Oxide ion conduction in the sintered oxides of MoO3-doped Bi2O3

In order to examine the conduction behaviour in the sintered oxides of MoO₃-doped Bi₂O₃, the electrical conductivity in air and the EMF of oxygen gas concentration cell were measured with respect to the phase relation determined by X-ray diffraction.The tetragonal single phase oxide containing 22 mol% MoO₃ was found to be a high oxide ion conductor, the conductivity of which was comparable to those of stabilized zirconias. The partial electronic conduction in this phase was negligibly small at relatively high oxygen pressure. The oxide ion conduction was considered to be attributable to an appreciable amount of oxygen vacancies present in the crystal. In the monoclinic compound 3Bi₂O₃·2MoO₃, the oxide ion conduction was also observed. Although the conductivity of this phase was somewhat lower than that of the tetragonal phase, the activation energy for conduction (53·5 kJ mol^–1) was much lower than the values for usual oxide ion conductors.     

Shear-rate dependence of first normal stress difference of poly(isoprene-b-styrene) in solution near the order-disorder transition temperature

Viscoelastic properties of poly(isoprene-b-styrene) in dioctylphthalate under steady shear flow were measured near the order—disorder transition temperature. In ordered states, first normal stress difference N₁ is proportional to shear rate at low region, but becomes proportional to at the high region, similar to the N₁ behaviour of polymer blends undergoing shear-induced homogenization. Because the existence of microdomains was confirmed at the high region by the flow birefringence method, it is concluded that the above N₁ behaviour is not caused by shear-induced homogenization, but is probably caused by the shear-induced alignment of the microdomain structure.     

The polymerization and copolymerization of nitroalkyl acrylates and nitroalkyl methacrylates

Nitroalkyl acrylates and methacrylates involving some new compounds were prepared. The homopolymerization of these monomers in toluene and their copolymerization with styrene in acetone were carried out with azobisisobutyronitrile as initiator. The rate of polymerization of the nitroalkyl acrylates showed a correlation with the number of nitro groups situated on the ester side chain. The apparent activation energies of the polymerization were found to be 22.0–27.5 kcal./mole for the nitroalkyl acrylates and about 11.5–13.0 kcal./mole for the nitroalkyl methacrylates. From the reactivity ratios and Q-e values of the copolymerization the following information was obtained. The copolymerization behavior of nitroalkyl acrylates and methacrylates showed an alternating tendency, and these monomers belong to the conjugative monomer groups. On the reactivities of these monomers, the polarity of vinyl group was affected a little by nitro group of ester bond side, and the resonance affected little. These monomers were crosslinked with 2-methyl-2-nitro-1,3-propylene diacrylate. Some of the polymers showed marked improvement in the physical properties of elastomers.     

Influence of chromium on the local structure and morphology of ferric oxyhydroxides

The extended X-ray absorption fine structure (EXAFS) method and transmission electron microscopy (TEM) have been used for characterizing the local structure and morphology of ferric oxyhydroxides, α-FeOOH and γ-FeOOH, with and without chromium. These ferric oxyhydroxide powders were prepared from aqueous solutions containing iron and chromium ions. Radial structural functions for iron obtained by Fe K edge EXAFS spectra showed that the linkage of structural units formed by FeO₆ octahedra in γ-FeOOH is distorted by chromium addition, while such distortion in α-FeOOH is not clearly detected. On the other hand, Cr K edge EXAFS spectra showed that the local structure around chromium does not necessarily correspond to the local structure around of iron, which is observed by Fe K edge EXAFS spectra. This suggests that the structural units containing iron and chromium are heterogeneously distributed in these ferric oxyhydroxides. The local structural information was discussed coupled with morphological features of these ferric oxyhydroxides observed by TEM.     

Linearized method: A new approach for kinetic analysis of central dopamine D(2) receptor specific binding

We proposed a new method (;linearized method') to analyze neuroleptic ligand-receptor specific binding in a human brain using positron emission tomography (PET). We derived the linear equation to solve four rate constants, k(3), k(4), k(5), k(6) from PET data. This method does not demand a radioactivity curve in plasma as an input function to the brain, and can perform fast calculations in order to determine rate constants. We also tested the nonlinearized method including nonlinear equations which is a conventional analysis using plasma radioactivity corrected for ligand metabolites as an input function. We applied these methods to evaluate dopamine D(2) receptor specific binding of [(11)C] YM-09151-2. The value of B(max)/K(d)=k(3)/k (4) obtained by the linearized method was 5.72+/-3.1 which was consistent with the value of 5.78+/-3.4 obtained by the nonlinearized method.     

Analysis of neutron yield produced by high-energy proton

Comparisons have been made between computational results obtained with the BNL code system and experimental data measured by Vasfl'kov et al. for 56 x 56 x 64 cm natural and depleted uranium blocks surrounded by lead walls and primary proton energies of 400 and 660 MeV. The energetic protons from a linear accelerator are used to produce an intensive neutron source inthe uraniumblocko The computercode system prepared at BNL to perform nuclear design analyses of linear accelerator reactors consists of six main programs: NMTC for spallation-evaporation processes above 15 MeV, HIST3D for the analysis of collision event records obtained by NMTC to get P₃ neutron source distribution, DLC-2 to compile 100 energy group cross sections, TAPEMAKER for format conversion, ANISN to collapse 100 group cross sections to fewer group P₃ cross section sets, and the principal code TWOTRAN-II which performs neutron reaction and transport calculations in the energy range below 15 MeV. Our computational method gives conservative total neutron yields, i.e., underestimates of about 16.8–29.8% in comparison with measured values depending on proton energy. Radiative capture²³⁸U(n,) density distributions have been compared between the calculation and experiment. The calculated distribution has the higher peak in the central part of the target system and the steeper gradient both in the r and z directions.Brookhaven National Laboratory, Upton, New York 11973. Published in Atomnaya Énergiya, Vol. 47, No. 2, pp. 83–91, August, 1979.     

Transfection of glutathione S-transferase (GST)-pi antisense complementary DNA increases the sensitivity of a colon cancer cell line to adriamycin, cisplatin, melphalan, and etoposide

The goal of this study was to demonstrate that glutathione S-transferase (GST)-pi is directly involved in the intrinsic and acquired resistance of cancer cells to anticancer drugs. To this end, GST-pi antisense cDNA was transfected into the cultured human colon cancer cell line M7609, which expresses an innately high level of GST-pi and shows intrinsic drug resistance, and into an M7609 strain with acquired resistance to Adriamycin (ADR;i.e., M7609/ADR cells). The changes in the sensitivity of these transfectants to various anticancer drugs were investigated. The intracellular concentrations of GST-pi in M7609/anti-1 cells and M7609/anti-2 cells, two clones that were established by transfection of GST-pi antisense cDNA into M7609 cells, were decreased to approximately half of those detected in the parent cells (M7609) and in the control cells transfected with vector alone (M7609/pLJ). The sensitivities of the antisense transfectants in relation to ADR, cisplatin, melphalan, and etoposide were increased -3.3-fold, 2.3-fold, 2.2-fold, and 2.1-fold, respectively, compared with those of M7609 and M7609/pLJ. On the other hand, the sensitivities of the antisense transfectants to Taxol, vincristine, 5-fluorouracil, and mitomycin C were not significantly changed. Similarly, the transfection of antisense cDNA into M7609/ADR cells resulted in the reduction of intracellular GST-pi concentration (by about half) and an increased sensitivity to ADR (4.4-fold), but no increase in 5-fluorouracil sensitivity. Thus, GST-pi is considered to be a multidrug resistance factor that is responsible for both the intrinsic and acquired resistance of cancer cells to anticancer drugs such as ADR, cisplatin, melphalan, and etoposide.     

Properties of Starch Films and their Improvement

The tensile strengths and elongations of starch films prepared from various unmodified and modified starches were measured. These properties were improved by addition of urea and polyvinyl alcohol to the starch paste. The results obtained were as follows.

• 1 The heating temperature greatly affected the tensile strength and elongation of various unmodified starches. Potato starch gave the best film.
• 2 Introduction of hydroxyethyl groups into corn starch had unexpectedly little affect on the properties of the films.
• 3 A combination of hydroxyethylation and acid-modification slightly improved the properties of the films.
• 4 No film could be obtained after combinations of hydroxyethylation and hypochlorite-oxidation, pyrodextrinization or α-amylase-dextrinization. However, addition of urea to these modified starches resulted in good films.
• 5 On addition of urea the elongation of starch films increased and the pastes adhered uniformly to water repellent surfaces.
• 6 A film with the best properties was prepared from a mixture of 67% acid-modified hydroxyethyl starch, 13% urea and 20% polyvinyl alcohol.