On the Kauffman skein modules

 Let k be a subring of the field of rational functions in α, s which contains α ^±1 ,s ^±1 . Let M be a compact oriented 3-manifold, and let K(M) denote the Kauffman skein module of M over k. Then K(M) is the k-module freely generated by isotopy classes of framed links in M modulo the Kauffman skein relations. In the case of , the field of rational functions in α, s, we give a basis for the Kauffman skein module of the solid torus and a basis for the relative Kauffman skein module of the solid torus with two points on the boundary. We then show that K(S ¹ × S ² is freely generated by the empty link, i.e., . Received: 20 October 2001 / Revised version: 20 March 2002     

Liquid crystal lens with focus movable in focal plane

A liquid crystal lens with focus movable in the focal plane is reported. There are three electrodes in the cell. One electrode with a hole in the center is divided into four subelectrodes. The potential of each subelectrode is adjusted to produce a desired asymmetrical phase transformation resulting in off-axis movement of the focus. The potential of another electrode is adjusted to maintain the focus in the focal plane. Movements of the focus in three directions in the focal plane are demonstrated experimentally, and off-axis movement as large as approximately 800 μm is realized.     

A highly sensitive and rapid assay for protein determination in human urine and penicillin using a Rayleigh light-scattering technique with benzeneazo-8-acetylamino-1-naphthol-3,6-disulfonic acid sodium salt.

A simple and sensitive method was conducted for the determination of trace amounts of proteins with benzeneazo-8-acetylamino-1-naphthol-3,6-disulfonic acid sodium salt (azophloxine, AP) using a Rayleigh light-scattering (RLS) technique. At pH 2.60 and in the presence of an emulsifier OP microemulsion, the RLS of AP can be greatly enhanced by proteins, owing to the interaction between AP and protein. The enhanced intensity is proportional to the concentration of proteins. Four proteins, including bovine serum albumin (BSA), human serum albumin (HSA), lysozyme (Lys) and gamma globulin (gamma-G) have been tested. For example, the linear range of BSA was 0 - 0.06 microg mL(-1) with detection limits of 2.38 ng mL(-1). The method was applied to the analysis of protein in human urine and penicillin samples with satisfactory results. The relative standard deviation was in all instances less than 4.0%, and the recovery was in the range of 97.5 - 104%.     

用分光光度法测定蜂胶超临界CO2萃取物中总黄酮含量

利用碱性条件下黄酮与Al3 生成粉红色络合物在可见光区510 nm处有最大吸收的特性,以芦丁为标样,采用分光光度法测定蜂胶超临界CO2萃取物中总黄酮含量,并与HPLC标准方法测定结果进行比较,发现各平行样的测定结果基本一致,最大偏差为268.38 mg/100 g,最小偏差为52.77 mg/100 g.该法简便快捷,结果相对准确,可作为蜂胶超临界CO2萃取物中总黄酮含量快速评估的一种方法.     

电荷量子比特与量子化光场之间的纠缠

研究了初态为混合态的电荷量子比特与量子化光场之间的纠缠.通过求解系统的concurrence下限, 研究初态的混合度λ和失谐量Δ对系统纠缠随时间演化的影响. 在弱场中, 电荷量子比特初始是激发态的系统, 其纠缠度远远大于电荷量子比特初始是基态的系统, 并且Δ对系统的纠缠有明显的抑制作用. 在强场中, 电荷量子比特初始分别为激发态和基态时系统的纠缠演化接近一致, 初态混合度最高时系统的纠缠度最小, 并且Δ对系统纠缠的影响变弱. 关键词： 约瑟夫森结 纠缠 混合态 concurrence下限     

EAST�ŵ����ֵģ�⼰����������

用TSC程序模拟了EAST装置等离子体放电的全过程。模拟中考虑了自举电流，并加入了离子回旋共振加热ICRH和快波电流驱动FWCD，得到了中心电子温度4.5keV、中心离子温度3.8keV、中心电子密度1.2×1020m–3的D形截面的等离子体。根据模拟结果对EAST装置进行了伏秒数分析，并研究了不同等离子体电流上升时间、有效电荷数Zeff对放电的影响。     

High-precision Monte Carlo test of the conformai-invariance predictions for two-dimensional mutually avoiding walks

Let _l be the critical exponent associated with the probability thatl independentN-step ordinary random walks, starting at nearby points, are mutually avoiding. Using Monte Carlo methods combined with a maximum-likelihood data analysis, we find that in two dimensions ₂=0.6240±0.0005±0.0011 and ₃=1.4575±0.0030±0.0052, where the first error bar represents systematic error due to corrections to scaling (subjective 95% confidence limits) and the second error bar represents statistical error (classical 95% confidence limits). These results are in good agreement with the conformal-invariance predictions ₂=5/8 and ₃=35/24.     

ACM-02型COD仪分光光度法快速测定废水中COD

水样在165℃下密封消解15 min,用ACM-2型COD仪测定.实验结果表明,本法既快速又节省试剂,加标回收率和相对标准偏差均能满足质量控制要求,具有一定适用性.     

聚(酪氨酸酯对苯二甲酰胺)碳酸酯药物控制释放材料的研究

报道了一类生物可降解聚（酪氨酸酯对苯二甲酰胺）碳酸酯的合成和结构表征，研究了聚合物的性质和体外降解性能，并以５ 氟脲嘧啶和牛血清白蛋为模型，对它们作为药物控制释放材料的性能进行了初步评价．