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   113篇
  免费   3篇
  国内免费   4篇
化学   79篇
力学   1篇
数学   32篇
物理学   8篇
  2023年   1篇
  2020年   2篇
  2019年   2篇
  2017年   1篇
  2016年   3篇
  2015年   5篇
  2014年   2篇
  2013年   10篇
  2012年   3篇
  2010年   3篇
  2009年   2篇
  2008年   5篇
  2007年   7篇
  2006年   4篇
  2005年   7篇
  2004年   6篇
  2003年   2篇
  2002年   2篇
  2000年   1篇
  1997年   1篇
  1996年   3篇
  1995年   4篇
  1994年   1篇
  1993年   2篇
  1992年   1篇
  1991年   2篇
  1988年   2篇
  1987年   1篇
  1984年   6篇
  1983年   3篇
  1982年   3篇
  1981年   2篇
  1980年   3篇
  1979年   3篇
  1978年   5篇
  1976年   1篇
  1971年   2篇
  1970年   1篇
  1965年   1篇
  1963年   1篇
  1928年   2篇
  1927年   1篇
  1926年   1篇
排序方式: 共有120条查询结果,搜索用时 15 毫秒
1.
The goal of our studies was to determine the nature of interactions between catalytic active samples, such as polypyrrole (PPy) doped with: chloride anions, heteropolyacids such as H5PMo10V2O40, or H4SiW12O40, and oxygen particles. In order to reveal the mechanism of the linkage between the catalysts and oxygen we provided the electron paramagnetic resonance (EPR) measurements of synthesized samples in O2 and N2 flow. Moreover, the X-ray photoelectron spectroscopy (XPS) measurements were performed to show the properties of doped heteropolyacids and the state of nitrogen in polypyrrole matrix. The results of EPR studies of PPy(Cl), PPy(H4SiW12O40), PPy(H5PMo10V2O40) samples, show that the polypyrrole doped with chloride anions interacts much easier with oxygen than polypyrrole doped with heteropolyacids (in the above given order, of preference with the most active polypyrrole system first). It correlates with XPS results, which show that a molybdenium-vanadium anion is more reduced than a silicon-tungsten one. The redox reactions of heteropolyacids involve the oxidation-reduction of the conjugated polymer chain, leaving no or little place for interactions with oxygen. Polypyrrole doped with H4SiW12O40 shows some oxygen sensitivity as observed in the EPR studies, as opposed to polypyrrole doped with H5PMo10V2O40, which is in line with the XPS results.  相似文献   
2.
In this paper, three new direct Mutually Orthogonal Latin Squares (MOLS) constructions are presented for 7 MOLS(24), 7 MOLS(75) and 8 MOLS(36); then using recursive methods, several new constructions for 7 and 8 MOLS are obtained. These reduce the largest value for which 7 MOLS are unknown from 780 to 570, and the largest odd value for which 8 MOLS are unknown from 1935 to 419. © 2003 Wiley Periodicals, Inc.  相似文献   
3.
A sensitive method of Co(II) determination by adsorptive stripping voltammetry is presented. The method exploits the enhancement of cobalt peak current observed in the system Co(II)-nioxime-cetyltrimethylammonium bromide-piperazine-N,N′-bis(2-ethanesulfonic acid). The calibration plot for an accumulation time of 60 s is linear from 5 × 10−11 to 3 × 10−9 mol L−1. The relative standard deviation is 3.8% for Co(II) determination at concentration 1 × 10−9 mol L−1. The detection limit is 1.7 × 10−11 mol L−1. The validation of the method is performed by the analyses of certified reference materials and comparing the result of Co(II) determination in river water sample by the proposed method with those obtained by ET AAS. The main advantage of this new system is the micro-trace Co(II) determination by adsorptive stripping voltammetry, as compared to those described before, a low concentration of the supporting electrolyte used, and so commercially available reagents without additional purification can be used.  相似文献   
4.
Procedures for trace cobalt determinations by adsorptive stripping voltammetry at in situ and ex situ plated bismuth film electrodes are presented. These exploit the enhancement of the cobalt peak obtained by using the Co(II)–dimethylglyoxime–cetyltrimethylammonium bromide–piperazine-N,N-bis(2-ethanesulfonic acid) system. The calibration graph for an accumulation time of 120 s was linear from 2 × 10–10 to 2 × 10–8 mol L–1. The relative standard deviation from five determinations of cobalt at a concentration of 5 × 10–9 mol L–1 was 5.2%. The detection limit for an accumulation time of 300 s was 1.8 × 10–11 mol L–1. The proposed procedure was applied to cobalt determination in certified reference materials and in tap and river water samples.  相似文献   
5.
6.
7.
8.
JPC – Journal of Planar Chromatography – Modern TLC - Recently, a growing interest has been observed in preventive and “anti-ageing” medicine, accompanied by a dynamic...  相似文献   
9.
10.
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