Controlled inert gas environment for enhanced chlorine and fluorine detection in the visible and near-infrared by laser-induced breakdown spectroscopy

被引:79
作者
Asimellis, G [1 ]
Hamilton, S
Giannoudakos, A
Kompitsas, M
机构
[1] Aristotle Univ Thessaloniki, Dept Phys, Solid State Sect, GR-54124 Thessaloniki, Greece
[2] Adnor Technol, Belfast B12 7AL, Antrim, North Ireland
[3] Natl Tech Univ Athens, Dept Chem Engn, Athens, Greece
[4] Natl Hellen Res Fdn, Inst Theoret & Phys Chem, GR-11635 Athens, Greece
关键词
halogen detection; infrared laser-induced breakdown spectroscopy; controlled ambient environment;
D O I
10.1016/j.sab.2005.05.035
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Efficient quantitative detection for halogens is necessary in a wide range of applications, ranging from pharmaceutical products to air polluting hazardous gases or organic compounds used as chemical weapons. Detection of the non-metallic elements such as fluorine (F) and chlorine (Cl) presents particular difficulty, because strong emission lines originating from their resonance states lie in the VUV spectral range (110-190 nm). In the present work we detect F and Cl in the upper visible and in the near IR (650-850 nm) under controlled inert gas ambient atmosphere. Investigation of the controlled atmosphere effects suggests that there exists an optimum pressure range that optimizes signal strength and quality. Ablation and ionization were achieved with a UV laser at 355 nm, and a gated GaAs photocathode-based detector was used for detection with quantum efficiency in the range of 20% in the wavelengths of interest. Our results indicate that our approach provides quantitative detection with linearity over at least two orders of magnitude that is achieved without the need for Internal Standardization Method, and improved limits of detection. In particular, fluorine has been detected for concentration values down to 0.03 wt.% Definite spectral assignment revealing all major emission lines centered around 837 nm for F and 687 nm for Cl has been obtained for the first time in Laser-induced breakdown spectroscopy application. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1132 / 1139
页数:8
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