宽带放大器用碲基掺铒光纤结构参量的设计考虑

利用光波导理论及均匀展宽四能级模型,研究了宽带放大器用阶跃型折射率分布碲基掺铒光纤的结构参量—纤芯半径和相对折射率差的设计考虑.理论研究表明,在单模传输条件下,为获取最大信号增益,宜选择相对折射率差大的碲基掺铒光纤来构建光纤放大器.相对折射率差一定的情况下,在高泵浦功率、小信号输入或光纤长度短于各信道最佳增益长度时,选择纤芯半径大的碲基掺铒光纤可以得到大的信号增益;反之,宜选择纤芯半径小的碲基掺铒光纤.     

温度/应变/扭曲三参量同时测量低成本传感系统

提出了一种利用布喇格光纤光栅反射光作信号源、高频CO2激光脉冲写入的长周期光纤光栅和超周期光纤光栅作传感器实现温度、应变和扭曲同时测量的全光栅型低成本强度解调传感方案.文中利用长周期光纤光栅边缘滤波效应实现了温度、应变和扭曲传感信号的实时解调.实验结果表明,其温度和应变的测量灵敏度分别为－0.211 dB/℃和－0.012 dB/10με;而扭曲率的测量灵敏度为0.4394 dB/(rad·m－1),是该法写入普通LPFG的4倍以上.     

新型三段高性能的长波段掺铒光纤超荧光光源的研究

提出了一种第一段无泵浦、第二段前向泵浦和第三段后向泵浦的三段级联掺铒光纤超荧光光纤光源的新结构.数值分析了泵浦光波长、铒光纤长度以及泵浦比例对新结构性能的影响.结果表明可以找到一组适合制作成本低廉、输出功率高、谱平坦的长波段掺铒光纤超荧光光源.     

光锥与TDI-CCD耦合监控中测试目标的一种实现方法

为了给光锥与时间延迟积分电荷耦合器件耦合监控装置提供有效的被测运动条纹,分析了传统推扫成像实验装置的不足之处,设计了电子显示目标滚屏运动装置.采用光学相机对印刷条纹静止成像,并用TDI-CCD数字相机对监视器屏幕上的运动条纹动态成像.实验结果表明,该方案解决了高分辨率的鉴别率图样无法在监视器或投影仪上精确显示的困难.与传统的实验室模拟装置相比,该方案提高了鉴别率条纹的运动稳定性,减小了条纹运动速率与TDI-CCD扫描行频间的失配误差,不仅能够对耦合过程实施监控,而且还能用于耦合系统的像质评价.     

光纤环形镜线形腔掺Er3+光纤激光器输出特性的数值分析

在分析光纤环形镜工作原理的基础上,给出了基于光纤环形镜的线形腔掺Er3+光纤激光器相位和幅度的振荡条件.通过求解速率方程,理论分析了其输出特性,获得了稳态条件下激光器输出功率、阈值泵浦功率和斜率效率的解析表达式.推导出激光器工作所需掺Er3+光纤最短长度,并在给定泵浦光功率时,在特定输出波长上获得最大输出功率所需最佳掺Er3+光纤长度的表达式,且通过实验进行了验证.     

高速双边缘光纤光栅波长解调技术

提出一种双边缘结构对光纤光栅传感进行波长解调的方案,利用被测光谱通过不同光谱特性的滤波器时输出不同光强的比值确定被测光的波长.该系统在解调时不存在任何机械移动部分,比扫描式的解调方法测量速度更快,运行时更稳定、更精确.     

晶须概念的泛化与学术影响

最初只称单晶短纤维为晶须,稍后结晶较好的多晶纤维也被称为"晶须",现在无定形纤维也归进了晶须专著,通过对晶须概念泛化过程的反思,希能澄清学术著作中10多年来相沿的一个模糊认知。     

Capillary-channeled polymer (C-CP) fibers as a stationary phase in microbore high-performance liquid chromatography columns

Microbore columns utilizing polypropylene capillary-channeled polymer (C-CP) fibers as the stationary phase in high-performance liquid chromatography (HPLC) have been investigated. The polypropylene C-CP fiber diameter is ∼50 μm, with eight channels along the periphery of the fiber ranging in diameter from ∼12 to 35 μm. The polypropylene C-CP fibers were packed into fluorinated ethylene propylene (FEP) tubing, 1.3 mm inner diameter, with lengths of 500, 750, and 1,000 mm, to examine the effects of increased column length with regards to plate height, resolution and analysis time. The low backpressures characteristic of the C-CP fiber stationary phases allow the length of the column to be increased without significantly decreasing the specific permeability. The high specific permeability (∼5×10⁻⁸ cm²) of the C-CP packed microbore columns yields a relatively low backpressure of 2.35 MPa at the highest flow rate of 17 μL/s (54 mm/s) for a 1,000 mm column. Radial compression of the soft-walled FEP tubing is accomplished by pulling the 1.7 mm o.d. column through a 1.4 mm diameter orifice. Reducing the inner diameter of the column from 1.3 to 1.0 mm lowered the interstitial fraction from 47% to 42%, decreased the A-term contributions to band broadening, resulted in a significant decrease in average plate height (∼30%), and increased resolution (∼36%) at identical linear velocities. Although the lower void volume of the radially compressed column increased the backpressure from 0.57 to 2.11 MPa at a linear velocity of ∼20 mm/s, the specific permeability only decreased from ∼7×10⁻⁸ to 4×10⁻⁸ cm².      

纤维素溶剂研究进展

概述了纤维素溶剂的重要研究进展,主要包括N-甲基吗啉-N-氧化物(NMMO)在85℃以上高温可破坏纤维素分子间氢键,导致溶解;氯化锂/二甲基乙酰胺(LiCl/DMAc)在100℃以上可溶解纤维素;1-丁基-3-甲基咪唑盐酸盐([BMIM]Cl)和1-烯丙基-3-甲基咪唑盐酸盐([AMIM]Cl)离子液体,含强氢键受体Cl-离子,通过它们与纤维素羟基作用而引起溶解.氨基甲酸酯体系则是通过尿素与纤维素在100℃以上反应转变为纤维素氨基甲酸酯,然后再溶解于NaOH水溶液中;氢氧化钠/水体系,只能溶解结晶度和聚合度较低的纤维素;NaOH/尿素、NaOH/硫脲和LiOH/尿素水溶液体系,它们预冷至-5~-12℃后可迅速溶解纤维素.主要是通过低温产生小分子和大分子间新的氢键网络结构,导致纤维素分子内和分子间氢键的破坏而溶解,同时尿素或者硫脲作为包合物客体阻止纤维素分子自聚集使纤维素溶液较稳定.低温溶解技术不仅突破了加热溶解的传统方法,而且可推进化学"绿色化"进程.共引用参考文献50篇.     

Pt Nanoparticle‐modified Carbon Fiber Microelectrode for Selective Electrochemical Sensing of Hydrogen Peroxide

We report a simple approach to the production of carbon fiber‐based amperometric microbiosensors for selective detection of hydrogen peroxide (H₂O₂), which was achieved by electrometallization of carbon fiber microelectrodes (CFMs) by electrodeposition of Pt nanoparticles. The Pt‐carbon hybrid sensing interface provided a sensitivity of 7711±587 μA ? mM^?1 ? cm^?2, a detection limit of 0.53±0.16 μM (S/N=3), a linear range of 0.8 μM–8.6 mM, and a response time of <2 sec. The morphologies of the Pt nanoparticle‐modified CFMs were characterized by scanning electron microscopy. To achieve selectivity, permseletive layers, polyphenylenediamine (PPD) and Nafion, were deposited resulting in exclusion of the anionic and cationic interferents, ascorbic acid and dopamine, respectively, at their physiologically relevant concentrations. The resultant sensors displayed a sensitivity to hydrogen peroxide of 1381±72 μA ? mM^?1 ? cm^?2, and a detection limit of 0.86±0.19 μM (S/N=3). This simple and rapid metallization method converts carbon fiber microelectrodes, which are readily accessible, to microscale Pt electrodes in 2 min, providing a platform for oxidase‐based amperometric biosensors with improved spatial resolution over more commonly used platinum electrode array microprobes.