首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   9004篇
  免费   1688篇
  国内免费   979篇
化学   6081篇
晶体学   92篇
力学   736篇
综合类   78篇
数学   1161篇
物理学   3523篇
  2024年   19篇
  2023年   196篇
  2022年   235篇
  2021年   308篇
  2020年   376篇
  2019年   336篇
  2018年   297篇
  2017年   293篇
  2016年   441篇
  2015年   428篇
  2014年   465篇
  2013年   661篇
  2012年   766篇
  2011年   859篇
  2010年   572篇
  2009年   553篇
  2008年   632篇
  2007年   487篇
  2006年   533篇
  2005年   388篇
  2004年   320篇
  2003年   256篇
  2002年   239篇
  2001年   205篇
  2000年   191篇
  1999年   195篇
  1998年   187篇
  1997年   183篇
  1996年   174篇
  1995年   141篇
  1994年   126篇
  1993年   114篇
  1992年   91篇
  1991年   69篇
  1990年   76篇
  1989年   61篇
  1988年   44篇
  1987年   34篇
  1986年   36篇
  1985年   22篇
  1984年   18篇
  1983年   14篇
  1982年   15篇
  1981年   3篇
  1980年   7篇
  1979年   2篇
  1975年   1篇
  1957年   2篇
排序方式: 共有10000条查询结果,搜索用时 250 毫秒
1.
Journal of Radioanalytical and Nuclear Chemistry - This study presents a time-efficient method of analysing 210Pb, 210Bi, and 210Po in natural waters. The optimum pH (1.00), temperature...  相似文献   
2.
赵金丰  周晋宇  张健 《合成化学》2022,30(11):861-869
针对大温差条件下固井水泥浆在固井过程中可能存在的悬浮失稳问题,本研究采用水溶液自由基聚合法来合成具有疏水缔合结构的聚合物作为悬浮稳定剂(PAAN)。通过红外光谱仪、凝胶渗透色谱仪、热重分析仪、高温流变仪、SEM、紫外分光光度计等表征PAAN的结构,发现PAAN随温度升高,形成分子间疏水缔合网状结构,保证了体系的粘度,从而起到有效的悬浮稳定作用。研究发现在40~110 ℃下,0.6%加量的PAAN可以保证固化后的水泥石柱顶部和底部密度差<0.01 g/cm3,且水泥浆稠化时间基本不变,表明PAAN可以保证水泥浆体系具有良好的悬浮稳定效果,且对水泥浆的其他性能无不良影响。  相似文献   
3.
A new A, D-seco limonoid, named 12-acetyloxyperforatin (1), along with three known ones, were isolated from the leaves of Harrisonia perforata. Their structures were elucidated on the basis of spectroscopic analysis, including extensive NMR techniques and computational modelling. These compounds showed no inhibitory activity against the 11β-HSD1 enzyme.  相似文献   
4.
Ding  Hao  Wang  Jin-Ting  Lu  Li-Qiao  Pan  Jian-Wen 《Nonlinear dynamics》2021,104(4):3365-3384
Nonlinear Dynamics - Conventional tuned liquid column dampers (TLCDs) are deficient in multidirectionality. In contrast, toroidal TLCDs are designed to extend the application to multidirectional...  相似文献   
5.
6.
Ding  Q.  Yao  M.  Wu  Sh.  Zeng  M.  Xue  N.  Wu  D.  Xu  J. 《Journal of Applied Spectroscopy》2022,89(4):712-718
Journal of Applied Spectroscopy - Based on partial least squares (PLS) analysis, the effects of different smoothing points and different preprocessing methods on the accuracy and precision of the...  相似文献   
7.
8.
The discharge of diverse pollutants has led to a complex water environment and posed a huge health threat to humans and animals. Self-propelled micromotors have recently attracted considerable attention for efficient water remediation due to their strong localized mass transfer effect. However, a single functionalized component is difficult to tackle with multiple contaminants and requires to combine different decontamination effects together. Here, we introduced a multifunctional micromotor to implement the adsorption and degradation roles simultaneously by integrating the poly(aspartic acid) (PASP) adsorbent with a MnO2-based catalyst. The as-prepared micromotors are well propelled in contaminated waters by MnO2 catalyzing hydrogen peroxide. In addition, the catalytic ramsdellite MnO2(R-MnO2) inner layer is decorated with Fe2O3 nanoparticles to improve their catalytic performance, contributing to an excellent degradation ability with 90% tetracycline (TC) removal in 50 minutes by enhanced Fenton-like reactions. Combining the attractive adsorption capability of poly (aspartic acid) (PASP), the composite micromotors offer an efficient removal of heavy metal ions in short time. Moreover, the designed micromotors are able to simultaneously remove antibiotic and heavy metals in mixed contaminants circumstance just in single treatment. This multifunctional micromotor with distinctive decontamination ability exhibits a promising prospective in treating multiple pollutants in the future.  相似文献   
9.
Fully utilizing solar energy for catalysis requires the integration of conversion mechanisms and therefore delicate design of catalyst structures and active species. Herein, a MOF crystal engineering method was developed to controllably synthesize a copper–ceria catalyst with well-dispersed photoactive Cu-[O]-Ce species. Using the preferential oxidation of CO as a model reaction, the catalyst showed remarkably efficient and stable photoactivated catalysis, which found practical application in feed gas treatment for fuel cell gas supply. The coexistence of photochemistry and thermochemistry effects contributes to the high efficiency. Our results demonstrate a catalyst design approach with atomic or molecular precision and a combinatorial photoactivation strategy for solar energy conversion.  相似文献   
10.
A sensitive and reliable LC–MS/MS method was developed and validated for simultaneous quantification of the major components of Huangqi–Honghua extact in rat plasma, including hydroxysafflor yellow A (HSYA), astragaloside IV (ASIV), calycosin‐7‐O‐β‐d ‐glucoside (CAG), calycosin, calycosin‐3′‐O‐glucuronide (C‐3′‐G) and calycosin‐3′‐O‐sulfate (C‐3′‐S). After extraction by protein precipitation with acetonitrile and methanol from plasma, the analytes were separated on a Hypersil BDS C18 column by gradient elution with acetonitrile and 5 mM ammonium acetate. The detection was carried out on a triple quadrupole tandem mass spectrometer equipped with electrospray ionization source switched between negative and positive modes. HSYA was monitored in negative ionization mode from 0 to 4.9 min, and ASIV, CAG, calycosin, C‐3′‐G and C‐3′‐S were determined in positive ionization mode from 4.9 to 10 min. The lower limits of quantification of the analytes were 6.25 ng/mL for HSYA, 0.781 ng/mL for CAG and 1.56 ng/mL for ASIV and calycosin. The intra‐ and inter‐assay precision (RSD) values were within 13.43%, and accuracy (RE) ranged from ?8.75 to 9.92%. The validated method was then applied to the pharmacokinetic study of HSYA, ASIV, CAG, calycosin, C‐3′‐G and C‐3′‐S in rat after an oral administration of Huangqi–Honghua extract.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号