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Intense Raman scattering by acetophenone molecules adsorbed on colloidal silver particles is reported. Greater enhancement is observed for the ring breathing and ring stretching vibrations. The orientation determination analysis shows that the adsorption of acetophenone molecule is neither through its co-ordinating site nor through itsπ-orbital system and there is no strong chemical interaction. However significant intensity enhancement for several vibrations suggests that the contribution is from classical electromagnetic field on the rough surface.  相似文献   
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The non axisymmetric motion produced by a buoyancy-induced secondary flow of a viscoelastic fluid over an infinite rotating disk in a verticalplane with a magnetic field applied normal to the disk has been studied.The governing Navier Stokes equations and the energy equation admit a self similar solution. The system of ordinary differential equations has been solved numerically using Runge-Kutta Gill subroutine.The turning moment for the viscoelastic fluid is found to be less than that of the Newtonian fluid but the turning moment is increased due to the magnetic parameter. The resultant force due to the buoyancy-induced secondary flow increases with the magnetic parameter but reduces as the viscoelastic parameter increases. The quantity of fluid, which is pumped outwards due to the centrifuging action of the disk, for the viscoelastic fluid is more than that of the Newtonian fluid. The buoyancy-induced secondary flow boundary layer is much thicker than the primary boundary layer thickness. The thermal boundary layer due to the primary flow increases with the magnetic parameter decreases as the viscoelastic parameter increases. The heat transfer increases with the viscoelastic parameter but decreases as the magnetic parameter increases. The effect of the viscoelastic parameter is more pronounced on the secondary flow than on the primary flow.  相似文献   
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Phase pure Zn1?x Co x O thin films grown by pulsed laser deposition have transmittance greater than 75 % in the visible region. Raman studies confirm the crystalline nature of Zn1?x Co x O thin films. Zn0.95Co0.05O thin films show room temperature ferromagnetism with saturation magnetization of 0.4μ B /Co atom. The possible origin of paramagnetism at higher Co doping concentrations can be attributed to the increased nearest-neighbor antiferromagnetic interactions between Co2+ ions in ZnO matrix. XPS confirms the substitution of Co2+ ions into the ZnO host lattice.  相似文献   
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In this paper we report the synthesis of highly luminescent ZnS and Mn-doped ZnS nanoparticles with uniform particle size distribution by liquid phase pulsed laser ablation. The formation of nanosized ZnS crystallites was confirmed by high-resolution transmission electron microscopy (HRTEM) images. The optical properties of these nanoparticles were studied by room temperature photoluminescence (PL) spectra. The PL emission from the ZnS nanoparticles shows a sharp peak in the UV region (334 nm) corresponding to the band edge and a broad peak in the visible region which can be attributed to the sulphur vacancies, cation vacancies and surface states in the nanocrystals. The yellow emission from the Mn-doped ZnS nanoparticles can be attributed to the radiative transition between 4T1 and 6A1 levels within the 3d5 orbital of Mn2+.  相似文献   
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In this report, we present methods of functionalization of AuNP's with deep-cavity cavitands that can include organic molecules. Two types of deep-cavity cavitand-functionalized AuNP's have been synthesized and characterized, one soluble in organic solvents and the other in water. Functionalized AuNP soluble in organic solvents forms a 1:1 host-guest complex where the guest is exposed to the exterior solvents. The one soluble in water forms a 2:1 host-guest complex where the guest is protected from solvent water. Phosphorescence from thiones and benzil included within heterocapsules attached to AuNP was quenched by gold atoms present closer to the guests included within deep-cavity cavitands. During this investigation, we have synthesized four new deep-cavity cavitands. Of these, two thiol-functionalized hosts allowed us to make stable AuNP's. However, AuNP's protected with two amine-functionalized cavitands tended to aggregate within a day.  相似文献   
17.
Photoinactivation of hepatitis A virus by synthetic porphyrins   总被引:1,自引:0,他引:1  
Porphyrins are photosensitizers and may be applicable in situations where viral inactivation is required, as for in vitro inactivation of nonenveloped viruses in blood components or in other aqueous media. No study has examined the efficacy of porphyrin inactivation on human pathogens such as hepatitis A virus (HAV) in plasma or other liquids. Experiments were conducted to evaluate the effect of synthetic porphyrins on HAV in porphyrin-containing human plasma and phosphate-buffered saline exposed to long-wavelength (365 nm) UV light. Inactivation of bacteriophage MS2 (MS2) also was determined in some trials. Solutions containing cationic, anionic or amphiphilic porphyrins irradiated with an average light dose of 4.3 J/cm(2) for 90 min resulted in >3 log(10) (>99.9%) to >4 log(10) (>99.99%) inactivation of both HAV and MS2. Viral inactivation may have been greater than observed because the limits of detection of the assay had been reached. Under ambient lighting conditions, none of the porphyrins was mutagenic in the Ames assay and only the congener with the longest chain-length, tetrakis (N-[n-hexadecyl]-4-pyridiniumyl) porphyrin, was appreciably toxic to mammalian cells. Disinfection by photoactivated synthetic porphyrins therefore can offer an effective and relatively safe approach to removal of nonenveloped viruses from aqueous media.  相似文献   
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It is of immense interest to exert spatial and temporal control of chemical reactions. It is now demonstrated that irradiation can trigger reactions specifically at the surface of a simple colloidal construct, obtained by adsorbing polyethyleneimine on fluorescent colloidal particles. Exciting the fluorescent dye in the colloid affords photoinduced electron transfer to spatially proximal amine groups on the adsorbed polymer to form free radical ions. It is demonstrated that these can be harnessed to polymerize acrylic acid monomer at the particle surface, or to break up colloidal assemblies by cleaving a cross‐linked polymer mesh. Formation of free radical ions is not a function of the size of the colloid, neither is it restricted to a specific fluorophore. Fluorophores with redox potentials that allow photoinduced electron transfer with amine groups show formation of free radical ions.  相似文献   
20.
This article has been retracted at the request of the Editors-in-Chief. Please see Elsevier Policy on Article Withdrawal (http://www.elsevier.com/locate/withdrawalpolicy). REASON: Considerable concern was raised about the research purportedly conducted at Sri Venkateswara University, India with the alleged involvement of Professor P. Chiranjeevi. Questions were raised as to the volume of publications, the actual capacity (equipment, orientation and chemicals) of the laboratory in which Professor Chiranjeevi worked, the validity of certain of the research data identified in the articles, the fact that a number of papers appear to have been plagiarized from other previously published papers, and some aspects of authorship. Professor Chiranjeevi was given the opportunity to respond to these allegations. Thereafter, a committee was constituted by the University to look into these allegations. Based on the enquiry committee report, we have been informed by the head of the Department of Chemistry at Sri Venkateswara University that the university authorities have taken disciplinary action against Professor Chiranjeevi, as the university considers that there are grounds for such action. Therefore, based on the results of this investigation, the Editors-in-Chief are retracting this article.  相似文献   
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