全文获取类型
收费全文 | 28820篇 |
免费 | 4193篇 |
国内免费 | 2412篇 |
专业分类
化学 | 20210篇 |
晶体学 | 552篇 |
力学 | 1064篇 |
综合类 | 273篇 |
数学 | 957篇 |
物理学 | 12369篇 |
出版年
2024年 | 52篇 |
2023年 | 249篇 |
2022年 | 613篇 |
2021年 | 782篇 |
2020年 | 901篇 |
2019年 | 861篇 |
2018年 | 789篇 |
2017年 | 1086篇 |
2016年 | 1327篇 |
2015年 | 1273篇 |
2014年 | 1463篇 |
2013年 | 2732篇 |
2012年 | 1813篇 |
2011年 | 1722篇 |
2010年 | 1478篇 |
2009年 | 1638篇 |
2008年 | 1654篇 |
2007年 | 1658篇 |
2006年 | 1554篇 |
2005年 | 1431篇 |
2004年 | 1384篇 |
2003年 | 1113篇 |
2002年 | 1151篇 |
2001年 | 789篇 |
2000年 | 801篇 |
1999年 | 692篇 |
1998年 | 585篇 |
1997年 | 486篇 |
1996年 | 436篇 |
1995年 | 471篇 |
1994年 | 340篇 |
1993年 | 308篇 |
1992年 | 286篇 |
1991年 | 197篇 |
1990年 | 198篇 |
1989年 | 150篇 |
1988年 | 167篇 |
1987年 | 141篇 |
1986年 | 124篇 |
1985年 | 108篇 |
1984年 | 95篇 |
1983年 | 49篇 |
1982年 | 83篇 |
1981年 | 43篇 |
1980年 | 35篇 |
1979年 | 47篇 |
1978年 | 15篇 |
1977年 | 7篇 |
1976年 | 7篇 |
1973年 | 17篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
831.
This work is a part of the systematic study of the ternary based chalcogenides systems. The aim is to determine the phase
equilibrium, and to determine the limits of the phase area. This is done in view to perfecting knowledge of elaboration conditions
for new materials and to study of their physical properties.
Few works have been devoted to the study of the ternary system Se-Te-Sn, only the cross section SnSe-SnTe has been studied
[1] and [2].
The experimental study by DTA, DSC and X-ray diffraction on powder performed at room temperature, exhibits a miscibility gap
in the liquid state which narrows as it goes through the Sn-Se binary system.
Three cross sections behave as ‘quasi-binary‘ system and six ternary invariants have been exhibited: three ternary eutectics
and three ternary quasi-peritectics.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
832.
杨始刚 《理化检验(化学分册)》2004,40(10):586-588,591
建立了农药中间体苯唑醇的分析方法,用指示剂法和电位法对苯唑醇进行了非水滴定的研究,测定结果与高效液相色谱(HPLC)法基本一致,相对标准偏差≤0.20%。 相似文献
833.
The binary system Li2Se-In2Se3 was investigated in the range of 40 to 100 mol% In2Se3 by thermoanalytical and X-ray methods. The system is characterized by two eutectic points. Beside the two binary components
and the known ternary compound LiInSe2 another ternary compound crystallizes in this binary system at 83.3 mol% In2Se3. This compound was identified as LiIn5Se8. In contrast to (Cu, Ag)IB5
IIIC8
VI compounds such as CuIn5S8 [1] it does not crystallize in the spinel structure. LiIn5Se8 shows a stratified structure. The melting point was determined to be at 810°C. Starting from room temperature up to the melting
point no phase transitions were observed.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
834.
固固相反应合成牛磺酸水杨醛钾与锑、铋的配合物 总被引:2,自引:0,他引:2
合成了牛磺酸水杨醛钾,并采用室温固固相反应法合成了牛磺酸水杨醛钾与三氯化锑和三氯化铋的配合物,其组成为:K2MC18H20O8N2S2 (M = Sb, Bi)。两种配合物的晶体结构均属于单斜晶系,锑配合物的晶胞参数为:a = 1.2869 nm, b = 1.7636 nm, c = 1.9917 nm, β= 93.79埃活榕浜衔锏木О问篴 = 1.4770 nm, b = 2.0334 nm, c = 2.0149 nm, β= 94.05。红外光谱表明N、Cl原子参与了配位,中心离子的配位数为5。 相似文献
835.
NiTiO3 shows an order-disorder transition from an ordered ilmenite structure to a corundum structure at high temperatures. The transition is followed by a strong increase of the specific electrical conductivity. The conductivity was investigated as a function of temperature and oxygen activity. An order parameter according to common phase transition theories can be used to describe the behaviour of the conductivity in the transition region and vice versa. A model for the defect structure of NiTiO3 is presented. 相似文献
836.
A multidimensional GC-system containing two capillary columns of different polarities, operated within a double oven instrument, was used for the optimized separation of complex isomeric mixtures of various types of chlorinated aromatic compounds such as PCB, PCDD, or PCDF. Electron capture was applied parallel to flame ionization detection to obtain sensitive signals of the PCB or PCDD and the n-alkane standards required for identification by Kovats indices, respectively. Electron capture detection within a valvelessly operated MDGC system forced changes in the usual instrumental set-up, the live-switching coupling piece being located within the second oven of the double oven instrument. This oven is operated isothermally to ensure optimal and interference-free detection, for stable flow conditions within the coupling piece and for the determination of the isothermal retention indices (Kovats), which are much more suitable for identification by retention than the so-called “linear” indices. 相似文献
837.
Determination of hydrazine and 1,1-dimethylhydrazine as salicyldehyde derivates by liquid chromatography with electrochemical detection 总被引:1,自引:0,他引:1
Summary Determination of hydrazine and 1,1-dimethylhydrazine after derivatization with salicylaldehyde was done using high-performance liquid chromatography with electrochemical detection. The oxidation of the phenolic group of salicylaldazine (S-HY) and salicylaldehyde-1,1-dimethylhydrazone (S-UDMH) was optimized with respect to ionic strength, pH, and applied potential. Less than 5 ng of S-HY and S-UDMH could be detected. The detection limits for hydrazine and 1,1-dimethylhydrazine solutions were estimated to be 0.025 and 0.20 ppm, respectively. 相似文献
838.
《Electroanalysis》2005,17(3):223-230
There is a need to develop analytical methods that are capable of rapidly measuring small biological markers in the field of metabolomics. Among others, carbohydrates play an important role biologically yet are traditionally hard to detect since they have no chromophore or fluorophore. In the present report, the first application of integrated pulsed amperometric detection (iPAD) coupled with microchip electrophoresis to the analysis of glucose, mannose, sucrose, maltose, glucosamine, lactose, maltotriose and galactose is demonstrated. iPAD is an electrochemical detection mode that can be used for direct detection of carbohydrates, amines and sulfur containing compounds. The effect of different solution parameters, including the buffer concentration, pH and the concentration of SDS on both separation and detection response was analyzed. In addition, a comparison study between PAD and iPAD was performed using glucose, glucosamine, sucrose and maltose as model carbohydrates. 相似文献
839.
Wei Jun Jin 《Analytica chimica acta》2004,522(1):1-8
Luminescent surface-modified CdSe semiconductor quantum dots (QDs), with nanoparticle (NP) size distribution in the order of 2-7 nm, have been synthesized for optical determination of cyanide ions. The nanoparticles have been functionalised with tert-butyl-N-(2-mercaptoethyl)-carbamate (BMC) groups and exhibit a strong fluorescent emission at about 580 nm with rather long fluorescence lifetimes (several hundred nanoseconds) in aerated methanolic solution. The observed luminescence emitted by the synthesized nanocrystals was tremendously increased by photo-activation under sunlight exposure. The functionalised QDs turned out to exhibit excellent long-term stability when stored in the dark (no significant changes in QDs luminescence emission intensity was observed even after two months from synthesis). The functionalisation of the NPs with carbamate ligand allowed a highly sensitive determination of free cyanide via analyte-induced changes in the photoluminescence (fluorescence quenching of intensity at 580 nm and lifetime changes) of the modified quantum dots (excited at 400 nm). A detection limit of 1.1 × 10−7 M (2.9 μg l−1) of cyanide ions was obtained, while the interfering effect of other inorganic anions (including NO3−, Cl− or SCN−) was negligible even at 200-fold level concentrations in excess of cyanide. 相似文献
840.
A one-step solid-phase extraction procedure, based on a new silica gel adsorbent modified with cholesterol groups, has been
investigated for measurement of cotinine in urine. Cotinine is the main metabolite of nicotine in the human body and is analyzed
as a biomarker for assessment of direct or passive exposure to tobacco smoke. New cholesterol-modified adsorbents have been
obtained by chemical modification of silica gel of different porosity with cholesterol ligands. Although recovery by this
extraction procedure were optimum over a relatively broad range of sample pH (3.1–8.0), analytical conditions such as sample
loading, washing and elution conditions, concentration of cotinine to be extracted, and the type of adsorbent used for extraction
were found to affect the efficiency of the procedure and had to be controlled for optimum recovery. When these conditions
were controlled, recovery of cotinine from spiked human urine was reproducible and depended on compound ionization. Quantitative
analysis of cotinine was performed by reversed-phase high-performance liquid chromatography with UV detection.
Presented at: Conference of the Hyphenation of Liquid Chromatography–Nuclear Magnetic Resonance Spectroscopy, Liquid Chromatography–Mass
Spectrometry and Related Topics, Tuebingen, Germany, March 25–29, 2006. 相似文献