新疆理化所提出一种基于模拟的使非线性光学晶体材料相匹配区间蓝移的方案

非线性光学晶体是通过频率转换拓宽固态激光器输出波段的关键材料。随着激光微加工,激光通讯和现代科学仪器的持续发展,对紫外/深紫外非线性光学晶体的需求日益增加。但是,很多拥有宽的紫外透过范围和大的倍频效应的晶体因其双折射无法满足深紫外相匹配而无法输出深紫外激光。     

The effects of ultrasound frequency and power on the activation energy in Si-KOH reaction system

The activation energy is the minimum amount of energy required to initiate a reaction. It is one of the important indexes for appraising a reaction. The chemical reaction rate is closely related to the value of activation energy, and reducing activation energy is propitious to promoting a chemical reaction. In the present paper, the relationship between the activation energy in Si-KOH reaction system and the ultrasound frequency and power has been discussed for the first time. The range of ultrasound frequency and power is 40-100kHz （interval by 20kHz） and 10-50W （interval by 10W）, respectively. The experimental clata indicate that the activation energy decreases with the increasing ultrasound power. Comparing with the activation energy without ultrasound irradiation, the results in our paper indicate that ultrasound irradiation could reduce the activation energy in Si-KOH reaction system and increase the reaction rate.     

数字离子阱质谱仪低质量截止值的改进方法

本研究在实验室自制的线形数字离子阱质量分析器上,通过改变数码电源的频率扫描方式,在CID过程中,通过扫描数字束缚方波电源的频率和数字激发方波的频率实现母体解离。例如对于利血平母体离子,当将离子数字束缚方波频率从500 kHz扫描到560 kHz,可以测量到低质荷比的碎片离子,成功实现了串级质谱分析的低质量碎片离子的分析。通过与利血平三重四极质谱串级质谱分析实验结果的比较,发现可以在数字离子阱质谱仪上获得与三重四极质谱相同的串级质谱测量结果。结果表明,本方法可以用于低质量离子的测量,克服了传统离子阱质谱进行串级质谱分析的一个主要难点,显著提高数字离子阱质谱的性能。     

气相中Co+催化N2O与C2H6循环反应催化剂活性的理论研究

采用密度泛函理论UB3LYP方法对Co⁺在三重态及五重态势能面上催化N₂O与C₂H₆进行循环反应的两态反应机理进行了研究. 运用Harvery方法优化了两自旋态势能面5个最低能量交叉点（MECP）,计算了MECP处自旋-轨道耦合作用. 采用Landau-Zener公式计算了自旋翻转处的系间窜越几率,各MECP处均可发生有效系间窜越. 通过应用Kozuch提出的能量跨度模型,Co⁺催化N₂O与C₂H₆在298K下反应生成CH₃CHO时有最大的TOF值3.35×10^-21 s^-1.     

Theory Study of the Adsorption of Hydrocyanic Acid onto Small Silver Clusters

Density functional theory calculations have been performed to study the interaction of small silver clusters, Ag2 ~Ag9, with HCN. The adsorption of HCN on-top site of the silver cluster, among various possible sites, is energetically preferred. The adsorption energies of HCN on the silver clusters reach a local maximum at n = 4, which is only about 0.450 eV, indicating that the adsorbed HCN molecule is weakly perturbed. The adsorbed C–N and C–H stretching frequencies are blue- and red-shifted compared with the values of free HCN, respectively.     

分布振子复合板的模态阻尼及多点激励下阻尼减振相关性

分布阻尼振子可拓宽结构减振频带,因此可将振子分布于板中以形成复合板（简称“分布振子复合板”）,进而实现较宽的减振频带．对于多点支撑处受到宽频非一致激励（例如在不同激励点处的激励频率、幅值与相位有差异）的分布振子复合板,目前还缺乏有效简便的优化控制指标．在作者之前的研究中,针对含分布振子的梁推导了基于模态应变能的模态阻尼计算理论,讨论了模态阻尼与单点激励下梁的减振效果的相关性,并应用于宽频减振设计优化．本文进一步将模态阻尼计算理论推广到分布振子复合板,并将研究从梁的单点激励扩展到板的多点非一致激励下的阻尼减振相关性．首先,在利用模态应变能法推导得到分布振子复合板的模态阻尼计算公式后,从理论上讨论了不同边界条件与模态阶次对计算结果的影响,以及计算理论的适用性．而后,进一步通过有限元参数分析了边界条件、频率比、模态阶次与质量比的影响．最后,通过算例分析了无振子板或分布振子复合板在四个激励点具有多种幅值与相位组合情况下的稳态响应．结果表明,推导的模态阻尼计算公式可正确预测不同边界条件下的模态阻尼,且理论预测的模态阻尼与基板的稳态平均加速度减小率、稳态峰值应变能减小率均有较高的相关性．     

典型无序结构芯体夹层梁的振动特性试验分析

通过悬臂梁模态试验研究了典型无序芯体(纤维毡、闭孔泡沫铝以及开孔泡沫铝)夹层结构的振动特性,并与夹层结构所对应等质量钢板进行振动特性对比分析。研究结果表明：无序芯体夹层结构相较于对应等质量钢板均有着更高的前三阶固有频率和阻尼比;等质量钢梁任一横截面上各点具有相同振动特性,而夹层结构任一横截面上各点振动特性受芯体结构影响较大。     

轧机主传动系统扭振响应数值模拟及结构失效研究

轧机主传动系统是轧制过程中传递运动和力矩的主要装置,其扭转振动(扭振)是影响钢铁生产质量并导致关键零部件异常破坏的重要原因之一。基于ANSYS有限元软件,针对轧机主传动扭振系统进行数值模拟及结构失效分析。首先,对轧机主传动系统进行模态分析,获得扭振系统固有属性关系;然后,通过谐响应分析得出不同位置零部件的频域响应曲线;最后,对易损部位关键零部件件进行结构失效原因分析,将数值计算结果与实际情况相结合,以验证分析结果的准确性与可靠性。研究结果可为轧机主传动扭振系统中零部件结构优化和进一步动态控制策略的制定提供重要理论参考。     

一种模拟动边界绕流的锐利界面浸入边界法

When the structural wall moves over a fixed grid, the structure coverage will change, resulting in many dead and emerging elements. To avoid the influence of malformation and reconstruction of body-fitted grids on the calculation efficiency and accuracy of the fluid-structure interaction problems with coupled boundary movement on the fixed grid, an improved numerical method for describing the interaction between an immersed rigid body and fluid based on a sharp-interface is proposed. In this method, both the fluid and solid are regarded as pure fluid domains in the whole computational domain, and the solid boundary is divided into several Lagrangian grid points. The flow parameter or velocity is reconstructed by interpolation at the interface element, which is then directly used as the boundary condition of the flow field, thus reflecting the influence of the wall boundary conditions. The method constructs the calculation structure of “virtual point, force point and vertical foot point”, and the velocity of the virtual point is obtained by bilinear interpolation. Then, the velocity of the force point is calculated by forcing the solid boundary to meet the no-slip condition, and the equations of the coupling system based on the immersion boundary method are finally solved to realize the numerical simulation of the flow with a complex moving boundary. The numerical program for this immersed boundary method is established using C++, then the accuracy and reliability of the proposed method are validated by comparison with the literature and experimental results of the basic numerical example of flow around a cylinder. Furthermore, the effects of the structural shape and the angle of attack on the trailing vortex structure, the vortex shedding frequency, and the lift/ coefficient characteristics of the flow around the elliptical cylinder have been analyzed. The anti-symmetric S-type, “P+S” Ⅰ-type and “P+S” Ⅱ-type trailing vortex shedding modes, as well as the variation laws of the vortex structure size, vortex shedding frequency and lift-drag coefficients ratio with axis ratio and angle of attack, are captured. The critical angle of attack (25°) corresponding to the maximum lift-drag ratio is determined as 25°.     

NMR Parameters and Vibrational Investigation of 2-Dicyanovinyl-5-（4-ethoxyphenyl） thiophene by ab initio HF and DFT Calculations

Optimized geometry and harmonic vibrational frequency of 2-dicyanovinyl-5-(4- ethoxyphenyl)thiophene (C16H12N2OS) are calculated at the HF/6-31++G(d,p) and B3LYP/6- 311++G(d,p) levels. Mulliken charges in the ground state are also calculated. The research shows the presence of intermolecular interaction in the title compound. The scaled harmonic vibrational frequencies have been compared with experimental FT-IR spectra. A detailed interpretation of the infrared spectra of the title compound is reported. The theoretical spectrograms for IR spectra of the title compound have been constructed. The isotropic chemical shift computed by 13C and 1H NMR analyses also shows good agreement with the experimental observations.