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   1867篇
  免费   36篇
  国内免费   312篇
化学   1793篇
晶体学   16篇
力学   18篇
综合类   4篇
数学   3篇
物理学   381篇
  2023年   82篇
  2022年   26篇
  2021年   62篇
  2020年   44篇
  2019年   61篇
  2018年   38篇
  2017年   54篇
  2016年   52篇
  2015年   52篇
  2014年   76篇
  2013年   112篇
  2012年   91篇
  2011年   141篇
  2010年   76篇
  2009年   103篇
  2008年   111篇
  2007年   125篇
  2006年   131篇
  2005年   80篇
  2004年   122篇
  2003年   89篇
  2002年   66篇
  2001年   64篇
  2000年   40篇
  1999年   50篇
  1998年   66篇
  1997年   44篇
  1996年   28篇
  1995年   23篇
  1994年   16篇
  1993年   21篇
  1992年   8篇
  1991年   13篇
  1990年   4篇
  1989年   5篇
  1988年   13篇
  1987年   3篇
  1986年   3篇
  1985年   4篇
  1982年   2篇
  1981年   2篇
  1980年   3篇
  1979年   2篇
  1978年   1篇
  1977年   2篇
  1976年   1篇
  1974年   1篇
  1968年   1篇
  1967年   1篇
排序方式: 共有2215条查询结果,搜索用时 31 毫秒
1.
原子吸收光谱法测定铝锂合金中锂   总被引:2,自引:0,他引:2  
本文研究了用原子吸收光谱法在笑气-乙炔火焰中测定铝锂合金中锂的最佳条件。其电离干扰可通过加进钾进盐来控制。应用本法测定合金中 锂的含量,获得了满意结果。  相似文献   
2.
曹宏杰 《光谱实验室》2006,23(3):616-618
用硫酸钠作掩蔽剂,火焰发射光谱法测定含锶卤水中的锂,有效的消除了锶对锂的干扰,方法测定检出限为1.18mg/L.加标回收率为98.5%-101.5%.对含锶卤水样品中锂进行11次平行测定,计算方法的精密度(RSD)为:0.39%.  相似文献   
3.
On a new calcium vanadate: synthesis, structure and Li insertion behavior   总被引:2,自引:0,他引:2  
A synthetic form of the mineral hewettite was prepared via a new route in aqueous medium, starting either from the crystalline compound Li1.1V3O8, or from its amorphous precursor. The anhydrous, crystalline derivative Ca0.5V3O8 was obtained by heating the synthetic hewettite at 250°C under dynamic vacuum. The diffraction studies show that the 2D structure of Ca0.5V3O8 involves the same V3O8 layers as in the hewettite or in Li1+αV3O8. The stacking of the layers is similar to that in the metahewettite. A structural model is proposed, where the Ca2+ ions occupy octahedral sites in the interlayer space. The electrochemical behavior of Ca0.5V3O8 vs. lithium insertion is presented. It is original and reveals particularly good performances in terms of stability during cycling at C/5 rate. The homologues obtained with Mg or Ba, instead of Ca, are briefly presented.  相似文献   
4.
In this work, we elucidate the effect of the less mobile ions on the dynamics of the more mobile ions by molecular dynamics simulations of lithium ions motion in lithium metasilicate glass by freezing some randomly chosen lithium ions (5%, 10% and 25%) at their initial locations at 700 K. A remarkable slowing down of the dynamics of the majority mobile Li ions was observed both in the self-part of the density–density correlation function, Fs(k,t), and in the diffusion coefficients. On the other hand, there is no significant change in the structure. These results show many similarities to the mixed alkali effect (MAE) with mixing of the small content of foreign alkali (10% and 25% of K2O), where large reduction of the dynamics was also observed in both experiments and MD simulations. This immobilization of faster ions causes the large MAE as already discussed in relation to the mechanism of the cooperative ion jump motions. Although of lesser importance, the ion dynamics are influenced by the matrix of oxygen atoms, because the jump motions of Li ions are assisted by the localized motions of oxygen atoms.  相似文献   
5.
The Mannich-type reaction of imines with (1-methoxy-2-methylpropenyloxy)trimethylsilane and aza-Diels-Alder reaction of imines with Danishefsky's diene can be carried out in scCO2 in the presence of lithium heptadecafluorooctanesulfonate which offer a way to synthesize β-amino carbonyl compounds and nitrogen-containing six-membered ring compounds under environmentally benign conditions.  相似文献   
6.
7.
8.
Experimental results are reported for a unique spectroscopic device called the Plasma Spectroscopy Cell. Optical absorption of lithium metal vapor was observed at high density and temperature. Absorption spectra are analyzed using theoretical calculations of absorption cross sections for lithium-helium interactions, and singlet and triplet state transitions of diatomic lithium in the visible spectral range. This is believed to be the most complex example yet calculated in which absolute bound-bound, bound-free, free-bound, and free-free contributions for all possible optically allowed transitions are all included, in quite respectable agreement with experiment.  相似文献   
9.
In this paper, we first report that a new proton source, glutaric acid, has been used to fabricate optical waveguides in Z-cut lithium niobate crystals. The relationship was experimentally established between proton-exchanged (PE) waveguide parameters and fabrication conditions. It is shown that this new organic acid can be used to obtain deep PE waveguides in fast diffusion speed (0.275 μm2/h at 221°C) and with low loss (0.2 dB/cm). It provides an alternative approach for fabricating PE waveguides in lithium niobate substrate.  相似文献   
10.
Spongy-like reticular structure is a unique morphology fabricated by electrostatic spray deposition (ESD) technique. The effects of solvent, substrate temperature, precursor feeding rate, static electric field strength, and deposition time on tailoring the reticular structure were investigated. Scanning electron microscopy was used to observe the film morphology. MnOx or LiMn2O4 were selected as the model materials. It is found that in addition to the conventional solvent butyl carbitol, other kinds of solvents such as ethylene glycol and propylene glycol can also be used to obtain reticular films at a suitable substrate temperature. Porous films with a low cross-linking degree pore structure can be prepared by increasing precursor feeding rate or decreasing substrate temperature. Increasing the deposition time or the electric field strength helps to obtain reticular films with more homogeneous pore size distribution. In addition, the addition of a high boiling-point solvent in mixed alcohol solvent results in the increase of proper substrate temperature. It is concluded that the fluidity of the spray droplets on the surface of a hot substrate is an important factor to form a reticular film.  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