Optimum structural design of CFRP isogrid cylindrical shell using genetic algorithm

This paper describes an optimum structural design of a CFRP isogrid cylindrical shell using a genetic algorithm (GA). When the CFRP isogrid cylindrical shell receives a prescribed uniaxial compressive load, an objective is to minimize weight of the CFRP isogrid cylindrical shell subjected to the constraint conditions of no buckling and no material failure. The buckling and material failure loads were approximated by a response surface method combined with partitioning of design spaces and these approximated values were used in the process of GA instead of FEM calculations in order to reduce the computational time. Furthermore, the differences from the constraint conditions of the linear or the non-linear (local) buckling loads were also calculated and their results were compared with each other.     

The structure of tartaric acid adsorbed over nickel catalyst observed by FT-IRAS

The structure of the L-tartaric acid adsorbed on the surface of a nickel metal catalyst with or without NaBr was studied by FT-IRAS. The carboxylic acid and carboxylate type adsorbed species were observed on nickel surface which was treated with only tartaric acid, while only one type of carboxylate ion was observed on the nickel surface which was treated with tartaric acid and NaBr.     

Miscibility in binary blends of aromatic and alicyclic polyamides

Miscibility was studied for four polyamide blends of 6I/6T [copolymer consisting of 1,6‐hexamethylene diamine and isophthalic acid (6I) (70 wt %) and terephthalic acid (6T) (30 wt %)] with MXD6 (polyamide of m‐xylenediamine and adipic acid), BAC6 (polyamide of 1,3‐bis(aminomethyl)cyclohexane and adipic acid), TR55 (copolymer consisting of nylon 11 (30 wt %), and polyamide of bis(3‐methyl, 4‐aminocyclohexyl)methane (30 wt %) and isophthalic acid (70 wt %), and CX7323 (polyamide of bis(4‐aminocyclohexyl)methane and dodecanedicarboxylic acid), using differential scanning calorimetry, X‐ray diffraction method, and electronmicroscopic observation. In quenched MXD6/(6I/6T) and BAC6/(6I/6T) blends, MXD6 and BAC6 components were miscible to 6I/6T, but TR55 and CX7323 components were completely phase‐separated from 6I/6T. Interestingly on electronmicroscopic observations, TR55 and CX7323 components were seen as droplets in 6I/6T medium when the content is low, but when 50 wt %, a layered structure was constructed with 6I/6T, reminiscent of morphological structure in block copolymer. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3971–3978, 2006     

Thermoplastic behavior of lignin with various synthetic plasticizers

The thermoplasticization of thiolignin (TL) and dioxane lignin (DL) with various synthetic plasticizers has been investigated. The thermal softening temperatures T_s of the lignin–plasticizer systems were measured applying the flow tester technique which is useful for investigating the thermal properties of polymers. It was found that the T_s of the lignins were lowered considerably as the solubility parameters (after Hildebrand) of the plasticizers approach close to that of lignin, namely, around 11. The lowering in the T_s of the lignins with the plasticizers was described by a linear equation with respect to the plasticizer concentration which ranged up to 20 wt-%. The sorption of the limited amounts (< 5%) of water to the lignins also considerably decreased the T_s, however, the extent of lowering in the T_s by water sorption is less than that by the plasticizer addition at their contents over about 15%. The relationship of T_s to water content (up to about 30%) was curved, not linear. It was clearly shown that a combined use of the plasticizer and water brought about the most effective plasticizing for the lignins compared with the use of either of those alone.     

Analyzing the Boundary Thermal Resistance of Epitaxially Grown Fe<Subscript>2</Subscript>VAl/W Layers by Picosecond Time-Domain Thermoreflectance

To gain deep insight into the mechanism of phonon scattering at grain boundaries, we investigated the boundary thermal resistance by using picosecond pulsed-laser time-domain thermoreflectance for epitaxially grown W/Fe₂VAl/W films. By using radio-frequency magnetron sputtering, we prepared a series of the three-layer films whose Fe₂VAl thickness ranged from 1 nm to 37 nm. The fine oscillation of reflectivity associated with the top W layer clearly appeared in synchrotron x-ray reflectivity measurements, indicating a less obvious mixture of elements at the boundary. The areal heat diffusion time, obtained from the time-domain thermoreflectance signal in the rear-heating front-detection configuration, reduced rapidly in samples whose Fe₂VAl layer was thinner than 15 nm. The ～ 10% mismatch in lattice constant between Fe₂VAl and W naturally produced the randomly distributed lattice stress near the boundary, causing an effective increase of boundary thermal resistance in the thick samples, but the stress became homogeneous in the thinner layers, which reduced the scattering probability of phonons.     

Effect of dehydration and urea on stability of homosulfamine in solid states

In the presence of urea in solid states, the stability of unpulverized homosulfamine hydrate (phase I; UHH) is significantly decreased whereas that of unpulverized homosulfamine anhydrate (UHA) is not. The stability of UHH is decreased slightly more by pulverization (PHH). The major objective of this study was to investigate the effects of urea, dehydration, and pulverization on the stability of homosulfamine in solid states. Binary mixtures of UHH and urea, PHH and urea, and UHA and urea in a ratio of 1:1 (wt/wt) were prepared as physical mixtures and were analyzed by scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), and Fourier transform infrared (FTIR) spectroscopy to study their appearance and structural changes before and after storage. PXRD analysis revealed that physical mixtures comprising UHH and urea and PHH and urea have the same diffraction pattern as that of the mixture of UHA and urea after preparation. The dehydration rate of the crystal water of UHH was accelerated by the presence of urea in addition to pulverization. Moreover, the PXRD patterns of the physical mixtures of UHH/urea and PHH/urea were significantly altered during storage, whereas that of UHA/urea was not, which was consistent with the SEM and FTIR results. The particle shape and appearance of UHH varied significantly as a result of pulverization. The stability of homosulfamine was influenced not only by the presence of urea and dehydration but also by the surface state and particle size of the crystalline form.     

Possible involvement of interleukin-1 in cyclooxygenase-2 induction after spinal cord injury in rats

A standardized compression injury of rat spinal cord brought about a time-dependent biphasic production of thromboxane A2 (detected as thromboxane B2) and prostaglandin I2 (detected as 6-ketoprostaglandin F1alpha). Thromboxane B2 was predominant during the first 1 h, whereas the 6-ketoprostaglandin F1alpha level exceeded that of thromboxane B2 at 8 h postinjury. As examined by inhibitor experiments and northern blotting, cyclooxygenase-1 was responsible for the first phase, and cyclooxygenase-2 was involved in the second phase. On compression injury the levels of interleukin-1alpha and -1beta detected as mRNA and protein increased and peaked at 2-4 h. Injection of exogenous interleukin-1alpha into the spinal cord resulted in an increase of cyclooxygenase-2 mRNA content and a predominant production of 6-ketoprostaglandin F1alpha resembling the second phase of eicosanoid production. Concomitantly, extravascular migration of polymorphonuclear leukocytes was enhanced after the interleukin-1alpha injection. These cells together with vascular endothelial cells and glial cells were stained positively with an anti-cyclooxygenase-2 antibody. The results suggest that the immediate eicosanoid synthesis after spinal cord injury was due to the constitutive cyclooxygenase-1 and the delayed synthesis of eicosanoids was attributable to the induction of cyclooxygenase-2 mediated by interleukin-1alpha.     

Catalytic transfer hydrogenation on a hydrogen-absorbing alloy (CaNi5) using hydriding–dehydriding properties

By using the characteristics of a hydrogen-absorbing alloy, the hydrogen produced by catalytic dehydrogenation of saturated compounds can be absorbed to form metal hydrides, and, vice versa, the resulting metal hydrides are able to hydrogenate efficiently unsaturated compounds upon dehydriding. Gas-phase reactions between 2-butene and 2-propanol on a hydrogen-absorbing alloy CaNi₅ have been studied in the temperature range of 393–473 K. CaNi₅ showed interesting characteristics as an active catalyst for the catalytic transfer hydrogenation of butene from propanol as a hydrogen donor. 2-propanol was effectively dehydrogenated at 423 K to yield acetone in which the dissociated hydrogen was completely absorbed by CaNi₅ to form the metal hydride. When the alloy was hydrided to some extent, butene was hydrogenated by the absorbed hydrogen in the metal hydride to produce butane. The overall reaction on CaNi₅ was expressed as catalytic transfer hydrogenation of 2-butene from 2-propanol through intermediate formation of metal hydrides, rather than the direct reaction between butene and propanol on the alloy. Thus, CaNi₅ effectively repeated hydriding–dehydriding cycles: hydriding of CaNi₅ by 2-propanol dehydrogenation with subsequent dehydriding for the hydrogenation of 2-butene. The use of hydrogen-absorbing CaNi₅ provides a novel reaction system for the catalytic transfer hydrogenation. This revised version was published online in July 2006 with corrections to the Cover Date.     

Tunable wavelength filter using nano-sized droplets of liquidcrystal

An electrically tunable optical filter has been developed that uses a polymer containing fine droplets of nematic liquid crystal as the active cavity in a Fabry-Perot interferometer (FPI). This FPI filter, whose finesse was 62, had a free spectral range of 37 nm in the 1.55-μm range with a full-width at half maximum of 0.6 nm and a transmission loss of 2.4 dB. The polarization dependent loss was smaller than 0.17 dB. The transmitted peak wavelength decreased with an electric field. This resulted in a tuning range of 10 nm at 300 V. The switching time was about 370 μs     

Tumor necrosis factor-alpha regulates in vivo expression of the rat UCP family differentially

A family of uncoupling proteins (UCPs), free fatty acid anion transporters, plays a crucial role in energy homeostatic thermoregulation. Tumor necrosis factor-alpha (TNF-alpha), a member of the cytokine family, is well known as an endogenous pyrogen. To evaluate the interaction of TNF-alpha with UCPs in thermogenesis, effects of TNF-alpha on rat UCP gene expression were examined in intrascapular brown adipose tissue (BAT), epididymal white adipose tissue (WAT) and soleus muscle (Muscle). Administration of TNF-alpha elevated rectal temperature by 0.7 degree C as well as serum leptin which peaked at 6 h, compared with saline controls. BAT UCP1 mRNA expression was increased by 1.2-fold at 6 h after the TNF-alpha treatment and decreased by 0.8-fold at 16 h after the treatment. In contrast to UCP1 expression in BAT, UCP2 mRNA expressions in BAT, WAT, and Muscle was increased to reach maximum levels of 1.3-, 1.6- and 1.8-fold, respectively, at 16 h after the treatment. UCP3 mRNA in Muscle, but not in BAT or WAT, was exclusively up-regulated by 1.7-fold at 16 h after the treatment. These results indicate that TNF-alpha up-regulates UCP gene expression differentially and tissue dependently, and add novel insights into thermogenesis under conditions of malignancy and inflammation.