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51.
Yoshitaka Ogiwara Yukie Ogiwara Hitoshi Kubota 《Journal of polymer science. Part A, Polymer chemistry》1968,6(6):1489-1499
Efforts were made in the present study to elucidate the mechanism of graft copolymerization of cellulose in the presence of a ceric salt as initiator. When cellulose is treated with an aqueous solution of the ceric salt, ceric ion is consumed in a roughly first-order reaction in the oxidation of cellulose and in the adsorption on cellulose, and the ratio of the rate constants of oxidation and adsorption is about 1:3 in the case of sulfite pulp. Ceric ion is adsorbed so strongly on cellulose as not to be readily desorbed by treatment with water, dilute acid, or dilute alkali. The number of moles of adsorbed ceric ion was approximately equal to the number of moles of the total carbonyl groups in the cases of cotton and sulfite pulp, which are low in hemicellulose content, and was several times as large in the cases of kraft pulp and semichemical pulp, which contain about 22% hemicellulose. In these samples, however, it was interesting to note that the amount of the adsorbed ceric ion was roughly equal to the amount consumed in oxidation. Cellulose on which ceric ion is adsorbed reacts with methyl methacrylate to yield graft copolymers; a higher molecular weight of grafts, smaller number of grafts, and lower graft efficiency than in a standard polymerization were observed. Since the stability of the adsorbed ceric ion is high, a contribution of the adsorbed ceric ion to the graft copolymerization appears small, and the oxidation reaction, which proceeds slightly more slowly than adsorption, seems more important to the graft copolymerization. 相似文献
52.
Yutaka Ado Yukie Suzuki Toshio Tadokoro Kazuo Kimura Hirotoshi Samejima 《Applied biochemistry and biotechnology》1979,4(1):43-55
A number of fermentative methods for the production of various important nucleotides from their precursors have been developed in Japan, and some of these nucleotides have been industrially produced for more than a decade. For the production of these nucleotides, required ATP is usually supplied to the fermentation media either exogenously or by the naturally occurring ATP regenerating system involved in microbial cells. In this paper, the authors describe an attempt to immobilize ATP-regenerating microbial cells and then utilize such immobilized cells for the continuous production of various nucleotides. 相似文献
53.
Shigeyuki S
miya Takao Kumaki Kazumitsu Hishinuma Zenjiro Nakai Tokuji Akiba Yukio Suwa 《Progress in Crystal Growth and Characterization of Materials》1991,21(1-4):195-198
Since 1980 much attention has been payed to hydrothermal processing. There are several papers related to hydrothermal fine Zirconia powders by authors 1), 2), 3) and 3).
The authors 3) prepared ZrO2 and Y2O3-ZrO2 powders under hydrothermal conditions. Several methods were used to prepare fine ZrO2 powders under hydrothermal conditions: hydrothermal precipatation, hydrothermal crystallization, hydrothermal oxidation, hydrothermal decomposition, hydrothermal synthesis, hydrothermal anodic oxidation, RESA (reactive electrode submerged arc) process, etc.
This paper describes hydrothermal precipatation processing of ZrO2 and Y-ZrO2 powder. 相似文献
54.
Takeshi Suwa Terutaka Watanabe Tadao Seguchi Jiro Okamoto Sueo Machi 《Journal of polymer science. Part A, Polymer chemistry》1979,17(1):111-127
The size, distribution, and number of PTFE particles formed by radiation-induced emulsifier-free polymerization were measured by electron microscope and automatic particle analyzer (centrifugation method). From the electron micrographs we found that the particles are formed within 5 min. The change in the number of polymer particles (np) with reaction time (t) depends on the relative concentration of growing polymer chains to stabilizing species produced by the radiolysis of water and monomer; that is, it was governed by TFE pressure/dose rate ratio and classified into three cases: case I, dnp/dt = 0 (e.g., at 3 × 104 rad/hr and 20 kg/cm2); case II, dnp/dt < 0 (e.g., at dose rate below 1.9 × 104 rad/hr and 20 kg/cm2); case III, dnp/dt > 0 (e.g., at 3 × 104 rad/hr and 2 kg/cm2). The polymer molecular weight above 106 is almost independent of the particle size. The polymerization loci are mainly on the surface of polymer particles dispersed in the aqueous phase in cases I and II except in the initial stage. In case III new particles are formed successively during polymerization. Therefore the polymerization loci are mainly in the aqueous phase. Especially in case I, we concluded that after the generation of particles the propagation proceeds mainly on the surface of polymer particles like the core shell model proposed by Granico and Williams. 相似文献
55.
Takeshi Suwa Tadao Seguchi Masaaki Takehisa Sueo Machi 《Journal of Polymer Science.Polymer Physics》1975,13(11):2183-2194
Melting and crystallization behavior of polytetrafluoroethylene as polymerized in emulsion and suspension is shown to depend on molecular weight. DSC heating curves for virgin PTFE with low molecular weight below 3 × 105 have a single peak, whereas curves for higher molecular weight samples have double peaks. With increasing heating rate the areas of higher melting peaks become larger than the lower melting peaks. The morphology of polymer exhibiting double melting peaks is mainly folded ribbons or granular particles. The phenomenon of double melting is explained on the basis of two different crystalline states which correspond to the “fold regions” and the “linear segments” in a folded ribbon. The melting temperature of virgin PTFE is almost constant at ca. 330°C for molecular weights below 1 × 106, and rises as the molecular weight increases above 1 × 106. The heat of melting of virgin PTFE is nearly independent of molecular weight. On the basis of these results, we propose a model for melting and crystallization of low and high molecular weight PTFE and for the crystal structure. 相似文献
56.
Mukai C Kobayashi M Kubota S Takahashi Y Kitagaki S 《The Journal of organic chemistry》2004,69(6):2128-2136
A new procedure for constructing monocyclic five- and six-membered azacycles by the endo-mode ring-closing reaction of allenylazido derivatives under neutral conditions has been developed. The azabicyclo[m.n.0] compounds were prepared by applying this newly developed procedure. The seven-membered azacycle was prepared when the allene possessing an unsubstituted carboxyl amido functionality was submitted to the basic conditions. In addition, indole and quinoline skeletons were synthesized using this procedure. 相似文献
57.
Masakatsu Matsumoto Naoyuki Hoshiya Ryo Isobe Yukie Watanabe Nobuko Watanabe 《Tetrahedron letters》2004,45(20):3895-3898
2-(Buta-1,3-dienyl)-3-methylpyrazines (5) and 3-(buta-1,3-dienyl)-4-methyl-1,2,5-oxadiazoles (10) were synthesized starting from base-induced reaction of 2,3-dimethylpyrazine or 3,4-dimethyl-1,2,5-oxadiazole with α,β-unsaturated carbonyls. The thus obtained heteroaromatics bearing a butadienyl moiety and a methyl at the adjacent position underwent intramolecular cyclization by the action of LDA to give the corresponding heteroaromatics fused with a seven-membered ring [7 (8)] and [11 (12)] in moderate to high yields. 相似文献
58.
J.-P. Brasselet D. Lehmann J. Seade T. Suwa 《Transactions of the American Mathematical Society》2002,354(4):1351-1371
Let be a compact local complete intersection defined as the zero set of a section of a holomorphic vector bundle over the ambient space. For each connected component of the singular set of , we define the Milnor class in the homology of . The difference between the Schwartz-MacPherson class and the Fulton-Johnson class of is shown to be equal to the sum of over the connected components of . This is done by proving Poincaré-Hopf type theorems for these classes with respect to suitable tangent frames. The -degree component coincides with the Milnor numbers already defined by various authors in particular situations. We also give an explicit formula for when is a non-singular component and satisfies the Whitney condition along .
59.
We propose that a chain of five-membered rings (polyaminotriazole) should be ferromagnetic with an appropriate doping that is envisaged to be feasible with a field-effect transistor structure. The ferromagnetism is confirmed by a spin density functional calculation, which also shows that ferromagnetism survives the Peierls instability. We explain the magnetism in terms of the Mielke and Tasaki flatband ferromagnetism with the Hubbard model. This opens a new possibility of band ferromagnetism in purely organic polymers. 相似文献
60.
Relative populations of S-form (D-E rings: boat-boat form) and F-form (D-E rings: chair-chair form) conformers, in equilibrium in CDCl3 solutions, of 20 derivatives (2-21) of bryonolic acid (D:C-friedoolean-8-en-3beta-ol-29-oic acid) (1) were calculated from NMR spectral data (J-values and chemical shifts), with the aid of molecular mechanic calculation using a MM2/CONFLEX program system. The principal deciding factor of the population ratio was found to be whether the functionality at C-29 is trigonal or tetrahedral; the S-form: F-form was 0:100-32:68 for the "trigonal" type and 48:52-100:0 for the "tetrahedral." The reliability of the results is discussed. 相似文献