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1.
We report on a luminescent phenomenon in Dy3+-doped SrSiO3 long-lasting phosphor. After irradiation by a 254-nm UV lamp for 5 min, the Dy3+-doped SrSiO3 phosphor emits white light-emitting long-lasting phosphorescence for more than 1 h even after the irradiation source has been removed. Photoluminescence, long-lasting phosphorescence and thermoluminescence (TL) spectra are used to explain this phenomenon. Photoluminescence spectra reveal that the white light-emitting long-lasting phosphorescence originated from the two mixtures of Dy3+ characteristic luminescence, the 480-nm blue emission (4F9/26H15/2) and the 572-nm yellow emission (4F9/26H13/2). TL spectra shows that the introduction of Dy3+ ions into the SrSiO3 host produces a highly dense trapping level at 377 K (0.59 eV), which is responsible for the long-lasting phosphorescence at room temperature. A possible mechanism of the long-lasting phosphorescence based on the experimental results is proposed. It is considered that the long-lasting phosphorescence is due to persistent energy transfer from the electron traps to the Dy3+ ions, which creates the persistent luminescence of Dy3+ to produce the white light-emitting long-lasting phosphorescence.  相似文献   
2.
When a poly(ethylene terephthalate), PET, film is heated in an aqueous solution of methacrylic acid in the presence of hydrogen peroxide as an initiator, it is found that the weight of the film is increased. The amount of methacrylic acid that may be added onto the film is dependent upon the concentration of the monomer, the initiator, and the temperature at which the reaction occurs. Pretreatment of the film with 1,1,2,2,tetrachloroethane causes swelling and the amount of add-on is increased as the swelling level increases. Methacrylic-acid-modified PET films hydrolyze at room temperature in aqueous sodium hydroxide; the rate of hydrolysis is dependent upon the amount of add-on and the concentration of the base. This procedure leads to a chemically induced blend of polymethacrylic acid and poly(ethylene terephthalate), and grafting of the monomer onto the polymer film does not occur. © 1995 John Wiley & Sons, Inc.  相似文献   
3.
以三氧化二铝陶瓷膜为载体,以钼酸根阴离子为模板离子,1-乙烯基咪唑为功能单体,1,6-二溴己烷为交联剂,采用表面印迹和接枝聚合方法制备了能选择性吸附Mo(Ⅵ)的新型印迹陶瓷膜(IIP-PVI/CM).采用红外光谱、X射线光电子能谱、热重分析及扫描电子显微镜等方法对陶瓷膜进行结构表征.研究了pH值对吸附性能的影响,当pH值范围为2~4时,IIP-PVI/CM具有良好吸附能力;动力学和热力学结果表明,IIP-PVI/CM对Mo(Ⅵ)的吸附符合准二级动力学模型和Langmuir吸附模型;当pH=4.0和温度为30℃时,IIP-PVI/CM对Mo(Ⅵ)具有良好选择性,Mo(Ⅵ)对W(Ⅵ)的选择性系数高达7.48;动态吸附结果表明,IIP-PVI/CM对W(Ⅵ)和Mo(Ⅵ)的吸附饱和时间分别为24和47 min,饱和吸附量分别为0.163和0.672 mmol/100 g,动态吸附时IIP-PVI/CM亦具有良好选择性;经9次吸附与解吸后,IIP-PVI/CM对Mo(Ⅵ)吸附容量仍可达到初始值的92%,再生和循环使用性能良好.  相似文献   
4.
A Cartesian grid method using immersed boundary technique to simulate the impact of body in fluid has become an important research topic in computational fluid dynamics because of its simplification, automation of grid generation, and accuracy of results. In the frame of Cartesian grid, one often uses finite volume method with second order accuracy or finite difference method. In this paper, an h‐adaptive Runge–Kutta discontinuous Galerkin (RKDG) method on Cartesian grid with ghost cell immersed boundary method for arbitrarily complex geometries is developed. A ghost cell immersed boundary treatment with the modification of normal velocity is presented. The method is validated versus well documented test problems involving both steady and unsteady compressible flows through complex bodies over a wide range of Mach numbers. The numerical results show that the present boundary treatment to some extent reduces the error of entropy and demonstrate the efficiency, robustness, and versatility of the proposed approach. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
5.
In this work, the K(l,p) equation is investigated. The sine-cosine method, the tanh method and the extended tanh method are efficiently used for analytic study of this equation. New solitary patterns solutions and compactons solutions are formally derived. The proposed schemes are reliable and manageable.  相似文献   
6.
A concise and efficient approach for the construction of the tetracyclic carbon skeleton of retigeranic acid A is described. The key transformations include a novel Rh‐catalyzed [3+2] cycloaddition of enyol to afford cyclopentanoid E , bearing two contiguous quaternary stereocenters at the bridgehead positions, and an intramolecular Pauson–Khand reaction to construct the advanced tetracyclic core structure of retigeranic acid A.  相似文献   
7.
Yang  Xiaobo  Huang  Weizhang  Qiu  Jianxian 《Numerical Algorithms》2019,82(4):1409-1440
Numerical Algorithms - A moving mesh finite difference method based on the moving mesh partial differential equation is proposed for the numerical solution of the 2T model for multi-material,...  相似文献   
8.
In this paper, we develop a simplified hybrid weighted essentially non-oscillatory (WENO) method combined with the modified ghost fluid method (MGFM) [31] to simulate the compressible two-medium flow problems. The MGFM can turn the two-medium flow problems into two single-medium cases by defining the ghost fluids state in terms of the predicted the interface state, which makes the material interface “invisible”. For the single medium flow case, we adapt between the linear upwind scheme and the WENO scheme automatically by identifying the regions of the extreme points for the reconstruction polynomial as same as the hybrid WENO scheme [55]. Instead of calculating their exact locations, we only need to know the regions of the extreme points based on the zero point existence theorem, which is simpler for implementation and saves computation time. Meanwhile, it still keeps the robustness and has high efficiency. Extensive numerical results for both one and two dimensional two-medium flow problems are performed to demonstrate the good performances of the proposed method.  相似文献   
9.
While conventional approaches have been studied for removal of ruthenium(III) ions (Ru(III)), this work focuses on the applicability of ion‐imprinted poly(methyl methacrylate‐vinyl pyrrolidone)/poly(vinylidene fluoride) blending membranes (Ru(III)–ion‐imprinted membrane[IIM]) for selective removal of Ru(III) from acidic water solutions. In order to measure the effectiveness of these imprinted membranes, after fabrication, binding experiments were done with aqueous Ru(III) solutions. The results showed that Ru(III)‐IIMs were fabricated successfully at various blending ratios, and their chemical components, microstructures, hydrophilicity, and water fluxes were measured. In pH range 0.5 to 5.0, binding capacity (Qe) of Ru(III) onto Ru(III)‐IIM increases remarkably with pH and then reaches to a maximum value (53.52 mg/g) at pH 1.5. After that, Qe gradually decreases. Compared with a nonimprinted membrane, Ru(III)‐IIM demonstrates higher selectivity for Ru(III) at pH 1.5 in the presence of Ni(II) and Cu(II) ions, and its selectivity coefficients for Ru(III)/Ni(II) and Ru(III)/Cu(II) are 3.70 and 3.32, respectively. Also, Ru(III)‐IIM shows a good chemical stability and reusability. C─N and C═O bonds within poly(vinyl pyrrolidone) segments of poly(methyl methacrylate‐vinyl pyrrolidone) (P(MMA‐VP)) participate the uptake of Ru(III). Ru(III)‐IIM exhibited excellent hydrophilicity and Ru(III) selective adsorption ability and reusability and has potential to be used for Ru(III) removal from acidic water solutions.  相似文献   
10.
In [J. Qiu, C.-W. Shu, Runge–Kutta discontinuous Galerkin method using WENO limiters, SIAM Journal on Scientific Computing 26 (2005) 907–929], Qiu and Shu investigated using weighted essentially non-oscillatory (WENO) finite volume methodology as limiters for the Runge–Kutta discontinuous Galerkin (RKDG) methods for solving nonlinear hyperbolic conservation law systems on structured meshes. In this continuation paper, we extend the method to solve two-dimensional problems on unstructured meshes, with the goal of obtaining a robust and high order limiting procedure to simultaneously obtain uniform high order accuracy and sharp, nonoscillatory shock transition for RKDG methods. Numerical results are provided to illustrate the behavior of this procedure.  相似文献   
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