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51.
提出了一种新的双正交磁光电流传感器技术,该技术可解决传统磁光电流传感器测量大电流脉冲时仅根据正弦或余弦信号无法唯一确定法拉第偏转角的技术难题。在该传感器中,起偏器的透光轴与两个偏振分束器的S分量偏振方向有0与45的夹角,四路输出信号两两之间有/2的相位差。针对该传感器,提出了大电流脉冲的一种反正切函数数据处理方法,该数据处理方法具有可避开正弦函数的不灵敏区间,从而提高数据处理精度的优点。采用双正交磁光电流传感器与罗果夫斯基线圈对比测量了FP-1装置的短路电流脉冲,两种测试技术的实验结果能很好地吻合,证实该光学电流传感器可有效地测量大电流脉冲。
相似文献52.
Ouyang Jinbo Wang Yun Li Tianqi Zhou Limin Liu Zhirong 《Journal of Radioanalytical and Nuclear Chemistry》2018,317(3):1419-1428
Journal of Radioanalytical and Nuclear Chemistry - The carboxyl-modified multiwalled carbon nanotubes were immobilized in chitosan-based composite membranes (CS-CNTs) which were used as efficient... 相似文献
53.
Recently, a polynomial-based (k, n) steganography and authenticated image sharing (SAIS) scheme was proposed to share a secret image into n stego-images. At the same time, one can reconstruct a secret image with any k or more than k stego-images, but one cannot obtain any information about the secret from fewer than k stego-images. The beauty of a (k, n)-SAIS scheme is that it provides the threshold property (i.e., k is the threshold value), the steganography (i.e., stego-images look like cover images), and authentication (i.e., detection of manipulated stego-images). All existing SAIS schemes require parity bits for authentication. In this paper, we present a novel approach without needing parity bits. In addition, our (k, n)-SAIS scheme provides better visual quality and has higher detection ratio with respect to all previous (k, n)-SAIS schemes. 相似文献
54.
A simple,rapid and reliable liquid chromatography–mass spectrometry method for determination of methotrexate in human plasma and its application to therapeutic drug monitoring 下载免费PDF全文
Dan Wu Yixuan Wang Yan Sun Nian Ouyang Jun Qian 《Biomedical chromatography : BMC》2015,29(8):1197-1202
A simple, rapid and reliable liquid chromatography–electrospray ionization tandem mass spectrometry method was established and validated for the determination of methotrexate in human plasma. After a straightforward protein precipitation by acetonitrile–water (70:30, v/v), methotrexate (MTX) and p‐aminoacetophenone (used as internal standard, IS) were separated on a Column C18 column (50 × 2.1 mm, 3 µm; Column Technology, Fremont, CA, USA) using a gradient elution with mobile phase of acetonitrile and 0.03% acetic acid aqueous solution at a flow rate of 0.5 mL/min. The total chromatographic runtime was 5 min for each injection. Quantification detection was performed in a triple‐quadruple tandem mass spectrometer under positive mode monitoring the following mass transitions: m/z 455.3 → 308.3 for MTX and m/z 136.1 → 94.4 for IS. The calibration curve was linear over the range of 0.05–25.0 µmol/L with a lower limit of quantification of 0.05 µmol/L. The intra‐ and interday precisions were <5.2%, the accuracy varied from ?4.1 to 4.5%. The recovery was >94%. The LC‐MS/MS method showed an excellent agreement with the existing HPLC‐UV method using Passing–Bablok regression and Bland–Altman difference plot analysis. The validated LC‐MS/MS can be successfully applied to the routine therapeutic drug monitoring of MTX in clinical laboratories. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
55.
Formation and dissociation of protonated cytosine–cytosine base pairs in i-motifs by ab initio quantum chemical calculations 下载免费PDF全文
Formation and dissociation mechanisms of C-C+ base pairs in acidic and alkaline environments are investigated, employing ab initio quantum chemical calculations. Our calculations suggest that, in an acidic environment, a cytosine monomer is first protonated and then dimerized with an unprotonated cytosine monomer to form a C-C+ base pair; in an alkaline environment, a protonated cytosine dimer is first unprotonated and then dissociated into two cytosine monomers. In addition, the force for detaching a C-C+ base pair was found to be inversely proportional to the distance between the two cytosine monomers. These results provide a microscopic mechanism to qualitatively explain the experimentally observed reversible formation and dissociation of i-motifs. 相似文献
56.
57.
Solid phase microextraction (SPME), a simple, fast and promising sampling technique, has been widely used for complex sample analysis. However, complex matrices could modify the absorption property of coatings as well as the uptake kinetics of analytes, eventually biasing the quantification results. In the current study, we demonstrated the feasibility of a developed calibration method for the analysis of polycyclic aromatic hydrocarbons (PAHs) in complex milk samples. Effects of the complex matrices on the SPME sampling process and the sampling conditions were investigated. Results showed that short exposure time (pre-equilibrium SPME, PE-SPME) could increase the lifetime of coatings, and the complex matrices in milk samples could significantly influence the sampling kinetics of SPME. In addition, the optimized sampling time, temperature and dilution factor for PAHs were 10 min, 85 °C and 20, respectively. The obtained LODs and LOQs of all the PAHs were 0.1–0.8 ng/mL and 1.4–4.7 ng/mL, respectively. Furthermore, the accuracy of the proposed PE-SPME method for milk sampling was validated by the recoveries of the studied compounds in two concentration levels, which ranged from 75% to 110% for all the compounds. Finally, the proposed method was applied to the screening of PAHs in milk samples. 相似文献
58.
正The Chang'E-3(CE-3)mission began with a smooth countdown and flawless launch on the Long March 3B rocket from the Xichang satellite launch center at 01:30 CST on December 2,2013.It landed on the northeastern Imbrium basin(340.49°E,44.12°N)at 21:11 CST on December 14,2013,and the Yutu rover was deployed from the lander the next morning at 04:35.The lander was equipped with a number of remote-sensing 相似文献
59.
Sandilya Garimella Xiaoyu Zhou Zheng Ouyang 《Journal of the American Society for Mass Spectrometry》2013,24(12):1890-1899
The understanding of the gas dynamics of the atmospheric pressure interface is very important for the development of mass spectrometry systems with high sensitivity. While the gas flows at high pressure (>1 Torr) and low pressure (<10–3 Torr) stages are relatively well understood and could be modeled using continuum and molecular flows, respectively, the theoretical modeling or numeric simulation of gas flow through the transition pressure stage (1 to 10–3 Torr) remains challenging. In this study, we used the direct simulation Monte Carlo (DMSC) method to develop the gas dynamic simulations for the continuous and discontinuous atmospheric pressure interfaces (API), with different focuses on the ion transfer by gas flows through a skimmer or directly from the atmospheric pressure to a vacuum stage, respectively. The impacts by the skimmer location in the continuous API and the temporal evolvement of the gas flow with a discontinuous API were characterized, which provide a solid base for the instrument design and performance improvement. Figure
? 相似文献
60.
Mi-Yeon Jang Xiao-Ping Song Mathy Froeyen Philippe Marlière Eveline Lescrinier Jef Rozenski Piet Herdewijn 《Chemistry & biology》2013,20(3):416-423
Highlights? A highly modified nucleotide as substrate for polymerases ? The reversibility of the polymerase reaction at the template level ? Synthesis of a nucleoside with two anomeric centers 相似文献