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981.
Surface status and size influences of nickel nanoparticles on sulfur compound adsorption 总被引:1,自引:0,他引:1
Metallic nickel nanoparticles were incorporated on mesoporous silica to remove sulfur compounds in diesel selectively. In the first method, nickel nanoparticles were formed on mesoporous silica SBA-15 by impregnation and subsequent reduction of nickel nitrate. The sulfur adsorption capacity was strongly dependent on the nickel loading and the average nickel particle size. In the second method, nickel nanoparticles were synthesized in solution in the presence of a capping agent and then incorporated in mesoporous silica MCF by sonication. Although these particles maintain their sizes on the MCF surface after heat treatment, capping agent remaining on the Ni particle surface might interfere the adsorption of sulfur compounds. 相似文献
982.
In this report, we demonstrate the efficient generation of collinearly propagating photon pairs in a bulk periodically poled potassium titanyl phosphate pumped by a cw laser. The detected coincidence counts are more than 7400/s with 3.58 mW pump power in a Hanbury-Brown-Twiss-type experiment. The estimated photon pair production rate is about 0.73 MHz/mW. This is very promising for some applications, such as quantum key distribution, proof of the Bell-inequality, preparation of single photon states in broadband wave packets, Franson-type interference and so on. 相似文献
983.
Al-doped ZnO (AZO) transparent conductive thin films were grown by magnetron sputtering with AZO (98 wt.% ZnO, 2 wt.% Al2O3) ceramic target in Ar + H2 ambient at a relatively low temperature of 100 °C. To investigate the dependence of crystalline and properties of as-grown AZO films on the H2-flux, X-ray diffraction (XRD), X-ray photoemission spectrometer (XPS), Hall and transmittance spectra measurements were employed to analyze the AZO samples deposited with different H2-flux. The results indicate that H2-flux has a considerable influence on the transparent conductive properties of AZO films. The resistivity of 4.15 × 10−4 Ω cm and the average transmittance of more than 94% in the visible range were obtained with the optimal H2-flux of 1.0 sccm. Such a low temperature growing method present here may be especially useful for some low-melting point photoelectric devices and substrates. 相似文献
984.
Electrodynamic Analysis of Dissipative Electromagnetic Materials Based on Fractional Derivative
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The generalized Lagrangian is defined in a dissipative electromagnetic medium on the basis of the combination of dynamical analysis and fractional derivative. Lorentz medium models are obtained by formulating relevant Euler-Lagrange equations. The invariance is obtained subsequently by investigating the invariance of time variation in the system, and then the relation between the related Hamiltonian and electromagnetic energy density is investigated. Canonical equations are obtained eventually. The electrodynamic interpretation on dissipative electromagnetic systems is revealed. 相似文献
985.
Kyung Ah Jeon Hyo Jeong Son Chang Eun Kim Jong Hoon Kim Sang Yeol Lee 《Physica E: Low-dimensional Systems and Nanostructures》2007,37(1-2):222
ZnO nanowires were fabricated on c-plane (0 0 0 1), a-plane (1 1 2¯ 0) sapphire, and boron doped p-type (1 0 0) Si substrates in vacuum furnace by simple physical vapor deposition. Room temperature photoluminescence spectra of the nanowires show the near band-edge emission and the deep-level green light emission. The ZnO nanowires formed on sapphire (1 1 2¯ 0) substrates exhibited enhancement on optical properties and better crystalline structures than those of nanowires grown on other substrates. The formation mechanism and the effect of substrate direction on structural and optical properties of the nanowires are discussed. 相似文献
986.
Yu-Lin Tsai Cheng-Chung Chang Chi-Chih Kang Ta-Chau Chang 《Journal of luminescence》2007,127(1):41-47
We have previously illustrated that the electron donor of carbazole moiety and the electron acceptor of methyl pyridinium cation in 3,6-bis(1-methyl-4-vinylpyridinium) carbazole diiodide (BMVC) molecule could form an intramolecular charge-transfer state. The intramolecular twist of the vinyl group in bridging the donor and acceptor plays an important role in the BMVC fluorescence. Here, we have synthesized three 9-aryl-substituted BMVC derivatives with different electronic properties for the design of the second generation of fluorescence probes. The steady-state solvatochromic studies show no appreciable change to the charge transfer of BMVC by substituting an anisole electron-donating group at 9-position of BMVC. However, substituting a 9-nitrobenzyl electron-withdrawing group in BMVC could restrict the charge transfer in the excited state. Moreover, the increase of the fluorescence yields of 9-anisole BMVC and 9-phenyl BMVC upon interaction with DNA is even higher than that in glycerol, while the fluorescence yield of 9-nitrobenzyl BMVC upon interaction with DNA is much lower than that in glycerol. Although 9-nitrobenzyl BMVC is a good G-quadruplex stabilizer, substituting an electron-withdrawing group at 9-position of BMVC is not recommended for the design of fluorescence probes. On the other hand, co-localization between 9-phenyl BMVC and MitoTracker Red in the merged image of cells indicates that the 9-phenyl BMVC is a potential fluorescent mitochondrial probe. 相似文献
987.
Geometries, relative energies, and stabilities of endo- and exohedral complexes, X@Si20H20 and XSi20H20, (X = H+, H, N, P, C?, and Si?) are calculated at B3LYP/6-31G* level. The energy minimum structure of Si20H21 + shows that the proton cannot be positioned in the Si20H20 centre, but prefers attach to Si20H20 exohedrally with C2v symmetry. Most investigated Ih endohedral complexes X@Si20H20 (X = H, N, P, C?, and Si?) are local minima, except for 2N@Si20H20, which is a high-order saddle point. Inclusions energies of the endohedral complexes are calculated, and it reveals that energy penalties caused by encapsulation are rather small. Exohedral complexes XSi20H20 (X = H, N, P, C?, and Si?) have C2v or Cs local minima, and most of them are more stable than their endohedral isomers with the exception of C2v 4PSi20H20 and 4Si?Si20H20. 相似文献
988.
989.
Hong Kyung Choi Jeong Ho Chang Il Hwan Ko Bong Yong Jeong Jung Bae Kim 《Journal of solid state chemistry》2011,184(4):805-2221
This work describes the development of highly efficient human DNA separation with functionalized mesoporous silica (FMS) materials. To demonstrate the electrostatic interaction effect between the target DNA molecules and FMS, three aminofunctionality types comprised of a mono-, a di-, and a tri-amine functional group were introduced on the inner surfaces of mesoporous silica particles. Systematic characterization of the synthesized materials was achieved by solid-state 29Si and 13C-NMR techniques, BET, FT-IR, and XPS. The DNA separation efficiency was explored via the function of the amino-group number, the amount used, and the added NaCl concentration. The DNA adsorption yields were high in terms of the use of triaminofunctionalized FMS at the 10 ng/L level, and the DNA desorption efficiency showed the optimum level at over 3.0 M NaCl concentration. The use of FMS in a DNA separation process provides numerous advantages over the conventional silica-based process. 相似文献
990.
Hyunpyo Lee Jun Beum Park Ji Young Chang 《Journal of polymer science. Part A, Polymer chemistry》2011,49(13):2859-2865
Core‐shell structured nanoparticles of poly(ethylene glycol) (PEG)/polypeptide/poly(D ,L ‐lactide) (PLA) copolymers were prepared and their properties were investigated. The copolymers had a poly(L ‐serine) or poly(L ‐phenylalanine) block as a linker between a hydrophilic PEG and a hydrophobic PLA unit. They formed core‐shell structured nanoparticles, where the polypeptide block resided at the interface between a hydrophilic PEG shell and a hydrophobic PLA core. In the synthesis, poly(ethylene glycol)‐b‐poly(L ‐serine) (PEG‐PSER) was prepared by ring opening polymerization of N‐carboxyanhydride of O‐(tert‐butyl)‐L ‐serine and subsequent removal of tert‐butyl groups. Poly(ethylene glycol)‐b‐poly(L ‐phenylalanine) (PEG‐PPA) was obtained by ring opening polymerization of N‐carboxyanhydride of L ‐phenylalanine. Methoxy‐poly(ethylene glycol)‐amine with a MW of 5000 was used as an initiator for both polymerizations. The polymerization of D ,L ‐lactide by initiation with PEG‐PSER and PEG‐PPA produced a comb‐like copolymer, poly(ethylene glycol)‐b‐[poly(L ‐serine)‐g‐poly(D ,L ‐lactide)] (PEG‐PSER‐PLA) and a linear copolymer, poly(ethylene glycol)‐b‐poly(L ‐phenylalanine)‐b‐poly(D ,L ‐lactide) (PEG‐PPA‐PLA), respectively. The nanoparticles obtained from PEG‐PPA‐PLA showed a negative zeta potential value of ?16.6 mV, while those of PEG‐PSER‐PLA exhibited a positive value of about 19.3 mV. In pH 7.0 phosphate buffer solution at 36 °C, the nanoparticles of PEG/polypeptide/PLA copolymers showed much better stability than those of a linear PEG‐PLA copolymer having a comparable molecular weight. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献