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1.
Ryohei Tsuda Sayaka Kaino Hisashi Kokubo Shin-Ichiro Imabayashi Masayoshi Watanabe 《Colloids and surfaces. B, Biointerfaces》2007,56(1-2):255-Optics
Redox properties of phenothiazine-labeled poly(ethyl glycidy ether)-block-poly(ethylene oxide) (PT-EGEn-b-EOm) are reversibly changed by core-shell micelle formation. In the temperature range higher than the critical micellization temperature (cmt), the anodic potential of PT group positively shifts and concomitantly its anodic current decrease, or levels off compared to those of the reference polymer PT-EOm without the thermo-responsive EGEn segment. The former alteration is caused by incorporation of hydrophobic PT groups into a core of the micelle and the latter by the decrease in the diffusion coefficient of PT groups due to formation of the core-shell micelles. The cmt value and the temperature-dependent alteration in the redox properties strongly depend on the polymer structure, especially the length of thermo-responsive EGEn segment. The electrochemically determined hydrodynamic radii of the polymer aggregates seem to be overestimated, compared to the values reported for the aggregates of other thermo-responsive polymers with similar molecular weights, implying the presence of electrochemically inactive PT groups in the copolymers having longer thermo-responsive segments. 相似文献
2.
Md. Nur Alam Per B. Zetterlund Masayoshi Okubo 《Journal of polymer science. Part A, Polymer chemistry》2007,45(21):4995-5004
Bimolecular termination in nitroxide‐mediated radical polymerization in miniemulsion has been investigated through the heating of a polystyrene–2,2,6,6‐tetramethylpiperidinyl‐1‐oxy macroinitiator and its 4‐hydroxy‐2,2,6,6‐tetramethylpiperidinyl‐1‐oxy analogue in an aqueous toluene dispersion with sodium dodecyl benzenesulfonate as a surfactant at 125 °C. The level of bimolecular termination by combination, evaluated from the high‐molecular‐weight shoulder, was higher in miniemulsion than in solution and increased with decreasing particle size. Quantitative analysis revealed that these results cannot be rationalized solely by nitroxide partitioning to the aqueous phase. The results are explained by an interface effect, by which nitroxide is adsorbed or located at the aqueous–organic interface. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4995–5004, 2007 相似文献
3.
Masayoshi Senba 《Hyperfine Interactions》1994,87(1):959-964
A study has been made of highly nitrogenated pure iron and iron-aluminum alloy powder containing 2 wt.% Al (Fe-2Al) using Mössbauer spectroscopy and X-ray diffraction. The samples were prepared by high-temperature, high-pressure diffusion of nitrogen. They were prepared in a hot-isostatic-pressure (HIP) furnace at 1000 °C at nitrogen pressures up to 200 MPa. The alloy powders contained up to 8 at.% nitrogen as determined by vacuum fusion analysis. XRD analysis indicates that for the pure iron powders, the lattice spacing remained independent of nitrogen concentration, but that for the Fe-2Al powders, it decreased with increasing nitrogen concentration. Mössbauer analysis showed that for the pure iron powders, most of the nitrogen was associated with the formation of the iron nitride Fe4N. For the alloy powders containing less than 5 at.% nitrogen, all of the nitrogen was contained interstitially. The presence of nitrogen completely eliminated the conduction-electron spin-density oscillations observed in many ferromagnetic alloys. 相似文献
4.
Masahiro?Okada Takumi?Matoba Masayoshi?OkuboEmail author 《Colloid and polymer science》2003,282(2):193-197
The influence of nonionic emulsifier, included inside styrene-methacrylic acid copolymer [P(S-MAA)] particles during emulsion copolymerization, on the formation of multihollow structure inside the particles via the alkali/cooling method (proposed by the authors) was examined in comparison to emulsifier-free particles. It was clarified that the nonionic emulsifier included inside the P(S-MAA) particles eased the formation of multihollow structure.Part CCL of the series studies on suspension and emulsion 相似文献
5.
Production of polyacrylonitrile particles by precipitation polymerization in supercritical carbon dioxide 总被引:2,自引:0,他引:2
Masayoshi?OkuboEmail author Syuji?Fujii Hiroshi?Maenaka Hideto?Minami 《Colloid and polymer science》2003,281(10):964-972
Polyacrylonitrile particles were produced by precipitation polymerization of acrylonitrile (AN) without any colloidal stabilizer in supercritical carbon dioxide as a polymerization medium at about 30 MPa for 24 h at 65 °C at different initiator concentrations (0.8–45.2 mmol/l) and at different AN concentrations (10–40% w/v). An increase in the initiator concentration led to increases in the conversion and in the degree of coagulation and to a decrease in the molecular weight. At AN concentration of 20% w/v, micron-sized, relatively monodisperse polyacrylonitrile particles with clean and uneven surfaces were produced. 相似文献
6.
Tomoya Kinumi Kazuo Tsujimoto Mamoru Ohashi Reiko Hara Tomiyuki Hara Koichi Ozaki Miho Saka Yuko Katsuta Akimori Wada Masayoshi Ito 《Photochemistry and photobiology》1993,58(3):409-412
Abstract— 3, 7-Dimethyl-2, 4, 6, 8, 10-dodecapentaenal was synthesized for reconstitution of the retinochrome analog. Its opsin shift was 1000 cm 1 smaller than that of native retinochrome, whose chromophore contains the same number of double bonds. The conformational change from 6-s-trans to 6-s-cis , as figured in a retinal molecule, plays an important role in the formation of the retinochrome analog, based on the estimation of opsin shifts for retinal analogs locked in the 6-s conformation. Thus the conformation of the 6–7 single bond in the native retinochrome was suggested to be 6 -cis . Analysis of the circular dichroic spectra of retinochrome analogs revealed that the 6-s conformation is independent of the appearance of the β-band. The stereoselectivity in the photoisomerization of the retinal analogs by a retinochrome template depends on the hydrophobic binding in the region of the β-ionone ring. 相似文献
7.
Akira Matsumoto Hisako Mano Masayoshi Oiwa George B. Butler 《Journal of polymer science. Part A, Polymer chemistry》1989,27(6):1811-1816
The radical polymerization of tetraallyl ammonium chloride (TAAC) was carried out in water using azo-initiator as compared to that of diallyl dimethyl ammonium chloride (DADMAC); the rate of polymerization was quite low for TAAC, around one-third of DADMAC. Kinetic discussion revealed the importance of degradative chain transfer in the polymerization of TAAC. The cyclopolymerizability of TAAC was estimated kinetically as the ability of 5-membered monocyclic radical to form a bicyclic ring, giving the cyclization constant of 21 mol/L at [M] = 2 mol/L. Gelation occurred at around 20% conversion. 相似文献
8.
Tetsuji Ohata Akira Matsumoto Masayoshi Oiwa 《Journal of polymer science. Part A, Polymer chemistry》1980,18(2):467-475
In order to elucidate the effect of the hydroxyl group on the polymerization of diallyl hydroxydicarboxylates, we investigated in detail the radical polymerizations of diallyl succinate (DASu), diallyl malate (DAMa), and diallyl tartrate (DATa), each of which have similar structure differing only in the number of hydroxyl groups present. The rate of polymerization (Rp) was quite enhanced in the order DASu < DAMa < DATa, in accord with the increase in the number of hydroxyl groups within a monomer unit. The enhanced ability of the allylic monomer radical to reinitiate chain growth was also in the same order, as was clear from the dependence of Rp on the initiator concentration. The dependence of the residual unsaturation of the polymer on the monomer concentration in the polymerizations of DAMa and DATa was abnormal in terms of cyclopolymerization. These results are discussed in connection with the formation of the intermolecular hydrogen bond through the hydroxyl groups. 相似文献
9.
Masayoshi Watanabe Tadashi Iida Kohei Sanui Naoya Ogata Tadahiko Kobayashi Zentaro Ohtaki 《Journal of polymer science. Part A, Polymer chemistry》1984,22(6):1299-1307
Novel polyamides that contain tetrathiafulvalene (TTF) moieties were synthesized by direct polycondensation of Δ2,2′ -bi-1,3-dithiole-4,4′(5′)-dicarboxylic acid with aromatic diamines in the presence of triphenylphosphine, hexachloroethane, and pyridine. Complexes of these polyamides with bromine were TTF cation radical () salts which resulted from the charge transfer of TTF moieties to bromine. The electrical conductivity of undoped polyamides increased with a decrease in diamine length. By doping the bromine the conductivity of the polyamides was enhanced by 3–5 orders of magnitude and reached 10?5–;10?9S cm?1. Maximum conductivity was observed at the doping ratio of [Br]/[repeat unit] < 1. The electrical conduction in the bromine complexes may be attributed to the hopping of odd electrons of between TTF moieties. 相似文献
10.
Yumi Arai Masayoshi Watanabe Kohei Sanui Naoya Ogata 《Journal of polymer science. Part A, Polymer chemistry》1985,23(12):3081-3093
Polycondensation methods greatly influence the molecular weight distribution of poly(hexamethylene sebacamide) (nylon 610) as determined by gel permeation chromatography (GPC). The ratio of weight average molecular weight to number average molecular weight (Mw/Mn) was used as a measure for estimating the molecular weight distribution. The Mw/Mn ratios of nylon 610 obtained from melt, solid phase, and high temperature polycondensation methods were 2 to 3.5, which were expected values for the most probable distribution. However, those for polymers obtained from the direct polycondensation in the presence of triphenylphosphine, interfacial polycondensation and low temperature polycondensation using an acid chloride varied over a wide range from 3.5 to 8.5. The effect of the kind of organic solvents in the interfacial method on the Mw/Mn ratios was especially large, and the molecular weight distribution could be controlled to some extent by selecting an appropriate solvent. 相似文献