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91.
In this study, we have developed a new numerical approach to solve differential-type viscoelastic fluid models for a commonly used benchmark problem, namely, the steady Taylor—Couette flow between eccentric cylinders. The proposed numerical approach is special in that the nonlinear system of discretized algebraic flow equations is solved iteratively using a Newton–Krylov method along with an inverse-based incomplete lower-upper preconditioner. The numerical approach has been validated by solving the benchmark problem for the upper-convected Maxwell model at a large Deborah number. Excellent agreement with the numerical data reported in the literature has been found. In addition, a parameter study was performed for an extended White–Metzner model. A large eccentricity ratio was chosen for the cylinder system in order to allow flow recirculation to occur. We detected several interesting phenomena caused by the large eccentricity ratio of the cylinder system and by the viscoelastic nature of the fluid. Encouraged by the results of this study, we intend to investigate other polymeric fluids having a more complex microstructure in an eccentric annular flow field. 相似文献
92.
Jos�� Fl��vio Marcelino Borges Marlon Luiz Hneda Andr�� Maur��cio Brinatti Jo?o Batista Marimon da Cunha Jadir Aparecido Rosa Jos�� Domingos Fabris 《Hyperfine Interactions》2011,203(1-3):9-15
A sample of the coarse sand fraction from the soil material of the A-horizon (0?C0.2 m from the soil surface) of a dusky red magnetic Oxisol was submitted to high-energy mechanical milling for different times. This assay aimed mainly at (a) monitoring the individualization of strongly aggregated mineral particles, and (b) measuring the effect of the milling pressure on the mineralogy changes of the material. These data are also intended to experimentally subside any physical model describing the mechanical behavior of the superficial soil layer that is subjected to intensive machine management, in agriculture fields. Powder X-ray data reveal that some mineralogical phases, notably gibbsite, disappear soon after the first few hours milling. The 298 K-transmission Mössbauer spectrum for the non-milled sand sample shows a qualitatively typical pattern for the sand fraction of basalt derived soils, with magnetically ordered sextets, assignable mainly to hematite and maghemite, and an intense central (super)paramagnetic Fe3?+? doublet. For the milled samples, spectra revealed progressive spectral reduction of the magnetic hyperfine structure, with concomitant increase of relative subspectral areas due to (super)paramagnetic phases, as the milling time increased. This result is consistent with the reduction of measured saturation magnetization, from 4.96(8) J T???1 kg???1, for the non-milled sample, to 3.26(7) J T???1 kg???1, for the sample milled for 8 hours. 相似文献
93.
94.
Nelson M. Larocca Edson N. Ito Carlos Triveño Rios Luiz A. Pessan Rosario E. S. Bretas Elias Hage Jr. 《Journal of Polymer Science.Polymer Physics》2010,48(21):2274-2287
Poly(butylene terephthalate) (PBT)/styrene‐acrylonitrile copolymer (SAN) blends were investigated with respect to their phase morphology. The SAN component was kept as dispersed phase and PBT as matrix phase and the PBT/SAN viscosity ratio was changed by using different PBT molecular weights. PBT/SAN blends were also compatibilized by adding methyl methacrylate‐co‐glycidyl methacrylate‐co‐ethyl acrylate terpolymer, MGE, which is an in situ reactive compatibilizer for melt blending. In noncompatibilized blends, the dispersed phase particle size increased with SAN concentration due to coalescence effects. Static coalescence experiments showed evidence of greater coalescence in blends with higher viscosity ratios. For noncompatibilized PBT/SAN/MGE blends with high molecular weight PBT as matrix phase, the average particle size of SAN phase does not depend on the SAN concentration in the blends. However noncompatibilized blends with low molecular weight PBT showed a significant increase in SAN particle size with the SAN concentration. The effect of MGE epoxy content and MGE molecular weight on the morphology of the PBT/SAN blend was also investigated. As the MGE epoxy content increased, the average particle size of SAN initially decreased with both high and low molecular weight PBT phase, thereafter leveling off with a critical content of epoxy groups in the blend. This critical content was higher in the blends containing low molecular weight PBT than in those with high molecular weight PBT. At a fixed MGE epoxy content, a decrease in MGE molecular weight yielded PBT/SAN blends with dispersed nanoparticles with an average size of about 40 nm. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2010 相似文献
95.
Cadmium determination in biological samples by direct solid sampling flame atomic absorption spectrometry 总被引:1,自引:0,他引:1
rico Marlon de Moraes Flores Jos Neri Gottfried Paniz Ayrton Figueiredo Martins Valderi L. Dressler Edson Irineu Müller Adilson Ben da Costa 《Spectrochimica Acta Part B: Atomic Spectroscopy》2002,57(12):2187-2193
A direct solid sampling flame atomic absorption spectrometric procedure for trace determination of cadmium in biological samples has been developed. Test samples (0.05–2.00 mg) were ground and weighed into small polyethylene vials, which were connected to the device for solid sample introduction into a conventional air/acetylene flame. Test samples were carried as a dry aerosol to a quartz cell, placed between the burner and the optical path, which had a perpendicular entrance and a slit in the upper part. The atomic vapor generated in the flame produced a transient signal that was totally integrated within 1 s. The effect of operating conditions and the extent of grinding on the analytical signal were evaluated. Background signals were always low and a characteristic mass of 0.29 ng Cd was obtained. Calibration was performed using different masses of solid certified reference materials. Results obtained for certified and in-house reference materials were typically within the 95% confidence interval of the certified and/or reference value, and the precision, expressed as relative standard deviation, was between 3.8 and 6.7%. The proposed system is simple and it might be adapted to conventional atomic absorption spectrometers allowing the determination of Cd in more than 80 test samples per hour, excluding weighing. 相似文献
96.
Luiz San Martin 《Semigroup Forum》1992,44(1):376-387
LetG be a connected semi-simple Lie group withfinite centre andS∋G a subsemigroup withnonvoid interior. The purpose of this article is to show thatS innot simultaneously leftand right reversible unlessS=G. 相似文献
97.
Heinrich R. Karfunkel Thomas Dressler Andreas Hirsch 《Journal of computer-aided molecular design》1992,6(5):521-535
Summary Substituting carbon atoms of fullerenes by heteroatoms and vacancies will lead to new and yet unknown spherical-shaped molecules termed hereafter as heterofullerenes. The enormous structural diversity of these molecules is investigated and their structural, electronic and thermochemical properties are predicted using semiempirical computations. Computational results for complexes with ions lead to the hypothesis that these molecules behave like microscopic Faraday cages in which the electrons concentrate on the outer side of the sphere. It is predicted that some of these heterofullerenes are structurally and electronically similar to phthalocyanines and related molecules but offer many additional advantages. Potential uses such as adding heterofullerenes to fullerene materials, as superior starting materials for the fabrication of diamonds, as catalysts in hydrogenation reactions, as components of materials dominated until now by phthalocyanines, etc., are discussed. Simple synthetic routes to these compounds that are based on minor alternations of existing methods for fullerene production are proposed. On the basis of the thermochemical calculations, we believe that the most promising possibility consists of using metal cyanide/graphite composite target rods instead of pure graphite rods as in a conventional fullerene synthesis. 相似文献
98.
99.
Marcela Cecilia González-Araya Luís Alberto Duncan Rangel Marcos Pereira Estellita Lins Luiz Flávio Autran Monteiro Gomes 《Annals of Operations Research》2002,116(1-4):271-288
This paper presents an application of the UTA method for building utility functions for the evaluation criteria defined by the Staff Evaluation Commission (CAD) of the Rio de Janeiro Federal University (UFRJ). Every year, the CAD-UFRJ gives the staff evaluation results for each Postgraduate Engineering Programme. However, the method used to generate the staff evaluation is assumed unknown. Trying to find the CAD-UFRJ preference structure, the evaluation results supplied by CAD-UFRJ are used to apply the UTA method. Some additional information obtained from the CAD-UFRJ data is incorporated in the optimal solutions analysis. 相似文献
100.
Luiz Augusto N. Barroso Márcia H.C. Fampa Rafael Kelman Mario V.F. Pereira Priscila Lino 《Annals of Operations Research》2002,117(1-4):247-270
The objective of this work is to investigate market power issues in bid-based hydrothermal scheduling. Initially, market power was simulated with a single stage Cournot–Nash equilibrium model. In this static model the equilibrium was calculated analytically. It was shown that the total production of N strategic agents is smaller than the least-cost solution by a factor of (N/(N+1)). Market power analysis for multiple stages was then carried through a stochastic dynamic programming scheme, where the decision in each stage and state is the Cournot–Nash equilibrium of a multi-agent game. Case studies with data taken from the Brazilian system are presented. 相似文献