全文获取类型
收费全文 | 9483篇 |
免费 | 654篇 |
国内免费 | 688篇 |
专业分类
化学 | 9334篇 |
晶体学 | 11篇 |
力学 | 63篇 |
综合类 | 113篇 |
数学 | 94篇 |
物理学 | 1210篇 |
出版年
2024年 | 6篇 |
2023年 | 118篇 |
2022年 | 231篇 |
2021年 | 327篇 |
2020年 | 280篇 |
2019年 | 299篇 |
2018年 | 299篇 |
2017年 | 435篇 |
2016年 | 526篇 |
2015年 | 474篇 |
2014年 | 440篇 |
2013年 | 632篇 |
2012年 | 766篇 |
2011年 | 645篇 |
2010年 | 529篇 |
2009年 | 617篇 |
2008年 | 481篇 |
2007年 | 621篇 |
2006年 | 452篇 |
2005年 | 453篇 |
2004年 | 424篇 |
2003年 | 248篇 |
2002年 | 197篇 |
2001年 | 173篇 |
2000年 | 132篇 |
1999年 | 130篇 |
1998年 | 104篇 |
1997年 | 100篇 |
1996年 | 107篇 |
1995年 | 91篇 |
1994年 | 73篇 |
1993年 | 65篇 |
1992年 | 68篇 |
1991年 | 56篇 |
1990年 | 66篇 |
1989年 | 36篇 |
1988年 | 25篇 |
1987年 | 30篇 |
1986年 | 15篇 |
1985年 | 6篇 |
1984年 | 13篇 |
1983年 | 7篇 |
1982年 | 9篇 |
1981年 | 2篇 |
1980年 | 5篇 |
1979年 | 4篇 |
1976年 | 3篇 |
1975年 | 1篇 |
1966年 | 1篇 |
1959年 | 2篇 |
排序方式: 共有10000条查询结果,搜索用时 171 毫秒
31.
32.
双(十二烷基亚磺酰)乙烷溶剂萃取钯及其机理的研究 总被引:2,自引:0,他引:2
本文研究用双(十二烷基亚磺酰)乙烷萃取钯的性能,在KI存在下从7mol/L盐酸介质中用含有BDSE的氯仿能定量萃取钯,有机的钯可被硫脲或氨溶液反萃继之用TMK-TritonX-100光度法测定,研究了萃取的最佳条件及干扰情况,斜率法测得萃合物组成为Pd:I:BDSE=1:2:1,红外光谱证实萃合物中BDSE的二个亚砜以硫原子与钯配位,萃合物为异位体络合物,提出了选择性萃取分离钯的新方法。 相似文献
33.
在GS-221高速摄影测量仪中,测角信息采集与处理速度的快慢是重要性能指标之一。本文讨论了如何在尽可能短的时间内对测角信息进行采集和处理的软件实现方法。 相似文献
34.
Arjan J. H. Louter Philo A. Jones J. David Jorritsma Jolan J. Vreuls Udo A. Th. Brinkman 《Journal of separation science》1997,20(7):363-368
An automated system for derivaatization was coupled on-line with solid-phase extraction-gas-chromatography (SPE-GC). The system was optimized for the determination of phenol and chlorinated phenols in aqueous samples. The test analytes were acetylated with acetic anhydride; proper buffering of the sample was a critical factor. Next, the phenol acetates were enriched on a SPE cartridge and transferred to a GC; two appraoaches were studied. In the first approach, the derivatives were enriched on disposable C18 cartridges (ASPEC type) and desorbed with methylacetate. Aan aliquot of the final eluate was injected on-line the GC by means of a loop-type interface. In the second approach, trace enrichment was performed on 10 × 2 mm i.d. LC-type precolumn packed with polystyrenedivinylbenzene copolymer (PLRP-S) this precolumn was dried with a mitrogen purge and the phenol acetates were desorbed with ethyl acetate which was injectedon-line into the retention gap of the GC under partially concurrent solvent evaporation (PCSE) conditions. The Derivatization-SPE-GC system which was based on the loop-type interface has the advantage of simplicity and easy operation, the main drawback is the impossibility to determine phenol acetates which elute prior to trichlorophenol acetates. With the derivatization-SPE-GC approach using PCSE-based desorption, even the most volatile analyte of the test series, phenol acetate, can be determined successfully. The entire procedure, including the derivatization step, was fully automated and integrated in one set-up. The precision data for the integrated on-line derivatization-SP-FID system were fully satisfactory, with RSD values of 1–12 % at the 1 μg/1 level. When a sample volume of 2.2 ml was analyzed, The detection limits for the chlorinated phenol acetates were in the 0.1–0.3 μg/1 range. 相似文献
35.
The solvent extraction of cobalt(II), nickel(II) and copper(II) using 2,4-pent-dione (Hacac) and 4-phenyl-2, 4-but-dione (Hbzac)
is carried out by varying the reagent concentration and pH of the aqueous phase. Each of these metals is quantitatively separated
(≈ 98%) from their binary mixtures with monovalent (Ag), divalent (Mn, Zn, Cd, Hg, Mg, Sn, Pb) and trivalent (Cr, Fe) metals.
The extraction constants are calculated from the metal distribution data using linear regression analysis. The extracted species
is MA2 in each case. A most significant result is separation of copper(II) from iron(III) which otherwise interferes when extracted
from the acidic medium. 相似文献
36.
This paper presents a fringe pattern normalization and noise-reduction algorithm. Locally the background noise is suppressed, the modulation normalized and the noise smoothed. An expression to calculate the cosine-only term is formulated. It is related to the directional derivatives of the intensity fringes. Two-dimensional Fourier series are used to calculate the parameters needed for the algorithm. Experimental work is presented using diffraction and ESPI images. The programming is relatively simple and involves mainly local convolutions. The processing time using a 2 GHz computer to normalize an image of 256 × 256 pixels is approximately one second. 相似文献
37.
38.
Anisha Gokarna Yong Hwan Kim Yong-Hoon Cho Min Su Lee In Cheol Kang Hyun Kyu Park Min Gon Kim Bong Hyun Chung 《Optical Review》2006,13(4):288-291
We demonstrate the fluorescence mapping of protein microarrays by the technique of scanning near-field optical microscopy
(SNOM) and confocal microscopy. Micron sized spots (300 μm) of human Immunoglobulin G (hIgG) protein with and without a Cy3
dye labeling have been fabricated on glass substrates by an immobilization method which makes use of calixcrown derivatives
termed Prolinker. We have also tried to probe into the well-known “doughnut effect” observed in fluorescence images of proteins
using the SNOM technique. The topographic and fluorescence SNOM images revealed that the number of proteins at the boundary
of the spot were more than at the center in the case of the microarray spot which showed brighter luminescence at the edge
than at the center in the confocal image. 相似文献
39.
Nadeem Saeed Basant K Puri Angela Oatridge Joseph V Hajnal Ian R Young 《Magnetic resonance imaging》1998,16(10):1237-1247
Two semi-automated methods for quantification of ventricular volume change from baseline and follow-up magnetic resonance imaging scans have been developed. Technique 1 employs direct segmentation of the ventricles from both the scans using thresholding and contour extraction. Technique 2 operates on difference images produced by voxel based intensity subtraction of the baseline from the registered follow-up images. Here, all voxels with intensities above a noise threshold and in a restricted area are monitored to compute volumetric changes. In phantom measurements the first technique was accurate to 0.0046%, the second to 0.167% of the phantom volume. Results from normal volunteers was that the average ventricular volume changed by 1.52% and 1.54% for images acquired within 9 months using techniques 1 and 2, respectively. With schizophrenic patients mean change of 10.78% and 9.43% were found employing the first and second procedures, respectively. All measurements agreed with a radiologist’s visual grading of the changes. Robust, objective, fast, easy-to-use, and fairly accurate procedures have been developed and validated to quantify volumetric changes. 相似文献
40.
C. N. Carducci S. E. Lucangioli V. G. Rodríguez G. C. Fernndez Otero 《Journal of chromatography. A》1996,730(1-2):313-319
Sample preparation procedures using octadecyl (C18) extraction disks were developed to obtain accurate and reproducible results for determinations of clenbuterol (20 μg per dose) and levothyroxine (100 μg per dose) in dissolution media of solid oral dosage forms. Preconcentration of samples allowed final concentrations of 1.1 μg/ml of clenbuterol and 4.0 μg/ml of levothyroxine to be reached prior to CE analysis. The results obtained by CE were in good agreement with those of HPLC. The precision of the migration time, peak area, peak height and accuracy were determined in both intea-day (n = 6) and inter-day (n =18) assays. Linearity was demonstrated over the ranges 0.5–80.0 μg/ml of clenbuterol and 1.0–30.0 μg/ml of levothyroxine. The mean recoveries were higher than 94.0%, ranging from 50 to 125% levels with respect to dose potencies. The proposed methodology may be generally applied to determine drugs at ng/ml concentrations. 相似文献