一种用于波分复用系统的ATM光交换模型

波分复用是增大通信容量,提高线路利用率的常用技术.本文提出了一种用于波分复用系统的ATM光交换模型.该结构利用波分复用的特点,采用内部多通道互连方式,使其具有易于实现、结构简单、对内部缓存要求较低等优点.并对该模型进行了性能分析,得出了结论.     

A massive-ion beam driver for high-energy-density physics and future inertial fusion

Several heavy ion drivers for heavy ion inertial fusion have been proposed in the US and Europe, based on linear induction accelerator technology [1] and existing RF technology [2], respectively, although they have not been realized on a large scale. Developing accelerator technology may provide an alternative efficient, robust, and relatively cheap massive-ion beam driver for future particle beam inertial fusion. Here, we propose an accelerator complex for accelerating giant cluster ions, instead of lead or bismuth ions, toward 120 GeV by using induction acceleration over the entire energy region. The proposed two-way multiplex induction synchrotron that is the main accelerator for the giant cluster ion beam would be equivalent to 10 synchrotrons of the same size for a single beam.     

A compact microfluidic geometry for multiplexing enzyme-linked immunosorbent assays

We have previously reported a novel approach to implementing multiplex enzyme-linked immunosorbent assay (ELISA) in connected microchannels by exploiting the slow diffusion of the enzyme reaction product across the different assay segments. This work builds on that report by implementing the noted assay in segments arranged along the circumference of a circular channel layout to reduce the footprint size and sample volume requirement. Using the current design, a 5-plex cytokine ELISA was demonstrated in a 1.5 × 1.5-cm region, which corresponded to a reduction in the footprint area by about a factor of 3 compared to that reported in our previous study. Additionally, the selective coating of our assay segments with the target molecules was realized in this work using electroosmosis instead of hydrodynamic flow as was the case in the previous report. This aspect of our experimental design is particularly significant as it permits the use of cross-sectional channel dimensions significantly shorter than those employed in the current work. Moreover, the use of an electric field for coating purposes enables the integration of functionalities such as electrokinetic preconcentration of analyte molecules during the sample incubation period that can further enhance the capabilities of our assay method.     

微流控芯片电泳-多重聚合酶链反应法同时测定多个单碱基多态性位点

以微流控芯片电泳为检测平台,建立了多重PCR扩增法同时测定多个单碱基多态性(SNP)位点的方法。先通过PCR扩增得一段含所有待测SNP位点的长片段;用限制性内切酶消化成短片段,再将酶切反应产物与脱氧核糖核酸适配器(DNAadapter)相连;以连接产物为模板,分成两管,分别用n条等位基因特异性引物和一条通用引物进行n重PCR扩增;最后用微流控芯片电泳法分离PCR扩增产物,根据两管扩增产物的芯片电泳图谱中扩增片段的大小判断SNP的类型。以细胞色素P4502D6(CYP2D6)基因中的5个SNP位点(100C>T、1661G>C、1758G>T、2470T>C和2850C>T)为检测对象,考察了各等位基因特异性引物之间的相互影响和扩增反应的特异性,采用微流控芯片电泳法成功测定了20名健康中国人的CYP2D6基因中5个SNP位点的基因多态性,与聚合酶链反应-限制性片段长度多态性法(PCR-RFLP)测定结果完全一致。     

光纤通信中有色散影响的受激喇曼散射信道特性研究

提出了在波分复用光纤通信系统中，考虑光纤色散“走离”时受激喇曼散射(SRS)信道的新模型,给出了计算中距离步长的选取公式。根据该模型，数值计算了各信道在随机数字序列调制下和在受激喇曼散射(SRS)非线性效应作用下经过有色散“走离”的波分复用光纤系统的传输功率。得出光纤色散会降低SRS效应引起的输出功率波动的结论,画出了在SRS效应作用下输出功率标准差随色散系数变化的曲线，并对产生该现象的机理进行了定性分析。该模型适合于任意光纤色散、任意输入功率和任意信道数目。     

利用交叉增益调制实现光时分复用波分复用波长变换

采用半导体光放大器的交叉增益调制效应 ,通过全光方法 ,实现了 1.2Gbit/s光时分复用信号转换成2× 6 2 2Mbit/s波分复用信号的解复用。它同样具有波分复用信号到光时分复用信号波长变换的功能。     

密集型波分复用薄膜干涉滤光片的设计

介绍了波分复用系统对薄膜干涉滤光片的基本要求，为了满足这些要求，一方面需要精心选择基板和薄膜材料，另一方面要寻找性能优良，制造容易的膜系，文中提出了二种适宜于设计这种滤光片的方法。     

Multi-scale mapping algorithm for INI cancellation and a novel mixed-numerologies OFDM transceiver

OFDM with mixed-numerologies enhances the system flexibility effectively to meet the demands of diversified application scenarios. However, the coexistence of waveforms with different numerologies leads to serious inter-numerology interference (INI), and the corresponding relationship between the number of guard subcarriers and the power of INI needs to be considered for scheduling subcarriers. In this paper, we propose a multi-scale mapping (MSM) and INI cancellation (MSM-INIC) algorithm as well as the corresponding de-MSM algorithm for mixed-numerologies OFDM system. Based on the proposed algorithms, we provide a novel transceiver in the scenario of multi-path fading channel, in which subcarrier scheduling does not need to consider whether the guard band is allocated. In the proposed transmitter, an additional MSM-INIC module is employed to pre-compensate signal distortion for downlink, and in the receiver, a de-MSM module is applied to de-map the received signals for recovering the original numerologies. Furthermore, we reveal the inherent property of the mapped signals, and propose a low computational complexity de-MSM algorithm accordingly. Simulation results verify the superiority of the proposed transceiver in BER performance as well as spectrum efficiency even without any guard band.     

Full utilization of a mass spectrometer using on‐demand sharing with multiple LC units

The applicability of liquid chromatography–mass spectrometry (LC/MS) is often limited by throughput. The sharing of a mass spectrometer with multiple LCs significantly improves throughput; however, the reported systems have not been designed to fully utilize the MS duty cycle, and as a result to achieve maximum throughput. To fully utilize the mass spectrometer, the number of LC units that a MS will need to recruit is application dependent and could be significantly larger than the current commercial or published implementations. For the example of a single analyte, the number may approach the peak capacity to a first degree approximation. Here, the construction of a MS system that flexibly recruits any number of LC units demanded by the application is discussed, followed by the method to port a previously developed LC/MS method to the system to fully utilize a mass spectrometer. To demonstrate the performance and operation, a prototypical MS system of eight LC units was constructed. When 1‐min chromatographic separations were performed in parallel on the eight LCs of the system, the average LC/MS analysis time per sample was 10.5 s when applied to the analysis of samples in 384‐well plate format. This system has been successfully used to conduct large‐volume biochemical assays with the analysis of a variety of molecular entities in support of drug discovery efforts. Allowing the recruitment of the number of LC units appropriate for a given application, this system has the potential to be a plug‐and‐play system to fully utilize a mass spectrometer. Copyright © 2012 John Wiley & Sons, Ltd.