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951.
Within the framework of microscopic fluctuation-dissipation theory, we obtain the stochastic equation describing the Brownian motion of an electron in the phonon field of the crystal lattice. An expression for the Green’s function of the phonon field is found in general form and for the case of linear phonon-variable interaction of an electron with the phonon field with allowance for the potential screening of crystal-lattice nuclei. An expression for the phonon drag acting on a conduction electron in the lattice field is found and analyzed with allowance for the interaction. Frequency dependence of the coefficient of the phonon drag acting on a conduction electron is studied and the contribution of the electron-phonon interaction to the effective mass of a charge carrier is determined.__________Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Radiofizika, Vol. 48, No. 3, pp. 249–268, March 2005. 相似文献
952.
Complex impedance spectra were obtained on a crystal of CaCu3Ti4O12 (CCTO) from 289 to 456 K. As in the case of ceramic CCTO, these spectra can be interpreted as arising from a conducting material containing insulating barriers. This is then further evidence for the existence of planar defects within crystals of CCTO that act as insulating barriers and produce the large dielectric constant through a space charge mechanism. 相似文献
953.
This article compares the performance of WDM lightpath protection and IP LSP protection schemes for IP-over-WDM networks. A mathematical formulation of the maximum throughput problem is presented and analytical expressions for recovery time are derived for both schemes. The throughputs and recovery times are analyzed and compared. Results show that the IP LSP protection scheme presents higher throughputs then WDM lightpath protection. The IP LSP protection scheme, providing individual IP LSP protection has, however, scalability problems. This scheme presents high recovery times when a failure affects many lightpaths and many hops are allowed for the primary routes of IP LSPs. 相似文献
954.
We consider the problem of determining the stress distributionin a finite rectangular elastic layer containing a Griffithcrack which is opened by internal shear stress acting alongthe length of the crack. The mode III crack is assumed to belocated in the middle plane of the rectangular layer. The followingtwo problems are considered: (A) the central crack is perpendicularto the two fixed lateral surfaces and parallel to the othertwo stress-free surfaces; (B) all the lateral surfaces of therectangular layer are clamped and the central crack is parallelto the two lateral surfaces. By using Fourier transformations,we reduce the solution of each problem to the solution of dualintegral equations with sine kernels and a weight function whichare solved exactly. Finally, we derive closed-form expressionsfor the stress intensity factor at the tip of the crack andthe numerical values for the stress intensity factor at theedges of the cracks are presented in the form of tables. 相似文献
955.
956.
957.
The oxides A(Ti0.5Te1.5)O6 (A = K, Rb, Cs, Tl), A(Ti0.5W1.5)O6 (A = Rb, Cs, Tl), and Cs(B0.5W1.5)O6 (B = Zr, Hf) have been obtained as polycrystalline powders giving X-ray diffraction patterns characteristic of defect cubic pyrochlores, space group
(No. 227), Z = 8. The best discrepancy R factors, from 0.0265 for Rb(Ti0.5Te1.5)O6 to 0.0554 for Cs(Zr0.5W1.5)O6, were obtained for the B cations randomly distributed at 16(d), A ions at one quarter of 32(e), and oxygen atoms at 48(f) positions. A linear relationship is observed between the a unit cell parameters and the ionic radii of the A cations, as well as the average ionic radii of the B atoms. The results of electrical resistivity measurements for A(Ti0.5Te1.5)O6 (A = K, Rb, Cs, Tl) are given. 相似文献
958.
V. A. Maihara M. B. A. Vasconcellos 《Journal of Radioanalytical and Nuclear Chemistry》1989,132(2):329-337
Instrumental neutron activation analysis was applied to the determination of the elements Na, K, Br, As, Rb, Zn, Co, Fe and Sc in Brazilian rice samples and in biological standards. Hg and Se concentrations were determined by using a simple radiochemical separation. The chemical procedure was carried out by means of distillation of Hg and Se in HBr medium and subsequent precipitation of selenium by sodium metabisulfite and mercury by thioacetamide. The accuracy of the instrumental and radiochemical methods was evaluated by means of analysis of the Reference Materials NBS-Bovine Liver, Bowen's Kale and NBS-Rice Flour. 相似文献
959.
Electrohydrodynamic instability in homeotropically oriented nematic samples of 4'-n-octyl-4-cyano-biphenyl and 4'n-alkyloxy-4-cyanobiphenyl, (n = 8.9) have been studied in an a.c. electric field. The domain patterns during the instability in these compounds in a very low frequency a.c. field are very similar to those in a d.c. field. The domain patterns observed at higher frequencies have been identified as 'maltese crosses' or 'crossed isogyres'. The electro-convective 'isotropic' flows near the electrode play an important role in the observed instability. 相似文献
960.
W M Niessen M A de Kraa E R Verheij P J Bergers G F La Vos U R Tjaden J van der Greef 《Rapid communications in mass spectrometry : RCM》1989,3(1):1-4
On-line sample pretreatment by means of the phase-system switching approach is an interesting technique for the analysis of aqueous samples, e.g., plasma, by means of supercritical-fluid chromatography. In order to analyse plasma samples the following analytical procedure is used. The plasma sample is injected on to a short precolumn, which is washed with water and subsequently dried with nitrogen. Next, the solutes are desorbed with the supercritical mobile phase, analysed with packed-column supercritical-fluid chromatography and detected with either a UV detector or a mass spectrometer, equipped with a moving-belt interface. The herbicide diuron is selected as a test compound to study the feasibility of this approach. Using a selective detector the procedure is sufficiently sensitive to detect diuron in plasma, but not appropriate to detect the diuron metabolites in a post-mortem plasma sample. These have been identified with liquid chromatography/mass spectrometry. The detection limit of diuron in plasma using the procedure described is about 30 ng/mL. 相似文献