Single-walled carbon nanohorns (SWCNHs) hybridized with palladium (Pd) nanoparticles were synthesized by a single-step gas-injected arc-in-water method (GI-AIW) with a Pd wire inserted inside the anode hole. In the arc zone, carbon and Pd were vaporized simultaneously, leading to the formation of hybrid material of SWCNHs and Pd nanoparticles due to effective quenching. Based on TEM and CO chemisorption analyses, Pd nanoparticles were found to be embedded inside SWCNH aggregates. The size of Pd nanoparticles, determined by X-ray diffraction, was in the range of 3–6 nm when Pd wires with diameters of 0.1 and 0.3 mm were used. Using a Pd wire with a diameter larger than 0.5 mm results in larger Pd nanoparticles which tend to be exposed to the outer surface of the hybrid material. According to thermogravimetric analyses, the weight fraction of Pd nanoparticles is increased by increasing the Pd wire diameter although the yield of Pd nanoparticles decreased. SWCNHs hybridized with dispersed Pd nanoparticles, synthesized with 0.1 mm Pd wire, exhibited strong anti-oxidation resistance with a highly graphitic structure. 相似文献
Polyethylene reactor powders prepared under different conditions were characterized using transmission electron microscopy, 1H nuclear magnetic resonance and X-ray diffraction techniques. The molecular weight of the polyethylene reactor powders was around 1 × 105. A unique domain morphology, quite different from the usual melt- or solution-crystallized lamellar structure, was observed, independent of polymerization temperature (Tpoly). Annealing of reactor powders caused the aggregation of these crystalline domains, due to the significant molecular motion of the amorphous chains, before melting. The critical temperature was 20 °C higher than each Tpoly, and corresponded to the temperature at the active catalyst site producing the chain growth. The morphologies of powders prepared at the lower Tpoly contained smaller crystals that exhibited a constrained monoclinic form. In contrast, only usual orthorhombic crystals of larger size were found within the powder prepared at the higher Tpoly. These results suggest that the competitive processes of chain propagation and crystal growth upon polymerization may lead to unique variations of the crystalline and amorphous phases, but with similar intermediate components in the phase that connects them. 相似文献
We have studied heat capacities of 4He adsorbed in straight nanopores 1.8, 2.2, and 2.8 nm in diameter. Heat capacities of the 4He fluid film on the solid layer at 0.08–0.4 K show power laws close to T in 1.8 nm pores, close to T2 in 2.8 nm pores, and a crossover from T to T2 with increasing temperature in 2.2 nm pores. These heat capacities are explained by a model assuming a phonon dispersion
with continuous one-dimensional (1D) states in the axial direction and discrete energy levels in the azimuthal direction.
By fitting experimental data to the model, the phonon velocity along the pore axis and the energy gap for propagation in the
cross section are derived. At temperatures sufficiently lower than the energy gap, where the thermal wave length of phonons
is much longer than the effective pore diameter, the 4He fluid films show a T-linear heat capacity of 1D phonons propagating only along the pore axis. At higher temperatures, a 1D-2D crossover of phonons
occurs.
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The notion of pseudo-free group was first introduced by Hohenberger (Master’s thesis, EECS Dept., MIT, 2003). Rivest (TCC
2004. LNCS 2951, 505–521, 2004) formalized it and showed that several standard cryptographic assumptions hold on pseudo-free groups, such
as the RSA assumption, the strong RSA assumption and the discrete logarithm assumption. Rivest (TCC 2004. LNCS 2951, 505–521, 2004) also proposed some variations of pseudo-free group, and those were formalized by Hirano and Tanaka (Research
Reports, Series C: Computer Science, C-239, Tokyo Institute of Technology, 2007). In this paper, we study the relationships
among such variations of pseudo-free group. We show that the pseudo-freeness implies the weak pseudo-freeness, and that the
pseudo-freeness is equivalent to the pseudo-freeness with generalized exponential expressions. We also show that the computational
Diffie-Hellman assumption holds on pseudo-free groups in a slightly varied form. 相似文献
Poly(9,10-dihydrophenanthrene-2,7-diyl)s with -OSi(R)2(R′) groups at the 9,10-positions were synthesized by dehalogenative polycondensation of the corresponding monomers by using a zerovalent nickel complex. They showed number average molecular weights (Mn's) of 9800-69,000 and high quantum yields (62%-quantitative) in photoluminescence. Palladium catalyzed copolymerization of 2,7-dibromo-9,10-dihydrophenanthrene having -OCH3 or -OSi(R)2(R′) groups at the 9,10-positions with diethynyl- or diboronic-aromatic compounds also gave photoluminescent polymers with high quantum yields. 相似文献
Great amounts of soil and waste contaminated with radioactive cesium have been generated due to the decontamination work after the Fukushima Daiichi Nuclear Power Plant accident. The aim of this study is to develop a sealing geomaterial for use at the disposal facilities of the soil and waste constructed in the maritime environment. The geomaterial consists of marine clay, bentonite, and zeolite. The hydraulic conductivity and cesium-adsorption performance of the geomaterial were examined through laboratory tests with different proportions of bentonite and zeolite added to marine clay. It was concluded that the hydraulic conductivity could be reduced to the required level by increasing the amount of bentonite and that the cesium-adsorption capacity could be enhanced by increasing the amount of zeolite. 相似文献
The iron(III) chloride‐catalyzed Friedel–Crafts arylation of 4‐aryl‐4‐methoxy‐2,5‐cyclohexadienones, which were easily prepared by the phenyliodine(III) diacetate (PIDA)‐mediated oxidation of 4‐arylphenols in methanol, proceeded site‐selectively to form meta‐terphenyl (2,4‐diarylphenol) derivatives in good yields. The subsequent PIDA‐mediated oxidation and iron(III) chloride‐catalyzed Friedel–Crafts arylation of the resulting products gave the corresponding 2,4,6‐triarylphenol derivatives. The present method provides useful highly substituted polyarylated compounds.