Determination of all elastic constants of orthotropic plate specimens from group velocity data

This paper presents a novel method of nondestructively determining all nine elastic constants of fiber-reinforced orthotropic plate specimens. Group velocities of bulk quasi-longitudinal (QL), pure transverse (PT), and surface skimming pseudo-longitudinal modes are measured in glass-fiber (GF) and carbon-fiber (CF) reinforced Poly Ether Ether Ketone (PEEK) specimens by a point-source/point-receiver (PS/PR) technique. First, the pure index longitudinal moduliC ₁₁,C ₂₂, andC ₃₃, are obtained from the longitudinal (L) group velocities measured in three principal directions. Next, the pure index shear moduli,C ₄₄,C ₅₅, andC ₆₆, are determined by measuring the shear horizontally (SH) polarized PT group velocities in the symmetry planes. Finally, the mixed index elastic constantsC _ij (i j) are calculated from QL group velocities measured in the symmetry planes and using analytic formulas.     

Mapping evapotranspiration using MODIS and MM5 Four-Dimensional Data Assimilation

Evapotranspiration (ET), the sum of evaporation from soil and transpiration from vegetation, is of vital importance in the hydrologic cycle and must be taken into consideration in assessments of the water resources of any region. The MODerate resolution Imaging Spectroradiometer (MODIS) sensor offers a promising opportunity for estimating daily ET with a 1 km spatial resolution, but is hampered by frequent cloud contamination or data gaps from other factors. In this study, 1) a stand-alone ET model was applied and tested during clear or partial cloudy sky conditions using MODIS-based inputs of land surface and atmospheric data and 2) meteorological simulations by using Four-Dimensional Data Assimilation (FDDA) system between MODIS and the 5th Generation Meso-scale Meteorological Model (MM5) was used in cloudy conditions to facilitate continuous daily ET estimates. The MODIS ET algorithm modified from Mu et al. (2007) is based on the Penman-Monteith equation and was applied to predict ET at flux measurement sites. This algorithm considers both the effects of surface energy partitioning processes and environmental constraints on ET. We devised gap-filling approaches for MODIS aerosol and albedo data that were identified as bottlenecks to determine retrieval rates of insolation and ET. MODIS-derived input variables (i.e., meteorological variables and radiation components) for estimating ET showed a good agreement with flux tower observations at each site. The retrieval rate of MODIS ET doubled at four flux measurement sites after gap-filling with negligible compensation was undertaken for accuracy. In spite of the high accuracy of MODIS-derived input variables, MODIS ET showed meaningful errors at the four flux measurement sites. These errors were mainly associated with errors in the estimated canopy conductance. During clear sky conditions, MODIS was used to calculate ET, while the MODIS-MM5 FDDA system provided input variables for the calculation of ET under cloudy sky conditions. The performance of the MODIS-MM5 FDDA system was evaluated by comparing ET based on MODIS, which showed a good agreement with the MODIS ET for various land cover types. Our results indicate that MODIS can be applied to monitor the land surface energy budget and ET with reasonable accuracy and that MODIS-MM5 FDDA has the potential to provide reasonable input data of ET estimation under cloudy conditions.     

A study of hypervelocity impact on cryogenic materials

This paper reports a result of hypervelocity impact experiments on cryogenically cooled aluminum alloys and a composite material. Experiments are carried out on a target palate at 122 K. Aluminum spheres at 1.95 km/s in 50 kPa air were impinged against the target plate at cryogenic temperature and the result was compared with room temperature target plates. Hypervelocity impact (HVI) processes were visualized with shadowgraph arrangement and recorded with high-speed video camera and to ensure the temperature dependence we compared HVI tests with metal target plates with AUTODYN 2D and SPH numerical simulations. We found that cryogenic impacts created slight differences of impact damage from room temperature ones, i.e., the shape and averaged diameters of HVI crater holes were less at cryogenic impacts.     

Thermodynamic evaluation of the phase equilibria and glass-forming ability of the Fe–Si–B system

A thermodynamic study has been carried out on the Fe–Si–B ternary system, which is important in the development of transformer core materials and Ni-based filler metals. A regular solution approximation based on the sublattice model was adopted to describe the Gibbs energy for the individual phases in the binary and ternary systems. Thermodynamic parameters for each phase were evaluated by combining the experimental results from differential scanning calorimetry with literature data. The evaluated parameters enabled us to obtain reproducible calculations of the isothermal and vertical section diagrams. Furthermore, the glass-forming ability of this ternary alloy was evaluated by introducing thermodynamic quantities obtained from the phase diagram calculations into Davies–Uhlmann kinetic formulations. In this evaluation, the time–temperature-transformation (TTT) curves were obtained, which are a measure of the time required to transform to the minimum detectable mass of crystal as a function of temperature. The critical cooling rates calculated on the basis of the TTT curves enabled us to evaluate the glass-forming ability of this ternary alloy. The results show good agreement with the experimental data in the compositional amorphization range.     

Pyrolysis Products of Lignin in Open and Sealed Vessels Studied by Py-GC-MS

The pyrolysis products of lignin in open and sealed vessels were studied by pyrolysis—gas chromatography—mass spectrometry (Py-GC-MS). Several kinds of phenolic derivatives were observed in the pyrolysates in both treatments, while phenolic compounds with alkenyl or acetyl groups had higher relative contents in the open vessel than those in the sealed vessel. Phenol and its alkyl or mono-methoxy substituted derivatives become the main pyrolysis products in the sealed vessel. Most of the lignin pyrolysis products in the open vessel could be detected by Py-GC-MS, but some active products would go through further reaction in the sealed vessel.     

Physiology and Pathophysiology of Heparan Sulfate in Animal Models: Its Biosynthesis and Degradation

Heparan sulfate (HS) is a type of glycosaminoglycan that plays a key role in a variety of biological functions in neurology, skeletal development, immunology, and tumor metastasis. Biosynthesis of HS is initiated by a link of xylose to Ser residue of HS proteoglycans, followed by the formation of a linker tetrasaccharide. Then, an extension reaction of HS disaccharide occurs through polymerization of many repetitive units consisting of iduronic acid and N-acetylglucosamine. Subsequently, several modification reactions take place to complete the maturation of HS. The sulfation positions of N-, 2-O-, 6-O-, and 3-O- are all mediated by specific enzymes that may have multiple isozymes. C5-epimerization is facilitated by the epimerase enzyme that converts glucuronic acid to iduronic acid. Once these enzymatic reactions have been completed, the desulfation reaction further modifies HS. Apart from HS biosynthesis, the degradation of HS is largely mediated by the lysosome, an intracellular organelle with acidic pH. Mucopolysaccharidosis is a genetic disorder characterized by an accumulation of glycosaminoglycans in the body associated with neuronal, skeletal, and visceral disorders. Genetically modified animal models have significantly contributed to the understanding of the in vivo role of these enzymes. Their role and potential link to diseases are also discussed.     

Oxidation kinetics for <Emphasis Type="Italic">cis</Emphasis>-9,<Emphasis Type="Italic">trans</Emphasis>-11 and <Emphasis Type="Italic">trans</Emphasis>-10,<Emphasis Type="Italic">cis</Emphasis>-12 isomers of CLA

The autoxidation processes of the cis-9,trans-11 (c9,t11) and trans-10,cis-12 (t10,c12) isomers of CLA were separately observed at ca. 0% RH and different temperatures. The t10,c12 CLA oxidized faster than the c9,t11 isomer at all tested temperatures. The first half of the oxidation process of t10,c12 CLA obeyed an autocatalytic-type rate expression, but the latter half followed first-order kinetics. On the other hand, the entire oxidation process of c9,t11 CLA could be expressed by the autocatalytic-type rate expression. The apparent activation energies and frequency factors for the autoxidation of the isomers were estimated from the rate constants obtained at various temperatures based on the Arrhenius equation. The apparent activation energies for the CLA isomers were greater than those for the nonconjugated n−6 and n−3 PUFA or their esters. However, the enthalpyentropy compensation held during the autoxidation of both the CLA and PUFA. This suggested that the autoxidation mechanisms for the CLA and PUFA were essentially the same.     

Guiding and blocking of highly charged ions through a single glass capillary

Highly charged ions produced in an electron beam ion trap, I^q+, q = 10-50, were transmitted through a tapered glass capillary having diameter of at the end. We found that for a particular beam current, there exists an optimum tilting angle of the capillary in which a steady output of ions is observed, while for smaller angles, the ion counts first rise, then gradually decay on a time scale of minutes. In the case of steady transmission, the charge state distribution is found to be slightly towards the lower side.     

Controlled radical polymerization with polyolefin macroinitiator: a convenient and versatile approach to polyolefin-based block and graft copolymers

This paper introduces the new synthetic methodology of polyolefin-based block and graft copolymers with polar segments [e.g., polystyrene and poly(meth)acrylates]. Various brominated polyolefins were prepared by bromination of polyolefins with N-bromosuccinimide. The resulting brominated polyolefins were able to initiate the controlled radical polymerization of polar monomers, such as methyl methacrylate, ethyl acrylate, t-butyl acrylate, styrene and 2-(dimethylamino)ethyl acrylate, using a CuBr/N,N,N′,N″,N″-pentamethyldiethylenetriamine catalyst system, leading to a variety of polyolefin-based copolymers with a different content of the corresponding polar segment. Because of the accessible synthesis of polyolefin macroinitiators, this synthetic methodology is expected to result in the preparation of a wide range of polyolefin-based block and graft copolymers.     

Classification of Geothermal Energy Resources in Japan Applying Exergy Concept

Higher demand for energy consumption and importance of environmental issues has encouraged researchers and policy makers to consider renewable energies more seriously. Geothermal resources are a green energy source that can make a considerable contribution in some countries. Japan has the third ranking geothermal energy potential, and its geothermal electricity production is currently eighth in the world. Since the nature of geothermal resources dictates its method of utilization, it is important to categorize available resources. There is no consensus on classification of geothermal resources. Most scientists, from geologist to engineers, agree on the term temperature. However, temperature or enthalpy alone cannot describe the nature of fluids; they can have same temperature with different phases, such as saturated water or saturated steam. Using exergy for resource classification benefits their comparison, according to their ability to do work. In this paper, exergetic classification of geothermal resources was applied to 18 under‐operating geothermal power plants in Japan. Six geothermal fields have high exergy resources according to their SExI values in excess of 0.5. The remaining geothermal fields in Japan are classified in the medium resources zone. Classification results can be used by decision makers as a reference for future geothermal development. Copyright © 2012 John Wiley & Sons, Ltd.