Ammonia production using iron nitride and water as hydrogen source under mild temperature and pressure

Ammonia generation was studied in the reaction between water and nitrogen-containing iron at 323 K and atmospheric pressure. Similar to metallic Fe, the interstitial compound Fe₃N reduced water through Fe oxidation to produce hydrogen gas, while the N combined with atomic hydrogen to produce ammonia as a byproduct. The addition of carbon dioxide to this system accelerated the reaction with concomitant consumption of carbon dioxide. The promoted ammonia production upon addition of carbon dioxide can be attributed to the generation of atomic hydrogen from the redox reaction of carbonic acid and Fe, as well as removal of used Fe from the reaction system through the formation of a soluble carbonato complex. When carbonate was added to the reaction system, the production rates of ammonia and hydrogen increased further. The results here confirmed that ammonia can be synthesized from iron nitride under mild conditions by utilizing carbon dioxide.     

Synthesis and properties of bismaleimide resins containing ether bonds

New bismaleimides containing ether bonds were prepared. The thermal properties of the bismaleimides were investigated by differential scanning calorimetry (DSC). The effects of structure of the bismaleimides and curing conditions on the thermal and mechanical properties of the cured resins such as initial decomposition temperature (T_d), glass transition temperature (T_g), and flexural strength were studied. The introduction of ether bonds to bismaleimide resins decreased the brittleness of the resins without reductions in their heat-resistant properties.     

Thermal Behavior of BaTiO3 Particles Synthesized by Plasma Chemical Vapor Deposition

The thermal behavior of nanoparticles BaTiO₃, prepared by a radio-frequency plasma chemical vapor deposition (RF-plasma CVD) method, was characterized by various analysis methods. The BaCO₃ phase was included in the powder as byproducts, which is also observed in hydrothermal BaTiO₃ powder. The BaCO₃ phase decomposed and disappeared by annealing at 873 K for 30 min. H₂O, N₂, CO₂ and H₂, were detected by a thermal desorption spectra measurement from BaTiO₃ powder. The annealed powder became well-crystallized particles without grain growth, although as-prepared powder included polycrystalline particles. We successfully observed in-situ grain growth for BaTiO₃ nanoparticles by thermal transmission electron microscope. At the initial step of normal grain growth, very fine particles with 40–60 nm diameters started to merge into the larger grains around 1083 K. The migration rate was measured by video images and a grain boundary diffusion coefficient D_gb was calculated.     

Effect of Grain Boundaries on Thermal Conductivity of Silicon Carbide Ceramic at 5 to 1300 K

The thermal conductivity of a SiC ceramic was measured as 270 W·m⁻¹·K⁻¹ at room temperature. At low temperatures ( T < 25 K), the decrease in the conductivity was proportional to T ³ on a logarithmic scale, which indicated that the conductivity was controlled by boundaries. The calculated phonon mean free path in the ceramic increased with decreased temperature, but was limited to ∼4 μm, a length almost equal to the grain size, at temperatures below 30 K. We concluded that the thermal conductivity of the ceramic below 30 K was influenced significantly by grain boundaries and grain junctions.     

Barium Carbonate Phase on the Surfaces of Barium Titanate Particles and in Situ Transmission Electron Microscopy Observation of Its Decomposition

A BaCO₃ phase is found on the surfaces of hydrothermally synthesized BaTiO₃ particles; it occurs as aggregates or small protuberances. A small proportion of the phase decomposes to BaO crystallites when heated by a convergent electron beam in a transmission electron microscope. The BaO and BaCO₃ crystallites disappear when they are irradiated successively by the convergent electron beam. The BaO crystallites and the BaCO₃ phase sublimate and/or react with BaTiO₃ crystals whose surface layers are deficient in Ba²⁺ ions.     

Relationship between oxidative stability of vitamin E and production of fatty acids in oils during microwave heating

Effects of microwave heating on the oxidative stability ofd-tocopherols were studied in relation to the production of fatty acids in oils. During microwave heating, the stability of tocopherols decreased in the orderδ>β>γ>α. This order did not depend on the types of ethyl esters of fatty acids or oils present. But, the shorter the chainlength and the lower the degree of unsaturation of the fatty acid ethyl esters, the greater was the reduction in amount of individual tocopherols. A similar tendency was observed when tocopherol-stripped vegetable oils, with equimolar mixtures of tocopherols added, were treated under the same conditions. The reduction in tocopherols became greater with increasing levels of free fatty acids.     

Structural Modulations in Monoclinic Tricalcium Silicate Solid Solutions Doped with Zinc Oxide, M(I), M(II), and M(III)

Structural modulations in solid solutions of C₃S doped with various amounts of ZnO were investigated via the selected-area electron diffraction method. Three monoclinic modifications (M(I), M(II), and M(III)) were identified in the solid solutions. The modifications had pseudohexagonal subcells that were modulated to form supercells. Coordinates of the reflections attributable to the supercells could be expressed by the following linear combinations of vectors of the reciprocal lattices: m₁(−2 a */5.4 + 2 b */5.4 − 7 c */5.4) for M(I), m₂(− a */5 + b */5 − c *) for M(II), and m₃(− a */6 + b */6 + 7 c */6) for M(III), m₁ and m₂=±1 and ±2, and m₃=±1, ±2, and ± 3. All the monoclinic modifications possessed structural modulations of a one-dimensional type. The modulation waves could be detected as wavy contrasts by high-resolution transmission electron microscopy.     

Preserving worker privacy in crowdsourcing

This paper proposes a crowdsourcing quality control method with worker-privacy preservation. Crowdsourcing allows us to outsource tasks to a number of workers. The results of tasks obtained in crowdsourcing are often low-quality due to the difference in the degree of skill. Therefore, we need quality control methods to estimate reliable results from low-quality results. In this paper, we point out privacy problems of workers in crowdsourcing. Personal information of workers can be inferred from the results provided by each worker. To formulate and to address the privacy problems, we define a worker-private quality control problem, a variation of the quality control problem that preserves privacy of workers. We propose a worker-private latent class protocol where a requester can estimate the true results with worker privacy preserved. The key ideas are decentralization of computation and introduction of secure computation. We theoretically guarantee the security of the proposed protocol and experimentally examine the computational efficiency and accuracy.     

Diffusion/adsorption model of cellulose dyeing. II. Ordinary cellulose–direct dye system

The diffusion and adsorption of C.I. Direct Yellow 12 and Blue 15 in water-swollen ordinary cellophane sheets were examined at various ionic strengths. The concentration dependence of apparent diffusion coefficients, D_c, for these dyes was obtained from the diffusion profiles in the substrate, which were measured by the use of the cylindrical film roll method. The decrease of apparent porosity with an increase in the amounts of adsorption was observed. To explain the diffusion/adsorption behaviors of these systems, a variable porosity model was proposed and was applied to analyze the concentration dependence of D_c's. The diffusion/adsorption behaviors of these dyes could be quantitatively described by this model at relatively low ionic strengths. At higher ionic strengths and/or lower values of C, i.e., at the large values of C_im/C_m, where the C's are the concentrations of immobilized (suffix im) and mobile (suffix m) species, it needed to introduce the concept of dynamic equilibria which occurred simultaneously with diffusion but deviated from the true equiliblia measured by the adsorption experiments.