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131.
M. M. Eisl B. M. Reichl S. D. Böhmig H. Störi 《Fresenius' Journal of Analytical Chemistry》1994,349(1-3):194-196
Using a discrete model for the segregation kinetics based on the Darken theory of diffusion and on the regular solution model (RSM), one and two dimensional simulations of interface segregation in binary and ternary systems have been performed. The aim of the calculations was to investigate the kinetics of segregation sequences in ternary systems, the segregation kinetics in discrete systems during the initial phase and finally the kinetics of surface segregation in the region of a grain boundary intersected by the surface. 相似文献
132.
R. D. Patel 《国际化学动力学杂志》1994,26(4):403-406
Pseudo-first-order rate constants and activation parameters have been measured for the solvolysis of 2-chloroquinoxaline in various aquo-organic mixtures using methanol, ethanol, and isopropanol as the organic solvent. Excellent linear correlations are found between lnk and the mol fraction of cosolvent and ln[H2O]. The medium effect on the rates of solvolysis is assessed by Grunwald–Winstein's mY correlationship. The estimated values of m (0.55–0.72) and the entropy of activation (148–212 J deg?1 mol?1) for the reactions are well in the range for a bimolecular aromatic substitution reactions. © 1994 John Wiley & Sons, Inc. 相似文献
133.
The kinetics of the thermal decomposition reaction of gaseous 3,3,6,6-tetramethyl-1,2,4,5-tetroxane (ACDP) in the presence of n-octane was studied in the 403.2–523.2 K temperature range. This reaction yields acetone as the organic product. Under optimum conditions, first-order kinetics were observed, included when the S/V ratio of the Pyrex reaction vessel was increased by a nearly six-fold factor. In the range 443.2–488.2 K the temperature dependence of the rate constants for the unimolecular reaction in conditioned vessels is given by In k1/(s?1) = (31.8 ± 2.5) ? [(39.0 ± 2.5)/RT]. The value of the energy of activation in kcal/mol correspond to one O? O bond homolysis of the ACDP molecule in a stepwise biradical initiated decomposition mechanism. At the lower reaction temperatures as well in preliminary experiments participation of a surface catalyzed ACDP decomposition process could be detected. © 1994 John Wiley & Sons, Inc. 相似文献
134.
A. Thomasson S. Geffroy E. Frejafon D. Weidauer R. Fabian Y. Godet M. Nominé T. Ménard P. Rairoux D. Moeller J.P. Wolf 《Applied physics. B, Lasers and optics》2002,74(4-5):453-459
Continuous mapping of an ozone episode in Paris in June 1999 has been performed using a differential absorption lidar system.
The 2D ozone concentration vertical maps recorded over 33 h at the Champ de Mars are compiled in a video clip that gives access
to local photochemical dynamics with unprecedented precision. The lidar data are compared over the whole period with point
monitors located at 0-, 50-, and 300-m altitudes on the Eiffel Tower. Very good agreement is found when spatial resolution,
acquisition time, and required concentration accuracy are optimized. Sensitivity to these parameters for successful intercomparison
in urban areas is discussed.
Received: 11 February 2002 / Published online: 14 March 2002 相似文献
135.
136.
Numerical methods for the efficient integration of both stiff and nonstiff equations of motion of multibody systems having
the form of differential-algebraic equations (DAE) of index 3 are discussed. Linear multi-step ABM and BDF methods are considered
for the non-iterational integration of nonstiff DAE. The Park method is proposed for integration of stiff equations.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
137.
It was shown by G. A. Jones and the first author in [8] that underlying any map on a compact orientable surface S there is a natural complex structure making S into a Riemann surface. In this paper we consider regular maps and enquire about the Weierstrass points on the underlying Riemann surface. We are particularly interested to know when these are geometric, i.e. whether they lie at vertices, face-centres or edge-centres of the map. 相似文献
138.
Distribution of melamine in polyester–melamine surface coatings cured under nonisothermal conditions
N. J. W. Gamage D. J. T. Hill C. A. Lukey P. J. Pomery 《Journal of polymer science. Part A, Polymer chemistry》2004,42(1):83-91
The influence of experimental cure parameters on the diffusion of reactive species in polyester–melamine thermoset coatings during curing has been investigated with X‐ray photoelectron spectroscopy and attenuated total reflectance Fourier transform infrared. The diffusion of melamine plays a vital role in the curing process and, therefore, in the ultimate properties of coatings. At a low (<20%) hexamethoxymethylmelamine (HMMM) crosslinker concentration, the matrix composition is uniform, but at high HMMM concentrations, excess HMMM rapidly segregates to the air–coating interface. The rate of migration is governed by the difference in the surface free energies of polyester and HMMM and the concentration gradient of HMMM between the bulk and the surface. An increased rate of energy absorption also increases the rate of migration of HMMM to the surface. A physical model has been proposed to explain this surface segregation phenomenon in terms of cocondensation and self‐condensation reactions. It suggests that an appropriate amount of melamine can be segregated on the surface and allowed to self‐condense to form a desired thickness of a melamine topcoat through the control of the binder composition and cure conditions. This technique can be implemented to apply a melamine topcoat during cure. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 83–91, 2004 相似文献
139.
140.
Rajnikant D. Watkin G. Tranter 《Acta Crystallographica. Section C, Structural Chemistry》1995,51(10):2071-2073