Concentration of docosahexaenoic acid in glyceride by hydrolysis of fish oil withcandida cylindracea lipase

In an attempt to concentrate the content of DHA (docosahexaenoic acid) in a glyceride mixture containing triglyceride, diglyceride and monoglyceride, fish oil was hydrolyzed with six kinds of microbial lipase. After the hydrolysis, free fatty acid was removed and fatty acid components of the glyceride mixtures were analyzed. When the hydrolysis withCandida cylindracea lipase was 70% complete, the DHA content in the glyceride mixture was three times more than that in the original fish oil. The EPA (eicosapentaenoic acid) content became almost 70% of the original fish oil. Hydrolysis with other lipases did not result in an increase in the DHA content in the glyceride mixtures. Hydrolysis of DHA-rich tuna oil (DHA content is about 25%) withCandida cylindracea lipase resulted in 53% DHA in the glyceride mixture. The EPA content, however, remained close to that of the original tuna oil. In this report, the acyl chain specificity of lipases is evaluated in terms of hydrolysis resistant value (HRV). HRV is the ratio between the DHA contents in the glyceride mixture of hydrolyzed oil and original oil. HRV clearly indicates differences in hydrolysis between DHA and other fatty acids (e.g., saturated and monoenoic acids).     

Preparation and characterization of membranes with positively charged main chain from polyethylenimine

A membrane, which has positively charged groups in the polymer main chain, was prepared from polyethylenimine by crosslinking and successive alkylation. Dibromoalkane was used as a crosslinking agent. The crosslinked membrane was alkylated using methyl iodide under several conditions. Elemental and ICP emission analyses were introduced to measure the rates of alkylation and quaternization. From the membrane potential measurement, the effective charge density was estimated. The highest value was about 1.0 M, which was obtained by a prolonged alkylation time. This value was larger than that of some commercial ion exchange membranes. The effective charge density, which was obtained by the last alkylation procedure, was 10 times larger than that of the former one, though the rate of quaternizing increased by less than a factor of two. This implies that the activity constant in the membrane increased when the charge density is increased. © 1993 John Wiley & Sons, Inc.     

Physicochemical properties of rare earth perovskite oxides used as gas sensor material

The change of the conductivity in the rare earth perovskite oxide took place after the chemisorption of flammable gases. The sensitivity for methanol was highest. From the conductivity change of these perovskite oxides after the injection of methanol, the energy needed to promote an electron from a conducting to a nonconducting state, E=E _c-E _t, could be derived from the equation=A ₀ exp (–E/kT). LnCoO₃ had the smallest E and H (metal-O), which is the binding energy of oxygen coordinating to the metal ions, but exhibited the highest activity for gas sensing. The gas sensing mechanism was also considered.     

Radiation grafting of α,β,β-trifluoroethylenesulfonyl fluoride onto low-density polyethylene film by simultaneous irradiation method. I. Kinetic study of simultaneous-irradiation grafting

α,β,β-Trifluoroethylenesulfonyl fluoride (TFESF) was grafted onto polyethylene (PE) film by a simultaneous-irradiation method. The influences of the grafting conditions were analyzed kinetically. The dependencies of the grafting rate on the dose rates and monomer concentrations ranging from 10 to 75% were found to be of 1 and 0 order, respectively. The overall activation energy for the graft polymerization was 2.05 × 10⁴ J/mol. The grafting rate was found to be independent of the film thicknesses ranging from 25 to 100 μm.     

Nanogrinding of multi-layered thin film amorphous Si solar panels

Nanogrinding was performed on the cross-sections of amorphous Si thin film solar panels, which are nanoscale multi-layer structures consisting of hard and brittle materials. The deformed structures of the panel cross-sectional surfaces after grinding were investigated using electron and atomic force microscopy. The nanogrinding results were compared with those obtained from polishing and nanoscratching, demonstrating that the three processes had produced consistent surface characteristics. Though nanogrinding produced nanometric surface roughness with ductile material removal, but could cause cracking, edge chipping and delamination at thin film interfaces. The results of this work are of value for developing the efficient machining process for thin film solar panels and other brittle multi-layer materials.     

Fabrication and characterizations of PCDTBT: PC71BM bulk heterojunction solar cell using air brush coating method

Organic solar cells have been significantly attracted due to the need to develop an inexpensive clean and sustainable renewable energy source. We report on the fabrication of poly [N-9″-hepta-decanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)]/[6, 6]-phenyl-C₇₁-butyric acid methyl ester blend active layer using airbrush spray-coating method in mixed solvents. Optical absorption of the active layers was analyzed using UV–visible spectral studies in the wavelength range from 300 to 800 nm. The surface morphology of the active layers deposited with different parameters (spraying time and substrate-nozzle distance) was examined using atomic force microscopy. The current density–voltage (J–V) characteristics of photovoltaic cells were measured under the illumination of simulated solar light with 100 mW cm^?2 (AM 1.5G) by an Oriel 1000 W solar simulator. The power conversion efficiency of the solar cell is more than 5 %.     

Study of crater formation and sputtering process with large gas cluster impact by molecular dynamics simulations

Molecular dynamics (MD) simulations of large argon clusters impacting on silicon solid targets were performed in order to study the transient process of crater formation and sputtering. The MD simulations demonstrate that the initial momentum of incident cluster is transferred to target surface atoms through multiple collision mechanism, where the initial momentum, which is along to the surface normal before impact, is deflected to lateral direction. This momentum transfer process was analyzed by the calculation of the velocity at the crater edge (the interface between cluster and target). In the case of Ar₁₀₀₀ cluster impact on Si(1 0 0) target at low energy per atom less than 40 eV/atom, the maximum value of lateral velocity of the crater edge increases in proportional to the velocity of incident cluster atoms. On the other hand, the crater edge velocity saturates over 40 eV/atom of incident energy per atom. In this case, the whole of constituent cluster atoms are implanted into the target and expand in both lateral and reflective directions at the subsurface region of the target. These MD simulations demonstrated that this collisional process result in the high yield sputtering of the target atoms.     

Thermally assisted recording of holographic gratings in semicrystalline azobenzene-containing polymers

We examine optically induced birefringence in semicrystalline azopolymer films that are held at glass-transition temperature Tg. The birefringence increases markedly after interception of the pump beam; the saturation value depends on exposure time. In addition, the induced birefringence is completely erased by irradiation with a circularly polarized beam at Tg. Using this thermally assisted method, we demonstrate the holographic recording of a test image. The intensity of the diffracted beam also increases after interception of the writing beams. Furthermore, the retrieved image is found to have a resolution of approximately 30 lp/mm. This resolution is comparable with that of the optical setup that is used. Accordingly, the thermally assisted recording by use of semicrystalline azopolymers is a promising method for reversible holographic storage.