DESIGN, CONSTRUCTION, AND EVALUATION OF AN INTEGRATING TRANSIENT RECORDER FOR DATA ACQUISITION IN CAPILLARY GAS-CHROMATOGRAPHY TIME-OF-FLIGHT MASS-SPECTROMETRY

被引:24
作者
HOLLAND, JF [1 ]
NEWCOMBE, B [1 ]
TECKLENBURG, RE [1 ]
DAVENPORT, M [1 ]
ALLISON, J [1 ]
WATSON, JT [1 ]
ENKE, CG [1 ]
机构
[1] MICHIGAN STATE UNIV,DEPT CHEM,E LANSING,MI 48824
关键词
D O I
10.1063/1.1142284
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
An integrating transient recorder (ITR) has been designed, constructed, and evaluated to accomplish time-array detection in gas chromatography time-of-flight mass spectrometry (GC-TOFMS) applications. The ITR consists of a 200-MHz flash analog-to-digital converter, 16 high-speed 100K emitter-couple logic (ECL) summing boards, three parallel processors for real-time data reduction, instrument control and routing functions, and a 300-Mbyte mass storage device. The ITR is capable of recording 80 mu-s bursts of transient information with a time resolution of 5 ns. For each transient, up to 16 384 sequential time-resolved channels may be recorded. An operator-selectable number of sequential transients may be summed in a locked time registry creating a summed scan file while maintaining the integrity of the transient time resolution. The information from each transient is read, summed, and stored in one of two summing registers (16 x 1024 x 24 bits). While incoming information is being stored in one summing register, the information in the other summing register is processed and read out to disk, thus permitting high-speed data collection continuously for long periods of time. The information from successive transients is summed in order to improve signal-to-noise, dynamic range, and sensitivity, and produces scan files at a rate sufficient to maintain all of the chromatographic information. GC-MS data collected at 1, 20, and 50 spectra per second are presented for a nine-component aliphatic/aromatic mixture. Although the ITR was specifically designed for GC-TOFMS studies, the overall design concepts of the ITR are universal and apply to any situation where information from two or more phenomena occur at the output of a single detector and occur over vastly different time domains.
引用
收藏
页码:69 / 76
页数:8
相关论文
共 11 条
[1]  
ALLISON J, 1987, ANAL INSTRUM, V16, P207
[2]  
BERRY RS, 1980, PHYSICAL CHEM, P279
[3]   EFFECT OF PEAK SENSING AND RANDOM NOISE ON PRECISION AND ACCURACY OF STATISTICAL MOMENT ANALYSES FROM DIGITAL CHROMATOGRAPHIC DATA [J].
CHESLER, SN ;
CRAM, SP .
ANALYTICAL CHEMISTRY, 1971, 43 (14) :1922-&
[4]  
ECKENRODE BA, IN PRESS INT J MASS
[5]  
ERICKSON E, IN PRESS ANAL CHEM
[6]   AN ELECTRON-IMPACT STORAGE ION-SOURCE FOR TIME-OF-FLIGHT MASS SPECTROMETERS [J].
GRIX, R ;
GRUNER, U ;
LI, G ;
STROH, H ;
WOLLNIK, H .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1989, 93 (03) :323-330
[7]   MASS-SPECTROMETRY ON THE CHROMATOGRAPHIC TIME SCALE - REALISTIC EXPECTATIONS [J].
HOLLAND, JF ;
ENKE, CG ;
ALLISON, J ;
STULTS, JT ;
PINKSTON, JD ;
NEWCOME, B ;
WATSON, JT .
ANALYTICAL CHEMISTRY, 1983, 55 (09) :A997-&
[8]  
MALMSTADT HV, 1981, ELECTRONICS INSTRUME, P128
[9]   NEW TIME-OF-FLIGHT MASS-SPECTROMETER FOR IMPROVED MASS RESOLUTION, VERSATILITY, AND MASS-SPECTROMETRY MASS-SPECTROMETRY STUDIES [J].
PINKSTON, JD ;
RABB, M ;
WATSON, JT ;
ALLISON, J .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1986, 57 (04) :583-592
[10]   MASS-SPECTROMETRY MASS-SPECTROMETRY BY TIME-RESOLVED MAGNETIC DISPERSION [J].
STULTS, JT ;
ENKE, CG ;
HOLLAND, JF .
ANALYTICAL CHEMISTRY, 1983, 55 (08) :1323-1330