基于光诱导荧光技术的浮游植物光合作用活性原位测量方法

根据浮游植物在不同光照下的荧光诱导特性,研究了叶绿素荧光作为浮游植物光合作用探针的特点,提出了原位测量活体叶绿素荧光值Ft和Fm获取浮游植物光合作用活性的方法。以淡水湖泊浮游植物中的普通小球藻、铜绿微囊藻和梅尼小环藻为实验对象,将原位测量方法得到的数据和实验室水样荧光仪的测试结果进行对比分析,结果表明:普通小球藻、梅尼小环藻和铜绿微囊藻的两组测试结果之间的相关系数分别为0.977 8,0.867 8和0.776 8,研究为进一步实现水体浮游植物光合作用活性的快速连续原位测量提供了方法。     

Large-Quantity Synthesis of Single-Crystalline Metal Indium Nano/Sub-Micron Wires

Large quantities of metal indium single-crystalline wires with diameters ranging from tens of nanometres to a few micrometres were synthesized on Si substrates. Unlike traditional methods for the fabrication of nanowires or nanorods, liquid indium was squeezed out of the pores and cracks from porous an InAlN layer to form the wires. Continuous pushing out of liquid metal indium under strength, lowering of liquid-solid interfaces and the confinement of the cracks all contribute to the growth of indium wires. Our experiments have shed some light on the possibility of synthesizing large quantities quasi-1D nano/sub-micron structures with specified cross-sectional geometry using the similar method.     

铋化物发光玻璃中银表面等离激元对铒离子的发光增强作用

局域表面等离激元可以由自由空间的光直接激发,这也是局域表面等离激元的优点所在。研究铋化物发光玻璃中纳米银颗粒的表面等离激元对铒离子发光的增强效应、进一步的提高铋化物发光玻璃中铒离子的发光性能很有意义。首先,测量了(A)Er 3+(0.5%)Ag(0.5%):铋化物发光玻璃与(B)Er 3+(0.5%):铋化物发光玻璃样品的吸收谱,发现(A)Er 3+(0.5%)Ag(0.5%):铋化物发光玻璃在约600.0 nm处有一个较弱的宽的银表面等离激元共振吸收峰。同时发现两者都有典型的铒离子的吸收峰,它们的吸收几乎完全一样:在波峰形状、峰值强度和峰值波长等方面都很相近。测量了(A)Er 3+(0.5%)Ag(0.5%):铋化物发光玻璃和(B)Er 3+(0.5%):铋化物发光玻璃样品的激发谱,发现有位于379.0,406.0,451.0,488.0和520.5 nm的5个550.0 nm可见光的可见激发谱峰,和位于379.0,406.5,451.0,488.5,520.5,544.0,651.5和798.0 nm的8个1531.0 nm红外光的红外激发谱峰,容易指认出依次为Er 3+的4I 15/2→4G 11/2,4I 15/2→2H 9/2,4I 15/2→(4F 3/2,4F 5/2),4I 15/2→4F 7/2,4I 15/2→2H 11/2,4I 15/2→4S 3/2,4I 15/2→4F 9/2和4I 15/2→4I 9/2跃迁的吸收峰,通过测量发现(A)Er 3+(0.5%)Ag(0.5%):铋化物发光玻璃相对于(B)Er 3+(0.5%):铋化物发光玻璃样品的可见和红外激发谱的最大增强依次分别是238%和133%。最后,测量了它们的发光谱,发现有位于534.0,547.5和658.5 nm的三组可见发光峰,容易指认出依次为Er 3+的2H 11/2→4I 15/2,4S 3/2→4I 15/2,4F 9/2→4I 15/2荧光跃迁。还发现红外发光峰位于978.0和1531.0 nm,依次为Er 3+的4I 11/2→4I 15/2和4I 13/2→4I 15/2的荧光跃迁。通过测量发现(A)Er 3+(0.5%)Ag(0.5%):铋化物发光玻璃相对于(B)Er 3+(0.5%):铋化物发光玻璃样品的可见和红外发光谱的最大增强依次分别是215%和138%。对于银表面等离激元增强铒离子发光的机理,认为主要为纳米银颗粒的局域表面等离激元共振,造成金属纳米结构附近产生的局域电场的强度要远大于入射光的电场强度,从而导致了金属纳米结构对入射光产生强烈的吸收和散射,进而导致了荧光的增强;即局域表面等离子体共振局域场的场增强效应。     

Nash平衡的存在性与稳定性

本文对Nash平衡的存在性与稳定性作了较为详细的研究和综述.     

广义病态方程的Tikhonov正则解

对于双方带扰动数据的病态方程(即所谓广义病态方程)，借助对Tikhonov正则化算法的改进，给出一种优良的正则化求解方法。     

An Optical Labeling Scheme with Novel DPSK/PPM Orthogonal Modulation

A novel differential-phase-shift-keying （DPSK）/pulse-position-modulation （PPM） orthogonal modulation is pro- posed for optical labeling applications, with PPM data as the high-speed payload and DPSK signal as the optical label. The systematic setup for the proposed scheme and research on bit-error rate is presented. The results show that at the bit-error rate of 10-~, the power penalties for 70kin fiber transmission are in the range of 1-3 dB to DPSK label and 5-6 dB to PPM payload in our simulation system. This is under the condition that the large extinction ratio of 18-19 dB is used for the intensity modulators of the PPM payload, with a well received DPSK label. Thus the feasibility of the proposed scheme for all optical transmission networks is clearly verified.     

冲击速度和轴向静载对红砂岩破碎及能耗的影响

地下岩体工程爆破开挖中,距爆源不同距离处岩体承受的地应力和动载荷大小不同,从动载荷的角度表征岩石动态破坏结果与工程实际更吻合。为研究动载荷和地应力大小对岩体破碎和能量耗散特性的影响,利用动静组合加载试验装置,分别设置7个冲击速度和轴向静应力等级,对红砂岩试件进行冲击试验。根据试件的破碎状况,分析不同静应力工况下冲击速度对岩石破坏模式和机理的影响。计算不同工况下的应力波能量值,研究冲击速度和轴向静应力对岩石能耗特性的影响。对破坏试件进行筛分试验,研究岩石破碎分形维数随冲击速度和轴向静应力的变化关系。结果表明,随着冲击速度的增大,试件的破坏程度逐渐加大。无轴压时岩石试件破坏后整体仍是一个圆柱体,属于张拉破坏;有轴压时岩石试件宏观破坏后呈沙漏状,属于拉剪破坏。岩石耗散能随冲击速度的升高呈二次函数关系递增;轴向静应力越高,递增幅度越小。随着冲击速度的升高,岩石分形维数由零逐渐增加;随着轴向静应力的升高,分形维数由零转为大于零的临界冲击速度先升高后降低。

     

二阶抽样总体比率的估计

本文研究二阶抽样下总体比率的估计问题, 就若干种情形给出总体比率的几种可行的估计量,讨论了它们的统计性质.     

高质量CdTe量子点的水相快速合成

系统考察了水相合成CdTe量子点的主要影响因素, 通过改变无水乙醇-水体系的体积, 提高NaHTe的合成质量, 并调整反应温度, 改变反应的初始pH值, 在水相中快速合成了量子产率高、粒径分布范围窄的CdTe量子点, 实现了对量子点发光性质的调控, 在最佳条件(无水乙醇3 mL, 水1 mL, 反应初始pH 8.0, 反应温度40 ℃)下, 最高量子产率达68%. 量子点胶体溶液在回流过程中有时产生白色沉淀, 放置7 d后, 未过滤白色沉淀的量子点比过滤后的量子点荧光强度提高15%, 白色沉淀还有减小粒径分布的作用.     

Sorption of Th(IV) ions onto TiO2: Effects of contact time, ionic strength, thorium concentration and phosphate

Summary The sorption of Th(IV) onto TiO₂ was studied by the batch technique as a function of pH and ionic strength at moderate concentration (10^-4-10^-5 mol/l) and in the presence and absence of phosphate. It was found that the sorption rate of Th(IV) was relatively slow, the sorption percent was abruptly increased from pH 2 to 4, and the sorption was decreased with increasing ionic strength as a whole. In the concentration range of Th(IV) from trace concentration to 1.4 ^. 10^-4 mol/l and in the absence of phosphate, the sorption isotherms were roughly fitted the Freundlich equation at different ionic strengths and approximately constant pH. These sorption characteristics of Th(IV) onto TiO₂ were compared with those of uranyl on the same sorbent. In addition, the positive effect of phosphate on the sorption of Th(IV) onto TiO₂ was demonstrated obviously and can be attributed to strong surface binding of phosphate, and the subsequent formation of ternary surface complexes of Th(IV). The difference between the sorption characteristics of Th(IV) ions and uranyl ions onto TiO₂ is discussed.