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   27976篇
  免费   874篇
  国内免费   164篇
化学   18711篇
晶体学   261篇
力学   944篇
综合类   1篇
数学   2500篇
物理学   6597篇
  2023年   154篇
  2022年   412篇
  2021年   499篇
  2020年   437篇
  2019年   452篇
  2018年   345篇
  2017年   322篇
  2016年   741篇
  2015年   639篇
  2014年   802篇
  2013年   1535篇
  2012年   1982篇
  2011年   2195篇
  2010年   1317篇
  2009年   1168篇
  2008年   1798篇
  2007年   1700篇
  2006年   1585篇
  2005年   1461篇
  2004年   1297篇
  2003年   1020篇
  2002年   988篇
  2001年   680篇
  2000年   591篇
  1999年   346篇
  1998年   265篇
  1997年   302篇
  1996年   342篇
  1995年   276篇
  1994年   285篇
  1993年   285篇
  1992年   279篇
  1991年   213篇
  1990年   158篇
  1989年   149篇
  1988年   147篇
  1987年   120篇
  1986年   103篇
  1985年   177篇
  1984年   123篇
  1983年   102篇
  1982年   135篇
  1981年   103篇
  1980年   86篇
  1978年   86篇
  1977年   89篇
  1976年   99篇
  1975年   105篇
  1974年   86篇
  1973年   103篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
31.
Cold-drawn Nylon-11 films, which were prepared by stretching the melt-quenched films to a draw ratio of 2.8: 1 at room temperature, were found to exhibit an electric displacement versus electric field hysteresis loop. The results confirmed that the Nylon-11 film exhibited ferroelectric behavior at or below room temperature. The coercive fields were 65, 98, 125, 160, and 215 MV/m at 20, 0, ?20, ?40, and ?60°C and the remanent polarization at ?20°C (where there was considerably less dc conduction) was 56 mC/m2. Switching of the polarization was almost completed within 20 ms.  相似文献   
32.
We have designed and synthesized novel perfluorinated polyimides with 3D controlled structure. At first, we successfully developed the new synthetic routes to diamines with pendant bulky perfluorinated aromatic units in a multi‐step synthetic procedure. Novel perfluorinated polyimides were prepared in a two‐step reaction in N‐methyl‐2‐pyrrolidinone (NMP) solution: The first step was for the synthesis of polyamic acids (PAAs) and the second reaction was for the imidization of PAA. The polymer yield was over 89% and the inherent viscosity of PAAs was in the range of 0.24–0.36 dL/g. The thin films were prepared by spin‐coating the PAA solution in NMP onto various substrates such as a Si wafer or a KBr pellet, dried at 80 °C and further cured at 230 °C. The resultant polyimides are thermally stable over 400 °C. The refractive index and birefringence of the resultant polyimides are 1.5858–1.6452 and 0.01–0.005, respectively. The refractive index of polyimide decreases with increasing the fluorine content. The copolymerization and the ether linkages into the backbone reduce the birefringence of polyimides. Surprisingly, the pendant ether linkage is not a crucial factor in reducing the polyimide birefringence. Their birefringence is comparatively very low, compared with that of previous polyimides. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 1326–1342, 2006  相似文献   
33.
34.
35.
36.
We construct functions Mα which are piecewise homogeneous polynomials on the (d+1)-dimensional torus Ud+1. These functions possess complete symmetry with respect to the independent variables. The symmetry and homogeneous relations for these functions are exploited to obtain a recurrence relation and explicit representations. Furthermore, we show that , where ω=e12x/k, 0≤jt≤k−1, are linearly independent. By restricting Mα to Ud, we obtain the complex analogue of polynomial box splines on a (d+1)-direction mesh on Ud, which is a multivariate analogue of B-splines on the circle studied by I.J. Schoenberg[8].  相似文献   
37.
38.
39.
The neutron irradiated potassium hexacyanoferrate(III) solutions were analyzed for Fe(CN)64?, Fe(CN)63?, and Prussian blue. The retention values (1.1%) were constant throughout the pH and concentration ranges studied, and did not change with the length of irradiation. The complex behavior of the radiochemical yield of the Fe(CN)64? and Prussian blue was attributed to the competition of the various reactions involved in the irradiation.  相似文献   
40.
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