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141.
Metallic Li in carbonaceous nanostructures was obtained in high concentration (as much as 33.4%) through metalorganic chemical vapor deposition involving certain lithium–aminoalkyl moieties, which are formed in situ , by decomposition of a precursor containing both cobalt and lithium. The bimetallic complex containing both lithium and cobalt was characterized by IR spectroscopy, mass spectroscopy, nuclear magnetic resonance spectroscopy, elemental analysis and thermogravimetric analysis. X‐ray photoelectron spectroscopy measurements performed on the as‐grown films demonstrate that lithium can be stable in metallic form in such a film. Results of X‐ray photoelectron spectroscopic analysis of the as‐grown films are presented as direct evidence of the formation and stabilization of metallic lithium in carbon nanotubes. Carbon nanotubes, encapsulating metallic lithium, can potentially act as a miniaturized nanobattery. Such a battery would be potentially useful in the next generation of communication and remote sensing devices, where a pulse of current is required for their operation. In addition, with metallic lithium, having an effective nuclear magnetic moment, such materials can be envisioned to show potential applications in devices based on nuclear magnetic resonances. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
142.
Theoretical and experimental research has been performed on the interaction curves and stress paths of crystallinepolymeric materials PE and POM under tensile-torsional stress with a linearly intensifying model and in terms of the yield points undergoing Von Mises criterion. 相似文献
143.
Akira Matsumoto Hiroyuki Hamamoto Yuta Miwa Hiroyuki Aota Satoshi Inoue Katsutoshi Yokoyama Yasuo Matoba Michirou Shibano 《Journal of polymer science. Part A, Polymer chemistry》2009,47(11):2871-2881
No difference in the actual gel points was substantially observed among three isomeric diallyl phthalates such as diallyl phthalate (DAP), diallyl isophthalate, and diallyl terephthalate (DAT); this interesting gelation behavior was discussed further in terms of the correlation between gelation and the difference in cyclization modes, and also, the difference in reactivity between the uncyclized and cyclized radicals for cross‐linking. In the present work, we tried to extend the preceding discussion to the polymerization of triallyl trimellitate (TAT) because the molecular structure of TAT is presumed to essentially involve the characteristics of three isomeric diallyl phthalates and, therefore, the enhanced gelation was expected in TAT polymerization. However, no enhancement of gelation was observed. For a full understanding of the gelation in multiallyl cross‐linking polymerization, we explored further the polymerizations of DAP, DAT, and TAT, especially focusing on the characterization of resultant network polymer precursors (NPPs) using SEC‐MALLS‐viscometry providing the correlation of [η] versus Mw of fractionated samples. Notably, the structure of NPP consisting of oligomeric primary polymer chains generated from specific allyl polymerization would become core‐shell type dendritic with the progress of polymerization. The correlation between delayed gelation and decreased reactivity of dendritic NPP for intermolecular cross‐linking is discussed. Conclusively, the reactivity for intermolecular cross‐linking between NPPs decreased with the progress of polymerization leading to a delayed gelation. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2871–2881, 2009 相似文献
144.
M. Biasini 《Il Nuovo Cimento D》1987,9(4):353-360
Summary The total and partial distribution functions of a metalloid/transition-metal amorphous alloy (Fe8B15) have been calculated by means of a ?nonstandard? hard-sphere dense-random-packing model. Based on these results, a comparison
with the ?canonical? dense-random-packing model is discussed.
Riassunto Si presenta un calcolo delle funzioni di distribuzione radiale parziali e totali di una lega metallo-metalloide amorfa (lega Fe-B) generate mediante simulazione numerica. La struttura viene realizzata tramite un modello ad impaccamento di sfere rigide basato su criteri di crescita probabilistici. I risultati sono confrontati con il modello ad impaccamento denso e casuale (dense random packing) ?canonico? di Bennet.
Резюме Вьічисляются полньіе и парциональньіе функции распределения для аморфного сплава ?металлоид-переходной металл? (Fe8B15), используя ?нестандартную⎴ модель плотной случайной упаковки твердых сфер. Полученные результаты сравниваются с результатами ?канонической? модели плотной случайной упаковки.相似文献
145.
Eri Yoshida 《Colloid and polymer science》2008,286(12):1435-1442
The novel synthesis of polyhedral particles was attained by the dispersion polymerization of styrene in supercritical carbon
dioxide using a polydimethylsiloxane-based macroazoinitiator as a precursor of the surfactant. The macroazoinitiator, VPS-1001,
composed of poly(dimethylsiloxane) and 6-8 molecules of the azo groups served as a precursor of the surfactant for the dispersion
polymerization by azobisisobutylonitrile as an initiator to produce 0.8-4 μm polyhedral particles. The size of the particles
decreased as a result of increasing the VPS-1001 concentration. Too high a concentration of VPS-1001 caused coagulation of
the particles. A decrease in the temperature increased the particle size and size distribution, while a decrease in the pressure
produced particles with nonspecific shapes. An increase in the stirring rotation speed tended to increase the size and size
distribution. However, too high a speed of rotation also caused coagulation of the particles. 相似文献
146.
The prediction of the high-cycle fatigue strength of polymeric and composite materials in asymmetric loading is considered.
The problem is solved on the basis of a nonlinear model of ultimate state allowing us to describe all typical forms of the
diagrams of ultimate stresses. The material constants of the model are determined from the results of fatigue tests in symmetric
reversed cycling, in a single fatigue test with the minimum stress equal to zero, and in a short-term strength test. The fatigue
strength characteristics of some polymers, glass-fiber laminates, glass-fiber-reinforced plastics, organic-fiber-reinforced
plastics, and wood laminates in asymmetric tension-compression, bending, and torsion have been calculated and approved experimentally.
__________
Translated from Mekhanika Kompozitnykh Materialov, Vol. 44, No. 1, pp. 87–102, January–February, 2008. 相似文献
147.
Russell Hooper Matthijs Toose Christopher W. Macosko Jeffrey J. Derby 《国际流体数值方法杂志》2001,37(7):837-864
A modified boundary element method (BEM) and the DEVSS‐G finite element method (FEM) are applied to model the deformation of a polymeric drop suspended in another fluid subjected to start‐up uniaxial extensional flow. The effects of viscoelasticity, via the Oldroyd‐B differential model, are considered for the drop phase using both FEM and BEM and for both the drop and matrix phases using FEM. Where possible, results are compared with the linear deformation theory. Consistent predictions are obtained among the BEM, FEM, and linear theory for purely Newtonian systems and between FEM and linear theory for fully viscoelastic systems. FEM and BEM predictions for viscoelastic drops in a Newtonian matrix agree very well at short times but differ at longer times, with worst agreement occurring as critical flow strength is approached. This suggests that the dominant computational advantages held by the BEM over the FEM for this and similar problems may diminish or even disappear when the issue of accuracy is appropriately considered. Fully viscoelastic problems, which are only feasible using the FEM formulation, shed new insight on the role of viscoelasticity of the matrix fluid in drop deformation. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
148.
The humidity and water tolerance of a sol-gel derived binder prepared using a cheap, multicomponent precursor has been studied.
The sol was prepared by dissolving the precursor in water under acidic conditions using either formic acid or a mixture of
formic acid and citric acid for pH adjustments. It is shown that a post-treatment temperature of 400 °C or higher is needed
in order to achieve full binder stability under excess water conditions, as thermal decomposition of metal carboxylates leads
to a pronounced decrease in water solubility of the gels. The mesoporous gel can be made hydrophobic by post-treatments with
either a silane or an organophosphonate, showing that both silica and metal oxides are exposed on the surface of the binder.
Surface functionalization is especially effective for gels heat-treated at higher temperatures where the metal carboxylates
have decomposed to the corresponding oxides or carbonates. The results are expected to be of great importance for the use
of this cheap binder in large scale industrial applications.
Electronic Supplementary Material The online version of this article () contains supplementary material, which is available to authorized users. 相似文献
149.
G. C. Boskovic A. R. Zarubica M. N. Kovacevic P. S. Putanov 《Journal of Thermal Analysis and Calorimetry》2008,91(3):849-854
Properties of two catalysts tailored in the laboratory conditions by sulfation of commercial Zr-hydroxide and Zr-hydroxide
of nitrate origin were compared with those of commercial SO4-Zr-hydroxide. Equally thermally treated samples in the temperature interval 500–700°C, and having the same amount of sulfur,
show different properties indicating memory effect of their solid parent materials. The catalyst obtained by sulfation of
commercial Zr-hydroxide differs in amount of residual sulfates upon calcination from other two catalysts. The instability
of sulfates in the previous case might be connected to the lowest surface area values of catalyst and the highest fraction
of monoclinic phase observed at all applied calcination temperatures. 相似文献
150.
相分离广泛存在于各种凝聚态物质中.根据局部浓度的变化形式,可将相分离分为固体模型(model B)和流体模型(model H),这两种模型适用于动力学对称的体系.近年来,Tanaka发现在一些动力学不对称的多组分高分子体系里存在一种新的相分离模式,其相分离过程分为动力学过程可用一个普适的粘弹模型来进行描述.动力学不对称可由体系中两组分间大的尺寸差异或玻璃化温度差异引起.本文介绍了多相高分子体系中产生粘弹相分离的原理及其基本特征,并讨论了模量、粘度、填料等因素对粘弹相分离动力学过程及多相体系微观结构的影响. 相似文献