Incorporation of linoleic acid and its conversion to λ-linolenic acid in fungi

The incorporation of [1-¹⁴C]linoleic acid (LA) into lipids ofMortierella ramanniana var.angulispora was studied to determine which lipid classes participated in the δ6-desaturation of [1-¹⁴C]LA. [1-¹⁴C]LA was rapidly taken up into fungal cells and esterified into various lipids. Comparison of the profile of [1-¹⁴C]LA incorporation between fungal cells at the exponential growth phase and the stationary growth phase showed that [1-¹⁴C]LA incorporation into most lipids—except for triacylglycerol (TG) and phosphatidylcholine (PC)—were greatly reduced at the stationary growth phase. Desaturation of [1-¹⁴C]LA into λ-linolenic acid (GLA) readily occurred at the exponential growth phase, but was greatly decreased at the stationary growth phase. Moreover, pulse-chase experiments revealed that the radiolabel incorporated into phosphatidylserine (PS) and PC rapidly turned over, while that in TG and diacylglycerol (DG) accumulated after the 4 hr chase. In addition to the change of the radiolabel in individual lipids, the content of radiolabeled GLA converted from [1-¹⁴C]LA varied with individual lipids. In phospholipids such as PC, phosphatidylethanolamine (PE) and PS, radiolabeled GLA rapidly increased after 1 hr and then decreased after 4 hr. On the other hand, a gradual increase in radiolabeled GLA until 4 hr was observed in TG. These results suggest that LA, which has been esterified into phospholipids such as PC, PE and PS, is readily desaturated to GLA, which is then transferred to TG. These differences in the fate of GLA derived from LA between phospholipids and neutral lipids may be reflected in the GLA content in the individual lipids.     

Coal liquefaction using iron complexes as catalysts

Hydroliquefaction of Japanese Miike and Taiheiyo coals was carried out using various iron complexes as catalysts in tetralin at 375–445 °C. Iron pentacarbonyl (Fe(CO)₅) showed the highest catalytic activity, increasing coal conversion by about 10% at 425 °C under an initial hydrogen pressure of 5 MPa. Amounts of hydrogen transferred to coal increased from 1.4–2.3 wt% of daf coal in the absence of the catalyst to 2.5–4.2 wt% of daf coal in the presence of Fe(CO)₅ at 425 °C.     

Rapidly mixed combustion of hydrogen/oxygen diluted by N2 and CO2 in a tubular flame combustor

In this study hydrogen flames have been attempted in a rapidly mixed tubular flame combustor for the first time, in which fuel and oxidizer are individually and tangentially injected into a cylindrical combustor to avoid flame flash back. Three different cases were designed to examine the effects of fuel and oxidizer feeding method, diluent property, oxygen content and equivalence ratio on the characteristics of hydrogen flame, including the flame structure, lean extinction limit, flame stability and temperature. The results show that by enhancing mixing rate through feeding system, the range of equivalence ratio for steady tubular flame can be much expanded for the N₂ diluted mixture, however, at the oxygen content of 0.21 (hydrogen/air) the steady tubular flame is achieved only up to equivalence ratio of 0.5; by decreasing oxygen content, the lean extinction limit slightly increases, and the upper limit for steady tubular flame establishment increases significantly, resulting in an expanded tubular flame range. For CO₂ diluted mixture, the stoichiometric combustion has been achieved within oxygen content of 0.1 and 0.25, for which the burned gas temperature is uniformly distributed inside the flame front; as oxygen content is below 0.21, a steady tubular flame can be obtained from the lean to rich limits; and the lean extinction limit increases from 0.17 to 0.4 as oxygen content decreases from 0.21 to 0.1, resulting in a shrunk tubular flame range. Laminar burning velocity, temperature and Damköhler number are calculated to examine the differences between N₂ and CO₂ diluted combustion as well as the requirement for hydrogen-fueled tubular flame establishment.     

Effect of sesamin on mitochondrial and peroxisomal β-oxidation of arachidonic and eicosapentaenoic acids in rat liver

The effects of dietary sesamin on the hepatic metabolism of arachidonic (AA) and eicosapentaenoic (EPA) acids, were investigated with respect to their β-oxidation and secretion as triacylglycerol (TG). For 2 wk, rats were fed three types of dietary oils: (i) corn oil (control) group; (ii) FPA group: FPA ethyl esters/rapeseed oil=2∶3; (iii) AA group: AA ethyl esters/palm oil/perilla oil=2∶2∶1, with or without 0.5% (w/w) of sesamin. Dietary sesamin significantly increased the activities of hepatic mitochondrial and peroxisomal fatty acid oxidation enzymes (mitochondrial carnitine acyltransferase I, acyl-CoA dehydrogenase, and peroxisomal acyl-CoA oxidase). Dietary FPA increased mitochondrial carnitine acyltransferase I and peroxisomal acyl-CoA oxidase. Dietary AA, however, had an effect on peroxisomal acyl-CoA oxidase only. In whole liver and the TG fraction, EPA and AA concentrations were significantly increased by dietary EPA and AA, respectively, and were decreased by dietary sesamin. In hepatic mitochondria and peroxisomes, EPA concentration was increased by dietary EPA, but AA was not changed by dietary AA. The addition of dietary sesamin to the EPA-supplemented diet significantly decreased the EPA concentration compared to concentrations found with consumption of dietary EPA alone. These results suggest that sesamin increased β-oxidation enzyme activities and reduced hepatic EPA and AA concentrations by degradation. The stimulating effect of sesamin on β-oxidation, however, was more significant in the EPA group than in the AA group. Hepatic AA concentration was altered by the joint effect of sesamin through esterification into TG and the stimulation of β-oxidation.     

Synthesis of poly(hemispherand) via cyclopolymerization of diepoxide

Summary Cyclopolymerization of 2,6-bis[3-(4,5-epoxy-2-oxapentyl)-2-methoxy-5-methylphenyl]-4-methylanisole was carried out with cationic, anionic, and coordination catalysts. The polymers obtained with BF₃·OEt₂ or SnCl₄ in dichloromethane and with t-BuOK in DMSO were soluble in benzene, chloroform, and THF. The mole fractions of the cyclic units in these polymers were from 0.65 to 0.75. The resulting poly(hemispherand) bound alkali metal cations and the selectivity was in the order of Rb⁺>K⁺>Cs⁺>Na⁺>Li⁺.     

Evaluation of molecular orientation in injection molded parts with microscale features by Raman spectroscopy

Molecular orientation of polycarbonate (PC) in injection‐molded parts with microscale features was characterized by means of polarized Raman spectroscopy, and the relationship between microstructure and replication was discussed. The microscale feature size of continuous v‐groove was 20 μm in depth and 50 μm in width. PC injection‐molded parts were molded with various molding conditions. The molecular orientation distribution along flow direction on the cross‐section of molding parts were evaluated by the intensity ratio of the bands at 635 to 703 cm^?1 (I₆₃₅/I₇₀₃) in the Raman spectra. Molecular orientation along the flow direction inside the v‐groove was higher than that of the core and the opposite surface region. In particular, the highest molecular orientation was at the surface of the v‐groove. Among the injection molding conditions, the mold temperature showed significant effect on the molecular orientation and replication. Higher mold temperature caused high replication and low molecular orientation. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Elongational viscosity in the isothermal melt spinning of polypropylene

The elongational viscosity of polypropylene has been investigated by isothermal melt spinning, carried out over a range of experimental conditions. The filament diameter and the elongational force were measured for running filaments and the relationship between elongational viscosity and elongational strain rate reported. The elongational viscosity was observed to decrease in the vicinity of the spinneret and then remained constant before increasing along the thread line. An increase in elongational viscosity did not occur within the isothermal zone until the elongational flow was fully developed. The onset of an increase in elongational viscosity was determined from the constant total elongational strain. The degree of molecular orientation was also studied by birefringence measurements and was investigated as a function of elongational stress. At a high elongational stress, the relation between birefringence and elongational stress departed from linearity and exhibited a rapid increase which can be related to the increase in elongational viscosity.     

Diameter controlled growth of fullerene nanowhiskers and their optical properties

The diameters of C₆₀ nanowhiskers (C₆₀NWs), which are prepared by a simple liquid–liquid interfacial precipitation method, can be tuned appropriately by controlling the area size of liquid–liquid interface. The diameters of C₆₀NWs decrease with decreasing the area size of liquid–liquid interface. The electronic spectra of C₆₀NWs show a dependence on the diameters of C₆₀NWs, reflecting strength of interaction among the C₆₀ molecules in each C₆₀NW.     

Estimation of dehumidifying performance of solid polymer electrolytic dehumidifier for practical application

A two-layer model for a solid polymer electrolytic (SPE) dehumidifier is applied to a system in which the chamber to be dehumidified has some leakage area. By introducing this area, the attainable humidity in the chamber, which is the steady-state humidity to be attained after a long-time dehumidification, can be defined. Experimental results of dehumidification by an SPE dehumidifier are compared to the calculations based on the two-layer model for the SPE dehumidifier, which was presented in our previous paper. Equations for the two-layer model are simplified by making use of assumptions for the current characteristics and a constant environmental condition, and it is reduced to equations including a differential equation on the time variation of the humidity in the chamber. The differential equation to describe the attainable humidity in the chamber and time constant for the dehumidification is obtained. The current flowing in the dehumidifier under steady state conditions is also given as a function of the humidities in the spaces facing the anode and the cathode. A diagram to estimate the attainable humidity and the time required for dehumidification from the dehumidifying area and leakage area is also given.     

Optimization of optical filters for ITER edge Thomson scattering diagnostics

In the ITER edge Thomson scattering measurement system, polychromators with optical band-pass filters and avalanche photodiodes are planned to be used. In this paper, we optimized the transmission wavelength ranges of the optical filters by a numerical method. Since measurements in a high electron temperature range are required for the measurement system, the Thomson spectrum could overlap a strong line emission of D_α when the electron temperature is rather high. It is shown that a filter whose transmission wavelength range is shorter than D_α becomes important to decrease the measurement error in the high temperature range. Moreover, it is found that a filter whose transmission wavelength range is above 1064 nm (laser wavelength) is useful to improve the measurement accuracy, in particular, when the number of filters is more than six.