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.     

A stable silicon congener of highly strained bicyclo[3.2.0]hepta-1,3,6-triene

A silicon-containing fused bicyclic compound with a highly strained bridgehead double bond, 2,3,6,7-tetra-tert-butyl-4-(tert-butyldimethylsilyl)-5-(tert-butyldimethylsiloxy)-5-silabicyclo[3.2.0]hepta-1,3,6-triene (2), was synthesized quantitatively by the reaction of 1,2-bis-tert-butyl-4,4-bis(tert-butyldimethylsilyl)-4-silatriafulvene (3) with di-tert-butylcyclopropenone (4) at 80 degrees C. An X-ray crystallographic analysis for 2 not only confirmed a bicyclic structure having a silacyclopentadiene (silole) ring fused with a silacyclobutene ring but also the remarkable deformation around the double bonds; the sum of the bond angles around the unsaturated bridgehead carbon was 333 degrees . The strain energy of a model 5-silabicyclo[3.2.0]hepta-1,3,6-triene was calculated at the MP2/6-31+G(d,p)//B3LYP/6-31+G(d) level (30.2 kcal/mol) to be comparable to that for parent bicyclo[3.2.0]hepta-1,3,6-triene (30.7 kcal/mol). Despite the high steric strain, 2 was stable enough to be kept intact for several months in the air. The high stability is ascribed to the effective steric protection of the ring system by the bulky substituents.     

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.     

Preparation and structures of novel silamacrocyclic compounds: silacalix[4]quinone and silacalix[4]hydroquinone octamethyl ether

X-ray crystallographic analysis revealed that novel silamacrocyclic compounds, 2,8,14,20-tetrasilacalix[4]quinone and 2,8,14,20-tetrasilacalix[4]hydroquinone octamethyl ether, adopted 1,3-alternate structures in the solid state.     

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     

Changes in light scattering from poly(ethylene terephthalate) and nylon 6 films upon stretching in relation to the deformation mechanism

Unoriented T-die flat films of nylon 6 and PET films annealed at 90°C were stretched in water at 80°C. Amorphous PET films were stretched in water at 65–75°C. Changes in the light scattering patterns from these samples upon stretching were investigated. One of the observed LS patterns from the stretched samples is the H_v eight-leaf pattern consisting of four lobes and streaks. In the nylon 6 and heat-treated PET showing this pattern, spherulitic patterns can be seen in polarization microscopy. The microscopic spherulitic superstructure may possibly be the factor responsible for producing the lobe-and-streak pattern. On the other hand, many microscopic eight-leaf patterns can be observed in amorphous unannealed PET showing the lobe-and-streak pattern. These microscopic patterns are due to retardation at stress concentrations around impurities and nuclei. The superstructure giving these microscopic patterns must be the origin of the lobe-and-streak pattern from unannealed PET. Another scattering pattern, the V_v cruciform pattern, was observed in both stretched nylon 6 and unannealed PET. This pattern is due to an orientation change across the slip lines observed under a polarizing microscope. It is noted (1) that the appearance of the slip lines in PET coincides with the occurrence of oriented crystallization on stretching, (2) that the lobe-and-streak pattern from PET in which orientation crystallization has taken place is fairly stable to heat treatment and does not disappear until just before melting, and (3) that the superstructures produced at low stretching seem to be deformed on further stretching, in accordance with affine deformation theory.     

Chemorheology of linear polymers

The structural changes brought about by chemical reactions are reflected in the viscoelastic behavior of polymers. Viscoelastic behavior induced by such chemical reactions is called chemorheology. This phenomenon is not readily observed in linear polymers, because molecular flow by diffusion is generally much more rapid than relaxation or flow caused by chemical reaction. It has become possible, however, to treat chemorheology of linear polymers theoretically by taking such physical flow into consideration. The experimental results for linear polystyrene compared with the theoretical ones are described in this paper. Good agreement between theoretical results and experimental ones is obtained for monodisperse polystyrene with low concentration of accelerators.     

The viscoelastic behavior of poly(isobutylene oxide) exposed to UV irradiation

The stress relaxation of poly(isobutylene oxide) in air was measured while it was exposed to UV irradiation. It was found that the relative stress increased markedly and the polymer degraded extensively with UV irradiation time. In other crystalline polymers that degrade easily, e.g., polyoxymethylene and polypropylene, the relative stress increased somewhat. However, such behavior was not found in another crystalline polymer that was difficult to degrade, polyethylene. It was also found that the increase in the relative stress depended on the strain imposed on the sample, exposure temperature, the degree of crystallinity of the sample, the degree of initial degradation of the sample, and the degree of orientation of the chain molecules in the sample. However, these changes were insignificant in experiments performed under N₂.