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991.
B. M. Forster J. M. Bailey G. A. Beer J. L. Beveridge J. H. Brewer W. N. Hardy T. M. Huber K. R. Kendall A. R. Kunselman J. A. Macdonald G. M. Marshall G. R. Mason A. Olin M. Senba J. B. Warren 《Hyperfine Interactions》1991,65(1-4):1007-1013
Muonic hydrogen isotopes (μ− p, μ− d, and μ−t) are simple quantum mechanical systems ideally suited for studies of numerous fundamental phenomena in electroweak and strong
interactions as well as in applied areas such as muon chemistry or muon catalyzed fusion.
Emission of muonic hydrogen isotopes into vacuum helps to overcome the limitations which are normally imposed on conventional
investigations with gaseous and liquid targets. A proof of principle experiment for this new technique was performed at TRIUMF
last year. Negative muons with 30 MeV/c momentum were stopped in a thin film of solid hydrogen and produced very low energy μ−d in vacuum. The distribution center of the normal velocity components of emitted μ−d atoms was measured to be ∼1 cm/μs. The yield of μ−d in vacuum is an increasing function of H2 film thickness δ up to a value of δ≥1 mm. 相似文献
992.
We have demonstrated a temperature switch based on an optically bistable device integrated with an optical fibre. The principle demonstrated here might lead to the development of new types of all-optical temperature sensors. 相似文献
993.
J P Kiplinger L Contillo W L Hendrick A Grodski 《Rapid communications in mass spectrometry : RCM》1992,6(12):747-752
Derivatization is used to increase both negative-ion sensitivity and positive-ion sequence information in the liquid secondary-ion mass spectra (LSIMS) of a series of peptides. The derivatization method involves acylation with pentafluorobenzoyl fluoride in a single-step reaction, and the reaction mixture is applied directly to the probe tip for analysis. Acylation takes place at the unprotected N-terminus, tyrosine, and lysine. The derivatives exhibit increased signal-to-noise ratio for [M-H]- ions, especially where there is not already an acidic amino acid residue in the peptide. In positive-ion LSIMS, the N-terminal group acts to retain the charge at the N-terminus, simplifying the fragmentation by producing N-terminal fragment ions. It also increases positive-ion fragmentation, sometimes very dramatically, making sequence determination more straightforward. The simplicity of the process, together with the enhancements it provides, make this a generally useful method for obtaining peptide structural information. 相似文献
994.
R. Klein R. Grieser L. Hoog G. Huber I. Klaft P. Merz T. Kühl S. Schröder M. Grieser D. Habs W. Petrich D. Schwalm 《Zeitschrift für Physik A Hadrons and Nuclei》1992,342(4):455-461
We have performed for the first time precision spectroscopy on a coasting fast7Li+ ion beam in a storage ring. The ion beam moving with 6.4% speed of light was first electron cooled and then merged with two counterpropagating laser beams acting on two different hyperfine transitions sharing a common upper level (λ-system). One laser was frequency locked to thea 3 127J2 hfs frequency component established as a secondary frequency standard at 514 nm. The second laser was tuned over theλ-resonance, which was recorded relative to127J2 hfs components. This experiment is sensitive to the time dilation in fast moving frames and will lead to new limits for the verification of special relatively. The present status of the experiment and perspectives in accuracy are discussed. 相似文献
995.
Fe2O3--V2O5 catalysts doped with Cs2SO4 (molar ratio: V:Fe:Cs=1:0.74:0.06) were found to be a rather inhomogeneous mixture of various crystalline and amorphous iron
vanadate phases. After calcination in air the catalyst was divided into three different parts which were analyzed separately
revealing the formation of FeVO4 in the top and bottom fraction of the crucible and Fe2V4O13 in the middle fraction. As compared to the well crystallized FeVO4 reference sample, the quadrupole splittings of FeVO4 in the Cs-doped catalysts were larger pointing to more distorted iron sites which were assumed to be responsible for high
catalytic selectivities. In contrast, the quadrupole splittings of FeVO4 in the less selective K- and Rb-doped Fe2O3--V2O5 catalysts were smaller. Additional components in the bottom fraction were also α-Fe2O3 and Fe1-xS. As indicated by the CEMS spectra the latter is located preferentially on the surface of the catalyst particles.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
996.
Ross W. Mair David G. Cory Sharon Peled Ching-Hua Tseng Samuel Patz Ronald L. Walsworth 《Journal of magnetic resonance (San Diego, Calif. : 1997)》1998,135(2):478-486
Pulsed-field-gradient NMR techniques are demonstrated for measurements of time-dependent gas diffusion. The standard PGSE technique and variants, applied to a free gas mixture of thermally polarized xenon and O2, are found to provide a reproducible measure of the xenon diffusion coefficient (5.71 × 10−6m2s−1for 1 atm of pure xenon), in excellent agreement with previous, non-NMR measurements. The utility of pulsed-field-gradient NMR techniques is demonstrated by the first measurement of time-dependent (i.e., restricted) gas diffusion inside a porous medium (a random pack of glass beads), with results that agree well with theory. Two modified NMR pulse sequences derived from the PGSE technique (named the Pulsed Gradient Echo, or PGE, and the Pulsed Gradient Multiple Spin Echo, or PGMSE) are also applied to measurements of time dependent diffusion of laser polarized xenon gas, with results in good agreement with previous measurements on thermally polarized gas. The PGMSE technique is found to be superior to the PGE method, and to standard PGSE techniques and variants, for efficiently measuring laser polarized noble gas diffusion over a wide range of diffusion times. 相似文献
997.
The line search method incorporating the Wolfe conditions is modified to ensure that a descent algorithm terminates in a finite number of steps at an approximate stationary point where the second-order conditions of optimality are satisfied. A simple procedure based on conjugate directions is proposed to determine directions of negative curvature. 相似文献
998.
J. A. Schramke Dhanpat Rai R. W. Fulton G. R. Choppin 《Journal of Radioanalytical and Nuclear Chemistry》1989,130(2):333-346
The reliability of two solvent extraction techniques for the determination of Pu oxidation states in solution was tested with low-ionic-strength solutions and with high-Na and high-Mg brines that contained Pu concentrations sufficient for spectrophotometric analysis. One procedure only differentiates between reduced Pu [Pu(III) and Pu(IV)] and oxidized Pu [Pu(V) and Pu(VI)], whereas the second procedure was designed to differentiate between Pu(IV), Pu(V), and Pu(VI) in solution. Both procedures successfully differentiated between oxidized and reduced Pu in both dilute solutions and brines when tested with samples that contained only the Pu(IV), Pu(V), or Pu(VI) oxidation states. However, when the second solvent extraction procedure, which differentiates between Pu(V) and Pu(VI), was employed for solutions that did not contain a strong oxidant to maintain the Pu(VI) oxidation state, significant quantities of Pu(VI) were reduced to Pu(V) during extraction, indicating that accurate quantification of Pu(V) and Pu(VI) is not possible with this procedure.Work supported by the U. S. Department of Energy under Contract DE-ACO6-76RLO 1830. 相似文献
999.
1000.