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81.
Bharat V. Bhut Kenneth A. Christensen Scott M. Husson 《Journal of chromatography. A》2010,1217(30):4946-4957
This contribution describes the purification of anthrax protective antigen (PA) protein from Escherichia coli lysate using bind-and-elute chromatography with newly designed weak anion-exchange membranes. Protein separation performance of the new AEX membrane adsorber was compared with the commercial Sartobind® D membrane adsorber and HiTrap™ DEAE FF resin column under preparative scale conditions. Dynamic protein binding capacities of all three stationary phases were determined using breakthrough curve analysis. The AEX membrane showed higher binding capacities than the Sartobind® D membrane at equivalent volumetric throughput and higher capacities than the HiTrap™ DEAE FF resin column at 15 times higher volumetric throughput. Anion-exchange chromatography was performed using all three stationary phases to purify PA protein. Quantitative SDS-PAGE analysis of effluent fractions showed that the purity of PA protein was higher for membrane adsorbers than the HiTrap™ DEAE FF resin column and was the same for the new AEX membrane and Sartobind® D membrane adsorbers. The effects of E. coli lysate load volume and volumetric flow rate on PA protein separation resolution using the membrane adsorbers were minor, and the peak elution profile remained un-changed even under conditions where >75% of the total protein dynamic binding capacity of the membranes had been utilized. PA protein peak resolution was higher using pH-gradient elution than with ionic strength gradient elution. Overall, the results clearly demonstrate that membrane chromatography is a high-capacity, high-throughput, high-resolution separation technique, and that resolution in membrane chromatography can be higher than resin column chromatography under preparative conditions and at much higher volumetric throughput. 相似文献
82.
The TRIUMF Injector CryoModule (ICM) adapted two superconducting single cavities as the capture section for the low injecting energy of 100 keV electrons. Coupler kick induced beam deflection and projected emittance growth are one of the prime concerns of the beam stability, especially at low energies. In low energy applications, the electron velocity changes rapidly inside the cavity, which makes the numerical analysis much more complicated. The commonly used theoretical formulas of the direct integral or the Panofsky- Wenzel theorem is not suitable for the kick calculation of β <1 electrons. Despite that, the above mentioned kick calculation method doesn't consider injecting electron energy, the beam offset due to the coupler kick may not be negligible because of the low injection energy even if the kick is optimized. Thus the beam dynamics code TRACK is used here for the simulation of the power coupler kick perturbation. The coupler kick can be compensated for by a judicious choice of the coupler position in successive cavities from upstream to downstream. The simulation shows that because of the adiabatic damping by the following superconducting 9-cell cavity, even for the worst orbit distortion case after two capture cavities, the kick is still acceptable at the exit of the ICM after reaching 10 MeV. This paper presents the analysis of the transverse kick and the projected emittance growth induced by the coupler for β <1 electrons. The simulated results of the TRIUMF ICM capture cavities are described and presented. 相似文献
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84.
The Gamow-Teller transitions for pf shell nuclei with proton number less than 40 and neutron number larger than 40 were believed to be blocked, due to the full filling of the neutron orbit. However, recent experimental research shows that the Gamow-Teller transitions for these kinds of nuclei are not blocked. In this paper, we systematically calculate the GT transition of pf shell nuclei 76Se in different truncations, and the results are compared with experimental results. It is shown that, due to correlations, the believed blocked GT transition occurs, and the shell model calculations reproduce the experimental GT strength. In addition, the electron capture rates in a stellar environment are calculated and discussed. 相似文献
85.
V.S. Kolhinen T. EronenD. Gorelov J. HakalaA. Jokinen A. KankainenJ. Rissanen J. SuhonenJ. Äystö 《Physics letters. [Part B]》2011
The double-electron-capture Q value for the 136Ce decay to 136Ba has been determined at JYFLTRAP. The measured value 2378.53(27) keV excludes the energy degeneracy with the 0+ excited state of the decay daughter 136Ba at 2315.32(7) keV in a resonant 0νECEC decay by 11.67 keV. The new Q value differs from the old adopted value 2419(13) keV (Atomic Mass Evaluation 2003) by 40 keV and is 50 times more precise. Our calculations show that the precise Q value renders the resonant 0νECEC decay of 136Ce undetectable by the future underground detectors. We measured also the double-β decay Q value of 136Xe to be 2457.86(48) keV which agrees well with the value 2457.83(37) keV measured at the Florida State University. 相似文献
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A model was developed to simulate permeability decrease induced by hydrodynamic effects when injecting a fluid in a reservoir with respect to particle release and capture mechanisms and the parameters of the fluid–rock system. The kinetics of particle release and capture were integrated after computing the initial permeability of the porous medium with a square lattice of a two–dimensional network model. The rate of particle release is related to the difference between a microscopic velocity of the fluid and a critical velocity. The permeability decrease shows a direct link to the reduction of pore throat radii by three mechanisms of particle capture: straining and particle accumulation through direct interception or diffusion. Comparison between the simulations and the experimental results shows that the model reproduces the physics of the permeability decrease phenomenon, although the values are overestimated. The difference between the two sets of results can be explained by the fact that the simulations are realized at constant pressure whereas the experiments are realized at constant flow rate, and that re–entrainment of the trapped particles was not taken into account in the model. 相似文献
88.
Yingchao Liu Jinsong Wu Sixiu Liu Dongxiao Zhuang Yongfei Wang Xuefei Shou Jianhong Zhu 《Colloids and surfaces. B, Biointerfaces》2009,71(2):187-193
Laser capture microdissection (LCM) technology combined with immunohistochemistry (immuno-LCM) is a valuable tool to obtain specific target cell populations and therefore this technique enables more accurate proteomic profile. In this study, we optimized the regular immuno-LCM technique to isolate and stain pure prolactin cells from either normal human pituitary (n = 6) or prolactioma (n = 11). Compared with the routine procedure, more intense and specific staining could be obtained when sections were pretreated with 0.2% Triton X-100 for 4 min. Interestingly, longer pretreatment (0.2% Triton X-100 for 10 min) or higher concentration (2% Triton X-100 for 4 and 10 min) greatly impaired labeling intensity and cell shape. Further scanning electron microscope study revealed that the component extracted from the cell surface by Triton X-100 was lipid. Using the optimized immuno-LCM technique, more pure prolactin cells could be isolated and prepared for further proteomic analysis. Taken together, we reported an optimized immuno-LCM technique that could effectively dissect pure target cells in different type pituitary adenomas for further proteomics analysis. 相似文献
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