马来酸酐接枝聚丙烯增容聚丙烯/碳酸钙复合物力学性能与增容机理

用在50L固相接枝反应器中合成的马来酸酐接枝聚丙烯(PP-g-MAH)作界面改性剂，制备了马来酸酐接枝聚丙烯／聚丙烯／碳酸钙(i-PP／PP-g-MAH／CaCO3)复合材料。研究了i-PP／PP-g-MAH／CaCO3复合材料的力学性能和增容机理。结果表明，PP-g-MAH对i-PP／CaCO3复合物的缺口冲击强度、弯曲强度和拉伸强度均有提高；PP-g-MAH与CaCO3反应形成PP-g-MAH的钙盐，实现反应性增容。     

变性淀粉取代聚乙烯醇生产Al2O3刚玉陶瓷的胶粘剂研究

论述了变性淀粉取代聚乙烯醇(PVA)生产Al2O3刚玉陶瓷的意义及聚乙烯醇结构与吸附性能的关系，并且根据胶粘机理，通过分析Al203胶粒的表面特性和变性淀粉的结构，说明了变性淀粉可以取代聚乙烯醇。     

纳米CaSiO_3填料的制备及其性能表征

以乙醇为溶剂,正硅酸乙酯(TEOS)为胶溶剂,CaCO3为主要试剂,采用溶胶-凝胶(Sol-Gel)技术制备纳米偏硅酸钙(CaSiO3)填料,考察主要工艺参数——初始水凝胶pH值、R值(H2O/TEOS)对粉体形貌、颗粒大小等性质的影响。研究表明:采用溶胶-凝胶法能合成纳米级的CaSiO3填料。     

Phenol adsorption on porous and non-porous carbons

Phenol physisorption on a series of porous and non-porous amorphous carbons was studied at 298 K. Grand Canonical Monte Carlo computer simulations were performed to simulate phenol adsorption from the gas phase. Phenol is adsorbed in a solid-like state within the pores and there is no well-developed multilayer regime. The ‘t’ plot method was adapted to phenol adsorption and the results obtained are in agreement with the model solids employed. The simulated adsorption isotherms were compared with experimental results obtained for adsorption from aqueous solutions of phenol. BET surface areas were calculated. Other characteristics of the adsorption system analyzed were: adsorption energy distribution functions, density profiles, distribution of molecules according to gas-solid energy, and local isotherms.     

采用主监视窗扩展技术的增强现实三维注册方法

在增强现实三维注册中,采用重新检测策略时顿卡现象严重。提出一种采用主监视窗扩展技术的增强现实三维注册方法。在检测阶段,引入特征点可信度和主监视窗,并设计主监视窗的分割、扩展和调控策略,大幅提升了计算速度;在跟踪阶段,采用基于图像金字塔的光流算法进行特征点跟踪。实验证明,该方法不仅有效缓解了顿卡现象,也提升了系统整体的实时性。     

基于自由运动一维标定物的多摄像机参数标定方法与实验

一维标定方法易于实现且标定效率高,为了克服现有一维标定方法的一些不足,本文提出一种用一维标定物标定多摄像机内外参数的方法,首先进行两两标定,在此过程中,假定主点坐标近似已知而仅考虑畸变、焦距、旋转和平移等参数,接着利用基本矩阵及一维标定物上特征点之间的几何约束,估计两摄像机的内外参数,两两标定完成后,采用Dijkstra最短路径法和捆绑调整对多摄像机系统进行全局标定(含主点坐标),仿真和真实实验表明本文的方法是切实有效的.     

Kinect体感控制性能优化方法

为提高基于Kinect体感应用程序控制识别的稳定性、准确性与鲁棒性,针对手臂光标延迟与身体控制场景内容稳定性的问题,提出在Unity3D平台下的体感控制性能优化方法。基于数据转化思想,通过放宽手臂光标触发成功条件,将单点稳定触发转化为范围稳定触发,实现手臂光标延迟性能优化;通过将身体位置控制场景内容转化为模拟键盘方向键输入的方法,实现身体控制场景内容稳定性优化。实验结果表明,该方法能够有效提高体感应用程序的相关性能。     

N,N,N-三甲基-2,3-二(硬脂酰氧基)丙基氯化铵(CDESA)的生物降解性

采用活性环氧中间体失水甘油基三甲基氯化铵合成了一种阳离子双酯表面活性剂——N,N,N-三甲基-2,3-二(硬脂酰氧基)丙基氯化铵(CDESA),来代替传统的难降解的表面活性剂型柔软剂,如目前国内仍在大量使用的双十八烷基二甲基氯化铵(D1821)。对CDESA的好氧降解性能进行了研究:以天然环境中的生活沉降污泥作为微生物源,用河水稀释,经培养、驯化后用于测试降解时间和半衰期,并与D1821的好氧降解性能作了对比。结果表明,CDESA的半衰期为3 d,容易降解,而D1821半衰期为7 d,较难降解,CDESA生物降解性能优于D1821。     

The preparation of coupled WO3/TiO2 photocatalyst by ball milling

The coupled photocatalyst WO₃/TiO₂ is prepared by ball milling by doping WO₃ into TiO₂ and using H₂O solution as disperser. The coupled photocatalyst WO₃/TiO₂ is characterized by UV–VIS diffuse reflection spectrum, X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD) and Transmission electron microscopy (TEM). The results show that the optimum percentage of WO₃ doped is 3% and that the photocatalytic activity of the coupled WO₃/TiO₂ photocatalyst is much higher than that of TiO₂ and WO₃–TiO₂ with no ball milling. Compared with TiO₂, the photoexcited wavelength range of the WO₃/TiO₂ photocatalyst red-shifts about 50 nm, and the light absorption intensity is also improved. The crystal phase of TiO₂ is not changed and new crystal phases are not found during the process of ball milling. WO₃ and TiO₂ coupled highly, forming the WO₃/TiO₂ photocatalyst. The increased photocatalytic activity of the coupled photocatalyst may be attributed to the enhance charge separation efficiency and the extend wavelength range of photoexcitation.     

Synthesis of hydroxyapatite nanoparticles in ultrasonic precipitation

Nanocrystalline hydroxyapatite (HAp) was prepared by a precipitation method with aid of ultrasonic irradiation using Ca(NO₃)₂ and NH₄H₂PO₄ as source material and carbamide (NH₂CONH₂) as precipitator. The crystallization and morphology of the prepared nanoparticles were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The mechanism and kinetics of the nano-hydroxyapatite were considered in particular, and the influence of the temperature and time on the HAp formation rate was also investigated. The results show that the needle-like HAp crystalline was prepared by the ultrasonic precipitation process. The HAp content increases with the preparation temperature and time. The adding of carbamide is helpful for formation of HAp nanoparticles. An Arrhenius relationship was found between the HAp formation rate and the temperature, and an apparent activation energy of 59.9 kJ/mol was obtained by calculation.