Research and development of liquid hydrogen (LH2) temperature monitoring system for marine applications

Monitoring the temperature in liquid hydrogen (LH₂) storage tanks on ships is important for the safety of maritime navigation. In addition, accurate temperature measurement is also required for commercial transactions. Temperature and pressure define the density of liquid hydrogen, which is directly linked to trading interests. In this study, we developed and tested a liquid hydrogen temperature monitoring system that uses platinum resistance sensors with a nominal electrical resistance of approximately 1000 Ω at room temperature, PT-1000, for marine applications. The temperature measurements were carried out using a newly developed temperature monitoring system under different pressure conditions. The measured values are compared with a calibrated reference PT-1000 resistance thermometer. We confirm a measurement accuracy of ±50 mK in a pressure range of 0.1 MPa–0.5 MPa.     

Fracture and deformation properties of Ni-Fe superalloy in cryogenic high magnetic field environments

The present paper includes experimental and analytical data on the fracture properties of a nickel-iron superalloy, a ferromagnetic austenite, at 4 K in magnetic fields of 0 and 6 T. The tensile, notch tensile and small punch tests are employed. A finite element analysis is also performed to convert the experimentally measured load-displacement data into useful engineering information. To interpret the results we review the available theory of the influence of magnetic field on the stress intensity factor for a crack in ferromagnetic materials.     

Effect of Forming Pressure on the Internal Structure of Alumina Green Bodies Examined with Immersion Liquid Technique

Green bodies prepared by compaction of alumina granules were made transparent by an immersion liquid technique, and the internal structure was characterized with an optical microscope to study the effect of forming pressure on the internal structure. Clear images obtained by the technique provide more detailed information than other existing methods for structures ranging from one to tens of micrometers. Intergranular pores were present between unfractured granules. Their sizes and concentration tended to decrease with increasing forming pressure. However, pores were clearly present even in the green body prepared at 600 MPa. A rod- and needlelike feature was also found and was concluded to correspond to a high-density region. The significance of large pores and high-density regions on processing as well as the details of the technique is discussed.     

Preparation and photoconduction of rapidly quenched films in the Bi2O31bM2O5 system (M=V,Nb and Ta)

The Bi₂O₃1bM₂O₅ films (M=V, Nb and Ta) were prepared by a rapid quenching technique using a twin-roller type equipment. Quenched film of pure Bi₂O₃ partially precipitated a tetragonal phase which differs from well-known β-Bi₂O₃ in structure. In every (Bi₂O₃)_0.975 (M₂O₅)_0.025 composition (2.5% M₂O₅), the tetragonal phase was obtained as single phase, and the tetragonality became greater than that of the pure Bi₂O₃. Beyond this composition, the tetragonality decreased to form δ-phase with a fcc structure with increasing the M₂O₅ content. The lowest V₂O₅ content forming a δ-phase was 5%, while a slight tetragonality still remained in the samples containing 10% Nb₂O₅ and 10% Ta₂O₅, respectively. From the measurement of the photoconductivities of the quenched films, it was proved that a photoconduction appeared in the tetragonal phase while no photoconductivity was observed in the cubic phase. The characteristic of the photoconduction was that a remarkable decrease in the resistivity was observed when a light of ca. 500 nm in wave length was irradiated on the films.     

Preparation and characterization of membranes with positively charged main chain from polyethylenimine

A membrane, which has positively charged groups in the polymer main chain, was prepared from polyethylenimine by crosslinking and successive alkylation. Dibromoalkane was used as a crosslinking agent. The crosslinked membrane was alkylated using methyl iodide under several conditions. Elemental and ICP emission analyses were introduced to measure the rates of alkylation and quaternization. From the membrane potential measurement, the effective charge density was estimated. The highest value was about 1.0 M, which was obtained by a prolonged alkylation time. This value was larger than that of some commercial ion exchange membranes. The effective charge density, which was obtained by the last alkylation procedure, was 10 times larger than that of the former one, though the rate of quaternizing increased by less than a factor of two. This implies that the activity constant in the membrane increased when the charge density is increased. © 1993 John Wiley & Sons, Inc.     

Stress analysis with arbitrary body force by boundary element method

Linear stress analysis without body force can be easily carried out by means of the boundary element method. Some cases of linear stress analysis with body force can also be solved without the domain integral. However domain integrals are generally necessary to solve the linear stress problems with complicated body forces. This paper shows that the linear stress problems with complicated body forces can be solved approximately without the domain integral. In order to solve these problems, the domain is divided into small areas using contour lines of body force. In these areas, the distributions of body force are assumed approximately to satisfy the Laplace equation.     

Preparation and photoconduction of rapidly quenched films in the Bi2O3-TiO2 system

The rapidly quenched films in the Bi₂O₃-TiO₂ system (0 to 60% TiO₂) were prepared using a twin-roller type apparatus. The films precipitated Bi₂O₃ solid solutions of different types in the composition ranges, with TiO₂ contents of 0 to 5, 7.5 to 10 and 12.5 to 40%, respectively. The first solid solution had a tetragonal structure of -form. The second, though also crystallized in the tetragonal structure, adopted a disordered modification of the -form. The third solid solution was -form (defect fluorite structure). The formation of amorphous phase commenced in the composition with 30% TiO₂, and the films became completely amorphous beyond 50% TiO₂. The quenched films showed a certain instability to decompose or transform into the different phase assemblage by annealing at higher temperatures (about 400 to 500° C, except 260° C for the pure Bi₂O₃ film). The quenched films were also characterized by a high photoconductivity. The photoconduction mechanism was suggested to be associated with a structural imperfection of Bi₂O₃ accompanied by a certain amount of pentavalent bismuth ion.     

X-ray CDF study on the behaviour of the amorphous chain under extension

The behaviour of the amorphous chain in vulcanized natural rubber (NR) and styrene-butadiene rubber (SBR) under extension is studied by means of the cylindrical distribution function (CDF) derived from wide angle X-ray scattering (WAXS). In the case of the highly stretched vulcanized NR where the orientation-induced crystallization took place, the observed WAXS intensity was separated into a crystalline peak component and a broad amorphous one from which the CDF was obtained. The CDF calculated from the broad component shows that some of the amorphous segments of the highly stretched vulcanized NR are extended as fully as the crystalline chains and that the fraction of the segments increases with increasing extension. In the case of SBR, such fully stretched segments as in the case of the vulcanized NR show higher degree of an interchain packing order than those in the vulcanized NR.     

Sorption and permeation of iodine in water-swollen poly(vinyl alcohol) membranes and iodine complex formation

The sorption and the permeation of iodine in water-swollen poly(vinyl alcohol) (PVA) membranes and the formation of PVA–iodine complexes were studied. The logarithms of the permeability and the diffusion coefficient decreased approximately linearly with the increase in polymer volume fraction. When the membrane was soaked in an aqueous I₂–KI solution, it contracted and Young's modulus increased. These findings were explained in terms of the formation of extra junction points due to the PVA–iodine complexes. These changes were reversible and could be recovered by replacing the solution with water. The length of the polyiodine chain increased with the increase in the degree of hydration of the membrane. At a fixed degree of hydration, Young's modulus of an iodine-sorbed membrane was much greater than that of a membrane soaked in pure water. This finding was explained on the basis of a double-network structure. The extension of the membrane promoted the complex formation, and the complex disappeared when the tension was released. The critical strain necessary for the complex formation was independent of the degree of hydration. The length of polyiodine chain increased with strain and became constant at higher strains.