全文获取类型
收费全文 | 13818篇 |
免费 | 1028篇 |
国内免费 | 861篇 |
专业分类
化学 | 11960篇 |
晶体学 | 28篇 |
力学 | 1046篇 |
综合类 | 52篇 |
数学 | 350篇 |
物理学 | 2271篇 |
出版年
2024年 | 40篇 |
2023年 | 229篇 |
2022年 | 477篇 |
2021年 | 356篇 |
2020年 | 542篇 |
2019年 | 509篇 |
2018年 | 471篇 |
2017年 | 587篇 |
2016年 | 677篇 |
2015年 | 669篇 |
2014年 | 647篇 |
2013年 | 892篇 |
2012年 | 950篇 |
2011年 | 885篇 |
2010年 | 704篇 |
2009年 | 799篇 |
2008年 | 745篇 |
2007年 | 778篇 |
2006年 | 685篇 |
2005年 | 646篇 |
2004年 | 596篇 |
2003年 | 494篇 |
2002年 | 380篇 |
2001年 | 269篇 |
2000年 | 234篇 |
1999年 | 201篇 |
1998年 | 176篇 |
1997年 | 136篇 |
1996年 | 141篇 |
1995年 | 139篇 |
1994年 | 120篇 |
1993年 | 84篇 |
1992年 | 74篇 |
1991年 | 69篇 |
1990年 | 54篇 |
1989年 | 50篇 |
1988年 | 38篇 |
1987年 | 29篇 |
1986年 | 21篇 |
1985年 | 19篇 |
1984年 | 19篇 |
1983年 | 14篇 |
1982年 | 18篇 |
1981年 | 13篇 |
1980年 | 7篇 |
1979年 | 8篇 |
1978年 | 6篇 |
1976年 | 5篇 |
1973年 | 2篇 |
1959年 | 2篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
51.
In order to better understand the early continental evolution of the Anshan area, one ofthe typical Precambrian distribution areas of the North China Craton, the geochronology and REEcomposition of the zircons from the meta-argillo-arenaceous rock occurred as enclave in 3.1 GaLishan trondhjemite are studied by using SHRIMP ll ion microprobe. It is indicated that the Pa-leoarchaean is a very important continental formation period in the Anshan area and 3.2 Ga can beregarded as the boundary between the Paleoarchaean and Mesoarchaean. 相似文献
52.
The precision of isotopic measurements of Pb by thermal ionization mass spectrometry (TIMS) is limited by the fact that this element does not possess an invariant isotope ratio that can be used for the correction of mass fractionation by internal normalization. Multiple-collector inductively coupled plasma mass spectrometry (MC-ICPMS) can overcome this limitation, because with plasma ionization, elements with overlapping mass ranges are thought to display identical mass discrimination. With respect to Pb, this can be exploited by the addition of Tl to the sample solutions; the mass discrimination factor obtained for Tl can then be used for the correction of the measured Pb isotope ratios. In this article we present the results of a detailed study that investigates the accuracy and precision of such an external correction technique for mass discrimination based upon the results of multiple analyses of a mixed standard solution of NIST SRM-981 Pb and SRM-997 Tl. Our data indicate that normalization of the Pb isotope ratios to the certified isotopic composition of SRM-997 Tl produces Pb isotopic results that are significantly lower than recently published reference values by TIMS. This systematic offset can be eliminated by renormalization of the Pb data to a different Tl isotopic composition to obtain an empirically determined mass discrimination factor for Pb that generates accurate results. It is furthermore shown that a linear law is least suited for the correction of mass discrimination, whereas a power or exponential law function provide significantly more accurate and precise results. In detail, it appears that a power law may provide the most appropriate correction procedure, because the corrected Pb isotope ratios display less residual correlations with mass discrimination compared to the exponentially corrected data. Using an exponential or power law correction our results, obtained over a period of over seven months, display a precision (2σ) of better than 60 parts per million (ppm) for 208Pb/206Pb and 207Pb/206Pb and of better than 350 ppm for 206Pb/204Pb, 207Pb/204Pb/204Pb, and 208Pb/204Pb. This represents a significant improvement compared to conventional TIMS techniques and demonstrates the potential of MC-ICPMS for routine, high-precision measurements of Pb isotopic compositions. 相似文献
53.
54.
Vora A. Riga A. Dollimore D Alexander K. 《Journal of Thermal Analysis and Calorimetry》2004,75(3):709-717
This study attempts to identify the degradative process which folic acid undergoes in the solid-state under thermal stress.
In order to facilitate the process, the various pieces of the chemical structure, namely, p-amino benzoic acid, pterin and glutamic acid as both its d- and l-isomers were investigated as separate entities. These structured solid-state pieces were then compared to the composite solid
state folic acid degradative curves in order to identify the peaks seen and provide direction for the interpolation of the
degradative mechanism. It was observed that none of the structural pieces could be superimposed as assumed earlier and hence
an attempt was made to identify the decomposition products using various analytical techniques such as infrared spectroscopy,
mass spectroscopy and X-ray diffraction which suggested that the glutamic acid fragment is lost first as evidenced by acid
loss and amide enhancement in the IR spectra. The vitamin was ultimately degrading to carbon fragments and that further identification
was not necessary.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
55.
Angelica pubescens and Angelica sinensis belong to the Umbelliferae family and both are used as traditional Chinese medicines. In the present study, headspace solid-phase microextraction (HS-SPME) with gas chromatography-mass spectrometry (GC-MS) was used for the analysis of the volatile constituents present in their roots. Eighty-seven compounds in Angelica pubescens and thirty-six compounds in Angelica sinensis were identified by GC-MS. Their relative contents were calculated by the peak area ratio. HS-SPME was compared to steam distillation (SD) by analyzing the volatile constituents of Angelica sinensis root. A good agreement between results obtained with both techniques was found. As a conclusion, HS-SPME is a powerful tool for determining the volatile constituents present in the TCMs. 相似文献
56.
57.
Haishan Bu Erqiang Chen Shengyong Xu Kexin Guo Bernhard Wunderlich 《Journal of Polymer Science.Polymer Physics》1994,32(8):1351-1357
Single-molecule single crystals were grown from amorphous droplets of fractionated isotactic polystyrene. The crystals were analyzed by electron microscopy and electron diffraction. The molecular mass distribution could be matched with a statistical analysis of single-molecule particles (amorphous and crystals). Proof was brought that single molecules of isotactic polystyrene do not reach equilibrium dimensions on crystallization, rather assume the lamellar morphology with chain-folded macroconformation, also known from crystallization of polymolecular crystals. © 1994 John Wiley & Sons, Inc. 1 This article is a US Government work and, as such, is in the public domain in the United States of America. US Government contract No. DE-AC05-840R-21400. 相似文献
58.
本文评述了表面热电离质谱(TIMS),特别是负离子质谱(NTI-MS)对非金属和具有高电离电位的金属元素的同位素测定的进展,引用文献34篇。 相似文献
59.
The Gas Complex MnAlF5 and its Influence on the Purification of AlF3 by Sublimation The gas complex MnAlF5 has been determined mass spectroscopically by the ions MnAlF5+ and MnAlF4+. The gas complex MnAlF5 is formed above 973 K by heating up mixtures of AlF3/MnF2 or AlF3 · 3 H2O endowed with Mn2+ or by heating up solid MnAlF5 too. At 1 008 K the enthalpie of dissociation is 197 kJ/mole. The equilibrium structures of the high spin molecule MnAlF5 (S = 5/2) were examined with ab initio calculations at the HF-level by comlete gradient optimizing. Two minimum structures were found on the potential energy surface. A bidentate fluorine bridged structure was found to be the most stable at the HF-level. Vibrational frequencies and thermodynamic functions of complex formation were estimated for both minimum structures. The importance of the formation of the gas complex for the separation of MnF2 and AlF3 by sublimation is discussed. 相似文献
60.
Analytical procedures for quantification of peptides in pharmaceutical research by liquid chromatography–mass spectrometry 总被引:6,自引:0,他引:6
John H Walden M Schäfer S Genz S Forssmann WG 《Analytical and bioanalytical chemistry》2004,378(4):883-897
Peptide quantification by liquid chromatography–mass spectrometry (LC–MS) combines the high resolving power of reversed-phase (RP) chromatography with the excellent selectivity and sensitivity of mass spectrometric detection. On the basis of comprehensive practical experience in the analysis of small molecules, pharmaceutical research is developing technologies for analysis of a growing number of peptidic drug candidates. This article is a detailed review of procedures based on LC–MS techniques for quantitative determination of peptides. With the focus on pharmaceutical applications several technologies for sample preparation, various aspects of peptide chromatography, important characteristics of ESI–MS, selectivity of MS-detection modes, the large variability of internal standards, and modern instrumentation are discussed. The demand for reliable, robust, sensitive, and accurate methods is discussed using numerous examples from the literature, complemented by experiments and results from our laboratory. 相似文献