Quality of Graphite Target for Biological/Biomedical/Environmental Applications of ~(14)C-Accelerator Mass Spectrometry

摘要

Catalytic graphitization for ~(14)C-accelerator mass spectrometry (~(14)C-AMS) produced various forms of elemental carbon. Our high-throughput Zn reduction method (C/Fe velence 1:5, 500 deg C, 3 h) produced the AMS target of graphite-coated iron powder (GCIP), a mix of non-graphitic carbon and Fe_(3)C. Crystallinity of the AMS targets of GCIP (nongraphitic carbon) was increased to turbostratic carbon by raising the C/Fe ratio from 1:5 to 1:1 and the graphitization temperature from 500 to 585 deg C. The AMS target of GCIP containing turbostratic carbon had a large isotopic fractionation and a low AMS ion current. The AMS target of GCIP containing turbostratic carbon also yielded less accurate/precise ~(14)C-AMS measurements because of the lower graphitization yield and lower thermal conductivity that were caused by the higher C/Fe ratio of 1:1. On the other hand, the AMS target of GCIP containing non-graphitic carbon had higher graphitization yield and better thermal conductivity over the AMS target of GCIP containing turbostratic carbon due to optimal surface area provided by the iron powder. Finally, graphitization yield and thermal conductivity were stronger determinants (over graphite crystallinity) for accurate/precise/high-throughput biological, biomedical, and environmental ~(14)C-AMS applications such as absorption, distribution, metabolism, elimination (ADME), and physiologically based pharmacokinetics (PBPK) of nutrients, drugs, phytochemicals, and environmental chemicals.