4.8 Article

Biological/biomedical accelerator mass spectrometry targets.: 1.: Optimizing the CO2 reduction step using zinc dust

期刊

ANALYTICAL CHEMISTRY
卷 80, 期 20, 页码 7651-7660

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ac801226g

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资金

  1. NIH [DK-45939, DK-48307]
  2. California Agricultural Experiment Station
  3. University of California-Lawrence Livermore National Laboratory [W-7405-Eng-48]
  4. NIH National Center for Research Resources [RR13461]

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Biological and biomedical applications of accelerator mass spectrometry (AMS) use isotope ratio mass spectrometry to quantify minute amounts of long-lived radioisotopes such as C-14. AMS target preparation involves first the oxidation of carbon (in sample of interest) to CO2 and second the reduction of CO2 to filamentous, fluffy, fuzzy, or firm graphite-like substances that coat a -400-mesh spherical iron powder (-400MSIP) catalyst. Until now, the quality of AMS targets has been variable; consequently, they often failed to produce robust ion currents that are required for reliable, accurate, precise, and high-throughput AMS for biological/biomedical applications. Therefore, we described our optimized method for reduction of CO2 to high-quality uniform AMS targets whose morphology we visualized using scanning electron microscope pictures. Key features of our optimized method were to reduce CO2 (from a sample of interest that provided 1 mg of C) using 100 +/- 1.3 mg of Zn dust, 5 +/- 0.4 mg of -400MSIP, and a reduction temperature of 500 degrees C for 3 h. The thermodynamics of our optimized method were more favorable for production of graphite-coated iron powders (GCIP) than those of previous methods. All AMS targets from our optimized method were of 100% GCIP, the graphitization yield exceeded 90%, and delta C-13 was -17.9 +/- 0.3 parts per thousand. The GCIP reliably produced strong C-12(-) currents and accurate and precise F-m values. The observed F-m value for oxalic acid II NIST SRM deviated from its accepted F-m value of 1.3407 by only 0.0003 +/- 0.0027 (mean +/- SE, n = 32), limit of detection of C-14 was 0.04 amol, and limit of quantification was 0.07 amol, and a skilled analyst can prepare as many as 270 AMS targets per day. More information on the physical (hardness/color), morphological (SEMs), and structural (FT-IR, Raman, XRD spectra) characteristics of our AMS targets that determine accurate, precise, and high-hroughput AMS measurement are in the companion paper.

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