A radical scavenging reaction of α-tocopherol with methyl radical

To study a radical scavenging reaction of α-tocopherol, it was reacted with methyl radical in dimethyl sulfoxide. Two main products, a geminal dimethyl cyclohexadienone and methyl ether of α-tocopherol, were obtained and these structures were determined by¹³C nuclear magnetic resonance spectroscopy. The radical methylation data of α-tocopherol suggested that a delocalized radical species would be an intermediate. TMIG-RI No. 3.     

Dipolar-decoupled carbon-13 NMR study of highly oriented polyethylene films

Summary High-resolution solid-state ¹³C NMR spectra and ¹³C relaxation times T₁ and T₁ have been measured at 40–100° C for uniaxially oriented polyethylene films with the drawing direction parallel to the magnetic field; this sample has a unique morphological structure that the noncrystalline chains are nearly disordered irrespective of the high degree of drawing. A sharp resonance line(line A) appears at the position corresponding to the principal value ₃₃ of the chemical shift tensor for the CH₂ carbons with the trans-trans conformation. Another sharp linedine B) is observed at almost the same chemical shift as for the CH₂ carbons of polyethylene in solution. Although these observations are similar to those for a cold-drawn polyethylene sample reported previously, line B is much enhanced in intensity and the linewidth is narrower in the present sample, reflecting the disorientation of the noncrystalline component. It is found from T₁ measurements that line A contains two components with different molecular mobility, both being assigned to the crystalline components. On the other hand, the line B is composed of a single component assignable to the noncrystalline component with liquid-like molecular mobility.     

Continuous hydrolysis of olive oil by lipase in microporous hydrophobic membrane bioreactor

Continuous hydrolysis of olive oil byCandida cylindracea’s lipase was studied in a microporous hydrophobic membrane bioreactor. Olive oil and buffer solution, fed continuously through two compartments partitioned by membrane, caused reaction at the interface of lipase-adsorbed membrane and buffer solution. Fatty acid was obtained in a single phase without being mixed with components of other phases. At all mean residence times, countercurrent flow mode was superior to cocurrent one. The lipase was adsorbed onto the membrane, and its adsorption was suggested to be partially specific from the experiments with enzymes having various levels of purity. The percent hydrolysis depended hyperbolically on the interfacial enzyme concentration. The hydrolysis seemed to be limited by diffusion of fat or fatty acid through the micropores of the membrane at higher interfacial enzyme concentrations. The lipase was stabilized significantly by glycerol added to the buffer solution. Satisfactory performance of the membrane bioreactor was obtained in a longterm continuous operation which lasted for 24 days by feeding buffer-glycerol (18.0%) solution over the adsorbed lipase. The operational half-life of the adsorbed enzyme was 15 days at 40 C.     

Reduction of nitric oxide with activated PAN fibres

The reductive removal of nitric oxide from flue gases by reaction with polyacrylonitrile-based active carbon fibres (PAN-ACF) activated with sulphuric acid has been studied at 423–632 K, using a circulating flow reactor. Nitric oxide (0.67 mmol) was completely removed via reduction with 1 g activated carbon under optimum conditions in 210 and 60 min at 423 and 623 K, respectively. N₂ was formed as NO was removed. Some oxygen remained on the carbon surface at 423 K, but was desorbed as CO or CO₂ on subsequent heating to 623 K. The bimolecular reaction of NO reduction over PAN-ACF, and the possible active sites of oxygen surface groups are discussed in the light of a kinetic study and a comparison of the fibre activation at different temperatures.     

An experimental study of energy dips for speech and music

Speech signals generally have many intervals with low energy “energy dips”. For music signals, energy dips are not always remarkable. We studied stochastic features of energy dips for speech and music signals. A certain difference was found between the signals in the length of energy dips. Also, the number of energy dips in a time window and their distribution were investigated. From this distribution, a threshold number of energy dips was estimated which provided a scheme for the discrimination of speech from music.     

The Effects of Conventional Stabilizers and Phenol Compounds Used as Antioxidants on the Stabilization of Nitrocellulose

The thermal behavior of nitrocellulose (NC) containing diphenylamine (DPA), 2‐nitrodiphenylamine (2‐NO₂‐DPA), N‐nitrosodiphenylamine (N‐NO‐DPA), ethyl centralite (EC), akardite II (AKII), 1,1,3‐tri‐(2‐methyl‐4‐hydroxy‐5‐tert‐butyl‐phenyl)‐butane (BP_less), 3‐(3,5‐di‐tert‐butyl‐4‐hydroxy‐phenyl)‐propionic acid octadecyl ester (BP_hin), and 3‐(3‐tert‐butyl‐4‐hydroxy‐5‐methyl‐phenyl)‐propionic acid 2‐(9‐{2‐[3‐(3‐tert‐butyl‐4‐hydroxy‐5‐methyl‐phenyl)‐propionyloxy]‐1,1‐dimethyl‐ethyl}‐2,4,8,10‐tetraoxa‐spiro [5.5] undec‐3‐yl)‐2‐methyl‐propyl ester (BP_semi) was observed during isothermal storage at 393 K using a C80 microcalorimeter. The results indicate that each stabilizer decreased NC's maximum heat release rate and increased the induction period of heat release. We also observed that the maximum heat release rate and the induction period were dependent on the amount of stabilizer. DPA decreased the maximum heat release rate to the greatest extent, with the other stabilizers having similar effects on the decrease of maximum heat release rate. AKII prolonged the induction period of heat release most. The order of prolongation of the induction period was AKII>2‐NO₂‐DPA≈DPA>N‐NO‐DPA≈EC>BP_less≈BP_semi≈BP_hin.     

Reusability, Durability and Treatability of Palladium Catalyst on a Semiconductor Plate: Comparison with Commercially Available Solid-Supported Palladium Catalysts

A palladium catalyst supported on a semiconductor plate underwent the Heck reaction effectively to afford a coupling product. The catalytic plate was easily recovered from the reaction mixture with tweezers and reused several times without any special treatment. Comparison of reusability, durability, and treatability of seven kinds of commercially available solid-supported palladium catalysts and the semiconductor-supported catalyst plate was studied.     

Pose-Invariant Facial Expression Recognition Using Variable-Intensity Templates

In this paper, we propose a method for pose-invariant facial expression recognition from monocular video sequences. The advantage of our method is that, unlike existing methods, our method uses a simple model, called the variable-intensity template, for describing different facial expressions. This makes it possible to prepare a model for each person with very little time and effort. Variable-intensity templates describe how the intensities of multiple points, defined in the vicinity of facial parts, vary with different facial expressions. By using this model in the framework of a particle filter, our method is capable of estimating facial poses and expressions simultaneously. Experiments demonstrate the effectiveness of our method. A recognition rate of over 90% is achieved for all facial orientations, horizontal, vertical, and in-plane, in the range of ±40 degrees, ±20 degrees, and ±40 degrees from the frontal view, respectively. Electronic Supplementary Material  The online version of this article () contains supplementary material, which is available to authorized users.     

V–I characteristics of solid polymer electrolytic (SPE) dehumidifier

Measurements of the V–I characteristics of a solid polymer electrolytic (SPE) dehumidifier were done using a modified SPE dehumidifier with four electrodes which included two electrodes to carry the main current and the other two electrodes to measure the voltages applied to the electrical double layer, which are the boundary voltages between the electrodes and the SPE membrane. The measured results were analyzed using the Butler-Volmer equation to examine the validity of the measurements. The current flowing in the dehumidifier is produced by the decomposition of water near the anode. Therefore, under a steady-state condition, the current should be proportional to the supply rate of water to the anode. On the other hand, a two-layer model for the SPE dehumidifier presented in our previous article showed that the current flowing in the dehumidifier was roughly proportional to the water content in the vicinity of the anode. These results were introduced for interpretation of the V–I measurements of the SPE dehumidifier. It was concluded that the dehumidifier current was expressed in the form of a Butler-Volmer equation as a function of the electrode boundary voltages which were the voltages across the boundary between the electrodes and the SPE membrane. An experimental formula for the current under a steady-state condition was developed as a function of the water content near the anode and the boundary voltages.     

Preparation of Titanium Nitride Films from Amide Precursors Synthesized by Electrolysis

A TiN precursor solution was synthesized by galvanostatic electrolysis of Ti metal and isopropylamine at a current density of 50 mA·cm⁻² at room temperature. TiN films were prepared by dip-coating of the precursor solution on a Si wafer, followed by two-stage heat treatment at 400°C and a fixed temperature of 800–1200°C in flowing N₂, N₂/NH₃, or NH₃ gas. The TiN films were characterized by XRD, chemical analysis, XPS, and electrical resistivity measurements. The TiN films were composed of uniform grains 20 to 200 nm in size with thicknesses ranging from 300 to 400 nm at temperatures of 800–1200°C. The effect of the heat treatment atmosphere (N₂ and NH₃) on the impurity content, crystallinity, particle size, and electrical resistivity is discussed.