首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   232篇
  免费   3篇
化学   95篇
晶体学   2篇
力学   11篇
数学   40篇
物理学   87篇
  2022年   5篇
  2021年   6篇
  2020年   2篇
  2018年   2篇
  2017年   2篇
  2016年   3篇
  2015年   4篇
  2014年   8篇
  2013年   10篇
  2012年   13篇
  2011年   8篇
  2010年   9篇
  2009年   2篇
  2008年   9篇
  2007年   6篇
  2006年   15篇
  2005年   7篇
  2004年   5篇
  2003年   10篇
  2002年   5篇
  2001年   4篇
  2000年   8篇
  1999年   6篇
  1998年   4篇
  1997年   3篇
  1996年   5篇
  1994年   2篇
  1993年   3篇
  1992年   7篇
  1991年   3篇
  1990年   2篇
  1989年   3篇
  1988年   3篇
  1985年   9篇
  1984年   4篇
  1983年   2篇
  1982年   4篇
  1981年   2篇
  1979年   3篇
  1978年   2篇
  1977年   4篇
  1974年   3篇
  1973年   3篇
  1972年   2篇
  1948年   1篇
  1936年   1篇
  1931年   2篇
  1930年   2篇
  1913年   1篇
  1896年   1篇
排序方式: 共有235条查询结果,搜索用时 15 毫秒
191.
192.
We study (symmetric) three-class association schemes. The graphs with four distinct eigenvalues which are one of the relations of such a scheme are characterized. We also give an overview of most known constructions, and obtain necessary conditions for existence. A list of feasible parameter sets on at most 100 vertices is generated.  相似文献   
193.
194.
Intercalation of C(70) with europium affords two kinds of magnetic compounds, a canted antiferromagnet Eu(x)C(70) (x approximately 3) and a ferromagnet Eu(x)C(70) (x approximately 9) with transition temperatures (T(C)) of 5 and 38 K, respectively. The Curie constants in the paramagnetic phase and the saturation moment in the ferromagnetic phase are both understood by the full moment of Eu(2+) for both systems. The structure of Eu(3)(-)(delta)C(70) (delta approximately 0.27) is pseudo-monoclinic, derived by a simple deformation of the parent face-centered cubic (fcc) structure. Eu(9)(-)(delta)C(70) (delta approximately 0.2) forms an fcc structure, in which cuboctahedral clustering of Eu(2+) ions is observed in the enhanced size octahedral holes. The observed T(C) of the Eu(9)(-)(delta)C(70) ferromagnet is comparable to or larger than those of simple binary Eu-based ferromagnets, such as Eu chalcogenides or carbides, despite the low atomic ratio of Eu in the chemical formulas. This can be understood by the short Eu(2+)-Eu(2+) distances and high coordination numbers permitted by the multiple occupation by Eu(2+) ions of the expanded octahedral interstitial sites in higher fullerene-based solids.  相似文献   
195.
196.
In this paper an LMS-gas is considered. This is an ideal gas with constant specific heats but with a special entropy distribution, so that generalized Riemann invariants r* and s* exist. A flow with r* and s* constant has the property that the gas moves as a rigid body with a constant acceleration or deceleration. It is shown that a flow composed of two domains, in each of which r* and s* are constant, separated by a plane normal shock-wave is admitted by the Rankine-Hugoniot equations. The path of the shock-wave is calculated exactly and a reasonably realistic situation is suggested to generate this composite flow.  相似文献   
197.
The structural, optical and dc electrical properties of MgxAl1-x (0.2≤x≤0.9) gradient thin films covered with Pd/Mg are investigated before and after exposure to hydrogen. We use hydrogenography, a novel high-throughput optical technique, to map simultaneously all the hydride forming compositions and the kinetics thereof in the gradient thin film. Metallic Mg in the MgxAl1-x layer undergoes a metal-to-semiconductor transition and MgH2 is formed for all Mg fractions x investigated. The presence of an amorphous Mg-Al phase in the thin film phase diagram enhances strongly the kinetics of hydrogenation. In the Al-rich part of the film, a complex H-induced segregation of MgH2 and Al occurs. This uncommon large-scale segregation is evidenced by metal and hydrogen profiling using Rutherford backscattering spectrometry and resonant nuclear analysis based on the reaction 1H(15N,αγ)12C. Besides MgH2, an additional semiconducting phase is found by electrical conductivity measurements around an atomic [Al]/[Mg] ratio of 2 (x=0.33). This suggests that the film is partially transformed into Mg(AlH4)2 at around this composition. PACS 78.20.-e; 68.55.-a; 64.75.+g  相似文献   
198.
An efficient, highly product selective, eco-friendly, one-pot multicomponent synthesis of dihydropyrimidine derivatives via Biginelli reaction has been described. The reaction was developed by greener nanoparticle-catalyzed organic synthesis enhancement (NOSE) chemistry and solvent free reaction condition (SFRC) approaches, which helped us in making the procedure greener. The reaction went smoothly with a diverse range of aromatic, aliphatic, hetero-aromatic aldehydes, different amine sources, as well as various β-dicarbonyl compounds, showing the flexibility of this methodology. Magnetically separable nano-Fe3O4@SiO2@SO3H, which acts as a potent solid acid catalyst, was characterized by FT-IR, SEM, EDX and TEM, VSM, and TGA analyses. The catalyst was recycled from the reaction mixture easily by an external magnet and reused in five more consecutive runs without much decrease in catalytic activity. Its catalytic efficiency was compared to other nano and bulk solid acid catalyst in order to ascertain the best combination for the conversion.  相似文献   
199.
This article presents a numerical model that was developed for the drying of ink-jet-printed polymer solutions after filling the pixels in a polymer LED display. The model extends earlier work presented in the literature while still maintaining a practical approach in limiting the number of input parameters needed. Despite some rigorous assumptions, the model is in fair agreement with experimental data from a pre-pilot ink-jet printing line. Comparison inside a single pixel is shown, as well as a general trend in which the amount of polymer that is transported out of the central part of the pixel decreases with the rate of viscosity increase as a function of polymer concentration. Moreover, the effect of a varying solute diffusion coefficient is studied.  相似文献   
200.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号