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961.
Alginate beads, often used for controlled release of enzymes and drugs, are usually produced by spraying sodium alginate liquid into a gelling agent using mechanical vibration nozzle or air jet. In this work an alternative method of electro-spray was employed to form droplets with desired size from a highly viscous sodium alginate solution using constant DC voltage. The droplets were then cured in a calcium chloride solution. The main objective was to produce mono-sized beads from such a highly viscous and non-Newtonian liquid (1000-5000 mPa s). The effects of nozzle diameter, flow rate and concentration of liquid on the size of the beads were investigated. Among the parameters studied, voltage had a pronounced effect on the size of beads as compared to flow rate zzle diameter and concentration of alginate liquid. The size of beads was reduced to a minimum value with increasing the voltage in the range of 0-10 kV. At the early stages of voltage increase (I.e. Up to about 4 kV), the rate of size reduction was relatively low, while the dripping mode dominated. However, in the middle part of the range of applied voltage, where the rate of size reduction was high (I.e. About 4-7 kV), an unstable transition occurred between dripping and jetting. At the end part of the range (I.e. 7-10 kV) jet mode of spray was observed. Increasing the height of fall of the droplets was found to improve the sphericity of the beads, because of the increased time of flight for the droplets. This was especially identifiable at higher concentrations of the alginate liquid (I.e. 3 w/v%)  相似文献   
962.
The mm-long carbon nanotube (CNT) arrays were grown in a floating catalyst reactor, using xylene-ferrocene and a small amount of acetic acid as the feed. The CNT arrays deposited on a quartz substrate at several positions along the reactor were extensively characterized using Raman spectroscopy, scanning electron microscopy, X-ray diffraction, high-resolution transmission electron microscopy, and optical microscopy. Various characterization methods consistently reveal that the acetic acid additive to the feed alleviates deposition of amorphous carbon layer, which gradually thickens CNTs along the reactor. The acetic acid also resulted in a higher growth rate along the so-called growth window, where CNT arrays are deposited on the quartz substrate. High-performance liquid chromatography of extracted byproducts (PAHs) confirmed the presence of some polycyclic aromatic hydrocarbons. The solid weight of PAHs decreased upon addition of ferrocene as the catalyst precursor, as well as of acetic acid to xylene feed. The results suggest that primary light products of xylene pyrolysis can be competitive reactants for both catalytic and subsequent pyrolytic reactions. They may also be more efficient feeds for CNT growth than xylene itself.  相似文献   
963.
964.
965.
We present a method to solve boundary value problems using artificial neural networks (ANN). A trial solution of the differential equation is written as a feed-forward neural network containing adjustable parameters (the weights and biases). From the differential equation and its boundary conditions we prepare the energy function which is used in the back-propagation method with momentum term to update the network parameters. We improved energy function of ANN which is derived from Schrodinger equation and the boundary conditions. With this improvement of energy function we can use unsupervised training method in the ANN for solving the equation. Unsupervised training aims to minimize a non-negative energy function. We used the ANN method to solve Schrodinger equation for few quantum systems. Eigenfunctions and energy eigenvalues are calculated. Our numerical results are in agreement with their corresponding analytical solution and show the efficiency of ANN method for solving eigenvalue problems.  相似文献   
966.
In this contribution, a novel dual-channel speech enhancement technique is introduced. The proposed approach uses the dissimilarity between the power of received signals in the two channels as a criterion for speech enhancement and noise reduction. We claim that in near field conditions, where the distances between microphones and sound source are short, the difference in the received power levels at the two microphones is an estimate of the clean speech signal power. Then, apply this theory to present an optimum method for speech enhancement. Fortunately, the method has the ability to cope with problems such as transient noise and nearby microphones which are two of the main problems of the proposed dual-microphone speech enhancement techniques. Using objective speech quality measures and spectrogram analysis, we show that the proposed method results in improved speech quality.  相似文献   
967.
In this project, Pt/NiO?GO nanocatalyst is grown on nickel foam (NF) and, its catalytic activity towards electrochemical oxidation of methanol in acidic media is studied. The first step is devoted to the synthesis of NiO?GO support by a hydrothermal method. Then Pt nanoparticles (~34.3 nm) are electrodeposited on this supporting material. Hydrothermal and electrochemical deposition conditions are optimized. Surface of modified NF was inspected for physical characterization and Chemical composition by some techniques such as field emission scanning electron microscopy (FESEM), energy‐dispersive X‐ray spectra (EDS), and X‐ray diffraction (XRD). In the electrochemical section, the catalytic performance of Pt/NiO?GO/NF towards methanol oxidation is investigated by cyclic voltammetry and chronoamperometry measurements. The electrochemical impedance spectroscopy (EIS) is elected to deliberate charge transfer resistance on the catalyst surface. Mass activity, electrochemical surface area (ECSA) and durability of prepared catalysts are compared with commercial Pt/C. Deliberations prove the superiority of Pt/NiO?GO/NF towards methanol oxidation in acidic media. The Superior quality of synthesized nanocatalyst that is attributed to the synergetic effect of the NiO?GO support material and Pt nanoparticles, indicate that Pt/NiO?GO/NF can be successfully used as the anode in the direct methanol fuel cell (DMFC).  相似文献   
968.
Polylactic acid (PLA) and thermoplastic starch (TPS) are known as bio‐based and biodegradable thermoplastic polymers that can be used in different applications owing to their inherent physical and mechanical properties. In order to reduce the higher costs of PLA and tuning its physical and mechanical properties suitable for short life packaging applications, blending of PLA with the TPS, more economical biodegradable polymer, has been considered in academic and industrial researches. However, melt blending of PLA with TPS without compatibilization process caused some drawbacks such as coarsening morphology and declining mechanical properties and ductility because of thermodynamic immiscibility, which may restrict its usage in packaging applications. Subsequently, our approach in this research is compatibilization of PLA/TPS blends by utilization of primary well tuning of TPS formulation with a combination of sorbitol and glycerol plasticizers. In this work, the wide composition range of melt mixed PLA/TPS blends was prepared using a laboratory twin screw extruder. The effects of microstructure on the rheological and mechanical properties of PLA/TPS blends were studied using different methods such as scanning electron microscopy (SEM) images, contact angle, oscillatory shear rheological measurements, and tensile and impact strength mechanical tests. The rheological and mechanical properties were interpreted according to the morphological features and considering the possibility of plasticizer migration from TPS to PLA phase during melt blending. Reduction in complex viscosity and storage modulus of PLA matrix samples indicates the improved melt processability of blends. Finally, in comparison with mechanical results reported in literature, our simple approach yielded the blends with elastic modulus and ductility comparable with those of chemically compatibilized PLA/TPS blends.  相似文献   
969.
Journal of Solid State Electrochemistry - A modified electrode PAN/PPY/cMWCNTs composed of polyaniline/polypyrrole (PAN/PPY) bilayer conducting polymer film, carboxylated multi-walled carbon...  相似文献   
970.
In this study, the photocatalytic degradation of Reactive Blue 81 (RB81) using synthesized NiO-doped ZnO–ZrO2 nanoparticles under UV irradiation was investigated. Then, the products were characterized by Scanning electron microscope (SEM), X-ray diffraction (XRD), and diffuse reflectance spectroscopy (DRS). The removal rate of RB81 using ZnO–ZrO2 after 180?min of irradiation was 96.7%. Nickel oxide (NiO) was used as an additive to ZnO–ZrO2 for improvement of RB81 degradation via photocatalysis process. Photodegradation of RB81 was achieved to 100% using ZnO–ZrO2–NiO nanoparticles with ratio of 1:2:0.3 after 180?min of irradiation. There was a red shift in absorption bands (from 410?nm to 435?nm) observed in increasing of NiO to ZnO–ZrO2 nanoparticle, that it might lead to a higher photocatalytic activity under visible light. Response surface methodology (RSM) was used for optimization of experimental and these results were obtained: solution pH = 3, ZnO–ZrO2–NiO dosage = 15?mg/L, and the initial RB81 concentration = 5?mg/L. The photodegredation of RB81 followed pseudo-first order kinetic according to the Langmuir–Hinshelwood model.  相似文献   
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