大学物理虚拟实验的网络教学系统

介绍了基于当前Internet网络环境实现仿真实验远程教学的方案和技术,为各种实验的远程教学开发与应用提供了一种可行的新模式。     

Generalized Steiner systems GS4 (2, 4, v,g) for g = 2, 3, 6

Generalized Steiner systems GS_d(t, k, v, g) were first introduced by Etzion and used to construct optimal constant‐weight codes over an alphabet of size g + 1 with minimum Hamming distance d, in which each codeword has length v and weight k. Much work has been done for the existence of generalized Steiner triple systems GS(2, 3, v, g). However, for block size four there is not much known on GS_d(2, 4, v, g). In this paper, the necessary conditions for the existence of a GS_d(t, k, v, g) are given, which answers an open problem of Etzion. Some singular indirect product constructions for GS_d(2, k, v, g) are also presented. By using both recursive and direct constructions, it is proved that the necessary conditions for the existence of a GS₄(2, 4, v, g) are also sufficient for g = 2, 3, 6. © 2001 John Wiley & Sons, Inc. J Combin Designs 9: 401–423, 2001     

Fe~(3 )/TiO_2/SiO_2复合纳米微粒的合成及光催化降解NO_2~-

采用溶胶 -凝胶法制备了 Ti O2 / Si O2 和不同浓度 Fe3 掺杂的 Fe3 / Ti O2 / Si O2 复合纳米粉末 ,并利用XRD、BET、UV-vis等手段研究了 Ti O2 / Si O2 及掺铁形成的 Fe3 / Ti O2 / Si O2 复合微粒的表面结构形态变化 ,以及对污染物 NO- 2 光催化降解的影响 .结果表明 ,Fe3 / Ti O2 / Si O2 (ω( Fe3 ) =1 .5 % ,m( Ti)∶ m( Si) =2∶ 1 )具有最佳活性 ,样品呈晶化度较低的锐钛矿结构 .Fe3 掺杂导致晶粒的增大 ,稳定性降低 ,大大提高了半导体的光催化活性 ,有利于对低浓度 NO- 2 的光催化降解     

α-Fe_2O_3掺杂对In_2O_3电导和气敏性能的影响

用化学共沉淀法制备了α－Ｆｅ２Ｏ３掺杂的Ｉｎ２Ｏ３纳米晶微粉,研究了α－Ｆｅ２Ｏ３掺杂对Ｉｎ２Ｏ３电导和气敏性能的影响．结果表明,α－Ｆｅ２Ｏ３和 Ｉｎ２Ｏ３间可形成有限固溶体Ｉｎ２－ｘＦｅｘＯ３（０≤ｘ≤０．４０）;Ｆｅ３＋对 Ｉｎ２Ｏ３晶格中Ｉｎ３＋格位的部分取代,大大增强了阴阳离子间的结合力,导致材料中氧空位Ｖｏｘ数骤降、自由电子的浓度变稀和电导下降．ｎ（Ｆｅ３＋）：ｎ（Ｉｎ３＋）＝５：５的共沉淀粉于 ８００℃下灼烧 ４ ｈ所得的 α－Ｆｅ２Ｏ３掺杂Ｉｎ２Ｏ３传感器元件,对 ４５μｍｏｌ·Ｌ－１Ｃ２Ｈ５ＯＨ的灵敏度达５４．０,为相同浓度干扰气体汽油的８倍多．     

氢化物发生微分电位溶出法测定人尿、头发及自来水中痕量锡

研究了氢化物发生微分电位溶出法测定人尿、头发及自来水中痕量锡的方法,该法能有效地消除共存离子的干扰。详细研究了锡化氢发生以及微分电位溶出法测定锡的最佳条件。方法的线性范围0－150mg.ml^-1,检出限2．5ng.ml^-1,成功地用于自来水、人尿及头发痕量锡的测定。测定发样中304．5ng.g^-1锡时,回收率为100．3％,相对标准偏差为5．1％（n=6)。     

Oxidative Dehydrogenation of Ethane to Ethylene over LiCl/MnOx/PC Catalysts

The catalytic stability of LiCl/MnO_x/PC catalyst have been investigated, the deactivation mechanism was discussed. The experimental results show that ethane conversion decreases and ethylene selectivity keeps about 90% as reaction time increases. The main deactivation reasons of LiCl/MnO_x/PC catalyst for oxidative dehydrogenation of ethane (ODHE) to ethylene are the transition of active species Mn₂O₃ to MnO species and the loss of active component Cl in catalyst. Instead of ethane with FCC tailed‐gas, the stability of LiCl/MnO_x/PC catalyst has been largely improved.     

一种弹-粘塑性本构模型材料常数的估计方法

推导了Ｂｏｄｎｅｒ－Ｐａｒｔｏｍ统一弹－粘性本构模型的材料常数估计公式,修正了国外有关文献的不当之处,发展了参数的优化估计方法与程序,并用算例验证了方法的可行性。     

材料交界面上连续应力分析的改进拉氏乘子法

引进材料界面的节理单元,以其刚度参数为罚参数,利用代表界面接触应力的拉氏乘子,通过迭代求解得到界面上的应力,为计算粘结在一起的不同材料交界面上的应力提供了一种非常有效的方法。     

信息系统中的可移动Agent

介绍了可移动Agent的特性,可移动Agent可在异质计算机网络中移动,它能感知网络的状态,监控系统并与其它Agent进行交互,导航模型可以让Agent适应网络的变化并自主制定导航计划,从而方便、有效、智能地完成信息检索的任务．     

RING-OPENING POLYMERIZATION OF TRIMETHYLENE CARBONATE BY CALIX[8]ARENE-NEODYMIUM*

Ring-opening polymerization of trimethylene carbonate (TMC) with a rare earth calixarene compound as catalysthas been studied for the first time. The effect of TMC/Nd (molar ratio) and polymerization conditions were investigated indetail. It was found that calix[8]arene-neodymium is a highly effective catalyst for the bulk polymerization of TMC and giveshigh molecular weight (M_v = 60,000) polymer. The optimum conditions of TMC polymerization were found to be asfollows:TMC/Nd (molar ratio) = 2,000, 80℃, 16 h. The polymers were characterized by NMR, GPC and DSC. Studying themechanism by NMR showed that the polymerization of TMC catalyzed by calix[8]arene-neodymium proceeds via a cationicmechanism.