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81.
Yiwang Chen Dongmei Liu Qilan Deng Xiaohui He Xiaofeng Wang 《Journal of polymer science. Part A, Polymer chemistry》2006,44(11):3434-3443
The direct preparation of grafting polymer brushes from commercial poly (vinylidene fluoride) (PVDF) films with surface‐initiated atom transfer radical polymerization (ATRP) is demonstrated. The direct initiation of the secondary fluorinated site of PVDF facilitated grafting of the hydrophilic monomers from the PVDF surface. Homopolymer brushes of 2‐(N,N‐dimethylamino)ethyl methacrylate (DMAEMA) and poly (ethylene glycol) monomethacrylate (PEGMA) were prepared by ATRP from the PVDF surface. The chemical composition and surface topography of the graft‐functionalized PVDF surfaces were characterized by X‐ray photoelectron spectroscopy, attenuated total reflectance/Fourier transform infrared spectroscopy, and atomic force microscopy. A kinetic study revealed a linear increase in the graft concentration of poly[2‐(N,N‐dimethylamino)ethyl methacrylate] (PDMAEMA) and poly[poly(ethylene glycol) monomethacrylate] (PPEGMA) with the reaction time, indicating that the chain growth from the surface was consistent with a controlled or living process. The living chain ends were used as macroinitiators for the synthesis of diblock copolymer brushes. The water contact angles on PVDF films were reduced by the surface grafting of DMAEMA and PEGMA. Protein adsorption experiments revealed a substantial antifouling property of PPEGMA‐grafted PVDF films and PDMAEMA‐grafted PVDF films in comparison with the pristine PVDF surface. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3434–3443, 2006 相似文献
82.
Peng Chen Jun Chen Baoqing Zhang Jun Zhang Jiasong He 《Journal of Polymer Science.Polymer Physics》2006,44(6):1020-1030
Polycarbonate (PC) was melt blended with small amount of liquid‐crystalline polymer (LCP) and various contents of glass beads (GB) having different diameters. The rheological measurements indicated that the GB addition increased the viscosity ratio and seemed unfavorable to the LCP fibrillation. However, the morphological observation showed that the LCP fibrillation was promoted by the GB addition and varied with the GB packing. With the increased GB packing by increasing the GB content and/or decreasing the GB diameter, LCP deformed from spheres and ellipsoids into stretched ellipsoids at lower shear rates and into long fibrils at higher shear rates. Although higher content of smaller GB jammed into the larger LCP droplets and inhibited the LCP fibrillation, very long LCP fibrils formed at higher shear rates at a high enough packing of GB. The relationship between GB packing and LCP fibrillation revealed two kinds of hydrodynamic effects of GB promoting the LCP fibrillation: at lower GB packing, the shear flow was enhanced by the high local shear between GB, in quantity; and for a high enough GB packing, the shear flow was changed, in quality, into elongational flow, which was more effective for the LCP fibrillation. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1020–1030, 2006 相似文献
83.
Xiaoqing Liu Chuncheng Li Dong Zhang Yaonan Xiao 《Journal of Polymer Science.Polymer Physics》2006,44(6):900-913
This article investigated the melting behaviors, crystallization kinetics, and spherulitic morphologies of poly(butylene succinate) (PBS) and its copolyester (PBSR) modified with rosin maleopimaric acid anhydride, using wide‐angle X‐ray diffraction, differential scanning calorimeter (DSC), and polarized optical microscope. Subsequent DSC scans of isothermally crystallized PBS and PBSR exhibited two melting endotherms, respectively, which was due to the melt‐recrystallization process occurring during the DSC scans. The equilibrium melting point of PBSR (125.9 °C) was lower than that of PBS (139 °C). The commonly used Avrami equation was used to describe the isothermal crystallization kinetics. For nonisothermal crystallization studies, the model combining Avrami equation and Ozawa equation was employed. The result showed a consistent trend in the crystallization process. The crystallization rate was decreased, the perfection of crystals was decreased, the recrystallization was reduced, and the spherulitic morphologies were changed when the huge hydrogenated phenanthrene ring was added into the chain of PBS. The activation energy (ΔE) for the isothermal crystallization process determined by Arrhenius method was 255.9 kJ/mol for PBS and 345.7 kJ/mol for PBSR. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 900–913, 2006 相似文献
84.
A. Subramanian T.-Y. Choi L.X. Dong J. Tharian U. Sennhauser D. Poulikakos B.J. Nelson 《Applied Physics A: Materials Science & Processing》2007,89(1):133-139
We report on a novel method for local control of shell engineering in multiwalled carbon nanotubes (MWNTs) using Joule-heating
induced electric breakdown. By modulating the heat dissipation along a nanotube, we can confine its thinning and shell breakdown
to occur within localized regions of peak temperatures, which are distributed over one-half of the NT length. The modulation
is achieved by using suitably designed nanomachined heat sinks with different degrees of thermal coupling at different parts
of a current-carrying nanotube. The location of electric breakdown occurs precisely at the regions of high temperatures predicted
by the classical finite-element model of Joule heating in the MWNT. The experiments herein provide new insight into the electric
breakdown mechanism and prove unambiguously that shell removal occurs due to thermal stress, underpinning the diffusive nature
of MWNTs. The method demonstrated here has the potential to be a powerful tool in realizing MWNT bearings with complex architectures
for use in integrated nanoelectromechanical systems (NEMS). In addition, the breakdown current and power in the nanotubes
are significantly higher than those observed in nanotubes without heat removal via additional heat sinks. This indicates future
avenues for enhancing the performance of MWNTs in electrical interconnect and nanoelectronic applications.
PACS 73.63.Fg; 65.80.+n 相似文献
85.
In this paper we prove the semialgebraic version of Palais' covering homotopy theorem, and use this to prove Bredon's covering mapping cylinder conjecture positively in the semialgebraic category. Bredon's conjecture was originally stated in the topological category, and a topological version of our semialgebraic proof of the conjecture answers the original topological conjecture for topological G-spaces over “simplicial” mapping cylinders. 相似文献
86.
Model and empirical study on some collaboration networks 总被引:8,自引:0,他引:8
Pei-Pei Zhang Kan Chen Yue He Tao Zhou Bei-Bei Su Yingdi Jin Hui Chang Yue-Ping Zhou Li-Cheng Sun Bing-Hong Wang Da-Ren He 《Physica A》2006,360(2):599-616
In this paper we present an empirical study of a few practical systems described by cooperation networks, and propose a model to understand the results obtained. We study four non-social systems, which are the Bus Route Networks of Beijing and Yangzhou, the Travel Route Network of China, Huai-Yang recipes of Chinese cooked food, and a social system, which is the Collaboration Network of Hollywood Actors. In order to explain the results related to the degree distribution, act-degree distribution and act-size distribution (especially about the degree distribution, which may be better fitted using a stretched exponential distribution (SED)), we suggest a simple model to show a possible evolutionary mechanism for the emergence of such networks. The analytic and numerical results obtained from the model are in good agreement with the empirical results. 相似文献
87.
对国民经济进行宏观调控,如同经济增长问题一样是一个永恒问题,对宏观调控的基本内容,手段,方法,国内外学者已进行了较多的规范性讨论,尤其是在数理分析方面,也已有许多具有普遍意义的成果,但是,要把那些成果转化为“生产力”从而变成清晰的,简明的,可操作的手段和方法,尚需人们不断的探索,本文通过对国民经济运行过程中若干宏观经济变量之间的数量关系分析,并以此建立了的国民经济宏观数量模型,就是尝试性的探索。 相似文献
88.
89.
90.
A new formulation of effective potential for local composite operators is given. The two-fermion condensate \(\langle \bar \Psi \Psi \rangle \) and four-fermion condensate \(\langle \bar \Psi \Psi \bar \Psi \Psi \rangle \) are calculated simultaneously in the Gross-Neveu model up to next-to-the-leading order in 1/N expansion. It is shown that factorization \(\langle \bar \Psi \Psi \bar \Psi \Psi \rangle = C_1 \langle \bar \Psi \Psi \rangle ^2 \) holds only in theN→∞ limit and the non-factorized part of \(\langle \bar \Psi \Psi \bar \Psi \Psi \rangle \) contributed by the order-1/N terms is comparable to \(C_1 \langle \bar \Psi \Psi \rangle ^2 \) when takingN=3. 相似文献