Effect of poly(acrylic acid) on the preparation of thick silica films by electrophoretic sol–gel deposition of re-dispersed silica particles

Thick silica films were prepared by the electrophoretic sol–gel deposition technique in the presence of poly(acrylic acid) (PAA) using monodispersed silica particles; the particles were prepared by the sol–gel method, pre-heat treated and then re-dispersed in the mixture of H2O and ethanol. The weight of deposited silica films was maximized when 0.2 mass % of PAA against the whole amount of sol was added. The particles constructing the thick silica films were packed densely when the amount of added PAA was less than 0.2 mass%. The weight of the film increased with decrease in the content of H2O in the sol when a fixed amount of PAA was added. After the heat treatment of deposited films at 800 °C, crack-free silica films of about 30 m thickness were prepared. © 1998 Chapman & Hall     

Discharge properties and chemical stability of SrZrO films

Abstract— MgO thin film is currently used as a surface protective layer for dielectric materials because MgO has a high resistance during ion sputtering and exhibits effective secondary electron emission. The secondary‐electron‐emission coefficient γ of MgO is high for Ne ions; however, it is low for Xe ions. The Xe content of the discharge gas of PDPs needs to be raised in order to increase the luminous efficiency. Thus, the development of high‐γ materials replacing MgO is required. The discharge properties and chemical surface stability of SrO containing Zr (SrZrO) as the candidate high‐γ protective layer for noble PDPs have been characterized. SrZrO films have superior chemical stability, especially the resistance to carbonation because of the existence of a few adsorption sites due to their amorphous structure. The firing voltage is 60 V lower than that of MgO films for a discharge gas of Ne/Xe = 85/15 at 60 kPa.     

Defect distribution near abraded surface of III–V compound semiconductors

Microstructures of damaged layers near the abraded surface of GaP, GaAs_0.6P_0.4 and GaAs single crystals have been observed with a transmission electron microscope. The damage due to 0.3 m Al₂O₃ abrasion consists of dislocations. Dislocation densities in the abrasion band and other regions are larger than 5×10¹¹ cm^–2 and about 10¹¹ cm^–2, respectively. Dislocation density decreases with increasing distance (depth) from the abraded surface. The depths of the damage layers for GaP, GaAs_0.6P_0.4 and GaAs are about 0.4, 0.55, and 0.8 m, respectively. The Burgers vector of dislocations is a/2[1 1 0], and A and B dislocations are observed. During annealing, the dislocations are rearranged and eliminated by the reaction of the dislocations with different Burgers vectors and climbing motion. The rearrangement temperatures for dislocations in GaP and GaAs are about 500 and 450° C, respectively. Electrical resistance changes in the damaged layer of GaP are recognized by electrical resistance measurements.     

Colorimetric microdetermination of sulphites in foods by use of the modified rankine apparatus. IV.

Summary Detection and determination of traces of sulphites in foods was attempted by use of the modified Rankine apparatus and pararosaniline colorimetry. Replacement of alkaline titration reported previously by pararosaniline colorimetry lowered the absolute detection limit from 30 g (titration method) to 2 g. In view of clean analysis, in the color developing system, 0.1 N-sodium hydroxide was used in place of mercuric chloride solution commonly used as an absorbant of sulphites. In order to prevent oxidative decomposition of sulphites during operation, nitrogen gas was used as carrier instead of air. Dimedone and sodium azide were used for the elimination of aldehydes and nitrites, respecitvely, in the sample, which will disturb the color development of sulphites with pararosaniline-formaldehyde reagents. With this improved method, it was possible to determine the residual sulphites in frozen peeled shrimps, sugared beans and other foods with low sulphite contents accurately.

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Colorimetrische Mikrobestimmung von Sulfiten in Lebensmitteln bei Anwendung der modifizierten IV. Rankine Apparatur

Zusammenfassung Geringe Sulfitmengen in Lebensmitteln (geschälte Garnelen, gezuckerte Bohnen) können colorimetrisch bestimmt werden. Die neuentwickelte Methode beruht auf einer Kombination von colorimetrischer Bestimmung mittels p-Rosanilin und der Bestimmungsmethode nach Rankine. Auf diese Weise lassen sich Gehalte von 2 g noch genau bestimmen. Bei der Farbentwicklung wurde das giftige Quecksilbertetrachlorid durch 0.1 n-NaOH ersetzt, anstelle von Luft Stickstoff als Trägergas verwendet und somit eine Oxydation des Sulfits während der Bestimmung vermieden. Da Nitrit und Aldehyde die Farbentwicklung stören, wurde ihr Einfluß durch Dimedon und Natriumazid ausgeschaltet.

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Studies on the Analyses of Sulphites in Foods (IV)     

Hot-water treatment of sol–gel derived SiO2–TiO2 microparticles and application to electrophoretic deposition for thick films

SiO₂–TiO₂ spherical microparticles of about 0.7 μm in diameter were prepared by the sol–gel method. Anatase nanocrystals were formed in the microparticles and their specific surface area was increased after a hot-water treatment at 90 °C. From the changes in the concentration of I₂ photocatalytically generated from KI aqueous solution, the activity of the SiO₂–TiO₂ microparticles was found to increase with increasing the hot-water treatment time. Particulate, thick films were electrophoretically deposited on indium tin oxide (ITO)-coated glass substrates using the anatase nanocrystal-precipitated SiO₂–TiO₂ microparticles. The thickness of the electrophoretically deposited particulate film increased to be approximately 10 μm with an increase in applied voltage. The resultant thick film showed a high photocatalytic activity.     

Satellite-Based Energy Balance to Assess Within-Population Variance of Crop Coefficient Curves

Quantifying evapotranspiration (ET) from agricultural fields is important for field water management, water resources planning, and water regulation. Traditionally, ET from agricultural fields has been estimated by multiplying the weather-based reference ET by crop coefficients (Kc) determined according to the crop type and the crop growth stage. Recent development of satellite remote sensing ET models has enabled us to estimate ET and Kc for large populations of fields. This study evaluated the distribution of Kc over space and time for a large number of individual fields by crop type using ET maps created by a satellite based energy balance (EB) model. Variation of Kc curves was found to be substantially larger than that for the normalized difference vegetation index because of the impacts of random wetting events on Kc, especially during initial and development growth stages. Two traditional Kc curves that are widely used in Idaho for crop management and water rights regulation were compared against the satellite-derived Kc curves. Simple adjustment of the traditional Kc curves by shifting dates for emergence, effective full cover, and termination enabled the traditional curves to better fit Kc curves as determined by the EB model. Applicability of the presented techniques in humid regions having higher chances of cloudy dates was discussed.     

Parallel processing circuit of line image using neuristor

A simultaneous detecting circuit system of centers and lengths of some lines in one dimension is presented applying an electronic circuit model of the nervous axon with respect to signal transmission. This model consists of series of one basic section, and has functions of Neuristor. The circuit system has a paralell processing function. It is constructed by three layers. In the first layer each visual signal of lines is changed to electric pulse signal. In the second layer edges of each line are detected, and in the third layer these detected signals are converted into voltages which correspond to lengths of the lines. These functions were confirmed experimentally using its hardware.     

Fuzzy Linear Programming with Interactive Uncertain Parameters

In this paper, we treat fuzzy linear programming problems with uncertain parameters whose ranges are specified as fuzzy polytopes. The problem is formulated based on fractile optimization model using a necessity measure. It is shown that the problem can be reduced to a semi-infinite linear programming problem and that a solution algorithm based on a relaxation procedure can be applied. A simple numerical example is given to illustrate the solution procedure. This revised version was published online in June 2006 with corrections to the Cover Date.     

A Technique to Eliminate Redundant Inter-Processor Communication on Parallelizing Compiler TINPAR

Optimizing inter-processor (PE) communication is crucial for parallelizing compilers for message-passing parallel machines to achieve high performance. In this paper, we propose a technique to eliminate redundant inter-PE messages. This technique utilizes data-flow analysis to find a definition point that corresponds to a use point where the definition and the use occur in different PEs. If several read accesses occurred in the same PE use the data defined at the same definition point in another PE, redundant inter-PE messages are eliminated as follows: only one inter-PE communication is performed for the earliest read access and the previously received data are used for the following read. In order to guarantee the consistency of the data, a valid flag and a sent flag are provided for each chunk of received data. The control of these flags is equivalent to the coherence control by the self invalidation on a compiler aided cache coherence scheme.     

Prediction of ethylene content in melt-state random and block polypropylene by near-infrared spectroscopy and chemometrics: comparison of a new calibration transfer method with a slope/bias correction method

This paper reports the prediction of the ethylene content (C2 content) in random polypropylene (RPP) and block polypropylene (BPP) in the melt state by near-infrared (NIR) spectroscopy and chemometrics. NIR spectra of RPP and BPP in the melt states were measured by a Fourier transform near-infrared (FT-NIR) on-line monitoring system. The NIR spectra of RPP and BPP were compared. Partial least-squares (PLS) regression calibration models predicting the ethylene (C2) content that were developed by using each RPP or BPP spectra set separately yielded good results (SECV (standard error of cross validation): RPP, 0.16%; BPP, 0.31%; correlation coefficient: RPP, 0.998; BPP, 0.996). We also built a common PLS calibration model by using both the RPP and the BPP spectra set. The results showed that the common calibration model has larger SECV values than the models based on the RPP or the BPP spectra sets individually and is not practical for the prediction of the C2 content. We further investigated whether a calibration model developed by using the BPP spectra set can predict the C2 contents in the RPP sample set. If this is possible, it can save a significant amount of work and cost. The results showed that the use of the BPP model for the RPP sample set is difficult, and vice versa, because there are some differences in the molar absorption coefficients between the RPP and BPP spectra. To solve this problem, a transfer method from one sample spectra (BPP) set to the other spectra (RPP) set was studied. A difference spectrum between an RPP spectrum and a BPP spectrum was used to transfer from the BPP calibration set to the RPP calibration set. The prediction result (SEP (standard error of prediction), 0.23%, correlation coefficient, 0.994) of RPP samples by the transferred calibration set and model showed that it is possible to transfer from the BPP calibration set to the RPP calibration set. We also studied the transfer from the RPP calibration set (the range of C2 content: 0-4.3%) to the BPP calibration set. The prediction result of C2 content (the range of C2 contents: 0-7.7%) in BPP by use of the calibration model based on the transferred BPP spectra from the RPP spectra showed that the transfer method is only effective for the interpolation of the C2 content range by the nonlinear change in the peak intensities with the C2 content.