聚类分析在髁突骨密度分析中的应用

本研究应用聚类分析的方法，对人离休髁突×片进行数字图像技术处理所获得的影像密度数值做了详细分析，取得人髁突不同区的骨密度分布及不同年龄阶段髁突密度变化的情况。该方法避免了人为因素的影响，其结果较客观地反映了髁突的骨质密度；为研究病理状态时髁突骨密度的改变提供参考。     

在BBO中产生217.3-2 21.4nm高功率和频输出

用Q-YAG激光的三次谐波(355nm)与调谐的Rh·6G染料激光在β-BaB2O4(BBO)晶体中和频,获得217.3～221.4nm连续调谐输出,和频输出的最大能量为250μJ,转换效率为11%.我们还讨论了获取最大和频输出能量的一些实验条件.     

Periodic solutions for p-Laplacian neutral functional differential equation with multiple deviating arguments

By using the theory of coincidence degree, we study a kind of periodic solutions to p-Laplacian neutral functional differential equation with multiple deviating arguments, a new result on the existence of periodic solutions is obtained.     

合肥同步辐射软X射线显微术研究

合肥国家同步辐射实验室首期建设的光束线之一用于软Ｘ射线显微成像研究。实验站现已装置初型的扫描透射Ｘ射线显微镜，并正在进行亲一代的扫描显微建设，同时还使同步辐射光进行接触软Ｘ射线呈微成像研究，并对选取的一些生物样品进行了成像试验。本文介绍了合肥同步辐射光源上软Ｘ射线显微术实验线站的建设及完成的一些实验结果。     

SrZnO_2∶Eu~(3+),Li~+长波紫外激发红光荧光体的合成及发光性能研究

采用高温固相法合成了一种长波紫外激发的SrZnO2∶Eu3+,Li+发光材料,用X射线衍射谱、荧光光谱对样品进行了表征。结果表明,Eu3+离子在SrZnO2基质中主要占据Sr2+离子不对称性格位,发射来源于5D0→7F2612 nm为主的红光。加入电荷补偿剂Li+离子能显著提高发光强度,350~400 nm内的激发峰也有明显提高,同时观察到来自Eu3+离子高能级5D1→7FJ(J=0~2)的跃迁发射,并对其产生机制进行了初步探讨。实验结果表明,SrZnO2∶Eu3+,Li+是一种有发展前途的长波紫外激发红光荧光体。     

稀土掺杂的(K, Sr)Cl·SiO2复合凝胶的荧光性能

采用sol gel法制备了单掺铕及共掺铕、铈的(K,Sr)Cl·SiO2复合凝胶,研究了复合凝胶的荧光性能。根据荧光测试结果,复合凝胶中,Eu3+在没有还原剂的作用下,可以与基质作用形成还原态的Eu2+,复合凝胶表现出相应的Eu2+荧光性能;研究认为,Ce3+,Eu3+共掺杂时,复合凝胶激发光谱与发射光谱峰位基本不变,但强度有所不同。330nm处的激发光谱明显增强,且发射光谱随Ce3+的掺杂量增加而增强。当Ce3+掺杂浓度为3.0%(原子分数)时,复合凝胶具有最大的荧光发射强度,表明Ce3+具有很好的敏化作用。在Ce3+,Eu3+共掺杂复合凝胶体系中,复合凝胶荧光强度增大的原因既可能是电子转移过程,也可能是Ce3+→Eu2+的能量传递过程所致。     

Complexation of well-controlled low-molecular weight polyelectrolytes with antisense oligonucleotides

The influences of polymer-related properties such as molecular weight, charge density, counter ion, and hydrophilic block on the complexation of polyelectrolytes and a fluorescein-labeled oligonucleotide (ON) were investigated. A series of well-defined and well-controlled 2-(N,N-dimethylamino)ethyl methacrylate (DMAEMA) polymers and block copolymers were prepared using living anionic and radical polymerization methods. Fluorescence measurement was used to reveal the effects of polymer molecular weight, charge density, and counter ion type on the complexation. PolyDMAEMA samples having double molecular weights of the chosen oligonucleotide gave the optimal complexation performance. Kinetic studies showed that high-molecular weight/high-charge density polymer samples produced very stable complexes. The fully charged polyDMAEMA displayed the strongest binding with the ON. These complexes were therefore less sensitive to the changes in the environment. PolyDMAEMA–DMSQ samples had slightly higher complexation ability than polyDMAEMA–MCQ (DMSQ: dimethylsulfate quat; MCQ: methylchloride quat). Both poly(DMAEMA-b-HEMA) and poly(DMAEMA–MCQ-b-PEG) block copolymers showed good complexation ability and steric stability [HEMA: 2-hydroxyethyl methacrylate; PEG: poly(ethylene glycol)]. PEG, but not HEMA block, enhanced the effectiveness of polyDMAEMA–MCQ binding with the ON.     

Molecular dynamics simulation of room-temperature ionic liquid mixture of [bmim][BF4] and acetonitrile by a refined force field

1-Butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4]) is one of the promising room-temperature ionic liquids. To test the refined force field for [bmim][BF4] proposed in our previously work (J. Phys. Chem. B, 2004, 108, 12978-12989), thermodynamic properties of mixtures of [bmim][BF4](1)+ acetonitrile (2) are presented by using molecular dynamics over the whole concentration range. The calculated densities are in good agreement with the experimental data with deviations less than 2%, indicating the force field is applicable to the mixtures. In addition, the diffusion constants, viscosities, heats of vaporization, cohesive energy densities and excess properties of the mixtures are reported. The microscopic structures are discussed in detail, corresponding to the thermodynamic properties.     

Synthesis and characterization of poly(amide sulfonamide)s (PASAs)

New diamino monomers IIa – IIg were synthesized in a two-step reaction sequence starting from p-acetamidobenzenesulfonyl chloride. Solution polymerization of these monomers in DMAC with terephthaloyl or isophthaloyl chloride resulted in the formation of a series of 14 poly(amide sulfonamide)s (PASAs) in excellent yield (> 95%). The polymers have in-trinsic viscosities of 0.32–1.11 dL g^?1. Except for polymers IIIa ? p and IIId - p , all other PASAs were readily soluble in aprotic polar solvents including DMAC, DMF, and DMSO. Thermogravimetric analyses of the polymers showed moderate thermal stability with 10% weight loss being recorded in the range of 325–408°C. In addition, these polymers exhibit moderate chemical stabilities toward alkali, acidic, and chromic acid solution. © 1995 John Wiley & Sons, Inc.     

ZnCl2熔盐的分子动力学模拟

近年来，若干作者根据几种粒子间函数，对ZnCl2熔盐结构做过分子动力学模拟［1－3］其出的Zn－Cl和Cl－Cl离子间的偏径向分布函数与中子衍射实测值符合较好，但Zn－Zn离子间距以及Zn－Zn间配位数计算值多偏高．鉴于Busing势函数在多价卤化物馆盐的分子动力学计算中应用效果较好[4],我们试用Busing势函数为基础对ZnCl2熔盐结构和能量做分子动力学计算．1研究方法计算所用粒子势为Busing势函数此处，Zi为离子的电行数（ZZn。＋＝2，Zcl－＝1），几；是离子有效半径，人为＊离子的“硬度”参数·据文献问，f二0．005071，尸zn。十二0．…