An improved setup for radiocarbon analysis of water-soluble organic carbon in environmental matrices

被引:0
|
作者
Strahl, Jan [1 ,2 ]
Lechleitner, Franziska A. [1 ,2 ]
Laemmel, Thomas [1 ,2 ]
Geissbuhler, Dylan [1 ,2 ]
Salazar, Gary A. [1 ,2 ,4 ,5 ]
Daellenbach, Kaspar R. [3 ]
Szidat, Sonke [1 ,2 ]
机构
[1] Univ Bern, Dept Chem Biochem & Pharmaceut Sci, CH-3012 Bern, Switzerland
[2] Univ Bern, Oeschger Ctr Climate Change Res, CH-3012 Bern, Switzerland
[3] Paul Scherrer Inst, Lab Atmospher Chem, CH-5232 Villigen, Switzerland
[4] Univ Ottawa, Dept Phys, Ottawa, ON K1N 6N5, Canada
[5] Univ Ottawa, AE Lalonde AMS Lab, Ottawa, ON K1N 6N5, Canada
关键词
radiocarbon; sample preparation; water-soluble organic carbon; wet chemical oxidation; C-14; ANALYSIS; SOURCE APPORTIONMENT; ELEMENTAL ANALYZER; SAMPLES; AEROSOLS; EXTRACTION; DELTA-C-13; OXIDATION; ACIDS; ICE;
D O I
10.1017/RDC.2024.113
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
This paper presents an improved setup for radiocarbon analysis of water-soluble organic carbon based on wetchemical oxidation as installed at the Laboratory for the Analysis of Radiocarbon with AMS (LARA) at theUniversity of Bern. The implementation of a non-dispersive infrared CO2detector allows more precise and accuratequantification of carbon amounts in samples and establishes the possibility of simple monitoring of the efficacy offlushing and sampling processes. A detailed blank assessment unveiled undesired oxidation of different materialsand sample temperature as critical factors regarding the level of constant contamination. Contamination arising fromoxidation of septum pieces and carbon-based glues in conventional sampling needles was minimized by developinga glass-sintered needle. This new needle was also designed to be longer, reducing the minimum amount of samplesolution needed to 2 mL. The oxidation time and temperature (1 hr at 75 degrees C) were optimized to further decreasecontamination during analyses of samples with carbon amounts of up to similar to 50 mu g. With these improvements, we nowreport low constant contamination levels of 0.62 +/- 0.12 mu g C (with F14C of 0.19 +/- 0.04), whereas the crosscontamination factor was determined to be 0.25 +/- 0.07%.
引用
收藏
页码:220 / 233
页数:14
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