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1.
P.A. Ramachandran 《Numerical Methods for Partial Differential Equations》2006,22(4):831-846
Time‐dependent differential equations can be solved using the concept of method of lines (MOL) together with the boundary element (BE) representation for the spatial linear part of the equation. The BE method alleviates the need for spatial discretization and casts the problem in an integral format. Hence errors associated with the numerical approximation of the spatial derivatives are totally eliminated. An element level local cubic approximation is used for the variable at each time step to facilitate the time marching and the nonlinear terms are represented in a semi‐implicit manner by a local linearization at each time step. The accuracy of the method has been illustrated on a number of test problems of engineering significance. © 2005 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq 2006 相似文献
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A new approach to identify the independent amplitudes along with their partial wave multipole expansions, for photo-and electro-production
is suggested, which is generally applicable to mesons with arbitrary spin-parity. These amplitudes facilitate direct identification
of different resonance contributions.
相似文献
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N. Ponpandian A. Narayanasamy D. Prabhu K. Ganesan M. Manivel Raja K. Chattopadhyay 《Journal of magnetism and magnetic materials》2006
The Fe73.5Cu1Nb3Si13.5B9 FINEMET alloy has been prepared by the rapid solidification technique. The critical behaviour of this alloy in the amorphous as well as in its nanocrystalline states has been studied near their respective Curie temperatures. From the values of the critical exponents one can conclude that the alloy behaves like a 3D Heisenberg ferromagnet in the amorphous and nanocrystalline states. But there exists a slight increase in the value of β for the alloy annealed at 823 K (the nanocrystalline state) as observed in most of the amorphous alloys. 相似文献
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This Note deals with the sensitivity analysis of a newtonian incompressible fluid driven by the Navier–Stokes equations with respect to the dynamic of the fluid domain boundary. The structure of the gradient with respect to the velocity of the domain for a given cost function is established. This result is obtained using new shape derivation tools for Eulerian functionals and the Min–Max derivation principle. To cite this article: R. Dziri et al., C. R. Acad. Sci. Paris, Ser. I 338 (2004). 相似文献
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Jacques Rouzaud MatthewD. Jones Robert Raja BrianF.G. Johnson John MeurigThomas MelindaJ. Duer 《Helvetica chimica acta》2003,86(5):1753-1759
A set of new, air‐stable, RhI‐based heterogeneous asymmetric hydrogenation catalysts have been synthesised, characterised, and tested. Individual members of this new family all exhibit good enantioselectivity. 相似文献
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The near flow field of small aspect ratio elliptic turbulent free jets (issuing from nozzle and orifice) was experimentally
studied using a 2D PIV Two point velocity correla tions in these jets revealed the extent and orientation of the large scale
structures in th e major and minor planes. The spatial filtering of the instantaneous velocity field using Gaussian convolution
kernel shows that while a single large vortex ring circumscribing the jet seems to be present at the exit of nozzle, the orifice
jet exhibited a number of smaller vortex ring pairs close to jet exit. The smaller length scale observed in the case of the
orifice jet is rep resentative of the smaller azimuthal vor tex rings that generate axial vortex field as they are convected.
This results in the axis-switching in th e case of orifice jet and may have a mechanism differ ent from the self induction
process as observed in the case of contoured nozzle jet flow. 相似文献
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The Ni(II) ion catalyzed thermal decomposition of peroxomonosulfate (PMS) was studied in the pH range 3.42–5.89. The rate is first order in [PMS] and Ni(II) ion concentrations. At pH greater than or equal to 5.23, the reaction becomes zero order in [PMS] and this changeover in the order of the reaction occurs at a higher concentration of nickel ions. The first‐order kinetics in PMS can be explained as a rate‐limiting step and is the transformation of nickel peroxomonosulfate into nickel peroxide. This peroxide intermediate reacts rapidly with another PMS to give oxygen and Ni(II). The formation of nickel peroxide is associated with a small negative or nearly zero entropy of activation. The zero‐order kinetics in [PMS] can be explained by the fact that the hydrolysis of aquated nickel(II) ions into hydroxocompounds is the rate‐limiting step. The turnover number is 2 at pH 3.42 and increases with pH. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 320–237, 2007 相似文献
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