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11.
    
We discuss the data sampling frequency, the spectral resolution, and the limit for non-aliasing in the static modulated Fourier transform spectrometer based on a modified Sagnac interferometer. The measurement was performed in a very short 4 ms, which is applicable for real time field operation. The improved spectrometer characteristics were used to investigate the spectral properties of an InGaAs light emitting diode. In addition, The measured spectral peak was shifted from 6420 cm−1 to 6365 cm−1, as the temperature increased from 25 °C to 40 °C, when the operating current is fixed to be 0.55 A. As the applied current increased from 0.30 A to 0.55 A at room temperature, the spectral width was broadened from 316 cm−1 to 384 cm−1. Compared to the conventional Fourier transform spectrometer, the measured spectral width by the static modulated Fourier transform spectrometer showed a deviation less than 10%, and the spectral peak shift according to the temperature rise showed a difference within 2%.  相似文献   
12.
The compressible steady state Navier–Stokes system with viscosity is considered on a plane polygonal domain. It is shown that if a solution satisfies certain reasonable regularity conditions, and if the velocity is non-zero and points into the domain at a vertex of the polygon, then the gradient of the density either becomes infinite or has a jump discontinuity at each point of the streamline emanating from the vertex.  相似文献   
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The effects of blending ratio on mixtures of an alcohol-to-jet (ATJ) fuel and a conventional petroleum-derived fuel on first stage ignition and overall ignition delay are examined at engine-relevant ambient conditions. Experiments are conducted in a high-temperature pressure vessel that maintains a small flow of dry air at the desired temperature (825 K and 900 K) and pressure (6 MPa and 9 MPa) for fuel injections from a custom single-hole, axially-oriented injector, representing medium (7.5 mg) and high (10 mg) engine loading. Formaldehyde, imaged using planar laser-induced fluorescence, is measured at discrete time steps throughout the first and second stage ignition process and is used as a marker of unburned short-chain hydrocarbons formed after the initial breakdown of the fuel. The formaldehyde images are used to calculate the first stage ignition delay for each ambient and fuel loading condition. Chemiluminescence imaging of excited hydroxyl radical at 75 kHz is used to determine the overall ignition delay. At all conditions, increased volume fraction of ATJ resulted in longer, but non-linearly increasing, overall ignition delay. Across all of the blends, first stage ignition delay accounted for about 15% of the increase in overall ignition delay compared to the military's aviation kerosene, F-24, which is Jet A with additives, while extended first stage ignition duration accounted for 85% of the increase. It is observed that blends consisting of 0–60% by volume of the low cetane number ATJ fuel produced nearly identical first stage ignition delays. These results will inform the development of ignition models that can capture the non-linear effects of fuel blending on ignition processes.  相似文献   
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Phase transformations in squaric acid (H2C4O4) have been investigated by thermogravimetry and differential scanning calorimetry with different heating rates β. The mass loss in TG apparently begins at onset temperatures Tdi=245±5 °C (β=5 °C min?1), 262±5 °C (β=10 °C min?1), and 275±5 °C (β=20 °C min?1). A polymorphic phase transition was recognized as a weak endothermic peak in DSC around 101 °C (Tc+). Further heating with β=10 °C min?1 in DSC revealed deviation of the baseline around 310 °C (Ti), and a large unusual exothermic peak around 355 °C (Tp), which are interpreted as an onset and a peak temperature of thermal decomposition, respectively. The activation energy of the thermal decomposition was obtained by employing relevant models. Thermal decomposition was recognized as a carbonization process, resulting in amorphous carbon.  相似文献   
17.
We study the Heat equation in the polyhedral cylinder with a non-convex edge. We construct the singularity functions depending on the time and edge axis, and the coefficient of the singularity, called the stress intensity distributions, and show regularity results for the solution and the coefficient. The regularity is achieved in the (not weighted) Sobolev space in the L2 and L q spaces, respectively. An application to the finite polyhedral cylinder is described.  相似文献   
18.
The barotropic compressible Navier–Stokes equations in an unbounded domain are studied. We prove the unique existence of the solution (u, p) of the system (1.1) in the Sobolev spaceHk + 3 × Hk + 2provided that the derivatives of the data of the problem are sufficiently small, wherek ≥ 0 is any integer. The proof follows from an analysis of the linearized problem, the solvability of the continuity equation, and the Schauder fixed point theory. Similar smoothness results are obtained for a linearized form of (1.1).  相似文献   
19.
The ion exchange membrane using polysulfone (PSf) and polyether ether ketone (PEEK) as a basic material was prepared to apply in the polymer electrolyte membrane electrolysis (PEME). The sulfonated block copolymer of PSf and poly(phenylene sulfide sulfone) (SPSf-co-PPSS) and the sulfonated PEEK (SPEEK) were blended with tungstophosphoric acid (TPA) to avoid water swelling at elevated temperatures led to decrease in mechanical strength. These prepared ion exchange membranes showed some interesting characteristics including physicochemical stabilities, mechanical and membrane properties.The prepared ion exchange membrane was utilized to prepare the membrane electrode assembly (MEA). MEA consisted of Pt/PEM/Pt was prepared by equilibrium and non-equilibrium impregnation–reduction (I–R) methods. The prepared MEA by non-equilibrium I–R method was used in the PEME unit cell. The cell voltages of the MEA using SPSf-co-PPSS/TPA and SPEEK/TPA membranes were 1.83 V and 1.90 V at 1 A/cm2 and 80 °C, with platinum loadings of 1.12 and 1.01 mg/cm2, respectively.  相似文献   
20.

Background  

Rieske non-heme iron aromatic ring-hydroxylating oxygenases (RHOs) are multi-component enzyme systems that are remarkably diverse in bacteria isolated from diverse habitats. Since the first classification in 1990, there has been a need to devise a new classification scheme for these enzymes because many RHOs have been discovered, which do not belong to any group in the previous classification. Here, we present a scheme for classification of RHOs reflecting new sequence information and interactions between RHO enzyme components.  相似文献   
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