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   168篇
  免费   13篇
  国内免费   1篇
化学   112篇
晶体学   3篇
力学   15篇
数学   22篇
物理学   30篇
  2023年   2篇
  2022年   1篇
  2021年   5篇
  2020年   11篇
  2019年   8篇
  2018年   12篇
  2017年   7篇
  2016年   13篇
  2015年   8篇
  2014年   11篇
  2013年   14篇
  2012年   12篇
  2011年   8篇
  2010年   15篇
  2009年   14篇
  2008年   8篇
  2007年   10篇
  2006年   5篇
  2005年   3篇
  2004年   1篇
  2003年   4篇
  2002年   2篇
  2001年   1篇
  2000年   1篇
  1996年   1篇
  1994年   1篇
  1989年   1篇
  1982年   1篇
  1979年   1篇
  1974年   1篇
排序方式: 共有182条查询结果,搜索用时 296 毫秒
81.
In this work, high aspect ratio zinc oxide nanowires are synthesized using templated one-step electrodeposition technique. Electrodeposition of the nanowires is done using a handcrafted electronic system. Nuclear track-etched polycarbonate membrane is used as a template to form the high aspect ratio nanowires. The result of X-ray diffraction and scanning electron microscopy shows that nanowires with a good crystallinity and an aspect ratio of more than 30 can be achieved in a suitable condition. The height of electrodeposited nanowires reaches to about 11 μm. Based on the obtained results, high aspect ratio ZnO nanowires can be formed using inexpensive electrodeposition setup with an acceptable quality.  相似文献   
82.
AC impedance spectroscopy was used to investigate the ionic conductivity of solution cast poly(ethylene oxide) (PEO)/poly(methyl methacrylate) (PMMA) blends doped with lithium perchlorate. At low PEO contents (below overlap weight fraction w*), ionic conductivities are almost low. This could be due to nearly distant PEO chains in blend, which means ion transportation cannot be performed adequately. However, at weight fractions well above w*, a significant increase in ionic conductivity was observed. This enhanced ionic conductivity mimics the PEO segmental relaxation in rigid PMMA matrix, which can be attributed to the accelerated motions of confined PEO chains in PMMA matrix. At PEO content higher than 20 wt % the conductivity measured at room temperature drops due to crystallization of PEO. However by increasing temperature to temperatures well above the melting point of PEO, a sudden increase of conductivity was observed which was attributed to phase transition from crystalline to amorphous state. The results indicate that some PEO/PMMA blends with well enough PEO content, which are structurally solid, can be considered as an interesting candidate for usage as solid‐state electrolytes in Lithium batteries. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 2065–2071, 2010  相似文献   
83.
Computational Optimization and Applications - A method, called an augmented subgradient method, is developed to solve unconstrained nonsmooth difference of convex (DC) optimization problems. At...  相似文献   
84.
The complexation reaction between UO2 2+ cation with macrocyclic ligand, 18-crown-6 (18C6), was studied in acetonitrile–methanol (AN–MeOH), nitromethane–methanol (NM–MeOH) and propylencarbonate–ethanol (PC–EtOH) binary mixed systems at 25 °C. In addition, the complexation process between UO2 2+ cation with diaza-18-crown-6 (DA18C6) was studied in acetonitrile–methanol (AN–MeOH), acetonitrile–ethanol (AN–EtOH), acetonitrile–ethylacetate (AN–EtOAc), methanol–water (MeOH–H2O), ethanol–water (EtOH–H2O), acetonitrile–water (AN–H2O), dimethylformamide–methanol (DMF–MeOH), dimethylformamide–ethanol (DMF–EtOH), and dimethylformamide–ethylacetate (DMF–EtOAc) binary solutions at 25 °C using the conductometric method. The conductance data show that the stoichiometry of the complexes formed between (18C6) and (DA18C6) with UO2 2+ cation in most cases is 1:1 [M:L], but in some solvent 1:2 [M:L2] complex is formed in solutions. The values of stability constants (log Kf) of (18C6 · UO2 2+) and (DA18C6 · UO2 2+) complexes which were obtained from conductometric data, show that the nature and also the composition of the solvent systems are important factors that are effective on the stability and even the stoichiometry of the complexes formed in solutions. In all cases, a non-linear relationship is observed for the changes of stability constants (log Kf) of the (18C6 · UO2 2+) and (DA18C6 · UO2 2+) complexes versus the composition of the binary mixed solvents. The stability order of (18C6 · UO2 2+) complex in pure studied solvents was found to be: EtOH > AN ≈ NM > PC ≈ MeOH, but in the case of (DA18C6 · UO2 2+) complex it was : H2O > MeOH > EtOH.  相似文献   
85.
2-(2-Formyl-1H-benzimidazol-1-yl)acetic acid, as a bifunctional formyl-acid was prepared in four steps. This compound underwent one-pot reaction with primary amines, and alkyl isocyanides under Ugi conditions. A series of novel 3-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]benzimidazole-1-carboxamides were obtained in moderate to excellent yields.  相似文献   
86.
In this study, a rapid flow injection-flame atomic absorption spectrometry for cyanide detection was developed. Different AgX (where X is Cl(-), Br(-), I(-) and N(3)(-)) solid-phase reagents (SPR) were tested for indirect determination of cyanide. In a single-line FIA system, the cyanide was allowed to react with AgX SPR, which in turn changed Ag ions in AgX to silver cyanide complexes in a sodium hydroxide carrier stream. The eluent containing the analyte as silver cyanide complexes was measured by FAAS. The calibration curve was linear up to 30 mg l(-1) with a detection limit of 0.05 mg l(-1) for cyanides. The sampling rate and the relative standard deviation were <1.09% and >200 h(-1), respectively. The method was applied to the determination of cyanide in electroplating wastewater.  相似文献   
87.
Parametric investigations were carried out on electrochemical etching (ECE) process of Lexan polycarbonate (PC) detector. Outstanding experimental results showing the enlargement of the registration energy range of α-particle tracks of the PC and decrease of ECE time are presented in this paper.In the experiment, major parameters such as etching solution and ECE conditions are focused. Ethylene diamine is applied as an additional chemical agent to increase the bulk etching rate (VB) which is maintained below a critical value . By using mixture of KOH, CH3OH (methanol), NH2(CH2)2NH2 (ethylene diamine) and H2O and applying interval-based ECE process in total duration of 70 min, expanded α-registration range of 0.5–4.7 MeV have been achieved, as well alpha track diameters decrease with increasing of alpha particle energy. In this process the density of background tracks also decreases comparably. In this paper, electric current is introduced as an effective ECE parameter for improving detection efficiency of low α-particles energy in the PC.  相似文献   
88.
In this paper 1,3-dipolar cycloaddition reaction has been studied. An efficient synthesis of 4′-[3-methyl-5-thioxo-1H-1,2,4-triazol-4(5H)-yl]-2′,5′-diphenyl-2′,4′-dihydro spiro(indolin-3,3′[1,2,4]triazol)-2-one derivatives using triethylamine in MeCN at room temperature is reported. The structures of the obtained compounds were confirmed by means of elemental analysis, MS and spectral (IR, 1H, and 13C NMR) methods.  相似文献   
89.
Titanium(IV) tetraisopropoxide was employed as a metal oxide sol–gel precursor to prepare ceramic composite nanofibers by the electrospinning system. To facilitate this process and obtain the desired nanofibers with higher aspect ratios and surface area, poly(vinylpyrrolidone) was added to the sol of titania. Four ceramic nanofibers sheets based on titania were prepared while each sheet contained different transition metals such as Fe‐Mn, Fe‐Ni, Fe‐Co, and Fe‐Mn‐Co‐Ni. The scanning electron microscope images showed good homogeneity for all the prepared ceramic composites with a diameter range of 100–250 nm. The sorption efficiency was investigated by a micro‐solid‐phase extraction setup in online combination with high‐performance liquid chromatography for the determination of naproxen and clobetasol. All the prepared composites exhibited comparable efficiencies for the desired analytes and the type of metal showed insignificant effect. For the selected composite with Fe‐Mn, the linearity of the analytes was in the range of 1–1000 μg/L and the limit of detection values were found to be 2 and 0.3 μg/L for naproxen and clobetasol, respectively. The developed method was extended to the analysis of urine and blood plasma samples and acceptable relative standard deviations were obtained at two concentration levels.  相似文献   
90.
Dynamic pricing has become a common form of electricity tariff, where the price of electricity varies in real time based on the realized electricity supply and demand. Hence, optimizing industrial operations to benefit from periods with low electricity prices is vital to maximizing the benefits of dynamic pricing. In the case of water networks, energy consumed by pumping is a substantial cost for water utilities, and optimizing pump schedules to accommodate for the changing price of energy while ensuring a continuous supply of water is essential. In this paper, a Mixed-Integer Non-linear Programming (MINLP) formulation of the optimal pump scheduling problem is presented. Due to the non-linearities, the typical size of water networks, and the discretization of the planning horizon, the problem is not solvable within reasonable time using standard optimization software. We present a Lagrangian decomposition approach that exploits the structure of the problem leading to smaller problems that are solved independently. The Lagrangian decomposition is coupled with a simulation-based, improved limited discrepancy search algorithm that is capable of finding high quality feasible solutions. The proposed approach finds solutions with guaranteed upper and lower bounds. These solutions are compared to those found by a mixed-integer linear programming approach, which uses a piecewise-linearization of the non-linear constraints to find a global optimal solution of the relaxation. Numerical testing is conducted on two real water networks and the results illustrate the significant costs savings due to optimizing pump schedules.  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