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991.
The cross-linked composite solid polymer electrolytes composed of poly(ethylene oxide), lithium salt (LiN(SO2CF3)2), and a hyperbranched polymer whose repeating units were connected by ether-linkage (hyperbranched polymer (HBP)-2) were prepared, and their ionic conductivity, thermal properties, electrochemical stability, mechanical property, and chemical stability were investigated in comparison with the non-cross-linked or cross-linked composite solid polymer electrolytes using hyperbranched polymers whose repeating units were connected by ester-linkage (HBP-1a, 1b). The cross-linked composite solid polymer electrolyte using HBP-2 exhibited higher ionic conductivity than the non-cross-linked and cross-linked composite solid polymer electrolytes using HBP-1a and HBP-1b, respectively. The structure of the hyperbranched polymer did not have a significant effect on the thermal properties and electrochemical stability of the composite solid polymer electrolytes. The tensile strength of the cross-linked composite solid polymer electrolyte using HBP-2 was lower than that of the cross-linked composite solid polymer electrolyte using HBP-1b, but higher than that of the non-cross-linked composite solid polymer electrolyte using HBP-1a. The HBP-2 with ether-linkage showed higher chemical stability against alkaline hydrolysis compared with HBP-1a with ester-linkage.  相似文献   
992.
993.
994.
Fluoroalkyl end‐capped cooligomers containing diphenylacetylene segments [RF‐(DPMA)x‐(Co‐M)yRF] were prepared by reaction of fluoroalkanoyl peroxide with 4‐(phenylethynyl)phenyl methacrylate (DPMA) and radical polymerizable comonomers such as N,N‐dimethylacrylamide (DMAA) and acryloylmorpholine (ACMO) under very mild conditions. Fluorinated cooligomers containing diphenylacetylene segments thus obtained exhibited a good solubility in a variety of organic solvents. These fluorinated cooligomers were also applied to the surface modification of traditional organic polymers such as poly(methyl methacrylate) (PMMA) to exhibit not only a good surface active property imparted by fluorine but also a fluorescent characteristic related to diphenylacetylene segments on their surface. In addition, these fluorinated cooligomers could form the nanometer size‐controlled fluorinated molecular aggregates in chloroform. Interestingly, some benzenes and biphenyl (BP) derivatives could interact with these fluorinated oligomeric aggregates as guest molecules, and in particular 2‐chloro‐5‐nitrobenzotrifluoride (CNB) was most effective for enhancing the fluorescent intensity of these guest molecules. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   
995.
Post-translational modifications (PTMs) of proteins are important in the activation, localization, and regulation of protein function in vivo. The usefulness of electron capture dissociation (ECD) and electron-transfer dissociation (ETD) in tandem mass spectrometry (MS/MS) using low-energy (LE) trap type mass spectrometer is associated with no loss of a labile PTM group regarding peptide and protein sequencing. The experimental results of high-energy (HE) collision induced dissociation (CID) using the Xe and Cs targets and LE-ETD were compared for doubly-phosphorylated peptides TGFLT(p)EY(p)VATR (1). Although HE-CID using the Xe target did not provide information on the amino acid sequence, HE-CID using the Cs target provided all the z-type ions without loss of the phosphate groups as a result of HE-ETD process, while LE-ETD using fluoranthene anion gave only z-type ions from z5 to z11. The difference in the results of HE-CID between the Xe and Cs targets demonstrated that HE-ETD process with the Cs target took place much more dominantly than collisional activation. The difference between HE-ETD using Cs targets and LE-ETD using the anion demonstrated that mass discrimination was much weaker in the high-energy process. HE-ETD was also applied to three other phosphopeptides YGGMHRQEX(p)VDC (2: X = S, 3: X = T, 4: X = Y). The HE-CID spectra of the doubly-protonated phosphopeptides (= [M + 2H]2+) of 2, 3, and 4 using the Cs target showed a very similar feature that the c-type ions from c7 to c11 and the z-type ions from z7 to z11 were formed via N-Cα bond cleavage without a loss of the phosphate group.  相似文献   
996.
We study scalar–tensor theory, k-essence and modified gravity with Lagrange multiplier constraint which role is to reduce the number of degrees of freedom. Dark Energy cosmology of different types (ΛCDM, unified inflation with DE, smooth non-phantom/phantom transition epoch) is reconstructed in such models. It is demonstrated that presence of Lagrange multiplier simplifies the reconstruction scenario. It is shown that mathematical equivalence between scalar theory and F(R)F(R) gravity is broken due to presence of constraint. The cosmological evolution is defined by the second F2(R)F2(R) function dictated by the constraint. The convenient F(R)F(R) gravity sector is relevant for local tests. This opens the possibility to make originally non-realistic theory to be viable by adding the corresponding constraint. A general discussion on the role of Lagrange multipliers to make higher-derivative gravity canonical is developed.  相似文献   
997.
We investigated the effects of indium doping on the superconducting properties of YBCO sintered samples and thin films. In2O3-doped YBCO and YBa2Cu3−xInxOy sintered samples showed a gradual decrease in the critical temperature (Tc) with increasing indium content; however, a Tc value above 80 K was maintained even up to 30 vol.% addition and x = 0.4, respectively. Ba3Cu3In4O12 was detected by X-ray diffractometry and energy-dispersive X-ray spectroscopy as a reaction product for both sintered samples. The normalized Jc under a magnetic field of 0.1 T showed a maximum at = 0.3. Indium-doped YBCO films prepared by pulsed laser deposition showed a similar dependence of Tc on indium content as the sintered samples.  相似文献   
998.
Emission characteristics of gadolinium (Gd) oxide are studied, using ns and fs laser pulses for ablation in double-pulse laser induced breakdown spectroscopy (LIBS). In the current conditions of pulse energy and signal detection timing, emission intensity enhancement in the reheating mode is 25-fold, but little effect can be observed in a pre-pulse mode. It is shown that the optimum focus position of the ablation pulse is about 5 mm apart from the sample surface in the reheating mode. Although little emission can be observed in the single-pulse configuration with fs ablation pulses, the intense emission can be observed in the reheating mode in the double-pulse configuration.  相似文献   
999.
Calcium graphite intercalation compounds (Ca-GICs; the composition is CaC6) and GICs containing CaC6 are synthesized from Grafoil and PGS graphite sheets, and the Seebeck coefficients are measured. The absolute values of the Seebeck coefficient of these GICs are very small; in some cases, the values are positive. This phenomenon observed in the Seebeck coefficient of GICs containing CaC6 is very different from that of general GICs such as alkali-metal GICs. The temperature dependence of the Seebeck coefficient of these GICs is to that of general GICs; that is, the absolute values of the Seebeck coefficient decrease with a decrease in the temperature.  相似文献   
1000.
Stoichiometric four-layered hexagonal (4H) (Sr1?x?yBaxLay)MnO3 was synthesized using a standard ceramic technique. Rietveld analysis at room temperature indicated that the Mn–O(1) distance increased and the Mn–O(2) distance decreased with the increase in x. The samples were n-type semiconductors and exhibited hopping conductivity in a small-polaron model below 533 K. The Mn3+ ion acted as a donor and the electron transfer became active through the Mn3+–O–Mn4+ path. The samples were antiferromagnetic and the Néel temperature (TN) was constant regardless of y when x was fixed to 0.3, whereas TN shifted to a high temperature when y was fixed to 0.02. The face-sharing Mn3+–O(2)–Mn4+ interaction strengthened as the Mn–O(2) distance decreased, and TN shifted to a high temperature as a result.  相似文献   
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