Characterization of phospholipid reverse micelles in relation to membrane processing of vegetable oils

Studies were conducted to determine the critical micelle concentration (CMC) of phospholipids in vegetable oils and the size of reverse micelles to understand their rejection phenomenon in the membrane process. The CMC values of phosphatidylcholine (PC) in triolein and phospholipids in crude soybean oil were determined to be 440 and 1020 mg/kg, respectively, by using TCNQ (7,7,8,8‐tetracyano‐quinodimethane) solubilization technique. The surface tension measurements of these samples gave similar values of CMC. From small‐angle X‐ray scattering (SAXS) analysis, the size of the PC micelles was determined to be in the range of 3.56 to 4.70 nm. The characterization of reverse micelles formed in the oil system was found useful in enhancing the understanding of the possible rejection phenomenon of phospholipids by non‐porous polymeric composite membranes used in our earlier studies on vegetable oils and in suggesting suitable types of membranes for the same.     

High-pressure synthesis and optical limiting property of cyclic diphenylacetylene oligomer

New conjugated oligomers were synthesized by reacting diphenylacetylene under high pressure of 0.13–0.76 GPa at 250 and 300°C for 1–10 h. The number-average molecular weight M _n, and the weight-average molecular weight M _w increased with pressure, but those values were independent of temperature and time (M _n, 320–490; M _w, 350–580). Elementary analysis, field desorption mass spectrometry, Fourier transform infrared, and ¹³C nuclear magnetic resonance experiments revealed that the oligomer above and including pentamer was a new compound having cyclic structure. Toluene solutions of the oligomer (400 M _n) contained within a quartz cell were irradiated with the pulse from a frequency-doubled Nd : Yag laser at 532 nm. The transmittance of the solution decreased with input fluence, and we observed an optical limiting property with saturated output fluence. As the concentration of the oligomer increased, the saturated output fluence decreased. The optical limiting property was analyzed according to the reverse saturable absorption mechanism. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68:129–135, 1998     

Development of high voltage harmonic measuring instruments for distribution systems using optical voltage sensor and current sensor

Application of an optical measuring technique was attempted in order to develop harmonic voltage and current measuring instruments for distribution systems. To develop the harmonic voltage measuring system using a Bi₁₂GeO₂₀ crystal as a sensing Pockels cell for high‐voltage distribution lines, zinc oxide elements were adopted as a voltage divider. Also, an optical current sensor system was improved on the harmonic current measuring system using an R₃Fe₅O₁₂ film as a Faraday device. In practical three‐phase distribution systems, the developed high voltage harmonic measuring devices using the optical voltage sensor and current sensor were compared with conventional harmonic analyzers for low voltage. As a result, it was confirmed that the developed high voltage harmonic measuring devices had satisfactory characteristics for practical use. © 1999 Scripta Technica, Electr Eng Jpn, 128(4): 84–93, 1999     

Development of an on‐line partial discharge monitoring system for gas insulated substations

This paper describes the results of tests and discussions carried out to develop a system for partial discharge monitoring in GIS. They include the propagation characteristics of partial discharge pulses in each GIS component, as well as the test results obtained using an actual 300‐kV GIS. We also report the results of verification test on the GIS partial discharge monitoring and location system developed by the authors. © 1999 Scripta Technica, Electr Eng Jpn, 129(2): 40–50, 1999     

High‐pressure synthesis of cyclic mesitylacetylene oligomer

Reaction of mesitylacetylene was carried out by annealing under high pressure (0.13 and 0.52 GPa). The products obtained were classified into soluble and insoluble products in chloroform. The insoluble product reacted under 0.13 GPa was the mesitylacetylene polymer. The soluble product reacted under 0.13 GPa was classified as the monomer and the oligomer [number‐average molecular weight (M̄_n): 390, weight‐average molecular weight (M̄_w): 453, Oligomer yield (O_y): 36%]. The oligomer yield was accelerated by pressure [pressure: 0.13–0.52 GPa, M̄_n: 390–315, M̄_w: 453–968, O_y: 36–98%]. Field desorption mass spectrum showed that the oligomer had cyclic structure. The result of the elementary analysis revealed that the insoluble product reacted under 0.52 GPa was a polycyclic aromatic compound. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 72: 1539–1542, 1999     

In situ Raman study on single- and double-walled carbon nanotubes as a function of lithium insertion

We investigated the electrochemical lithium ion (Li(+)) insertion/desertion behavior on highly pure and bundled single- and double-walled carbon nanotubes (SWNTs and DWNTs) using an in situ Raman technique. In general, two storage sites could host Li(+) in SWNT and DWNT bundles when varying an external potential: a) the outer surface sites, and b) the interstitial spaces within the bundles. The most sensitive changes in the tangential mode (TM) of the Raman spectra upon doping with Li(+) can be divided into two regions. The first region was found from 2.8 to 1.0 V (the coverage of Li(+) on the outer surface of a bundled nanotube) and was characterized by the loss of resonant conditions via partial charge transfer, where the G(+) line of the SWNT and the TM of the outer tube of DWNTs experienced a highly depressed intensity, but remained almost constant in frequency. The appearance of a Breit-Wigner-Fano (BWF) profile provided strong evidence of metallic inner tubes within DWNTs. The second region was observed when the applied potentials ranged from 0.9 to 0 V and was characterized by Li(+) diffusion into the interstitial sites of the bundled nanotube material. This phenomenon invoked a large downshift of the G(-) band in SWNTs, and a small downshift of the TM of the inner tube of DWNTs caused by expansion of the C--C bonds due to the charge transferred to the nanotubes, and the disappearance of the BWF profile through the screening effect of the interstitial Li(+) layers.