Effects of Solvents in the Polyethylene Glycol Series on the Bonding of Copper Joints Using Ag2O Paste

The effects of reducing solvents on the bonding process using silver oxide paste in a copper joint were investigated. Three solvent types were tested: diethylene glycol (DEG), triethylene glycol (TEG), and polyethylene glycol (PEG). The strength of the joints was assessed by fracturing, which occurred at the interface of the copper oxide layer and the copper substrate in DEG and TEG samples and at the bonded interface in the PEG sample. Analysis of the samples revealed that, in the DEG and TEG samples, the copper substrate was oxidized during the bonding process, which compromised the shear strength of the joints. In contrast, the PEG sample exhibited nonuniform sintering of the silver layer while retaining good shear strength. It was found that the combination of DEG and PEG produced optimum shear strength in the copper joint, as PEG suppressed the growth of copper oxide and DEG promoted the formation of a dense sintered silver layer. The bonding strength achieved was higher than that of the gold-to-gold joint made using standard Pb-5Sn solder.     

Apatite mineralization abilities and mechanical properties of covalently cross-linked pectin hydrogels

Natural bone has features such as high fracture toughness and bone-bonding bioactivity, and is organic–inorganic hybrid composed of collagen and apatite crystals. Therefore, apatite-polymer hybrids designed to mimic the structure of bone represent candidates for high-performance bone substitutes. In this study, we prepared pectin hydrogels through covalent cross-linking using divinylsulfone (DVS) and investigated their apatite-forming abilities of the gels in simulated body fluid (SBF) and mechanical properties by tensile test. The obtained results were interpreted in terms of surface charge of the gels and chemical reaction with SBF. The apple- and citrus-derived gels formed the apatite on their surfaces in SBF within 3 days. These gels showed tensile strength around 30 MPa.     

Mechanical relaxation processes of wood in the low-temperature range

The dynamic viscoelastic properties of untreated and chemically modified wood specimens were determined in the temperature range 123 to 293 K and at constant frequencies. Absolutely dry wood specimens exhibited one relaxation process labeled γ at around 180 K, being attributed to the motions of methylol groups in the amorphous region of the wood constituents. The changes in the γ process due to the chemical modifications were explained by the reduction in the original γ loss peak due to the decrease of methylol groups, and an additional relaxation induced by the other groups introduced. With moisture adsorption, an additional relaxation labeled β was induced at 220–240 K. It appeared only when the wood adsorbed moisture irrespective of chemical modifications, and its characteristics were not affected by the formaldehyde and PEG treatments involving the remarkable changes in the mobility of amorphous molecules. These results suggested that the dominant mechanism of β relaxation was not the segmental motions of the main chain, but the motion of the adsorbed water molecules. The positive activation entropy of the β relaxation was interpreted to reflect rearrangement of the adsorption sites required for the rotation of the adsorbed water molecules. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 3338–3347, 2001     

Changes of spin–spin relaxation time for EPR composites during mixing process

The changes of the mobility of rubber molecules for carbon black-filled EPR composites during mixing process in an internal mixer have been elucidated from T₂ measurement using pulsed nuclear magnetic resonance (NMR). The thickness of the tightly bound region which is formed by the direct interaction with carbon black was stabilized with mixing but the restriction of the molecular mobility increased with further mixing. The amount of the loosely bound region increased considerably throughout the mixing, indicating that this region is formed by entanglement and crosslinking of the molecules. T₂ of the mobile region which is a predominant part in the composites is independent of the mixing time. EPR has the thinner tightly bound shell and longer T_2S compared with EPDM, showing the effect of unsaturated bond in EPDM which can become a strong bond site with carbon black.     

On the Application of Modern Control Theory to Automotive Engine Control

This study deals with how modern control theory can be applied to automotive engine control. Appropriate models are indispensable in the application of modern control theory, the present study achieves engine modeling using physical and statistical approaches. Also, for a concrete application of modern control theory, the present focus is on a torque servo engine, because torque is the output most necessary for an engine. Modern control techniques are used to control a torque servo engine to obtain the most fuel-saving operation possible. It is found that a high potential could be achieved compared with conventional control methods.     

AFM picking-up manipulation of the metaphase chromosome fragment by using the tweezers-type probe

We have studied the development of a new procedure based on atomic force microscopy (AFM) for the analysis of metaphase chromosome. The aim of this study was to obtain detailed information about the specific locations of genes on the metaphase chromosome. In this research, we performed the manipulation of the metaphase chromosome by using novel AFM probes to obtain chromosome fragments of a smaller size than the ones obtained using the conventional methods, such as glass microneedles. We could pick up the fragment of the metaphase chromosome dissected by the knife-edged probe by using our tweezers-type probe.     

Reaction and oxygen permeation studies in Sm0.4Ba0.6Fe0.8Co0.2O3 − δ membrane reactor for partial oxidation of methane to syngas

A disk-type Sm_0.4Ba_0.6Co_0.2Fe_0.8O_3 − δ perovskite-type mixed-conducting membrane was applied to a membrane reactor for the partial oxidation of methane to syngas (CO + H₂). The reaction was carried out using Rh (1 wt%)/MgO catalyst by feeding CH₄ diluted with Ar. While CH₄ conversion increased and CO selectivity slightly decreased with increasing temperature, a high level of CH₄ conversion (90%) and a high selectivity to CO (98%) were observed at 1173 K. The oxygen flux was increased under the conditions for the catalytic partial oxidation of CH₄ compared with that measured when Ar was fed to the permeation side. We investigated the reaction pathways in the membrane reactor using different membrane reactor configurations and different kinds of gas. In the membrane reactor without the catalyst, the oxygen flux was not improved even when CH₄ was fed to the permeation side, whereas the oxygen flux was enhanced when CO or H₂ was fed. It is implied that the oxidation of CO and H₂ with the surface oxygen on the permeation side improves the oxygen flux through the membrane, and that CO₂ and H₂O react with CH₄ by reforming reactions to form syngas.     

Studies of the fractionation of polyoxymethylene

The precipitation of polyoxymethylene in p-chlorophenol solution and the molecular weight fractionation of the polymer by mechanical agitation were investigated. The agitation of the solution was carried out in a glass vessel with a stirrer, usually at 60°C. After agitation for several minutes a fibrous polymer precipitated. High molecular weight polymer precipitated around the stirrer in an early stage, and therefore the method might be applied to the fractionation of polyoxymethylene. The method was applied to the fractionation of polyoxymethylene prepared in a solid-state and in a solution polymerization of trioxane, catalyzed by BF₃.OEt₂. It was found that the polymer from the solid state contained a small amount of extremely high molecular weight fraction, and that obtained from the solution had a relatively narrow distribution of molecular weight.