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91.
Most developed countries support farming activities through policies that are tailored to meet their specific social, economic and environmental objectives. Economic and environmental efficiency have recently become relevant targets of most of these policies, whose sound implementation can be enhanced by monitoring farm performance from a multidimensional perspective. This paper proposes farm-level technical and environmental efficiency measures that recognize the stochastic conditions in which production takes place. A state-contingent framework is used to model production uncertainty. An implementable representation of the technology is developed using data envelopment analysis. The application focuses on a sample of Catalan arable crop farms. Results suggest that technical efficiency is slightly lower in bad than in good growing conditions. Nitrogen pollution can decrease substantially more under good than bad growing conditions.  相似文献   
92.
We present a compact and stable dual-wavelength laser source for onboard atom interferometry with two different atomic species. It is based on frequency-doubled telecom lasers locked on a femtosecond optical frequency comb. We take advantage of the maturity of fiber telecom technology to reduce the number of free-space optical components, which are intrinsically less stable, and to make the setup immune to vibrations and thermal fluctuations. The source provides the frequency agility and phase stability required for atom interferometry and can easily be adapted to other cold atom experiments. We have shown its robustness by achieving the first dual-species K-Rb magneto-optical trap in microgravity during parabolic flights.  相似文献   
93.
Ultracold atomic physics experiments offer a nearly ideal context for the investigation of quantum systems far from equilibrium. We describe three related emerging directions of research into extreme non‐equilibrium phenomena in atom traps: quantum emulation of ultrafast atom‐light interactions, coherent phasonic spectroscopy in tunable quasicrystals, and realization of Floquet matter in strongly‐driven lattice systems. We show that all three should enable quantum emulation in parameter regimes inaccessible in solid‐state experiments, facilitating a complementary approach to open problems in non‐equilibrium condensed matter.  相似文献   
94.
Advances in robustness, selectivity and sensitivity in organic solvent vapour detection can be achieved by the application of β-cyclodextrines as coatings for mass sensitive chemical sensors. Linking the cyclodextrines with e.g. diiodooctane combines the molecular recognition capabilities of host-guest chemistry with the high stability of polymeric layers. Special increase in selectivity is achieved with anhydro cyclodextrines, since their flattened conus is adapted to benzene derivatives as can also be shown by computer modelling. Furthermore methylation elongates the cavity, guaranteeing an optimised engulfing of the analytes. In this way even a differentiation between p- and m-xylene vapours and a QMB detection limit of some μL/L is possible.  相似文献   
95.
Structural effects in the chiral base and the influence of some key reaction parameters (catalyst type and solvent) in the Pd-induced enantioselective decarboxylation (cascade reaction) of three different ,-disubstituted benzyl β-ketoesters were explored. The reaction intermediate after debenzylation (β-keto-carboxylic acid) was synthesized and its decarboxylation studied independently. The highest ee (up to 60%) in the cascade reaction was achieved with those substrates that contained an aromatic ring system and with chiral amino alcohols that possessed an extended aromatic ring (quinine and quinidine). Polar solvents with weak H-bond donor and acceptor properties favor enantioselection.  相似文献   
96.
We present a new finite element – finite volume (FEFV) method combined with a realistic equation of state for NaCl–H2O to model fluid convection driven by temperature and salinity gradients. This method can deal with the nonlinear variations in fluid properties, separation of a saline fluid into a high-density, high-salinity brine phase and low-density, low-salinity vapor phase well above the critical point of pure H2O, and geometrically complex geological structures. Similar to the well-known implicit pressure explicit saturation formulation, this approach decouples the governing equations. We formulate a fluid pressure equation that is solved using an implicit finite element method. We derive the fluid velocities from the updated pressure field and employ them in a higher-order, mass conserving finite volume formulation to solve hyperbolic parts of the conservation laws. The parabolic parts are solved by finite element methods. This FEFV method provides for geometric flexibility and numerical efficiency. The equation of state for NaCl–H2O is valid from 0 to 750°C, 0 to 4000 bar, and 0–100 wt.% NaCl. This allows the simulation of thermohaline convection in high-temperature and high-pressure environments, such as continental or oceanic hydrothermal systems where phase separation is common.  相似文献   
97.
K. Geiger 《Rheologica Acta》1988,27(2):209-211
Zusammenfassung Basierend auf dem das Fließverhalten strukturviskoser Fluide sehr genau beschreibenden sogenannten Carreau-Ansatz wird eine Näherungsformel für die Drehmoment-Schergeschwindigkeit-Charakteristik (scheinbare Fließkurve) des Platte-Platte-Rotationsrheometers (PPR) im stationären Versuch vorgeschlagen. Die gewonnenen Resultate können in die Auswertungseinheit des Platte-Platte-Systems leicht integriert werden und damit das Anwendungsgebiet des PPR-Systems für konzentrierte Polymerlösungen und Polymerschmelzen beträchtlich erweitern.
A new simplified, but very accurate, formula is proposed for the torque-rate characteristic (apparent flow curve) of the parallel-disk rotational rheometer (PDR) in steady-shear mode, based on the Carreau formula for the viscosity of pseudoplastic fluids. The results can easily be incorporated into the evaluation of the parallel-disk system and therefore the application field of the PDR-system can be extended considerably for concentrated polymer solutions and polymer melts.
  相似文献   
98.
This work characterizes the adsorption, structure, and binding mechanism of oxygenated organic species from cyclohexane solution at the liquid/solid interface of optically flat alumina-supported palladium nanoparticle surfaces prepared by atomic layer deposition (ALD). The surface-specific nonlinear optical vibrational spectroscopy, sum-frequency generation (SFG), was used as a probe for adsorption and interfacial molecular structure. 1-Hexanoic acid is an overoxidation product and possible catalyst poison for the aerobic heterogeneous oxidation of 1-hexanol at the liquid/solid interface of Pd/Al(2)O(3) catalysts. Single component and competitive adsorption experiments show that 1-hexanoic acid adsorbs to both ALD-prepared alumina surfaces and alumina surfaces with palladium nanoparticles, that were also prepared by ALD, more strongly than does 1-hexanol. Furthermore, 1-hexanoic acid adsorbs with conformational order on ALD-prepared alumina surfaces, but on surfaces with palladium particles the adsorbates exhibit relative disorder at low surface coverage and become more ordered, on average, at higher surface coverage. Although significant differences in binding constant were not observed between surfaces with and without palladium nanoparticles, the palladium particles play an apparent role in controlling adsorbate structures. The disordered adsorption of 1-hexanoic acid most likely occurs on the alumina support, and probably results from modification of binding sites on the alumina, adjacent to the particles. In addition to providing insight on the possibility of catalyst poisoning by the overoxidation product and characterizing changes in its structure that result in only small adsorption energy changes, this work represents a step toward using surface science techniques that bridge the complexity gap between fundamental studies and realistic catalyst models.  相似文献   
99.
We present a method to accurately measure the electrophoretic mobility of spherical colloids at high volume fractions in real space using confocal laser scanning microscopy (CLSM) and particle tracking. We show that for polymethylmethacrylate (PMMA) particles in a low-polar, density- and refractive-index-matched mixture of cyclohexylbromide and cis-decahydronaphthalene, the electrophoretic mobility decreases nonlinearly with increasing volume fraction. From the electrophoretic mobilities, we calculate the ζ-potential and the particle charge with and without correcting for volume fraction effects. For both cases, we find a decreasing particle charge as a function of volume fraction. This is in accordance with the fact that the charges originate from chemical equilibria that represent so-called weak association and/or dissociation reactions. Finally, as our methodology also provides data on particle self-diffusion in the presence of an electric field, we also analyze the diffusion at different volume fractions and identify a nonlinear decreasing trend for increasing volume fraction.  相似文献   
100.
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