A rapid method for determination of hydrogen and oxygen isotope ratios from water and hydrous minerals

被引:281
作者
Sharp, ZD
Atudorei, V
Durakiewicz, T
机构
[1] Univ New Mexico, Dept Earth & Planetary Sci, Albuquerque, NM 87131 USA
[2] Marie Curie Sklodowska Univ, Inst Phys, Mass Spectrometry Lab, PL-20031 Lublin, Poland
基金
美国国家科学基金会;
关键词
stable isotopes; gas chromatography; methodology; carbon reduction; in situ; fluid inclusions;
D O I
10.1016/S0009-2541(01)00262-5
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
A general-purpose, on-line, continuous flow method for determination of delta and delta O-18 values of water and hydrous minerals is described. Minor modifications of commercially available equipment allow for analyses of water and solid samples, fluid inclusions and in situ hydrogen isotope determinations of hydrous minerals using a laser. The technique involves reduction of H2O or solid hydrous samples by reaction with glassy carbon at high temperatures. H-2 and CO are produced by reaction with the carbon at 1450 degreesC in a helium carrier gas. Product gases are separated in a gas chromatograph and analyzed in a mass spectrometer configured to make hydrogen isotope analyses in continuous flow mode. Sample size is as small as 0.1 mul of water (or equivalent from hydrous phases) for both hydrogen and oxygen isotope ratio determinations. Waters are injected through a heated septa into the He stream; solid materials are wrapped in silver foil and dropped into the furnace using an autosampler. Using standard correction procedures, results obtained with this method are identical to those obtained conventionally with a precision for water samples of +/- 2 parts per thousand (1 sigma) for hydrogen and +/- 0.2 parts per thousand (1 delta) for oxygen. Saline waters can be analyzed without any additional preparation. Reproducibility of deltaD values from hydrous silicates is also +/- 2 parts per thousand The delta O-18 values of 'dehydration' water evolved from biotite during heating is variable and irreproducible. Total time of analysis is less than 2 min for a single hydrogen isotope analysis. Sample size can be reduced an order of magnitude by using a low He-flow rate, a narrow-bore reduction column, a capillary GC column and a more efficient open split. With the high sensitivity design, in situ measurements can be made on hydrous minerals using a CO2 laser for sample heating. Stable isotope determinations of fluid inclusions can be made by decrepitating samples in the He-stream. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:197 / 210
页数:14
相关论文
共 28 条
[21]   ISOTOPE-RATIO-MONITORING GAS CHROMATOGRAPHY-MASS SPECTROMETRY [J].
MATTHEWS, DE ;
HAYES, JM .
ANALYTICAL CHEMISTRY, 1978, 50 (11) :1465-1473
[22]  
Nelson ST, 2000, RAPID COMMUN MASS SP, V14, P1044, DOI 10.1002/1097-0231(20000630)14:12<1044::AID-RCM987>3.0.CO
[23]  
2-3
[24]   HIGH-PRECISION DETERMINATION OF H-2/H-1 IN H-2 AND H2O BY CONTINUOUS-FLOW ISOTOPE RATIO MASS-SPECTROMETRY [J].
PROSSER, SJ ;
SCRIMGEOUR, CM .
ANALYTICAL CHEMISTRY, 1995, 67 (13) :1992-1997
[25]   Fractionation of hydrogen isotopes in lipid biosynthesis [J].
Sessions, AL ;
Burgoyne, TW ;
Schimmelmann, A ;
Hayes, JM .
ORGANIC GEOCHEMISTRY, 1999, 30 (09) :1193-1200
[26]  
SHARP ZD, 1989, LASER BASED CARBON R, V21, P72
[27]   Reduction of microliter amounts of water with manganese for D/H isotope ratio measurement by mass spectrometry [J].
Tanweer, A ;
Han, LF .
ISOTOPES IN ENVIRONMENTAL AND HEALTH STUDIES, 1996, 32 (01) :97-103
[28]   HIGH-PRECISION D/H MEASUREMENT FROM HYDROGEN GAS AND WATER BY CONTINUOUS-FLOW ISOTOPE RATIO MASS-SPECTROMETRY [J].
TOBIAS, HJ ;
GOODMAN, KJ ;
BLACKEN, CE ;
BRENNA, JT .
ANALYTICAL CHEMISTRY, 1995, 67 (14) :2486-2492