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基于交流耦合方式的双模式离子迁移谱仪

Dual ion mobility spectrometer based on AC coupling
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摘要 为了快速检测并区分未知大分子(如毒品、爆炸物、化学战剂、DNA残片、酶等),并解决在高压电路中提取极弱电信号时,使用变压器导致的电路系统设计复杂、体积庞大的问题,设计了结构紧凑、装配简便、操作简便的双模式离子迁移谱仪。谱仪的正负迁移管能够检测具备正、负离子亲和力的大分子。采用了交流耦合的方式来提取Faraday盘上的10-13 C弱电信号。谱仪仅需要12V直流电源及标准的TLL脉冲便可以被驱动且易于控制。实验表明:该谱仪能够长时间稳定地工作,能够检测到多种复杂分子。以国际上常用的参考分子三硝基甲苯(TNT)来衡量,则仪器的检测灵敏度好于1ng TNT。当单侧迁移区长度为50mm时,其TNT的分辨率可达到21,当单侧迁移区长度为90mm时,其TNT的分辨率为32。 A dual ion mobility spectrometer is developed to quickly detect and analyze complex molecules (such as explosives, drugs, DNA compounds and enzymes), which simplifies the large, complex circuit required when using transformers to measure a weak signal in a high voltage. The spectrometer has an integrated structure, is simple to manufacture and is easily operated. Positive and negative drift tubes in the spectrometer can detect both positive and negative ion affinity molecules. The weak signal of 10-3 C on the Faraday plate is driven by an AC coupling circuit. The spectrometer is driven by a 12 V DC, TTL pulse and can be easily controlled. The spectrometer can work continuously with many complex molecules detected by the system. The sensitivity when used to detect TNT (a reference molecular used world wide) is better than 1 ng and the relative resolution for TNT can reach 21 when the drift tube is 50 mm long and 32 when the drift tube is 90 mm long.
出处 《清华大学学报(自然科学版)》 EI CAS CSCD 北大核心 2013年第10期1374-1379,共6页 Journal of Tsinghua University(Science and Technology)
关键词 离子迁移谱仪(IMS) 双模式 正负离子 爆炸物 分辨率 灵敏度 ion mobility spectrometry (IMS) dual mode positive and negative ions explosive resolution sensitivity
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  • 1Gorshkov M P. Analysis of Impurities in Gases [P]. No. 9666583. Russia, G01N27/62, 1982.
  • 2Shvartsburg A A, Hudgins R R, Dugourd P, et al Structural information from ion mobility measurements Applications to semiconductor clusters [J]. Chem Soc Rev 2001, 30: 26-35.
  • 3Vautz W, Sielemann S, Baumbach J I. Determination of terpenes in humid Ambient air using ultraviolet absorbance ion mobility spectrometry [J]. Analytica Chimica Acta, 2004, 513(2): 393-399.
  • 4贾建,郭会勇,高晓光,何秀丽,李建平.漂移管工作温度对离子迁移率谱的影响[J].分析化学,2006,34(12):1783-1786. 被引量:11
  • 5Sielemann S, Baumbach J I, Schmidt H, et al. Detection of alcohols using UV-ion mobility spectrometers [J]. Analytica Chimica Acta, 2001, 431(2) : 293 - 301.
  • 6Steiner W E, Clowers B H, Matz L M, et al. Rapid screening of aqueous chemical warfare agent degradation products: Ambient pressure ion mobility mass spectrometry [J]. Anal Chem, 2002, 74(17) 4343-4352.
  • 7李芳,邵士勇,姚琏,李安林,李海洋.紫外离子迁移谱在线监测芳香族化合物[J].分析化学,2008,36(3):361-364. 被引量:17
  • 8Henderson S C, Valentine S J, Counterman A E, et al. ESl/ion trap/ion mobility/time-of-flight mass spectrometry for rapid and sensitive analysis of biomeolecular mixtures [J]. Anal Chem, 1999, 71(2): 291-301.
  • 9Hoaglund C S, Valentine S J, Sporleder C R, et al. Three dimensional ion mobility/TOFMS analysis of electrosprayed biomolecules [J]. Anal Chem, 1998, 70(11): 2236 - 2242.
  • 10] WU Ching, Siems W F, Asbury G R, et al. Electrospray ionization high-resolution ion mobility spectrometry-mass spectrometry [J]. Anal Chern, 1998, 70(23) 4929 - 4938.

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