Micro gas preconcentrator using metal organic framework embedded metal foam for detection of low-concentration volatile organic compounds

被引:28
|
作者
Lee, Janghyeon [1 ]
Lee, Junsuk [1 ]
Lim, Si-Hyung [2 ]
机构
[1] Kookmin Univ, Dept Mech & Design, Seoul 02707, South Korea
[2] Kookmin Univ, Sch Mech Engn, Seoul 02707, South Korea
基金
新加坡国家研究基金会;
关键词
Environmental monitoring; Toxic chemicals; Gas preconcentration; VOCs adsorbents; THERMAL-DESORPTION; PRE-CONCENTRATORS; TRACE DETECTION; RISK-ASSESSMENT; HEALTH-RISK; BTEX; SENSOR; BREATH; ARRAY; MOF-5;
D O I
10.1016/j.jhazmat.2020.122145
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Analysis of volatile organic compounds (VOCs) is essential for on-site environmental monitoring and toxic chemicals detection. However, quantitatively detecting VOC gases is difficult because of their low gas concentration (< 100 ppb), and preconcentration is necessary to overcome the detection limitations of various gas sensors. Many studies on micro preconcentrators (mu-PC) have been reported, however, these devices suffer from high desorption temperatures and significant pressure drops, which degrade sensing ability and increase operating costs, respectively. Due to these disadvantages, such devices are not yet commercially available. In this study, a mu-PC was developed using metal organic framework embedded metal foam (MOFM) as an adsorbent. The preconcentration performance of the mu-PC was evaluated based on several key parameters, such as desorption temperature, adsorption time, and initial sample concentration. In addition, the MOFM and commercial adsorbents were each packed in the same mu-PC chip, respectively, to compare their preconcentration and pressure drop performances. The MOFM-adsorbent-packed mu-PC demonstrated the preconcentration factors were 2.6 and 4 times higher, and the pressure drops were 4 and 3 times lower than those of the commercial adsorbents under the same conditions owing to the high specific surface area and the efficient flow distribution of the MOFM adsorbent.
引用
收藏
页数:12
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