高速列车受电弓气动噪声分析与空腔降噪研究

随着高速列车运行速度的不断提高,受电弓气动噪声也愈加严重。针对这一问题,文中采用LES大涡模拟、边界层噪声源模型和FW-H声类比法,通过建立某型号受电弓局部1:1气动噪声分析模型进行数值模拟。文中研究了受电弓各部位的气动噪声贡献量,还探究了针对较大噪声位置空腔采用射流降噪方法的降噪效果。结果表明,当网格总数为4 323万个时,数值模拟精确度满足要求。受电弓空腔上游和空腔中部绝缘子是气动噪声的主要来源。在射流降噪前后,空腔内部气动噪声均为宽频带噪声,主要能量集中在0~4 500 Hz。对250 km·h^-1行驶速度下的空腔进行主动射流降噪,距列车25 m远处的垂向监测点声压级最小值为81.65 dB,比降噪前降低了2.64 dB。     

Solvent-free reactions of fullerenes and N-alkylglycines with and without aldehydes under high-speed vibration milling

The solvent-free reactions of fullerenes and N-alkylglycines with and without aldehydes (RCHO) 2a-e under high-speed vibration milling (HSVM) conditions have been investigated. Fulleropyrrolidines 4a-e (C₆₀(CH₂N(CH₃)CHR), R=H (4a), C₆H₅ (4b), p-NO₂-C₆H₄ (4c), p-CH₃O-C₆H₄ (4d), p-(CH₃)₂N-C₆H₄ (4e)) were obtained in moderate yields from reactions of C₆₀ with aldehydes 2a-e and N-methylglycine (Prato reaction). In all these solvent-free reactions, 4a was found to be formed besides 4b-e, indicating that fullerenes can react with N-substituted glycines in the absence of aldehyde to give fulleropyrrolidines. For this novel reaction, a possible reaction mechanism involving an electron transfer process has been proposed. Intrigued by this observation, the dependence of the yield on the reagent ratio for the reaction of C₆₀ with paraformaldehyde and/or N-methylglycine was examined to search the optimal conditions. The reaction of C₇₀ with paraformaldehyde and/or N-methylglycine under HSVM conditions was also studied and was found to give the positional isomers of [70]fulleropyrrolidines.     

12bit 800MSPS电流舵结构的高速DAC设计

本文设计了一个分辨率为12位，采样频率为800MHz的高速电流舵结构DAC。该设计基于TSMC0．18umCMOS工艺，采用了二进制码控制和温度计码译码控制相结合的方式，从而在降低DNL误差和减小毛刺的同时，又能实现较小的芯片面积和功耗。为达到高的精度和高的转换速度，该设计在系统结构、电路结构以及芯片版图等方面都做了优化。     

Adaptive beamforming of massive MIMO based on DoA in high mobility scenarios

A direction of arrival based (DoA-based) beamforming of massive MIMO was proposed for high-speed railway scenarios.In order to guarantee that the optimal system capacity can be obtained during traveling,an iterative multi-beams scheme was proposed.It aimed to design different beams for different mobile carriage terminals (MCT) respectively.The proposal adaptively selected the number of antennas for each beam,and adaptively designed the number of beams according to system capacity.Moreover,the scheme didn’t need channel state information (CSI) that can reduce system implementation complexity and cost.Numerical results indicate that the proposed scheme is suitable for high-speed scenarios,the system performance can be improved more efficiently compared to conventional methods.     

高速信号采集记录仪设计

针对高速信号实时采集存储的需求,设计了一种高速信号采集记录仪。记录仪通过高速A/D转换器对信号进行采样,并实时存入NAND FLASH存储阵列中。为提高数据存储速率,综合采用并行总线、交错双平面页编程、多级流水线等技术,大幅提升FLASH的写入速度。记录仪可实现8bit、200MSPS的采样速率,并可将速率为200MB/s的采样数据实时存储。     

基于DDR2 SDRAM乒乓双缓冲的高速数据收发系统设计

在高速数据收发系统设计中,首先需要解决的问题是实时数据的高速缓存,然而FPGA内部有限的存储资源无法满足海量数据缓存的要求。为了解决系统中海量数据的缓存问题,系统创新提出了一种基于DDR2 SDRAM的乒乓双缓冲设计方案。方案设计了两路基于DDR2 SDRAM的大容量异步FIFO,通过FPGA内部选择逻辑实现两条通路间的乒乓操作,从而实现数据的高速缓存。实验结果表明,基于DDR2 SDRAM的数据收发系统实现了每路512 Mbit的缓存空间和200 MHz的总线速率,解决了海量数据的高速缓存问题。     

高速铁路场景移动通信系统切换研究综述

高铁的高速、全封闭特性给移动通信系统的越区切换性能带来了极大挑战,直接影响用户体验。阐述了移动通信系统中越区切换的概念,并指出高速铁路场景下越区切换面临的问题。回顾了国内外为解决这些问题所进行的相关研究及最新进展,包括网络架构优化和切换流程中测量、参数设置、执行策略、数据传输环节的优化,并指出群切换机制是未来值得关注的研究方向。     

Isolation of three glucaric acids from Leonurus japonicus Houtt. by using high-speed countercurrent chromatography combined with semi-preparative high-performance liquid chromatography

The isomerism of glucaric acids and the complexity of the composition of Leonurus japonicus Houtt. increased the difficulty of the separation of glucaric acids from the herb. In the present study, three glucaric acids were isolated from Leonurus japonicus Houtt. by using high-speed countercurrent chromatography combined with semi-preparative high-performance liquid chromatography. Cation exchange resin chromatography was applied to remove the alkaloids and enrich the glucaric acid fractions. Preliminary separation of the glucaric acid extract by high-speed countercurrent chromatography was carried out at 45℃ by using an optimized solvent system of ethyl acetate/n-butanol/formic acid/water (1:1:0.01:2, v/v/v/v) with satisfied stationary phase retention and separation factor. The semi-preparative high-performance liquid chromatography was used for further separation and purification of the target fractions, and three monomeric compounds were obtained with purities of 90.0, 91.0, and 95.3%. UV spectroscopy, NMR spectroscopy, and mass spectrometry were employed to identify their structures, which were assigned as 2-syringyl glucaric acid, 2,4-disyringyl glucaric acid, and 3,4-disyringyl glucaric acid, respectively, and 2,4-disyringyl glucaric acid was reported for the first time.     

Scale-Up Preparation of Crocins I and II from Gardenia jasminoides by a Two-Step Chromatographic Approach and Their Inhibitory Activity Against ATP Citrate Lyase

Crocins are highly valuable natural compounds for treating human disorders, and they are also high-end spices and colorants in the food industry. Due to the limitation of obtaining this type of highly polar compound, the commercial prices of crocins I and II are expensive. In this study, macroporous resin column chromatography combined with high-speed counter-current chromatography (HSCCC) was used to purify crocins I and II from natural sources. With only two chromatographic steps, both compounds were simultaneously isolated from the dry fruit of Gardenia jasminoides, which is a cheap herbal medicine distributed in a number of countries. In an effort to shorten the isolation time and reduce solvent usage, forward and reverse rotations were successively utilized in the HSCCC isolation procedure. Crocins I and II were simultaneously obtained from a herbal resource with high recoveries of 0.5% and 0.1%, respectively, and high purities of 98.7% and 99.1%, respectively, by HPLC analysis. The optimized preparation method was proven to be highly efficient, convenient, and cost-effective. Crocins I and II exhibited inhibitory activity against ATP citrate lyase, and their IC₅₀ values were determined to be 36.3 ± 6.24 and 29.7 ± 7.41 μM, respectively.