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   2036篇
  免费   229篇
  国内免费   228篇
化学   2107篇
晶体学   11篇
力学   12篇
综合类   29篇
数学   83篇
物理学   251篇
  2024年   13篇
  2023年   62篇
  2022年   219篇
  2021年   183篇
  2020年   152篇
  2019年   116篇
  2018年   125篇
  2017年   103篇
  2016年   130篇
  2015年   82篇
  2014年   122篇
  2013年   232篇
  2012年   102篇
  2011年   73篇
  2010年   86篇
  2009年   68篇
  2008年   94篇
  2007年   80篇
  2006年   77篇
  2005年   76篇
  2004年   56篇
  2003年   59篇
  2002年   36篇
  2001年   31篇
  2000年   16篇
  1999年   13篇
  1998年   15篇
  1997年   8篇
  1996年   11篇
  1995年   9篇
  1994年   8篇
  1993年   10篇
  1992年   6篇
  1991年   6篇
  1990年   6篇
  1989年   3篇
  1988年   1篇
  1987年   1篇
  1986年   2篇
  1981年   1篇
排序方式: 共有2493条查询结果,搜索用时 8 毫秒
1.
FED器件的发展迫切需要具有化学和热稳定性 ,高亮度 ,长寿命的新型荧光材料。本文合成了Gd3 +离子共掺杂的YAGG∶Tb获得了YAGG∶Tb ,Gd ,并将其用于 0~ 30 0 0V低压范围 ,对其在不同电压和电流密度下的发光特性进行了测试。结果表明 ,该种材料特性优于ZnO∶Zn并且不存在电压与电流饱和  相似文献   
2.
The glycosidations of glucopyranosyl diethyl phosphite and alcohols using an ionic liquid, 1-n-hexyl-3-methylimidazolium trifluoromethanesulfonimidide (C6mim[NTf2]) containing a protic acid, trifluoromethanesulfonimide (HNTf2), as a novel solvent-catalyst system, effectively proceeded under mild conditions to give the corresponding glycosides in good to high yields. Furthermore, this acid-ionic liquid combination could be reused many times for the glycosidations without any loss in efficiency.  相似文献   
3.
在碱性介质中,加热时空气氧化Mn为Mn,Mn与二安替比林苯基甲烷反应生成橙色产物,吐温20和乳酸起到协同增敏作用,λmax=460nm,ε=7.8×10^4L.mol^-1.cm^-1,锰量在0-12μg/25ml范围内符合比尔定律。  相似文献   
4.
The aim of this work was to investigate, for the first time, the potential of the enzyme glutathione S-transferase I (isoenzyme GST-I) for uses in analytical chemistry. A novel fiber-optic biosensor for the detection and determination of the triazine herbicide atrazine was developed based on maize GST-I expressed in E. coli. The sensing bioactive material was a three-layer mini-sandwich. The enzyme was immobilized on the outer layer that consisted of a hydrophilic polyvinylidenefluoride membrane. This membrane was supported on an inner glass disk by means of an intermediate binder sol–gel layer that incorporated bromcresol green (BCG). The biosensor operated in a static mode at 25 °C and the rate of the enzymatic reaction, using atrazine as a substrate, served as an analytical signal. A calibration curve was obtained for atrazine, with analytically useful concentration range 2.52–125 μM. The sensor detection limit was 0.84 μM. The reproducibility of atrazine sensing was in the order of ±3–5%. The method was successfully applied to the determination of this herbicide in real water samples, without sample preparation steps. Atrazine recovery ranged between 85 and 110%. No interference from other pesticides, such as alachlor and carbaryl was observed in the absence of atrazine. The immobilized enzyme retained about 75% of its original activity after 1 month use. Simply unscrewing the terminal holding ring of the probe and placing a new bioactive sandwich could easily replace a deteriorated mini-sandwich.  相似文献   
5.
本文研究了Os-SnCl_2-PVA-亮绿离子缔合体系的显色反应,摩尔吸光系数ε_(434)为5.6×10~6L·mol~(-1)·cm~(-1),锇含量在0.1~0.7μg/25mL范围内遵守比耳定律,室温下显色后,吸光度在110min内稳定。研究了30种外来离子的影响,并进行了高纯镍中微量锇的测定。  相似文献   
6.
停流流动注射催化光度法测定痕量钒   总被引:6,自引:0,他引:6  
王术皓  张爱梅 《分析化学》1996,24(7):832-834
  相似文献   
7.
Green Chemistry and Modern Technology   总被引:4,自引:0,他引:4  
The basic principles, approaches, and early achievements of green chemistry are considered. The definition of green chemistry as a branch of chemistry that studies the laws of passing of chemical reactions and the properties of substances participating in such reactions, with the aim of acquiring basic knowledge that provides a basis for designing chemical technologies that eliminate (sharply curtail) the use and production of materials that pose a risk to the environment.  相似文献   
8.
SDS胶束对孔雀绿褪色反应的影响   总被引:4,自引:0,他引:4  
研究了十二烷基硫酸钠(SDS)表而活性剂胶束和预胶束对孔雀绿褪色可逆反应的影响,建立了1-1型可逆反应的胶束催化模型和预胶束催化模型,获得了胶束相中正逆反应的速率常数和预胶束的平均聚集数.结果表明,SDS胶束和预胶束对正反应有禁阻作用,而对逆反应有催化作用.  相似文献   
9.
The reactions of two triphenyl methane (TPM) dyes—crystal violet (CV+) and malachite green (MG+)—with N3 and OH radicals were studied by pulse radiolytic kinetic spectrophotometry. The rate constants for the reaction of the cationic dyes (D+) with N3 are (9.0±0.6)×109 and (3.0±0.2)×109 dm3 mol−1 s−1 respectively and those for the reaction with OH are obtained as (8.0±0.6)×109 and (1.1±0.1)×109 dm3 mol−1 s−1 respectively. The transient spectra resulting from the oxidation of the dyes were characterized. The time-resolved spectra indicate that the reaction with OH radicals initially generates an adduct which subsequently dissociates to form the radical dication D•2+. The D•2+ species decay by further reaction with the parent dye.  相似文献   
10.
Poly(malachite green) film modified Nafion‐coated glassy carbon electrodes have been prepared by potentiodynamic cycling in malachite green solution. The pH of polymerisation solution has only minor effect on film formation. Electrochemical quartz crystal microbalance (EQCM) was used to monitor the growth of the poly(malachite green) film. Cyclic voltammogram of the poly(malachite green) film shows a redox couple with well‐defined peaks. The redox response of the modified electrode was found to be depending on the pH of the contacting solution. The peak potentials were shifted to a less positive region with increasing pH and the dependence of the peak potential was found to be 56 mV per pH unit. The electrocatalytic behavior of poly(malachite green) film modified Nafion‐coated glassy carbon electrodes was tested towards oxidation of NADH, dopamine, and ascorbic acid. The oxidation of dopamine and ascorbic acid occurred at less positive potential on poly(malachite green) film compared to bare glassy carbon electrode. In the case of NADH, the overpotential was reduced substantially on modified electrode. Finally, the feasibility of utilizing poly(malachite green) film electrode in analytical estimation of ascorbic acid was demonstrated in flow injection analysis.  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