A segmented ring, cylindrical ion trap source for time-of-flight mass spectrometry

被引:19
作者
Ji, QC
Davenport, MR
Enke, CG
Holland, JF
机构
[1] UNIV NEW MEXICO,DEPT CHEM,ALBUQUERQUE,NM 87131
[2] MICHIGAN STATE UNIV,DEPT BIOCHEM,E LANSING,MI 48824
基金
美国国家卫生研究院;
关键词
D O I
10.1016/1044-0305(96)00044-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An ion trap source has been designed for use with time-of-flight (TOF) mass analysis. Two thin diaphragms make up a segmented ring electrode; the end cap electrodes are planar wire mesh. The potential field produced by the rf voltage applied between the ring and end cap electrodes resembles that of the cylindrical ion trap. The trapped ion population for ions created by electron impact exhibits linear growth against a first-order loss that has a time constant of about 50 mu s; no ion loss occurs when the electron beam is off. The observed value of q(z) at low-mass cutoff for rf ion storage is -0.84. Pulsed extraction of all ions is accomplished by switching the trap electrodes from rf to voltages required to provide a linear de extraction field. The TOF flight path includes a wide energy range reflectron. Better than unit mass resolution is achieved through m/z 500 without collisional ion cooling. With an extraction rate of 1 kHz and a recording rate of 4 spectra per second, a linear working curve is obtained between 36 pg and 18 ng of chlorobenzene delivered chromatographically. The system has demonstrated the potential to achieve a very high sample utilization efficiency at high spectral generation rates.
引用
收藏
页码:1009 / 1017
页数:9
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