Narrow Band FLIP for Liquid Simulations

The Fluid Implicit Particle method (FLIP) for liquid simulations uses particles to reduce numerical dissipation and provide important visual cues for events like complex splashes and small‐scale features near the liquid surface. Unfortunately, FLIP simulations can be computationally expensive, because they require a dense sampling of particles to fill the entire liquid volume. Furthermore, the vast majority of these FLIP particles contribute nothing to the fluid's visual appearance, especially for larger volumes of liquid. We present a method that only uses FLIP particles within a narrow band of the liquid surface, while efficiently representing the remaining inner volume on a regular grid. We show that a naïve realization of this idea introduces unstable and uncontrollable energy fluctuations, and we propose a novel coupling scheme between FLIP particles and regular grid which overcomes this problem. Our method drastically reduces the particle count and simulation times while yielding results that are nearly indistinguishable from regular FLIP simulations. Our approach is easy to integrate into any existing FLIP implementation.     

Hydrocarbons with a homoconjugated polyene system and their monoepoxy derivatives: Sex attractants of geometrid and noctuid moths distributed in Japan

Although several sex pheromones of the family Geometridae have been characterized, investigations on Japanese species are limited. In order to obtain more information, screening using known sex pheromones and their analogs was carried out. The (Z,Z,Z)-3,6,9-triunsaturated and (Z,Z)-6,9-diunsaturated hydrocarbons with straight C¹⁹-C²¹ chains were synthesized by the Grignard coupling reaction as a key step starting from linolenic and linoleic acids, respectively. Oxidation of the homoconjugated trienes withm-chloroperoxybenzoic acid yielded a 111 mixture of three monoepoxy derivatives that could be separated by silica gel chromatography. The chemical structure of each positional isomer was confirmed using two-dimensional NMR techniques and MS measurements, which enabled characteristic fragment ions from the isomers to be identified. Field tests using lures incorporating only one of the above six hydrocarbons or nine epoxides were carried out in a forest in Tokyo. Consequently, attraction of male moths of 14 geometrid species in addition to four species in another family, the Noctuidae, was observed. It was concluded that hydrocarbons with a homoconjugated polyene system and the monoepoxy derivatives are important components of sex pheromones produced by Japanese lepidopterous insects, particularly the geometrid moths.     

Zr-Hf interdiffusion in polycrystalline Y2O3-(Zr+Hf)O2

Lattice and grain-boundary interdiffusion coefficients were calculated from the concentration distributions determined for Zr-Hf interdiffusion in polycrystalline 16Y₂O₃·84(Zr_1–x Hf _x )O₂ withx=0.020 and 0.100. The lattice interdiffusion coefficients were described byD=0.031 exp [–391 (kJ mol^–1)/RT] cm² sec^–1 and the grain-boundary diffusion parameters byD=1.5×10^–6exp [–309(kJ mol^–1)/RT] cm³ sec^–1 in the temperature range 1584–2116° C. Comparison of the results with those for the systems CaO-(Zr+Hf)O₂ and MgO-(Zr+Hf)O₂ indicated that the Zr self-diffusion coefficient was insensitive to the dopants in the fluorite-cubic ZrO₂ solid solutions.     

Tensile properties of iron-based P/M steels with ferrite + martensite microstructure

The effect of intercritical heat treatments on the tensile properties of iron-based P/M steels was investigated. For this purpose, atomized iron powder (Ancorsteel 1000) was admixed with 0.3 wt.% graphite powder. Tensile test specimens were cold pressed at 700 MPa and sintered at 1120 °C for 30 min under pure argon gas atmosphere. After sintering, ∼20% pearlite volume fraction in a ferrite matrix was obtained. To produce coarse ferrite + martensite microstructures, the sintered specimens were intercritically annealed at 724 and 760 °C and quenched in water. To obtain fine ferrite + martensite microstructures, the sintered specimens were first austenitized at 890 °C and water-quenched to produce a fully martensitic structure. These specimens were then intercritically annealed at 724 and 760 °C and re-quenched. After the intercritical annealing at 724 and 760 °C and quenching, martensite volume fractions were ∼ 18% and 43%, respectively, in both the coarse- and fine-grained specimens. Although the intercritically annealed specimens exhibited higher yield and tensile strength than the as-sintered specimens, their elongation values were lower. Specimens with a fine ferrite + martensite microstructure showed high yield and tensile strength and ductility in comparison to specimens with a coarse ferrite + martensite microstructure. The strength values of specimens increased with increasing martensite volume fraction.     

Preparation and characterization of Z-type hexaferrites, Ba3(1−x)Sr3x Co2Fe24O41 with x = 0–0.5, via a two-step calcination with an intermediate wet milling

Z-type hexaferrites (Ba_{3(1 − x)}Sr_3x Co₂Fe₂₄O₄₁with x = 0–0.5, Z-hex) were prepared in a nearly phase pure state by a two-step calcination with an intermediate wet milling. The first calcination of the starting mixture comprising oxides or hydroxides at temperatures below 1100^∘C brought about a mixture of layer-structured M and Y-type hexaferrite phases, together with a spinel phase of Co ferrite. Z-hex was fully crystallized after the second calcination up to 1230^∘C. Wet milling between the two calcination steps was decisive for the phase purity. Emphasis was laid on the quantitative analyses of Z-hex, together with the evaluation of anisotropic growth of the crystallites. Sr addition stabilizes Z-hex, while decreases degree of anisotropy simultaneously.     

"Residence times difference" fluxgate magnetometers

We present analytical and experimental results on fluxgate magnetometers that make use of a readout technique based on residence times. This approach allows for enhancing sensitivity to weak target signals in particular when the reduction of the sensor dimensions are considered. Our approach, exploiting the inherent nonlinear character of the bistable core dynamics, is based on the time domain characterization of the transitions between the two saturation states of the hysteresis loop that is inherent in the ferromagnetic core dynamics. This readout technique can be implemented with bias signals having lower amplitude and frequency than those used in conventional fluxgate processing schemes, thus reducing the device power requirements. The efficacy of this strategy is shown through an analytical approach and via experimental results which suggests guidelines for optimal device design and realization. The experiments have been carried out on a miniaturized laboratory fluxgate prototype; this device shows numerous desirable characteristics, including very good sensitivity and resolution, as well as ease of operation and a very low cost.     

Preparation of porous membranes by selective decomposition of adamantane unit in ABA‐type triblock copolymer

The mechanism of pore formation by selective decomposition of adamantane unit in an ABA‐type triblock copolymer derived from 4,4‐(hexafluoroisopropylidene)diphthalic anhydride‐2,3,5,6‐tetramethyl‐1,4‐phenylenediamine (6FDA‐TeMPD) and poly(2‐methyl‐2‐adamantylmethacrylate) (PMAdMA) was investigated on this basis. This study aims to developing a novel method of material design for high‐precision gas separation membranes and application to electric devices by improving dielectric constant. Scanning electron microscopy images showed that the membrane structure changed considerably after heating; the difference increased with the increase in adamantane content. Interestingly, the internal structure of Block(36 mol%6FDA‐TeMPD/64 mol%PMAdMA) membrane was almost unchanged although its surface structure was changed. These results suggest that the mechanism of formation of porous membrane involves the decomposition of adamantane unit from surface. In addition, more adamantane units inside the membrane were discharged to the surface of the membrane through a path formed by decomposed adamantane units. POLYM. ENG. SCI., 56:1191–1200, 2016. © 2016 Society of Plastics Engineers     

Development of biobased microwave absorbing composites with various magnetic metals and carbons

The preparation and characterization of a biobased electromagnetic absorbing composites derived from natural lacquer as a renewable resource with microwave‐absorption fillers, including Ni–Zn ferrite and carbonyl iron (CI) as magnetic metals and soot and carbon nanotube (CNT) as carbon materials, were investigated in terms of the gel content, hardness, drying properties, and electromagnetic absorption properties. Interestingly, composites with ferrite and CI contained up to 320 and 550 wt %, respectively, of these compounds. This quite high loading capacity of the metal fillers in a natural‐lacquer base could have been due to the high compatibility between the filler and the natural lacquer; this indicated that the natural lacquer worked as a binder for these metals. The morphology of the biobased composite was characterized by scanning electron microscopy. The electromagnetic absorption properties of composites were characterized in the frequency range from 0.05 and 20 GHz by the reflection loss (RL) measurement method in terms of the kind of fillers and filler loading. The natural lacquer did not affect the absorption properties of the fillers. Biobased composites showed over 99% electromagnetic absorption in the frequency range 3.0–4.0 GHz for 280 wt % ferrite and 8.9–9.7 GHz for 200 wt % CI. Conversely, 10 and 20 wt % soot exhibited good performance (RL < ?20 dB) between 16.5 and 17.3 and between 8.8 and 9.2 GHz, respectively. The areas with RL values of less than ?20 dB of the CNT composites were 10.4–11.0 GHz for 5 wt % and 14.6–15.2 GHz for 10 wt %. Hence, natural lacquer can be used as a binder material for electromagnetic absorption composites. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44131.     

Thermal and optical properties of hyperbranched fluorinated polyimide/mesoporous SiO2 nanocomposites exhibiting high transparency and reduced thermo-optical coefficients

A series of hyper-branched polyimide (HBPI)/mesoporous SiO₂ nanocomposite films were prepared from a fluorinated anhydride (6FDA), a fluorinated triamine (TFAPOB), and mesoporous SiO₂ nanoparticles (NPs). The anhydride-terminated precursor of HBPI was functionalized using a coupling agent prior to mixing with SiO₂ NPs. The morphologies and thermal-optical properties of the nanocomposite films were investigated, with particular focus on their optical transparency, refractive indices (n), and thermo-optical (TO) coefficients. The absolute values of TO coefficients (|dn/dT|) of HBPI film (50.8 ppm/K) were significantly reduced to 13.4 ppm/K by homogeneous dispersion of 15 wt% of SiO₂ NPs. The HBPI/SiO₂ composite films exhibited high thermal stability without significant weight loss of up to 400 °C in air. The films also exhibited small coefficients of linear thermal expansion (CTEs) within the range 30–40 ppm/K. In addition, enhanced interfacial interactions between SiO₂ and HBPI significantly improve the optical transparency with cutoff wavelengths shorter than 450 nm. The refractive indices of HBPI/SiO₂ composite films were found to range from 1.477 to 1.502, which agrees well with the calculated values. This study shows that the incorporation of SiO₂ NPs in multi-functional HBPI matrix is a promising approach to prepare high performance thermally stable films for thermo-optic applications.