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1.
Human brain bacterial meningitis is a life-threatening disease caused mainly by Neisseria meningitidis, lead to damage of the outer membrane covering (meninges) of brain or even death. The usual methods of diagnosis are either time-consuming or have some limitations. The specific rmpM (reduction-modifiable protein M) virulent gene based genosensor is more sensitive, specific, and can detect N. meningitidis directly from the patient cerebrospinal fluid in 30 min including 1-min response time. 5′-Thiol-labeled single-stranded DNA (ssDNA) probe was immobilized onto screen-printed gold electrode (SPGE) and hybridized with denatured (95 °C) single-stranded genomic DNA (ssG-DNA) for 10 min at 25 °C. The electrochemical response was measured by cyclic voltammetry, differential pulse voltammetry (DPV) and electrochemical impedance using redox indicators. The sensitivity of the genosensor was 9.5087?(μA/cm2)/ng with DPV and limit of detection was 3 ng/6 μL ssG-DNA. The immobilization of the ssDNA probe and hybridization with ssG-DNA from N. meningitidis was characterized by atomic force microscopy and Fourier transform infrared spectroscopy. The rmpM genosensor was stable for 6 months at 4 °C with 10 % loss in initial DPV current. The advantage of rmpM genosensor is to detect bacterial meningitis simultaneously in multiple patients using SPGE array during an outbreak of the disease.  相似文献   
2.
A novel class of multifunctional and multinucleate chalcogen (selenium and tellurium) containing derivatives (1-10) has been developed based on sequential chloride substitution of 2,4,6-trichloro-1,3,5-triazine with chalcogen-bearing amines. The structure of compound 1 has been determined in the solid state by X-ray crystallography.  相似文献   
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The influence of oxides in the hydrogen evolution on Raney nickel electrocatalysts was characterized by electrochemical impedance measurements. In addition, these materials show competitive overpotentials for hydrogen evolution with a modified Watts bath as a binder for the Raney nickel. The optimum result was ?190?mV of overpotential at 100?mA?cm?2. Oxygen in the Raney Ni catalyst affects its electroactivity toward hydrogen evolution. The source of oxygen is related to the presence of chloride ions in the modified Watts bath. A Watts bath binds Raney Ni particles to the surface of the catalysts and chloride regulates the oxygen content in the nickel binder during electrodeposition. High oxygen content increases the hydrogen evolution overpotential of the electrode. The electroactivity of the synthesized porous coatings was evaluated by polarization curves and impedance plots. In addition, surface characterization by X-ray diffraction, field emission–scanning electron microscopy equipped with energy-dispersive analysis, and X-ray photoelectron spectroscopy is reported.  相似文献   
5.
Macrophages are one of the principal immune effector cells that play essential roles as secretory, phagocytic, and antigen-presenting cells in the immune system. In this study, we address the issue of cytotoxicity and immunogenic effects of gold nanoparticles on RAW264.7 macrophage cells. The cytotoxicity of gold nanoparticles has been correlated with a detailed study of their endocytotic uptake using various microscopy tools such as atomic force microscopy (AFM), confocal-laser-scanning microscopy (CFLSM), and transmission electron microscopy (TEM). Our findings suggest that Au(0) nanoparticles are not cytotoxic, reduce the production of reactive oxygen and nitrite species, and do not elicit secretion of proinflammatory cytokines TNF-alpha and IL1-beta, making them suitable candidates for nanomedicine. AFM measurements suggest that gold nanoparticles are internalized inside the cell via a mechanism involving pinocytosis, while CFLSM and TEM studies indicate their internalization in lysosomal bodies arranged in perinuclear fashion. Our studies thus underline the noncytotoxic, nonimmunogenic, and biocompatible properties of gold nanoparticles with the potential for application in nanoimmunology, nanomedicine, and nanobiotechnology.  相似文献   
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The structural characteristics of olivine-type lithium orthophosphate Li(Mg0.5Ni0.5)PO4 synthesized via solid-state reaction have been studied using X-ray diffraction, ion beam technique, scanning electron microscopy, infrared spectroscopy, transmission electron microscopy and energy dispersive X-ray analysis. The parent LiNiPO4 compound can be synthesized in olivine structure without any evidence of secondary phases as impurities. The structural quality of the parent LiNiPO4 in the absence of secondary component phases resulted in the formation of hexagonal closed packed structure. The olivine analogue compound containing mixed M (M?=?Mg, Ni) cations, Li(Mg0.5Ni0.5)PO4 contained Li3PO4 as a second phase upon synthesis, however a carbothermal reduction method produced a single-phase compound. The redox behaviour of carbon-coated Li(Mg0.5Ni0.5)PO4 cathode in aqueous lithium hydroxide as the electrolyte showed reversible lithium intercalation.  相似文献   
8.
Earth experiments must be carried out on terrain that deforms similarly to the lunar terrain to assess the tractive performances of lunar vehicles. Most notably, terrain compaction and shear response underneath the lunar vehicle wheels must represent that of the Moon. This paper discusses the development of a new lunar soil simulant, Glenn Research Center lunar soil simulant #1 (GRC-1), which meets this need. A semi-empirical design approach was followed in which the soil was created by mixing readily available manufactured sands to a particle size distribution similar to the coarse fraction of lunar soil. By varying terrain density, a broad range of in situ cone penetration measurements collected by the Apollo mission astronauts can be replicated. An extensive set of characterization data is provided in this article to facilitate the use of this material. For reference, the index and geotechnical properties of GRC-1 are compared to the lunar soil and existing lunar soil simulants.  相似文献   
9.
In this paper we critically examine a recently posed paradox (tippe top paradox in relativity) and its suggested resolution. A tippe top when spun on a table, tips over after a few rotations and eventually stands spinning on its stem. The ability of the top to demonstrate this charming feat depends on its geometry (all tops are not tippe tops). To a rocket-bound observer the top geometry should change because of the Lorentz contraction. This gives rise to the possibility that for a sufficiently fast observer the geometry of the top may get altered to such an extent that the top may not tip over! This is certainly paradoxical since a mere change of the observer cannot alter the fact that the top tips over on the table. In an effort to resolve the issue the authors of the paradox compare the equations of motion of the particles of the top from the perspective of the inertial frames of the rocket and the table and observe among other things that (1) the relativity of simultaneity plays an essential role in resolving the paradox and (2) the puzzle in some way is connected with one of the corrolaries of special relativity that the notion of rigidity is inconsistent with the theory. We show here that the question of the incompatibility of the notion of rigidity with special relativity has nothing to do with the current paradox and the role of the lack of synchronization of clocks in the context of the paradox is grossly over-emphasized. The conventionality of simultaneity of special relativity and the notion of the standard (Einstein) synchrony in the Galilean world have been used to throw light on some subtle issues concerning the paradox.  相似文献   
10.
In study of polymer-salt complexes usually one is interested in the dc conductivity, which can be extracted from impedance spectroscopy. However, impedance spectroscopy yields a host of additional information, for example, frequency variation of the measured admittance or impedance, nature of the Cole-Cole plot and dielectric function. Proper analysis of this information reveals details of the microstructure and transport processes in the sample. This in turn, will lead to development of better solid electrolytes with tailor-made properties. The polymer electrolyte PEO-NH4ClO4 shows an interesting variation in its properties in two different regimes, (1) where salt concentration is below ∼ 19 wt.% and (2) above this concentration. In the present paper we suggest an equivalent circuit incorporating a constant phase element (CPE), which reproduces the complex admittance behavior at different salt fractions. Paper presented at the 2nd International Conference on Ionic Devices, Anna University, Chennai, India, Nov. 28–30, 2003.  相似文献   
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