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   2252篇
  免费   253篇
  国内免费   199篇
化学   1693篇
晶体学   27篇
力学   99篇
综合类   14篇
数学   223篇
物理学   648篇
  2023年   39篇
  2022年   41篇
  2021年   63篇
  2020年   80篇
  2019年   97篇
  2018年   69篇
  2017年   55篇
  2016年   91篇
  2015年   83篇
  2014年   112篇
  2013年   152篇
  2012年   188篇
  2011年   202篇
  2010年   127篇
  2009年   110篇
  2008年   143篇
  2007年   137篇
  2006年   122篇
  2005年   121篇
  2004年   70篇
  2003年   56篇
  2002年   75篇
  2001年   47篇
  2000年   34篇
  1999年   34篇
  1998年   30篇
  1997年   29篇
  1996年   32篇
  1995年   32篇
  1994年   21篇
  1993年   18篇
  1992年   30篇
  1991年   12篇
  1990年   23篇
  1989年   17篇
  1988年   15篇
  1987年   15篇
  1986年   8篇
  1985年   13篇
  1984年   14篇
  1983年   9篇
  1982年   6篇
  1981年   7篇
  1980年   4篇
  1979年   5篇
  1978年   4篇
  1975年   3篇
  1962年   1篇
  1961年   1篇
  1954年   1篇
排序方式: 共有2704条查询结果,搜索用时 175 毫秒
21.
The study focused on determining the effect of acidic and basic cold activation on hydrochar (HC) for the removal of methyl orange (MO). HC was prepared by hawthorn seeds (HS) under hydrothermal carbonization. HC was cold-activated with HCl and NaOH, respectively, and they were grafted with aminopropyltriethoxysilane (APTES) and protonated to obtain AHC-N+ (acid-activated and modified HC) and BHC-N+ (base-activated and modified HC) to determine the effect of acidic and basic activation. They were characterized by elemental analysis, IR, thermal analysis, zeta potential, N2 adsorption–desorption measurements, and SEM–EDX analysis. The prepared adsorbents displayed MO adsorption due to abundant protonated amine groups. BHC-N+ showed higher MO adsorption than AHC-N+. The result showed that more protonated APTES groups grafted on the surface of HC via NaOH activation. The obtained data had a good fitting with the Langmuir isotherm and pseudo-second-order kinetic. The maximum adsorption capacity of BHC-N+ was 250.38 mg g−1. The adsorption mechanism could be attributed to the electrostatic interactions between MO and protonated amine groups of APTES and hydrogen bonding.  相似文献   
22.
Here,the selective adsorption behaviors of guest molecule COR in two hexamer host grids were investigated by means of scanning tunnelling microscope(STM).The assembled structures of small functional organic molecules TTBTA and TATBA were thermodynamically stable.Interestingly,the introduction of the guest molecule COR destroyed the original hexamer structure of TTBTA and combined with it to form a new triangular host-guest system.Different from TTBTA,the introduction of the guest molecule COR did not affect the six-membered ring structure of TATBA.Furthermore,the co-assembly structure of TTBTA/TATBA/COR was established and the guest molecule COR showed preferential adsorption to the TATBA host grid.Density functional theory(DFT) calculations had been performed to disclose the mechanism of the involved assemblies.  相似文献   
23.
Journal of Structural Chemistry - We report a comprehensive study of the effect of the chemical structure of boron carbonitride films on the variability of their functional characteristics. The...  相似文献   
24.
This paper describes a novel approach to detect Cd(II) using the combination of the differential pulse anodic stripping voltammetry and magnetic nanoparticle based dispersive solid phase microextraction as an efficient, green and accurate method. Currents of Cd(II) increased linearly in the range from 75 to 2000 ng L−1 Cd(II) with a detection limit of 21.6 ng L−1. The RSD values of 2.6 and 6.0 % for 1.00 and 0.10 μg L−1 respectively showed that proposed method has an acceptable repeatability. Recovery values between 92.3 and 98.6 % showed that this approach can be successfully used for determination of Cd(II) in water samples.  相似文献   
25.
Journal of Thermal Analysis and Calorimetry - As high heat dissipation has increasingly become the primary factor restricting the capability of electronic elements, and the high temperature of the...  相似文献   
26.
An accurate and fast spectrophotometric method for the determination of acetylcysteine by silicomolybdenum blue has been established. The various effect factors on the determination of acetylcysteine by silicomolybdenum blue spectrophotometry are investigated in detail. The results show that under the optimum reaction conditions, SiO32‐ reacts with Mo7O246‐ to form silicon molybdenum heteropoly acid (H4Si(Mo3O10)4). Then H4Si(Mo3O10)4 is reduced by hydrosulfuryl (‐SH) in acetylcysteine to form silicomolybdenum blue (H4Si(Mo3O10)2(Mo3O9)2). The absorbance of silicomolybdenum blue is measured at the maximal absorption wavelength of 735 nm, and the content of acetylcysteine can be calculated based on this absorbance. A good linear relationship is obtained between the absorbance of silicomolybdenum blue and the concentration of acetylcysteine in the range of 5.040∼25.20 μg⋅mL‐1. The linear regression equation is A = 0.0272 + 21.484C (mg⋅mL‐1), with a linear correlation coefficient of 0.9995. This proposed method has been successfully applied to the determination of acetylcysteine in pharmaceutical samples, and the results agree well with those obtained by pharmacopoeial method.  相似文献   
27.
Two metal‐organic frameworks, [Co2(ABTC)(bimh)(OH)] · 2H2O ( 1 ) and [Co3(ABTC)2(dimb)4]n ( 2 ) [H3ABTC = 3,4′,5‐azobenzenetricarboxylic acid, bimh = 1,1′‐(1,4‐hexanediy)bis(imidazole), dimb = 1,4‐bis(1H‐imidazol‐1‐yl)benzene], were prepared under solvothermal conditions and structurally characterized. Complex 1 demonstrates a complicated 3D (3,8)‐connected tfz‐d net with (43)2(46.617.85) topology. The framework of 2 can be classified as a rare 3D (3,6,6)‐connected net with the Schäfli symbol of (4.62)2(42.610.83)(44.610.8), and exhibits an intriguing self‐penetrating motif. Meanwhile, the thermal stabilities and magnetic properties for 1 and 2 were also probed.  相似文献   
28.
With the aim of obtaining high corrosion resistant Zn–Sn alloy coatings from an ionic liquid, the effects of electrodeposition potential and electrolyte composition on the electrodeposition behavior, film composition, morphology and corrosion performance were investigated. Cyclic voltammograms indicate that Zn and Sn were co‐deposited at distinct reduction potentials as pure Zn and Sn elements. In addition, the phase composition analysis also showed that the obtained Zn–Sn alloy deposits (8 wt.%–45 wt.% Zn) consist of a two‐phase mechanical mixture of small aggregates of Zn and Sn metals. The Zn content of the alloy significantly increases as the electrodeposition potential and electrolyte Zn (II)/Sn (II) ratio increase. The corrosion performance study of the obtained Zn–Sn coatings showed that they have a passivation behavior and their corrosion resistance increases as the alloy‐Sn content increases. To improve their morphological properties, ethylene diamine tetraacetic acid additive was introduced into the electrolyte and greatly improved the morphology and corrosion resistance of the deposits. For the first time, it was shown that high corrosion resistance Zn–Sn coatings can be obtained from ionic liquids. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   
29.
纳米TiO2修饰的La0.6Sr0.4Co0.2Fe0.8O3-δ(LSCF)阴极被直接应用于YSZ电解质电池上. TiO2可阻止LSCF和YSZ间的化学反应,抑制SrZrO3的形成. LSCF-0.25 wt% TiO2阴极电池在0.7 V和600°C下的电流密度是LSCF阴极电池的1.6倍.电化学阻抗谱结果表明, TiO2修饰显著加快了氧离子注入电解质的过程,这可能与TiO2抑制了阴极/电解质界面处高电阻SrZrO3层的形成有关.本文为在ZrO2基电解质上使用高性能的(La,Sr)(Co,Fe)O3阴极材料提供了一种简单有效的方法.  相似文献   
30.
A novel and efficient strategy to build α‐benzylic quaternary cyclopentanones with excellent enantioselectivities (up to 96 % ee) and high yields (up to 99 % yield) has been developed, and its application demonstrated by the first catalytic asymmetric total synthesis of (?)‐1,14‐herbertenediol and the formal synthesis of (?)‐aphanorphine.  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