自适应频率和二维波达方向角跟踪估计算法

运用特征子空间分析方法的关键问题在于信号或噪声子空间的估计,在实际中有些信号的统计特性通常是随时间变化的,这时需要随时根据新的阵列接收数据对信号或噪声子空间进行更新,以得到参数的实时估计值,在该文中建立了多维信号参量联合估计的3D Unitary ESPRIT算法,然后提出了基于球面平均 ULV分解的子空间跟踪算法,将子空间跟踪算法与多维信号多量联合估计算法相结合,得到多维时变信号参数的跟踪估计算法,仿真计算结果验证了该算法的有效性。     

色噪声背景下正弦参量估计的互谱矩和SVD方法

互谱估计方法是用于色噪声背景下正弦信号参量估计的一个十分有效的方法。但以往互谱估计都是采用FFT方法和互周期图法。本文首次将现代谱估计方法引入到互谱估计中,从理论上建立了互相关函数的Yule-Walker方程,并在此基础上进而提出了互谱估计的矩估计法和SVD方法。给出了仿真实例结果。     

利用信号重构的全球导航卫星系统欺骗干扰抑制方法

欺骗式干扰通过发射与真实卫星信号相似的信号误导接收机产生错误的定位结果,具有极大的危害。该文针对转发式欺骗干扰,提出一种基于信号重构的单天线欺骗干扰抑制方法。该方法首先通过参数估计方法估计出欺骗信号载波频率和码相位,然后构建欺骗信号子空间正交投影矩阵以抑制干扰。仿真实验结果表明该方法对欺骗干扰具有良好的抑制效果,能够保障接收机在干扰环境中实现有效定位,并具有较低的运算复杂度。

     

基于酪胺信号放大的新型免疫传感器

将酪胺应用于酶联免疫分析,建立了一种新的高灵敏伏安型免疫传感器。利用纳米金的静电吸咐和己二硫醇、巯基乙胺的自组装,将羊抗人IgG抗体固定到金电极表面上,以辣根过氧化物酶标记羊抗人IgG抗体为酶标抗体,以生物素化酪胺为酶底物,利用催化酪胺沉积反应,在传感界面沉积大量生物素,使原始信号得到几何级数的放大。结果表明,通过生物素化酪胺催化放大后,制得的免疫传感器对H2O2的催化能力增大近20倍,检测hIgG在1.5μg/L～22 mg/L范围内有良好的线性关系,检出限为0.1μg/L。用于实际试样的回收率的测定,结果良好。     

舰船辐射噪声模拟发射系统的设计研究

本文依据典型舰船噪声的频谱特性规律,设计研制了一套舰船辐射噪声发射系统实验样机,包括信号结构设计、换能器选择配置、系统构成设计等,本噪声模拟发射系统具有100Hz～16kHz频带噪声的模拟发射功能,包括线谱、连续谱成分,频谱分配和谱线形式可调可控,信号总声源级动态范围达60dB。     

2019年中华人民共和国第二届青年运动会IBC调度中心系统设计与实践

本文以2019年中华人民共和国第二届青年运动会IBC信号调度系统为例,介绍了二青会赛事转播调度中心系统的功能,15个赛事直播场馆的信号传输、汇聚、发布的组成及技术方案,为电视台转播大型运动会转播信号的回传发布系统建设进行了有益实践。     

铁电存储器FM3808在TMS320VC5402系统中的应用

FM3808是Ramtron公司生产的新型超低功耗非易失铁电存储器，该器件可支持对存储区的高速读写，并可进行近乎无限次的写入。FM3808内部除具有256kB的存储阵列外还集成了实时时钟和系统监控模块，因而功能十分强大。文中介绍了FM3808的性能特点、内部结构和工作原理，分析了TMS320VC5402 DSP的并行引导装载模式。给出了DSP与FM3808组成的并行引导接口方案。     

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.     

Sensitive pseudobienzyme electrocatalytic DNA biosensor for mercury(II) ion by using the autonomously assembled hemin/G-quadruplex DNAzyme nanowires for signal amplification

Herein, a novel sensitive pseudobienzyme electrocatalytic DNA biosensor was proposed for mercury ion (Hg²⁺) detection by using autonomously assembled hemin/G-quadruplex DNAzyme nanowires for signal amplification. Thiol functionalized capture DNA was firstly immobilized on a nano-Au modified glass carbon electrode (GCE). In presence of Hg²⁺, the specific coordination between Hg²⁺ and T could result in the assembly of primer DNA on the electrode, which successfully triggered the HCR to form the hemin/G-quadruplex DNAzyme nanowires with substantial redox probe thionine (Thi). In the electrolyte of PBS containing NADH, the hemin/G-quadruplex nanowires firstly acted as an NADH oxidase to assist the concomitant formation of H₂O₂ in the presence of dissolved O₂. Then, with the redox probe Thi as electron mediator, the hemin/G-quadruplex nanowires acted as an HRP-mimicking DNAzyme that quickly bioelectrocatalyzed the reduction of produced H₂O₂, which finally led to a dramatically amplified electrochemical signal. This method has demonstrated a high sensitivity of Hg²⁺ detection with the dynamic concentration range spanning from 1.0 ng L⁻¹ to 10 mg L⁻¹ Hg²⁺ and a detection limit of 0.5 ng L⁻¹ (2.5 pM) at the 3S_blank level, and it also demonstrated excellent selectivity against other interferential metal ions.     

Ultrasensitive electrochemical biosensor for specific detection of DNA based on molecular beacon mediated circular strand displacement polymerization and hyperbranched rolling circle amplification

Using a cascade signal amplification strategy, an ultrasensitive electrochemical biosensor for specific detection of DNA based on molecular beacon (MB) mediated circular strand displacement polymerization (CSDP) and hyperbranched rolling circle amplification (HRCA) was proposed. The hybridization of MB probe to target DNA resulted in a conformational change of the MB and triggered the CSDP in the presence of bio-primer and Klenow fragment (KF exo⁻), leading to multiple biotin-tagged DNA duplex. Furthermore, the HRCA was implemented to product amounts of double-stranded DNA (ds-DNA) fragments using phi29 DNA polymerase via biotin-streptavidin interaction. After the product of HRCA binded numerous biotinylated detection probes, an ultrasensitive electrochemical readout by further employing the streptavidin-alkaline phosphatase. The proposed biosensor exhibited excellent detection sensitivity and specificity with a log-linear response to target DNA from 0.01 fM to 10 pM as low as 8.9 aM. The proposed method allowed DNA detection with simplicity, rapidness, low cost and high specificity, which might have the potential for application in clinical molecular diagnostics and environmental monitoring.