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   16397篇
  免费   1186篇
  国内免费   1195篇
化学   9236篇
晶体学   357篇
力学   1080篇
综合类   136篇
数学   1854篇
物理学   6115篇
  2023年   141篇
  2022年   303篇
  2021年   296篇
  2020年   351篇
  2019年   364篇
  2018年   347篇
  2017年   297篇
  2016年   512篇
  2015年   459篇
  2014年   650篇
  2013年   928篇
  2012年   1165篇
  2011年   1332篇
  2010年   1080篇
  2009年   1003篇
  2008年   1086篇
  2007年   1028篇
  2006年   1015篇
  2005年   727篇
  2004年   706篇
  2003年   551篇
  2002年   525篇
  2001年   665篇
  2000年   511篇
  1999年   371篇
  1998年   285篇
  1997年   250篇
  1996年   245篇
  1995年   178篇
  1994年   162篇
  1993年   132篇
  1992年   132篇
  1991年   131篇
  1990年   123篇
  1989年   91篇
  1988年   68篇
  1987年   51篇
  1986年   45篇
  1985年   56篇
  1984年   42篇
  1983年   34篇
  1982年   38篇
  1981年   35篇
  1980年   33篇
  1979年   21篇
  1978年   31篇
  1977年   20篇
  1976年   21篇
  1975年   20篇
  1974年   19篇
排序方式: 共有10000条查询结果,搜索用时 46 毫秒
11.
A green and sustainable strategy synthesizes clinical medicine warfarin anticoagulant by using lipase‐supported metal–organic framework (MOF) bioreactors (see scheme). These findings may be beneficial for future studies in the industrial production of chemical, pharmaceutical, and agrochemical precursors.  相似文献   
12.
A uniform dispersion of reactants is necessary to achieve a complete reaction involving multicomponents. In this study, we have examined the role of plasticizer in the reaction of two seemingly unlikely reactants: a highly crystalline hexamethylenetetramine (HMTA) and a strongly hydrogen bonded phenol formaldehyde resin. By combining information from NMR, infrared spectroscopy and differential scanning calorimetry, we were able to determine the role of specific intermolecular interactions necessary for the plasticizer to dissolve the highly crystalline HMTA and to plasticize the phenol formaldehyde resin in this crosslinking reaction. The presence of the plasticizer increased the segmental mobility, disrupted the hydrogen bonded matrix, and freed the hydroxyl units, which further increased the solubility of the HMTA. Both the endothermic and exothermic transitions are accounted for in the calorimetric data obtained. For the first time, it is possible to obtain the effective molar ratio of each component needed to complete the crosslinking reaction efficiently. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1519–1526  相似文献   
13.
Kim  F. H.  Moylan  S. P.  Phan  T. Q.  Garboczi  E. J. 《Experimental Mechanics》2020,60(7):987-1004
Experimental Mechanics - Insufficient data are available to fully understand the effects of metal additive manufacturing (AM) defects for widespread adoption of the emerging technology....  相似文献   
14.
15.
光束发散度对紫外写入光纤光栅的影响   总被引:1,自引:0,他引:1  
李琳  赵岭  高侃  黄锐  方祖捷 《光学学报》2002,22(6):49-752
用傅里叶衍射光学分析了准分子激光束发散度对于光纤光栅制备的影响,发现光束发散角使光纤光栅的布拉格波长发生改变,相位版后干涉场沿光纤轴向和径向不均匀,对制备30dB高反射率光纤光栅造成困难。实验结果与理论分析基本一致,相对于理想平行光束情况,会聚光束使得光纤光栅布拉格波长出现在短波一边,发射光束使得光纤光栅布拉格波长出现在长波一边。  相似文献   
16.
Supposa that f(x) is a quasidifferentiable function, defined on S(?)R~n where S is an open set, with a -equivalent bounded quasidifferential subfam ily. Lenma I  相似文献   
17.
In this paper, an MILP formulation is proposed for the design of a reverse logistics network based on a warehouse location–allocation model, which optimizes, simultaneously, the forward and reverse networks. A single product model with unlimited capacity is first defined. Subsequently, the model is extended to a multi-product capacitated recovery network model, where capacity limitations and a multi-product system can be considered. The proposed model is compared to published work in the field, where different model assumptions have been proposed. Two cases are described so as to gain a better insight into the model and allow a comparative analysis.  相似文献   
18.
The paper introduces a special system calibration technology in s-parameters measurement of microwave and millimeter wave devices. The 8-term errors module is built by analyzing the signals flowing in the measurement system. Then the calibration technology using non-standard kits is designed on the base. Finally, the experiment using the calibration technology is introduced.  相似文献   
19.
An amphiphilic poly(ethylene oxide)‐block‐poly(dimethylsiloxane) (PEO–PDMS) diblock copolymer was used to template a bisphenol A type epoxy resin (ER); nanostructured thermoset blends of ER and PEO–PDMS were prepared with 4,4′‐methylenedianiline (MDA) as the curing agent. The phase behavior, crystallization, hydrogen‐bonding interactions, and nanoscale structures were investigated with differential scanning calorimetry, Fourier transform infrared spectroscopy, transmission electron microscopy, and small‐angle X‐ray scattering. The uncured ER was miscible with the poly(ethylene oxide) block of PEO–PDMS, and the uncured blends were not macroscopically phase‐separated. Macroscopic phase separation took place in the MDA‐cured ER/PEO–PDMS blends containing 60–80 wt % PEO–PDMS diblock copolymer. However, the composition‐dependent nanostructures were formed in the cured blends with 10–50 wt % PEO–PDMS, which did not show macroscopic phase separation. The poly(dimethylsiloxane) microdomains with sizes of 10–20 nm were dispersed in a continuous ER‐rich phase; the average distance between the neighboring microdomains was in the range of 20–50 nm. The miscibility between the cured ER and the poly(ethylene oxide) block of PEO–PDMS was ascribed to the favorable hydrogen‐bonding interaction. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 3042–3052, 2006  相似文献   
20.
Free-standing and supported hydrogenated amorphous carbon films (a:C–H) were prepared upon pyrolysis of the polymer formed by ethanolamine (EA) and citric acid (CA), under an ambient atmosphere at 300 °C. EA facilitates the formation of the macroscopic films, while CA is essential for obtaining the a:C–H microstructure, which comprises a mixture of sp2 and sp3 carbon. Received: 29 May 2001 / Accepted: 17 August 2001 / Published online: 20 December 2001  相似文献   
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