Analysis of solute distribution in dendrites of carbon steel with δ/γ transformation during solidification

Solute distribution in dendrites during solidification of carbon steel was analyzed by unidirectional solidification experiments and mathematical analysis. The characteristic of the mathematical analysis is that diffusion of solutes in solid and redistribution of solutes at solid/liquid andδ/γ interfaces are taken into consideration. Based on the observed and calculated results, it was found that phosphorus was redistributed fromγ-phase toδ-phase, and that manganese was slightly redistributed fromδ-phase toγ-phase. Therefore the concentrated region of phosphorus can be separated from that of manganese duringδ/γ transformation in the case of slow cooling. Moreover, it was concluded that rapid diffusion inδ-phase and the redistribution duringδ/γ transformation played an important role in the variation of the interdendritic concentrations of solutes with lower carbon concentration.     

An investigation into the relationship between processing,structure and properties for high-modulus PBO fibres: part 3: analysis of fibre microstructure using transmission electron microscopy

A detailed morphological study of the microstructure of poly(p-phenylene benzobisoxazole) (PBO) fibres (HM and HM+) and a polypyridobisimidazole (PIPD) (HT) fibre has been undertaken using transmission electron microscopy. Both PBO and PIPD fibres are composed of rigid-rod polymers having p-phenylene rings in the molecular backbone and show high modulus (280–360 GPa) and high strength (4–6 GPa). It is found that the PBO HM+ fibre has the highest degree of molecular orientation of the three fibres and the longest crystal length along the fibre axis, while the PIPD fibre shows a lower degree of orientation and a shorter crystal length than the PBO fibres. To understand the effect of crystalline size and fine structure of the fibres upon mechanical properties, dark-field and high-resolution lattice images were obtained and analysed in detail.     

Low Temperature Phase Transition in C70 and Solvation Effects

The heat capacity of C₇₀ has been measured by adiabatic calorimetry between 14 and 320 K. The orientational phase transition is observed as a broad hump in the heat capacity curve, which is strongly influenced by small amount of solvent remaining in the sample.     

“Click Peptide“: pH‐Triggered in Situ Production and Aggregation of Monomer Aβ1–42

Into neutral : We demonstrate the unique features of a pH click peptide based on an O‐acyl isopeptide method. Under acidic conditions, the click peptide remains in a monomeric form. Upon increase of the pH to 7.4, the click peptide is quickly able to convert into Aβ1–42 through an O‐to‐N intramolecular acyl migration. Further study using this pH click peptide would elucidate the pathological role of Aβ1–42 in Alzheimer's disease.

     

Development of a method to lower recontamination after chemical decontamination by depositing Pt nano particles: (I) Consideration of the suppression mechanism using a quantum dynamics calculation

The Pt coating (Pt-C) process has been developed to lower the recontamination by radioactive elements after chemical decontamination of piping surfaces. In this process, a layer of fine Pt nano particles is formed in an aqueous solution on the base metal of the piping following the chemical decontamination. In this study, we confirmed that the suppression effect by the Pt-C toward ⁶⁰Co deposition on type 316 stainless steel using a ⁶⁰Co deposition test under hydrogen water chemistry. Furthermore, we investigated the suppression mechanism of deposition of radioactive elements by a quantum molecular simulation. The deposition amounts of ⁶⁰Co which were incorporated in oxides after 1000 h with and without the Pt-C process were about 90 and 10.2 Bq/cm², respectively. The amount of ⁶⁰Co deposition with Pt-C is about 10% that of non-coated specimens. The ⁶⁰Co incorporation for the Pt-C specimen was suppressed by decreasing the formation of oxides. We considered this phenomenon using a quantum dynamics calculation and concluded that the Fe–O bonds in oxides were weakened by the effect of Pt and hydrogen radicals which were produced in the reaction between H₂ and Pt, and then oxides were dissolved into the water.     

Fabrication and properties of one-mask-patterned ferroelectric integrated capacitors

A one-mask-patterned ferroelectric capacitor test structure designed with a 0.5-μm feature size was fabricated. Oxygen plasma treatment after dry etching decreased the leakage current to as low as that of as-deposited film. These one-mask-patterned ferroelectric capacitors, with switching charge almost equal to as-deposited film, were successfully fabricated. Ferroelectric memories as dense as dynamic random access memories will become possible with this technology. However, the leakage current density for micron-sized capacitors is 2 to 10 times that of large capacitors. The leakage current in small capacitors is increased due to perimeter leakage that runs through the damaged region on the capacitor sidewall. © Scripta Technica, Inc. Electr Eng Jpn, 121(1): 43–50, 1997     

Thermal strain of high strength polyethylene fiber in low temperature

High strength polyethylene fiber (Toyobo, Dyneema® fiber: hereinafter abbreviated to DF) has a negative thermal expansion coefficient. Relation between fiber structure and thermal strain of DF used as reinforcement of DF reinforced plastic (DFRP) for cryogenic use was investigated. The crystallinities and orientation angles of several kinds of polyethylene fibers having different modulus from 15 to 134Gpa (herein after abbreviated to DFs) were measured by NMR and X‐ray. We obtained the parameters of the mechanical series‐parallel model composed of crystal and amorphous by crystallinity and modulus. Thermal expansion coefficients of DFs were estimated by mechanical series‐parallel model. All DFs having different modulus showed negative thermal expansion coefficients in the temperature range from 180 to 300K, and absolute values of those markedly increased by increasing tensile modulus of DF. The estimated thermal expansion coefficients showed negative values, and thermal strains showed a similar curve to observed ones mostly. Average thermal expansion coefficients in the temperature range from 180 to 300K estimated by mechanical model agreed with the observed ones. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2918–2925, 2004     

Identification of Cross-linking Site(s) of Myosin Heavy Chains in Oxidatively Stressed Chicken Myofibrils

ABSTRACT: The cross-linking site(s) of myosin heavy chains (MHC) in chicken myofibrils exposed to non-enzymatic, hydroxyl radical-generation oxidizing systems (HRGS) was investigated by means of chymotryptic digestion and subsequent electrophoresis. Oxidation of the chymotryptic digests resulted in cross-linking of the rod or light meromyosin (LMM) segment of MHC mostly via disulfide bonds, while subfragment-1 (S-1) or heavy meromyosin (HMM) was not affected. A mixture of cross-linked rod or LMM and uncross-linked S-1 or HMM was also produced when myofibrils were 1st oxidized and then digested with chymotrypsin, confirming that cross-linking of myosin in HRGS-oxidized myofibrils occurred initially in the LMM portion of the myosin rod.     

Conductimetric titration of polyelectrolytes having sulfate and carboxyl groups

Summary Conductimetric titration of polyelectrolyte solutions was carried out to determine the contents of sulfate and carboxyl groups. In the mixtures of poly(acrylic acid) and poly(vinyl sulfate), and of alginic acid and dextran sulfate, the contents of sulfate and carboxyl groups observed by the conductimetric titration were in agreement with those derived from the concentration of the original homopolymers. This method was applied to a viscous polysaccharide from red algae, funoran, which contains both the sulfate and carboxyl groups. These results suggested that this method is applicable to either the samples consisting of the mixture of homopolymers or those of copolymers containing both ionic species.     

Degradation mechanism of galvanized steel in wet-dry cyclic environment containing chloride ions

The wet-dry cyclic test of a galvanized steel (GI) and pure zinc (ZN), which simulates marine atmospheric environment, has been conducted to clarify the degradation mechanism of galvanized steel. The samples were exposed to alternate conditions of 1 h-immersion in a 0.05 M NaCl solution and 7 h-drying at 25 °C and 60%RH, and the corrosion was monitored for 10 days (30 cycles) using a two-electrode type probe. Simultaneously, the corrosion potential was measured every three cycles only during the immersed conditions. The reciprocal of polarization resistance R_p⁻¹ was taken as an index of the corrosion rate. Several sample plates of GI and ZN were exposed, together with the monitoring probes. They were removed from the test chamber at the end of 1st, 3rd, 9th, 18th, and 30th cycles of exposure and were analyzed for the corrosion products with XRD and laser Raman spectroscopy. Further, their cross sections were analyzed with FESEM-EDS. The FESEM photographs and elemental analysis of cross sections confirmed that the R_p⁻¹ value commences to decrease when the corrosion front reaches Zn-Fe alloy layers (boundary layers of zinc coating and steel substrate) due to localized nature of attack. A schematic model of degradation mechanism and the role of galvanic protection have been discussed.