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101.
In this paper, the numerical modelling of the flow through the low‐pressure steam turbine last stage was presented. On the basis of predicted wet steam flow‐field, the aerodynamic as well as thermodynamic losses were estimated. For calculations of the wet steam steady flow‐field three numerical methods were employed. The first method was a streamline curvature method (SCM). The commercial CFD code (CFX‐TACflow) and an in‐house code, both solving the 3‐D RANS equations, were the next two methods. In the wet steam region, by means of all three methods, the equilibrium flow was modelled. Additionally, the in‐house CFD code was used for modelling of the non‐equilibrium steam condensing flow. In this work, the comparison of the cascade loss coefficient for stator and rotor and selected flow parameters for the stage were presented, compared and discussed. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   
102.
We perform summation of ladder diagrams in the high energy, large momentum limit. This leads to new results for both perturbative and non-perturbative approaches. In particular, an explicit expression for any diagram's contribution is given, the non-perturbative form of asymptotically non-analytic terms is found and representation of amplitude as a series of Regge poles is presented.Supported in part by Polish Ministery of National Education, grant no. CPBP 01.03  相似文献   
103.
Summary Diffusion of a fractal cluster of dimensiond f in a three-dimensional space is investigated. The diffusion process is assumed to be modelled by a standard parabolic diffusion equation, although a more general case represented by the Fokker-Planck-Kolmogoroff equation is also introduced. The mean-square displacement of the cluster mass centre is analysed and its anomalous behaviour is presented and critically discussed. The results obtained can be applied to describe some effects which may occur during the diffusion-limited cluster-cluster aggregation process, especially when the viscosity of the solvent is changed in time and/or a directed transport of clusters is present in the system. Paper presented at the I International Conference on Scaling Concepts and Complex Fluids, Copanello, Italy, July 4–8, 1994.  相似文献   
104.
Szymański  K.  SatuŁa  D.  Dobrzyński  L. 《Hyperfine Interactions》2004,159(1-4):21-27
Nuclear resonance studies of the two different types impurity doped potassium hexachloro-stannates, the isomorphic system such as (K–Rb)2SnCl6 and K2(Sn–Re)Cl6 and the nonisomorphic system K2SnCl6:Al3+ in the high temperature cubic phase revealed contrasting features with one the other characterized by static in the former and dynamic feature in the latter case respectively. The resonance spectra of the nonisomorphic system indicate additionally a sign of the local structural transition above the conventional structural phase transition temperature. This seems to be triggered by the ligand-deficient octahedral defects and can be explained in terms of the enhanced activity of the octahedral defects for the hindered rotation.  相似文献   
105.
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107.
Kalska  B.  Szymański  K.  Dobrzyński  L.  SatuŁa  D.  Wäppling  R.  Broddefalk  A.  Nordblad  P. 《Hyperfine Interactions》2002,141(1-4):169-173
Properties of amorphous alloy Fe0.66Er0.19B0.15 are reported. A reorientation of the Fe and Er magnetic moments during sample cooling through the compensation point in a large magnetic field is found by means of monochromatic circularly polarised radiation. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   
108.
The dilution of tert‐butylamine (tBA) with water and subsequent cooling leads to a large series of different crystalline hydrates by an in situ IR laser melting‐zone procedure. The crystal structures were determined for tBA?n H2O, with n=0, , 1, 7 , 7 , 9 , 11, and 17. For the two lower hydrates (n= , 1), one‐ and two‐dimensional hydrogen‐bonded networks are formed, respectively. The higher hydrates (n>1) exhibit a clathrate‐like three‐dimensional water framework with the tBA molecules as part of, or sitting inside, the cages. In all cases, tBA is hydrogen‐bonded to the H2O framework. In the intermediate range (1相似文献   
109.
Microtubules are regulated by microtubule‐associated proteins. However, little is known about the structure of microtubule‐associated proteins in complex with microtubules. Herein we show that the microtubule‐associated protein Tau, which is intrinsically disordered in solution, locally folds into a stable structure upon binding to microtubules. While Tau is highly flexible in solution and adopts a β‐sheet structure in amyloid fibrils, in complex with microtubules the conserved hexapeptides at the beginning of the Tau repeats two and three convert into a hairpin conformation. Thus, binding to microtubules stabilizes a unique conformation in Tau.  相似文献   
110.
This text presents a novel method for the separation and detection of phosphorothioate oligonucleotides with the use of ion pair ultra high performance liquid chromatography coupled with inductively coupled plasma mass spectrometry The research showed that hexafluoroisopropanol/triethylamine based mobile phases may be successfully used when liquid chromatography is coupled with such elemental detection. However, the concentration of both HFIP and TEA influences the final result. The lower concentration of HFIP, the lower the background in ICP-MS and the greater the sensitivity. The method applied for the analysis of serum samples was based on high resolution inductively coupled plasma mass spectrometry. Utilization of this method allows determination of fifty times lower quantity of phosphorothioate oligonucleotides than in the case of quadrupole mass analyzer. Monitoring of 31P may be used to quantify these compounds at the level of 80 μg L−1, while simultaneous determination of sulfur is very useful for qualitative analysis. Moreover, the results presented in this paper demonstrate the practical applicability of coupling LC with ICP-MS in determining phosphorothioate oligonucleotides and their metabolites in serum within 7 min with a very good sensitivity. The method was linear in the concentration range between 0.2 and 3 mg L−1. The limit of detection was in the range of 0.07 and 0.13 mg L−1. Accuracy varied with concentration, but was in the range of 3%.  相似文献   
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