. A semi‐empirical model with three parameters was proposed to describe the equilibrium behavior, in which the non‐idealities in both aqueous and organic phases were considered. Over the ranges studied, the model agreed reasonably well with the experimental data (standard deviation, 15%). The forward and backward reaction rate constants were determined as (5.31 ± 0.16)×10^?6 m^9/4 mol^?3/4 s^?1 and (2.62 ± 0.09)×10^?7 s^?1, respectively, at 298 K. An interfacial reaction mechanism was proposed, which revealed that the reaction between the chelated anions and trimeric amine molecules at the interface was rate limiting. The derived rate laws were consistent with the experimental results. © 2002 Society of Chemical Industry     

Li NMR, ionic conductivity and self-diffusion coefficients of lithium ion and solvent of plasticized organic-inorganic hybrid electrolyte based on PPG-PEG-PPG diamine and alkoxysilanes

Organic-inorganic hybrid electrolytes based on poly(propylene glycol)-block-poly(ethylene glycol)-block-poly(propylene glycol) bis(2-aminopropyl ether) (D2000) complexed with LiClO₄ via the co-condensation of an epoxy trialkoxysilane and tetraethoxysilane have been prepared and plasticized by a solution of ethylene carbonate (EC)/propylene carbonate (PC) mixture (1:1 by weight). The cross-linked hybrid network shows no solvent exudation and retains a large amount of plasticizer over 70 wt.% in stable state. The in situ built in silica network provides the hybrid electrolytes with good mechanical properties. The ionic conductivity of the dry hybrid electrolyte films was enhanced by two orders of magnitude via plasticization, reaching a maximum conductivity value of 4.0 × 10⁻³ S/cm at 30 °C. Variable temperature ⁷Li-{¹H} magic angle spinning (MAS) NMR demonstrated that the Li⁺ cations can be complexed by the polymer network as well as by the plasticizing solvents, but not with the incorporated silica network. Furthermore, the ⁷Li chemical shift change indicated a progressive change in the lithium coordination from lithium-polymer to lithium-solvent with increasing temperatures. The role of the solvents and the mobility of the lithium ions were investigated by pulsed gradient spin echo (PGSE) NMR measurements to elucidate the behavior of the ionic conductivity.     

Identification of intra-individual variation in intracranial arterial flow by MRI and the effect on computed hemodynamic descriptors

Magnetic Resonance Materials in Physics, Biology and Medicine - To determine the intra-individual flow variation in serially acquired studies, and the influence of this variation on subsequent...     

Evaluation on wear behavior of Cr-Ag-N and Cr-W-N PVD nanocomposite coatings using two different types of tribometer

Practice has proven that CrN performs better than TiN under some specific tribological applications. Nevertheless, the relatively soft nature of CrN still remains a problem. This paper reports experimental results on increases in hardness of sputtered PVD CrN coatings by means of additions of varying content of Ag or W. The resulting Cr-Ag-N and Cr-W-N coatings, grown on JIS SKH51 steel substrates, were characterized using SEM, EDS, WDS, XRD, micro-indentation hardness testing and scratch adhesion tests. Moreover, wear behavior was studied on two types of tribometer, employing different contact regimes — a ‘cylinder-on-disk’ line-contact reciprocating-sliding regime and a ‘ball-on-disk’ point-contact rotating-sliding regime.The experimental results can be summarized as follows: The hardness of Cr-W-N coatings increased with increasing W content; reversely, that of Cr-Ag-N coatings decreased with increasing Ag content. The additions of Ag and W resulted in a formation of secondary phases, elemental Ag and WN, respectively, uniformly embedded in the CrN coatings. With the two different types of tribometer, the observed trends for wear behavior, wear and friction coefficient, were nearly identical, indicating that both Ag and W additions to CrN coatings were beneficial. However, the Cr-W-N coatings were significantly more wear resistant than the Cr-Ag-N coatings. With the addition of W at 6.8 at.%, the largest wear improvement of 73%-85% was achieved.     

REACTIVE DIFFUSION BETWEEN Si AND NbC AT 1300℃

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Enhancing the accuracy of WLAN-based location determination systems using predicted orientation information

Indoor location determination has emerged as a significant research topic due to the wide-spread deployment of wireless local area networks (WLANs) and the demand for context-aware services inside buildings. However, prediction accuracy remains a primary issue surrounding the practicality of WLAN-based location determination systems. This study proposes a novel scheme that utilizes mobile user orientation information to improve prediction accuracy. Theoretically, if the precise orientation of a user can be identified, then the location determination system can predict that user’s location with a high degree of accuracy by using the training data of this specific-orientation. In reality, a mobile user’s orientation can be estimated only by comparing variations in received signal strength; and nevertheless the predicted orientation may be incorrect. Incorrect orientation information causes the accuracy of the entire system to decrease. Therefore, this study presents an accumulated orientation strength algorithm which can utilize uncertain estimated orientation information to improve prediction accuracy. Implementation of this system is based on the Bayesian model, and the experimental results indeed show the effectiveness of our proposed approach.