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91.
Some Properties of Residuated Lattices   总被引:1,自引:0,他引:1  
We investigate some (universal algebraic) properties of residuated lattices--algebras which play the role of structures of truth values of various systems of fuzzy logic.  相似文献   
92.
If there are correlations between two qubits, then the results of the measurement on one of them can help to predict measurement results on the other one. It is an interesting question as to what can be predicted about the results of two complementary projective measurements on the first qubit. To quantify these predictions the complementary knowledge excesses are used. A nontrivial constraint restricting them is derived. For any mixed state and for arbitrary measurements the knowledge excesses are bounded by a factor depending only on the maximal violation of Bell's inequalities. This result is experimentally verified on two-photon Werner states prepared by means of spontaneous parametric down-conversion.  相似文献   
93.
We propose a quantum device that can approximate any projective measurement on a qubit-a quantum "multimeter." The desired measurement basis is selected by the quantum state of a "program register." Two different kinds of programs are considered and in both cases the device is optimized with respect to maximal average fidelity (assuming uniform distribution of measurement bases). Quantum multimeters exhibiting the covariance property are introduced and an optimal covariant multimeter with a single-qubit program register is found. Possible experimental realization of the simplest proposed device is presented.  相似文献   
94.
Electrophoretic mobilities and shapes of zones of sanguinarine and chelerythrine in aqueous media around pH 7 are affected by limited solubility of their uncharged forms and by the pH-dependent chemical equilibrium between cationic and uncharged forms of these alkaloids. The sanguinarine solubility in sodium MOPS of pH 7.4 was estimated at 50 micromol x L(-1). Sanguinarine zones in this buffer have the shape of tailed peak with concentration-independent mobility if the injected sanguinarine concentration exceeds this solubility limit only slightly. The chelerythrine solubility is higher because of lower dissociation constants of its cations. Precipitation of sanguinarine and chelerythrine with the phosphate anions decelerates their electrophoretic transport in phosphate buffer. Sanguinarine solubility is 5 micromol x L(-1) at the most in 13 mmol x L(-1) sodium phosphate buffer of pH 7.4. Acidifying of the sample up to pH 3 decreases the tailing of the peaks of sanguinarine and chelerythrine and contributes to the rise of sharp maxima of their migrating zones. Any capillary coating deteriorates the peak shape.  相似文献   
95.
The unique optical and photoredox properties of heptazine-based polymeric carbon nitride (PCN) materials make them promising semiconductors for driving various productive photocatalytic conversions. However, their typical absorption onset at ca. 430–450 nm is still far from optimum for efficient sunlight harvesting. Despite many reports of successful attempts to extend the light absorption range of PCNs, the determination of the structural features responsible for the red shift of the light absorption edge beyond 450 nm has often been obstructed by the highly disordered structure of PCNs and/or low content of the moieties responsible for changes in optical and electronic properties. In this work, we implement a high-temperature (900 °C) treatment procedure for turning the conventional melamine-derived yellow PCN into a red carbon nitride. This approach preserves the typical PCN structure but incorporates a new functionality that promotes visible light absorption. A detailed characterization of the prepared material reveals that partial heptazine fragmentation accompanied by de-ammonification leads to the formation of azo-groups in the red PCN, a chromophore moiety whose role in shifting the optical absorption edge of PCNs has been overlooked so far. These azo moieties can be activated under visible-light (470 nm) for H2 evolution even without any additional co-catalyst, but are also responsible for enhanced charge-trapping and radiative recombination, as shown by spectroscopic studies.  相似文献   
96.
M. Knob  V. Uruba 《PAMM》2008,8(1):10621-10622
In a blind trough cavity subject to a jet– impingement, the jet switching phenomenon has been known for decades. The large vortices, formed by the Kelvin– Helmholtz instability play a crucial role in this phenomenon– they are the main cause of the fluid entrainment phenomenon, which consequently evoke the Coanda effect and finally results in the jet switch. As the jet swings, the vortical structure inside the cavity changes together with the impinigement point. The aim of this article is to describe the relationship between the wall shear stress, i.e. the motion of the impingement point, and the vortical structure.The analysed data were obtained using the TR PIV system, the caity aspect ratios 16:24 and 18:24, jet hydraulic diameter based Reynolds numbers 3000, 11200 and 19600, and the impingement angles 0°, 5°, 10° and 15°. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   
97.

A set of 31 structurally different chiral pharmaceutical compounds was used as model analytes for investigation of the enantioselective potential of two immobilized polysaccharide-based chiral stationary phases under normal and reversed phase separation conditions. These chiral stationary phases differed in the polymeric backbone, amylose or cellulose, but possessed the same derivatization functionality. The results showed that the tris(3,5-dimethylphenylcarbamate) of amylose and cellulose have very broad, and often complementary, enantiorecognition abilities. In general, normal phase separation mode seemed to be more advantageous for separation of the majority of studied pharmaceuticals no matter if amylose- or cellulose-based columns were used. However, in certain cases the reversed phase separation system yielded better results. The combination of these two immobilized chiral stationary phases offers a powerful tool for enantioseparation of different types of pharmaceuticals in the normal and/or reversed phase mode.

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