Effects of phenylenediamines and alkoxysilanes on gas transport properties of polyimide - silica hybrid membranes

Gas transport properties of polyimides (PIs) and their silica hybrids were investigated. The PIs synthesized with several methyl-substituted phenylenediamines were hybridized with silica via a sol–gel process with different alkoxysilanes. The prepared hybrid membranes showed controlled gas permselectivity, depending on the selected phenylenediamines and alkoxysilanes. It was worth noting that the hybrids prepared with tetraethoxysilane possessed improved CO₂ permselectivity with increasing silica content, which tended to exceed the upper-bound trade-off line. This fact suggested the additional formation of free volume holes especially favorable for the CO₂/CH₄ separation around the polymer/silica interfacial area.     

Effect of Sliding History on Super-Low Friction of Diamond-Like Carbon Coating in Water Lubrication

Water lubrication using diamond-like carbon (DLC) coatings is regarded as being a promising eco-friendly technology. However, it has been reported that delamination of DLC coatings occurs in water. The authors clarified that the application of friction in ambient air prior to self-mating DLC water lubrication, in addition to the suppression of DLC delamination, caused the friction coefficient to decrease more than when no processing is performed in the boundary lubrication region. When compared to the case when there was no pre-sliding, in terms of the wear scar, in this case, a much more hydrophilic and smoother surface was formed. Therefore, the friction-reducing process in water due to the presence of a sliding history (pre-sliding in ambient air) was clarified by an analysis of the DLC geometry, structure, chemical state and an in situ analysis that can measure the friction properties and the chemical state of DLC. We clarified that the process in which the oxidation and structural changes of the DLC proceed at the time of pre-sliding in ambient air using in situ Fourier transform infrared spectroscopy–attenuated total reflection. It was also revealed that the OH termination subsequently accelerated rapidly due to the friction in water after pre-sliding process. In addition, a time-of-flight secondary ion mass spectrometry analysis revealed that this OH group was derived from the lubricating water and unlike the case in which there was no pre-sliding in ambient air, the rate at which OH terminates increased considerably.     

Thermophysical properties of (U,Y)O2

We prepared polycrystalline pellets of (U,Y)O₂, containing YO_1.5 up to 11 mol.%. We performed indentation tests on the pellets, and evaluated the Young’s modulus and hardness. We measured the heat capacity and the thermal diffusivity, and evaluated the thermal conductivity. We succeeded in evaluating the effect of Y content on the thermophysical properties of (U,Y)O₂. We revealed that the Young’s modulus, hardness, and thermal conductivity of (U,Y)O₂ decreased with increasing the Y content.     

Measurement of Young’s Modulus and Poisson’s Ratio of Thermal Barrier Coating Based on Bending of Three-Layered Plate

Thermal barrier coatings (TBCs) are used to protect the hot sections of gas turbine engines and airplane engines. A TBC system comprises a substrate, bond coat, and TBC topcoat. The development of an accurate method for determining the Young’s modulus and Poisson’s ratio of TBC using a multilayered specimen is of importance. In this study, we applied the bending theory of a laminated plate to a three-layered material and proposed models to determine the Young’s modulus and Poisson’s ratio of the TBC layer using the bending strain of the TBC system specimen. Three methods were developed by utilizing (i) the coating biaxial strain, (ii) substrate biaxial strain, or (iii) coating and substrate biaxial strains. Subsequently, we determined appropriate dimensions of the specimen and span by using three-dimensional finite element analysis, and numerically verified the usefulness of the three proposed methods. However, the Young’s modulus and Poisson’s ratio determined using the multilayered specimen with a substrate are sensitive to experimental errors. Therefore, we evaluated the sensitivity of the three proposed methods to experimental error, and we determined the most insensitive method among them. Finally, we experimentally demonstrated the usefulness of this method.     

Simulation of the fracture behavior of Zircaloy-4 cladding under reactivity-initiated accident conditions with a damage mechanics model combined with fuel performance codes FEMAXI-7 and RANNS

A continuum damage mechanics model using FEM calculations was proposed to be applied to an analysis of the fuel failure due to pellet cladding mechanical interaction (PCMI) under reactivity-initiated accident conditions. The model expressed ductile fracture via two processes: damage nucleation related to void nucleation and damage evolution related to void growth and linkage. The boundary conditions for the simulations were input from the fuel performance codes FEMAXI-7 and RANNS. The simulation made reasonable predictions for the cladding hoop strain at failure and reproduced the typical fracture behavior of the fuel cladding under the PCMI loading, characterized by a ductile shear zone in the inner region of the cladding wall. It was shown that occurrence of a through-wall crack is determined at an early stage of crack propagation, and the rest of the through-wall penetration process is achieved with a negligible increment in strain. The effect of a local temperature rise in the cladding inner region on the failure strain was found to be less than 5% for the conditions investigated. Failure strains predicted under a plane strain loading were smaller by 20%–30% than those predicted under equibiaxial tensions between the hoop and the axial directions.     

Synthesis of the Bi-2222 Compounds of Bi–Sr–Ln(Zr)–Cu–O (Ln = Sm,Eu, Gd,and Dy)

Bi-based superconducting compounds with the 2222 structure has been already synthesized in the Bi₂Sr₂- (Ln_1−x Ce _x )₂Cu₂O_10+y (Ln = Sm, Eu, and Gd) systems. One of the characteristics of these compounds is the existence of the fluorite-like (Ln_1−x Ce _x )₂O₂ block between two CuO₅ pyramids in the crystal structure. The tetravalent ions of Ce⁴⁺ are reported to be necessary to stabilize the 2222 structure. Recently, we have discovered that the Bi-2222 phase could be composed in the Bi₂Sr₂(Ln_2−x Zr _x )Cu₂O _z (Ln = Sm, Eu, Gd, and Dy) systems, where Zr⁴⁺ is used as a new tetravalent ion stabilizing the 2222 structure in stead of Ce⁴⁺. In the new system, nearly single 2222 phase samples have been obtained at the nominal composition of x=0.5 (Ln = Sm, Eu, and Gd) and in the range of 0.1≤x≤0.3 (Ln = Dy). Among them, the sample with Ln = Gd has the smallest resistivity at 273 K. But it is a semiconductor, and the conduction process at low temperatures is assumed to be followed by a two-dimensional VRH. The experimental results for the Gd samples with a partial substitution of Pb for Bi in the Bi₂Sr₂(Gd_2−x Zr _x )Cu₂O _z system are also reported.     

Isolation and structural analysis of efficient autonomously replicating sequences (ARSs) of the yeast Candida utilis

The industrially important yeast Candida utilis is widely used in production of food and medical materials, but its host-vector system has not been well developed. We screened for compact and efficient ARSs to construct practically useful vectors. The C. utilis strain AHU3053 was found to be efficiently transformed by the conventional lithium acetate method and was used as the host. The C. utilis IAM4264 genomic library was constructed by inserting the partial Sau3AI digests in pRI51, which has a kanMX gene expressible in C. utilis. By examining 98 C. utilis G418-resistant transformants, five plasmids had the highest ARS activity. By trimming of the inserts, the 1490 and 552 bp fragments with transformation activity of over 10(3)/microg DNA were obtained from ARS3 and ARS4, respectively. Although several sequences identical to S. cerevisiae ARS consensus sequences (ACSs) were found in ARS3 and ARS4, our deletion analysis indicated that these were not essential for the activity. Because the minimal functional ARS fragment was also several-fold larger than that of S. cerevisiae, the C. utilis ARSs have some unique characteristics resembling the Sz. pombe ARSs. These ARSs were functional in other C. utilis strains tested and useful for constructing practical vectors.     

Acceptor recognition of kojibiose phosphorylase from Thermoanaerobacter brockii: syntheses of glycosyl glycerol and myo-inositol

The glucosyl transfer reaction of kojibiose phosphorylase (KP; EC 2.4.1.230) was examined using glycerol or myo-inositol as an acceptor. In the case of glycerol, KP produced two main transfer products: saccharides A and B. The structure of saccharide A was O-alpha-D-glucopyranosyl-(1-->1)-glycerol and that of saccharide B was O-alpha-D-glucopyranosyl-(1-->2)-O-alpha-D-glucopyranosyl-(1-->1)-glycerol. These results show that KP transferred a glucose residue to the hydroxyl group at position 1 of glycerol. On the other hand, when myo-inositol was used as an acceptor, KP produced four transfer products: saccharides 1-4. The structures of saccharides 1 and 2 were O-alpha-D-glucopyranosyl-(1-->1)- and O-alpha-D-glucopyranosyl-(1-->5)-myo-inositol, respectively; those of saccharides 3 and 4 were O-alpha-D-glucopyranosyl-(1-->2)-O-alpha-D-glucopyranosyl-(1-->1)- and O-alpha-D-glucopyranosyl-(1-->2)-O-alpha-D-glucopyranosyl-(1-->5)-myo-inositol, respectively. KP transferred a glucose residue to the hydroxyl group at position 1 or 5 of myo-inositol. On the basis of the structures of their glucosyl transfer products, glycerol and myo-inositol were found to have a common structure with three hydroxyl groups corresponding to the hydroxyl group of the glucose molecule at positions 2, 3 and 4. The conformation of these three hydroxyl groups in the structure is equatorial. This structure is the substrate recognition site of KP. It has been suggested that KP strictly recognizes the structures of glycerol and myo-inositol, and catalyzes the transfer reaction of a glucose residue to the hydroxyl group at position 1 in glycerol, and at position 1 or 5 in myo-inositol, corresponding to position 2 in glucose.     

Optimal production-inventory policy for make-to-order versus make-to-stock based on the M/Er/1 queuing model

This paper analyzes a multi-product production / inventory system where demands for each item arrive according to a Poisson process and the production time for each product has an Erlang distribution. The paper proposes an optimality condition that specifies whether each product should be produced make-to-stock or make-to-order. In the event a product should be produced make-to-stock, an approach for computing the optimal base-stock level is proposed. Numerical examples are given for illustrative purpose.