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   202339篇
  免费   1960篇
  国内免费   502篇
化学   110619篇
晶体学   3647篇
力学   7996篇
综合类   11篇
数学   19200篇
物理学   63328篇
  2020年   1724篇
  2019年   1920篇
  2018年   2237篇
  2017年   2356篇
  2016年   3516篇
  2015年   2194篇
  2014年   3548篇
  2013年   9079篇
  2012年   6507篇
  2011年   8019篇
  2010年   5699篇
  2009年   5658篇
  2008年   7162篇
  2007年   7071篇
  2006年   6698篇
  2005年   6064篇
  2004年   5529篇
  2003年   5111篇
  2002年   4873篇
  2001年   6141篇
  2000年   4626篇
  1999年   3521篇
  1998年   2745篇
  1997年   2703篇
  1996年   2591篇
  1995年   2440篇
  1994年   2330篇
  1993年   2165篇
  1992年   2826篇
  1991年   2730篇
  1990年   2672篇
  1989年   2690篇
  1988年   2713篇
  1987年   2721篇
  1986年   2591篇
  1985年   3303篇
  1984年   3313篇
  1983年   2598篇
  1982年   2709篇
  1981年   2763篇
  1980年   2533篇
  1979年   2875篇
  1978年   2860篇
  1977年   2980篇
  1976年   2816篇
  1975年   2553篇
  1974年   2509篇
  1973年   2465篇
  1972年   1702篇
  1968年   1703篇
排序方式: 共有10000条查询结果,搜索用时 10 毫秒
991.
Dubby PS  Tandon KN 《Talanta》1966,13(5):765-766
Alizarin Red S, Pyrocatechol Violet and Xylenol Orange are shown to be effective adsorption indicators for the titrations of hexacyanoferrate(II) and oxalate with Thorium(IV) solution. The action of the indicators can be explained by the theory of surface compound formation.  相似文献   
992.
The principle of back-titration with EDTA is applied to rapid radiometric methods. A suitable vessel for performing the reaction, filtration and count-rate measurement is described. The optimal conditions for the use of solid 110mAgIO3 as indicator were studied: the time for solubility-equilibrium of solid silver iodate, the reaction time of EDTA with silver iodate, and the pH-dependence of the silver-EDTA reaction rate. Procedures are given for calibration curves and for rapid radiometric determinations of copper(II). nickel(II), lead(II) and zinc(II). The method is suitable for the range 1–100μg.  相似文献   
993.
Summary The structures of two pregnane glycosides fromCynanchum sibiricum Willd. have been established. Sibiricoside D (II) is sibirigenin (cynanchogenin) 3-D-glucosido-D-cymarosido-D-cymarosido-D-cymarosido-D-oleandroside. Sibiricoside E (I) is sibirigenin (or cynanchogenin) 3-D-glucosido-D-glucosido-D-cymarosido-D-cymarosido-D-cymarosido-D-oleandroside.The hypothesis has been put forward that glycosides of isolinoleone are present in the native state which are isomerized into linoleone derivatives in the process of isolation and treatment with acid and alkaline agents.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 171–177, March–April, 1975.  相似文献   
994.
The principal decomposition routes of molecular ions of cis, cis, cis-2,4,6-octatriene, cis, cis, trans-2,4,6-octatriene, trans, cis, trans-2,4,6-octatriene, trans-5,6-dimethyl-1,3-cyclohexadiene and cis-5,6-dimethyl-1,3-cyclohexadiene were studied using ion kinetic spectroscopy. The loss of radicals from [M]+· appears to proceed via a ground state, while loss of a neutral molecule appears to involve either complete equilibration of structure within the system or both ground state and excited state pathways.  相似文献   
995.
Zusammenfassung Bei der Reaktion von BaCO3 mit NiO bildet sich unter bestimmten Bedingungen ein kristallines Pulver der Zusammensetzung 9 BaNiO2 · 2 BaCO3. Die Verbindung zeigt scharfe Röntgeninterferenzen, die sich kubisch indizieren lassen. Es wurden elektronenmikroskopische Aufnahmen gemacht sowie Elektronenstrahlfeinbereichsbeugungen durchgeführt. Das IR-Spektrum wurde aufgenommen und die magnetische Suszeptibilität bestimmt.
A new compound 9 BaNiO2·2 BaCO3
During the reaction of BaCO3 with NiO under special conditions a crystalline powder with the composition 9 BaNiO2 · 2 BaCO3 is formed. This compound shows clear X-ray patterns which can be indexed using a cubic cell. Electron microscopic investigations have been carried out and selected area diffraction patterns have been taken. The IR-spectrum and the magnetic susceptibility have been proved.


Mit 3 Abbildungen  相似文献   
996.
Isopiestic measurements of mixed electrolyte solutions involving sodium hydroxide and other components of Bayer liquors were performed at 50?°C and 100?°C. Most of the systems studied obey Zdanovskii’s rule exactly or very closely. However, those with sodium chloride as one of their components show deviations from Zdanovskii’s rule, which are well predicted by our thermodynamic modelling software based on Pitzer’s equations.  相似文献   
997.
Applicability of the nitromethane selective quenching rule for discriminating between alternant versus nonalternant polycyclic aromatic hydrocarbons (PAHs) is examined for 20 representative PAH solutes dissolved in micellar sodium dodecylsulfate (SDS) + cetyltrimethylammonium bromide (CTAB), SDS + dodecyltrimethylammonium bromide (DTAB), SDS + Brij-35, and SDS + sodium octanoate (SO) mixed surfactant solvent media. Experimental results show that nitromethane quenched fluorescence of all 8 alternant PAHs studied in the four different solvent systems. Unexpected quenching behavior was observed, however, in the case of nonalternant PAHs. Nitromethane quenched fluorescence emission of nonalternant PAHs dissolved in the SDS + SO solvent media, which is contrary to the selective quenching rule. In the case of the mixed anionic + cationic surfactant solvent media, nitromethane quenching selectivity was restored at concentration ratios of approximately 4 : 1 (anionic:cationic) or less. Received: 22 May 1997 / Revised: 29 September 1997 / Accepted: 3 October 1997  相似文献   
998.
Summary The essential oils have been isolated from tobacco leaves using a simple gas co-distillation apparatus. The method involves co-distillation with water under the continuous stream of an inert gas with subsequent single solvent extraction of the distillate. The extract is analysed on GC and GC/MS in splitless injection mode without further concentration. The method was evaluated for reproducibility using n-octadecane as an internal standard. The distillation-extraction procedure was reporducible with an average deviation of ±3% for the major constituents. The present method was applied to the analyses of the essential oils of other agricultural products.Dedicated to Dr. L. S. Ettre on the occasion of his 60th birthday.  相似文献   
999.
A comparison of an established gas chromatographic assay for 4-hydroxydebrisoquine and debrisoquine and a modified high-performance liquid chromatographic assay was made. Both assays used guanoxan as the internal standard and required derivatization of all three compounds with acetylacetone at 96 degrees C for 2.5 h and subsequent ethereal extraction and cleaning steps before chromatographic analysis. For detailed pharmacokinetic studies the gas chromatographic assay was more sensitive in the measurement of low concentrations in plasma, but the liquid chromatographic assay was adequate for phenotyping the 4-hydroxylation of debrisoquine in a population. In the latter assay a mobile phase consisting of 70% methanol in water at pH 3.5 (adjusted with orthophosphoric acid containing 10 mM 1-pentanesulphonic acid was employed (flow-rate 1.5 ml/min) with a pre-column (C8) linked to a reversed-phase muBondapak C18 cartridge in a Z-module. The eluate was detected at 248 nm. With this assay it was observed that the buccal absorption of debrisoquine and 4-hydroxy-debrisoquine was affected by the pH of the buccal medium. This indicates that urinary pH may influence the excretion of both substances at high pH. The debrisoquine-to-4-hydroxydebrisoquine ratio may be dose-dependent.  相似文献   
1000.
Previous animal experiments suggested that the Magos cold vapor atomic absorption spectroscopic (CVAAS) method might overestimate the concentrations of inorganic mercury (I-Hg) in the presence of methylmercury (MeHg). In the present study it is shown that this error is due to a fast degradation of MeHg during the formation of the analytical signal. For brain samples, about 5% of the total amount of MeHg in the reaction vessel is degraded to I-Hg. Speciation of Hg in aqueous solution of MeHg chloride, after purification with ionexchange chromatography using the Magos method, showed that about 9% was I-Hg. Analysis by NMR of MeHg chloride and MeHg hydroxide showed that less than 1% was in the form of I-Hg. The absolute magnitude of the error in the CVAAS method is dependent on the amounts of SnCl2 and MeHg in the reaction vessel; however, the ratio of I-Hg to total (T-Hg) is shown to be independent of the amount of MeHg (25.5–255 ng as Hg) in the reaction vessel. A procedure for corrections is proposed, based on the results from these studies and empirical data from speciation analyses of brain tissue from MeHg-exposed rats and rabbits.  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