Sparse Localized Decomposition of Deformation Gradients

Sparse localized decomposition is a useful technique to extract meaningful deformation components out of a training set of mesh data. However, existing methods cannot capture large rotational motion in the given mesh dataset. In this paper we present a new decomposition technique based on deformation gradients. Given a mesh dataset, the deformation gradient field is extracted, and decomposed into two groups: rotation field and stretching field, through polar decomposition. These two groups of deformation information are further processed through the sparse localized decomposition into the desired components. These sparse localized components can be linearly combined to form a meaningful deformation gradient field, and can be used to reconstruct the mesh through a least squares optimization step. Our experiments show that the proposed method addresses the rotation problem associated with traditional deformation decomposition techniques, making it suitable to handle not only stretched deformations, but also articulated motions that involve large rotations.     

Phase Assemblages of Pr α-sialon Derived from SHS-ed Powders and TEM Study on the Nucleation of Pr α-sialon

The Pr α-sialon powders prepared by self-propagating high-temperature synthesis (SHS), consisting of 55 wt% Pr α-sialon and 45 wt% of β-sialon (abbreviated as α' and β'), were hot-pressed at 1800°C for 1 h. The results showed that Pr α' phase would transfer to β' with the appearance of JEM phase (Pr(Si_{6− z} Al _z )(N_{10− z} O _z )) after sintering, thus resulting in the increase of β' phase to 86 wt%. The addition of Y₂O₃ into SHS-ed Pr α' powders as the starting materials restrains the transformation of α' to β' and prevents the formation of JEM phase as well. The nucleation mechanism of Pr α' grain during hot-pressing was investigated in terms of transmission electron microscope and energy-dispersive spectrometer analysis. Two nucleation modes of Pr α' grains were found, i.e., nucleating on the undissolved Pr α' grains and on the nuclei of (Pr, Y) α' grains precipitated from liquid phase.     

国际泥沙计划案例研究综述

在全球变化等多种因素的影响下,许多流域的泥沙问题严重,泥沙管理的重要性日益突出。通过对联合国教科文组织国际泥沙计划所开展的案例研究进行综述,认识到自然地理特征、社会经济条件、水利工程建设对流域产沙、输沙和水资源利用有重要影响。土壤侵蚀加速、水库淤积、下游输沙量减少和生态平衡破坏是目前全球各大流域面临的主要问题。综合各项案例,研究泥沙管理技术,提出流域综合泥沙管理的策略,包括水库淤积管理、推移质泥沙管理、土地管理和水土保持等技术手段,以及法律、行政和组织措施。     

YS-842催化剂在Hypol工艺PP中试装置上的应用

将Ziegler-Natta高效载体催化剂YS—842在Hypol工艺聚丙烯(PP)中试装置上进行应用考核，考察了该催化剂的适应性及共聚合性能。试验表明，YS—842催化剂活性高(达1．2Mg／g)、寿命长、氢调敏感性好：用YS—842催化剂生产的聚合物流动性好，粒径分布窄，细粉少，平均粒径为640μm；等规指数大于98．5％，堆密度大于0．45g／mL；试生产的F401、J340，其机械性能与使用进口催化剂生产的产品相当。     

射流流化床内流体力学行为的模拟研究

以流化床应用为代表的气固流动系统是许多化工过程中的重要组成部分 ,CFD( computational fluid dynamics)方法能够为其优化设计和放大提供所需要的信息 .本文采用双欧拉模型 ,与 Gidaspow等的实验结果进行了对比 ,模拟了二维射流流化床内气泡的形成规律 ,得到了带锥型分布器的流化床内瞬时空隙率和气固相速度分布等流体力学参数 .对锥型分布器流化床的实验结果表明 ,模拟得到的气泡的形状与实验现象相接近 .     

圆盘反应器中的PET缩聚过程

利用薄膜实验研究了PET缩聚过程反应和传质规律 ,建立了链增长、链降解反应动力学模型和泡沫脱挥时的传质速率方程 ;通过冷模实验研究了圆盘反应器中PET的混合、流动、成膜、膜表面更新以及传质规律 ;综合了反应和反应器研究结果 ,建立了圆盘反应器中的PET缩聚过程模型 ,对圆盘反应器中的PET缩聚过程进行了仿真分析 ,考察了温度、压力、停留时间、转速、催化剂浓度、负荷大小等各种因素的影响     

林产化学加工学科的现况与发展前景

本文了介绍了并论述了林产化学加工学科所含的五个专业方向，木材化学加工工程，树木提取物化学工程，林产生物化工，木材保护与改性，林产化工装备与控制的研究内容，工业现状，存在问题与发展前景。     

合成丁酸异戊酯的新方法

采用超强酸代替浓硫酸作催化剂，对丁酸异戊酯合成反应进行了研究，讨论了影响收率的多种因素，在最佳条件下，酯化反应时间短，催化剂可以重复使用，丁酸异戊酯收率达到９８％。     

Selectivities in methanol oxidation over silica supported molybdena

Selectivities in methanol oxidation over silica supported molybdenum oxide catalysts were investigated in relation with the phase distribution. The supported catalysts were prepared by impregnation with ammonium heptamolybdate. In addition to crystalline MoO₃, Mo containing cluster species of 1–2 nm size were observed by STEM even from a used catalyst with 13% catalyst loading. The percentage of Mo present as crystalline MoO₃ increases with the catalyst loading. An ESCA study indicates that part of surface Mo in the supported catalysts is reduced to Mo⁵⁺. The dimethyl ether selectivity increases with the catalyst loading and its formation occurs over the crystalline MoO₃ phase. The Selectivities to CO and methyl formate are greatly enhanced because of the presence of support, and are relatively independent of the catalyst loading and phase distribution. The dependence and independence of the Selectivities of different byproducts on the loading make the silica supported catalysts with high catalyst loadings less selective for the partial oxidation of methanol to formaldehyde.     

Rapid Formation of Active Mesoporous TiO2 Photocatalysts via Micelle in a Microwave Hydrothermal Process

Rapid formation of active, mesoporous, and crystalline TiO₂ photocatalysts via a novel microwave hydrothermal process is presented. Crystalline anatase mesoporous nanopowders 100–300 nm in size with worm hole-like pore sizes of 3–5 nm were prepared by a modified sol–gel of titanium tetra-isopropoxide, accelerated by a microwave hydrothermal process. The organic surfactant, tetradecylamine, which is used as a self-assembly micelle in the sol–gel and microwave hydrothermal process, enables to harvest crystallized mesoporous anatase nanoparticles with a high-surface area. Mesoporous worm hole-like and crystalline powders with surface areas of 243–622 m²/g are obtained. X-ray diffraction, N₂-adsorption isotherms (Barrett–Joyner–Halenda and Brunauer–Emmet–Teller method), scanning electron microscope, and transmission electron microscope are used to identify the characteristics and morphologies of the powders. It is shown that crystallization by calcination at 400°C/3 h inevitably reduced the surface area, while the microwave hydrothermal process demonstrated a rapid formation of crystalline mesoporous TiO₂ nanopowders with a high-surface area and excellent photocatalytic effects.