Promotion of CO2 methanation activity and CH4 selectivity at low temperatures over Ru/CeO2/Al2O3 catalysts

The effect of CeO₂ loading amount of Ru/CeO₂/Al₂O₃ on CO₂ methanation activity and CH₄ selectivity was studied. The CO₂ reaction rate was increased by adding CeO₂ to Ru/Al₂O₃, and the order of CO₂ reaction rate at 250 °C is Ru/30%CeO₂/Al₂O₃ > Ru/60%CeO₂/Al₂O₃ > Ru/CeO₂ > Ru/Al₂O₃. With a decrease in CeO₂ loading of Ru/CeO₂/Al₂O₃ from 98% to 30%, partial reduction of CeO₂ surface was promoted and the specific surface area was enlarged. Furthermore, it was observed using FTIR technique that intermediates of CO₂ methanation, such as formate and carbonate species, reacted with H₂ faster over Ru/30%CeO₂/Al₂O₃ and Ru/CeO₂ than over Ru/Al₂O₃. These could result in the high CO₂ reaction rate over CeO₂-containing catalysts. As for the selectivity to CH₄, Ru/30%CeO₂/Al₂O₃ exhibited high CH₄ selectivity compared with Ru/CeO₂, due to prompt CO conversion into CH₄ over Ru/30%CeO₂/Al₂O₃.     

HPLC Elution Behavior of La-Fullerenes Investigated by Radiochemical Method

HPLC elution behaviors of La-fullerenes were investigated by use of the radiochemical methods. Elution curves of La-fullerenes could be observed in detail for the first time, and the persistent presence of La in the whole elution curve was demonstrated. Production of La-fullerenes containing a radioactive ¹⁴⁰La could be achieved for the first time.     

Influence of cold-rolling and annealing conditions on formability of aluminium alloy sheet

Using an Al-Mg-Cu alloy developed for auto body panels, strip sheets are experimentally produced by various cold-rolling and annealing procedures. Tensile and metallographic properties of the sheets and their relations are examined to attain high formability. The elongation is closely related to the grain size, and increases with the final annealing temperature. The rolling texture influences the plastic anisotropy, the Lankford value of the sheets. The comparatively high Lankford values are obtained under the condition that both the intermediate and the final annealing temperatures are higher and the reduction ratio after the intermediate annealing is smaller.     

Serum selenium contents and the risk of cancer

To investigate the relationship between serum Se contents and the risk of cancer, 4857 serum samples were obtained from cancerous (2730) and non-cancerous patients (2127). In this cohort, the incidence of cancer in the non-cancerous patients was followed for the subsequent 3 years. The serum Se level of non-cancerous patients who later developed cancer during the 3 years was determined and compared with that of the non-cancerous patients. A high incidence of cancer was observed in the lower serum Se patients of the non-cancerous group. The serum Se levels of cancerous patients were significantly lower than in non-cancerous patients. These results suggest that the low serum Se level in cancerous patients may not be induced by the tumor but it was more likely already present before the tumor. To calculate the odds ratio, cancerous and non-cancerous patients were divided into group of less than 110 ppb and more than 111 ppb group in serum Se. The odds ratio was estimated to be 1.95, suggesting the high risk of cancer in the low serum Se group.     

Effect of insulin fragments on biological activity of insulin and desoctapeptide insulin. I. Potentiation of biological activities

Four derivatives of the insuln B-chain COOH-terminal pentapeptide Arg-Gly-Phe-Phe-Tyr (B22-26) were synthesized and shown to be inactive alone. In the presence of submaximal concentrations of insulin or desoctapeptide insulin, peptides at concentrations of 10(-4) M and higher, markedly stimulated the actions of insulin on rat adipocytes including labeled glucose oxidation, activation of glycogen synthase, and stimulation of 2-deoxyglucose transport. The B-chain COOH-terminal heptapeptide, Gly-Phe-Phe-Tyr-Thr-Pro-Lys (B23-29) was inactive alone or in the presence of submaximal concentrations of insulin or desoctapeptide insulin, suggesting that argnine is required. Dose response curves of insulin, and desoctapeptide insulin for labeled glucose oxidation by rat adipocytes were shifted 1 log concentration unit to the left in the presence of peptide. Peptide shortened the lag time of labeled glucose oxidation and markedly enhanced the rate of 14CO2 production following the lag time. Peptides also enhanced insulin-like activities of concanavalin A and nonsuppressible insulin-like activity P.     

High-speed GaN growth and compositional control of GaN-AlGaNsuperlattice quasi-ternary compounds by RF-radical source molecular beamepitaxy

Novel growth technologies of III-nitrides for fabricating optical devices by molecular beam epitaxy using RF-plasma excited nitrogen (RF-MBE) were investigated. A relatively high-growth rate, up to 1.4 μm/h of GaN with high-electrical and high-optical quality was obtained. The concept of AlGaN quasi-ternary (QT) compounds, consisting of GaN-AlGaN short period superlattice, was demonstrated and the Al composition was controlled with a shutter control method in the range of 0-0.47. Using the QT technology, a GaN-Al_0.07Ga_0.933N-Al_0.3Ga_0.7 N multiquantum-well heterostructure was fabricated to show the effectiveness of the method     

Remarkable enhancement in durability of Pd/H-ZSM-5 zeolite catalysts for CH4-SCR

Effect of second components on the catalytic performance of Pd/H-ZSM-5 zeolite (Pd: 0.4 wt.%) was evaluated by a durability test of NO reduction with CH₄ at a relatively high temperature of 500°C in the presence of water vapor for a prolonged period. The Pd/H-ZSM-5 showed high stable activity for this reaction without H₂O in the reactant feed, while immediate and irreversible deactivation was observed in the presence of H₂O, resulting in no activity after 7 h. The second components such as Co, Rh, Ag, Ce, and Fe introduced individually to the Pd/H-ZSM-5 enhanced the durability, and in particular the addition of 3.3 wt.% Co led to a stable NO conversion for more than 40 h in the presence of H₂O.     

Functionalized Bilayer Membranes as Artificial Transaminase: Modification of the Active Site and Its Consequence in Catalytic Efficiency

The transamination reaction of l-phenylalanine with pyruvate as catalyzed by the artificial transaminase formed with synthetic bilayer aggregates was examined in aqueous media under mild kinetic conditions. Each catalyst system was constructed with a combination of a synthetic peptide lipid, a hydrophobic vitamin B₆ derivative, and metal ions. Modification of the active site in the present artificial transaminase was performed by changing a combination of molecular components constituting the catalytic system. While the catalytic activity was scarcely influenced by differences in aggregate structure, single- or multi-walled bilayer, and in copper-(II) concentration, molecular structures of the hydrophobic vitamin B₆ and an amino acid residue of the peptide lipid had significant effects on the reactivity.