基于均匀化理论的多孔板弯曲问题新解

由于密集型分布孔的存在,通常的有限元法不能有效地分析多孔板的弯曲问题.该文基于均匀化理论建立了该类问题的新解法.对含密集型分布的阶梯型圆孔板的分析结果,说明了该文方法是有效的.     

水中爆炸冲击波作用下混凝土墩动态响应初步分析

用水下爆炸冲击分析（ＵＳＡ）方法,在假设条件下,数值模拟了混凝土结构物水中爆炸冲击波作用下的加速度及压力响应,是对浅层水中爆炸流－固耦合动力学问题数值解的初步尝试。     

Magnetic Order and Its Interplay with Structure Phase Transition in van der Waals Ferromagnet Ⅵ3

Van der Waals magnet Ⅵ3 demonstrates intriguing magnetic properties that render it great for use in various applications.However,its microscopic magnetic struct...     

Evolution of domain structure in Fe_3GeTe_2

Two-dimensional(2D)magnets provide an ideal platform to explore new physical phenomena in fundamental magnetism and to realize the miniaturization of magnetic devices.The study on its domain structure evolution with thickness is of great significance for better understanding the 2D magnetism.Here,we investigate the magnetization reversal and domain structure evolution in 2D ferromagnet Fe₃GeTe₂(FGT)with a thickness range of 11.2-112 nm.Three types of domain structures and their corresponding hysteresis loops can be obtained.The magnetic domain varies from a circular domain via a dendritic domain to a labyrinthian domain with increasing FGT thickness,which is accompanied by a transition from squared to slanted hysteresis loops with reduced coercive fields.These features can be ascribed to the total energy changes from exchange interaction-dominated to dipolar interaction-dominated with increasing FGT thickness.Our finding not only enriches the fundamental magnetism,but also paves a way towards spintronics based on 2D magnet.     

对称正定问题多搜索方向共轭梯度法的收敛性理论

In this paper, we give the convergence and consistence theory of multiple search direction conjugate gradient method (see [10]) and give some upper bound estimations of iterative value and error of our method.     

热结构稳态响应的耦合灵敏度分析方法

研究结构稳态热变形和热应力的灵敏度分析方法,给出了直接法和伴随法两种算法。考虑了温度场的耦合作用,在直接法中需要计算温度场对设计变量的导数,在伴随法中需要计算热载荷对温度场的导数。对尺寸和形状两类设计变量的灵敏度分析算例,验证了本文方法的精度。伴随法在应用程序中的实现,为大型结构优化提供了高效率的灵敏度计算方法。     

Preparation and characterization of superfine ammonium perchlorate (AP) crystals through ceramic membrane anti-solvent crystallization

In this paper, a novel ceramic membrane anti-solvent crystallization (CMASC) method was proposed for the safe and rapid preparation ammonium perchlorate (AP) crystals, in which the acetone and ethyl acetate were chosen as solvent and anti-solvent, respectively. Comparing with the conventional liquid anti-solvent crystallization (LASC), CMASC which successfully introduces ceramic membrane with regular pore structure to the LASC as feeding medium, is favorable to control the rate of feeding rate and, therefore, to obtain size and morphology controllable AP. Several kinds of micro-sized AP particles with different morphology were obtained including polyhedral-like, quadrate-like to rod-like. The effect of processing parameters on the crystal size and shape of AP crystals such as volume ratio of anti-solvent to solvent, feeding pressure and crystallization temperature were investigated. It is found that higher volume ratio of anti-solvent to solvent, higher feeding pressure and higher temperature result in smaller particle size. Scaning electron microscopy (SEM) and X-ray diffraction (XRD) were used to characterize the resulting AP crystals. The nucleation and growth kinetic of the resulting AP crystals were also discussed.     

Controlled chemical co-precipitation and solid phase synthesis,microstructure and photoluminescence of La3PO7:Eu3+ phosphors

Eu³⁺-doped oxy-phosphate (La₃PO₇:Eu³⁺) with monoclinic phase has been synthesized via solid phase and co-precipitation methods. The products present various regular morphologies after high temperature thermal treatment, such as bulk with holes, leaf-like flake, nano-rod and so on. All the phosphors exhibit the characteristic fluorescence of Eu ion, the electric dipole transition ⁵D₀→⁷F₂ of Eu³⁺ ions is dominant indicating that the sites of Eu³⁺ ions in La₃PO₇ have no the inversion center. Furthermore, the intensity of ⁵D₀→⁷F₂ increases due to the introducing of surfactant and increasing of the calcination temperature.