HIGH-PRECISION D/H MEASUREMENT FROM HYDROGEN GAS AND WATER BY CONTINUOUS-FLOW ISOTOPE RATIO MASS-SPECTROMETRY

被引:35
作者
TOBIAS, HJ [1 ]
GOODMAN, KJ [1 ]
BLACKEN, CE [1 ]
BRENNA, JT [1 ]
机构
[1] CORNELL UNIV,DIV NUTR SCI,ITHACA,NY 14853
关键词
D O I
10.1021/ac00110a025
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two instrumental approaches are described for continuous-flow high-precision determinations of D/H ratios from hydrogen gas or via on-line reduction of water. In the first system, Ar is used as a carrier gas, with a Ni reduction furnace and a water trap to remove minor levels of unreduced water that are a potential source of memory effects. Precisions of SD < 10 parts per thousand (delta D-SMOW) over a 600 parts per thousand range from -55 to +532 parts per thousand are obtained for liquid water (0.4 mu L). Linearity is excellent over 4 orders of magnitude of D concentration in tap water (r(2) > 0.9999), although precision degrades at enrichments delta D-SMOW > 5000 parts per thousand. In the second system, a heated Pd metal foil functions as a filter to admit purified hydrogen into the mass spectrometer. Hydrogen gas injections are made into flowing Ar and are directed to the Pd filter (similar to 330 degrees C) which passes hydrogen isotopes only while diverting the carrier now to waste. Precisions of these measurements are SD < 6 parts per thousand over the D enrichment range -213 to 340 parts per thousand, with excellent linearity (r(2) > 0.9999) and accuracy (<2 parts per thousand). Similar precision is obtained using the on-line reduction apparatus and a water trap prior to the Pd filter with injections of 0.4 mu L of liquid water, with acceptable linearity (r(2) > 0.999) over 3 orders of magnitude of D concentration. Neither system shows any sign of memory effects when water is analyzed. The data indicate that either one of these systems is a useful means for continuous-now IRMS of D/H isotope ratio determinations.
引用
收藏
页码:2486 / 2492
页数:7
相关论文
共 15 条
[1]   HIGH-PRECISION GAS ISOTOPE RATIO MASS-SPECTROMETRY - RECENT ADVANCES IN INSTRUMENTATION AND BIOMEDICAL APPLICATIONS [J].
BRENNA, JT .
ACCOUNTS OF CHEMICAL RESEARCH, 1994, 27 (11) :340-346
[2]   HIGH-PRECISION LIQUID CHROMATOGRAPHY-COMBUSTION ISOTOPE RATIO MASS-SPECTROMETRY [J].
CAIMI, RJ ;
BRENNA, JT .
ANALYTICAL CHEMISTRY, 1993, 65 (23) :3497-3500
[3]   IMPROVEMENTS IN THE GASEOUS-HYDROGEN WATER EQUILIBRATION TECHNIQUE FOR HYDROGEN ISOTOPE RATIO ANALYSIS [J].
COPLEN, TB ;
WILDMAN, JD ;
CHEN, J .
ANALYTICAL CHEMISTRY, 1991, 63 (09) :910-912
[4]  
EHLERINGER JR, 1988, STABLE ISOTOPES HIST
[5]   HIGH-SENSITIVITY TRACER DETECTION USING HIGH-PRECISION GAS-CHROMATOGRAPHY COMBUSTION ISOTOPE RATIO MASS-SPECTROMETRY AND HIGHLY ENRICHED [U-C-13]-LABELED PRECURSORS [J].
GOODMAN, KJ ;
BRENNA, JT .
ANALYTICAL CHEMISTRY, 1992, 64 (10) :1088-1095
[6]   ISOTOPE-RATIO-MONITORING GAS CHROMATOGRAPHY-MASS SPECTROMETRY [J].
MATTHEWS, DE ;
HAYES, JM .
ANALYTICAL CHEMISTRY, 1978, 50 (11) :1465-1473
[7]   NITROGEN ISOTOPIC ANALYSES BY ISOTOPE-RATIO-MONITORING GAS-CHROMATOGRAPHY MASS-SPECTROMETRY [J].
MERRITT, DA ;
HAYES, JM .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (05) :387-397
[8]   FACTORS CONTROLLING PRECISION AND ACCURACY IN ISOTOPE-RATIO-MONITORING MASS-SPECTROMETRY [J].
MERRITT, DA ;
HAYES, JM .
ANALYTICAL CHEMISTRY, 1994, 66 (14) :2336-2347
[9]   INTERFACING AN AUTOMATIC ELEMENTAL ANALYZER WITH AN ISOTOPE RATIO MASS-SPECTROMETER - THE POTENTIAL FOR FULLY AUTOMATED TOTAL NITROGEN AND N-15 ANALYSIS [J].
PRESTON, T ;
OWENS, NJP .
ANALYST, 1983, 108 (1289) :971-977
[10]   MASS-SPECTROMETRIC ANALYSIS OF STABLE-ISOTOPE-LABELED AMINO-ACID TRACERS [J].
PRESTON, T ;
SLATER, C .
PROCEEDINGS OF THE NUTRITION SOCIETY, 1994, 53 (02) :363-372