Chemical Reactions and Kinetics of the Carbon Monoxide Coupling in the Presence of

The chemical reactions and kinetics of the catalytic coupling reaction of carbon monoxide to diethyl oxalate were studied in the presence of hydrogen over a supported palladium catalyst in the gaseous phase at the typical coupling reaction conditions. The experiments were performed in a continuous flow fixed-bed reactor. The results indicated that hydrogen only reacts with ethyl nitrite to form ethanol, and kinetic studies revealed that the rate-determining step is the surface reaction of adsorbed hydrogen and the ethoxy radical (EtO-). A kinetic model is proposed and a comparison of the observed and calculated conversions showed that the rate expressions are of rather high confidence.     

国家治理的家户逻辑：基于田野政治学的分析进路

家户是中国社会的细胞,也是国家治理的基本单元。从历史上看,家户单元以独立的个体家庭的产生为基础,并经由“编户齐民”制度而成熟定型。与其他治理单元不同,家户具有极强的自主性,并从中汲取动能与活力。家户自主性是基于家户自身生存和发展需要而产生的内在能动性,包括意识自主性、目标自主性和行动自主性。中国国家治理的重要特征,不是对家户单元的控制与形塑,而是对家户自主性的认同与调适。家户自主性的产生,主要源于家户单元的自组织特性,包括联结方式的血缘性、个体需求的内生性、组织形态的灵活性以及国家权力的外在性。从历史上看,正是家户单元的自主性治理,为“集家为国”的中国国家治理提供了动力,其不仅创造了灿烂的农业文明,也实现了国家的长治久安。进入近代以后,家户作为国家治理单元的功能不断弱化甚至一度被取代,但其内在价值并未因此消解,反而在改革实践中展现独特魅力与光芒。在推进国家治理体系和治理能力现代化的进程中,应当高度重视家户单元及其蕴含的自主性价值,并赋予其新的时代意义。     

Differential algebraic method for time of flight property of electrostatic electron lenses

Differential algebraic method is a powerful technique in computer numerical analysis. It presents a straightforward method for computing arbitrary order derivatives of functions with extreme high accuracy limited only by the truncation error of the computer. When applied to nonlinear dynamical systems, the arbitrary high-order transfer properties of the systems can be computed directly with high precision. In this article, the time of flight (TOF) property of electrostatic electron lens systems is studied by differential algebraic method and their arbitrary order TOF transfer properties can be numerically calculated. As an example, Schiske's model electrostatic lens has been studied by the efficient differential algebraic TOF method.     

预裂爆破设计参数的理论分析

本文在分析不偶合装药爆破物理过程和动态冲击压力的基础上,研究了预裂孔的破坏型态;利用相应的破坏准则,推导了预裂孔临界和允许体积装药密度的理论计算式,并在总结已有的预裂成缝理论和实验成果的基础上,用裂断力学理论对成缝机理作了进一步探讨。考虑了岩体初始应力的影响,对裂缝扩展进行了定量描述,提出了预裂爆破炮孔间距的计算表达式。     

基于隐马尔科夫模型的汉语韵律词基频模型

提出了一种基于隐马尔科夫模型(HMM)的汉语韵律词的统计基频模型。模型能反映韵律环境和基频曲线参数之间的映射关系,从模型可以估计一段基频曲线和一段文本之间的相关度,也可以从文本生成相应的基频曲线。本方法使用HMM作为基木框架,具有HMM理论体系所能支配的各种优点。同时将韵律作为模型单元,使得模型能够反映韵律层次级的连续变调。最后给出了实验结果并对模型的应用前景进行了展望。     

曙光一号自由电子激光器的理论计算

系统总结曙光一号自由电子激光器理论计算的主要结果:包括曙光一号装置主要参数的选取和理解;磁场失谐曲线的计算;常参数摇摆器和变参数摇摆器的主要结果;高阶波导模的贡献;电子束参数扰动对激光性能的影响;空间电荷效应等。计算结果表明,常参数摇摆器激光输出功率可达80MW,效率约50％;变参数摇摆器激光输出功率可达250MW左右,效率约16％。     

自由电子激光振荡器的二维数值模拟

在柱二维坐标系中,用数值计算方法求解了摇摆器内电子模拟方程组、光场方程组和无源区(不含摇摆器区)经非自适应方法变换后的无源旁轴波动方程并设计了相应的程序R_2D。用该程序计算的数值结果表明,在有源条件下二维数值模拟结果与高斯光束近似下的数值模拟结果符合较好;取完全相同的计算条件R-2D程序与洛斯阿拉莫斯实验室(LANL)的FELEX程序的计算结果符合较好;初步认为LANL实验数据的物理图象合理,数值结果基本可信;最后给出北京自由电子激光器(BFEL)的一些物理数据。     

An experimental and modeling study of the autoignition of 3-methylheptane

An experimental and kinetic modeling study of the autoignition of 3-methylheptane, a compound representative of the high molecular weight lightly branched alkanes found in large quantities in conventional and synthetic aviation kerosene and diesel fuels, is reported. Shock tube and rapid compression machine ignition delay time measurements are reported over a wide range of conditions of relevance to combustion engine applications: temperatures from 678 to 1356 K; pressures of 6.5, 10, 20, and 50 atm; and equivalence ratios of 0.5, 1.0, and 2.0. The wide range of temperatures examined provides observation of autoignition in three reactivity regimes, including the negative temperature coefficient (NTC) regime characteristic of paraffinic fuels. Comparisons made between the current ignition delay measurements for 3-methylheptane and previous results for n-octane and 2-methylheptane quantifies the influence of a single methyl substitution and its location on the reactivity of alkanes. It is found that the three C₈ alkane isomers have indistinguishable high-temperature ignition delay but their ignition delay times deviate in the NTC and low-temperature regimes in correlation with their research octane numbers. The experimental results are compared with the predictions of a proposed kinetic model that includes both high- and low-temperature oxidation chemistry. The model mechanistically explains the differences in reactivity for n-octane, 2-methylheptane, and 3-methylheptane in the NTC through the influence of the methyl substitution on the rates of isomerization reactions in the low-temperature chain branching pathway, that ultimately leads to ketohydroperoxide species, and the competition between low-temperature chain branching and the formation of cyclic ethers, in a chain propagating pathway.