Mechanism of Mechanical Strength Increase of Soda–Lime Glass by Aging

Two models have been proposed to explain the mechanical strength increase of abraded or indented soda–lime glasses upon aging, namely, crack tip blunting and the release of residual tensile stress near the crack tip. To clarify the mechanism, the time dependence of the strengthening of an abraded soda–lime glass was investigated. Effects of aging media, such as moist air, distilled water, 1 N HCI and 1 N NaOH solutions, as well as the abrasion flaw depth, were determined. The strength increase rate in water of abraded soda–lime glass was compared with those of borosilicate and high-silica glasses. The effect of stressing during aging was also investigated. It was found that the rate of strength increase was faster with decreasing abrasion flaw depth and with decreasing chemical durability. For a given flaw depth, an acidic solution produced the fastest strengthening. The strengthening rate was found to accelerate because of the "coaxing'effect of stressing during aging. From these observations, it was concluded that the strengthening rates relate to the diffusion process and chemical reactions, especially the alkali–hydrogen (or hydronium) ion-exchange reaction, near the crack tip. The role of the residual tensile stress appears to be similar to that of the applied tensile stress, helping the diffusion process near the crack tip. The observed strength increase of soda–lime glass by aging was thus attributed to the effective blunting of the crack tip geometry by the glass–water reaction.     

Oxidation Resistance Evaluation of Silicon Carbide Ceramics with Various Additives

Five silicon carbide ceramics with various additives were evaluated for oxidation resistance at 1300°C in flowing dry and wet air. In the dry atmosphere, the oxidation of the five samples was diffusion-controlled, and in wet atmosphere they exhibited a linear relation beween weight gain by oxidation and water vapor content. Water vapor in the atmosphere strongly accelerated oxidation. The influence of oxidation on room-temperature strength was complex, but the samples were not as affected by oxidation.     

Properties of networks obtained by internal plasticization of epoxy resin with aromatic and aliphatic glycidyl compounds

In order to improve the fracture properties of p, p′-diaminodiphenylmethane-cured epoxy resin, various kinds of aromatic and aliphatic glycidyl compounds were investigated as a modifier at an amount of 30 wt %. Several compounds promoted the fracture toughness. In any glycidyl compounds, however, heat resistance was decreased by the modification. The dynamic mechanical properties of the modified epoxy resins were measured. The crosslinking density ρ was calculated from the theory of rubber elasticity, and the mechanical properties of the resins were discussed in regard to the crosslinking density. Tensile strength was scarcely affected by the crosslinking density. Elongation at break and Izod impact strength increased remarkably with decrease in crosslinking density. The fracture toughness K_Ic- increased with decrease in crosslinking density except at small ρ.     

Pervaporation separation of water/ethanol mixtures through polysaccharide membranes. II. The permselectivity of chitosan membrane

The separation of water/alcohol mixtures through chitosan membrane was investigated. The degree of the deacetylation of chitosan did not affect the selectivity of the membrane in the separation of the water/ethanol mixture. The selectivity of the chitosan membrane was affected by the specific salts such as CoSO₄, ZnSO₄, and MnSO₄ and it increased when the salts were present in the feed mixture or the membrane was pretreated with the salt solution. This behavior would be explained by the contraction of the “holes” produced by the thermal motion of polymer chains and this contraction would be correlated with the conformation change of chitosan molecule due to the formation of complexes with metal ions.     

H2O-tolerant monolithic catalysts for preferential oxidation of carbon monoxide in the presence of hydrogen

Pt–Fe/mordenite (4 wt% Pt–0.5 wt% Fe) powder catalysts were wash-coated onto ceramic straight-channel monoliths by using silica- and/or alumina-sol as a binder, and were evaluated for the preferential oxidation of carbon monoxide (PROX) in a hydrogen-rich gas. In a synthetic reformate gas (1% CO, 1% O₂, 5% H₂O, 20% CO₂, and balance H₂), the CO concentration was reduced to less than 20 ppm at temperatures ranging from 100 to 130 °C. After a certain period of the PROX reaction, condensation of H₂O in the pores of the mordenite-support occurred over the monolithic catalyst, which was wash-coated with alumina-sol, in the lower temperature range (100–120 °C), resulting in a rapid increase in CO concentration. The monolithic catalyst wash-coated with silica-sol, however, showed an excellent tolerance against H₂O condensation and offered a stable catalytic performance, maintaining a CO concentration of ca. 20 ppm for 200 h. The H₂O-tolerant characteristic was attributed to the relatively small adsorption amount of H₂O over the silica-modified monolithic catalyst.     

High temperature water–gas shift reaction over hollow Ni–Fe–Al oxide nano-composite catalysts prepared by the solution-spray plasma technique

The effect of Fe content in Ni–Fe–Al oxide nano-composites prepared by the solution-spray plasma technique on their catalytic activity for the high temperature water–gas shift reaction was investigated. The composites showed a hollow sphere structure, with highly dispersed Fe–Ni particles supported on the outer surface of the spheres. When the water–gas shift reaction was performed over an Ni–Al oxide composite catalyst without Fe, undesired CO methanation took place predominantly compared to the water–gas shift reaction, and significant amounts of hydrogen were consumed. When appropriate amounts of Fe were added to the Ni–Al oxide composite catalyst during the plasma process, methanation was suppressed remarkably, without serious loss of activity for the water–gas shift reaction. The catalyst was characterized by STEM, XRD and H₂ chemisorption measurements.     

Kinetic roughening transition and missing regime transition of melt crystallized polybutene-1 tetragonal phase: growth kinetics analysis

The morphology and lateral growth rate of isotactic polybutene-1 (it-PB1) have been investigated for crystallization from the melt over a wide range of crystallization temperatures from 50 to 110°C. The morphology of it-PB1 crystals is a rounded shape at crystallization temperatures lower than 85°C, while lamellar single crystals possess faceted morphology at higher crystallization temperatures. The kinetic roughening transition occurs around 85°C. The nucleation and growth mechanism for crystallization does not work below 85°C, since the growth face is rough. However, the growth rate shows the supercooling dependence derived from the nucleation and growth mechanism. The nucleation theory seems still to work even for rough surface growth. Possible mechanisms for the crystal growth of this polymer are discussed.     

Designed RNAs with Two Peptide‐Binding Units as Artificial Templates for Native Chemical Ligation of RNA‐Binding Peptides

The template effect plays important roles not only in modern synthetic and enzymatic catalysis but also in the ancient “RNA‐polypeptide (RNP) world,” which has been postulated to be a crucial stage in the origin of life. To mimic primitive template catalysis of peptide ligations by RNAs, we previously reported the design and synthesis of a ternary RNP complex in which the ligation of two peptides was significantly facilitated by a template RNA with two peptide‐binding units. However, RNA molecules also promoted the ligation reaction in a nonspecific manner through electrostatic interactions between RNA and basic peptides. In this study, we suppressed this effect by reducing the length of the original template derived from the Tetrahymena intron RNA. This modification, however, decreased the template ability for the specific reaction. As an alternative RNA that was as effective as the original template, we found that a self‐dimerizing RNA was a promising template for peptide ligation without a nonspecific effect.     

Synthesis of Nano-Sized Platinum Metal Particles on Ti-Containing Mesoporous Silica Using Microwave-Assisted Deposition Method

Using microwave-assisted deposition method the uniform and nano-sized platinum metal particles were prepared on the tetrahedrally coordinated Ti-oxide moieties isolated within the framework of mesoporous silica supports. The present nano-sized metal catalyst exhibited a higher activity for hydrogenation of nitrobenzene than the catalyst prepared by a conventional impregnation method.     

Pt and Sn Doped Sputtered CeO2 Electrodes for Fuel Cell Applications

The interaction of Pt with CeO₂ layers was investigated by using photoelectron spectroscopy. Thirty‐nanometre‐thick Pt and Sn doped CeO₂ layers were deposited simultaneously by rf‐magnetron sputtering on a Si(001) substrate and a carbon diffusion layer of a polymer membrane fuel cell by using a composite CeO₂–Pt–Sn target. The laboratory XPS and synchrotron radiation soft X‐ray and hard X‐ray photoemission spectra showed the formation of cerium oxide with completely ionised Pt^2+,4+ species, and with Pt⁴⁺ embedded in the film bulk. Hydrogen/air fuel cell activity measurements normalised to the amount of Pt used revealed high specific power of up to 5.4 × 10⁴ mW mg^–1 (Pt). The activity of these materials is explained by the strong activity of embedded Ptⁿ⁺ cations.