Electromigration of sodium ions and electro-osmotic flow in water-saturated, compacted Na-montmorillonite

Sodium ions spiked with ²²Na as a tracer were migrated by electromigration and electro-osmosis in the water-saturated compacted Na-montmorillonite at dry densities 1.0×10³ kg m⁻³, under an electric potential gradient. Dissolved helium was also migrated by electro-osmosis in the montmorillonite. After migration, concentration profiles of the sodium ions and helium were obtained by γ-spectrometry and mass-spectrometric methods, respectively. From the profiles of both chemical species, not only migration due to electrokinetic phenomena but also mechanical dispersion was observed in the montmorillonite. The dispersion coefficients, D_i, and apparent migration rates, U_i^a, of ²²Na and helium were found in the compacted Na-montmorillonite at 1.0×10³ kg m⁻³. The migration of helium in the montmorillonite under an electric potential gradient reflects that of water because helium migrates as an electrically neutral species. The parameters D_He^m, U_He^a, and α_He correspond to those of water. The mechanical dispersion coefficients, D_Na^m, of ²²Na⁺ ions are much smaller than those of water obtained by helium. The dispersivity parameters, α_Na, for ²²Na⁺ obtained from these D_Na and U_Na^a values are 10⁻⁵ m and those for water (α_He) are 10⁻³ m. This indicates that ²²Na⁺ ions migrate in different spaces than water in the compacted montmorillonite under a potential gradient. This finding suggests that the migration of Na⁺ ions occurs in the interlayer and/or on the outer surfaces of the montmorillonite; whereas dissolved helium migrates in the pore water.     

Advantages of counter-current operation for hydrodesulfurization in trickle bed reactors

The deep desulfurization of oil fraction is a central matter of concern to every refinery. Hydrogen sulfide is the product of hydrodesulfurization reaction and it is the inhibiter of the reaction. When products inhibit the reaction, the counter-current operation is expected to have an advantage over the co-current operation. Hydrodesulfurization of vacuum gas oil in a trickle bed reactor was simulated for both models of co-current operation and counter-current operation. The models were simulated on high and low gas and liquid velocities. Hydrogen sulfide was affected by mass transfer resistance in both gas-liquid and liquid-catalyst interface. The other component mass transfer resistances were negligible. When the deep desulfurization was required, simulation results showed that the counter-current operation was superior to the co-current operation in organic sulfur conversion     

Effect of Phosphorus Ions on the Proton Conductivity in the Sol–Gel-Derived Porous Glasses

The effect of phosphorus ions on the proton conductivity was examined for the sol–gel-derived glasses. The porous glasses were prepared through hydrolysis of PO(OCH₃)₃ and Si(OC₂H₅)₄, in which the phosphorus ions consisted of the POH bonds and were dissolved into the silica matrix without any P-O-Si bond. The electrical conductivity increased in a humid atmosphere and reached ∼30 mS/cm at 50°C under 70% RH. High conductivity is achieved by both the POH bonds and the molecular water bonded to the POH bonds. The conductivity increased with a change in humidity from 40% to 80% RH. The phosphorus ions were selectively dissolved in water, resulting in a lower conductivity.     

Phase transformation and interface segregation behavior in Si3N4 ceramics sintered with La2O3–Lu2O3 mixed additive

Microstructure and mechanical property of silicon nitride (Si₃N₄) ceramic are strongly dependent on the selection of sintering additives. When rare‐earth (RE) oxide is used as the sintering additive, segregation of RE ions at interface between Si₃N₄ grain and intergranular glassy film (IGF) is believed to play a critical role. Although the ionic radius of RE ion is known to be an empirical parameter to modify the mechanical property, the correlation between the segregated ions and their ionic radii is still under controversy. In order to address this issue, (i) rate of α‐β phase transformation and (ii) segregation behavior at the interface were studied for Si₃N₄ ceramics sintered using mixture of La₂O₃ and Lu₂O₃ as additives in this study. Specimens of Lu content 30% and higher exhibited lower activation energies for the α‐β phase transformation as compared with those of Lu content 20% and lower. In terms of the segregation behavior, La was preferably segregated at one site and Lu at the other site along β‐Si₃N₄/IGF interface in the specimens of Lu content 30% and higher. It is understood from these results that Lu segregation site should be more closely related with grain growth.     

SPRAY DRYING CHARACTERISTICS BY A CENTRIFUGAL PRESSURE NOZZLE WITH LARGE ORIFICE DIAMETER

A study was made of a centrifugal pressure nozzle with large orifice diameter (8-10 nun) for producing dry milk in capacity of 2-3 tons per hour to develop some performance data on spray distribution, drop size distribution, and capacity with changing spray drying conditions such as nozzle pressure, orifice diameter and spray angle.

Experimental results were shown as follows.

(1) A centrifugal pressure nozzle of large capacity such as 5,000- 5,500 l/hr at 150 kg/cm2 spray pressure and 110°s ray angle was designed by using the nozzle parameter Si/dedi√di/di.

(2) Atomization characteristics were greatly affected by the ratio of orifice diameter (de) to the length (L) of the nozzle core. The smaller the ratio, around 0.125, the better are the atomizing effects.

(3) The large orifice can be used at least 3,000 hr in the spray drying operation for milk without any wear in the orifice although it is only made of stainless steel.

As a result, a spray dryer of large capacity for dry milk has been operated by a mono nozzle with a large orifice without any trouble for a long time     

Thermotropic and Barotropic Phase Behavior of Phosphatidylcholine Bilayers

Bilayers formed by phospholipids are frequently used as model biological membranes in various life science studies. A characteristic feature of phospholipid bilayers is to undergo a structural change called a phase transition in response to environmental changes of their surroundings. In this review, we focus our attention on phase transitions of some major phospholipids contained in biological membranes, phosphatidylcholines (PCs), depending on temperature and pressure. Bilayers of dipalmitoylphosphatidylcholine (DPPC), which is the most representative lipid in model membrane studies, will first be explained. Then, the bilayer phase behavior of various kinds of PCs with different molecular structures is revealed from the temperature–pressure phase diagrams, and the difference in phase stability among these PC bilayers is discussed in connection with the molecular structure of the PC molecules. Furthermore, the solvent effect on the phase behavior is also described briefly.     

Growth and microstructure of Ba β-alumina films by laser chemical vapor deposition

Ba β-alumina films were prepared by laser chemical vapor deposition. Mostly single-phase Ba β-alumina films were obtained at 1125–1200 K and for an Al/Ba molar ratio of 12.4–16.6. BaAl₂O₄ and α-Al₂O₃ were codeposited with Ba β-alumina under Ba- and Al-rich conditions, respectively. The Ba β-alumina films consisted of hexagonal grains, and the (1 1 0)-oriented Ba β-alumina films had a fin-like columnar structure. The highest deposition rate reached 120 μm h^?1 at around 1200 K. A thin layer of Ba-rich superstructure was formed on the surface of the (1 1 0)-oriented columnar grains.     

Transparent Lu3NbO7 bodies prepared by reactive spark plasma sintering and their optical and mechanical properties

Transparent lutetium niobate (Lu₃NbO₇) bodies were prepared by reactive spark plasma sintering using Lu₂O₃ and Nb₂O₅ powders. Fully dense Lu₃NbO₇ bodies with density greater than 99.5% of the theoretical were obtained at 1300–1650 °C. The grains steadily grew from 0.1 to 0.6 μm with increasing sintering temperature from 1200 to 1450 °C and significant grain growth from 2.2 to 9.2 μm occurred at 1550–1650 °C. The Lu₃NbO₇ body sintered at 1450 °C showed the highest transmittance of 63% at 550 nm after heat treatment at 850 °C in air for 6 h. Fully dense, submicron-size transparent Lu₃NbO₇ exhibited Vickers hardness of ～13.0 GPa and indentation fracture toughness of 1.0 MPa m^1/2.     

A Practical Model for the Interactions Between Hydrating Portland Cements and Poly-β-Naphthalene Sulfonate Condensate Superplasticizers

The performance of poly-β-naphthalene sulfonate condensate superplasticizer (BNS) as a dispersant for cement in concrete is affected severely by slight differences in the characteristics of the cement. In order to be able to predict these effects, a model for estimating the fluidity of cement paste containing BNS is proposed. This model is based on an assumption that the fluidity of cement paste is proportional to the BNS adsorption amount per surface area of hydrated cement (Ad/Hy). BNS is known to show two types of sorption on hydrated cement: one is the bulk absorption into initial hydrates and the other one is the superficial adsorption onto hydrates. Only the superficially adsorbed BNS is expected to work as a dispersant. By assuming a competitive Langmuir-type adsorption on hydrates between BNS and SO₄²⁻, a simple method to estimate Ad/Hy is developed, with the concentrations of BNS and SO₄²⁻ as the only two independent parameters. The resulting estimates of Ad/Hy show a good correlation with paste flow and its change with elapsed time for a broad range of cements. The SO₄²⁻ concentration in the aqueous phase of the cement paste just after the beginning of the mixing is known to affect the performance of BNS as a dispersant. By using the proposed model to discriminate between the superficial adsorption and bulk absorption of BNS, this phenomenon is explained quantitatively.