Er3+-Yb3+共掺磷酸盐玻璃(LGS-L)波导放大器设计

就作者自行研制的Er3 + Yb3 + 共掺磷酸盐玻璃 (LGS L) ,用重叠积分方法进行放大器设计。在Er3 + 、Yb3 + 掺杂浓度分别为 1.5 1× 10 2 6ions/m3 、19.1× 10 2 6ions/m3 的情况下可获得 2 .6dB/cm的增益 ;Er3 + 掺杂浓度为2× 10 2 6ions/m3 时 ,在 4cm的器件上可获得超过 15dB的增益。此外 ,讨论了信号光和抽运光光场强度的横向分布与Er3 + 、Yb3 + 横向掺杂浓度分布之间的重叠对放大器增益的影响 ,放大器的最佳长度 ,以及在 980nm抽运下 ,Yb3 + 、Er3 + 掺杂浓度比对放大器增益的影响。     

Metamaterial absorber and extending absorbance bandwidth based on multi-cross resonators

In this paper, we report the design, simulation, and measurements of a broadband metamaterial absorber (MA) based on a periodic array of multi-layer cross-structure resonators. A perfect narrowband MA consists of cross-structure resonator, dielectric substrate, and continuous metal films, and the absorption frequency can be tunable by changing the geometrical parameters based on L-C resonance circuit theory. Furthermore, the absorption band of our design is effectively extended by simply stacking several such structural layers with different geometrical dimensions. Finally, the 4-layer cross-structure MA is only 2 mm, which can achieve a full width at half maximum (FWHM) bandwidth of 2 GHz by numerical simulations, and 90 % bandwidth of 1.9 GHz by experiments.     

范德瓦耳斯气液状态方程纵横谈

首先强调了范氏方程是气液系统的状态方程,范氏方程可以很好地说明物质气态和液态的相互转变．分析了焦-汤效应,简述了气体的液化与低温的获得．     

The propagation problem and far-field patterns in a stratified finite-depth ocean

In this paper we investigate the direct problem associated with the scattering of ‘plane waves’ from an object submerged in an ocean of finite depth. An integral representation for the Dirichlet problem is found, from which a formula for the far-field pattern evolves. A density theorem is established concerning the set of all far-field patterns. This theorem is essential for the reconstruction of the submerged object, the ‘inverse’ problem [2], [4], [5].     

64通道一维位置灵敏电流分布探测器及其数据获取系统

针对高流强粒子束与绝缘毛细管相互作用的特点, 设计制作了一套64通道一维位置灵敏电流分布探测器及其配套的数据获取系统, 该探测器可分辨最小直径为1 mm的束斑, 通过数据获取系统可实现可视化自动数据采集。 用2 nA和200—2000 eV电子对探测器进行了定标, 并用10 μA和2000 eV的电子束穿越锥形毛细管后的出射电子, 对探测器及数据获取系统进行测试, 获得了出射粒子的位置分布谱及能量信息。 A 64 channel position sensitive current distribution detector with 1 mm position resolution was developed, while the data acquisition system is based on the LabVIEW software. The test result obtained by using a 2 nA, 200—2000 eV electron beam deflecting by different voltages and the position spectra of 10 μA, 2000 eV electrons transmitted through a glass capillary was measured. The result indicated that the detector can be used to detect the charged particles with strong beam current through the capillary.     

Backward heat equation with time dependent variable coefficient

Backward heat equation with time dependent variable coefficient is severely ill‐posed in the sense of Hadamard, so we need regularization. In this paper, we consider Backward heat equation with time dependent variable coefficient, and by small perturbing, we obtain an approximation problem. We show this approximation problem is well‐posed with small parameter. Also, we show this approximation system converges to the original problem when parameter goes to zero. Here, we use modified‐quasi boundary value method to regularize this problem. Copyright © 2016 John Wiley & Sons, Ltd.     

纳米复合固体超强酸SO42-/CoFe2O4的制备和表征

采用纳米化学制备技术合成了新型的纳米复合团体超强酸催化剂ＳＯ４２－／ＣｏＦｅ２Ｏ４。用ＸＲＤ、ＴＥＭ、ＸＰＳ、红 外光谱和比表面测定等技术研究了该催化剂的结构形态,结果表明：所研制的ＳＯ４２－／ＣｏＦｅ２Ｏ４催化剂为晶态纳 米粒子（＜ ５０ｎｍ）,比表面积很大（１５７ｍ２· ｇ－１）,ＳＯ４２－与氧化物的金属离子呈无机双齿螯合状配位化合物的结 合形式。以乙酸乙酯合成为模型反应考察了该催化剂的催化活性,比较了酸性和酸强度,推断出该催化剂的酸 强度Ｈ０＜－１４．５。     

高效液相色谱-串联质谱法测定黄瓜与土壤中烯酰吗啉和氰霜唑及其代谢物的残留量

为评价烯酰吗啉和氰霜唑在黄瓜和土壤中的安全性,建立了同时检测烯酰吗啉和氰霜唑及其代谢物4-氯-5-(4-甲苯基)-1H-咪唑-2-腈(CCIM)的高效液相色谱-串联质谱法。样品经乙腈提取,乙二胺-N-丙基硅烷键合相(PSA)和十八烷基硅烷键合相(C18)净化后,质谱多反应监测模式扫描,基质匹配标准曲线外标法定量。烯酰吗啉、氰霜唑和CCIM在0. 01～0. 5 mg/L范围内均具有良好的线性关系,相关系数(r)均大于0. 994 0,在0. 05、0. 1、0. 5 mg/kg加标浓度下,3种待测物在黄瓜和土壤中的平均回收率为78%～105%,相对标准偏差(RSD)为1. 3%～14. 8%,定量下限为0. 05 mg/kg。对35%氰霜唑·烯酰吗啉悬浮剂在黄瓜和土壤中的残留动态及最终残留量进行分析,发现烯酰吗啉、氰霜唑及CCIM之和在黄瓜和土壤中消解较快,烯酰吗啉在黄瓜和土壤中的半衰期分别为1. 2～2. 1、3. 0～9. 6 d;氰霜唑及CCIM之和在黄瓜和土壤中的半衰期为0. 9～2. 3、1. 8～6. 2 d。该方法简单、快速、灵敏度及准确度高,能够满足黄瓜和土壤中烯酰吗啉、氰霜唑及CCIM残留量的检测要求。     

Synthesis, Crystal Structure and Antiproliferative Activity of 2,2-Dimethyl-4-oxochroman-3-ylmorpholine-4-carbodithioate

The crystal structure of the new title compound 2,2-dimethyl-4-oxochroman-3-ylmorpholine-4-carbodithioate(C16H19NO3S2,Mr = 337.44) has been prepared and determined by single-crystal X-ray diffraction.The crystal is of triclinic,space group P1 with a = 9.5518(7),b = 9.7172(7),c = 11.0220(8),α = 67.08(1),β = 74.66(1),= 61.31(1)°,V = 822.72(10)3,Z = 2,Dc = 1.362 g/cm3,F(000) = 356,μ = 0.092 mm-1,MoKa radiation(λ = 0.71073),R = 0.0515 and wR = 0.1389 for 2623 observed reflections with I > 2(I).X-ray diffraction analysis reveals that the chroman ring adopts a half-chair conformation while the morpholine ring shows a chair conformation.Intramolecular and intermolecular C-H···S and C-H···O hydrogen bonds together with π-π interations are found in the structure.The result of MTT assay shows the title compound displays good antiproliferative activity against two human cancer cell lines.