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1.
Yan Yin Otoo Yamada Shunsuke Hayashi Kazuhiro Tanaka Hidetoshi Kita Ken‐Ichi Okamoto 《Journal of polymer science. Part A, Polymer chemistry》2006,44(12):3751-3762
A series of branched/crosslinked sulfonated polyimide (B/C‐SPI) membranes were prepared and evaluated as proton‐conducting ionomers based on the new concept of in situ crosslinking from sulfonated polyimide (SPI) oligomers and triamine monomers. Chemical branching and crosslinking in SPI oligomers with 1,3,5‐tris(4‐aminophenoxy)benzene as a crosslinker gave the polymer membranes very good water stability and mechanical properties under an accelerated aging treatment in water at 130 °C, despite their high ion‐exchange capacity (2.2–2.6 mequiv g?1). The resulting polymer electrolytes displayed high proton conductivities of 0.2–0.3 S cm?1 at 120 °C in water and reasonably high conductivities of 0.02–0.03 S cm?1 at 50% relative humidity. In a single H2/O2 fuel‐cell system at 90 °C, they exhibited high fuel‐cell performances comparable to those of Nafion 112. The B/C‐SPI membranes also displayed good performances in a direct methanol fuel cell with methanol concentrations as high as 50 wt % that were superior to those of Nafion 112. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3751–3762, 2006 相似文献
2.
The influence of NCS? ion concentration on the rate of base hydrolysis of trans-[Cr(NK3)2(NCS)4]? complex has been examined. The form of the pseudo-first-order rate constants dependence on [NCS?] is used as a criterion of the reaction mechanism. The mass-law (rate) retardation effect in the rate determining reaction stage suggests the DCB mechanism for the alkali dependent path. 相似文献
3.
Hiromitsu Terao Yoshihiko Kai Kazuyo Kita Yoshihiro Furukawa 《Hyperfine Interactions》2010,198(1-3):93-101
The crystals of 4-NH2PyHSbI4 (Py = C5H4N) have been investigated by means of 127I NQR, 1H NMR T 1 and DTA. The crystals can exist in two modifications of β and α(I) at room temperatures. The α(I)-phase is a metastable state which is obtained when the stable β form is heated. The α(I)-phase undergoes a first-order type phase transition of α(I) $\leftrightarrow \alpha $ (II) at 272 K (on heating), while the β-phase is stable down to 77 K. Four and two 127I (m = ±1/2 $\leftrightarrow \pm $ 3/2) NQR lines have been found for the β- and α(II)-phases, respectively. One half of them is assignable to the terminal I atom(s) and the other to the bridging I atom(s) in each phase. All the resonance lines of the α(II)-phase underwent a disappearance above ca. 240 K and no resonance line was observed in the α(I)-phase. The second moment M 2 value of 1H NMR spectra with 8 G2 at 290 K shows that the 4-NH2PyH?+? cations reside in the rigid lattice in the β-phase. In contrast, in the α(I)-phase the cation rotates about an axis more symmetric than pseudo threefold axis. The activation energy of 21 kJ mol???1 was estimated for the reorientational motion in the α(I)-phase from the 1H NMR T 1 measurements. The nature of phase transitions in the 4-NH2PyHSbI4 is discussed in comparison with that in 4-NH2PyHSbBr4. 相似文献
4.
Y. Yamamoto K. Fujisawa T. Takemura S. Kita 《International Journal of Infrared and Millimeter Waves》1988,9(1):29-40
Measurements have been done in the millimeter wave region on a composite waveguide which comprises a dielectric rod waveguide connecting two metal rectangular waveguides. Such a waveguide has been used by us in a Josephson harmonic mixer installed in a small metal cryostat, to prevent the thermal invasion from outside environment and to transmit both signal and LO waves with small losses. The measured transmission loss, that is caused mainly by the coupling loss between metal rectangular waveguides (TE10 mode) and a dielectric rod waveguide (HE11 mode), has been less than 2dB in the frequency range of 52–104 GHz. 相似文献
5.
The Mermin-Ho and Anderson-Toulouse coreless vortices are demonstrated to be thermodynamically stable in ferromagnetic F = 1 spinor Bose-Einstein condensates under rotation. We have carried out extensive calculations of the Gross-Pitaevskii equations by assuming uniform density along the z axis and comparing the energies of other competing non-axis-symmetric or singular vortices. The phase diagram is thereby established in a plane of the rotation drive vs the total magnetization. Their stability is also checked by calculating collective modes based on the Bogoliubov equations. 相似文献
6.
Thermal diffusion forced Rayleigh scattering results on thermal diffusion of poly(ethylene oxide) (PEO) in ethanol/water mixtures are presented. In water-rich solvent mixtures, PEO is found to migrate towards regions of lower temperature. This is typical for polymer solutions and corresponds to a positive Soret coefficient of PEO. In solvent mixtures with low water content, however, the polymer is found to migrate towards higher temperatures, corresponding to a negative Soret coefficient of PEO in ethanol-rich solutions. To our knowledge, this is the first observed sign change of the Soret coefficient of a polymer in solution. We also present a simple lattice model for the polymer solvent system and calculate Soret coefficients with statistical mechanics methods. The calculated values agree qualitatively with the experimental results. 相似文献
7.
On the basis of the theory developed in a previous paper (Part I), the angle and speed distributions of D2 molecules desorbing thermally from the Ni(111) surface are numerically calculated in the present paper (Part II). The dynamical motion of the activated complex of the recombinative desorption process is calculated by using a model potential surface, which involves a few parameters introduced to describe the necessary features of the potential surface at the transition state. Numerical calculations are carried out, and the results show that the present dynamical theory reproduces very well a variety of the characteristic features of the experimental results, e.g., sharply focused angular distribution, mean translational energy lower than 2k
B
T at grazing angle, and the non-Maxwellian profile of the TOF distribution. 相似文献
8.
Bailly J. L. Caso C. Chiba Y. Dibon H. Epp B. Ferrando A. Fontanelli F. Ganguli S. N. Gémesy T. Gurtu A. Hamatsu R. Hidas P. Hirose T. Hrubec J. Ivanyshenkov Yu. Kageya T. Khalatyan N. Kistenev E. Kita I. Kitamura S. Kubik V. MacNaughton J. Malhotra P. K. Matsumoto S. Mittra I. S. Montanet L. Neuhofer G. Pinter G. Porth P. Raghavan R. Rodrigo T. Singh J. Squarcia S. Takahashi K. Tanaka R. Tikhonova L. A. Trevisan U. Yamagata T. Zholobov G. Zotkin S. A. 《Zeitschrift fur Physik C Particles and Fields》1989,43(3):341-348
Zeitschrift für Physik C Particles and Fields - Correlations among identically charged pions were measured for pions produced inp p collisions at 360 GeV/c using the EHS spectrometer. The... 相似文献
9.
Hongyuan Wang Toshinari Ugomori Yong Wang Kazuhiro Tanaka Hidetoshi Kita Ken‐Ichi Okamoto Yasunori Suma 《Journal of Polymer Science.Polymer Physics》2000,38(13):1800-1811
Poly(ethylene oxide imide) segmented copolymer (PEO‐PI) membranes were crosslinked by the chemical reaction between ethylene glycol diglycidyl ether and benzylalcohol groups of diamine moieties in polyimide segments at high temperatures. Sorption and diffusion of penetrants took place in poly(ethylene oxide) segment microdomains. Sorption and desorption behavior of pure vapors such as benzene (Bz), cyclohexane (Cx) and n‐hexane (Hx) was classified as the Fickian diffusion. Sorption isotherms of binary liquid mixtures could be represented by the Flory–Rehner model, but the model overpredicted the sorption amounts of Cx and Hx, leading to small predictions of sorption selectivity αS for Bz/Cx and Bz/Hx systems. UNIFAC‐FV model fairly well predicted the sorption amounts of aromatic hydrocarbons, but significantly overestimated those of nonaromatic ones, leading to too small predictions of αS. Pervaporation (PV) behavior of PEO‐PI membranes was governed by sorption behavior followed by membrane swelling. Diffusion coefficient weakly depended on the minimum cross section of a penetrant. The diffusivity selectivity αD hardly depended on the feed composition and was about 1.4 and 0.75 for Bz/Cx and Bz/Hx, respectively. PV selectivity αPV was larger for Bz/Hx than for Bz/Cx because of larger αS. PEO‐PI membranes displayed high specific permeation flux Ql and reasonably high αPV for aromatic/nonaromatic hydrocarbons; for example, Ql = 60 Kg μm/(m2 h) and αPV = 8 for a feed mixture containing Bz, Tol, Hx, n‐Ot and i‐Ot of 20 wt % at 353 K. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 1800–1811, 2000 相似文献
10.
Fujioka H Okitsu T Sawama Y Murata N Li R Kita Y 《Journal of the American Chemical Society》2006,128(17):5930-5938
We report here unexpected highly chemoselective deprotection of the acetals from aldehydes. Treatment of acetal compounds from aldehydes with TESOTf-2,6-lutidine or TESOTf-2,4,6-collidine in CH2Cl2 at 0 degrees C followed by H2O workup at the same temperature caused the conversion of the acetal functions to aldehyde functions. The reaction had generality and was applied to many acetal compounds. Study using various bases revealed the reaction and reached the best combination of TESOTf-base. It was very mild and highly chemoselective and proceeded under weakly basic conditions. Then, many functional groups such as allyl alcohol, silyl ether, acetate, methyl ether, triphenylmethyl (Tr) ether, 1,3-dithiolane, methyl ester, and tert-butyl ester could survive under these conditions. Furthermore, this methodology could selectively deprotect the acetals in the presence of ketals as the most characteristic feature, although this chemoselectivity is difficult to achieve by other previously reported methods. A detailed study of the reaction including MS and NMR studies revealed the reaction mechanism for determining the structures of the intermediates, pyridinium-type salts. These intermediates had a weak electrophilicity and were successfully applied to the efficient formation of the mixed acetals in high yields. 相似文献