基于几何特征的流体动画控制方法

在流体动画中,流体控制是生成可控流体运动的关键技术.为产生视觉逼真、行为可控的流体动画效果,提出一种基于几何特征的流体控制方法.首先通过构建流体形状的时变几何分区,实现对可控流体形状的表达及动态跟踪;在此基础上设计异构控制模型,以增强流体运动控制的灵活性,该模型采用了带约束优化的刚性控制和基于弹簧模型的柔性控制2种方法;最后将异构控制模型与高精度流体物理模型相耦合,生成视觉逼真的可控流体运动效果.实验结果表明,该方法能够在保持流体角色形状的同时产生丰富的流体细节,满足动画师的设计需求.     

基于内容重要性的Storyline可视化局部变形框架

针对Storyline可视化局部放大问题,提出一种基于内容重要性的局部变形框架.首先对可视化领域中局部变形技术进行对比和分析;然后给出了Storyline可视化可视元素及其重要性计算方法,并对重要性较大的实体元素进行放大显示,在高斯函数的指导下对重要会话元素进行局部放大和过渡平滑处理,根据不同位置的权重对线条进行重新定位;最后以Inception交互会话数据为实验数据,将该方法应用到Storyline可视化视图中.实验结果表明,文中方法能够在有限的显示空间中对Storyline可视化视图的整体结构和局部详细信息同时进行协调、友好的可视化.     

稀疏表示分类中遮挡字典构造方法的改进

针对稀疏表示分类算法中遮挡字典维数高且无冗余的问题,提出一种遮挡字典构造方法.首先通过图像分块得到各级的遮挡基图像;然后将所有互不相同的遮挡基图像按字典顺序转化为向量,并用这些向量作为遮挡字典的列,从而构造出维数相对较低且具有一定冗余度的遮挡字典.实验结果表明,该方法不仅明显提高了稀疏表示分类算法对遮挡人脸的识别率,而且还能通过减少图像的分块级数降低稀疏分解的耗时量,提高运算效率.     

秋季太湖叶绿素a浓度荧光反演研究

基于2007年11~12月太湖全湖实测水质参数和光谱数据,首先利用高斯方程对遥感反射率进行过滤分解,找出叶绿素a(chl\|a)吸收峰675 nm以后的荧光反射峰(Fluorescence Peak:FP),再以662 nm处的反射率为基准,采用归一化荧光高度法进行叶绿素a浓度(C chl-a)反演,得到chl-a反演模型。基于高斯分解获取的chl-a的荧光反射峰值R(FP)与662 nm处的反射率R (662)比值［R(FP)/R(662)］与C chl-a之间存在显著的相关性,该模型为秋季太湖水体C chl-a的最佳反演模型。在高悬浮泥沙条件下,该模型能够较好地表示出叶绿素荧光高度与叶绿素浓度之间的关系,为C chl-a反演提供新的方法和依据,并为传感器敏感波段的选取和设置提供参考。     

衣架式机头口模设计公式的修正探讨

基于表征值方法和熔体等压线平行于模唇这一流动模型,对衣架式机头口模进行了流动分析,并发现了文献[1]提出的口模设计公式中的一个缺陷,即计算的扇形狭缝区域与歧管发生了分离,针对该缺陷给出了修正公式。     

常减压蒸馏装置配剂方法比较

对常减压装置的三种配剂方法进行分析比较，从而选出经济、合理的配剂方法。     

ENR／CSM的自硫化研究

研究在没有任何硫化剂的情况下环氧化天然橡胶（ＥＮＲ－５０）和氯磺化聚乙烯（ＣＳＭ－４０）共混物的自硫化，以及共混比、填料品种及用量、间苯撑双马来酰亚胺与马来酸酐等活性剂、硫化温度和时间对交联程度和性能的影响。结果表明ＥＮＲ／ＣＳＭ共混体可以产生自硫化；共混比为５０／５０时交联密度最大，性能最佳，炭黑和白炭黑对该体系有好的补强作用，但白炭黑的补强作用比炭黑的好；间苯撑双马来酰亚胺及马来酸酐能活化自硫化体系；延长硫化时间及提高硫化温度均可增加交联作用，该自硫化体系没有返原现象。     

Effects of the o‐aromatic ring in the molecular chain on the properties of polyester polyols

A series of liquid polyester polyols from adipic acid (AA), phthalic anhydride (PA), ethylene glycol, propanediol‐1,2, and trihydroxymethylpropane, varying in the molar ratio of PA to AA, were prepared. The effects of the o‐aromatic ring in the molecular chain, which came from PA, on the viscosity, glass‐transition temperature, and thermal degradation temperature of the polyester polyols were studied with viscometry, differential scanning calorimetry, and thermogravimetry. The intrinsic viscosity and glass‐transition temperature increased with the concentration of the o‐aromatic ring increasing. The temperature of the maximum thermal degradation rate for aliphatic polyester polyols was 434.20°C. Two steps of thermal degradation were found when there were o‐aromatic rings in the molecular chain. One thermal degradation temperature was 358.36–360.48°C, and the other was 412.85–427.18°C. Polyester polyols with o‐aromatic rings had higher stability at lower temperatures (<240.00°C). However, aliphatic polyester polyols had higher stability at higher temperatures (300.00–480.00°C). The activation energy and order of degradation were calculated from thermogravimetric curves. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1617–1624, 2002     

工业变换炉最佳催化剂粒度

本文在建立数学模型的基础上，用计算机模拟变换炉的操作工况，考察改变催化剂粒度对经济效益的影响，从而得到工业变换炉催化剂颗粒最佳尺寸，开发了以经济效益为考察依据，工业反应器中催化剂颗粒最佳尺寸的计算方法。     

Copolymerization of trimethylene carbonate and 2,2-dimethyltrimethylene carbonate by rare earth calixarene complexes

Rare earth (Nd, Y, La) p-tert-butylcalix[n]arene (n=4, 6, and 8) complexes alone have been developed to catalyze random and block copolymerizations of trimethylene carbonate (TMC) and 2,2-dimethyltrimethylene carbonate (DTC). The random or block structure and thermal behavior of the copolymers have been characterized by SEC, NMR, DSC, XRD and PLM. Random copolymer with M_w of 14,100 and M_w/M_n of 1.36 was prepared by neodymium p-tert-butylcalix[6]arene complex under the conditions: [TMC+DTC]₀/[Nd]=400, 80 °C, 8 h. The reactivity ratios of TMC and DTC are measured to be r_TMC=4.68 and r_DTC=0.163, respectively. Random copolymerization could be well designed by the feeding ratio to prepare copolymers with controlled T_m and T_g. Only 8% TMC units in the polymer chain destroyed the crystallization of PDTC showing no T_m of the copolymer in the DSC analysis.