全文获取类型
收费全文 | 1060篇 |
免费 | 38篇 |
国内免费 | 7篇 |
专业分类
化学 | 796篇 |
晶体学 | 5篇 |
力学 | 16篇 |
数学 | 132篇 |
物理学 | 156篇 |
出版年
2023年 | 3篇 |
2022年 | 8篇 |
2021年 | 15篇 |
2020年 | 18篇 |
2019年 | 10篇 |
2018年 | 14篇 |
2017年 | 7篇 |
2016年 | 21篇 |
2015年 | 32篇 |
2014年 | 27篇 |
2013年 | 55篇 |
2012年 | 67篇 |
2011年 | 97篇 |
2010年 | 34篇 |
2009年 | 35篇 |
2008年 | 68篇 |
2007年 | 72篇 |
2006年 | 62篇 |
2005年 | 53篇 |
2004年 | 50篇 |
2003年 | 51篇 |
2002年 | 47篇 |
2001年 | 16篇 |
2000年 | 20篇 |
1999年 | 10篇 |
1998年 | 11篇 |
1997年 | 12篇 |
1996年 | 12篇 |
1995年 | 12篇 |
1994年 | 17篇 |
1993年 | 12篇 |
1992年 | 11篇 |
1991年 | 9篇 |
1990年 | 4篇 |
1989年 | 5篇 |
1988年 | 4篇 |
1987年 | 5篇 |
1986年 | 9篇 |
1985年 | 11篇 |
1984年 | 9篇 |
1983年 | 3篇 |
1982年 | 5篇 |
1981年 | 6篇 |
1980年 | 8篇 |
1978年 | 6篇 |
1976年 | 5篇 |
1975年 | 7篇 |
1974年 | 5篇 |
1973年 | 4篇 |
1942年 | 3篇 |
排序方式: 共有1105条查询结果,搜索用时 22 毫秒
101.
Nathalie L. Lévêque Sylvie Héron Alain Tchapla 《Journal of mass spectrometry : JMS》2010,45(3):284-296
Triacylglycerols (TAGs) provide a challenge for mass spectrometry (MS) analysis because of their complexity. In particular, for dietary, nutritional and metabolic purposes, the positional placement of fatty acids on the glycerol backbone of TAGs is a crucial aspect. To solve this problem, we have investigated the TAGs' fragmentation patterns using an ion trap mass spectrometer. A series of pure regioisomeric pairs of TAGs (POP/PPO, POO/OPO and OSO/SOO) were cationized by Ag+ after their separation by non‐aqueous reversed‐phase liquid chromatography (NARP‐LC) before MS to improve MS sensitivity. Electrospray ionization–MS (ESI‐MS) conditions were optimized in order to produce characteristic [M + Ag + AgNO3]+ ions from each TAG, which were then fragmented to produce MS/MS spectra and then fragmented further to produce up to MS5 spectra. The observation of ions produced by LC‐MS5 of on‐line Ag+‐cationized TAG provided unambiguous information on the fatty acid distribution on the glycerol backbone. These strategies of MS to MS5 experiments were applied to identify components and to determine the regiospecificity of TAG within a complex mixture of lipids in natural oils. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
102.
103.
The purpose of this work is to identify the effect of the cation nature on mechanisms of the sand consolidation with alkaline silicate solution at low temperature (70 °C). Three diluted lithium, sodium and potassium silicate solutions with [Si] = 2.8 mol/l were used to agglomerate sand composed of grains which mean diameter is 340 μm. According to the cation, different behaviors were observed in terms of the drying time and the material cohesion. Essentially, the drying time increases with decreasing cation size. In contrast, the compressive strength raises when the cation size increases inducing intra-granular rupture highlighted by SEM observations. This could find an explanation in the cation hydration sphere of cations. The strength of the cation–water electrostatic interaction becomes less important as the size of the cations increase leading to more ionic bonds. Despite their strong consolidation, potassium-based materials have a high solubility in water. This result is consistent with the ionic nature of bonds. 相似文献
104.
105.
Racha El Debs Maguy Abi Jaoudé Nicolas Morin Cécile Miege Jérôme Randon 《Journal of separation science》2011,34(15):1805-1810
In recent years, metal oxides such as titania have been commercially available as chromatographic beds that can potentially be used to achieve novel separations of polar compounds. For example β blockers, which are more often encountered in environmental sciences, have a wide range of polarity, and their basic character leads to difficult sample treatment and separation on conventional silica‐based sorbents. The contribution of titania to the selective analysis of nine β blockers was evaluated in terms of retention mechanisms observed in hydrophilic interaction LC using acetonitrile/water mobile phases with various additives. The mobile phase additives enabled to control the β blocker charge as well as the titania surface charge. Depending on their respective ionic state, various retention mechanisms were identified at low water contents (<40%), including mainly adsorption mixed with hydrophilic interaction LC partition, ion exchange and ion exclusion. An unexpected retention was also observed for high water content and high pH, changing the selectivity of the support. 相似文献
106.
Numerical programs may require a high level of guarantee. This can be achieved by applying formal methods, such as machine-checked
proofs. But these tools handle mathematical theorems while we are interested in C code, in which numerical computations are
performed using floating-point arithmetic, whereas proof tools typically handle exact real arithmetic. To achieve this high
level of confidence on C programs, we use a chain of tools: Frama-C, its Jessie plugin, Why and provers among Coq, Gappa,
Alt-Ergo, CVC3 and Z3. This approach requires the C program to be annotated: each function must be precisely specified, and
we prove the correctness of the program by proving both that it meets its specifications and that no runtime error may occur.
The purpose of this paper is to illustrate, on various examples, the features of this approach. 相似文献
107.
108.
We present a new approach to describe the rheological properties of dispersions with non-hydrodynamic interactions (steric, electrostatic and Van der Waals interactions) in the linear viscoelastic domain. Our model is based on the calculation of additional stresses resulting from interaction potentials between spheres and Brownian motion. We start from the statistical mechanical approaches which have been developed by Batchelor and Green and later Lionberger and Russel, to model the viscoelastic properties of emulsions and suspensions. We have extended their calculations to the more general case of viscoelastic deformable inclusions in a viscoelastic matrix. Our contribution lies in the computation of the hydrodynamic functions involved in the term describing interaction stresses. This computation is based on Palierne's results on the deformation field around a viscoelastic inclusion embedded in a viscoelastic matrix. We have also rewritten the conservation equation in the case of interest, over the whole frequency domain. We finally express the complex shear modulus of the dispersion as the sum of two terms : Palierne's complex shear modulus gives the purely hydrodynamic contribution; the interaction contribution depends on both the hydrodynamic properties and the interaction potential. 相似文献
109.