Preparation of thermoplastic elastomer from natural rubber grafted with polystyrene

Thermoplastic elastomer was prepared from deproteinized natural rubber (DPNR) by graft-copolymerization of styrene, which was performed onto rubber particles of about 1 μm in diameter in latex stage with tert-butyl hydroperoxide/tetraethylenepentamine as an initiator. Suitable initiator concentrations were determined to be 3.3 × 10⁻² and 20 × 10⁻² mol/kg-rubber for the graft-coplymerization of styrene of 1.5 and 5.5 mol/kg-rubber, respectively, in which conversion and grafting efficiency of styrene were more than 90 mol% and 80 mol%, respectively. The resulting polystyrene, grafted onto the rubber particles, was characterized by size exclusion chromatography after ozonolysis. Morphology of the DPNR grafted with polystyrene (DPNR-graft-PS) was observed by transmission electron microscopy (TEM). Change in morphology after processing the DPNR-graft-PS at 150 °C was associated with change in mechanical properties, i.e. stress at strain of 1 and stress at break. The outstanding mechanical properties, maintained even after processing, were assigned to the thermoplasticity of the DPNR-graft-PS, based on the high conversion and high grafting efficiency.     

Surface segregation of poly(2-methoxyethyl acrylate) in a mixture with poly(methyl methacrylate)

Poly(2-methoxyethyl acrylate) (PMEA) exhibits excellent blood compatibility. To understand why such a surface functionality exists, the surface of PMEA should be characterized in detail, structurally and dynamically, under not only ambient conditions, but also in water. However, a thin film of PMEA supported on a solid substrate can be easily broken, namely it is dewetted. Our strategy to overcome this difficulty is to mix PMEA with poly(methyl methacrylate) (PMMA). Differential scanning calorimetry and cloud point measurements revealed that the PMEA/PMMA blend has a phase diagram with a lower critical solution temperature. The blend surface was also characterized by X-ray photoelectron spectroscopy in conjunction with microscopic observations. Although PMEA is preferentially segregated over PMMA at the blend surface due to its lower surface free energy, the extent of segregation in the as-prepared films was not sufficient to cover the surface. Annealing the blend film at an appropriate temperature, higher than the glass transition temperature and lower than the phase-separation temperature of the blend, enabled us to prepare a stable and flat surface that was perfectly covered with PMEA.     

Sharp photonic Crystal Defect Modes and Their Response to Ultrashort Optical Pulses

Single photonic crystal defects based on an air-bridge structure were fabricated. We obtained sharp defect modes with quality factors higher than 600 and observed their response to ultrashort optical pulses by utilizing two-photon absorption.     

Optical Storage Media with Dye-Doped Minute Spheres on Polymer Films

We have fabricated a new optical storage media using minute spheres arranged on a surface relief grating (SRG). Using minute spheres as recording bits, we can limit recordable regions by sphere size, and can realize high resolution reproduction in the plane direction. Surface relief structures were made on a polymer thin film on which we performed diffusion arrangement and adsorptive fixation of minute spheres. The stability of the arranged spheres was confirmed for heating and washing. Furthermore, we used a dipping method for a more simple arrangement of minute spheres on a large area of the substrate and made a monolayer sample of the spheres. We were able to realize a highly sensitive reconstruction of the medium using a confocal optical system as a record and readout system.     

Diffusion controlled formation of husk-like microcapsules

 Solid microspheres consisting of thermal heterocomplex molecules made from heating a mixture of aspartic acid and proline were transformed into husk-like microcapsules in their aqueous suspensions when pH value increased. The thickness of the outer shell of the husk-like microcapsule decreased as pH increased. Formation of the husk-like microcapsules is discussed to be due to both diffusion of the constituent molecules from the inside of the microspheres and conformational changes of those molecules in the process. Received: 16 October 1996 Accepted: 16 January 1997     

Selection of spectral lines and transition probability data in plasma temperature measurements by photoelectric scanning spectrometry

A strict, comparative investigation of published transition probabilities for thermometric lines and an experimental study of determinations of plasma temperatures were made for improving the accuracy in temperature measurements by the well-known slope method. Four sets of FeI lines which satisfy the requirements for the thermometric lines were selected in the wavelength region of 200–400 nm. A statistical method was used to evaluate degrees of agreement among different sets of transition probabilities. In the experimental study, excitation temperatures of a stabilized arc plasma were determined from relative line-intensities recorded by photoelectric scanning spectrometry. In conclusion, two recommended combinations of lines and transition probability data are presented for the slope temperature measurement. Line pairs used in combination of selected transition probabilities suitable for the two-line method are also given.     

Molecular rotation and lattice dynamical properties for cyclodextrin-ferrocene and some its ring-substituted derivative clathrates

This paper reports the unusual relaxation effect in the⁵⁷Fe Mössbauer spectra of -cyclodextrin(-cyclopentadienyl)(-ethylcyclopentadienyl)iron(II) clathrate. At low temperatures it consists of a simple quadrupole doublet. However, the Mössbauer spectrum collapses to a broad peak at 320 K. This behavior is interpreted in terms of a model that a ferrocene molecule in the cavity of clathrate lattices rotates as temperature is raised. The relaxation reaches a critical rate, a lifetime of the excited nuclear state. The relaxation time for the reorientation of (-cyclopentadienyl)(-ethylcyclopentadienyl)iron(II) in a cavity was 1.2×10^–7 s at 320 K and a barrier to rotation of about 8.8 KJ/mol was estimated.