Restraint Method for Overcoming Heating Irregularity and Improving Heating Equipment Efficiency for Beverage Cans Using High‐Frequency Induction Heating

We were able to reduce heating irregularities in equipment for heating beverage cans by using the high‐frequency induction heating method and determining the resulting improvement in the heating efficiency. The heating irregularity between the top and bottom of the can was reduced to less than 3°C by improving the arrangement of the heating coils for the beverage can by thinning the winding and changing the circuit configuration. The efficiency of power conversion was improved from 93.0% to 97.4%. In this paper, the configuration of the equipment and the experimental results are reported.     

AREM Shop Evaluation Method

A new tool has been developed to evaluate the reliability of assembly shop operation. It is a subsystem of AREM (Assembly Reliability Evaluation Method) [1] that can evaluate assembly fault occurrence rates by using product design information. This new tool uses approximately forty questions to assess quantitatively the influence of assembly shop operation reliability on assembly fault occurrence. This method is being used both to improve shop operation reliability and to select preferable shop, and is proven to be effective. The entire AREM system supports efficiently systematic improvement in assembly quality by examining both product design and assembly shop.     

Reaction Phases and Strength of AlN/V Diffusion Couples

Diffusion couples of AlN/V were experimentally examined after annealing in a temperature range of 1373 K1773 K for a bonding time range of 0.9 ks21.6 ks. The interfacial reaction, reaction mechanism, and bond strength of the bonded AlN/V couples have been explained on the basis of phase relations at different bonding conditions, making use of elemental analysis, XRD, and shear testing method. Formation of V(Al) solid solution and V₂N nitride controls the interfacial joining of the AlN/V couples. A complete diffusion path between AlN and V could be predicted at 1573 K before 0.9 ks, following a sequence of AlN/V(Al)/V₂N/V. This sequence can be discussed during the Al-V-N ternary phase diagram. At a high temperature of 1573 K, AlN decomposition at the interface took place. A maximum bond strength could be obtained for a joint bonded at 1573 K after 5.4 ks, having a structure of AlN/V(Al)/V₂N + V.     

Tiered Electron Anions in Multiple Voids of LaScSi and Their Applications to Ammonia Synthesis

Electrides—compounds in which electrons localized in interstitial spaces periodically serve as anions—have attracted broad attention for their exotic properties, such as extraordinary electron‐donating ability. In our efforts to expand this small family of phases, LaScSi emerges as a promising candidate. Its electron count is 2e^? f.u.^?1 in excess of that expected from the Zintl concept, while its structure offers interstitial spaces that can accommodate these extra electrons. Herein, this potential is explored through density functional theory (DFT) calculations and property measurements on LaScSi. DFT calculations (validated by heat capacity and electrical transport measurements) reveal electron density peaks at two symmetry‐distinct interstitial sites. Importantly, this electride‐like character is combined with chemical stability in air and water, an advantage for catalysis. Ru‐loaded LaScSi shows outstanding catalytic activity for ammonia synthesis, with a turnover frequency (0.1 s^?1 at 0.1 MPa, 400 °C) an order of magnitude higher than those of oxide‐based Ru catalysts, e.g., Ru/MgO. As with other electrides, LaScSi's ability to reversibly store hydrogen prevents the hydrogen poisoning of Ru surfaces. The better performance of LaScSi, however, hints at the importance of the high concentration (>1.6 × 10²² cm^?3) and tiered nature of its anionic electrons, which offers guidance toward new catalysts.     

Effect of W-Mo balance and boron nitrides on creep rupture ductility of 9Cr steel

The effect of W-Mo balance and boron nitrides (BN) on creep rupture ductility has been investigated for five heats of 9% Cr steel with 1.5% Mo equivalent, 0.003% boron and 0.05% nitrogen at 600^oC, 650^oC and 700^oC. The maximum time to rupture was 68,718 h at 650^oC. The reduction of area (RA) slightly decreases for up to about 8000 and 1000 h at 600 and 650^oC, respectively, while it significantly decreases above those. The BN particles are responsible for the degradation in RA at low stresses and long times by accelerating the formation of creep voids. At high stresses and short times, the RA decreases with increasing time to rupture and with increasing W concentration and concomitantly with decreasing Mo concentration. The rupture ductility is evaluated by using a semi-logarithmic diagram of the RA and total elongation, showing the necking dominant and void swelling dominant regions.     

Effects of Samarium Oxide Addition on the Phase Composition, Microstructure, and Electrical Resistivity of Aluminum Nitride Ceramics

The phase composition, microstructure, and electrical resistivity of hot-pressed AlN ceramics with 0–4.8 wt% Sm₂O₃ additive were investigated. The phase composition was approximately consistent with that estimated from the Sm₂O₃–Al₂O₃ phase diagram using the amount of added Sm₂O₃ and oxygen content of the AlN raw material. When sintered at more than 1800°C, the AlN ceramics with 1.0–2.9 wt% Sm₂O₃ additive contained an Sm-β-alumina phase wetting the grain boundaries, and their electrical resistivity considerably decreased to 10¹⁰–10¹²Ω·cm. This resistivity decrease was caused by the continuity of the Sm-β-alumina phase with a resistivity lower than that of bulk AlN.     

Radiation-induced polymerization of ethylene in a pilot plant. I. Bulk process

Radiation-induced bulk polymerization of ethylene was carried out with use of a pilot plant with a 10 liter reactor at pressures of 225–400 kg/cm², temperatures of 30–95°C, ethylene feed rates of 5–28 kg/hr, and dose rate of 3.8 × 10⁵ rad/hr. Characteristics of the process are mild polymerization conditions and capability of producing medium density polyethylene in powder form. The spacetime yield and molecular weight of polymer were in the range of 3.5 to 13.1 g/liter hr and 2.2 × 10⁴ to 14 × 10⁴, respectively. The space-time yield increased with mean residence time and 2.4 powders of pressure, and decreased with temperature. Molecular weight changed similarly with the reaction conditions. These results were consistent with those of the bench plant experiment and the scale effect was small. Polymer deposit to the reactor wall limited a period of continuous operation of the plant. The amount of deposited polymer was increased with the square of reaction time. The rate of polymer deposit was proportional to polymer concentration and to the cube of pressure. The polymer deposit cannot be solved in the bulk process.     

Narrow multi-walled carbon nanotubes produced by chemical vapor deposition using graphene layer encapsulated catalytic metal particles

The use of graphene layer encapsulated catalytic metal particles for the growth of narrower multi-walled carbon nanotubes (MWCNTs) has been studied using plasma-enhanced chemical vapor deposition and conventional thermal CVD. Ni–C or Fe–C composite nanoclusters were fabricated using the dc arc discharge technique with metal–graphite composite electrodes carrying a current of 100–200 A in a stainless-steel chamber filled with He and CH₄ mixture gas at 27 kPa. Nano-sized grains with diameters less than 10 nm were fabricated and deposited on a Si substrate, and were used as a catalyst for MWCNT growth. Structural analyses of the composite nanoclusters and MWCNTs were carried out using transmission electron microscopy. The results show that the diameters of the MWCNTs were reduced from 50–100 nm for a conventional Ni thin film-evaporated Si substrate to a minimum of roughly 2–4 nm in the present study.     

Porous cellulose acetate membrane prepared by thermally induced phase separation

Microporous cellulose acetate membranes were prepared by a thermally induced phase separation (TIPS) process. Two kinds of cellulose acetate with acetyl content of 51 and 55 mol % and two kinds of diluents, such as 2‐methyl‐2,4‐pentandiol and 2‐ethyl‐1,3‐hexanediol, were used. In all polymer‐diluent systems, cloud points were observed, which indicated that liquid–liquid phase separation occurred during the TIPS process. The growth of droplets formed after the phase separation was followed using three cooling conditions. The obtained pore structure was isotropic, that is, the pore size did not vary across the membrane. In addition, no macrovoids were formed. These pore structures were in contrast with those usually obtained by the immersion precipitation method. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3951–3955, 2003