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   297篇
  免费   8篇
  国内免费   3篇
化学   197篇
力学   9篇
数学   69篇
物理学   33篇
  2023年   3篇
  2022年   3篇
  2021年   8篇
  2020年   4篇
  2019年   3篇
  2018年   4篇
  2017年   2篇
  2016年   10篇
  2015年   9篇
  2014年   3篇
  2013年   17篇
  2012年   16篇
  2011年   23篇
  2010年   13篇
  2009年   4篇
  2008年   17篇
  2007年   18篇
  2006年   13篇
  2005年   13篇
  2004年   11篇
  2003年   13篇
  2002年   9篇
  2001年   6篇
  2000年   10篇
  1999年   2篇
  1998年   2篇
  1997年   3篇
  1993年   2篇
  1992年   3篇
  1990年   1篇
  1989年   1篇
  1986年   1篇
  1985年   4篇
  1984年   5篇
  1983年   4篇
  1982年   3篇
  1981年   3篇
  1980年   4篇
  1979年   4篇
  1978年   4篇
  1977年   4篇
  1976年   7篇
  1975年   1篇
  1974年   1篇
  1973年   7篇
  1972年   3篇
  1971年   1篇
  1970年   1篇
  1968年   1篇
  1966年   2篇
排序方式: 共有308条查询结果,搜索用时 187 毫秒
1.
2.
In this paper, to test goodness of fit to any fixed distribution of errors in multivariate linear models, we consider a weighted integral of the squared modulus of the difference between the empirical characteristic function of the residuals and the characteristic function under the null hypothesis. We study the limiting behaviour of this test statistic under the null hypothesis and under alternatives. In the asymptotics, the rank of the design matrix is allowed to grow with the sample size.  相似文献   
3.
The aromatic composition of sugar cane spirits and, in general, of alcoholic beverages, is mainly influenced by the ageing process in wood barrels. There are several factors that affect the quality of the final aged product, but the time of the storage in the barrel is perhaps the most important one. Ageing time must therefore be controlled in order to detect counterfeits; however, this parameter is very difficult to control and, at present, there is no analytical method available to determine it. We propose a quantitative method for determining the ageing time of sugar cane spirits in oak barrels by using an electronic nose based on coupling directly a headspace sampler to a mass spectrometer (HS-MS), and multivariate calibration. The method developed is simple and provides, in 5 min, the ageing time of spirits with an accuracy of about 1 month.  相似文献   
4.
5-vinylisoxazole     
Cycloaddition of fulminic acid to 1-butyn-3-ol gave a mixture of 5-α-hydroxyethylisoxazole (I) and 4-α-hydroxyethylisoxazole (II) in the ratio 9:1. By the dehydration of 1, 5-vinylisoxazole (III) was obtained. Compound III has also been prepared by cyclization of 4-penten-2-ynal as well as its diethylacetal with hydroxylamine hydrochloride; in both instances no isomers have been obtained. Compound III spontaneously polymerizes even at room temperature yielding a polymer still containing isoxazole rings.  相似文献   
5.
In the hydroformylation of ethylene with approximately equimolar H2/D2 mixtures and Rh4(CO)12 or Co2(CO)8 as the catalyst precursor about 50% of propionaldehyde-d1 was formed. The propionaldehyde-d0/d2 ratio was ~ 3 for rhodium and ~ 2.6 for the cobalt catalyst. On the basis of the results and assuming that there is no rapid M(H)2/M(D)2 scrambling, activation of hydrogen through M(H)2 or M(H)2(olefin) complexes can be excluded.  相似文献   
6.
Temperature has great impact on the structure and size of the linked crystallites of the conducting topmost layer formed at the surface of a polycarbonate film via the reaction BEDT-TTF+IBr [BEDT-TTF=bis(ethylenedithio)tetrathiafulvalene]. We show that fine temperature control permits formation of a semiconducting topmost layer of alpha'-(BEDT-TTF)(2)(I(x)Br(1-x))(3) crystallites with either micro- or nanometre size, a result that opens a route to miniaturized conducting plastic materials.  相似文献   
7.
In this work, the nonionic surfactant polyoxyethylene-10-lauryl ether has been used for the extraction and preconcentration of 14 polycyclic aromatic hydrocarbons, classified as priority pollutants by the US Environmental Protection Agency, from seawater samples. The cloud-point preconcentration previous separation by HPLC and quantification using fluorimetric detection and wavelength programming allow to determine these pollutants with detection limits ranging from 1.0 to 1.5 x 10(2) ng/l with RSDs better than 10.4%. The methodology is evaluated using well-established extraction and preconcentration methods and GC-MS.  相似文献   
8.
With a view to the use of picolinealdehyde salicyloylhydrazone as analytical reagent, a study of the physical properties and chemical reactions of this substance has been carried out. It reacts with nickel (λmax = 375 nm, ? = 3.9 × 104M?1cm?1) or zinc (λmax = 365 nm, ? = 4.8 × 104M?1cm?1) to produce a yellow 1:2 complex in both cases. Spectrophotometric determinations of trace amounts of nickel and zinc have been established.  相似文献   
9.
Summary An absorption method for the collection of acid and condensable volcanic gases is described. A Cd(OH)2 suspension allows the simultaneous sampling of sulfide and sulfur dioxide. A complete scheme for chemical analysis of H2O, CO2, H2S, SO2, HCl and HF is presented.The method is relatively simple and accurate and requires only simple equipment. Moreover, separate samples of the condensable part of the volcanic gas may be used for analysis of trace elements.
Probenahme und Analyse vulkanischer Gase
Zusammenfassung Eine Absorptionsmethode zur Probenahme saurer und kondensierbarer Vulkangase wurde beschrieben. Eine Cd(OH)2-Suspension ermöglicht die gleichzeitige Probenahme von H2S und SO2. Ein Analysenschema für die chemische Analyse von H2O, CO2, H2S, SO2, HCl und HF wurde angegeben. Das Verfahren ist relativ einfach und genau; es erfordert nur eine einfache Ausrüstung. Proben des kondensierbaren Anteils der Gase dienen zur Bestimmung der Spurenanteile.
  相似文献   
10.
Bearing in mind the insight into the Hohenberg–Kohn theorem for Coulomb systems provided recently by Kryachko (Int J Quantum Chem 103:818, 2005), we present a re-statement of this theorem through an elaboration on Lieb’s proof as well as an extension of this theorem to finite subspaces. Contribution to the Serafin Fraga Memorial Issue.  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