A defect correction approach to turbulence modeling

A method for resolving turbulent flow problems is presented, aiming at competing with the existing mathematical tractable Approximate Deconvolution Models in terms of accuracy, and outperforming these models in terms of the computational time needed. Full numerical analysis is performed, and the method is shown to be stable, easy to implement and parallelize, and computationally fast. The proposed method employs the defect correction approach to solve spatially filtered Navier–Stokes equations. A simple numerical test is provided that compares the method against the approximate deconvolution turbulence model (ADM). When resolving a fluid flow at high Reynolds number, the numerical example verifies the key feature of the method: while having the accuracy comparable to that of the ADM, the method computes in less than 80% of the time needed for the turbulence model—even before the parallelization.© 2014 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq 31: 268–288, 2015     

基于波导、金和氧化锌的随机激光器的研究

通过将金属金嵌入到上下两层波导结构中,与ZnO随机粒子相结合,设计出一种新型结构的随机激光器。采用时域有限差分法(FDTD),数值模拟了该随机激光器系统的光场分布和模式频谱图,并针对金粒子和金薄膜两种情况进行对比分析。结果显示,采用金粒子作夹层时,出射激光模式数量减少,单色性较好;采用金薄膜作夹层时,出射激光光强较大。     

聚丙烯腈基碳纤维原丝在纺丝过程中纳米孔变化规律与机理研究

应用小角X射线散射等方法, 系统、定量地测试表征了聚丙烯腈基碳纤维原丝中纳米孔的尺寸、形状、体积分数、单位体积中纳米孔绝对数量以及纤维总孔洞率等形态结构参量, 并对这些参量在水洗、水洗牵伸、热致密化、高压蒸汽牵伸及热稳定化等工艺过程中的变化规律及原因进行了研究. 结果表明, 纺丝过程中牵伸及高温热处理均可使纤维总孔洞率逐步下降. 纳米孔尺寸体积分数V_i测试表明, 对于小于10 nm³的小纳米孔和大于10³ nm³的较大纳米孔, 两者的V_i在纺丝初期水洗牵伸工艺中分别为0.217和0.369, 而在纺丝后期热稳定化处理后发生大幅度改变, 分别为0.948 与0.015. 其原因并不是在高压蒸汽牵伸及热稳定处理中较小纳米孔含量的增加, 而是较大纳米孔含量的大幅度减少. 纳米孔形状研究表明, 纺丝工艺中的多次牵伸处理均使纳米孔的长短轴比加大, 而大于玻璃化温度的热处理均使纳米孔长短轴比收缩, 并且对于较小纳米孔来说这种收缩更为显著.     

基于频带分解和距离加权的单矢量水听器浅海被动测距方法研究

本文针对浅海环境下中低频宽带脉冲声源被动测距问题, 提出了一种声压和水平振速联合处理的被动测距方法. 在浅海波导中, 声压和质点振速的自相关函数卷绕(warping)谱具有稳定的频率特征. 声压和水平振速的自相关卷绕谱具有相同的准线谱特征, 垂直振速自相关卷绕谱具有宽谱叠加线谱的特征, 与声压自相关卷绕谱相比, 其尖峰个数比更多, 且尖峰宽度更宽. 利用引导源, 本文提出了基于频带分解和距离加权的声压和水平振速联合被动测距方法. 利用该方法对2008年冬季青岛海域综合实验中单矢量水听器接收的气枪信号进行处理, 结果表明, 该方法能够实现气枪声源的有效测距. 与传统单声压水听器被动测距方法相比, 该方法可以有效减小代价函数的主瓣宽度、提高测距精度.     

Two lower bounds for the Stanley depth of monomial ideals

Let be two monomial ideals of the polynomial ring . In this paper, we provide two lower bounds for the Stanley depth of . On the one hand, we introduce the notion of lcm number of , denoted by , and prove that the inequality holds. On the other hand, we show that , where denotes the order dimension of the lcm lattice of . We show that I and satisfy Stanley's conjecture, if either the lcm number of I or the order dimension of the lcm lattice of I is small enough. Among other results, we also prove that the Stanley–Reisner ideal of a vertex decomposable simplicial complex satisfies Stanley's conjecture.     

Pointwise versus equal (quasi-normal) convergence via ideals

We prove a characterization showing when the ideal pointwise convergence does not imply the ideal equal (aka quasi-normal) convergence. The characterization is expressed in terms of a cardinal coefficient related to the bounding number b$\mathfrak{b}$. We also prove a characterization showing when the ideal equal limit is unique.     

部分相干平顶光束在非Kolmogorov湍流中的湍流距离

给出了部分相干平顶光束通过非Kolmogorov湍流传输的湍流距离解析表达式,并研究了非Kolmogorov湍流的湍流广义指数、内尺度、外尺度和光束参数对部分相干平顶光束湍流距离的影响。研究表明:湍流距离随相干参数、束腰、外尺度(当湍流广义指数的取值为3.6~4.0时)的增大而减小;随光束阶数、内尺度的增大而增大;随湍流广义指数先减小后增大,且在湍流广义指数取3.11时存在极小值,即光束扩展的极大值。同时利用湍流广义指数及光束参数,具体比较了湍流距离与瑞利区间的大小,并指出光束参数及湍流广义指数决定了湍流是否在瑞利区间内就能对光束扩展构成明显的影响。     

Experimental validation of an effective carbon number-based approach for the gas chromatography–mass spectrometry quantification of ‘compounds lacking authentic standards or surrogates’

For the quantitative analysis of ‘compounds lacking authentic standards or surrogates’ (CLASS) in environmental media, we previously introduced an effective carbon number (ECN) approach to develop an empirical equation for the prediction of their response factor (RF). In this research, a series of laboratory experiments were carried out to benchmark the reliability of an ECN approach for sorbent tube/thermal desorption/gas chromatography (GC)/mass spectrometry (MS) applications. First, the ECN values were determined using external calibration data from 25 reference volatile organic compounds (VOCs) using two MS dectectors (quadrupole (Q) and time-of-flight (TOF)). Then, a certified standard mixture of 54 VOCs was analyzed by each system as a simulated unknown sample. The analytical bias, assessed in terms of percentage difference (PD) between the certified and ECN-predicted mass values, averaged 19.2 ± 16.1% (TOF-MS) and 28.2 ± 27.6% (Q-MS). The bias using a more simplified carbon number (CN)-based prediction increased considerably, yielding 53.4 ± 53.3% (TOF-MS) and 61.7 ± 81.3% (Q-MS). However, the bias obtained using the ECN-based prediction decreased significantly to yield average PD values of 9.84 ± 7.28% (TOF-MS) and 16.8 ± 8.35% (Q-MS), if the comparison was limited to 26 (out of 54) VOCs with CN ≥ 4 (i.e., 25 aromatics and hexachlorobutadiene).     

On some compound distributions with Borel summands

The generalized Poisson distribution is well known to be a compound Poisson distribution with Borel summands. As a generalization we present closed formulas for compound Bartlett and Delaporte distributions with Borel summands and a recursive structure for certain compound shifted Delaporte mixtures with Borel summands. Our models are introduced in an actuarial context as claim number distributions and are derived only with probabilistic arguments and elementary combinatorial identities. In the actuarial context related compound distributions are of importance as models for the total size of insurance claims for which we present simple recursion formulas of Panjer type.     

Solubility of HFCs in lower alcohols

This work is inserted in a research program that consists mainly in the experimental and theoretical study of the effect of association between solute and solvent molecules in the solubility of gases in liquids.The solubilities of hydrofluorocarbons, HFCs, (CH₃F, CH₂F₂, CHF₃) in lower alcohols (methanol, ethanol, 1-propanol, 1-butanol) have been determined in the temperature range [284, 313] K, at atmospheric pressure. An automated apparatus based on Ben-Naim-Baer and Tominaga et al. designs was used, which provides an accuracy of 0.6%. A precision of the same order of magnitude was achieved.To represent the temperature dependence of the mole fraction solubilities, the equation R ln x₂ = A + B/T + C ln T was used. From this equation, the experimental Gibbs energies, enthalpies and entropies of solution at 298 K and 1 atm partial pressure of the gas, were calculated.A semiempirical correlation has been developed between the solubilities of HFCs in alcohols at 298 K and the Gutmann acceptor number of solvents, AN, and reduced dipole moment of the gases, μ*.