N-, O- and P-selective on-column atomic emission detection in capillary gas chromatography

N-, O- and P-selective on-column atomic emission detection in capillary gas chromatography
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毛细管气相色谱中的 N、O 和 P 选择性柱上原子发射检测

DOI:
10.1016/0021-9673(94)00072-7
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发表时间:
1994
影响因子:
4.1
通讯作者:
T. Greibrokk
T. Greibrokk
中科院分区:
化学2区
文献类型:
--
作者:
S. Pedersen‐Bjergaard;T. Greibrokk

文献摘要

被引文献

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评估了柱上持续的 350 kHz He 等离子体,用于毛细管气相色谱中的 N、O 和 P 选择性原子发射检测。由于当维持在 2.0 ml/min 的载气中时,等离子体会引起峰拖尾,因此在放电中添加了 15 ml/min 的辅助氦气。对于N-和O-选择性检测,分别使用CH4与O2或N2混合作为等离子体掺杂剂。即使采用这种广泛的等离子体掺杂,由于原子 N 和 O 背景水平的暂时变化,洗脱碳氢化合物也会产生非特异性响应。如果没有背景校正,N 和 O 的元素与碳选择性分别限制为 100:1 和 40:1。对于这两种元素,获得了 50 pg/s 水平的检测限和 5 · 102 的线性度。以H2-CH4为等离子体掺杂剂进行P选择性检测,P的检出限为39 pg/s。磷碳选择性为2300:1,线性为2·102。经过背景校正,选择性和检出限有望显着提高。
A 350-kHz He plasma sustained on-column was evaluated for N-, O- and P-selective atomic emission detection in capillary gas chromatography. As the plasma caused peak tailing when sustained in 2.0 ml/min of carrier gas, 15 ml/min of auxiliary helium was added to the discharge. For N- and O-selective detection, CH4mixed with O2or N2, respectively, were used as plasma dopant. Even with this extensive plasma doping, non-specific responses arose from eluting hydrocarbons due to temporary changes in the background level of atomic N and O. Without background correction, element-to-carbon selectivities for N and O were limited to 100:1 and 40:1, respectively. For both elements, detection limits at the 50 pg/s level and linearities of 5 · 102were obtained. P-selective detection was carried out with H2-CH4as plasma dopant, and provided a 39 pg/s detection limit for P. The phosphorus-to-carbon selectivity was 2300:1 and the linearity was 2 · 102. With background correction, both selectivities and detection limits are expected to improve significantly.