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791.
792.
Exact solutions of the Navier-Stokes equations are derived by a Laplace-transform technique for two-dimensional, incompressible flow of an electrically conducting fluid past an infinite porous plate under the action of a transverse magnetic field subject to the conditions: (i) the magnetic Prandtl number Pm is unity, and (ii) the Alfven velocity is less than the suction velocity. It is assumed that the flow is independent of the distance parallel to the plate and that the velocity component normal to the plate is constant. General formulae are derived for the velocity distribution and the magnetic field in terms of the given external velocity. The skin-friction is obtained and some special cases are considered. 相似文献
793.
The two-dimensional, incompressible flow past an infinite plate of a weakly conducting fluid in the presence of a transverse magnetic field is discussed when the suction velocity normal to the plate as well as the external flow velocity vary periodically with time. Expressions for the velocity and the skin-friction in the boundary layer have been obtained in a non-dimensional form. 相似文献
794.
This paper deals with the two-dimensional unsteady flow of a conducting viscous incompressible fluid between two parallel, porous plates, one of which is fixed, while the other is uniformly accelerated, when there is a transverse magnetic field. It is shown that, for a given Hartmann number M, as suction parameter β increases, the velocity at any point of the fluid increases, the Skin friction at the stationary plate increases, while that at the accelerated plate decreases. The results are true, as time T increases, for given Hartmann number M and the suction parameter β. The results also hold good for a given β, as M increases when the magnetic lines of force are fixed relative to the plate, while they are just opposite for the magnetic lines of force fixed relative to the fluid. 相似文献
795.
796.
Extensive randomization of the substituents is found in mono- and disubstituted diphenylacetylenes under electron impact conditions. The study of diphenylacetylenes with a variety of substituents indicates that the electron-withdrawing groups favour the substituent scrambling, AH the substituted diphenylacetylenes give an ion at m/z 176, having a common ion-structure, arising as a result of the expulsion of a hydrogen radical and the substituent in monosubstituted diphenylacetylenes and the expulsion of both the substituents in disubstituted diphenylacetylenes. A ring-expanded structure is postulated for this common fragment. 相似文献
797.
Effective atomic numbers (Zeff) for different materials of dosimetric interest have been calculated for total photon interaction in the energy region 1 keV–20 MeV. The calculations are made using the mass attenuation coefficients data from Tables of X-ray Mass Attenuation Coefficients and Mass Energy-absorption Coefficients 1 keV to 20 MeV for elements Z = 1 to 92 and 48 Additional Substances of Dosimetric Interest, J. H. Hubbell and S. M. Seltzer (Hubbell and Seltzer, 1995), NISTIR-5632. The variation of Zeff value with energy is discussed. 相似文献
798.
Sanjiv Kumar J. V. Ramana V. S. Raju J. Arunachalam S. Gangadharan 《Fresenius' Journal of Analytical Chemistry》1992,343(12):879-880
Summary The stoichiometry of cadmium telluride has been determined by the non-destructive technique of XPS. The determination has been based on differential photoionisation cross-sections, electron mean free paths and areas due to M5 electrons of Cd and Te. The stoichiometry of Cd and Te determined by XPS has been found to be in good agreement with that obtained by analysing Cd and Te independently by chemical methods. 相似文献
799.
K. Venkata Ramiah C. A. Indira Chary P. Usha Bai 《Proceedings Mathematical Sciences》1967,66(5):279-286
Hydrogen bonding of O-H ... O=C and S-H ... O=C type has been studied in parachlorophenol and thiophenol with dimethyl and diphenyl amides and from the equilibrium constants, variation in the integrated absorption intensities and frequency shifts, the strength of the interaction in these complexes is discussed. In these systems diphenyl amides form weaker H-bond compared to that with the corresponding dimethyl amides. In dimethyl amides, the interaction is in the order dimethyl acetamide > dimethyl propionamide > dimethyl formamide. Similar results are obtained with diphenyl amides. 相似文献
800.
A convenient method for determination of thallium(III) is based on photochemical reduction with hydrogen peroxide in the presence of bromide as catalyst, followed by oxidation of thallium(I) with potassium bromate. 相似文献