Modification of cyanate ester resin by soluble polyimides

Soluble polyimides (PIs) were prepared as random or multiblock types with 4,4′‐(hexafluoroisopropylidene) diphthalic anhydride (6FDA) and 3,3′,4,4′‐biphenyltetracarboxylic dianhydride (s‐BPDA) as acid dianhydride components and 4,4′‐bis(m‐aminophenoxy) diphenyl sulfone (m‐BAPS) as a diamine component by a one‐pot process and used to improve the brittleness of the cyanate ester resin. Random‐type PIs were more effective as modifiers than multiblock‐type PIs. The morphologies of the modified resins depended on PI structure, molecular weight, and concentration. The most effective modification of the cyanate ester resin was attained because of a heterogeneous phase structure composed of a flat matrix phase and phase‐inverted structures of the modified resin; a 15 wt % inclusion of a random PI (weight‐average molecular weight = 63,400) composed of 6FDA, s‐BPDA, and m‐BAPS (0.5/0.5/1.0 molar ratio) led to a 65% increase in the fracture toughness for the modified resin with a slight loss of flexural strength and a retention of flexural modulus and glass‐transition temperature, compared with the values for the unmodified resin. Water absorptivity of the modified resin was comparable to that of the unmodified resin up to 400 h, and then, water absorption of the modified resins increased considerably. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1–11, 2003     

An efficient method for the two-dimensional elastostatic boundary element method

In order to obtain accurate results and to reduce computation time, we have proposed in this paper a new strategic method, where quadratic elements are used at the corner points and linear elements at the points off the corner points. A computer program using this method has been developed and applied to several problems of various shapes. The usefulness of this method was illustrated by the application results.     

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.     

Encapsulation of lead-free Sn/Zn/Bi solder alloy particles by coating with wax powder for improving oxidation resistance

An encapsulation treatment of lead-free Sn/Zn/Bi solder powder was investigated for improving the oxidation resistance. Sn-8mass%Zn-3mass%Bi alloy particles were coated with a wax (12-hydroxystearic acid) powder by means of a dry mechanical treatment method using a ball mill. In order to determine the optimum operating conditions of the ball mill in the wax-coating treatments, the compressive energy required for deforming a single Sn/Zn/Bi alloy particle was measured with an unconfined compression tester and the mechanical energy applied to the alloy particles in the ball mill was estimated using the results of the compression test. The optimum operating conditions were determined based on both the applied energy and the flowability of solder pastes, and the wax-coated alloy particles maintaining the spherical shape were obtained under the conditions. The wettability test and the solder balling test for the solder pastes containing the wax-coated alloy particles stored at room temperature in air were carried out to evaluate the oxidation resistance performance. The wax-coated alloy particles had an excellent wettability compared with the original alloy particles, and the oxidation resistance of the Sn/Zn/Bi solder powder was improved by the encapsulation treatment.     

Slip mechanism in optical fiber coating with open-cup applicators

The allowable maximum coating speed of optical fibers has been correlated to the flow properties of the coating material itself. The maximum smooth coating speed has been measured from the coating thickness fluctuation-coating speed curves using several types of silicone resins. Flow curves of the silicone resins also have been measured by two different viscometers, i.e., cone-plate and capillary viscometers. The maximum smooth coating speed, at which the coating thickness fluctuation begins to increase, has been found to correspond to the critical shear rate at which the flow curve deviates from a power law. This correspondence probably results from the fact that the slip occurs both at the fiber-coating material interface and at the viscometer (cone, plate, or capillary)-coating material interface. Accordingly, the maximum smooth coating speed can be predicted from the critical shear rate value without the actual fiber coating experiments.     

Changing Microspatial Patterns of Sulfate-Reducing Microorganisms (SRM) during Cycling of Marine Stromatolite Mats

Microspatial arrangements of sulfate-reducing microorganisms (SRM) in surface microbial mats (~1.5 mm) forming open marine stromatolites were investigated. Previous research revealed three different mat types associated with these stromatolites, each with a unique petrographic signature. Here we focused on comparing “non-lithifying” (Type-1) and “lithifying” (Type-2) mats. Our results revealed three major trends: (1) Molecular typing using the dsrA probe revealed a shift in the SRM community composition between Type-1 and Type-2 mats. Fluorescence in-situ hybridization (FISH) coupled to confocal scanning-laser microscopy (CSLM)-based image analyses, and ³⁵SO₄ ²⁻-silver foil patterns showed that SRM were present in surfaces of both mat types, but in significantly (p < 0.05) higher abundances in Type-2 mats. Over 85% of SRM cells in the top 0.5 mm of Type-2 mats were contained in a dense 130 μm thick horizontal layer comprised of clusters of varying sizes; (2) Microspatial mapping revealed that locations of SRM and CaCO₃ precipitation were significantly correlated (p < 0.05); (3) Extracts from Type-2 mats contained acylhomoserine-lactones (C4-, C6-, oxo-C6 C7-, C8-, C10-, C12-, C14-AHLs) involved in cell-cell communication. Similar AHLs were produced by SRM mat-isolates. These trends suggest that development of a microspatially-organized SRM community is closely-associated with the hallmark transition of stromatolite surface mats from a non-lithifying to a lithifying state.     

Palladium‐Catalyzed Hydroxymethylation of Aryl‐ and Heteroarylboronic Acids using Aqueous Formaldehyde

Cyclometallated NHC palladium complexes prepared from palladium(II) acetate [Pd(OAc)₂] and unsymmetrical 1,3‐diarylimidazolinium salts catalyzed the hydroxymethylation of (hetero)arylboronic acids using an excess amount of formalin to afford (hetero)arylmethanols in good to satisfactory yields.

     

Ironmaking with ammonia at low temperature

This paper describes the reduction of hematite with ammonia for ironmaking, in which the effect of temperature on the products was examined. The results showed that the reduction process began at 430 °C during heating, and with an increase in temperature, the reduction mechanism changed apparently from a direct reduction of ammonia (Fe(2)O(3) + 2NH(3) → 2Fe + N(2) + 3H(2)O) to an indirect reduction via the thermal decomposition of ammonia (2NH(3) → N(2) + 3H(2), Fe(2)O(3) + 3H(2) → 2Fe + 3H(2)O) at temperatures over 530 °C. The final product obtained at 600 and 700 °C was pure metallic iron, in contrast with that formed at 450 °C, that is, a mixture of metallic iron and iron nitride. The results suggest the possibility of using ammonia as a reducing agent for carbonless ironmaking, which is operated at a much lower temperature than 900 °C in conventional coal-based ironmaking.