Property of TS-16N solid state nuclear track detectors as an imaging medium for macroautoradiography of alpha-emitters in biological specimens

Feasibility of TS-16N solid state nuclear track detectors for an imaging medium of rapid autoradiography of alpha-emitters is described. Though a little longer etching time was required, the contrast of autoradiographic image on this detector proved to be superior to CR-39 detectors whose property for macroautoradiography was previously reported by the authors. The resolutions of these two different type detectors were almost equivalent to each other. The autoradiography taken by way of trial proved that this detector could be used to study metabolism and dosimetry of internally deposited alpha-emitters. With further study, the inherent properties of this detector such as low background or high sensitivity should extend the field of track etch imaging technique such as fast neutron radiography.     

19F- and 1H-NMR spectra of tetrafluoroethylene–propylene copolymers

High resolution 94-MHz ¹⁹F- and 100-MHz ¹H-NMR spectra were measured on a series of tetrafluoroethylene (TFE)-propylene (P) copolymers having a range of composition (TFE/P molar ratio = 37/63–55/45) and polymerized at different temperatures (?23, 25 and 65°C). The spectra were analyzed in relation to copolymer compositions. The assignment of ¹⁹F resonance in terms of tetrads proposed previously was confirmed, and the tentative assignment of ¹H resonances was proposed in terms of triads. The spectra thus interpreted revealed the sequence distribution of the copolymers. Copolymer compositions calculated from NMR spectra and elemental analysis agreed rather well with each other. Monomer reactivity ratios were calculated from the sequence distributions and compared with those obtained from the elemental analysis. It was observed that highly alternating copolymers are obtained in this system over a wide range of monomer composition at lower temperatures and that a deviation from alternancy increases slightly with rising polymerization temperature.     

The Radiation-Induced Polymerization and Copolymerization of Butadiene in Emulsion

Abstract

The polymerization of butadiene in emulsion initiated by ^{6 0}Co gamma radiation has been studied in some detail. Similar studies with styrene and styrene-butadiene comonomer mixtures were also conducted. The rates of polymerization were found to be much lower than anticipated from the reported k_p values for butadiene and for the comonomer mixtures. Styrene, on the other hand, polymerizes at normal rates. A number of possible explanations for this behavior is discussed.     

Improvement of corrosion resistance of carbon steel using chemical vapor deposition from the mixture of Mo(CO)6 and Cr(CO)6 with an ArF-excimer laser

The corrosion resistance of carbon steel has been improved by the deposition from the mixture of Mo(CO)₆ and Cr(CO)₆ as well as from each carbonyl alone with an ArF-excimer laser (193 nm). The corrosion resistance attained by coating with the films from the mixture is higher than from Mo(CO)₆ alone, while lower than from Cr(CO)₆ alone. While the corrosion resistance increases with beam intensity monotonically over the range 4–25 MW cm^–2 for the deposition from Cr(CO)₆ alone, it tends to decrease slightly above 15 MW cm^–2 for the deposition from Mo(CO)₆ alone and from the mixture. SEM (Scanning Electron Microscope) photographs show that the films from each carbonyl and their mixture consist of small grains that are more densely packed at higher beam intensities. The comparison of the film thickness evaluated from sputtering time to remove the films with that from direct observation with SEM suggests that the density of the film increases with beam intensity. In the films deposited from the mixture, molybdenum is preferentially incorporated from the gas phase. Present name: Department of Quantum Engineering and Systems Science     

Status and dreams of photonics polymer for IT

We have proposed a low-loss, high-bandwidth and large-core graded-index plastic optical fiber (GI POF) in data-corn, area. The GI POF enables us to eliminate the “modal noise” problem which is observed in medium-core silica fibers. Therefore, stable high-speed data transmission can be realized by the GI POF rather than medium-core silica fibers. Furthermore, advent of perfluorinated (PF) polymer based GI POF network can support higher transmission than silica fibers network because of the small material dispersion of PF polymer compared with silica. In addition, we proposed a “highly scattering optical transmission (HSOT) polymer” and applied it to a light guide plate of a liquid crystal display backlight. The HSOT polymer backlight that was designed using the HSOT designing simulator demonstrated twice the brightness of the conventional taransparent backlight with sufficient color uniformity. Furthermore, we proposed the two types of zero-birefringence polymers synthesized by the random copolymerization method and the anisotropic molecule dopant method. Both of the polymers exhibited no orientational birefringence for any orientation of polymer chains.     

Radiation-Induced Copolymerization of Chlorotrifluoroethylene with Olefins

The copolymerizations of chlorotrifluoroethylene with propylene and isobutylene were carried out at 0 ～ ?78°C by γ-ray irradiation. It was found that alternating copolymers are obtained over a wide range of monomer composition for both systems. The alternating copolymer of chlorotrifluoroethylene with isobutylene was found to be highly crystalline, but the copolymer of chlorotrifluoroethylene with propylene was found to be amorphous. The copolymerizations were considered to proceed via a radical mechanism, but in the case of the isobutylene-chlorotrifluoroethylene system a cationic polymerization also takes place simultaneously at ?78°C.     

Phospholipid-linked quinones-mediated electron transfer on an electrode modified with lipid bilayers

Phospholipid-linked naphthoquinones separated by spacer methylene groups (C(n)), PE-C(n)-NQ (n=0, 5, 11), were synthesized to investigate the quinone-mediated electron transfers on a glassy carbon (GC) electrode covered with phospholipids membrane. The PE-C(n)-NQ could be incorporated in lipid bilayer composed of phosphatidylcholine and exhibited characteristic absorption spectral change corresponding to their redox state, quinone/hydroquinone. The cyclic voltammogram of PE-C(n)-NQ-containing lipid bilayer modified on a GC electrode indicated a set of waves corresponding to the consecutive two-electron and two-proton transfer reduction of the quinone moiety. The peak currents of PE-C(n)-NQ as a function of temperature showed a sharp break point in the current-temperature behavior, reflecting the gel-fluid phase transition. The shape of the cyclic voltammograms changed with the pH of the buffer solution. Below pH 6 the first step of the reduction of quinone was a monoprotonation of quinone, whereas above pH 10 the first step of the oxidation was a monodeprotonation of hydroquinone. This indicates that reaction sequences of quinone/hydroquinone were different with the change of the pH. These results showed that the PE-C(n)-NQ exhibited electron transfer associated with proton transfer in the lipid membranes, depending on the diffusivity of the redox species in the membrane and pH. Interestingly, less effect of the number of methylene of the spacer group on the peak currents was observed. Comparison of manganese porphyrin-mediated electron transfer that depends on the spacer methylene lengths [M. Nango, T. Hikita, T. Nakano, T. Yamada, M. Nagata, Y. Kurono, T. Ohtsuka, Langmuir 14 (1998) 407] is made.     

Efficient peroxide decoloration of azo dye catalyzed by polyethylene glycol-linked manganese chlorin derivative

We reported here that polyethylene glycol (PEG)-linked manganese pyrochlorophyllide a (PEG-MnPChlide a) possesses remarkable catalytic activity comparable to horseradish peroxidase (HRP). The PEG-MnPChlide a catalyzed the oxidation decoloration reaction of C.I. Acid Orange 7 by hydrogen peroxide under a mild aqueous condition, pH 8.0 at 25 °C. The manganese pyrochlorophyride a methylester (MnPChlide a ME) dissolved in a Triton X-100 micellar solution also exhibited the catalytic activity, indicating the micellar environment plays an important role in the catalytic reaction. The reaction rate was accelerated by addition of imidazole. The catalytic reactions were analyzed by Michaelis–Menten kinetics, revealing that the higher reactivity of catalyst–substrate complex is responsible for the present catalytic reaction system.     

Light-energy conversion systems for hydrogen production and photocurrent generation using zinc chlorin derivatives

To develop efficient systems for light-energy conversion, monomeric and dimeric zinc chlorin derivatives were synthesized. These derivatives act as photosensitizers for light-induced hydrogen production with methylviologen as the electron mediator and Pt nanoparticles as the hydrogen-evolution catalyst. The monomeric derivative exhibited ~1.5-times higher activity than the dimeric derivative. The photocurrent-generating activity of the Zn chlorin derivatives assembled on a chemically modified indium tin oxide electrode was investigated; the dimeric derivative exhibited significant activity compared to the monomeric derivative. The photosensitizing activity of the derivatives in dye-sensitized solar cells was also investigated. The dimeric derivative exhibited two-fold higher performance than the monomeric derivative. The dimerization effect on the photosensitizing activities is briefly discussed in terms of stacking conformations based on the results of absorption and fluorescence spectroscopies.     

Observation of stimulated Brillouin scattering in polymer optical fiber with pump-probe technique

Stimulated Brillouin scattering (SBS) in a perfluorinated graded-index polymer optical fiber (POF) with 120 μm core diameter was experimentally observed for the first time, to the best of our knowledge, at 1.55 μm wavelength with the pump-probe technique. Compared to spontaneous Brillouin scattering previously reported, the Brillouin gain spectrum (BGS) was detected with an extremely high signal-to-noise ratio, even with a short POF (1 m) and scrambled polarization state. We also investigated the BGS dependences on probe power and temperature, which indicate that SBS in a POF measured with this technique can be utilized to develop high-accuracy temperature sensing systems.