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931.
David P. Kratz 《Journal of Quantitative Spectroscopy & Radiative Transfer》2008,109(6):1060-1080
Over the last quarter century, improvements in the determination of the spectroscopic characteristics of the infrared-active trace species have enhanced our ability to retrieve quantitative distributions of temperatures, clouds, and abundances for various trace species within the Earth's atmosphere. These improvements have also allowed for refinements in the estimates of climatic effects attributed to changes in the Earth's atmospheric composition. Modeling efforts, however, have frequently experienced significant delays in assimilating improved spectroscopic information. Such is the case for highly parameterized models, where considerable effort is typically required to incorporate any revisions. Thus, a line-by-line radiative transfer model has been used to investigate the magnitude of the effects resulting from modifications to the spectroscopic information. Calculations from this line-by-line model have demonstrated that recent modifications to the HITRAN (High Resolution Transmission) line parameters, the continuum formulation, and the CO2 line-mixing formulation can significantly affect the interpretation of the high spectral resolution radiance and brightness temperature retrievals. For certain moderate-resolution satellite remote sensing channels, modifications to these spectroscopic parameters and formulations have shown the capacity to induce changes in the calculated radiances equivalent to brightness temperature differences of 1-2 K. Model calculations have further shown that modifications of the spectroscopic characteristics tend to have a modest effect on the determination of spectrally integrated radiances, fluxes, and radiative forcing estimates, with the largest differences being of order 1 W m−2 for the total thermal infrared fluxes, and of order 2-3% of the calculated radiative forcing at the tropopause attributed to the combined doubling of CO2, N2O, and CH4. The results from this investigation are intended to function as a guide to differentiate between cases where older parameterizations provide acceptable results, within specified accuracy bounds, and cases where upgrades to the latest spectroscopic database are necessary. 相似文献
932.
Recently we have proposed a phenomenological approach in terms of two coexisting macroscopic order parameters corresponding
to the superconducting and insulating states and have discussed the electrodynamical responses of the superconducting ceramics.
In this paper we discuss the fluctuations of the order parameters both in static and dynamical situations in the mean field
approach and obtain results for the electrical conductivity which possesses anomalies as in granular materials. 相似文献
933.
A kinetic study of the tumor-associated galactopyranosyl-(1→3)-2-acetamido-2-deoxy-α-d-galactopyranoside (T-antigen) with lectin peanut agglutinin is described. The disaccharide antigen was synthesized by chemical
methods and was functionalized suitably for immobilization onto a carboxy-methylated sensor chip. The ligand immobilized surface
was allowed interaction with the lectin peanut agglutinin, which acted as the analyte and the interaction was studied by the
surface plasmon resonance method. The ligand—lectin interaction was characterized by the kinetic on-off rates and a bivalent
analyte binding model was found to describe the observed kinetic constants. It was identified that the antigen-lectin interaction
had a faster association rate constant (k
a1) and a slower dissociation rate constant (k
d1) in the initial binding step. The subsequent binding step showed much reduced kinetic rates. The antigen-lectin interaction
was compared with the kinetic rates of the interaction of a galactopyranosyl-(1→4)-β-d-galactopyranoside derivative and a mannopyranoside derivative with the lectin. 相似文献
934.
Band structure parameters such as the conduction band edge, the valence band edge and the quasi‐particle gap of diffusing CdSe quantum dots (Q‐dots) of various sizes were determined using cyclic voltammetry. These parameters are strongly dependent on the size of the Q‐dots. The results obtained from voltammetric measurements are compared to spectroscopic and theoretical data. The fit obtained to the reported calculations based on the semi‐empirical pseudopotential method (SEPM)—especially in the strong size‐confinement region, is the best reported so far, according to our knowledge. For the smallest CdSe Q‐dots, the difference between the quasi‐particle gap and the optical band gap gives the electron–hole Coulombic interaction energy (Je1,h1). Interband states seen in the photoluminescence spectra were verified with cyclic voltammetry measurements. 相似文献
935.
A. Yu. Fishkin 《Functional Analysis and Its Applications》2009,43(1):78-80
We consider a nondegenerate one-parameter family of germs of conformal maps of (?, 0) into (?, 0). We prove that such a family is analytically linearizable whenever it is formally linearizable. In this case, the linearizing coordinate change analytically depends on the parameter. 相似文献
936.
Kalska B. Häggström L. Lindgren B. Blomquist P. Wäppling R. Andreeva M. A. Nikitenko Yu. V. Proglyado V. V. Aksenov V. L. Semenov V. G. Chumakov A. I. Leupold O. Rüffer R. 《Hyperfine Interactions》2001,136(3-8):295-300
Hyperfine Interactions - We have performed a depth selective investigation of monocrystalline samples with composition [57Fe(10 ML)/V(5 ML)]20 and [57Fe(7 ML)/V(10 ML)]29 by means of synchrotron... 相似文献
937.
Concetta De Stefano Antonio Gianguzza Ottavia Giuffr Alberto Pettignano Silvio Sammartano 《应用有机金属化学》2008,22(1):30-38
Thermodynamic data of mono‐, di‐ and tri‐methyltin(IV)‐carboxylate complexes (acetate, malonate, succinate, oxydiacetate, diethylenetrioxydiacetate, malate, citrate, 1,2,3‐tricarballylate, 1,2,3,4‐butanetetracarboxylate, 1,2,3,4,5,6‐benzenehexacarboxylate) in aqueous solution are reported at t = 25 °C and I = 0 mol l−1. Thermodynamic parameters obtained were analysed to formulate empirical predictive relationships as a function of different parameters, such as the number of carboxylate groups of the ligand and the charge of the alkyltin(IV) cation. Sequestration diagrams of citrate and 1,2,3‐tricarballylate towards alkyltin(IV) cations at different pH values are also reported and discussed. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
938.
Marianne Gaborieau Hank De bruyn Siyabonga Mange Patrice Castignolles Andreas Brockmeyer Robert G. Gilbert 《Journal of polymer science. Part A, Polymer chemistry》2009,47(7):1836-1852
A method is developed for anchoring enzymatically degraded cationized starch as electrosteric stabilizers onto synthetic latices, using cerium(IV) to create free‐radical grafting sites on the starch. Direct anchoring of debranched starch onto a poly(methyl methacrylate) seed latex yields a latex stabilized by well‐defined oligosaccharides. Using α‐amylase to randomly cleave starch to form (1→4)‐α‐glucans, and a comonomer, N‐isopropyl acrylamide (NIPAM), whose corresponding polymer exhibits a lower critical solution temperature (LCST), creates a means to synthesize block (or graft) oligomers of oligosaccharide and synthetic polymer, which are water soluble at room temperature. Above 30 °C, they become amphiphilic and form self‐emulsifying nanoparticles (sometimes termed “frozen micelles”) from which a synthetic latex is grown after addition of methyl methacrylate, the collapsed NIPAM‐containing entities functioning as a type of in situ seed. This synthesis of stable synthetic latex particles is shown to have a high grafting efficiency. The starch fragments were characterized by 1H solution‐state NMR before grafting, and 13C solid‐state cross‐polarization magic‐angle spinning (CP‐MAS) NMR was used to characterize the starch oligomers actually grafted on the final latex. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1836–1852, 2009 相似文献
939.
讨论了一类二阶非线性微分方程多点共振边值问题,通过运用Mawhin连续定理,我们在一个较简单的条件下得到了问题的解的存在性结果. 相似文献
940.
Banjong Boonchom Chanaiporn Danvirutai 《Journal of Thermal Analysis and Calorimetry》2009,96(3):771-775
Cumene hydroperoxide (CHP) and its derivatives have caused many serious explosions and fires in Taiwan as a consequence of
thermal instability, chemical contamination, and even mechanical shock. It has been employed in polymerization for producing
phenol and dicumyl peroxide (DCPO). Differential scanning calorimetry (DSC) was used to analyze the thermal hazard of CHP
in the presence of sodium hydroxide (NaOH), sulfuric acid (H2SO4), and sodium bisulfite (Na2SO3). Thermokinetic parameters for decomposition, such as exothermic onset temperature (T
0
), maximum temperature (T
max
), and enthalpy (ΔH), were obtained from the thermal curves. Isothermal microcalorimetry (thermal activity monitor, TAM) was employed to investigate
the thermal hazards during CHP storage and CHP mixed with NaOH, H2SO4, and Na2SO3 under isothermal conditions in a reactor or container. Tests by TAM indicated that from 70 to 90 °C an autocatalytic reaction
was apparent in the thermal curves. According to the results from the TAM test, high performance liquid chromatography (HPLC)
was, in turn, adopted to analyze the result of concentration versus time. By the Arrhenius equation, the activation energy
(E
a
) and rate constant (k) were calculated. Depending on the process conditions, NaOH was one of the incompatible chemicals or catalysts for CHP. When
CHP is mixed with NaOH, the T
0
is induced earlier and the reactions become more complex than for pure CHP, and the E
a
is lower than for pure CHP. 相似文献