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61.
《Physics letters. A》2014,378(30-31):2308-2311
62.
Thermomagnetoelectroelastic crack branching of magnetoelectro thermoelastic materials is theoretically investigated based on Stroh formalism and continuous distribution of dislocation approach. The crack face boundary condition is assumed to be fully thermally, electrically and magnetically impermeable. Explicit Green’s functions for the interaction of a crack and a thermomagnetoelectroelastic dislocation (i.e., a thermal dislocation, a mechanical dislocation, an electric dipole and a magnetic dipole located at a same point) are presented. The problem is reduced to two sets of coupled singular integral equations with the thermal dislocation and magnetoelectroelastic dislocation densities along the branched crack line as the unknown variables. As a result, the formulations for the stress, electric displacement and magnetic induction intensity factors and energy release rate at the branched crack tip are expressed in terms of the dislocation density functions and the branch angle. Numerical results are presented to study the effect of applied thermal flux, electric field and magnetic field on the crack propagation path by using the maximum energy release rate criterion. 相似文献
63.
Esa Kokko Pirjo Pietikinen Jari Koivunen Jukka V. Seppl 《Journal of polymer science. Part A, Polymer chemistry》2001,39(21):3805-3817
Ethene was copolymerized (1) with 1,5‐hexadiene with rac‐ethylenebis(indenyl)zirconium dichloride/methylaluminoxane (MAO) used as a catalyst and (2) with 1,7‐octadiene with bis(n‐butylcyclopentadienyl)zirconium dichloride/MAO and rac‐ethylenebis(indenyl)hafnium dichloride (Et[Ind]2HfCl2)/MAO used as catalysts at 80 °C in toluene. The copolymer microstructure and the influence of diene incorporation on the rheological properties were examined. Ethene and 1,5‐hexadiene formed a copolymer in which a major fraction of the 1,5‐hexadiene was incorporated into rings and a small fraction formed 1‐butenyl branches. The copolymerization of ethene with 1,7‐octadiene resulted in a higher selectivity toward branch formation. Some of the branches formed long‐chain‐branching (LCB) structures. The ring formation selectivity increased with decreasing ethene concentration in the polymerization reactor. Melt rheological properties of the diene copolymers resembled those of metallocene‐catalyzed LCB homopolyethenes and depended on the vinyl content, the catalyst, and the polymerization conditions. At high diene contents, all three catalysts produced crosslinked polyethene. This was especially pronounced with Et[Ind]2HfCl2, where only 0.2 mol % 1,7‐octadiene in the copolymer was required to achieve significantly modified rheological properties. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3805–3817, 2001 相似文献
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65.
At each time be a random sequence of non-negative numbers that are ultimately zero in a random environment . The existence and uniqueness of the nonnegative fixed points of the associated smoothing transformation in random environment are considered. These fixed points are solutions to the distributional equation for ,where are random variables in random environment which satisfy that for any environment ; under ; are independent of each other and , and have the same conditional distribution where T is the shift operator. This extends the classical results of J. D. Biggins [J. Appl. Probab., 1977, 14: 25-37] to the random environment case. As an application, the martingale convergence of the branching random walk in random environment is given as well. 相似文献
66.
In this paper,we consider the(L,1) state-dependent reflecting random walk(RW) on the half line,which is an RW allowing jumps to the left at a maximal size L.For this model,we provide an explicit criterion for(positive) recurrence and an explicit expression for the stationary distribution.As an application,we prove the geometric tail asymptotic behavior of the stationary distribution under certain conditions.The main tool employed in the paper is the intrinsic branching structure within the(L,1)-random walk. 相似文献
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69.
Carolina Toloza Porras Dagmar R. D'hooge Marie‐Franoise Reyniers Guy B. Marin 《Macromolecular theory and simulations》2013,22(2):136-149
The potential of initiators for continuous activator regeneration atom transfer radical polymerization (ICAR ATRP) for the synthesis of well‐defined poly(n‐butyl acrylate) is analyzed by means of simulations. The kinetic model accounts for reactivity differences between secondary and tertiary macrospecies and considers the possible influence of diffusional limitations. CuBr2 is used as transition metal salt and the commercially available N,N,N′,N″,N″‐pentamethyldiethylenetriamine as ligand. For targeted chain lengths (TCLs) up to 1000, the ICAR ATRP can be performed relatively quickly, and with ppm levels of ATRP catalyst. For moderate TCLs, slightly higher ppm levels are required if excellent control over chain length is also desired. In all cases, limited loss of end‐group functionality (EGF) results.
70.